Literature DB >> 21629274

Family-based designs for genome-wide association studies.

Jurg Ott1, Yoichiro Kamatani, Mark Lathrop.   

Abstract

Association mapping has successfully identified common SNPs associated with many diseases. However, the inability of this class of variation to account for most of the supposed heritability has led to a renewed interest in methods - primarily linkage analysis - to detect rare variants. Family designs allow for control of population stratification, investigations of questions such as parent-of-origin effects and other applications that are imperfectly or not readily addressed in case-control association studies. This article guides readers through the interface between linkage and association analysis, reviews the new methodologies and provides useful guidelines for applications. Just as effective SNP-genotyping tools helped to realize the potential of association studies, next-generation sequencing tools will benefit genetic studies by improving the power of family-based approaches.

Mesh:

Year:  2011        PMID: 21629274     DOI: 10.1038/nrg2989

Source DB:  PubMed          Journal:  Nat Rev Genet        ISSN: 1471-0056            Impact factor:   53.242


  127 in total

1.  Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified.

Authors:  H H Göring; J D Terwilliger
Journal:  Am J Hum Genet       Date:  2000-03-23       Impact factor: 11.025

2.  Genomic control for association studies.

Authors:  B Devlin; K Roeder
Journal:  Biometrics       Date:  1999-12       Impact factor: 2.571

3.  Personal genomes: The case of the missing heritability.

Authors:  Brendan Maher
Journal:  Nature       Date:  2008-11-06       Impact factor: 49.962

Review 4.  The TDT and other family-based tests for linkage disequilibrium and association.

Authors:  R S Spielman; W J Ewens
Journal:  Am J Hum Genet       Date:  1996-11       Impact factor: 11.025

5.  Detection of putative functional angiotensinogen (AGT) gene variants controlling plasma AGT levels by combined segregation-linkage analysis.

Authors:  Eva Brand; Nathalie Chatelain; Françoise Paillard; Laurence Tiret; Sophie Visvikis; Mark Lathrop; Florent Soubrier; Florence Demenais
Journal:  Eur J Hum Genet       Date:  2002-11       Impact factor: 4.246

6.  CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs.

Authors:  Anne-Christine Merveille; Erica E Davis; Anita Becker-Heck; Marie Legendre; Israel Amirav; Géraldine Bataille; John Belmont; Nicole Beydon; Frédéric Billen; Annick Clément; Cécile Clercx; André Coste; Rachelle Crosbie; Jacques de Blic; Stephane Deleuze; Philippe Duquesnoy; Denise Escalier; Estelle Escudier; Manfred Fliegauf; Judith Horvath; Kent Hill; Mark Jorissen; Jocelyne Just; Andreas Kispert; Mark Lathrop; Niki Tomas Loges; June K Marthin; Yukihide Momozawa; Guy Montantin; Kim G Nielsen; Heike Olbrich; Jean-François Papon; Isabelle Rayet; Gilles Roger; Miriam Schmidts; Henrique Tenreiro; Jeffrey A Towbin; Diana Zelenika; Hanswalter Zentgraf; Michel Georges; Anne-Sophie Lequarré; Nicholas Katsanis; Heymut Omran; Serge Amselem
Journal:  Nat Genet       Date:  2010-12-05       Impact factor: 38.330

7.  A novel approach to detect parent-of-origin effects from pedigree data with application to Beckwith-Wiedemann syndrome.

Authors:  Sanjay Shete; Robert C Elston; Yue Lu
Journal:  Ann Hum Genet       Date:  2007-06-18       Impact factor: 1.670

8.  High-resolution genetic mapping of the ACE-linked QTL influencing circulating ACE activity.

Authors:  Florent Soubrier; Sabrina Martin; Amalia Alonso; Sophie Visvikis; Laurence Tiret; Fumihiko Matsuda; G Mark Lathrop; Martin Farrall
Journal:  Eur J Hum Genet       Date:  2002-09       Impact factor: 4.246

9.  MHC fine mapping of human type 1 diabetes using the T1DGC data.

Authors:  C He; S Hamon; D Li; S Barral-Rodriguez; J Ott
Journal:  Diabetes Obes Metab       Date:  2009-02       Impact factor: 6.577

Review 10.  Exome sequencing: the sweet spot before whole genomes.

Authors:  Jamie K Teer; James C Mullikin
Journal:  Hum Mol Genet       Date:  2010-08-12       Impact factor: 6.150

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  132 in total

Review 1.  Genetic contributions to behavioural diversity at the gene-environment interface.

Authors:  Andres Bendesky; Cornelia I Bargmann
Journal:  Nat Rev Genet       Date:  2011-11-08       Impact factor: 53.242

2.  Family-based association studies for next-generation sequencing.

Authors:  Yun Zhu; Momiao Xiong
Journal:  Am J Hum Genet       Date:  2012-06-08       Impact factor: 11.025

Review 3.  A guide on gene prioritization in studies of psychiatric disorders.

Authors:  Sven Stringer; Kim C Cerrone; Wim van den Brink; Julia F van den Berg; Damiaan Denys; Rene S Kahn; Eske M Derks
Journal:  Int J Methods Psychiatr Res       Date:  2015-07-31       Impact factor: 4.035

4.  Rare-variant extensions of the transmission disequilibrium test: application to autism exome sequence data.

Authors:  Zongxiao He; Brian J O'Roak; Joshua D Smith; Gao Wang; Stanley Hooker; Regie Lyn P Santos-Cortez; Biao Li; Mengyuan Kan; Nik Krumm; Deborah A Nickerson; Jay Shendure; Evan E Eichler; Suzanne M Leal
Journal:  Am J Hum Genet       Date:  2013-12-19       Impact factor: 11.025

5.  Combined linkage disequilibrium and linkage mapping: Bayesian multilocus approach.

Authors:  P Pikkuhookana; M J Sillanpää
Journal:  Heredity (Edinb)       Date:  2013-11-20       Impact factor: 3.821

6.  A SNP in the HTT promoter alters NF-κB binding and is a bidirectional genetic modifier of Huntington disease.

Authors:  Kristina Bečanović; Anne Nørremølle; Scott J Neal; Chris Kay; Jennifer A Collins; David Arenillas; Tobias Lilja; Giulia Gaudenzi; Shiana Manoharan; Crystal N Doty; Jessalyn Beck; Nayana Lahiri; Elodie Portales-Casamar; Simon C Warby; Colúm Connolly; Rebecca A G De Souza; Sarah J Tabrizi; Ola Hermanson; Douglas R Langbehn; Michael R Hayden; Wyeth W Wasserman; Blair R Leavitt
Journal:  Nat Neurosci       Date:  2015-05-04       Impact factor: 24.884

Review 7.  The role of replicates for error mitigation in next-generation sequencing.

Authors:  Kimberly Robasky; Nathan E Lewis; George M Church
Journal:  Nat Rev Genet       Date:  2013-12-10       Impact factor: 53.242

8.  Cohort profile: Wisconsin longitudinal study (WLS).

Authors:  Pamela Herd; Deborah Carr; Carol Roan
Journal:  Int J Epidemiol       Date:  2014-02       Impact factor: 7.196

Review 9.  The genetic basis of female reproductive disorders: etiology and clinical testing.

Authors:  Lawrence C Layman
Journal:  Mol Cell Endocrinol       Date:  2013-03-14       Impact factor: 4.102

10.  Fast Genome-Wide QTL Association Mapping on Pedigree and Population Data.

Authors:  Hua Zhou; John Blangero; Thomas D Dyer; Kei-Hang K Chan; Kenneth Lange; Eric M Sobel
Journal:  Genet Epidemiol       Date:  2016-12-12       Impact factor: 2.135

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