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Camille W Brune

Showing results (1-10 of 14) with videos related to

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Neuroscience Letters|March 27, 2007
Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autismSuma Jacob, Camille W Brune, C S Carter, et al.
The American Journal of Psychiatry|December 8, 2006
5-HTTLPR Genotype-Specific Phenotype in Children and Adolescents With AutismCamille W Brune, Soo-Jeong Kim, Jeff Salt, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 9, 2011
Parent-of-origin effects of the serotonin transporter gene associated with autismEmily Kistner-Griffin, Camille W Brune, Lea K Davis, et al.
Autism Research : Official Journal of the International Society for Autism Research|April 11, 2009
Family-Based Association Testing of OCD-associated SNPs of SLC1A1 in an autism sampleCamille W Brune, Soo-Jeong Kim, Gregory L Hanna, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2008
Transmission disequilibrium testing of the chromosome 15q11-q13 region in autismSoo-Jeong Kim, Camille W Brune, Emily O Kistner, et al.
Autism Research : Official Journal of the International Society for Autism Research|December 19, 2009
A pharmacogenetic study of escitalopram in autism spectrum disordersThomas Owley, Camille W Brune, Jeff Salt, et al.
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.
Journal of Medical Genetics|June 24, 2009
A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autismRavinesh A Kumar, Jyotsna Sudi, Timothy D Babatz, 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.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Neuroscience Letters|March 27, 2007
Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autismSuma Jacob, Camille W Brune, C S Carter, et al.
The American Journal of Psychiatry|December 8, 2006
5-HTTLPR Genotype-Specific Phenotype in Children and Adolescents With AutismCamille W Brune, Soo-Jeong Kim, Jeff Salt, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 9, 2011
Parent-of-origin effects of the serotonin transporter gene associated with autismEmily Kistner-Griffin, Camille W Brune, Lea K Davis, et al.
Autism Research : Official Journal of the International Society for Autism Research|April 11, 2009
Family-Based Association Testing of OCD-associated SNPs of SLC1A1 in an autism sampleCamille W Brune, Soo-Jeong Kim, Gregory L Hanna, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2008
Transmission disequilibrium testing of the chromosome 15q11-q13 region in autismSoo-Jeong Kim, Camille W Brune, Emily O Kistner, et al.
Autism Research : Official Journal of the International Society for Autism Research|December 19, 2009
A pharmacogenetic study of escitalopram in autism spectrum disordersThomas Owley, Camille W Brune, Jeff Salt, et al.
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.
Journal of Medical Genetics|June 24, 2009
A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autismRavinesh A Kumar, Jyotsna Sudi, Timothy D Babatz, 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.
Pageof 2