Comparison of statistical tests for association between rare variants and binary traits (Q34388775)

1 August 2017

Comparison of statistical tests for association between rare variants and binary traits (English)

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1 August 2017

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1 reference

John C Whittaker

3

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author name string

Silviu-Alin Bacanu

series ordinal

1

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PubMed ID

22912707

1 August 2017

Matthew R Nelson

series ordinal

2

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PubMed ID

22912707

1 August 2017

language of work or name

English

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publication date

9 August 2012

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1 August 2017

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1 August 2017

7

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1 August 2017

8

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1 August 2017

e42530

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Creative Commons Attribution 4.0 International

1 August 2017

start time

9 August 2012

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression

6 July 2018

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

6 July 2018

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An increased burden of common and rare lipid-associated risk alleles contributes to the phenotypic spectrum of hypertriglyceridemia

6 July 2018

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Testing for an unusual distribution of rare variants

6 July 2018

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A new testing strategy to identify rare variants with either risk or protective effect on disease

6 July 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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Hundreds of variants clustered in genomic loci and biological pathways affect human height

6 July 2018

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

6 July 2018

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

6 July 2018

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

6 July 2018

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Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

6 July 2018

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Common genetic variation and human traits

6 July 2018

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Genetic and metabolic determinants of plasma PCSK9 levels

6 July 2018

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

6 July 2018

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Assessing the evolutionary impact of amino acid mutations in the human genome

6 July 2018

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

6 July 2018

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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

6 July 2018

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Medical sequencing at the extremes of human body mass

6 July 2018

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A genome-wide association study identifies novel risk loci for type 2 diabetes

6 July 2018

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A spectrum of PCSK9 alleles contributes to plasma levels of low-density lipoprotein cholesterol.

6 July 2018

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Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample

6 July 2018

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Mutations in PCSK9 cause autosomal dominant hypercholesterolemia

6 July 2018

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Incorporation of covariates in multipoint model-free linkage analysis of binary traits: how important are unaffecteds?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3415421

Are rare variants responsible for susceptibility to complex diseases?

6 July 2018

1 reference

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NCBI's LocusLink and RefSeq

6 July 2018

1 reference

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An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3415421

Comparison of methods and sampling designs to test for association between rare variants and quantitative traits.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3415421

10.1371/JOURNAL.PONE.0042530

27 October 2018

Identifiers

DOI

1 reference

1 August 2017

0 references

1 reference

1 August 2017

1 reference

PubMed ID

22912707