A large data resource of genomic copy number variation across neurodevelopmental disorders

Zarrei, Mehdi; L. Burton, Christie; Engchuan, Worrawat; J. Young, Edwin; J. Higginbotham, Edward; R. MacDonald, Jeffrey; Trost, Brett; J. S. Chan, Ada; Walker, Susan; Lamoureux, Sylvia; Heung, Tracy; A. Mojarad, Bahareh; Kellam, Barbara; Paton, Tara; Faheem, Muhammad; Miron, Karin; Lu, Chao; Wang, Ting; Samler, Kozue; Wang, Xiaolin; Costain, Gregory; Hoang, Ny; Pellecchia, Giovanna; Wei, John; Patel, Rohan; Thiruvahindrapuram, Bhooma; Roifman, Maian; Merico, Daniele; Goodale, Tara; Drmic, Irene; Speevak, Marsha; Howe, Jennifer; K. C. Yuen, Ryan; A. Buchanan, Janet; Vorstman, Jacob; R. Marshall, Christian; F. Wintle, Richard; R. Rosenberg, David; L. Hanna, Gregory; Woodbury‐Smith, Marc; Cytrynbaum, Cheryl; Zwaigenbaum, Lonnie; Elsabbagh, Mayada; Flanagan, Janine; A. Fernandez, Bridget; T. Carter, Melissa; Szatmári, Péter; Roberts, Wendy; P. Lerch, Jason; Liu, Xudong; Nicolson, Rob; Georgiades, Stelios; Weksberg, Rosanna; Arnold, Paul; S. Bassett, Anne; Crosbie, Jennifer; Schachar, Russell; J. Stavropoulos, Dimitri; Anagnostou, Evdokia; W. Scherer, Stephen

doi:10.1038/s41525-019-0098-3

Public

A large data resource of genomic copy number variation across neurodevelopmental disorders

Published in npj Genomic Medicine • Oct 7, 2019

Authors:

Mehdi Zarrei

Christie L. Burton

Worrawat Engchuan

Abstract

Abstract Copy number variations (CNVs) are implicated across many neurodevelopmental disorders (NDDs) and contribute to their shared genetic etiology. Multiple studies have attempted to identify shared etiology among NDDs, but this is the first genome-wide CNV analysis across autism spectrum disorde...

Subject

Copy-number variation

Autism spectrum disorder

Autism

Research Assistant

AI chat, annotations, notes & similar papers

Finding related papers...

Discussions

(0)

No comments yet

Be the first to share your thoughts!