Literature DB >> 28120836

From exomes to genomes: challenges and solutions in population-based genetic association studies.

Paul L Auer1, Suzanne M Leal2.   

Abstract

Mesh:

Year:  2017        PMID: 28120836      PMCID: PMC5386426          DOI: 10.1038/ejhg.2016.206

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


× No keyword cloud information.
  32 in total

1.  Pooled association tests for rare variants in exon-resequencing studies.

Authors:  Alkes L Price; Gregory V Kryukov; Paul I W de Bakker; Shaun M Purcell; Jeff Staples; Lee-Jen Wei; Shamil R Sunyaev
Journal:  Am J Hum Genet       Date:  2010-05-13       Impact factor: 11.025

2.  Power of deep, all-exon resequencing for discovery of human trait genes.

Authors:  Gregory V Kryukov; Alexander Shpunt; John A Stamatoyannopoulos; Shamil R Sunyaev
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-06       Impact factor: 11.205

3.  Linkage analysis of quantitative traits: increased power by using selected samples.

Authors:  G Carey; J Williamson
Journal:  Am J Hum Genet       Date:  1991-10       Impact factor: 11.025

4.  Low-coverage sequencing: implications for design of complex trait association studies.

Authors:  Yun Li; Carlo Sidore; Hyun Min Kang; Michael Boehnke; Gonçalo R Abecasis
Journal:  Genome Res       Date:  2011-04-01       Impact factor: 9.043

5.  Obama's Precision Medicine Initiative.

Authors:  Sharon F Terry
Journal:  Genet Test Mol Biomarkers       Date:  2015-03

6.  A global reference for human genetic variation.

Authors:  Adam Auton; Lisa D Brooks; Richard M Durbin; Erik P Garrison; Hyun Min Kang; Jan O Korbel; Jonathan L Marchini; Shane McCarthy; Gil A McVean; Gonçalo R Abecasis
Journal:  Nature       Date:  2015-10-01       Impact factor: 49.962

7.  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

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

Authors:  Andrew P Morris; Eleftheria Zeggini
Journal:  Genet Epidemiol       Date:  2010-02       Impact factor: 2.135

9.  Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.

Authors:  Paul L Auer; Alexander Teumer; Ursula Schick; Andrew O'Shaughnessy; Ken Sin Lo; Nathalie Chami; Chris Carlson; Simon de Denus; Marie-Pierre Dubé; Jeff Haessler; Rebecca D Jackson; Charles Kooperberg; Louis-Philippe Lemieux Perreault; Matthias Nauck; Ulrike Peters; John D Rioux; Frank Schmidt; Valérie Turcot; Uwe Völker; Henry Völzke; Andreas Greinacher; Li Hsu; Jean-Claude Tardif; George A Diaz; Alexander P Reiner; Guillaume Lettre
Journal:  Nat Genet       Date:  2014-04-28       Impact factor: 38.330

10.  The UK10K project identifies rare variants in health and disease.

Authors:  Klaudia Walter; Josine L Min; Jie Huang; Lucy Crooks; Yasin Memari; Shane McCarthy; John R B Perry; ChangJiang Xu; Marta Futema; Daniel Lawson; Valentina Iotchkova; Stephan Schiffels; Audrey E Hendricks; Petr Danecek; Rui Li; James Floyd; Louise V Wain; Inês Barroso; Steve E Humphries; Matthew E Hurles; Eleftheria Zeggini; Jeffrey C Barrett; Vincent Plagnol; J Brent Richards; Celia M T Greenwood; Nicholas J Timpson; Richard Durbin; Nicole Soranzo
Journal:  Nature       Date:  2015-09-14       Impact factor: 49.962

View more
  1 in total

1.  Whole genome sequence association with E-selectin levels reveals loss-of-function variant in African Americans.

Authors:  Linda M Polfus; Laura M Raffield; Marsha M Wheeler; Russell P Tracy; Leslie A Lange; Guillaume Lettre; Amanda Miller; Adolfo Correa; Russell P Bowler; Joshua C Bis; Shabnam Salimi; Nancy Swords Jenny; Nathan Pankratz; Biqi Wang; Michael H Preuss; Lisheng Zhou; Arden Moscati; Girish N Nadkarni; Ruth J F Loos; Xue Zhong; Bingshan Li; Jill M Johnsen; Deborah A Nickerson; Alex P Reiner; Paul L Auer
Journal:  Hum Mol Genet       Date:  2019-02-01       Impact factor: 6.150

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.