A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

Human Genetics

Volumn 131, Issue 4, 2012, Pages 565-579

  Casey, Jillian P ^a   Magalhaes, Tiago ^b,c,d   Conroy, Judith M ^a   Regan, Regina ^a   Shah, Naisha ^a   Anney, Richard ^e   Shields, Denis C ^a   Abrahams, Brett S ^f   Almeida, Joana ^g   Bacchelli, Elena ^h   Bailey, Anthony J ⁱ   Baird, Gillian ^j   Battaglia, Agatino ^k   Berney, Tom ^l   Bolshakova, Nadia ^e   Bolton, Patrick F ^m   Bourgeron, Thomas ⁿ   Brennan, Sean ^e   Cali, Phil ^o   Correia, Catarina ^b,c,d   Corsello, Christina ^p   Coutanche, Marc ^q   Dawson, Geraldine ^r,s   De Jonge, Maretha ^t   Delorme, Richard ^u   Duketis, Eftichia ^v   Duque, Frederico ^g   Estes, Annette ^w   Farrar, Penny ^x   Fernandez, Bridget A ^y   Folstein, Susan E ^z   Foley, Suzanne ^q   Fombonne, Eric ^aa   Freitag, Christine M ^v   Gilbert, John ^z   Gillberg, Christopher ^ab   Glessner, Joseph T ^ac   Green, Jonathan ^ad   Guter, Stephen J ^o   Hakonarson, Hakon ^ac,ae   Holt, Richard ^x   Hughes, Gillian ^e   Hus, Vanessa ^p   Igliozzi, Roberta ^k   Kim, Cecilia ^ac   Klauck, Sabine M ^af   Kolevzon, Alexander ^ag   Lamb, Janine A ^ah   Leboyer, Marion ^ai   Couteur, Ann Le ^l   Leventhal, Bennett L ^aj,ak   Lord, Catherine ^p   Lund, Sabata C ^al   Maestrini, Elena ^h   Mantoulan, Carine ^am   Marshall, Christian R ^an   McConachie, Helen ^l   McDougle, Christopher J ^ao   McGrath, Jane ^e   McMahon, William M ^ap   Merikangas, Alison ^e   Miller, Judith ^ap   Minopoli, Fiorella ^h   Mirza, Ghazala K ^x   Munson, Jeff ^w   Nelson, Stanley F ^aq   Nygren, Gudrun ^ab   Oliveira, Guiomar ^g   Pagnamenta, Alistair T ^x   Papanikolaou, Katerina ^ar   Parr, Jeremy R ^l   Parrini, Barbara ^k   Pickles, Andrew ^ah   Pinto, Dalila ^an   Piven, Joseph ^s   Posey, David J ^ao   Poustka, Annemarie ^af   Poustka, Fritz ^v   Ragoussis, Jiannis ^x   Roge, Bernadette ^am   Rutter, Michael L ^m   Sequeira, Ana F ^b,c,d   Soorya, Latha ^ag   Sousa, Inês ^x   Sykes, Nuala ^x   Stoppioni, Vera ^as   Tancredi, Raffaella ^k   Tauber, Maïté ^am   Thompson, Ann P ^at   Thomson, Susanne ^al   Tsiantis, John ^ar   Van Engeland, Herman ^t   Vincent, John B ^au   Volkmar, Fred ^av   Vorstman, Jacob A S ^t   Wallace, Simon ^q   Wang, Kai ^ac   Wassink, Thomas H ^aw   White, Kathy ^q   Wing, Kirsty ^x   Wittemeyer, Kerstin ^ax   Yaspan, Brian L ^al   Zwaigenbaum, Lonnie ^ay   Betancur, Catalina ^az   Buxbaum, Joseph D ^ag   Cantor, Rita M ^aq   Cook, Edwin H ^o   Coon, Hilary ^ap   Cuccaro, Michael L ^z   Geschwind, Daniel H ^f   Haines, Jonathan L ^al   Hallmayer, Joachim ^ba   Monaco, Anthony P ^x   Nurnberger Jr , John I ^ao   Pericak Vance, Margaret A ^z   Schellenberg, Gerard D ^bb   Scherer, Stephen W ^an,bc   Sutcliffe, James S ^al   Szatmari, Peter ^at   Vieland, Veronica J ^bd   Wijsman, Ellen M ^w   Green, Andrew ^a   Gill, Michael ^e   Gallagher, Louise ^e   Vicente, Astrid ^b,c,d   Ennis, Sean ^a,be   more..

^a UNIVERSITY COLLEGE DUBLIN   (Ireland)

^b NATIONAL INSTITUTE OF HEALTH DR RICARDO JORGE   (Portugal)

^c UNIVERSITY OF LISBON   (Portugal)

^d INSTITUTO GULBENKIAN DE CIÊNCIA   (Portugal)

^e TRINITY COLLEGE DUBLIN   (Ireland)

^f Center for Autism Research and Treatment   (United States)

^g CENTRO HOSPITALAR E UNIVERSITÁRIO DE COIMBRA   (Portugal)

^h UNIVERSITY OF BOLOGNA   (Italy)

ⁱ UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^j GUY S HOSPITAL   (United Kingdom)

^k DEPARTMENT OF DEVELOPMENTAL NEUROSCIENCE   (Italy)

^l NEWCASTLE UNIVERSITY   (United Kingdom)

^m KING'S COLLEGE LONDON   (United Kingdom)

ⁿ INSTITUT PASTEUR   (France)

^o UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

^p UNIVERSITY OF MICHIGAN   (United States)

^q UNIVERSITY OF OXFORD   (United Kingdom)

^r Autism Speaks Inc   (United States)

^s UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^t UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^u HÔPITAL ROBERT DEBRÉ   (France)

^v GOETHE UNIVERSITY   (Germany)

^w UNIVERSITY OF WASHINGTON   (United States)

^x UNIVERSITY OF OXFORD   (United Kingdom)

^y MEMORIAL UNIVERSITY OF NEWFOUNDLAND   (Canada)

^z UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

^aa MCGILL UNIVERSITY   (Canada)

^ab UNIVERSITY OF GOTHENBURG   (Sweden)

^ac CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^ad BOOTH HALL CHILDREN S HOSPITAL   (United Kingdom)

^ae UNIVERSITY OF PENNSYLVANIA   (United States)

^af GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

^ag MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^ah UNIVERSITY OF MANCHESTER   (United Kingdom)

^ai FONDATION FONDAMENTAL   (France)

^aj NATHAN S KLINE INSTITUTE FOR PSYCHIATRIC RESEARCH   (United States)

^ak NEW YORK UNIVERSITY CHILD STUDY CENTER   (United States)

^al VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

^am UNIVERSITÉ DE TOULOUSE   (France)

^an HOSPITAL FOR SICK CHILDREN   (Canada)

^ao INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^ap UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^aq UNIVERSITY OF CALIFORNIA   (United States)

^ar UNIVERSITY OF ATHENS   (Greece)

^as S CROCE E CARLE HOSPITAL   (Italy)

^at MCMASTER UNIVERSITY   (Canada)

^au UNIVERSITY OF TORONTO   (Canada)

^av YALE UNIVERSITY   (United States)

^aw UNIVERSITY OF IOWA   (United States)

^ax UNIVERSITY OF BIRMINGHAM   (United Kingdom)

^ay UNIVERSITY OF ALBERTA   (Canada)

^az INSERM   (France)

^ba STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^bb UNIVERSITY OF PENNSYLVANIA   (United States)

^bc UNIVERSITY OF TORONTO   (Canada)

^bd OHIO STATE UNIVERSITY   (United States)

^be UNIVERSITY COLLEGE DUBLIN   (Ireland)

more..

Author keywords

[No Author keywords available]

Indexed keywords

EPHRIN RECEPTOR A3; FIBROBLAST GROWTH FACTOR 10; SHAL POTASSIUM CHANNEL; SHAL POTASSIUM CHANNEL 2; UNCLASSIFIED DRUG;

ABHD14A GENE; ARTICLE; AUTISM; CADM2 GENE; CHILD; CHRFAM7A GENE; COGNITION; COMPARATIVE STUDY; CONTROLLED STUDY; DISEASE ASSOCIATION; GENE FREQUENCY; GENE IDENTIFICATION; GENE MAPPING; GENE STRUCTURE; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; GENETIC VARIABILITY; GENOTYPE; GRIK2 GENE; GRM3 GENE; HAPLOTYPE; HOMOZYGOSITY; HOMOZYGOUS HAPLOTYPE; HUMAN; HUMAN GENOME PROJECT; IMMP2L GENE; LARGE SCALE PRODUCTION; MAJOR CLINICAL STUDY; PDZK1 GENE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; ADULT; CLUSTER ANALYSIS; COHORT ANALYSIS; COPY NUMBER VARIATION; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENETIC PREDISPOSITION; GENETICS; HOMOZYGOTE; MALE; METHODOLOGY; MIDDLE AGED; NUCLEAR FAMILY;

ADULT; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CLUSTER ANALYSIS; COHORT STUDIES; DNA COPY NUMBER VARIATIONS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HAPLOTYPES; HOMOZYGOTE; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; MIDDLE AGED; NUCLEAR FAMILY; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84860879137     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/s00439-011-1094-6     Document Type: Article

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