Accès ouvert déclaré 2022 article

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

Jack Fu, F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Brie Wamsley, Lambertus Klei, Lily Wang, Stephanie P. Hao, Christine Stevens, Caroline Cusick, Mehrtash Babadi, Eric Banks, Brett Collins, Sheila Dodge, Stacey B. Gabriel, Laura D. Gauthier, Samuel K. Lee, Lindsay Liang, Alicia Ljungdahl, Behrang Mahjani, Laura Sloofman, Andrey N. Smirnov, Mafalda Barbosa, Catalina Betancur, Alfredo Brusco, Brian Hon‐Yin Chung, Edwin H. Cook, Michael L. Cuccaro, Enrico Domenici, Giovanni Battista Ferrero, J. Jay Gargus, Gail E. Herman, Irva Hertz‐Picciotto, Patrı́cia Maciel, Dara S. Manoach, Maria Rita Passos‐Bueno, Antonio M. Persico, Alessandra Renieri, James S. Sutcliffe, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Simona Cardaropoli, Diana Carli, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina De Sanctis Girardi, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Rebecca J. Schmidt, Moyra Smith, Claudia Ismania Samogy Costa, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, Branko Aleksić, Mykyta Artomov, Elisa Benetti, Monica Biscaldi-Schafer, Anders D. Børglum, Ãngel Carracedo, Andreas G. Chiocchetti, Hilary Coon, Ryan N. Doan, Montse Fernández‐Prieto, Christine M. Freitag, Sherif Gerges, Stephen J. Guter, David M. Hougaard, Christina M. Hultman, Suma Jacob, Miia Kaartinen, Alexander Kolevzon, Itaru Kushima, Terho Lehtimäki, Caterina Lo Rizzo, Nell Maltman, Marianna Manara, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Matthew W. Mosconi, Norio Ozaki, Aarno Palotie, Mara Parellada, Kaija Puura, Abraham Reichenberg, Sven Sandin, Stephen W. Scherer, Sabine Schlitt, Lauren Schmitt, Katja Schneider-Momm, Paige M. Siper, Pål Surén, John A. Sweeney, Karoline Teufel, Maria del Pilar Trelles, Lauren A. Weiss, Ryan K. C. Yuen, David J. Cutler, Silvia De Rubeis, Joseph D. Buxbaum, Mark J. Daly, Bernie Devlin, Kathryn Roeder, Stephan Sanders, Michael E. Talkowski

657Citations signalées — pas une note de qualité

63Institutions déclarées

17Pays d’affiliation déclarés

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DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.

Titre Crossref: Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Date Crossref: 18/08/2022
Éditeur: Springer Science and Business Media LLC
Type: journal-article

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Institutions déclarées

Broad Institute Harvard University Massachusetts General Hospital Carnegie Mellon University University of California, San Francisco University of California, Los Angeles University of Pittsburgh Child Health and Development Institute Icahn School of Medicine at Mount Sinai Duchess of Kent Children's Hospital University of Hong Kong Karolinska Institutet Centre National de la Recherche Scientifique Inserm Sorbonne Université Institut de Biologie Paris-Seine Neurosciences Paris-Seine Azienda Ospedaliera Citta' della Salute e della Scienza di Torino Department of Medical Sciences University of Turin University of Illinois Chicago University of Miami University of Trento University of California, Irvine Center for Autism and Related Disorders Nationwide Children's Hospital University of California, Davis University of Minho Universidade de São Paulo University of Messina University of Siena Azienda Ospedaliera Universitaria Senese Vanderbilt University University of Verona The University of Texas Health Science Center at Houston Università Campus Bio-Medico Nagoya University Goethe University Frankfurt Lundbeck Foundation Universidade de Santiago de Compostela Centre for Biomedical Network Research on Rare Diseases Center for Research in Molecular Medicine and Chronic Diseases University of Utah Boston Children's Hospital Tampere University Hospital Tampere University Tampere University Fimlab (Finland)Ben-Gurion University of the Negev Children's Hospital of Philadelphia University of Kansas University of Helsinki Institute for Molecular Medicine Finland Hospital General Universitario Gregorio Marañón Centro de Investigación Biomédica en Red de Salud Mental Hospital for Sick Children Norwegian Institute of Public Health University of Cincinnati Emory University Allen Institute for Brain Science Center for Systems Biology UPMC Health System University of Pittsburgh Medical Center

Une affiliation ne permet pas de déduire la nationalité d’un auteur.

Sujets associés

Autism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalitiesCongenital heart defects research

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