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Nature Genetics|June 27, 2017
The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disabilityTarjinder Singh, James T R Walters, Mandy Johnstone, et al.
Brain : a Journal of Neurology|February 1, 2013
SGCE mutations cause psychiatric disorders: clinical and genetic characterizationKathryn J Peall, Daniel J Smith, Manju A Kurian, et al.
Bjpsych Open|February 8, 2023
DRAGON-Data: a platform and protocol for integrating genomic and phenotypic data across large psychiatric cohortsAmy J Lynham, Sarah Knott, Jack F G Underwood, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 20, 2010
Fine-mapping reveals novel alternative splicing of the dopamine transporterMichael E Talkowski, Kathleen L McCann, Michael Chen, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 15, 2015
Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illnessTim B Bigdeli, Stephan Ripke, Silviu-Alin Bacanu, et al.
JAMA Psychiatry|July 30, 2013
A comprehensive family-based replication study of schizophrenia genesKarolina A Aberg, Youfang Liu, Jozsef Bukszár, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|May 26, 2007
Genetics of epilepsy: epilepsy research foundation workshop reportSanjay Sisodiya, J Helen Cross, Ingmar Blümcke, et al.
European Journal of Human Genetics : EJHG|October 27, 2011
Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areataLina M Forstbauer, Felix F Brockschmidt, Valentina Moskvina, et al.
Human Molecular Genetics|February 9, 2013
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizuresAnath C Lionel, Andrea K Vaags, Daisuke Sato, 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.
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