Genome-wide linkage scan of a pedigree with familial hypercholesterolemia suggests susceptibility loci on chromosomes 3q25-26 and 21q22. (Q34055467)

30 July 2017

title

Genome-wide linkage scan of a pedigree with familial hypercholesterolemia suggests susceptibility loci on chromosomes 3q25-26 and 21q22. (English)

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familial hypercholesterolemia

30 July 2017

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1 reference

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Xu Wang

1

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30 July 2017

Xin Li

2

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30 July 2017

Yong-Biao Zhang

3

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30 July 2017

Feng Zhang

4

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30 July 2017

Liyuan Sun

5

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30 July 2017

Jie Lin

6

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30 July 2017

Duen-Mei Wang

7

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30 July 2017

Lu-Ya Wang

8

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30 July 2017

language of work or name

English

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publication date

14 October 2011

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30 July 2017

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30 July 2017

volume

6

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30 July 2017

issue

10

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30 July 2017

page(s)

e24838

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Creative Commons Attribution 4.0 International

30 July 2017

copyright license

start time

14 October 2011

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

Mutations in the LDL receptor gene in four Chinese homozygous familial hypercholesterolemia phenotype patients

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The first genomewide interaction and locus-heterogeneity linkage scan in bipolar affective disorder: strong evidence of epistatic effects between loci on chromosomes 2q and 6q.

5 July 2018

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Mechanisms of disease: genetic causes of familial hypercholesterolemia

5 July 2018

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Diagnosis and screening for familial hypercholesterolaemia: finding the patients, finding the genes

5 July 2018

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ABCA1 and ABCG1 or ABCG4 act sequentially to remove cellular cholesterol and generate cholesterol-rich HDL.

5 July 2018

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How to model a complex trait. 1. General considerations and suggestions

5 July 2018

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Mutations in PCSK9 cause autosomal dominant hypercholesterolemia

5 July 2018

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Mutation in the ARH gene and a chromosome 13q locus influence cholesterol levels in a new form of digenic-recessive familial hypercholesterolemia

5 July 2018

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Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

5 July 2018

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Use of homozygosity mapping to identify a region on chromosome 1 bearing a defective gene that causes autosomal recessive homozygous hypercholesterolemia in two unrelated families

5 July 2018

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A new locus for autosomal recessive hypercholesterolemia maps to human chromosome 15q25-q26

5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia

5 July 2018

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5 July 2018

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Familial defective apolipoprotein B-100: low density lipoproteins with abnormal receptor binding

5 July 2018

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5 July 2018

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Genetic heterogeneity of autosomal dominant hypercholesterolemia in Mexico

5 July 2018

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Update of the Portuguese Familial Hypercholesterolaemia Study

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024838

High factor VIII levels in venous thromboembolism show linkage to imprinted loci on chromosomes 5 and 11

21 January 2018

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ABCG1 has a critical role in mediating cholesterol efflux to HDL and preventing cellular lipid accumulation

21 January 2018

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Genotypic Effect of ABCG1 gene promoter -257T>G polymorphism on coronary artery disease severity in Japanese men.

21 January 2018

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Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics

21 January 2018

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Replication of Linkage of Familial Combined Hyperlipidemia to Chromosome 1q With Additional Heterogeneous Effect of Apolipoprotein A-I/C-III/A-IV Locus

21 January 2018

1 reference

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How to model a complex trait. 2. Analysis with two disease loci

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22022364

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0024838

1 reference

30 July 2017

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30 July 2017

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