Literature DB >> 20862653

Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies.

Andrew Crossett1, Brian P Kent, Lambertus Klei, Steven Ringquist, Massimo Trucco, Kathryn Roeder, Bernie Devlin.   

Abstract

We propose a method to analyze family-based samples together with unrelated cases and controls. The method builds on the idea of matched case-control analysis using conditional logistic regression (CLR). For each trio within the family, a case (the proband) and matched pseudo-controls are constructed, based upon the transmitted and untransmitted alleles. Unrelated controls, matched by genetic ancestry, supplement the sample of pseudo-controls; likewise unrelated cases are also paired with genetically matched controls. Within each matched stratum, the case genotype is contrasted with control/pseudo-control genotypes via CLR, using a method we call matched-CLR (mCLR). Eigenanalysis of numerous SNP genotypes provides a tool for mapping genetic ancestry. The result of such an analysis can be thought of as a multidimensional map, or eigenmap, in which the relative genetic similarities and differences amongst individuals is encoded in the map. Once constructed, new individuals can be projected onto the ancestry map based on their genotypes. Successful differentiation of individuals of distinct ancestry depends on having a diverse, yet representative sample from which to construct the ancestry map. Once samples are well-matched, mCLR yields comparable power to competing methods while ensuring excellent control over Type I error.

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Year:  2010        PMID: 20862653      PMCID: PMC4629477          DOI: 10.1002/sim.4057

Source DB:  PubMed          Journal:  Stat Med        ISSN: 0277-6715            Impact factor:   2.373


  42 in total

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2.  Case-control association studies with matching and genomic controlling.

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Journal:  Neural Comput       Date:  2004-10       Impact factor: 2.026

4.  The transmission/disequilibrium test and parental-genotype reconstruction: the reconstruction-combined transmission/ disequilibrium test.

Authors:  M Knapp
Journal:  Am J Hum Genet       Date:  1999-03       Impact factor: 11.025

5.  Principal components analysis corrects for stratification in genome-wide association studies.

Authors:  Alkes L Price; Nick J Patterson; Robert M Plenge; Michael E Weinblatt; Nancy A Shadick; David Reich
Journal:  Nat Genet       Date:  2006-07-23       Impact factor: 38.330

6.  Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.

Authors:  Lucia A Hindorff; Praveen Sethupathy; Heather A Junkins; Erin M Ramos; Jayashri P Mehta; Francis S Collins; Teri A Manolio
Journal:  Proc Natl Acad Sci U S A       Date:  2009-05-27       Impact factor: 11.205

7.  A simple and improved correction for population stratification in case-control studies.

Authors:  Michael P Epstein; Andrew S Allen; Glen A Satten
Journal:  Am J Hum Genet       Date:  2007-03-29       Impact factor: 11.025

8.  Genotype-based matching to correct for population stratification in large-scale case-control genetic association studies.

Authors:  Weihua Guan; Liming Liang; Michael Boehnke; Gonçalo R Abecasis
Journal:  Genet Epidemiol       Date:  2009-09       Impact factor: 2.135

9.  Discovering genetic ancestry using spectral graph theory.

Authors:  Ann B Lee; Diana Luca; Lambertus Klei; Bernie Devlin; Kathryn Roeder
Journal:  Genet Epidemiol       Date:  2010-01       Impact factor: 2.135

10.  Population structure and eigenanalysis.

Authors:  Nick Patterson; Alkes L Price; David Reich
Journal:  PLoS Genet       Date:  2006-12       Impact factor: 5.917

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1.  Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism.

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Review 2.  Do common variants play a role in risk for autism? Evidence and theoretical musings.

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Journal:  Brain Res       Date:  2010-11-12       Impact factor: 3.252

3.  A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?

Authors:  Pauline Chaste; Lambertus Klei; Stephan J Sanders; Vanessa Hus; Michael T Murtha; Jennifer K Lowe; A Jeremy Willsey; Daniel Moreno-De-Luca; Timothy W Yu; Eric Fombonne; Daniel Geschwind; Dorothy E Grice; David H Ledbetter; Shrikant M Mane; Donna M Martin; Eric M Morrow; Christopher A Walsh; James S Sutcliffe; Christa Lese Martin; Arthur L Beaudet; Catherine Lord; Matthew W State; Edwin H Cook; Bernie Devlin
Journal:  Biol Psychiatry       Date:  2014-09-30       Impact factor: 13.382

4.  Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.

Authors:  Stephan J Sanders; A Gulhan Ercan-Sencicek; Vanessa Hus; Rui Luo; Michael T Murtha; Daniel Moreno-De-Luca; Su H Chu; Michael P Moreau; Abha R Gupta; Susanne A Thomson; Christopher E Mason; Kaya Bilguvar; Patricia B S Celestino-Soper; Murim Choi; Emily L Crawford; Lea Davis; Nicole R Davis Wright; Rahul M Dhodapkar; Michael DiCola; Nicholas M DiLullo; Thomas V Fernandez; Vikram Fielding-Singh; Daniel O Fishman; Stephanie Frahm; Rouben Garagaloyan; Gerald S Goh; Sindhuja Kammela; Lambertus Klei; Jennifer K Lowe; Sabata C Lund; Anna D McGrew; Kyle A Meyer; William J Moffat; John D Murdoch; Brian J O'Roak; Gordon T Ober; Rebecca S Pottenger; Melanie J Raubeson; Youeun Song; Qi Wang; Brian L Yaspan; Timothy W Yu; Ilana R Yurkiewicz; Arthur L Beaudet; Rita M Cantor; Martin Curland; Dorothy E Grice; Murat Günel; Richard P Lifton; Shrikant M Mane; Donna M Martin; Chad A Shaw; Michael Sheldon; Jay A Tischfield; Christopher A Walsh; Eric M Morrow; David H Ledbetter; Eric Fombonne; Catherine Lord; Christa Lese Martin; Andrew I Brooks; James S Sutcliffe; Edwin H Cook; Daniel Geschwind; Kathryn Roeder; Bernie Devlin; Matthew W State
Journal:  Neuron       Date:  2011-06-09       Impact factor: 17.173

5.  The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum.

Authors:  Behrang Mahjani; Lambertus Klei; Manuel Mattheisen; Matthew W Halvorsen; Abraham Reichenberg; Kathryn Roeder; Nancy L Pedersen; Julia Boberg; Elles de Schipper; Cynthia M Bulik; Mikael Landén; Bengt Fundín; David Mataix-Cols; Sven Sandin; Christina M Hultman; James J Crowley; Joseph D Buxbaum; Christian Rück; Bernie Devlin; Dorothy E Grice
Journal:  Am J Psychiatry       Date:  2021-11-18       Impact factor: 18.112

6.  Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.

Authors:  Günter U Höglinger; Nadine M Melhem; Dennis W Dickson; Patrick M A Sleiman; Li-San Wang; Lambertus Klei; Rosa Rademakers; Rohan de Silva; Irene Litvan; David E Riley; John C van Swieten; Peter Heutink; Zbigniew K Wszolek; Ryan J Uitti; Jana Vandrovcova; Howard I Hurtig; Rachel G Gross; Walter Maetzler; Stefano Goldwurm; Eduardo Tolosa; Barbara Borroni; Pau Pastor; Laura B Cantwell; Mi Ryung Han; Allissa Dillman; Marcel P van der Brug; J Raphael Gibbs; Mark R Cookson; Dena G Hernandez; Andrew B Singleton; Matthew J Farrer; Chang-En Yu; Lawrence I Golbe; Tamas Revesz; John Hardy; Andrew J Lees; Bernie Devlin; Hakon Hakonarson; Ulrich Müller; Gerard D Schellenberg
Journal:  Nat Genet       Date:  2011-06-19       Impact factor: 38.330

7.  A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies.

Authors:  Corneliu A Bodea; Benjamin M Neale; Stephan Ripke; Mark J Daly; Bernie Devlin; Kathryn Roeder
Journal:  Am J Hum Genet       Date:  2016-04-14       Impact factor: 11.025

8.  A genome-wide scan for common alleles affecting risk for autism.

Authors:  Richard Anney; Lambertus Klei; Dalila Pinto; Regina Regan; Judith Conroy; Tiago R Magalhaes; Catarina Correia; Brett S Abrahams; Nuala Sykes; Alistair T Pagnamenta; Joana Almeida; Elena Bacchelli; Anthony J Bailey; Gillian Baird; Agatino Battaglia; Tom Berney; Nadia Bolshakova; Sven Bölte; Patrick F Bolton; Thomas Bourgeron; Sean Brennan; Jessica Brian; Andrew R Carson; Guillermo Casallo; Jillian Casey; Su H Chu; Lynne Cochrane; Christina Corsello; Emily L Crawford; Andrew Crossett; Geraldine Dawson; Maretha de Jonge; Richard Delorme; Irene Drmic; Eftichia Duketis; Frederico Duque; Annette Estes; Penny Farrar; Bridget A Fernandez; Susan E Folstein; Eric Fombonne; Christine M Freitag; John Gilbert; Christopher Gillberg; Joseph T Glessner; Jeremy Goldberg; Jonathan Green; Stephen J Guter; Hakon Hakonarson; Elizabeth A Heron; Matthew Hill; Richard Holt; Jennifer L Howe; Gillian Hughes; Vanessa Hus; Roberta Igliozzi; Cecilia Kim; Sabine M Klauck; Alexander Kolevzon; Olena Korvatska; Vlad Kustanovich; Clara M Lajonchere; Janine A Lamb; Magdalena Laskawiec; Marion Leboyer; Ann Le Couteur; Bennett L Leventhal; Anath C Lionel; Xiao-Qing Liu; Catherine Lord; Linda Lotspeich; Sabata C Lund; Elena Maestrini; William Mahoney; Carine Mantoulan; Christian R Marshall; Helen McConachie; Christopher J McDougle; Jane McGrath; William M McMahon; Nadine M Melhem; Alison Merikangas; Ohsuke Migita; Nancy J Minshew; Ghazala K Mirza; Jeff Munson; Stanley F Nelson; Carolyn Noakes; Abdul Noor; Gudrun Nygren; Guiomar Oliveira; Katerina Papanikolaou; Jeremy R Parr; Barbara Parrini; Tara Paton; Andrew Pickles; Joseph Piven; David J Posey; Annemarie Poustka; Fritz Poustka; Aparna Prasad; Jiannis Ragoussis; Katy Renshaw; Jessica Rickaby; Wendy Roberts; Kathryn Roeder; Bernadette Roge; Michael L Rutter; Laura J Bierut; John P Rice; Jeff Salt; Katherine Sansom; Daisuke Sato; Ricardo Segurado; Lili Senman; Naisha Shah; Val C Sheffield; Latha Soorya; Inês Sousa; Vera Stoppioni; Christina Strawbridge; Raffaella Tancredi; Katherine Tansey; Bhooma Thiruvahindrapduram; Ann P Thompson; Susanne Thomson; Ana Tryfon; John Tsiantis; Herman Van Engeland; John B Vincent; Fred Volkmar; Simon Wallace; Kai Wang; Zhouzhi Wang; Thomas H Wassink; Kirsty Wing; Kerstin Wittemeyer; Shawn Wood; Brian L Yaspan; Danielle Zurawiecki; Lonnie Zwaigenbaum; Catalina Betancur; Joseph D Buxbaum; Rita M Cantor; Edwin H Cook; Hilary Coon; Michael L Cuccaro; Louise Gallagher; Daniel H Geschwind; Michael Gill; Jonathan L Haines; Judith Miller; Anthony P Monaco; John I Nurnberger; Andrew D Paterson; Margaret A Pericak-Vance; Gerard D Schellenberg; Stephen W Scherer; James S Sutcliffe; Peter Szatmari; Astrid M Vicente; Veronica J Vieland; Ellen M Wijsman; Bernie Devlin; Sean Ennis; Joachim Hallmayer
Journal:  Hum Mol Genet       Date:  2010-07-27       Impact factor: 6.150

9.  Functional rare and low frequency variants in BLK and BANK1 contribute to human lupus.

Authors:  Simon H Jiang; Vicki Athanasopoulos; Julia I Ellyard; Aaron Chuah; Jean Cappello; Amelia Cook; Savit B Prabhu; Jacob Cardenas; Jinghua Gu; Maurice Stanley; Jonathan A Roco; Ilenia Papa; Mehmet Yabas; Giles D Walters; Gaetan Burgio; Kathryn McKeon; James M Byers; Charlotte Burrin; Anselm Enders; Lisa A Miosge; Pablo F Canete; Marija Jelusic; Velibor Tasic; Adrian C Lungu; Stephen I Alexander; Arthur R Kitching; David A Fulcher; Nan Shen; Todor Arsov; Paul A Gatenby; Jeff J Babon; Dominic F Mallon; Carmen de Lucas Collantes; Eric A Stone; Philip Wu; Matthew A Field; Thomas D Andrews; Eun Cho; Virginia Pascual; Matthew C Cook; Carola G Vinuesa
Journal:  Nat Commun       Date:  2019-05-17       Impact factor: 14.919

10.  Individual common variants exert weak effects on the risk for autism spectrum disorders.

Authors:  Richard Anney; Lambertus Klei; Dalila Pinto; Joana Almeida; Elena Bacchelli; Gillian Baird; Nadia Bolshakova; Sven Bölte; Patrick F Bolton; Thomas Bourgeron; Sean Brennan; Jessica Brian; Jillian Casey; Judith Conroy; Catarina Correia; Christina Corsello; Emily L Crawford; Maretha de Jonge; Richard Delorme; Eftichia Duketis; Frederico Duque; Annette Estes; Penny Farrar; Bridget A Fernandez; Susan E Folstein; Eric Fombonne; John Gilbert; Christopher Gillberg; Joseph T Glessner; Andrew Green; Jonathan Green; Stephen J Guter; Elizabeth A Heron; Richard Holt; Jennifer L Howe; Gillian Hughes; Vanessa Hus; Roberta Igliozzi; Suma Jacob; Graham P Kenny; Cecilia Kim; Alexander Kolevzon; Vlad Kustanovich; Clara M Lajonchere; Janine A Lamb; Miriam Law-Smith; Marion Leboyer; Ann Le Couteur; Bennett L Leventhal; Xiao-Qing Liu; Frances Lombard; Catherine Lord; Linda Lotspeich; Sabata C Lund; Tiago R Magalhaes; Carine Mantoulan; Christopher J McDougle; Nadine M Melhem; Alison Merikangas; Nancy J Minshew; Ghazala K Mirza; Jeff Munson; Carolyn Noakes; Gudrun Nygren; Katerina Papanikolaou; Alistair T Pagnamenta; Barbara Parrini; Tara Paton; Andrew Pickles; David J Posey; Fritz Poustka; Jiannis Ragoussis; Regina Regan; Wendy Roberts; Kathryn Roeder; Bernadette Roge; Michael L Rutter; Sabine Schlitt; Naisha Shah; Val C Sheffield; Latha Soorya; Inês Sousa; Vera Stoppioni; Nuala Sykes; Raffaella Tancredi; Ann P Thompson; Susanne Thomson; Ana Tryfon; John Tsiantis; Herman Van Engeland; John B Vincent; Fred Volkmar; J A S Vorstman; Simon Wallace; Kirsty Wing; Kerstin Wittemeyer; Shawn Wood; Danielle Zurawiecki; Lonnie Zwaigenbaum; Anthony J Bailey; Agatino Battaglia; Rita M Cantor; Hilary Coon; Michael L Cuccaro; Geraldine Dawson; Sean Ennis; Christine M Freitag; Daniel H Geschwind; Jonathan L Haines; Sabine M Klauck; William M McMahon; Elena Maestrini; Judith Miller; Anthony P Monaco; Stanley F Nelson; John I Nurnberger; Guiomar Oliveira; Jeremy R Parr; Margaret A Pericak-Vance; Joseph Piven; Gerard D Schellenberg; Stephen W Scherer; Astrid M Vicente; Thomas H Wassink; Ellen M Wijsman; Catalina Betancur; Joseph D Buxbaum; Edwin H Cook; Louise Gallagher; Michael Gill; Joachim Hallmayer; Andrew D Paterson; James S Sutcliffe; Peter Szatmari; Veronica J Vieland; Hakon Hakonarson; Bernie Devlin
Journal:  Hum Mol Genet       Date:  2012-07-26       Impact factor: 6.150

  10 in total

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