(Q33511799)

27 July 2017

title

Detecting rare variants for complex traits using family and unrelated data. (English)

1 reference

27 July 2017

1 reference

Xiaofeng Zhu

1

1 reference

27 July 2017

Tao Feng

2

1 reference

27 July 2017

Yali Li

3

1 reference

27 July 2017

Qing Lu

4

1 reference

27 July 2017

Robert C Elston

5

1 reference

27 July 2017

publication date

1 February 2010

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27 July 2017

1 reference

27 July 2017

volume

34

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27 July 2017

issue

2

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27 July 2017

page(s)

171-187

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Generalized linear modeling with regularization for detecting common disease rare haplotype association

27 July 2017

cites work

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A common allele on chromosome 9 associated with coronary heart disease

21 June 2018

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Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Are rare variants responsible for susceptibility to complex diseases?

21 June 2018

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21 June 2018

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A New Statistical Method for Haplotype Reconstruction from Population Data

21 June 2018

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

21 June 2018

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How many diseases does it take to map a gene with SNPs?

21 June 2018

1 reference

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21 June 2018

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Searching for genetic determinants in the new millennium

21 June 2018

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The future of genetic studies of complex human diseases

21 June 2018

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Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

21 June 2018

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Sizing up human height variation

21 June 2018

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Ten genes for inherited breast cancer.

31 October 2018

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New susceptibility locus for hypertension on chromosome 8q by efficient pedigree-breaking in an Italian isolate

31 October 2018

1 reference

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

31 October 2018

1 reference

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A genome-wide scan for obesity in African-Americans

31 October 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2811752

The emerging landscape of breast cancer susceptibility

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2811752

Haplotypes produced from rare variants in the promoter and coding regions of angiotensinogen contribute to variation in angiotensinogen levels

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2811752

The new genomics: global views of biology

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19847924

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Population genetics--making sense out of sequence

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19847924

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/GEPI.20449

1 reference

27 July 2017

1 reference

27 July 2017

1 reference