Literature DB >> 21047260

Rare variant association analysis methods for complex traits.

Jennifer Asimit1, Eleftheria Zeggini.   

Abstract

There has been increasing interest in rare variants and their association with disease, and several rare variant-disease associations have already been detected. The usual association tests for common variants are underpowered for detecting variants of lower frequency, so alternative approaches are required. In addition to reviewing the association analysis methods for rare variants, we discuss the limitations of genome-wide association studies in identifying rare variants and the problems that arise in the imputation of rare variants.

Mesh:

Year:  2010        PMID: 21047260     DOI: 10.1146/annurev-genet-102209-163421

Source DB:  PubMed          Journal:  Annu Rev Genet        ISSN: 0066-4197            Impact factor:   16.830


  135 in total

1.  Rare versus common variants in pharmacogenetics: SLCO1B1 variation and methotrexate disposition.

Authors:  Laura B Ramsey; Gitte H Bruun; Wenjian Yang; Lisa R Treviño; Selina Vattathil; Paul Scheet; Cheng Cheng; Gary L Rosner; Kathleen M Giacomini; Yiping Fan; Alex Sparreboom; Torben S Mikkelsen; Thomas J Corydon; Ching-Hon Pui; William E Evans; Mary V Relling
Journal:  Genome Res       Date:  2011-12-06       Impact factor: 9.043

Review 2.  Natural variation in Arabidopsis: from molecular genetics to ecological genomics.

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Journal:  Plant Physiol       Date:  2011-12-06       Impact factor: 8.340

3.  Exome sequencing and the genetic basis of complex traits.

Authors:  Adam Kiezun; Kiran Garimella; Ron Do; Nathan O Stitziel; Benjamin M Neale; Paul J McLaren; Namrata Gupta; Pamela Sklar; Patrick F Sullivan; Jennifer L Moran; Christina M Hultman; Paul Lichtenstein; Patrik Magnusson; Thomas Lehner; Yin Yao Shugart; Alkes L Price; Paul I W de Bakker; Shaun M Purcell; Shamil R Sunyaev
Journal:  Nat Genet       Date:  2012-05-29       Impact factor: 38.330

4.  Comprehensive evaluation of imputation performance in African Americans.

Authors:  Pritam Chanda; Naoya Yuhki; Man Li; Joel S Bader; Alex Hartz; Eric Boerwinkle; W H Linda Kao; Dan E Arking
Journal:  J Hum Genet       Date:  2012-05-31       Impact factor: 3.172

5.  Incorporating model uncertainty in detecting rare variants: the Bayesian risk index.

Authors:  Melanie A Quintana; Jonine L Berstein; Duncan C Thomas; David V Conti
Journal:  Genet Epidemiol       Date:  2011-08-26       Impact factor: 2.135

6.  Tests of association for rare variants: case control mutation screening.

Authors:  Sean V Tavtigian; Mia Hashibe; Alun Thomas
Journal:  Nat Rev Genet       Date:  2011-02-01       Impact factor: 53.242

7.  Incorporating molecular and functional context into the analysis and prioritization of human variants associated with cancer.

Authors:  Thomas A Peterson; Nathan L Nehrt; Dohwan Park; Maricel G Kann
Journal:  J Am Med Inform Assoc       Date:  2012 Mar-Apr       Impact factor: 4.497

8.  KALRN Rare and Common Variants and Susceptibility to Ischemic Stroke in Chinese Han Population.

Authors:  Meizheng Dang; Zhenzhen Wang; Ruyou Zhang; Xiaoying Li; Yanqing Peng; Xuesong Han; Litao Sun; Jiawei Tian
Journal:  Neuromolecular Med       Date:  2015-04-28       Impact factor: 3.843

9.  Rare nonsynonymous exonic variants in addiction and behavioral disinhibition.

Authors:  Scott I Vrieze; Shuang Feng; Michael B Miller; Brian M Hicks; Nathan Pankratz; Gonçalo R Abecasis; William G Iacono; Matt McGue
Journal:  Biol Psychiatry       Date:  2013-10-04       Impact factor: 13.382

10.  Family-based study of AVPR1B association and interaction with stressful life events on depression and anxiety in suicide attempts.

Authors:  Yair J Ben-Efraim; Danuta Wasserman; Jerzy Wasserman; Marcus Sokolowski
Journal:  Neuropsychopharmacology       Date:  2013-02-19       Impact factor: 7.853

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