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Thomas M Werge

Showing results (11-20 of 38) with videos related to

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Frontiers in Neuroscience|December 7, 2016
Investigation of SNP rs2060546 Immediately Upstream to <i>NTN4</i> in a Danish Gilles de la Tourette Syndrome CohortShanmukha S Padmanabhuni, Rayan Houssari, Ann-Louise Esserlind, et al.
Focus (American Psychiatric Publishing)|February 5, 2020
Shared Molecular Neuropathology Across Major Psychiatric Disorders Parallels Polygenic OverlapMichael J Gandal, Jillian R Haney, Neelroop N Parikshak, et al.
Translational Psychiatry|December 1, 2017
A mouse model of the schizophrenia-associated 1q21.1 microdeletion syndrome exhibits altered mesolimbic dopamine transmissionJacob Nielsen, Kim Fejgin, Florence Sotty, et al.
Science (New York, N.Y.)|February 14, 2018
Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlapMichael J Gandal, Jillian R Haney, Neelroop N Parikshak, et al.
Brain Communications|January 25, 2023
The genetic background of hydrocephalus in a population-based cohort: implication of ciliary involvementTina N Munch, Paula L Hedley, Christian M Hagen, et al.
Scientific Reports|September 1, 2021
Genetic regulation of spermine oxidase activity and cancer risk: a Mendelian randomization studyJoão Fadista, Victor Yakimov, Urmo Võsa, et al.
Biological Psychiatry|October 5, 2013
A mouse model that recapitulates cardinal features of the 15q13.3 microdeletion syndrome including schizophrenia- and epilepsy-related alterationsKim Fejgin, Jacob Nielsen, Michelle R Birknow, et al.
Journal of Psychiatry & Neuroscience : JPN|July 9, 2016
Persistent gating deficit and increased sensitivity to NMDA receptor antagonism after puberty in a new mouse model of the human 22q11.2 microdeletion syndrome: a study in male miceMichael Didriksen, Kim Fejgin, Simon R O Nilsson, et al.
Plos One|December 12, 2018
Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to diseaseChristian M Hagen, Vanessa F Gonçalves, Paula L Hedley, et al.
Plos One|December 14, 2018
Complex spatio-temporal distribution and genomic ancestry of mitochondrial DNA haplogroups in 24,216 DanesJonas Bybjerg-Grauholm, Christian M Hagen, Vanessa F Gonçalves, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Frontiers in Neuroscience|December 7, 2016
Investigation of SNP rs2060546 Immediately Upstream to <i>NTN4</i> in a Danish Gilles de la Tourette Syndrome CohortShanmukha S Padmanabhuni, Rayan Houssari, Ann-Louise Esserlind, et al.
Focus (American Psychiatric Publishing)|February 5, 2020
Shared Molecular Neuropathology Across Major Psychiatric Disorders Parallels Polygenic OverlapMichael J Gandal, Jillian R Haney, Neelroop N Parikshak, et al.
Translational Psychiatry|December 1, 2017
A mouse model of the schizophrenia-associated 1q21.1 microdeletion syndrome exhibits altered mesolimbic dopamine transmissionJacob Nielsen, Kim Fejgin, Florence Sotty, et al.
Science (New York, N.Y.)|February 14, 2018
Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlapMichael J Gandal, Jillian R Haney, Neelroop N Parikshak, et al.
Brain Communications|January 25, 2023
The genetic background of hydrocephalus in a population-based cohort: implication of ciliary involvementTina N Munch, Paula L Hedley, Christian M Hagen, et al.
Scientific Reports|September 1, 2021
Genetic regulation of spermine oxidase activity and cancer risk: a Mendelian randomization studyJoão Fadista, Victor Yakimov, Urmo Võsa, et al.
Biological Psychiatry|October 5, 2013
A mouse model that recapitulates cardinal features of the 15q13.3 microdeletion syndrome including schizophrenia- and epilepsy-related alterationsKim Fejgin, Jacob Nielsen, Michelle R Birknow, et al.
Journal of Psychiatry & Neuroscience : JPN|July 9, 2016
Persistent gating deficit and increased sensitivity to NMDA receptor antagonism after puberty in a new mouse model of the human 22q11.2 microdeletion syndrome: a study in male miceMichael Didriksen, Kim Fejgin, Simon R O Nilsson, et al.
Plos One|December 12, 2018
Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to diseaseChristian M Hagen, Vanessa F Gonçalves, Paula L Hedley, et al.
Plos One|December 14, 2018
Complex spatio-temporal distribution and genomic ancestry of mitochondrial DNA haplogroups in 24,216 DanesJonas Bybjerg-Grauholm, Christian M Hagen, Vanessa F Gonçalves, et al.
Pageof 4