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Michael E Talkowski

Showing results (121-130 of 184) with videos related to

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European Journal of Human Genetics : EJHG|May 2, 2013
Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorderSureni V Mullegama, Jill A Rosenfeld, Carmen Orellana, et al.
Archives of General Psychiatry|October 10, 2012
Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesityCarl Ernst, Christian R Marshall, Yiping Shen, et al.
Genome Biology|March 7, 2017
Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genomeRyan L Collins, Harrison Brand, Claire E Redin, et al.
Nature Communications|June 6, 2023
Chromatin alternates between A and B compartments at kilobase scale for subgenic organizationHannah L Harris, Huiya Gu, Moshe Olshansky, et al.
Nature Communications|September 27, 2024
A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disordersArthur S Lee, Lauren J Ayers, Michael Kosicki, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Therapeutic targeting of alternative splicing caused by a lethal noncoding structural variant in X-linked dystonia parkinsonismRachita Yadav, Christine A Vaine, Aloysius Domingo, et al.
Annals of Medicine|December 13, 2005
Serotonin gene polymorphisms and bipolar I disorder: focus on the serotonin transporterHader A Mansour, Michael E Talkowski, Joel Wood, et al.
American Journal of Human Genetics|December 11, 2012
Disruption of a large intergenic noncoding RNA in subjects with neurodevelopmental disabilitiesMichael E Talkowski, Gilles Maussion, Liam Crapper, et al.
American Journal of Medical Genetics. Part A|October 21, 2016
Implication of LRRC4C and DPP6 in neurodevelopmental disordersGilles Maussion, Cristiana Cruceanu, Jill A Rosenfeld, et al.
Plos One|June 14, 2018
Traditional and systems biology based drug discovery for the rare tumor syndrome neurofibromatosis type 2, Robert Allaway, Steve P Angus, et al.
Pageof 19

Showing results (121-130 of 184) with videos related to

Sort By:
Pageof 19
European Journal of Human Genetics : EJHG|May 2, 2013
Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorderSureni V Mullegama, Jill A Rosenfeld, Carmen Orellana, et al.
Archives of General Psychiatry|October 10, 2012
Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesityCarl Ernst, Christian R Marshall, Yiping Shen, et al.
Genome Biology|March 7, 2017
Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genomeRyan L Collins, Harrison Brand, Claire E Redin, et al.
Nature Communications|June 6, 2023
Chromatin alternates between A and B compartments at kilobase scale for subgenic organizationHannah L Harris, Huiya Gu, Moshe Olshansky, et al.
Nature Communications|September 27, 2024
A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disordersArthur S Lee, Lauren J Ayers, Michael Kosicki, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Therapeutic targeting of alternative splicing caused by a lethal noncoding structural variant in X-linked dystonia parkinsonismRachita Yadav, Christine A Vaine, Aloysius Domingo, et al.
Annals of Medicine|December 13, 2005
Serotonin gene polymorphisms and bipolar I disorder: focus on the serotonin transporterHader A Mansour, Michael E Talkowski, Joel Wood, et al.
American Journal of Human Genetics|December 11, 2012
Disruption of a large intergenic noncoding RNA in subjects with neurodevelopmental disabilitiesMichael E Talkowski, Gilles Maussion, Liam Crapper, et al.
American Journal of Medical Genetics. Part A|October 21, 2016
Implication of LRRC4C and DPP6 in neurodevelopmental disordersGilles Maussion, Cristiana Cruceanu, Jill A Rosenfeld, et al.
Plos One|June 14, 2018
Traditional and systems biology based drug discovery for the rare tumor syndrome neurofibromatosis type 2, Robert Allaway, Steve P Angus, et al.
Pageof 19