Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders-Reference-Cited by-同舟云学术

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Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders

Published:2019-02-07 Issue:1 Volume:11 Page:
ISSN:1866-1947
Container-title:Journal of Neurodevelopmental Disorders
language:en
Short-container-title:J Neurodevelop Disord

Author:

Costain Gregory,Walker Susan,Argiropoulos Bob,Baribeau Danielle A.,Bassett Anne S.,Boot Erik,Devriendt Koen,Kellam Barbara,Marshall Christian R.,Prasad Aparna,Serrano Moises A.,Stavropoulos D. James,Twede Hope,Vermeesch Joris R.,Vorstman Jacob A. S.,Scherer Stephen W.^ORCID

Funder

The Centre for Applied Genomics

The Hospital for Sick Children

Genome Canada

Autism Speaks

Canadian Institutes of Health Research

Canadian Institutes for Advanced Research

University of Toronto McLaughlin Centre

Publisher

Springer Science and Business Media LLC

Subject

Cognitive Neuroscience,Neurology (clinical),Pathology and Forensic Medicine,Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1186/s11689-019-9263-3.pdf

Reference88 articles.

1. Yuen RKC, Merico D, Bookman M, Howe LJ, Thiruvahindrapuram B, Patel RV, Whitney J, Deflaux N, Bingham J, Wang Z, et al. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder. Nat Neurosci. 2017;20(4):602–11.

2. Tammimies K, Marshall CR, Walker S, Kaur G, Thiruvahindrapuram B, Lionel AC, Yuen RK, Uddin M, Roberts W, Weksberg R, et al. Molecular diagnostic yield of chromosomal microarray analysis and whole-exome sequencing in children with autism spectrum disorder. JAMA. 2015;314(9):895–903.

3. Yuen RK, Thiruvahindrapuram B, Merico D, Walker S, Tammimies K, Hoang N, Chrysler C, Nalpathamkalam T, Pellecchia G, Liu Y, et al. Whole-genome sequencing of quartet families with autism spectrum disorder. Nat Med. 2015;21(2):185–91.

4. De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, Cicek AE, Kou Y, Liu L, Fromer M, Walker S, et al. Synaptic, transcriptional and chromatin genes disrupted in autism. Nature. 2014;515(7526):209–15.

5. Iossifov I, O'Roak BJ, Sanders SJ, Ronemus M, Krumm N, Levy D, Stessman HA, Witherspoon KT, Vives L, Patterson KE, et al. The contribution of de novo coding mutations to autism spectrum disorder. Nature. 2014;515(7526):216–21.

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