(Q34175418)

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Methods for adjusting population structure and familial relatedness in association test for collective effect of multiple rare variants on quantitative traits

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Europe PubMed Central

PubMed publication ID

31 July 2017

Methods for adjusting population structure and familial relatedness in association test for collective effect of multiple rare variants on quantitative traits (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

population structure

1 reference

based on heuristic

inferred from title

quantitative trait

1 reference

based on heuristic

inferred from title

Michael A Province

5

object named as

Michael A Province

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Europe PubMed Central

PubMed publication ID

31 July 2017

author name string

Qunyuan Zhang

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Doyoung Chung

2

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Aldi Kraja

3

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Ingrid I Borecki

4

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

publication date

29 November 2011

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Europe PubMed Central

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31 July 2017

BMC Proceedings

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Europe PubMed Central

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31 July 2017

5 Suppl 9

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Europe PubMed Central

PubMed publication ID

31 July 2017

S35

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Europe PubMed Central

PubMed publication ID

31 July 2017

copyright license

Creative Commons Attribution 2.0 Generic

29 November 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

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Genetic Analysis Workshop 17 mini-exome simulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287871

5 July 2018

Genomics: In search of rare human variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287871

5 July 2018

Statistical analysis strategies for association studies involving rare variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287871

5 July 2018

Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287871

5 July 2018

Pooled association tests for rare variants in exon-resequencing studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287871

5 July 2018

A data-adaptive sum test for disease association with multiple common or rare variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287871

5 July 2018

An evaluation of statistical approaches to rare variant analysis in genetic association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287871

5 July 2018

Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287871

5 July 2018

A groupwise association test for rare mutations using a weighted sum statistic

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287871

5 July 2018

Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287871

5 July 2018

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287871

5 July 2018

Efficient control of population structure in model organism association mapping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287871

5 July 2018

Medical sequencing at the extremes of human body mass

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287871

5 July 2018

Principal components analysis corrects for stratification in genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287871

5 July 2018

Sequence variations in PCSK9, low LDL, and protection against coronary heart disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287871

5 July 2018

A unified mixed-model method for association mapping that accounts for multiple levels of relatedness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287871

5 July 2018

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3287871

5 July 2018

A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST).

1 reference

https://api.crossref.org/works/10.1186%2F1753-6561-5-S9-S35

21 January 2018

Identifiers

10.1186/1753-6561-5-S9-S35

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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https://api.fatcat.wiki/v0/release/vl53che6gnd5ha7ydpx2haxm3m

24 November 2022

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PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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