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Michael E Talkowski

Showing results (141-150 of 184) with videos related to

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Bipolar Disorders|October 21, 2009
Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophreniaHader A Mansour, Michael E Talkowski, Joel Wood, et al.
American Journal of Human Genetics|October 11, 2011
Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorderMichael E Talkowski, Sureni V Mullegama, Jill A Rosenfeld, et al.
Cell|January 26, 2020
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of AutismF Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, et al.
Annals of Neurology|January 25, 2023
Genome-Wide Analysis of Structural Variants in Parkinson DiseaseKimberley J Billingsley, Jinhui Ding, Pilar Alvarez Jerez, et al.
Human Mutation|February 1, 2012
Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic featuresAllen N Lamb, Jill A Rosenfeld, Nicholas J Neill, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2024
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disordersJulie A Jurgens, Brenda J Barry, Wai-Man Chan, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disordersJulie A Jurgens, Brenda J Barry, Wai-Man Chan, et al.
Medrxiv : the Preprint Server for Health Sciences|May 18, 2026
NeuroDev: etiology and experience of neurodevelopmental disorders in Kenya and South AfricaPatricia Kipkemoi, Emily O'Heir, Mutaz Amin, et al.
Medrxiv : the Preprint Server for Health Sciences|November 19, 2025
Population-scale Long-read Sequencing in the <i>All of Us</i> Research ProgramKiran V Garimella, Qiuhui Li, Julie Wertz, et al.
Medrxiv : the Preprint Server for Health Sciences|December 3, 2025
Common and rare variant genetic contributions in African Americans with autismMatilde Cirnigliaro, Jennifer K Lowe, Alexander O Flynn-Carroll, et al.
Pageof 19

Showing results (141-150 of 184) with videos related to

Sort By:
Pageof 19
Bipolar Disorders|October 21, 2009
Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophreniaHader A Mansour, Michael E Talkowski, Joel Wood, et al.
American Journal of Human Genetics|October 11, 2011
Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorderMichael E Talkowski, Sureni V Mullegama, Jill A Rosenfeld, et al.
Cell|January 26, 2020
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of AutismF Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, et al.
Annals of Neurology|January 25, 2023
Genome-Wide Analysis of Structural Variants in Parkinson DiseaseKimberley J Billingsley, Jinhui Ding, Pilar Alvarez Jerez, et al.
Human Mutation|February 1, 2012
Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic featuresAllen N Lamb, Jill A Rosenfeld, Nicholas J Neill, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2024
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disordersJulie A Jurgens, Brenda J Barry, Wai-Man Chan, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disordersJulie A Jurgens, Brenda J Barry, Wai-Man Chan, et al.
Medrxiv : the Preprint Server for Health Sciences|May 18, 2026
NeuroDev: etiology and experience of neurodevelopmental disorders in Kenya and South AfricaPatricia Kipkemoi, Emily O'Heir, Mutaz Amin, et al.
Medrxiv : the Preprint Server for Health Sciences|November 19, 2025
Population-scale Long-read Sequencing in the <i>All of Us</i> Research ProgramKiran V Garimella, Qiuhui Li, Julie Wertz, et al.
Medrxiv : the Preprint Server for Health Sciences|December 3, 2025
Common and rare variant genetic contributions in African Americans with autismMatilde Cirnigliaro, Jennifer K Lowe, Alexander O Flynn-Carroll, et al.
Pageof 19