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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 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.Biological Psychiatry|April 25, 2006
Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samplesMichael E Talkowski, Howard Seltman, Anne S Bassett, et al.Molecular Psychiatry|November 12, 2024
Genome-wide copy number variation association study in anorexia nervosaAlicia Walker, Robert Karlsson, Jin P Szatkiewicz, et al.The American Journal of Psychiatry|February 18, 2011
Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illnessAndrés Ingason, George Kirov, Ina Giegling, et al.Nature Genetics|August 5, 2008
Identification of loci associated with schizophrenia by genome-wide association and follow-upMichael C O'Donovan, Nicholas Craddock, Nadine Norton, et al.European Archives of Psychiatry and Clinical Neuroscience|December 6, 2019
International Consortium on the Genetics of Electroconvulsive Therapy and Severe Depressive Disorders (Gen-ECT-ic)Takahiro Soda, Declan M McLoughlin, Scott R Clark, et al.Nature|April 9, 2022
Rare coding variants in ten genes confer substantial risk for schizophreniaTarjinder Singh, Timothy Poterba, David Curtis, 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.Pageof 20