A unified method for detecting secondary trait associations with rare variants: application to sequence data (Q30578001)

14 August 2017

A unified method for detecting secondary trait associations with rare variants: application to sequence data (English)

1 reference

14 August 2017

2

Suzanne M Leal

1 reference

14 August 2017

Dajiang J Liu

1

1 reference

14 August 2017

15 November 2012

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14 August 2017

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14 August 2017

8

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14 August 2017

11

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14 August 2017

e1003075

1 reference

Creative Commons Attribution 4.0 International

14 August 2017

start time

15 November 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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A flexible likelihood framework for detecting associations with secondary phenotypes in genetic studies using selected samples: application to sequence data

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A rare penetrant mutation in CFH confers high risk of age-related macular degeneration.

20 June 2018

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Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability

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Comparison of statistical tests for disease association with rare variants

20 June 2018

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Rare-variant association testing for sequencing data with the sequence kernel association test

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Population sequencing of two endocannabinoid metabolic genes identifies rare and common regulatory variants associated with extreme obesity and metabolite level

20 June 2018

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A Novel Adaptive Method for the Analysis of Next-Generation Sequencing Data to Detect Complex Trait Associations with Rare Variants Due to Gene Main Effects and Interactions

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A covering method for detecting genetic associations between rare variants and common phenotypes

20 June 2018

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Biological, clinical and population relevance of 95 loci for blood lipids

20 June 2018

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

20 June 2018

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Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease

20 June 2018

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Genome-wide association study of blood pressure and hypertension

20 June 2018

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Validating, augmenting and refining genome-wide association signals

20 June 2018

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

20 June 2018

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20 June 2018

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20 June 2018

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

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The genetic susceptibility to type 2 diabetes may be modulated by obesity status: implications for association studies

20 June 2018

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20 June 2018

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

20 June 2018

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Maximum-likelihood estimation of demographic parameters using the frequency spectrum of unlinked single-nucleotide polymorphisms

20 June 2018

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Single nucleotide polymorphisms in the apolipoprotein B and low density lipoprotein receptor genes affect response to antihypertensive treatment

20 June 2018

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Mutation rates differ among regions of the mammalian genome

20 June 2018

1 reference

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A polymorphism within the G6PC2 gene is associated with fasting plasma glucose levels

20 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003075

Meta-analysis of genetic association studies.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003075

Common disorders are quantitative traits

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003075

Are common disease susceptibility alleles the same in outbred and founder populations?

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23166519

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Closing in on complex traits

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23166519

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PGEN.1003075

1 reference

release_xv4gtb4xr5eofbzlvgowxdbfc4

14 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/xv4gtb4xr5eofbzlvgowxdbfc4

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMC publication ID

3499373

1 reference

PMC publication ID

3499373

14 August 2017

PubMed publication ID

23166519

1 reference

PMC publication ID

3499373