Tests of linkage and/or association of the LEPR gene polymorphisms with obesity phenotypes in Caucasian nuclear families (Q47199978)

11 January 2018

title

Tests of linkage and/or association of the LEPR gene polymorphisms with obesity phenotypes in Caucasian nuclear families (English)

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8

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author name string

Yong-Jun Liu

1

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Sonia M S Rocha-Sanchez

2

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Peng-Yuan Liu

3

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Ji-Rong Long

4

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Yan Lu

5

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Leo Elze

6

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Robert R Recker

7

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publication date

13 April 2004

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published in

Physiological Genomics

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volume

17

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page(s)

101-106

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issue

2

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A general test of association for quantitative traits in nuclear families

cites work

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

Linkages and associations between the leptin receptor (LEPR) gene and human body composition in the Québec Family Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

The human obesity gene map: the 2002 update

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

Genomic structure of the human OB receptor and identification of two novel intronic microsatellites.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

A genomewide linkage scan for quantitative-trait loci for obesity phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

Tests of linkage and/or association of genes for vitamin D receptor, osteocalcin, and parathyroid hormone with bone mineral density

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

A comparison of linkage disequilibrium measures for fine-scale mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

Leptin and the regulation of body weight in mammals

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

Combined linkage and association sib-pair analysis for quantitative traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

A meta-analytic investigation of linkage and association of common leptin receptor (LEPR) polymorphisms with body mass index and waist circumference

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

Abnormal splicing of the leptin receptor in diabetic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

A follow-up linkage study for quantitative trait loci contributing to obesity-related phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

Human leptin receptor gene in obese Japanese subjects: evidence against either obesity-causing mutations or association of sequence variants with obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

Absence of linkage of obesity and energy metabolism to markers flanking homologues of rodent obesity genes in Pima Indians

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

The future of genetic studies of complex human diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

Structure and sequence variation at the human leptin receptor gene in lean and obese Pima Indians

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

Association studies in psychiatric genetics: what are we doing?

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

Positional cloning of a quantitative trait locus on chromosome 13q14 that influences immunoglobulin E levels and asthma

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

Genome scans and candidate gene approaches in the study of common diseases and variable drug responses

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

Haplotype tagging for the identification of common disease genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00213.2003

10.1152/PHYSIOLGENOMICS.00213.2003

21 January 2018

Identifiers

DOI

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11 January 2018

PubMed ID

14970363

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11 January 2018