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Deborah L Levy

Showing results (41-50 of 49) with videos related to

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American Journal of Human Genetics|August 7, 2012
Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophreniaAnna C Need, Joseph P McEvoy, Massimo Gennarelli, et al.
Neuron|December 27, 2011
High frequencies of de novo CNVs in bipolar disorder and schizophreniaDheeraj Malhotra, Shane McCarthy, Jacob J Michaelson, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|June 3, 2019
New insights into tardive dyskinesia genetics: Implementation of whole-exome sequencing approachAnna Alkelai, Lior Greenbaum, Erin L Heinzen, et al.
Nature|February 25, 2011
Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophreniaVladimir Vacic, Shane McCarthy, Dheeraj Malhotra, et al.
Biological Psychiatry|July 8, 2019
Targeted Treatment of Individuals With Psychosis Carrying a Copy Number Variant Containing a Genomic Triplication of the Glycine Decarboxylase GeneJ Alexander Bodkin, Michael J Coleman, Laura J Godfrey, 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.
Nature Genetics|February 16, 2010
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delaySanthosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, et al.
Nature Genetics|October 27, 2009
Microduplications of 16p11.2 are associated with schizophreniaShane E McCarthy, Vladimir Makarov, George Kirov, et al.
Nature Genetics|November 22, 2016
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjectsChristian R Marshall, Daniel P Howrigan, Daniele Merico, et al.
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Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
American Journal of Human Genetics|August 7, 2012
Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophreniaAnna C Need, Joseph P McEvoy, Massimo Gennarelli, et al.
Neuron|December 27, 2011
High frequencies of de novo CNVs in bipolar disorder and schizophreniaDheeraj Malhotra, Shane McCarthy, Jacob J Michaelson, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|June 3, 2019
New insights into tardive dyskinesia genetics: Implementation of whole-exome sequencing approachAnna Alkelai, Lior Greenbaum, Erin L Heinzen, et al.
Nature|February 25, 2011
Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophreniaVladimir Vacic, Shane McCarthy, Dheeraj Malhotra, et al.
Biological Psychiatry|July 8, 2019
Targeted Treatment of Individuals With Psychosis Carrying a Copy Number Variant Containing a Genomic Triplication of the Glycine Decarboxylase GeneJ Alexander Bodkin, Michael J Coleman, Laura J Godfrey, 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.
Nature Genetics|February 16, 2010
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delaySanthosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, et al.
Nature Genetics|October 27, 2009
Microduplications of 16p11.2 are associated with schizophreniaShane E McCarthy, Vladimir Makarov, George Kirov, et al.
Nature Genetics|November 22, 2016
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjectsChristian R Marshall, Daniel P Howrigan, Daniele Merico, et al.
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