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Joseph D Buxbaum

Showing results (271-280 of 361) with videos related to

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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 13, 2026
Black EquaLity in OCD NeuroGenomics (BELONG): Study ProtocolIasha J Williams, Dalia Y Marquez, Kara E Lopez-Lengowski, et al.
American Journal of Medical Genetics. Part A|September 11, 2024
Aortic Root Dilation and Genotype Associations in Phelan-McDermid SyndromeJake Gluckman, Tess Levy, Kate Friedman, et al.
Annals of Neurology|July 22, 2014
PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylationGyungah Jun, Hirohide Asai, Ella Zeldich, et al.
Neuron|November 28, 2023
An evolutionary perspective on complex neuropsychiatric diseaseJon M McClellan, Anthony W Zoghbi, Joseph D Buxbaum, et al.
American Journal of Human Genetics|February 8, 2011
Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosaStephan Züchner, Julia Dallman, Rong Wen, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 16, 2025
Genome Sequencing Uncovers Additional Findings in Phelan-McDermid SyndromeRachel Gore Moses, Morgan Similuk, Alexandra Hehn, et al.
Molecular Autism|November 14, 2014
The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analysesJoseph D Buxbaum, Nadia Bolshakova, Jessica M Brownfeld, et al.
Genome Medicine|December 22, 2017
Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disordersHoang T Nguyen, Julien Bryois, April Kim, et al.
American Journal of Human Genetics|October 19, 2010
A genome-wide study reveals copy number variants exclusive to childhood obesity casesJoseph T Glessner, Jonathan P Bradfield, Kai Wang, et al.
European Journal of Human Genetics : EJHG|March 6, 2023
Skewed X-chromosome inactivation in unsolved neurodevelopmental disease cases can guide re-evaluation For X-linked genesChiara Giovenino, Slavica Trajkova, Lisa Pavinato, et al.
Pageof 37

Showing results (271-280 of 361) with videos related to

Sort By:
Pageof 37
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 13, 2026
Black EquaLity in OCD NeuroGenomics (BELONG): Study ProtocolIasha J Williams, Dalia Y Marquez, Kara E Lopez-Lengowski, et al.
American Journal of Medical Genetics. Part A|September 11, 2024
Aortic Root Dilation and Genotype Associations in Phelan-McDermid SyndromeJake Gluckman, Tess Levy, Kate Friedman, et al.
Annals of Neurology|July 22, 2014
PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylationGyungah Jun, Hirohide Asai, Ella Zeldich, et al.
Neuron|November 28, 2023
An evolutionary perspective on complex neuropsychiatric diseaseJon M McClellan, Anthony W Zoghbi, Joseph D Buxbaum, et al.
American Journal of Human Genetics|February 8, 2011
Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosaStephan Züchner, Julia Dallman, Rong Wen, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 16, 2025
Genome Sequencing Uncovers Additional Findings in Phelan-McDermid SyndromeRachel Gore Moses, Morgan Similuk, Alexandra Hehn, et al.
Molecular Autism|November 14, 2014
The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analysesJoseph D Buxbaum, Nadia Bolshakova, Jessica M Brownfeld, et al.
Genome Medicine|December 22, 2017
Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disordersHoang T Nguyen, Julien Bryois, April Kim, et al.
American Journal of Human Genetics|October 19, 2010
A genome-wide study reveals copy number variants exclusive to childhood obesity casesJoseph T Glessner, Jonathan P Bradfield, Kai Wang, et al.
European Journal of Human Genetics : EJHG|March 6, 2023
Skewed X-chromosome inactivation in unsolved neurodevelopmental disease cases can guide re-evaluation For X-linked genesChiara Giovenino, Slavica Trajkova, Lisa Pavinato, et al.
Pageof 37