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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.Nature|July 3, 2009
Common variants on chromosome 6p22.1 are associated with schizophreniaJianxin Shi, Douglas F Levinson, Jubao Duan, et al.Human Molecular Genetics|October 29, 2013
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1Elliott Rees, James T R Walters, Kimberly D Chambert, et al.American Journal of Human Genetics|January 10, 2006
Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sampleBrian K Suarez, Jubao Duan, Alan R Sanders, 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.Biological Psychiatry|April 21, 2019
Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four CohortsXianglong Zhang, Abdel Abdellaoui, James Rucker, 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.The American Journal of Psychiatry|August 14, 2012
Genome-wide association study of multiplex schizophrenia pedigreesDouglas F Levinson, Jianxin Shi, Kai Wang, 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.Nature Genetics|May 5, 2009
Narcolepsy is strongly associated with the T-cell receptor alpha locusJoachim Hallmayer, Juliette Faraco, Ling Lin, et al.Pageof 8