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Genetics of autism spectrum disorders

author

Daniel Geschwind

published in: Trends in Cognitive Sciences

date of publication: 2011-08-18

main subject: autism spectrum disorder, autism

Cites articles 81

Date

Title

Authors

2012-03-01

Neurocognitive and behavioral outcomes of younger siblings of children with autism spectrum disorder at age five

Julie A Crittendon
2011-03-01

CNTNAP2 variants affect early language development in the general population

Dorothy Bishop, Simon Fisher, Andrew Whitehouse, Craig E. Pennell
2011-03-22

Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting
2011-10

Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

Guy A. Rouleau, Tabrez J. Siddiqui, Marie-Odile Krebs, Éric Fombonne, Laurent Mottron, Dan Spiegelman, Julie Gauthier, Jacques L. Michaud, Ann Marie Craig, Pierre Drapeau, Anne Noreau, Nathalie Champagne, Mathieu Lapointe, Ronald G. Lafrenière, Ferid Fathalli, Salvatore Carbonetto
2011-06-16

Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patients.

Andrea Poretti, Thierry A.G.M. Huisman
2011-11-01

Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism
2011-06

Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

Michael Wigler, Michael Ronemus, Abba M. Krieger, Ivan Iossifov, Anthony Leotta, Jude Kendall, Jennifer Troge, Linda H Rodgers
2011-05-25

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

Irina Voineagu, Xinchen Wang, Jonathan Mill, Daniel Geschwind, Benjamin J. Blencowe, Steve Horvath, Rita M. Cantor
2011-04-01

Cilia in the nervous system: linking cilia function and neurodevelopmental disorders
2011-03-29

Next-generation association studies for complex traits

Eleftheria Zeggini
2011-03

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

Hakon Hakonarson, Itsik Pe'er, Nancy G. Buccola, Sarah E Bergen, Donald W. Black, Peter Holmans, Kenneth Kendler, Frank Dudbridge, Ann Olincy, C. Robert Cloninger, Kai Wang, Jeremy Silverman, Douglas F Levinson, Jubao Duan, Alan R. Sanders, Bryan Mowry, Ayman Fanous, Pablo V Gejman
2011-06-01

Pragmatic language and school related linguistic abilities in siblings of children with autism

Catherine Lord, Nurit Yirmiya, Marian Sigman
2011-06-01

Disrupted neural synchronization in toddlers with autism

Ilan Dinstein, Marlene Behrmann, Karen Pierce, Eric Courchesne
2011-04-01

Mechanisms of neurocognitive dysfunction and therapeutic considerations in tuberous sclerosis complex

Mustafa Sahin
2011-06-01

Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses

Michael Wigler, Michael Ronemus, Ivan Iossifov
2011-06-01

Protein interactome reveals converging molecular pathways among autism disorders

Chad Shaw, Yasunari Sakai, Huda Zoghbi
2011-06-01

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

Stephan J. Sanders, Su Chu, Thomas V. Fernandez, Gerald Goh, Sabata Lund, Brian J O'Roak, Brian L. Yaspan, Dorothy E Grice, Chad Shaw, Jay A. Tischfield, Eric M. Morrow, Éric Fombonne, James S. Sutcliffe, Kathryn Roeder, Daniel Geschwind, Christopher A. Walsh, Catherine Lord, Christopher E. Mason, Rita M. Cantor, David H. Ledbetter
2011-05-01

The erosion of phenotypic specificity in psychiatric genetics: emerging lessons from CNTNAP2
2011-05-01

The quantitative nature of autistic social impairment

John N Constantino
2010-06-29

Penetrance for copy number variants associated with schizophrenia.

Christine Patch, Cathryn Lewis, Dan Rujescu, David St Clair, Evangelos Vassos, David Collier
2010-02-20

Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2

John Ashburner, Richard S. J. Frackowiak, Nicholas W. Wood
2010-12-30

A common genetic variant in the neurexin superfamily member CNTNAP2 is associated with increased risk for selective mutism and social anxiety-related traits

Joel Gelernter
2010-11-04

Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia

Daniel Moreno-De-Luca, Christa Lese Martin, David H. Ledbetter
2010-10-01

The genetics of child psychiatric disorders: focus on autism and Tourette syndrome
2010-11-09

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample

Ellen M. Wijsman, Virginia W. Berninger
2010-05-20

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies

Stefan Schreiber, Heather C. Mefford, Evan E. Eichler, Andre Franke
2010-10-26

Defining the cognitive phenotype of autism

Tony Charman, Catherine R. Jones, Andrew Pickles, Emily Simonoff, Francesca Happé
2010-07-20

A twin study of autism symptoms in Sweden.

Angelica Ronald, Henrik Larsson, Henrik Anckarsäter, Paul Lichtenstein
2010-09-08

Traits contributing to the autistic spectrum

Jean Golding
2010-09-01

Self-referenced processing, neurodevelopment and joint attention in autism
2010-10-15

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

Richard Anney, Lambertus Klei, Dalila Pinto, Regina Regan, Judith Conroy, Catarina Correia, Nuala Sykes, Alistair T Pagnamenta, Elena Bacchelli, Gillian Baird, Agatino Battaglia, Tom Berney, Nadia Bolshakova, Sven Bölte, Thomas Bourgeron, Jessica Brian, Andrew Carson-Stevens, Guillermo Casallo, Jillian P Casey, Christina Corsello, Andrew Crossett, Geraldine Dawson, Richard Delorme, Irene Drmic, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A. Fernandez, Susan Folstein, Éric Fombonne, Christine M Freitag, Christopher Gillberg, Joseph Glessner, Jonathan Green, Hakon Hakonarson, Elizabeth A Heron, Matthew J Hill, Vanessa Hus Bal, Roberta Igliozzi, Sabine M Klauck, Janine A Lamb, Olena Korvatska, Vlad Kustanovich, Clara M. Lajonchere, Magdalena Laskawiec, Marion Leboyer, Ann Le Couteur, Bennett L Leventhal, Anath C. Lionel, Xiao-Qing Liu, Catherine Lord, Linda Lotspeich, Sabata Lund, Elena Maestrini, Carine Mantoulan, Christian Marshall, Helen McConachie, Christopher J McDougle, Jane McGrath, Nadine M Melhem, Alison K Merikangas, Ohsuke Migita, Ghazala K. Mirza, Jeff Munson, Stanley F Nelson, Gudrun Nygren, Guiomar Oliveira, Katerina Papanikolaou, Jeremy R Parr, Barbara Parrini, Tara A Paton, Andrew Pickles, Joseph Piven, Annemarie Poustka, Fritz Poustka, Aparna Prasad, Jiannis Ragoussis, Katy Renshaw, Jessica Rickaby, Wendy Roberts, Kathryn Roeder, Michael Rutter, Laura J. Bierut, Jeff Salt, Katherine Sansom, Ricardo Segurado, Lili Senman, Naisha Shah, Val C Sheffield, Latha Soorya, Vera Stoppioni, Christina Strawbridge, Raffaella Tancredi, Katherine E. Tansey, Bhooma Thiruvahindrapduram, Susanne Thomson, Ana Tryfon, John Tsiantis, Fred R. Volkmar, Rachel Wallace, Kai Wang, Zhouzhi Wang, Thomas H Wassink, Kirsty Wing, Brian L. Yaspan, Danielle Zurawiecki, Lonnie Zwaigenbaum, Catalina Betancur, Joseph Buxbaum, Rita M. Cantor, Edwin H Cook, Hilary Coon, Michael L Cuccaro, Louise Gallagher, Daniel Geschwind, Michael Gill, Jonathan L Haines, Anthony 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, William M. McMahon, John B Vincent, Maretha de Jonge, Stephen J Guter, John P Rice, João A B Sousa
2010-11-01

Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2

Russell A. Poldrack, Jeanette A. Mumford, Mirella Dapretto, Susan Y. Bookheimer, Daniel Geschwind

Article - wd:Q84797519

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