Showing results (71-80 of 81) with videos related to
Sort By:
Pageof 9
Nature Neuroscience|April 5, 2022
Exome sequencing of individuals with Huntington's disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onsetBranduff McAllister, Jasmine Donaldson, Caroline S Binda, et al.Diabetes|June 23, 2012
Association testing of previously reported variants in a large case-control meta-analysis of diabetic nephropathyWinfred W Williams, Rany M Salem, Amy Jayne McKnight, et al.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|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 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|April 9, 2022
Rare coding variants in ten genes confer substantial risk for schizophreniaTarjinder Singh, Timothy Poterba, David Curtis, et al.Pageof 9