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W Brune

Showing results (21-30 of 27) with videos related to

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American Journal of Human Genetics|January 9, 2008
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autismDan E Arking, David J Cutler, Camille W Brune, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 24, 2007
Heterogeneous association between engrailed-2 and autism in the CPEA networkCamille W Brune, Elena Korvatska, Kristina Allen-Brady, et al.
Biological Psychiatry|April 1, 2008
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorderSusan L Christian, Camille W Brune, Jyotsna Sudi, et al.
Plos One|February 27, 2009
Association and mutation analyses of 16p11.2 autism candidate genesRavinesh A Kumar, Christian R Marshall, Judith A Badner, et al.
American Journal on Intellectual and Developmental Disabilities|August 26, 2025
Characterizing Developmental and Behavioral Profiles in Developmental Synaptopathies to Inform Clinical Trial EndpointsLatha Valluripalli Soorya, Camille W Brune, Cristan A Farmer, et al.
Nature|May 1, 2009
Autism genome-wide copy number variation reveals ubiquitin and neuronal genesJoseph T Glessner, Kai Wang, Guiqing Cai, et al.
Nature|May 1, 2009
Common genetic variants on 5p14.1 associate with autism spectrum disordersKai Wang, Haitao Zhang, Deqiong Ma, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
American Journal of Human Genetics|January 9, 2008
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autismDan E Arking, David J Cutler, Camille W Brune, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 24, 2007
Heterogeneous association between engrailed-2 and autism in the CPEA networkCamille W Brune, Elena Korvatska, Kristina Allen-Brady, et al.
Biological Psychiatry|April 1, 2008
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorderSusan L Christian, Camille W Brune, Jyotsna Sudi, et al.
Plos One|February 27, 2009
Association and mutation analyses of 16p11.2 autism candidate genesRavinesh A Kumar, Christian R Marshall, Judith A Badner, et al.
American Journal on Intellectual and Developmental Disabilities|August 26, 2025
Characterizing Developmental and Behavioral Profiles in Developmental Synaptopathies to Inform Clinical Trial EndpointsLatha Valluripalli Soorya, Camille W Brune, Cristan A Farmer, et al.
Nature|May 1, 2009
Autism genome-wide copy number variation reveals ubiquitin and neuronal genesJoseph T Glessner, Kai Wang, Guiqing Cai, et al.
Nature|May 1, 2009
Common genetic variants on 5p14.1 associate with autism spectrum disordersKai Wang, Haitao Zhang, Deqiong Ma, et al.
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