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Joseph D Buxbaum

Showing results (101-110 of 376) with videos related to

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Autism Research : Official Journal of the International Society for Autism Research|June 29, 2026
Prevalence of Phelan McDermid Syndrome Estimated To Be ~1:7300 Using a Multisource ModelTess Levy, David Lapidus, Kate Friedman, et al.
Biological Psychiatry|March 23, 2020
Maternal Effects as Causes of Risk for Obsessive-Compulsive DisorderBehrang Mahjani, Lambertus Klei, Christina M Hultman, et al.
Experimental Neurology|August 3, 2016
New translational perspectives for blood-based biomarkers of PTSD: From glucocorticoid to immune mediators of stress susceptibilityNikolaos P Daskalakis, Hagit Cohen, Caroline M Nievergelt, et al.
Psychiatric Genetics|June 5, 2010
PCDH11X variation is not associated with late-onset Alzheimer disease susceptibilityGary W Beecham, Adam C Naj, John R Gilbert, et al.
Biological Psychiatry|April 18, 2006
Lack of evidence for association of the serotonin transporter gene SLC6A4 with autismNicolas Ramoz, Jennifer G Reichert, Thomas E Corwin, et al.
Brain Research|November 11, 2010
Analysis of a purported SHANK3 mutation in a boy with autism: clinical impact of rare variant research in neurodevelopmental disabilitiesAlexander Kolevzon, Guiqing Cai, Latha Soorya, et al.
Psychiatric Genetics|August 12, 2005
Fine mapping of the 5p13 locus linked to schizophrenia and schizotypal personality disorder in a Puerto Rican familyIrina N Bespalova, Gary W Angelo, Martina Durner, et al.
American Journal of Human Genetics|May 5, 2018
FUN-LDA: A Latent Dirichlet Allocation Model for Predicting Tissue-Specific Functional Effects of Noncoding Variation: Methods and ApplicationsDaniel Backenroth, Zihuai He, Krzysztof Kiryluk, et al.
Human Genetics|July 16, 2023
Prospective phenotyping of CHAMP1 disorder indicates that coding mutations may not act through haploinsufficiencyTess Levy, Thariana Pichardo, Hailey Silver, et al.
Human Molecular Genetics|March 10, 2022
CHAMP1 disorder is associated with a complex neurobehavioral phenotype including autism, ADHD, repetitive behaviors and sensory symptomsTess Levy, Bonnie Lerman, Danielle Halpern, et al.
Pageof 38

Showing results (101-110 of 376) with videos related to

Sort By:
Pageof 38
Autism Research : Official Journal of the International Society for Autism Research|June 29, 2026
Prevalence of Phelan McDermid Syndrome Estimated To Be ~1:7300 Using a Multisource ModelTess Levy, David Lapidus, Kate Friedman, et al.
Biological Psychiatry|March 23, 2020
Maternal Effects as Causes of Risk for Obsessive-Compulsive DisorderBehrang Mahjani, Lambertus Klei, Christina M Hultman, et al.
Experimental Neurology|August 3, 2016
New translational perspectives for blood-based biomarkers of PTSD: From glucocorticoid to immune mediators of stress susceptibilityNikolaos P Daskalakis, Hagit Cohen, Caroline M Nievergelt, et al.
Psychiatric Genetics|June 5, 2010
PCDH11X variation is not associated with late-onset Alzheimer disease susceptibilityGary W Beecham, Adam C Naj, John R Gilbert, et al.
Biological Psychiatry|April 18, 2006
Lack of evidence for association of the serotonin transporter gene SLC6A4 with autismNicolas Ramoz, Jennifer G Reichert, Thomas E Corwin, et al.
Brain Research|November 11, 2010
Analysis of a purported SHANK3 mutation in a boy with autism: clinical impact of rare variant research in neurodevelopmental disabilitiesAlexander Kolevzon, Guiqing Cai, Latha Soorya, et al.
Psychiatric Genetics|August 12, 2005
Fine mapping of the 5p13 locus linked to schizophrenia and schizotypal personality disorder in a Puerto Rican familyIrina N Bespalova, Gary W Angelo, Martina Durner, et al.
American Journal of Human Genetics|May 5, 2018
FUN-LDA: A Latent Dirichlet Allocation Model for Predicting Tissue-Specific Functional Effects of Noncoding Variation: Methods and ApplicationsDaniel Backenroth, Zihuai He, Krzysztof Kiryluk, et al.
Human Genetics|July 16, 2023
Prospective phenotyping of CHAMP1 disorder indicates that coding mutations may not act through haploinsufficiencyTess Levy, Thariana Pichardo, Hailey Silver, et al.
Human Molecular Genetics|March 10, 2022
CHAMP1 disorder is associated with a complex neurobehavioral phenotype including autism, ADHD, repetitive behaviors and sensory symptomsTess Levy, Bonnie Lerman, Danielle Halpern, et al.
Pageof 38