Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases

Holly A.F. Stessman; Bo Xiong; Bradley P. Coe; Tianyun Wang; Kendra Hoekzema; Michaela Fencková; Malin Kvarnung; Jennifer Gerdts; Sandy Trinh; Nele Cosemans; Laura Vives; Janice Lin; Tychele N. Turner; Gijs W.E. Santen; Claudia Ruivenkamp; Marjolein Kriek; Arie van Haeringen; Emmelien Aten; Kathryn Friend; Jan Liebelt; Christopher Barnett; Eric Haan; Marie Shaw; Jozef Gécz; Britt-Marie Anderlid; Ann Nordgren; Anna Lindstrand; Charles E. Schwartz; R. Frank Kooy; Geert Vandeweyer; Céline Helsmoortel; Corrado Romano; A Alberti; Mirella Vinci; Emanuela Avola; Stefania Giusto; Eric Courchesne; Tiziano Pramparo; Karen Pierce; Srinivasa Nalabolu; David G. Amaral; Ingrid E. Scheffer; Martin B. Delatycki; Paul J. Lockhart; Fereydoun Hormozdiari; Benjamin Harich; Anna Castells‐Nobau; Kun Xia; Hilde Peeters; Magnus Nordenskjöld; Annette Schenck; Raphael Bernier; Evan E. Eichler

doi:10.1038/ng.3792

Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases

Holly A.F. Stessman(University of Washington), Bo Xiong(University of Washington), Bradley P. Coe(University of Washington), Tianyun Wang(Central South University), Kendra Hoekzema(University of Washington), Michaela Fencková(Radboud University Nijmegen), Malin Kvarnung(Karolinska University Hospital), Jennifer Gerdts(University of Washington), Sandy Trinh(University of Washington), Nele Cosemans(KU Leuven), Laura Vives(University of Washington), Janice Lin(University of Washington), Tychele N. Turner(University of Washington), Gijs W.E. Santen(Leiden University Medical Center), Claudia Ruivenkamp(Leiden University Medical Center), Marjolein Kriek(Leiden University Medical Center), Arie van Haeringen(Leiden University Medical Center), Emmelien Aten(Leiden University Medical Center), Kathryn Friend(South Australia Pathology), Jan Liebelt(South Australia Pathology), Christopher Barnett(South Australia Pathology), Eric Haan(South Australia Pathology), Marie Shaw(Women's and Children's Hospital), Jozef Gécz(South Australia Pathology), Britt-Marie Anderlid(Karolinska University Hospital), Ann Nordgren(Karolinska University Hospital), Anna Lindstrand(Karolinska University Hospital), Charles E. Schwartz(Greenwood Genetic Center), R. Frank Kooy(University of Antwerp), Geert Vandeweyer(University of Antwerp), Céline Helsmoortel(University of Antwerp), Corrado Romano(Oasi Maria SS), A Alberti(Oasi Maria SS), Mirella Vinci(Oasi Maria SS), Emanuela Avola(Oasi Maria SS), Stefania Giusto(Oasi Maria SS), Eric Courchesne(University of California San Diego), Tiziano Pramparo(University of California San Diego), Karen Pierce(University of California San Diego), Srinivasa Nalabolu(University of California San Diego), David G. Amaral(University of California, Davis), Ingrid E. Scheffer(Royal Children's Hospital), Martin B. Delatycki(Royal Children's Hospital), Paul J. Lockhart(Royal Children's Hospital), Fereydoun Hormozdiari(University of California, Davis), Benjamin Harich(Radboud University Nijmegen), Anna Castells‐Nobau(Radboud University Nijmegen), Kun Xia(Central South University), Hilde Peeters(KU Leuven), Magnus Nordenskjöld(Karolinska University Hospital), Annette Schenck(Radboud University Nijmegen), Raphael Bernier(University of Washington), Evan E. Eichler(Howard Hughes Medical Institute)

Nature Genetics

February 13, 2017

10.1038/ng.3792

Cited by 577Open Access

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