The human obesity gene map: the 2003 update (Q35715184)

9 August 2017

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title

The human obesity gene map: the 2003 update (English)

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9 August 2017

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Brandon Walts

2

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Louis Pérusse

object named as

Louis Pérusse

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3

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Claude Bouchard

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7

object named as

Claude Bouchard

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9 August 2017

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Tuomo Rankinen

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9 August 2017

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Yvon C Chagnon

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9 August 2017

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S John Weisnagel

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9 August 2017

Eric E Snyder

1

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9 August 2017

1 March 2004

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9 August 2017

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9 August 2017

12

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9 August 2017

369-439

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9 August 2017

3

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Current status of the human obesity gene map.

9 August 2017

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https://api.crossref.org/works/10.1038%2FOBY.2004.47

The human obesity gene map: the 1996 update

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The human obesity gene map: the 1997 update

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The human obesity gene map: the 1998 update

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The human obesity gene map: the 1999 update.

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The human obesity gene map: the 2000 update

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The human obesity gene map: the 2001 update

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The human obesity gene map: the 2002 update

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

ACEDB: a database for genome information

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Getting started with Acedb

31 March 2020

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The genome of Caenorhabditis elegans

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The SNP Consortium website: past, present and future

31 March 2020

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Scriptable Access to theCaenorhabditis elegansGenome Sequence and Other ACEDB Databases

31 March 2020

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Creating the gene ontology resource: design and implementation

31 March 2020

1 reference

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Clinical spectrum of obesity and mutations in the melanocortin 4 receptor gene

31 March 2020

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Genetic predisposition to obesity in bulimia nervosa: a mutation screen of the melanocortin-4 receptor gene

31 March 2020

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Melanocortin-4 receptor gene: case-control study and transmission disequilibrium test confirm that functionally relevant mutations are compatible with a major gene effect for extreme obesity.

31 March 2020

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A novel nonsense mutation in the melanocortin-4 receptor associated with obesity in a Spanish population

31 March 2020

1 reference

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Functional characterization of melanocortin-4 receptor mutations associated with childhood obesity

31 March 2020

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Mutations in the human melanocortin-4 receptor gene associated with severe familial obesity disrupts receptor function through multiple molecular mechanisms

31 March 2020

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Poor Cell Surface Expression of Human Melanocortin-4 Receptor Mutations Associated with Obesity

31 March 2020

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Molecular genetics of human obesity-associated MC4R mutations

31 March 2020

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Binge eating as a major phenotype of melanocortin 4 receptor gene mutations

31 March 2020

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A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism

31 March 2020

1 reference

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Digenic inheritance of severe insulin resistance in a human pedigree

31 March 2020

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GNAS1 lesions in pseudohypoparathyroidism Ia and Ic: genotype phenotype relationship and evidence of the maternal transmission of the hormonal resistance

31 March 2020

1 reference

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Mutational analysis of the GNAS1 exons encoding the stimulatory G protein in five patients with pseudohypoparathyroidism type 1a.

31 March 2020

1 reference

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Analysis of GNAS1 and overlapping transcripts identifies the parental origin of mutations in patients with sporadic Albright hereditary osteodystrophy and reveals a model system in which to observe the effects of splicing mutations on translated and

31 March 2020

1 reference

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Albright hereditary osteodystrophy and del(2)(q37.3) in four unrelated individuals

31 March 2020

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STK25 is a candidate gene for pseudopseudohypoparathyroidism

31 March 2020

1 reference

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Multisystem dystrophy syndrome due to novel missense mutations in the amino-terminal head and alpha-helical rod domains of the lamin A/C gene

31 March 2020

1 reference

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Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy

31 March 2020

1 reference

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A new clinical condition linked to a novel mutation in lamins A and C with generalized lipoatrophy, insulin-resistant diabetes, disseminated leukomelanodermic papules, liver steatosis, and cardiomyopathy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

PPARG F388L, a transactivation-deficient mutant, in familial partial lipodystrophy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Human metabolic syndrome resulting from dominant-negative mutations in the nuclear receptor peroxisome proliferator-activated receptor-gamma

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

VSX1: a gene for posterior polymorphous dystrophy and keratoconus

31 March 2020

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https://api.crossref.org/works/10.1038%2FOBY.2004.47

Haploinsufficiency of TBX3 causes ulnar-mammary syndrome in a large Turkish family

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Morbid obesity and hyperphagia in the WAGR syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Missense mutations in the DNA-binding region and termination codon in PAX6.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutations of the PRKAR1A gene in Cushing's syndrome due to sporadic primary pigmented nodular adrenocortical disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Human tumors associated with Carney complex and germline PRKAR1A mutations: a protein kinase A disease!

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Clinical genetics of multiple endocrine neoplasias, Carney complex and related syndromes

31 March 2020

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Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic interaction of BBS1 mutations with alleles at other BBS loci can result in non-Mendelian Bardet-Biedl syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1)

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Phenotypic and genetic heterogeneity in congenital generalized lipodystrophy.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Cohen Syndrome Is Caused by Mutations in a Novel Gene, COH1, Encoding a Transmembrane Protein with a Presumed Role in Vesicle-Mediated Sorting and Intracellular Protein Transport

31 March 2020

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A secondary respiratory chain defect in a patient with Fanconi-Bickel syndrome

31 March 2020

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A novel mutation (N32K) of GLUT2 gene in a Japanese patient with Fanconi-Bickel syndrome

31 March 2020

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Novel PHF6 mutation p.D333del causes Börjeson-Forssman-Lehmann syndrome

31 March 2020

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Shashi XLMR syndrome: report of a second family.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome

31 March 2020

1 reference

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Genotype/phenotype correlations of males affected by Simpson-Golabi-Behmel syndrome with GPC3 gene mutations: patient report and review of the literature.

31 March 2020

1 reference

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A peculiar subphenotype in the fra(X) syndrome: extreme obesity-short stature-stubby hands and feet-diffuse hyperpigmentation. Further evidence of disturbed hypothalamic function in the fra(X) syndrome?

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Prader-Willi-like phenotype in fragile X syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The mouse mahoganoid coat color mutation disrupts a novel C3HC4 RING domain protein

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Obesity in transgenic female mice with constitutively elevated luteinizing hormone secretion

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Androgen receptor functions from reverse genetic models

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

SPARC-null mice exhibit increased adiposity without significant differences in overall body weight

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Interleukin-6-deficient mice develop mature-onset obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Transgenic mice with dominant negative PKC-theta in skeletal muscle: a new model of insulin resistance and obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A central role for JNK in obesity and insulin resistance

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) contiguous gene syndromes by chromosome engineering in mice: phenotypic consequences of gene dosage imbalance.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Human/mouse homology relationships

31 March 2020

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https://api.crossref.org/works/10.1038%2FOBY.2004.47

A rat genetic linkage map and comparative maps for mouse or human homologous rat genes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A genetic linkage map of the laboratory rat, Rattus norvegicus

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

QTL analysis of self-selected macronutrient diet intake: fat, carbohydrate, and total kilocalories

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic contributions to body weight in mice: relationship of exploratory behavior to weight.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Loci on chromosomes 2, 4, 9, and 16 for body weight, body length, and adiposity identified in a genome scan of an F2 intercross between the 129P3/J and C57BL/6ByJ mouse strains

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Identification of interactive loci linked to insulin and leptin in mice with genetic insulin resistance

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Quantitative trait loci for insulin-like growth factor I, leptin, thyroxine, and corticosterone in genetically heterogeneous mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic variation in the renin-angiotensin system and abdominal adiposity in men: the Olivetti Prospective Heart Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Beta2 adrenoceptor functional gene variants, obesity, and blood pressure level interactions in the general population

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Effect of Trp64Arg mutation of the β3‐adrenergic receptor gene and C161T substitution of the peroxisome proliferator activated receptor γ gene on obesity in Japanese children

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Allele-specific differential expression of a common adiponectin gene polymorphism related to obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutations in the adiponectin gene in lean and obese subjects from the Swedish obese subjects cohort

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of two apolipoprotein A-I gene MspI polymorphisms with high density lipoprotein (HDL)-cholesterol levels and indices of obesity in selected healthy Chinese subjects and in patients with early-onset type 2 diabetes.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Further evidence for the association between obesity-related traits and the apolipoprotein A-IV gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Na+-K+-ATPase alpha 2-gene and skeletal muscle characteristics in response to long-term overfeeding

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of the SNP-19 genotype 22 in the calpain-10 gene with elevated body mass index and hemoglobin A1c levels in Japanese

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of polymorphisms in the estrogen receptor alpha gene with body fat distribution

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic variation in the human winged helix/forkhead transcription factor gene FOXC2 in Pima Indians

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

An epidemiological study of blood pressure and metabolic phenotypes in relation to the Gbeta3 C825T polymorphism.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Associations between a polymorphism in the 11 beta hydroxysteroid dehydrogenase type I gene and body composition

31 March 2020

1 reference

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The interleukin 6-174G/C polymorphism is associated with indices of obesity in men.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of polymorphisms in the interleukin 6 receptor complex with obesity and hyperandrogenism

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Metabolic effects of the Gly1057Asp polymorphism in IRS-2 and interactions with obesity

31 March 2020

1 reference

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Visceral obesity attenuates the effect of the hepatic lipase -514C>T polymorphism on plasma HDL-cholesterol levels in French-Canadian men.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

No linkage to obesity in candidate regions of chromosome 2 and 10 in a selected sample of Swedish twins.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

An acyl-CoA synthetase gene family in chromosome 16p12 may contribute to multiple risk factors

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Correlates of obesity in postmenopausal women with breast cancer: comparison of genetic, demographic, disease-related, life history and dietary factors

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Contribution of variants in the small heterodimer partner gene to birthweight, adiposity, and insulin levels: mutational analysis and association studies in multiple populations

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The relation between two polymorphisms in the glucocorticoid receptor gene and body mass index, blood pressure and cholesterol in obese patients

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The N363S polymorphism in the glucocorticoid receptor gene is associated with overweight in subjects with type 2 diabetes mellitus.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The peroxisome proliferator-activated receptor alpha L162V mutation is associated with reduced adiposity.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The Pro12Ala PPARgamma2 gene missense mutation is associated with obesity and insulin resistance in Swedish middle-aged men.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Haplotype analysis of the PPARgamma Pro12Ala and C1431T variants reveals opposing associations with body weight.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Pilot study examining the frequency of several gene polymorphisms in a morbidly obese population.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The PPAR-gamma P12A polymorphism modulates the relationship between dietary fat intake and components of the metabolic syndrome: results from the Québec Family Study.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Pro12Ala of the peroxisome proliferator-activated receptor-gamma2 gene is associated with lower serum insulin levels in nonobese African Americans: the Atherosclerosis Risk in Communities Study.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Dopamine transporter genotype as a risk factor for obesity in African-American smokers

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

High frequency of mutations in the HNF-1alpha gene in non-obese patients with diabetes of youth in Japanese and identification of a case of digenic inheritance

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Increased abdominal obesity, insulin and glucose levels in nondiabetic subjects with a T29C polymorphism of the transforming growth factor-beta1 gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The CAG repeat polymorphism in the androgen receptor gene modulates body fat mass and serum concentrations of leptin and insulin in men.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

C174T polymorphism in the CNTF receptor gene is associated with fat-free mass in men and women.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Beta(2)-adrenergic receptor mutation and abdominal obesity risk: effect modification by gender and HDL-cholesterol

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The glutamine 27 glutamic acid polymorphism of the beta2-adrenoceptor gene is associated with abdominal obesity and greater risk of impaired glucose tolerance in men but not in women: a population-based study in Spain

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Androgen receptor gene repeats and indices of obesity in older adults

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The CYP19 gene and associations with androgens and abdominal obesity in premenopausal women

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic variation at the adipsin locus and response to long-term overfeeding

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Uncoupling protein 1 and 3 polymorphisms are associated with waist-to-hip ratio.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Arg64β3‐Adrenoceptor Variant and the Components of Energy Expenditure

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The C-174G promoter polymorphism of the IL-6 gene affects energy expenditure and insulin sensitivity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The Gln223Arg polymorphism of the leptin receptor in Pima Indians: influence on energy expenditure, physical activity and lipid metabolism

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A functional variant in the peroxisome proliferator-activated receptor gamma2 promoter is associated with predictors of obesity and type 2 diabetes in Pima Indians

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A Gly482Ser missense mutation in the peroxisome proliferator-activated receptor gamma coactivator-1 is associated with altered lipid oxidation and early insulin secretion in Pima Indians

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Evidence for an important role of perilipin in the regulation of human adipocyte lipolysis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

K121Q PC‐1 Gene Polymorphism Is Not Associated with Insulin Resistance in a Spanish Population

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Melanocortin-3-receptor gene variants in morbid obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Pro-opiomelanocortin gene is associated with serum leptin levels in lean but not in obese individuals

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Effects of uncoupling protein 1 and ß3-adrenergic receptor gene polymorphisms on body size and serum lipid concentrations in Japanese women

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Long-term adiposity changes are related to a glucocorticoid receptor polymorphism in young females

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Prediction of successful weight reduction under sibutramine therapy through genotyping of the G-protein beta3 subunit gene (GNB3) C825T polymorphism

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Phenylethanolamine N-methyltransferase G-148A genetic variant and weight loss in obese women

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Difficulty in losing weight by behavioral intervention for women with Trp64Arg polymorphism of the beta3-adrenergic receptor gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Effects of beta2-adrenergic receptor gene variants on adiposity: the HERITAGE Family Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

No evidence for involvement of the promoter polymorphism -866 G/A of the UCP2 gene in childhood-onset obesity in humans.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A 45‐bp Insertion/Deletion Polymorphism of Uncoupling Protein 2 in Relation to Obesity in Tongans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A common polymorphism in the promoter of UCP2 contributes to the variation in insulin secretion in glucose-tolerant subjects

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Lack of association between the uncoupling protein-2 Ala55Val gene polymorphism and phenotypic features of the Metabolic Syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A deletion in the alpha2B-adrenergic receptor gene and autonomic nervous function in central obesity.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Alpha(2B)-adrenergic receptor deletion polymorphism associates with autonomic nervous system activity in young healthy Japanese

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Obesity risk is associated with carbohydrate intake in women carrying the Gln27Glu beta2-adrenoceptor polymorphism.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Relationship of beta2-adrenergic receptor polymorphism with obesity in type 2 diabetes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Obesity, Type II diabetes and the beta 2 adrenoceptor gene Gln27Glu polymorphism in the Tongan population

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The influence of the Pro12Ala mutation of the PPAR-gamma receptor gene on metabolic and clinical characteristics in treatment-naïve patients with type 2 diabetes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Analysis of the Relationship between PPAR-γ 2 Gene Variants and Severe Insulin Resistance in Obese Patients with Impaired Glucose Tolerance

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Variation in resistin gene promoter not associated with polycystic ovary syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The absence of evidence for major effects of the frequent SNP +299G>A in the resistin gene on susceptibility to insulin resistance syndrome associated with Japanese type 2 diabetes.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A promoter genotype and oxidative stress potentially link resistin to human insulin resistance

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Polymorphism of angiotensin-converting enzyme gene and BMI in obese Korean women

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The polymorphism of the beta3-adrenergic receptor gene is associated with reduced low-density lipoprotein particle size

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Obesity and alcohol modulate the effect of apolipoprotein E polymorphism on lipids and insulin

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Influence of apolipoprotein e polymorphism on cardiovascular risk factors in obese children

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian Caucasians

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association study of the vitamin D: 1alpha-hydroxylase (CYP1alpha) gene and type 2 diabetes mellitus in a Polish population

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Role of the DGAT Gene C79T Single‐Nucleotide Polymorphism in French Obese Subjects

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Endothelin-1 gene Lys198Asn polymorphism and blood pressure reactivity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of endothelin-1 gene variant with hypertension

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Influence of dietary and genetic factors on metabolic status in obese and lean postmenopausal women

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Effect of the factor VII R353Q missense mutation on plasma apolipoprotein B levels: impact of visceral obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Obesity, Type II diabetes and the Ala54Thr polymorphism of fatty acid binding protein 2 in the Tongan population

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of polymorphisms in GPR10, the gene encoding the prolactin-releasing peptide receptor with blood pressure, but not obesity, in a U.K. Caucasian population

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Linkage and association of the CA repeat polymorphism of the IL6 gene, obesity-related phenotypes, and bone mineral density (BMD) in two independent Caucasian populations

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The interleukin-6 promoter polymorphism is associated with elevated leukocyte, lymphocyte, and monocyte counts and reduced physical fitness in young healthy smokers

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Increased insulin resistance in obese children who have both 972 IRS-1 and 1057 IRS-2 polymorphisms

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic variation in the leptin receptor gene, leptin, and weight gain in young Dutch adults

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The lipoprotein lipase gene HindIII polymorphism is associated with lipid levels in early-onset type 2 diabetic patients.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Endothelial nitric oxide synthase polymorphisms are associated with type 2 diabetes and the insulin resistance syndrome.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic Variation in the Small Heterodimer Partner Gene and Young-Onset Type 2 Diabetes, Obesity, and Birth Weight in U.K. Subjects

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Frequency of the T228A polymorphism in the SORBS1 gene in children with premature pubarche and in adolescent girls with hyperandrogenism

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The effect of the -308A allele of the TNF-alpha gene on insulin action is dependent on obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A genome-wide scan for body mass index among Nigerian families.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic linkage and imprinting effects on body mass index in children and young adults

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A whole-genome scan for obstructive sleep apnea and obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A study of linkage and association of body mass index in the Old Order Amish.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Linkage for BMI at 3q27 region confirmed in an African-American population.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Linkage and linkage disequilibrium mapping of genes influencing human obesity in chromosome region 7q22.1-7q35

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Interacting genetic loci on chromosomes 20 and 10 influence extreme human obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genome scan for childhood and adolescent obesity in German families.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A genome-wide scan for human obesity genes reveals a major susceptibility locus on chromosome 10

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Quantitative trait loci on chromosomes 3 and 17 influence phenotypes of the metabolic syndrome.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Congenital leptin deficiency is associated with severe early-onset obesity in humans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A leptin missense mutation associated with hypogonadism and morbid obesity.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutational analysis of melanocortin-4 receptor, agouti-related protein, and α-melanocyte-stimulating hormone genes in severely obese children

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor deficiency

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Missense variants in the human cholecystokinin type A receptor gene: no evidence for association with early-onset obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Identification and functional analysis of novel human melanocortin-4 receptor variants

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Several mutations in the melanocortin-4 receptor gene including a nonsense and a frameshift mutation associated with dominantly inherited obesity in humans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Phenotypes in three pedigrees with autosomal dominant obesity caused by haploinsufficiency mutations in the melanocortin-4 receptor gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Melanocortin 4 Receptor Sequence Variations Are Seldom a Cause of Human Obesity: The Swedish Obese Subjects, the HERITAGE Family Study, and a Memphis Cohort

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A Novel homozygous missense mutation of melanocortin-4 receptor (MC4R) in a Japanese woman with severe obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Intracellular retention is a common characteristic of childhood obesity-associated MC4R mutations

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A frameshift mutation in human MC4R is associated with a dominant form of obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A frameshift mutation in MC4R associated with dominantly inherited human obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Alström syndrome: further evidence for linkage to human chromosome 2p13.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alström syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Refinement of genetic localization of the Alström syndrome on chromosome 2p12-13 by linkage analysis in a North African family.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Delineation of the critical interval of Bardet-Biedl syndrome 1 (BBS1) to a small region of 11q13, through linkage and haplotype analysis of 91 pedigrees

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A founder effect in the newfoundland population reduces the Bardet-Biedl syndrome I (BBS1) interval to 1 cM

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic and mutational analyses of a large multiethnic Bardet-Biedl cohort reveal a minor involvement of BBS6 and delineate the critical intervals of other loci

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Canadian Bardet-Biedl syndrome family reduces the critical region of BBS3 (3p) and presents with a variable phenotype.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The cloning and developmental expression of unconventional myosin IXA (MYO9A) a gene in the Bardet-Biedl syndrome (BBS4) region at chromosome 15q22-q23

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

BBS4 is a minor contributor to Bardet-Biedl syndrome and may also participate in triallelic inheritance

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Identification of the gene that, when mutated, causes the human obesity syndrome BBS4.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic heterogeneity of Bardet-Biedl syndrome in a distinct Canadian population: evidence for a fifth locus

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A fifth locus for Bardet-Biedl syndrome maps to chromosome 2q31

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutations in MKKS cause Bardet-Biedl syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutation analysis of the MKKS gene in McKusick-Kaufman syndrome and selected Bardet-Biedl syndrome patients

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A Gene for Congenital Generalized Lipodystrophy Maps to Human Chromosome 9q34

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Molecular analysis of Berardinelli-Seip congenital lipodystrophy in Oman: evidence for multiple loci

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Heterogeneity for congenital generalized lipodystrophy in seventeen patients from Oman.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Cohen syndrome: essential features, natural history, and heterogeneity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutation analysis of two Japanese patients with Fanconi-Bickel syndrome.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutation analysis of the GLUT2 gene in patients with Fanconi-Bickel syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A newly recognized missense mutation in the GLUT2 gene in a patient with Fanconi-Bickel syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Nonsense mutation in the human growth hormone-releasing hormone receptor causes growth failure analogous to the little (lit) mouse

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A glycine 375-to-cysteine substitution in the transmembrane domain of the fibroblast growth factor receptor-3 in a newborn with achondroplasia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Pseudohypoparathyroidism, a novel mutation in the betagamma-contact region of Gsalpha impairs receptor stimulation

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Rapid GDP release from Gs alpha in patients with gain and loss of endocrine function

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Two mutations of the Gsalpha gene in two Japanese patients with sporadic pseudohypoparathyroidism type Ia.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A novel mutation in the switch 3 region of Gsalpha in a patient with Albright hereditary osteodystrophy impairs GDP binding and receptor activation

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A heterozygous 4-bp deletion mutation in the Gs alpha gene (GNAS1) in a patient with Albright hereditary osteodystrophy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Parental origin of Gs alpha gene mutations in Albright's hereditary osteodystrophy.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Pseudohypoparathyroidism type I and Albright's hereditary osteodystrophy with a proximal 15q chromosomal deletion in mother and daughter

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A previously unrecognised phenotype characterised by obesity, muscular hypotonia, and ability to speak in patients with Angelman syndrome caused by an imprinting defect

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Confirmation of linkage of hereditary partial lipodystrophy to chromosome 1q21-22

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Localization of the gene for familial partial lipodystrophy (Dunnigan variety) to chromosome 1q21–22

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A mutation in the tyrosine kinase domain of the insulin receptor associated with insulin resistance in an obese woman

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Analysis of the insulin receptor gene tyrosine kinase domain in obese patients with hyperandrogenism, insulin resistance and acanthosis nigricans (type C insulin resistance)

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Detection of mutations in the insulin receptor gene in patients with insulin resistance by analysis of single-stranded conformational polymorphisms

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Molecular scanning of the insulin receptor gene in syndromes of insulin resistance

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Prevalence of mutations in the insulin receptor gene in subjects with features of the type A syndrome of insulin resistance.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Insulin-resistant diabetes associated with partial deletion of insulin-receptor gene.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Abnormal messenger ribonucleic acid (mRNA) transcribed from a mutant insulin receptor gene in a patient with type A insulin resistance

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Linkage of posterior polymorphous corneal dystrophy to 20q11

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brain

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Evidence for the role of PWCR1/HBII-85 C/D box small nucleolar RNAs in Prader-Willi syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Maternal uniparental disomy for chromosome 14 in a boy with a normal karyotype

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Prader-Willi syndrome is caused by disruption of the SNRPN gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genes.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Submicroscopic deletion in cousins with Prader-Willi syndrome causes a grandmatrilineal inheritance pattern: effects of imprinting

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Imprinting-mutation mechanisms in Prader-Willi syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Identification of a novel paternally expressed gene in the Prader-Willi syndrome region

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

De novo interstitial deletion q16.2q21 on chromosome 6.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Profound obesity associated with a balanced translocation that disrupts the SIM1 gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Familial complex chromosomal rearrangement resulting in duplication/deletion of 6q14 to 6q16.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The diagnosis of Prader-Willi syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Third case of WAGR syndrome with severe obesity and constitutional deletion of chromosome (11)(p12p14)

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Börjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patient

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

MEHMO (Mental retardation, Epileptic seizures, Hypogenitalism, Microcephaly, Obesity): a new X-linked mitochondrial disorder

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

MEHMO (mental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly, obesity), a novel syndrome: assignment of disease locus to xp21.1-p22.13.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

MEHMO, a novel syndrome: assignment of disease locus to Xp21.1-p22.13. Mental retardation, epileptic seizures, hypogonadism and genitalism, microcephaly, obesity.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Linkage mapping of a new syndromic form of X-linked mental retardation, MRXS7, associated with obesity.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Prader-Willi-like syndrome in a patient with an Xq23q25 duplication

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Simpson-Golabi-Behmel syndrome: genotype/phenotype analysis of 18 affected males from 7 unrelated families

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Clinical and molecular aspects of the Simpson-Golabi-Behmel syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A clinical and molecular study of a patient with Simpson-Golabi-Behmel syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

GPC4, the gene for human K-glypican, flanks GPC3 on xq26: deletion of the GPC3-GPC4 gene cluster in one family with Simpson-Golabi-Behmel syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mapping of a new SGBS locus to chromosome Xp22 in a family with a severe form of Simpson-Golabi-Behmel syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Gene localisation for Wilson-Turner syndrome (WTS:MIM 309585)

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

New X-linked syndrome of mental retardation, gynecomastia, and obesity is linked to DXS255.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Evidence that the diabetes gene encodes the leptin receptor: identification of a mutation in the leptin receptor gene in db/db mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Identification and expression cloning of a leptin receptor, OB-R

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Lipodystrophy in the fld mouse results from mutation of a new gene encoding a nuclear protein, lipin

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Hyperproinsulinaemia in obese fat/fat mice associated with a carboxypeptidase E mutation which reduces enzyme activity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

An animal model of congenital defect of gene expression of cholecystokinin (CCK)-A receptor

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Growth hormone deficiency in 'little' mice results in aberrant body composition, reduced insulin-like growth factor-I and insulin-like growth factor-binding protein-3 (IGFBP-3), but does not affect IGFBP-2, -1 or -4

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Positional cloning of the mouse obese gene and its human homologue

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Tyrosine phosphorylation of tub and its association with Src homology 2 domain-containing proteins implicate tub in intracellular signaling by insulin

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Identification and characterization of the mouse obesity gene tubby: a member of a novel gene family

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A candidate gene for the mouse mutation tubby

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The mahogany protein is a receptor involved in suppression of obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The mouse mahogany locus encodes a transmembrane form of human attractin

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Structure and function of ASP, the human homolog of the mouse agouti gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Continuous fatty acid oxidation and reduced fat storage in mice lacking acetyl-CoA carboxylase 2

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Protection from obesity and insulin resistance in mice overexpressing human apolipoprotein C1.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Life without white fat: a transgenic mouse

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mice lacking bombesin receptor subtype-3 develop metabolic defects and obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Impaired energy homeostasis in C/EBP alpha knockout mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Defective adipocyte differentiation in mice lacking the C/EBPbeta and/or C/EBPdelta gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mice lacking the M3 muscarinic acetylcholine receptor are hypophagic and lean.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Aromatase-deficient (ArKO) mice have a phenotype of increased adiposity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Abnormal brown and white fat development in transgenic mice overexpressing glycerol 3-phosphate dehydrogenase

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Dopamine-deficient mice are severely hypoactive, adipsic, and aphagic

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Uncoupling of obesity from insulin resistance through a targeted mutation in aP2, the adipocyte fatty acid binding protein

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Obesity resistance and multiple mechanisms of triglyceride synthesis in mice lacking Dgat

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Estrogen deficiency, obesity, and skeletal abnormalities in follicle-stimulating hormone receptor knockout (FORKO) female mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Transgenic mice overexpressing gamma-aminobutyric acid transporter subtype I develop obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Adipose tissue reduction in mice lacking the translational inhibitor 4E-BP1.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Melanin-concentrating hormone 1 receptor-deficient mice are lean, hyperactive, and hyperphagic and have altered metabolism

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Targeted disruption of histamine H1-receptor attenuates regulatory effects of leptin on feeding, adiposity, and UCP family in mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic ablation of orexin neurons in mice results in narcolepsy, hypophagia, and obesity.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Abnormalities in the functioning of adipocytes from R6/2 mice that are transgenic for the Huntington's disease mutation

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

In vivo modulation of Hmgic reduces obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A transgenic model of visceral obesity and the metabolic syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A new class of obesity genes encodes leukocyte adhesion receptors

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Functions of interleukin 1 receptor antagonist in gene knockout and overproducing mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Obesity and hyperleptinemia in metallothionein (-I and -II) null mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Hypogonadism and obesity in mice with a targeted deletion of the Nhlh2 gene.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetically lean mice result from targeted disruption of the RII beta subunit of protein kinase A

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Absence of perilipin results in leanness and reverses obesity in Lepr(db/db) mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Perilipin ablation results in a lean mouse with aberrant adipocyte lipolysis, enhanced leptin production, and resistance to diet-induced obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Melanin-concentrating hormone overexpression in transgenic mice leads to obesity and insulin resistance

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mice lacking melanin-concentrating hormone are hypophagic and lean

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Decreased food intake and body weight in pancreatic polypeptide-overexpressing mice.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Increased insulin sensitivity and obesity resistance in mice lacking the protein tyrosine phosphatase-1B gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Transgenic expression of syndecan-1 uncovers a physiological control of feeding behavior by syndecan-3.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Overproduction of cholesterol and fatty acids causes massive liver enlargement in transgenic mice expressing truncated SREBP-1a

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Insulin resistance and diabetes mellitus in transgenic mice expressing nuclear SREBP-1c in adipose tissue: model for congenital generalized lipodystrophy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Requirement of STAT5b for sexual dimorphism of body growth rates and liver gene expression

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Hepatic fibrosis, glomerulosclerosis, and a lipodystrophy-like syndrome in PEPCK-TGF-beta1 transgenic mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Targeted deletion of the Vgf gene indicates that the encoded secretory peptide precursor plays a novel role in the regulation of energy balance

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mapping of body weight loci on mouse chromosome X.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Detection of obesity QTLs on mouse chromosomes 1 and 7 by selective DNA pooling.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Obesity QTLs on mouse chromosomes 2 and 17.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Dietary obesity linked to genetic loci on chromosomes 9 and 15 in a polygenic mouse model

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetics of dietary obesity in AKR/J x SWR/J mice: segregation of the trait and identification of a linked locus on chromosome 4

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic loci controlling body fat, lipoprotein metabolism, and insulin levels in a multifactorial mouse model

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic dissection of obesity in polygenic animal models

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Quantitative trait loci affecting growth in high growth (hg) mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Test of candidate gene--quantitative trait locus association applied to fatness in mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Single QTL effects, epistasis, and pleiotropy account for two-thirds of the phenotypic F(2) variance of growth and obesity in DU6i x DBA/2 mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mapping of obesity QTLs in a cross between mouse lines divergently selected on fat content

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetics of obesity in KK mouse and effects of A(y) allele on quantitative regulation.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Gender-influenced obesity QTLs identified in a cross involving the KK type II diabetes-prone mouse strain

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Identification of four chromosomal loci determining obesity in a multifactorial mouse model

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic analysis of late-onset type 2 diabetes in a mouse model of human complex trait

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Identification of an obesity quantitative trait locus on mouse chromosome 2 and evidence of linkage to body fat and insulin on the human homologous region 20q.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Quantitative trait loci for obesity and insulin resistance (Nob1, Nob2) and their interaction with the leptin receptor allele (LeprA720T/T1044I) in New Zealand obese mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Multiple obesity QTLs identified in an intercross between the NZO (New Zealand obese) and the SM (small) mouse strains

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Maternal environment and genotype interact to establish diabesity in mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Growth quantitative trait loci (QTL) on mouse chromosome 10 in a Quackenbush-Swiss x C57BL/6J backcross

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Quantitative trait loci for body weight in the intercross between SM/J and A/J mice.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic architecture of adiposity in the cross of LG/J and SM/J inbred mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mapping quantitative trait loci for murine growth: a closer look at genetic architecture

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic analysis of obese diabetes in the TSOD mouse

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Detection of quantitative trait loci for body weight at 10 weeks from Philippine wild mice.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic dissection of "OLETF," a rat model for non-insulin-dependent diabetes mellitus: quantitative trait locus analysis of (OLETF x BN) x OLETF.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Complete genome searches for quantitative trait loci controlling blood pressure and related traits in four segregating populations derived from Dahl hypertensive rats

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Chromosomal mapping of genetic loci associated with non-insulin dependent diabetes in the GK rat

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic analysis of non-insulin dependent diabetes mellitus in the GK rat.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic modifiers of Leprfa associated with variability in insulin production and susceptibility to NIDDM

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic dissection of "OLETF", a rat model for non-insulin-dependent diabetes mellitus.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic evidence for obesity loci involved in the regulation of body fat distribution in obese type 2 diabetes rat, OLETF

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Detection of a quantitative trait locus for intramuscular fat accumulation using the OLETF rat

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Quantitative trait loci for body weight, blood pressure, blood glucose, and serum lipids: linkage analysis with wild rats (Rattus norvegicus).

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Sex-specific and sex-independent quantitative trait loci for facets of the metabolic syndrome in WOKW rats

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A molecular genome scan analysis to identify chromosomal regions influencing economic traits in the pig. II. Meat and muscle composition.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic mapping of quantitative trait loci for growth and fatness in pigs

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Confirmed quantitative trait loci for fatness and growth on pig chromosome 4

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A QTL on pig chromosome 4 affects fatty acid metabolism: evidence from an Iberian by Landrace intercross

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Fine mapping and imprinting analysis for fatness trait QTLs in pigs

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A directed search for quantitative trait loci on chromosomes 4 and 7 in pigs

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genome-wide scan for body composition in pigs reveals important role of imprinting

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The X Chromosome harbors quantitative trait loci for backfat thickness and intramuscular fat content in pigs

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Quantitative trait loci (QTL) analysis in a Meishan x Göttingen cross population

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mapping of quantitative trait loci on porcine chromosome 4.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Detection of quantitative trait loci for growth and fatness in pigs.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Identification of quantitative trait loci affecting birth characters and accumulation of backfat and weight in a Meishan-White Composite resource population.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Identification of quantitative trait loci affecting carcass composition in swine: I. Fat deposition traits

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A paternally expressed QTL affecting skeletal and cardiac muscle mass in pigs maps to the IGF2 locus

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

An imprinted QTL with major effect on muscle mass and fat deposition maps to the IGF2 locus in pigs

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Sensitivity to dietary obesity linked to a locus on chromosome 15 in a CAST/Ei x C57BL/6J F2 intercross

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic studies of the sulfonylurea receptor gene locus in NIDDM and in morbid obesity among French Caucasians

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A possible genetic component of obesity in childhood. Observations on acid phosphatase polymorphism

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Adenosine deaminase and body mass index in non-insulin-dependent diabetes mellitus

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The alpha 2-adrenergic receptor gene and body fat content and distribution: the HERITAGE Family Study.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

DNA polymorphisms in the alpha 2- and beta 2-adrenoceptor genes and regional fat distribution in humans: association and linkage studies

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Effect of a three-amino acid deletion in the α2B-adrenergic receptor gene on long-term body weight change in Finnish non-diabetic and type 2 diabetic subjects

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association between obesity and a polymorphism in the β1-adrenoceptor gene (Gly389Arg ADRB1) in Caucasian women

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The risk of obesity and the Trp64Arg polymorphism of the beta(3)-adrenergic receptor: effect modification by age.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The Q/E27 polymorphism in the beta2-adrenoceptor gene is associated with increased body weight and dyslipoproteinaemia involving triglyceride-rich lipoproteins.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Influence of the beta2-adrenergic receptor Arg16Gly polymorphism on longitudinal changes in obesity from childhood through young adulthood in a biracial cohort: the Bogalusa Heart Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The effect of the beta(2) adrenoceptor gene Thr164Ile polymorphism on human adipose tissue lipolytic function

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of polymorphisms in the beta2-adrenergic receptor gene with obesity, hypertriglyceridaemia, and diabetes mellitus

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Human beta-2 adrenoceptor gene polymorphisms are highly frequent in obesity and associate with altered adipocyte beta-2 adrenoceptor function

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Impact of polymorphisms of the human β 2 -adrenoceptor gene on obesity in a French population

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Beta2-adrenoceptor gene polymorphism, body weight, and physical activity.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Obesity gene variant and elite endurance performance

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The Gln27Glu beta2-adrenergic receptor variant is associated with obesity due to subcutaneous fat accumulation in Japanese men

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Polymorphisms of the beta2-adrenergic receptor gene (ADRB2) in relation to cardiovascular risk factors in men.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Interactions among the α2-, β2-, and β3-adrenergic receptor genes and obesity-related phenotypes in the Quebec Family Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Beta-2 adrenergic receptor variants are associated with subcutaneous fat accumulation in response to long-term overfeeding

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic factors as predictors of weight gain in young adult Dutch men and women

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic variation in the beta 3-adrenergic receptor and an increased capacity to gain weight in patients with morbid obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Gender specific associations of the Trp64Arg mutation in the beta3-adrenergic receptor gene with obesity-related phenotypes in a Mediterranean population: interaction with a common lipoprotein lipase gene variation

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of Trp64Arg polymorphism of the beta3-adrenergic receptor gene and no association of Gln223Arg polymorphism of the leptin receptor gene in Japanese schoolchildren with obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of Trp64Arg mutation of the ?3-adrenergic-receptor with NIDDM and body weight gain

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of a genetic variation in the beta 3-adrenergic receptor gene with coronary heart disease among Japanese

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Polymorphism of the human beta3-adrenoceptor gene forms a well-conserved haplotype that is associated with moderate obesity and altered receptor function

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Expression of the beta 3-adrenoceptor gene polymorphism (Trp64Arg) in obese diabetic and non-diabetic subjects.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A mutation in the beta 3-adrenergic receptor gene is associated with obesity and hyperinsulinemia in Japanese subjects.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A mutation of the b3-adrenergic receptor is associated with visceral obesity but decreased serum triglyceride

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

TRP64ARG polymorphism of the beta3-adrenergic receptor gene and obesity risk: effect modification by a sedentary lifestyle

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The Trp64Arg mutation of the beta3-adrenergic receptor is associated with hyperglycemia and current body mass index in Jamaican women

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A paired sibling analysis of the beta-3 adrenergic receptor and obesity in Mexican Americans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genotype Arg/Arg, but not Trp/Arg, of the Trp64Arg polymorphism of the beta(3)-adrenergic receptor is associated with type 2 diabetes and obesity in a large Japanese sample

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Relation of beta3-adrenergic receptor gene mutation to total body fat but not percent body fat and insulin levels in Thais.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Beta 3-adrenergic-receptor polymorphism: a genetic marker for visceral fat obesity and the insulin resistance syndrome.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of the Trp64Arg mutation of the beta3-adrenergic receptor with fatty liver and mild glucose intolerance in Japanese subjects.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Relationship of the Trp64Arg polymorphism of the beta3-adrenoceptor gene to central adiposity and high blood pressure: interaction with age. Cross-sectional and longitudinal findings of the Olivetti Prospective Heart Study.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The Trp64Arg polymorphism of the β3-adrenergic receptor gene and obesity in Chinese subjects with components of the metabolic syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Insulin sensitivity and body weight changes in young white carriers of the codon 64 amino acid polymorphism of the beta 3-adrenergic receptor gene.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of a polymorphism in the beta 3-adrenergic-receptor gene with features of the insulin resistance syndrome in Finns.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A polymorphism in the human agouti-related protein is associated with late-onset obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Body weight changes and the A-6G polymorphism of the angiotensinogen gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic variation on chromosome 1 associated with variation in body fat distribution in men.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Body fat, resting and exercise blood pressure and the angiotensinogen M235T polymorphism: the heritage family study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A haplotype at the adiponectin locus is associated with obesity and other features of the insulin resistance syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of the T-G polymorphism in adiponectin (exon 2) with obesity and insulin sensitivity: interaction with family history of type 2 diabetes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Human evidence that the apolipoprotein a-II gene is implicated in visceral fat accumulation and metabolism of triglyceride-rich lipoproteins

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Common apolipoprotein A-IV variants are associated with differences in body mass index levels and percentage body fat

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

ApoB-100 gene EcoRI polymorphism. Relations to plasma lipoprotein changes associated with abdominal visceral obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Variation of apolipoprotein-B gene is associated with obesity, high blood cholesterol levels, and increased risk of coronary heart disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

DNA polymorphisms of the apolipoprotein B gene are associated with obesity and serum lipids in healthy Indians in Singapore.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Apolipoprotein E polymorphism and lipid levels differ by gender and family history of diabetes: the Rancho Bernardo Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

DNA variation in the genes of the Na,K-adenosine triphosphatase and its relation with resting metabolic rate, respiratory quotient, and body fat

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The CART gene and human obesity: mutational analysis and population genetics.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Sequencing of the putative promoter region of the cocaine- and amphetamine-regulated-transcript gene and identification of polymorphic sites associated with obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Polymorphism in the 3' untranslated region of MTG8 is associated with obesity in Pima Indian males

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Gene structure of human cholecystokinin (CCK) type-A receptor: body fat content is related to CCK type-A receptor gene promoter polymorphism

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Candidate genes involved in cardiovascular risk factors by a family-based association study on the island of Kosrae, Federated States of Micronesia.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The dopamine D2 receptor (DRD2) as a major gene in obesity and height

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A Ser311Cys mutation in the human dopamine receptor D2 gene is associated with reduced energy expenditure

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Modulation of blood pressure and obesity with the dopamine D2 receptor gene TaqI polymorphism.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Relationships between the taqI polymorphism of the dopamine D2 receptor and blood pressure in hyperglycaemic and normoglycaemic Chinese subjects.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Vitamin D and estrogen receptor gene polymorphisms in type 2 diabetes mellitus and in android type obesity.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association between Ala54Thr substitution of the fatty acid-binding protein 2 gene with insulin resistance and intra-abdominal fat thickness in Japanese men.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Gly40Ser polymorphism of the glucagon receptor gene is associated with central adiposity in men.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutations in the glucokinase gene of the fetus result in reduced birth weight.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A variation in the ghrelin gene increases weight and decreases insulin secretion in tall, obese children

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutations in the preproghrelin/ghrelin gene associated with obesity in humans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

G protein beta3 subunit 825 TT genotype and post-pregnancy weight retention.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Effects of the G-protein beta3 subunit 825T allele on adipogenesis and lipolysis in cultured human preadipocytes and adipocytes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

G-protein beta3 subunit gene splice variant and body fat distribution in Nunavut Inuit

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of maternal G protein β3 subunit 825T allele with low birthweight

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of the G protein beta3 subunit T allele with insulin resistance in essential hypertension

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

G protein beta 3 polymorphism and hemodynamic and body composition phenotypes in the HERITAGE Family Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Effect of the (C825T) Gbeta(3) polymorphism on adrenoceptor-mediated lipolysis in human fat cells

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

G protein beta3 subunit 825T allele and its potential association with obesity in hypertensive individuals

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A paired-sibling analysis of the XbaI polymorphism in the muscle glycogen synthase gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Relation between BglII polymorphism in 3beta-hydroxysteroid dehydrogenase gene and adipose tissue distribution in humans.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic variation in the stress protein hsp70-2 gene is highly associated with obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Polymorphism of the serotonin 5-HT1B receptor gene (HTR1B) associated with minimum lifetime body mass index in women with bulimia nervosa

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

5-HT2A receptor gene polymorphism is associated with food and alcohol intake in obese people

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

5-HT2A receptor gene promoter polymorphism in relation to abdominal obesity and cortisol

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of antipsychotic drug-induced weight gain with a 5-HT2C receptor gene polymorphism

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association between a polymorphism of the 5-HT2C receptor and weight loss in teenage girls

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Identification of polymorphic loci in the promoter region of the serotonin 5-HT2C receptor gene and their association with obesity and type II diabetes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association and linkage between an insulin-like growth FACTOR-1 GENE polymorphism and fat free mass in the HERITAGE Family Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Apal polymorphism in insulin-like growth factor II (IGF2) gene and weight in middle-aged males

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

IGF2 genotype and obesity in men and women across the adult age span

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of the INS VNTR with size at birth. ALSPAC Study Team. Avon Longitudinal Study of Pregnancy and Childhood.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Evidence of multiple causal sites affecting weight in the IGF2-INS-TH region of human chromosome 11.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Paternal transmission of the very common class I INS VNTR alleles predisposes to childhood obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Associations of IGF2 ApaI RFLP and INS VNTR class I allele size with obesity.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Central obesity and hyperinsulinaemia in women are associated with polymorphism in the 5' flanking region of the human insulin gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Plasma leptin levels: interaction of obesity with a common variant of insulin receptor substrate-1.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Variants of the insulin receptor substrate-1 and fatty acid binding protein 2 genes and the risk of type 2 diabetes, obesity, and hyperinsulinemia in African-Americans: the Atherosclerosis Risk in Communities Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Cross-sectional study of a microsatellite marker in the low density lipoprotein receptor gene in obese normotensives.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of the low-density lipoprotein receptor gene with obesity in Native American populations

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of a low density lipoprotein receptor microsatellite variant with obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Marked association of a RFLP for the low density lipoprotein receptor gene with obesity in essential hypertensives

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of HincII RFLP of low density lipoprotein receptor gene with obesity in essential hypertensives

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic variants of the human obesity (OB) gene in subjects with and without Prader-Willi syndrome: comparison with body mass index and weight.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A polymorphism in the 5' untranslated region of the human ob gene is associated with low leptin levels

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A polymorphism in the leptin promoter region (-2548 G/A) influences gene expression and adipose tissue secretion of leptin

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A common promoter variant of the leptin gene is associated with changes in the relationship between serum leptin and fat mass in obese girls.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Sequence variants in the 5' flanking region of the leptin gene are associated with obesity in women

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Novel polymorphisms in the 5' region of the LEP gene: association with leptin levels and response to low-calorie diet in human obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Markers for the gene ob and serum leptin levels in human morbid obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A novel microsatellite polymorphism in the human OB gene: a highly polymorphic marker for linkage analysis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Linkages and associations between the leptin receptor (LEPR) gene and human body composition in the Québec Family Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

LEPR gene polymorphisms: associations with overweight, fat mass and response to diet in women

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association analysis of genes involved in the leptin-signaling pathway with obesity in Brazil

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A single nucleotide polymorphism (SNP) in the leptin receptor is associated with BMI, fat mass and leptin levels in postmenopausal Caucasian women

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Transmission disequilibrium and sequence variants at the leptin receptor gene in extremely obese German children and adolescents

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Structure and sequence variation at the human leptin receptor gene in lean and obese Pima Indians

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Polymorphisms in the leptin receptor gene, body composition and fat distribution in overweight and obese women

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The hormone-sensitive lipase gene and body composition: the HERITAGE Family Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A common hormone-sensitive lipase i6 gene polymorphism is associated with decreased human adipocyte lipolytic function

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The hormone-sensitive lipase i6 gene polymorphism and body fat accumulation

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Human hormone-sensitive lipase: genetic mapping, identification of a new dinucleotide repeat, and association with obesity and NIDDM.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The hormone sensitive lipase gene in familial combined hyperlipidemia and insulin resistance

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic variation in LMNA modulates plasma leptin and indices of obesity in aboriginal Canadians

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association between nuclear lamin A/C R482Q mutation and partial lipodystrophy with hyperinsulinemia, dyslipidemia, hypertension, and diabetes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Evidence of LPL gene-exercise interaction for body fat and LPL activity: the HERITAGE Family Study.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Linkage and association studies between the melanocortin receptors 4 and 5 genes and obesity-related phenotypes in the Québec Family Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A missense mutation in the human melanocortin-4 receptor gene in relation to abdominal obesity and salivary cortisol

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Sequence variation within the neuropeptide Y gene and obesity in Mexican Americans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Novel polymorphisms in the neuropeptide-Y Y5 receptor associated with obesity in Pima Indians

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Mutations in the small heterodimer partner gene are associated with mild obesity in Japanese subjects

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Abdominal visceral fat is associated with a BclI restriction fragment length polymorphism at the glucocorticoid receptor gene locus

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A glucocorticoid receptor gene marker is associated with abdominal obesity, leptin, and dysregulation of the hypothalamic-pituitary-adrenal axis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Interactions among the glucocorticoid receptor, lipoprotein lipase and adrenergic receptor genes and abdominal fat in the Québec Family Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Glucocorticoid receptor Bcl I variant is associated with an increased atherogenic profile in response to long-term overfeeding

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Molecular screening of the proopiomelanocortin (POMC ) gene in Italian obese children: report of three new mutations

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A polymorphism, L162V, in the peroxisome proliferator-activated receptor alpha (PPARalpha) gene is associated with lower body mass index in patients with non-insulin-dependent diabetes mellitus

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The Pro12Ala variant of peroxisome proliferator-activated receptor-gamma2 (PPAR-gamma2) is associated with measures of obesity in Mexican Americans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A Pro12Ala substitution in PPARgamma2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Homozygosity of the Pro12Ala variant of the peroxisome proliferation-activated receptor-gamma2 (PPAR-gamma2): divergent modulating effects on body mass index in obese and lean Caucasian men.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Effect of the Pro12Ala polymorphism of the peroxisome proliferator-activated receptor gamma-2 gene on adiposity, insulin sensitivity and lipid profile in the Spanish population

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Effect of the Pro12Ala polymorphism of the PPAR-gamma2 gene on long-term weight change in Finnish non-diabetic subjects

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of the Pro12Ala polymorphism in the PPAR-gamma2 gene with 3-year incidence of type 2 diabetes and body weight change in the Finnish Diabetes Prevention Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Impact of the Peroxisome Proliferator Activated Receptor γ2 Pro12Ala polymorphism on adiposity, lipids and non-insulin-dependent diabetes mellitus

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A genetic polymorphism of the peroxisome proliferator-activated receptor gamma gene influences plasma leptin levels in obese humans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic variation in the peroxisome proliferator-activated receptor-gamma2 gene (Pro12Ala) affects metabolic responses to weight loss and subsequent weight regain

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Obesity associated with a mutation in a genetic regulator of adipocyte differentiation

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Pro12Ala mutation in the peroxisome proliferator-activated receptor gamma2 (PPARgamma2) and severe obesity: a case-control study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Peroxisome proliferator-activated receptor-gamma coactivator-1 gene locus: associations with obesity indices in middle-aged women

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

5' flanking variants of resistin are associated with obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association between SAH, an acyl-CoA synthetase gene, and hypertriglyceridemia, obesity, and hypertension

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of polymorphisms at the SR-BI gene locus with plasma lipid levels and body mass index in a white population

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The common -675 4G/5G polymorphism in the plasminogen activator inhibitor -1 gene is strongly associated with obesity.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Molecular scanning of the human sorbin and SH3-domain-containing-1 (SORBS1) gene: positive association of the T228A polymorphism with obesity and type 2 diabetes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Tumor necrosis factor-alpha--308 G/A polymorphism in obese Caucasians

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of the TNF-alpha -308 G/A promoter polymorphism with insulin resistance in obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The TNF-alpha gene Nco I polymorphism influences the relationship among insulin resistance, percent body fat, and increased serum leptin levels

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Polymorphisms of the tumour necrosis factor-alpha gene, coronary heart disease and obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Excessive fat accumulation is associated with the TNFα -308 G/A promoter polymorphism in women but not in men

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Susceptible locus for obese type 2 diabetes mellitus in the 5'-flanking region of the tumor necrosis factor-alpha gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Linkage between obesity and a marker near the tumor necrosis factor-alpha locus in Pima Indians

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Role of tumor necrosis factor-alpha gene locus in obesity and obesity-associated hypertension in French Canadians

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Polymorphism of the tumor necrosis factor-alpha receptor 2 gene is associated with obesity, leptin levels, and insulin resistance in young subjects and diet-treated type 2 diabetic patients

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The association of a HOPA polymorphism with major depression and phobia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association of -3826 G variant in uncoupling protein-1 with increased BMI in overweight Australian women.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Synergic effect of polymorphisms in uncoupling protein 1 and beta3-adrenergic receptor genes on weight loss in obese Japanese.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic variation at the uncoupling protein 1, 2 and 3 loci and the response to long-term overfeeding.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Impact of the v/v 55 polymorphism of the uncoupling protein 2 gene on 24-h energy expenditure and substrate oxidation

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

An uncoupling protein 2 gene variant is associated with a raised body mass index but not Type II diabetes.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A common polymorphism in the promoter of UCP2 is associated with decreased risk of obesity in middle-aged humans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Frequency of and interaction between polymorphisms in the beta3-adrenergic receptor and in uncoupling proteins 1 and 2 and obesity in Germans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association between polymorphisms in candidate genes and morbid obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Fat tissue accumulation during peritoneal dialysis is associated with a polymorphism in uncoupling protein 2

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association between uncoupling protein polymorphisms (UCP2-UCP3) and energy metabolism/obesity in Pima indians.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Associations between uncoupling protein 2, body composition, and resting energy expenditure in lean and obese African American, white, and Asian children

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Effects of mutations in the human uncoupling protein 3 gene on the respiratory quotient and fat oxidation in severe obesity and type 2 diabetes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Evidence that single nucleotide polymorphism in the uncoupling protein 3 (UCP3) gene influences fat distribution in women of European and Asian origin.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Uncoupling protein 3 genetic variants in human obesity: the c-55t promoter polymorphism is negatively correlated with body mass index in a UK Caucasian population

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Racial differences in the relation between uncoupling protein genes and resting energy expenditure

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Association between uncoupling protein 3 gene and obesity-related phenotypes in the Québec Family Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Uncoupling protein 3 gene is associated with body composition changes with training in HERITAGE study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A genetic variation in the 5' flanking region of the UCP3 gene is associated with body mass index in humans in interaction with physical activity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Uncoupling protein 3 and peroxisome proliferator-activated receptor gamma2 contribute to obesity and diabetes in palauans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A genomewide linkage scan for quantitative-trait loci for obesity phenotypes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A major predisposition locus for severe obesity, at 4p15-p14

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Suggestive linkages between markers on human 1p32-p22 and body fat and insulin levels in the Quebec Family Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genome scan for adiposity in Dutch dyslipidemic families reveals novel quantitative trait loci for leptin, body mass index and soluble tumor necrosis factor receptor superfamily 1A

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Autosomal genomic scan for loci linked to obesity and energy metabolism in Pima Indians

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A Genome-Wide Scan for Abdominal Fat Assessed by Computed Tomography in the Quebec Family Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Quantitative-trait loci influencing body-mass index reside on chromosomes 7 and 13: the National Heart, Lung, and Blood Institute Family Heart Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Subcutaneous abdominal adipocyte size, a predictor of type 2 diabetes, is linked to chromosome 1q21--q23 and is associated with a common polymorphism in LMNA in Pima Indians.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Linkage analysis in a large pedigree ascertained due to essential familial hypercholesterolemia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Linkage and association studies between the proopiomelanocortin (POMC) gene and obesity in caucasian families

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The Genetic Basis of Plasma Variation in Adiponectin, a Global Endophenotype for Obesity and the Metabolic Syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

The quantitative trait locus on chromosome 2 for serum leptin levels is confirmed in African-Americans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A genomewide linkage scan for abdominal subcutaneous and visceral fat in black and white families: The HERITAGE Family Study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A combined analysis of genomewide linkage scans for body mass index from the National Heart, Lung, and Blood Institute Family Blood Pressure Program

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A genome-wide scan for obesity in African-Americans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

An exploratory investigation of genetic linkage with body composition and fatness phenotypes: the Québec Family Study.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genome-Wide Linkage Analysis Assessing Parent-of-Origin Effects in the Inheritance of Type 2 Diabetes and BMI in Pima Indians

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A sib-pair analysis study of 15 candidate genes in French families with morbid obesity: indication for linkage with islet 1 locus on chromosome 5q.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Eating behavior in the Old Order Amish: heritability analysis and a genome-wide linkage analysis.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A polymorphism in the gene encoding CART is not associated with obesity in Pima Indians

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Factors of insulin resistance syndrome--related phenotypes are linked to genetic locations on chromosomes 6 and 7 in nondiabetic mexican-americans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genome-wide search for genes related to the fat-free body mass in the Québec family study

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Indication for linkage of the human OB gene region with extreme obesity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genetic markers at the leptin (OB) locus are not significantly linked to hypertension in African Americans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Extreme obesity may be linked to markers flanking the human OB gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Further support for linkage of extreme obesity to the obese gene in a study group of obese children and adolescents

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Relationship of a novel polymorphic marker near the human obese (OB) gene to fat mass in healthy women

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A quantitative trait locus influencing BMI maps to the region of the beta-3 adrenergic receptor

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genomic scan for genes affecting body composition before and after training in Caucasians from HERITAGE

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Independent confirmation of a major locus for obesity on chromosome 10.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

A locus affecting obesity in human chromosome region 10p12.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Linkage Between Markers in the Vicinity of the Uncoupling Protein 2 Gene and Resting Metabolic Rate in Humans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Linkage of body mass index to chromosome 20 in Utah pedigrees.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Genome scan for human obesity and linkage to markers in 20q13.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

An X-chromosome scan reveals a locus for fat distribution in chromosome region Xp21-22.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

Variation in the FABP2 promoter alters transcriptional activity and is associated with body composition and plasma lipid levels

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

7 January 2021

The alpha2B adrenergic receptor deletion/insertion polymorphism in morbid obesity

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

7 January 2021

6q1 monosomy: a distinctive syndrome

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

7 January 2021

Obesity and WAGR syndrome

1 reference

https://api.crossref.org/works/10.1038%2FOBY.2004.47

7 January 2021

Identifiers

DOI

10.1038/OBY.2004.47

1 reference

9 August 2017

1 reference

PubMed ID

15044658