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Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 1, 2014
Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literatureChelsea Lowther, Gregory Costain, Dimitri J Stavropoulos, et al.
Journal of Neurodevelopmental Disorders|February 21, 2023
Deep phenotypic analysis of psychiatric features in genetically defined cohorts: application to XYY syndromeArmin Raznahan, Srishti Rau, Luke Schaffer, et al.
Communications Biology|January 30, 2021
Multimodal in vivo recording using transparent graphene microelectrodes illuminates spatiotemporal seizure dynamics at the microscaleNicolette Driscoll, Richard E Rosch, Brendan B Murphy, et al.
Eneuro|February 2, 2022
Neurophysiological Evidence for Cognitive Map Formation during Sequence LearningJennifer Stiso, Christopher W Lynn, Ari E Kahn, et al.
Human Brain Mapping|July 18, 2019
Brain-based ranking of cognitive domains to predict schizophreniaTeresa M Karrer, Danielle S Bassett, Birgit Derntl, et al.
American Journal of Medical Genetics. Part A|March 26, 2018
Elucidating the diagnostic odyssey of 22q11.2 deletion syndromeLisa D Palmer, Nancy J Butcher, Erik Boot, et al.
Genome Medicine|December 1, 2017
Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophreniaChelsea Lowther, Daniele Merico, Gregory Costain, et al.
Biorxiv : the Preprint Server for Biology|November 1, 2024
Network analysis of α-synuclein pathology progression reveals p21-activated kinases as regulators of vulnerabilityNaman Vatsa, Julia K Brynildsen, Thomas M Goralski, et al.
Science Advances|June 22, 2022
Cortical-subcortical structural connections support transcranial magnetic stimulation engagement of the amygdalaValerie J Sydnor, Matthew Cieslak, Romain Duprat, et al.
Cell|August 1, 2020
Memory Sequencing Reveals Heritable Single-Cell Gene Expression Programs Associated with Distinct Cellular BehaviorsSydney M Shaffer, Benjamin L Emert, Raúl A Reyes Hueros, et al.
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