Literature DB >> 23147383

Combined analysis of exome sequencing points toward a major role for transcription regulation during brain development in autism.

E Ben-David1, S Shifman.   

Abstract

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Year:  2012        PMID： 23147383     DOI： 10.1038/mp.2012.148

Source DB:  PubMed          Journal:  Mol Psychiatry        ISSN： 1359-4184            Impact factor:   15.992


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  66 in total

1.  Meta-Analysis of Gene Expression in Autism Spectrum Disorder.

Authors:  Carolyn Ch'ng; Willie Kwok; Sanja Rogic; Paul Pavlidis
Journal:  Autism Res       Date:  2015-02-26       Impact factor: 5.216

2.  Loss-of-function variants in schizophrenia risk and SETD1A as a candidate susceptibility gene.

Authors:  Atsushi Takata; Bin Xu; Iuliana Ionita-Laza; J Louw Roos; Joseph A Gogos; Maria Karayiorgou
Journal:  Neuron       Date:  2014-05-21       Impact factor: 17.173

3.  Autism genes keep turning up chromatin.

Authors:  Janine M Lasalle
Journal:  OA Autism       Date:  2013-06-19

4.  Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database.

Authors:  Jinchen Li; Tao Cai; Yi Jiang; Huiqian Chen; Xin He; Chao Chen; Xianfeng Li; Qianzhi Shao; Xia Ran; Zhongshan Li; Kun Xia; Chunyu Liu; Zhong Sheng Sun; Jinyu Wu
Journal:  Mol Psychiatry       Date:  2015-04-07       Impact factor: 15.992

Review 5.  The developmental transcriptome of the human brain: implications for neurodevelopmental disorders.

Authors:  Andrew T N Tebbenkamp; A Jeremy Willsey; Matthew W State; Nenad Sestan
Journal:  Curr Opin Neurol       Date:  2014-04       Impact factor: 5.710

Review 6.  Lost in Translation: Traversing the Complex Path from Genomics to Therapeutics in Autism Spectrum Disorder.

Authors:  Nenad Sestan; Matthew W State
Journal:  Neuron       Date:  2018-10-24       Impact factor: 17.173

Review 7.  Advancing the understanding of autism disease mechanisms through genetics.

Authors:  Luis de la Torre-Ubieta; Hyejung Won; Jason L Stein; Daniel H Geschwind
Journal:  Nat Med       Date:  2016-04       Impact factor: 53.440

8.  Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay.

Authors:  Keren Machol; Justine Rousseau; Sophie Ehresmann; Thomas Garcia; Thi Tuyet Mai Nguyen; Rebecca C Spillmann; Jennifer A Sullivan; Vandana Shashi; Yong-Hui Jiang; Nicholas Stong; Elise Fiala; Marcia Willing; Rolph Pfundt; Tjitske Kleefstra; Megan T Cho; Heather McLaughlin; Monica Rosello Piera; Carmen Orellana; Francisco Martínez; Alfonso Caro-Llopis; Sandra Monfort; Tony Roscioli; Cheng Yee Nixon; Michael F Buckley; Anne Turner; Wendy D Jones; Peter M van Hasselt; Floris C Hofstede; Koen L I van Gassen; Alice S Brooks; Marjon A van Slegtenhorst; Katherine Lachlan; Jessica Sebastian; Suneeta Madan-Khetarpal; Desai Sonal; Naidu Sakkubai; Julien Thevenon; Laurence Faivre; Alice Maurel; Slavé Petrovski; Ian D Krantz; Jennifer M Tarpinian; Jill A Rosenfeld; Brendan H Lee; Philippe M Campeau
Journal:  Am J Hum Genet       Date:  2018-12-20       Impact factor: 11.025

9.  Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder.

Authors:  N H Chapman; R A Bernier; S J Webb; J Munson; E M Blue; D-H Chen; E Heigham; W H Raskind; Ellen M Wijsman
Journal:  Hum Genet       Date:  2018-10-01       Impact factor: 4.132

10.  NETWORK ASSISTED ANALYSIS TO REVEAL THE GENETIC BASIS OF AUTISM.

Authors:  Li Liu; Jing Lei; Kathryn Roeder
Journal:  Ann Appl Stat       Date:  2015-11-02       Impact factor: 2.083
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