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Science (New York, N.Y.)
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December 15, 2018
Integrative functional genomic analysis of human brain development and neuropsychiatric risks
Mingfeng Li, Gabriel Santpere, Yuka Imamura Kawasawa, et al.
Nature Genetics
|
April 28, 2018
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
Donna M Werling, Harrison Brand, Joon-Yong An, et al.
Neuron
|
January 29, 2013
Using whole-exome sequencing to identify inherited causes of autism
Timothy W Yu, Maria H Chahrour, Michael E Coulter, et al.
Neuron
|
September 25, 2015
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
Stephan J Sanders, Xin He, A Jeremy Willsey, et al.
Journal of Psychiatric Research
|
August 6, 2016
Pre- and perinatal complications in relation to Tourette syndrome and co-occurring obsessive-compulsive disorder and attention-deficit/hyperactivity disorder
Mohamed Abdulkadir, Jay A Tischfield, Robert A King, et al.
Nature
|
May 1, 2009
Common genetic variants on 5p14.1 associate with autism spectrum disorders
Kai Wang, Haitao Zhang, Deqiong Ma, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 24, 2025
Rare coding mutations identify 36 large-effect risk genes in obsessive-compulsive disorder and chronic tic disorders
Belinda Wang, Matthew N Tran, Sheng Wang, et al.
Nature Genetics
|
April 6, 2010
Genome-wide association study of intracranial aneurysm identifies three new risk loci
Katsuhito Yasuno, Kaya Bilguvar, Philippe Bijlenga, et al.
Biological Psychiatry
|
June 28, 2016
Constance E. Lieber, Theodore R. Stanley, and the Enduring Impact of Philanthropy on Psychiatry Research
John H Krystal, Anissa Abi-Dargham, Schahram Akbarian, et al.
Neuron
|
June 11, 2011
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, et al.
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of 13
Search research articles
Search
Showing results (111-120 of 123) with videos related to
Sort By:
Page
of 13
Science (New York, N.Y.)
|
December 15, 2018
Integrative functional genomic analysis of human brain development and neuropsychiatric risks
Mingfeng Li, Gabriel Santpere, Yuka Imamura Kawasawa, et al.
Nature Genetics
|
April 28, 2018
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
Donna M Werling, Harrison Brand, Joon-Yong An, et al.
Neuron
|
January 29, 2013
Using whole-exome sequencing to identify inherited causes of autism
Timothy W Yu, Maria H Chahrour, Michael E Coulter, et al.
Neuron
|
September 25, 2015
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
Stephan J Sanders, Xin He, A Jeremy Willsey, et al.
Journal of Psychiatric Research
|
August 6, 2016
Pre- and perinatal complications in relation to Tourette syndrome and co-occurring obsessive-compulsive disorder and attention-deficit/hyperactivity disorder
Mohamed Abdulkadir, Jay A Tischfield, Robert A King, et al.
Nature
|
May 1, 2009
Common genetic variants on 5p14.1 associate with autism spectrum disorders
Kai Wang, Haitao Zhang, Deqiong Ma, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 24, 2025
Rare coding mutations identify 36 large-effect risk genes in obsessive-compulsive disorder and chronic tic disorders
Belinda Wang, Matthew N Tran, Sheng Wang, et al.
Nature Genetics
|
April 6, 2010
Genome-wide association study of intracranial aneurysm identifies three new risk loci
Katsuhito Yasuno, Kaya Bilguvar, Philippe Bijlenga, et al.
Biological Psychiatry
|
June 28, 2016
Constance E. Lieber, Theodore R. Stanley, and the Enduring Impact of Philanthropy on Psychiatry Research
John H Krystal, Anissa Abi-Dargham, Schahram Akbarian, et al.
Neuron
|
June 11, 2011
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, et al.
Page
of 13