An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder-Reference-Cited by-同舟云学术

An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder

Published:2018-04-26 Issue:5 Volume:50 Page:727-736
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Werling Donna M.^ORCID,Brand Harrison,An Joon-Yong^ORCID,Stone Matthew R.,Zhu Lingxue,Glessner Joseph T.,Collins Ryan L.^ORCID,Dong Shan,Layer Ryan M.^ORCID,Markenscoff-Papadimitriou Eirene,Farrell Andrew,Schwartz Grace B.,Wang Harold Z.,Currall Benjamin B.,Zhao Xuefang,Dea Jeanselle,Duhn Clif,Erdman Carolyn A.,Gilson Michael C.,Yadav Rachita,Handsaker Robert E.^ORCID,Kashin Seva,Klei Lambertus,Mandell Jeffrey D.,Nowakowski Tomasz J.,Liu Yuwen,Pochareddy Sirisha,Smith Louw,Walker Michael F.,Waterman Matthew J.,He Xin^ORCID,Kriegstein Arnold R.,Rubenstein John L.,Sestan Nenad^ORCID,McCarroll Steven A.,Neale Benjamin M.^ORCID,Coon Hilary,Willsey A. Jeremy,Buxbaum Joseph D.,Daly Mark J.^ORCID,State Matthew W.,Quinlan Aaron R.^ORCID,Marth Gabor T.^ORCID,Roeder Kathryn,Devlin Bernie,Talkowski Michael E.^ORCID,Sanders Stephan J.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/s41588-018-0107-y.pdf

Reference78 articles.

1. Schizophrenia Working Group of the Psychiatric Genomics Consortium. Biological insights from 108 schizophrenia-associated genetic loci. Nature 511, 421–427 (2014).

2. Astle, W. J. et al. The allelic landscape of human blood cell trait variation and links to common complex disease. Cell 167, 1415–1429 (2016).

3. de Lange, K. M. et al. Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. Nat. Genet. 49, 256–261 (2017).

4. Sanders, S. J. et al. Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci. Neuron 87, 1215–1233 (2015).

5. Deciphering Developmental Disorders Study. Prevalence and architecture of de novo mutations in developmental disorders. Nature 542, 433–438 (2017).

Cited by 240 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Gene therapy for polygenic or complex diseases;Biomarker Research;2024-09-04

2. Genetic modifiers and ascertainment drive variable expressivity of complex disorders;2024-08-28

3. Decomposition of phenotypic heterogeneity in autism reveals distinct and coherent genetic programs;2024-08-16

4. Complex de novo structural variants are an underestimated cause of rare disorders;2024-08-07

5. Investigating copy number variants in schizophrenia pedigrees using a new consensus pipeline called PECAN;Scientific Reports;2024-07-30