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Patrick F Sullivan

Showing results (391-400 of 468) with videos related to

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Nature Neuroscience|August 6, 2013
Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disordersGeorg Stoll, Olli P H Pietiläinen, Bastian Linder, et al.
Nature Genetics|October 10, 2017
Genome-wide association analysis identifies 30 new susceptibility loci for schizophreniaZhiqiang Li, Jianhua Chen, Hao Yu, 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.
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.
Cell|October 15, 2019
Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and RecommendationsRoseann E Peterson, Karoline Kuchenbaecker, Raymond K Walters, et al.
Medrxiv : the Preprint Server for Health Sciences|August 12, 2025
Genome-wide study of somatic symptom and related disorders identifies novel genomic loci and map genetic architectureVera Fominykh, Piotr Jaholkowski, Alexey A Shadrin, et al.
The Lancet Regional Health. Europe|December 20, 2023
COVID-19 illness severity and 2-year prevalence of physical symptoms: an observational study in Iceland, Sweden, Norway and DenmarkQing Shen, Emily E Joyce, Omid V Ebrahimi, et al.
Biological Psychiatry|November 14, 2017
Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics ConsortiumWouter J Peyrot, Sandra Van der Auwera, Yuri Milaneschi, et al.
Nature|January 28, 2014
A polygenic burden of rare disruptive mutations in schizophreniaShaun M Purcell, Jennifer L Moran, Menachem Fromer, et al.
Nature Communications|September 5, 2014
Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B allelesJacqueline I Goldstein, L Fredrik Jarskog, Chris Hilliard, et al.
Pageof 47

Showing results (391-400 of 468) with videos related to

Sort By:
Pageof 47
Nature Neuroscience|August 6, 2013
Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disordersGeorg Stoll, Olli P H Pietiläinen, Bastian Linder, et al.
Nature Genetics|October 10, 2017
Genome-wide association analysis identifies 30 new susceptibility loci for schizophreniaZhiqiang Li, Jianhua Chen, Hao Yu, 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.
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.
Cell|October 15, 2019
Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and RecommendationsRoseann E Peterson, Karoline Kuchenbaecker, Raymond K Walters, et al.
Medrxiv : the Preprint Server for Health Sciences|August 12, 2025
Genome-wide study of somatic symptom and related disorders identifies novel genomic loci and map genetic architectureVera Fominykh, Piotr Jaholkowski, Alexey A Shadrin, et al.
The Lancet Regional Health. Europe|December 20, 2023
COVID-19 illness severity and 2-year prevalence of physical symptoms: an observational study in Iceland, Sweden, Norway and DenmarkQing Shen, Emily E Joyce, Omid V Ebrahimi, et al.
Biological Psychiatry|November 14, 2017
Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics ConsortiumWouter J Peyrot, Sandra Van der Auwera, Yuri Milaneschi, et al.
Nature|January 28, 2014
A polygenic burden of rare disruptive mutations in schizophreniaShaun M Purcell, Jennifer L Moran, Menachem Fromer, et al.
Nature Communications|September 5, 2014
Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B allelesJacqueline I Goldstein, L Fredrik Jarskog, Chris Hilliard, et al.
Pageof 47