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Stephen T Warren

Showing results (91-100 of 99) with videos related to

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Science Advances|August 16, 2023
Cross-species analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletionRyan H Purcell, Esra Sefik, Erica Werner, et al.
Biorxiv : the Preprint Server for Biology|February 7, 2023
Cross-species transcriptomic analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletionRyan H Purcell, Esra Sefik, Erica Werner, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 26, 2022
Identification of <i>PSMB5</i> as a genetic modifier of fragile X-associated tremor/ataxia syndromeHa Eun Kong, Junghwa Lim, Alexander Linsalata, et al.
Fertility and Sterility|May 21, 2021
Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutationCristina E Trevino, J Christopher Rounds, Krista Charen, et al.
Biological Psychiatry|July 23, 2013
Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophreniaJennifer Gladys Mulle, Ann E Pulver, John A McGrath, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilitiesErin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
American Journal of Human Genetics|November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophreniaDaniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Plos Genetics|March 14, 2012
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility lociEimear E Kenny, Itsik Pe'er, Amir Karban, et al.
Molecular Psychiatry|February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletionIsabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
Pageof 10

Showing results (91-100 of 99) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 99 results.
Science Advances|August 16, 2023
Cross-species analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletionRyan H Purcell, Esra Sefik, Erica Werner, et al.
Biorxiv : the Preprint Server for Biology|February 7, 2023
Cross-species transcriptomic analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletionRyan H Purcell, Esra Sefik, Erica Werner, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 26, 2022
Identification of <i>PSMB5</i> as a genetic modifier of fragile X-associated tremor/ataxia syndromeHa Eun Kong, Junghwa Lim, Alexander Linsalata, et al.
Fertility and Sterility|May 21, 2021
Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutationCristina E Trevino, J Christopher Rounds, Krista Charen, et al.
Biological Psychiatry|July 23, 2013
Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophreniaJennifer Gladys Mulle, Ann E Pulver, John A McGrath, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilitiesErin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
American Journal of Human Genetics|November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophreniaDaniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Plos Genetics|March 14, 2012
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility lociEimear E Kenny, Itsik Pe'er, Amir Karban, et al.
Molecular Psychiatry|February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletionIsabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
Pageof 10