Literature DB >> 21522172

Defining rare variants by their frequencies in controls may increase type I error.

Mathieu Lemire.   

Abstract

Mesh：

Year:  2011        PMID： 21522172     DOI： 10.1038/ng.818

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


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  5 in total

1.  Are rare variants responsible for susceptibility to complex diseases?

Authors:  J K Pritchard
Journal:  Am J Hum Genet       Date:  2001-06-12       Impact factor: 11.025

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

Authors:  Bingshan Li; Suzanne M Leal
Journal:  Am J Hum Genet       Date:  2008-08-07       Impact factor: 11.025

3.  From genotypes to genes: doubling the sample size.

Authors:  P D Sasieni
Journal:  Biometrics       Date:  1997-12       Impact factor: 2.571

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

Authors:  Christopher T Johansen; Jian Wang; Matthew B Lanktree; Henian Cao; Adam D McIntyre; Matthew R Ban; Rebecca A Martins; Brooke A Kennedy; Reina G Hassell; Maartje E Visser; Stephen M Schwartz; Benjamin F Voight; Roberto Elosua; Veikko Salomaa; Christopher J O'Donnell; Geesje M Dallinga-Thie; Sonia S Anand; Salim Yusuf; Murray W Huff; Sekar Kathiresan; Robert A Hegele
Journal:  Nat Genet       Date:  2010-07-25       Impact factor: 38.330

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

Authors:  Bo Eskerod Madsen; Sharon R Browning
Journal:  PLoS Genet       Date:  2009-02-13       Impact factor: 5.917
  5 in total
  8 in total

1.  The role of SHANK2 rare variants in schizophrenia susceptibility.

Authors:  J Costas
Journal:  Mol Psychiatry       Date:  2015-08-25       Impact factor: 15.992

2.  Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders.

Authors:  E M Kenny; P Cormican; S Furlong; E Heron; G Kenny; C Fahey; E Kelleher; S Ennis; D Tropea; R Anney; A P Corvin; G Donohoe; L Gallagher; M Gill; D W Morris
Journal:  Mol Psychiatry       Date:  2013-10-15       Impact factor: 15.992

3.  Excess of rare variants in non-genome-wide association study candidate genes in patients with hypertriglyceridemia.

Authors:  Christopher T Johansen; Jian Wang; Adam D McIntyre; Rebecca A Martins; Matthew R Ban; Matthew B Lanktree; Murray W Huff; Miklós Péterfy; Margarete Mehrabian; Aldons J Lusis; Sekar Kathiresan; Sonia S Anand; Salim Yusuf; Ann-Hwee Lee; Laurie H Glimcher; Henian Cao; Robert A Hegele
Journal:  Circ Cardiovasc Genet       Date:  2011-12-01

4.  Role of rare variants in undetermined multiple adenomatous polyposis and early-onset colorectal cancer.

Authors:  Jérémie H Lefevre; Carolina Bonilla; Chrystelle Colas; Bruce Winney; Elaine Johnstone; Susan Tonks; Tammy Day; Katarzyna Hutnik; Abdelhamid Boumertit; Florent Soubrier; Rachel Midgley; David Kerr; Yann Parc; Walter F Bodmer
Journal:  J Hum Genet       Date:  2012-08-09       Impact factor: 3.172

5.  Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study.

Authors:  Z Hawi; T D R Cummins; J Tong; M Arcos-Burgos; Q Zhao; N Matthews; D P Newman; B Johnson; A Vance; H S Heussler; F Levy; S Easteal; N R Wray; E Kenny; D Morris; L Kent; M Gill; M A Bellgrove
Journal:  Mol Psychiatry       Date:  2016-07-26       Impact factor: 15.992

6.  A fast and noise-resilient approach to detect rare-variant associations with deep sequencing data for complex disorders.

Authors:  Yee Him Cheung; Gao Wang; Suzanne M Leal; Shuang Wang
Journal:  Genet Epidemiol       Date:  2012-08-03       Impact factor: 2.135

7.  A biologically informed method for detecting rare variant associations.

Authors:  Carrie Colleen Buchanan Moore; Anna Okula Basile; John Robert Wallace; Alex Thomas Frase; Marylyn DeRiggi Ritchie
Journal:  BioData Min       Date:  2016-08-30       Impact factor: 2.522

8.  Rare SHANK2 variants in schizophrenia.

Authors:  S Peykov; S Berkel; F Degenhardt; M Rietschel; M M Nöthen; G A Rappold
Journal:  Mol Psychiatry       Date:  2015-08-25       Impact factor: 15.992
  8 in total

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