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

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

doi:10.1093/hmg/ddq307

Public

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

Published in Human Molecular Genetics • Jul 27, 2010

Authors:

Richard Anney

Lambertus Klei

Dalila Pinto

Abstract

Although autism spectrum disorders (ASDs) have a substantial genetic basis, most of the known genetic risk has been traced to rare variants, principally copy number variants (CNVs). To identify common risk variation, the Autism Genome Project (AGP) Consortium genotyped 1558 rigorously defined ASD fa...

Subject

Biology

Genetics

Single-nucleotide polymorphism

Research Assistant

AI chat, annotations, notes & similar papers

Finding related papers...

Discussions

(0)

No comments yet

Be the first to share your thoughts!