Refining analyses of copy number variation identifies specific genes associated with developmental delay

被引:0
|
作者
Bradley P Coe
Kali Witherspoon
Jill A Rosenfeld
Bregje W M van Bon
Anneke T Vulto-van Silfhout
Paolo Bosco
Kathryn L Friend
Carl Baker
Serafino Buono
Lisenka E L M Vissers
Janneke H Schuurs-Hoeijmakers
Alex Hoischen
Rolph Pfundt
Nik Krumm
Gemma L Carvill
Deana Li
David Amaral
Natasha Brown
Paul J Lockhart
Ingrid E Scheffer
Antonino Alberti
Marie Shaw
Rosa Pettinato
Raymond Tervo
Nicole de Leeuw
Margot R F Reijnders
Beth S Torchia
Hilde Peeters
Elizabeth Thompson
Brian J O'Roak
Marco Fichera
Jayne Y Hehir-Kwa
Jay Shendure
Heather C Mefford
Eric Haan
Jozef Gécz
Bert B A de Vries
Corrado Romano
Evan E Eichler
机构
[1] University of Washington School of Medicine,Department of Genome Sciences
[2] Signature Genomics Laboratories,Department of Human Genetics
[3] LLC,Department of Pediatrics
[4] PerkinElmer,Department of Paediatrics
[5] Inc.,Division of Developmental and Behavioral Pediatrics
[6] Radboud University Medical Center,undefined
[7] SA Pathology,undefined
[8] IRCCS (Istituto di Ricovero e Cura a Carattere Scientifico) Associazione Oasi Maria Santissima,undefined
[9] University of Washington,undefined
[10] Representing the Autism Phenome Project,undefined
[11] MIND Institute,undefined
[12] University of California,undefined
[13] Davis,undefined
[14] University of Melbourne,undefined
[15] Royal Children's Hospital,undefined
[16] Barwon Child Health Unit,undefined
[17] Barwon Health,undefined
[18] Murdoch Childrens Research Institute,undefined
[19] University of Melbourne,undefined
[20] Royal Children's Hospital,undefined
[21] Florey Institute,undefined
[22] University of Melbourne,undefined
[23] Austin Health and Royal Children's Hospital,undefined
[24] Mayo Clinic,undefined
[25] Center for Human Genetics,undefined
[26] University Hospitals Leuven,undefined
[27] KU Leuven,undefined
[28] Leuven Autism Research (LAuRes),undefined
[29] School of Paediatrics and Reproductive Health,undefined
[30] University of Adelaide,undefined
[31] Robinson Institute,undefined
[32] University of Adelaide,undefined
[33] Howard Hughes Medical Institute,undefined
[34] Present addresses: Molecular and Medical Genetics,undefined
[35] Oregon Health and Science University (OHSU),undefined
[36] Portland,undefined
[37] Oregon,undefined
[38] USA (B.J.O.) and Medical Genetics,undefined
[39] University of Catania,undefined
[40] Catania,undefined
[41] Italy (M.F.).,undefined
来源
Nature Genetics | 2014年 / 46卷
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摘要
Evan Eichler and colleagues report an expanded copy number variation (CNV) morbidity map of developmental delay, with additional resequencing of candidate genes in regions implicated by large CNVs. They identify several new disease-associated CNVs and show how their combined approach facilitates discovery of new developmental syndromes and disease genes.
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页码:1063 / 1071
页数:8
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