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Elliott Rees

Showing results (61-70 of 68) with videos related to

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Plos Genetics|May 7, 2016
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental DisordersAnthony R Isles, Andrés Ingason, Chelsea Lowther, et al.
JAMA Psychiatry|January 18, 2013
Implication of a rare deletion at distal 16p11.2 in schizophreniaSaurav Guha, Elliott Rees, Ariel Darvasi, et al.
Human Molecular Genetics|January 30, 2014
An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosisDerek W Morris, Richard D Pearson, Paul Cormican, et al.
Neuron|June 23, 2017
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette SyndromeAlden Y Huang, Dongmei Yu, Lea K Davis, et al.
Nature Neuroscience|March 15, 2016
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disordersTarjinder Singh, Mitja I Kurki, David Curtis, et al.
Nature Genetics|February 28, 2018
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selectionAntonio F Pardiñas, Peter Holmans, Andrew J Pocklington, et al.
Nature Genetics|June 5, 2019
Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selectionAntonio F Pardiñas, Peter Holmans, Andrew J Pocklington, et al.
Nature|April 9, 2022
Rare coding variants in ten genes confer substantial risk for schizophreniaTarjinder Singh, Timothy Poterba, David Curtis, et al.
Pageof 7

Showing results (61-70 of 68) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 68 results.
Plos Genetics|May 7, 2016
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental DisordersAnthony R Isles, Andrés Ingason, Chelsea Lowther, et al.
JAMA Psychiatry|January 18, 2013
Implication of a rare deletion at distal 16p11.2 in schizophreniaSaurav Guha, Elliott Rees, Ariel Darvasi, et al.
Human Molecular Genetics|January 30, 2014
An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosisDerek W Morris, Richard D Pearson, Paul Cormican, et al.
Neuron|June 23, 2017
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette SyndromeAlden Y Huang, Dongmei Yu, Lea K Davis, et al.
Nature Neuroscience|March 15, 2016
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disordersTarjinder Singh, Mitja I Kurki, David Curtis, et al.
Nature Genetics|February 28, 2018
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selectionAntonio F Pardiñas, Peter Holmans, Andrew J Pocklington, et al.
Nature Genetics|June 5, 2019
Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selectionAntonio F Pardiñas, Peter Holmans, Andrew J Pocklington, et al.
Nature|April 9, 2022
Rare coding variants in ten genes confer substantial risk for schizophreniaTarjinder Singh, Timothy Poterba, David Curtis, et al.
Pageof 7