(Q34154481)

31 July 2017

title

The empirical power of rare variant association methods: results from sanger sequencing in 1,998 individuals (English)

1 reference

31 July 2017

3

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31 July 2017

Martin Ladouceur

1

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31 July 2017

Zari Dastani

series ordinal

2

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31 July 2017

Celia M T Greenwood

series ordinal

4

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31 July 2017

J Brent Richards

series ordinal

5

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31 July 2017

publication date

2 February 2012

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31 July 2017

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31 July 2017

volume

8

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31 July 2017

issue

2

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31 July 2017

page(s)

e1002496

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Creative Commons Attribution 4.0 International

31 July 2017

copyright license

start time

2 February 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Testing for an unusual distribution of rare variants

5 July 2018

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

5 July 2018

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Replication strategies for rare variant complex trait association studies via next-generation sequencing

5 July 2018

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Progress and promise of genome-wide association studies for human complex trait genetics

5 July 2018

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To identify associations with rare variants, just WHaIT: Weighted haplotype and imputation-based tests

5 July 2018

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Rare variant association analysis methods for complex traits

5 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

5 July 2018

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

5 July 2018

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Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability

5 July 2018

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5 July 2018

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

5 July 2018

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Approaches for evaluating rare polymorphisms in genetic association studies

5 July 2018

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A genome-wide association study reveals variants in ARL15 that influence adiponectin levels

5 July 2018

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Detecting rare variants for complex traits using family and unrelated data

5 July 2018

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

5 July 2018

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Association tests using kernel-based measures of multi-locus genotype similarity between individuals

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Discovery of rare variants via sequencing: implications for the design of complex trait association studies

5 July 2018

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

5 July 2018

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Next-generation sequencing: from basic research to diagnostics

5 July 2018

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5 July 2018

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5 July 2018

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

5 July 2018

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Common and rare variants in multifactorial susceptibility to common diseases

5 July 2018

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Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.

5 July 2018

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The CoLaus study: a population-based study to investigate the epidemiology and genetic determinants of cardiovascular risk factors and metabolic syndrome

5 July 2018

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Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses

5 July 2018

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Genetic variation in ABC transporter A1 contributes to HDL cholesterol in the general population

5 July 2018

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Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

5 July 2018

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The APC variants I1307K and E1317Q are associated with colorectal tumors, but not always with a family history.

5 July 2018

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Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC.

5 July 2018

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Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002496

Using SIFT and PolyPhen to predict loss-of-function and gain-of-function mutations

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002496

Modelling evolutionary processes in small populations: not as ideal as you think

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002496

10.1371/JOURNAL.PGEN.1002496

21 January 2018

Identifiers

DOI

1 reference

31 July 2017

1 reference

31 July 2017

1 reference