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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 14, 2025. (Total: 235269Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Schizophrenia and NIPA2[original query]
Rare CNVs and tag SNPs at 15q11.2 are associated with schizophrenia in the Han Chinese population.
Schizophrenia bulletin 2012 Feb .
Zhao Q, Li T, Zhao X, Huang K, Wang T, Li Z, Ji J, Zeng Z, Zhang Z, Li K, Feng G, St Clair D, He L, Shi Y
Genetic counseling for susceptibility loci and neurodevelopmental disorders: the del15q11.2 as an example.
American journal of medical genetics. Part A 2013 Nov 161A (11): 2846-54.
De Wolf Veerle, Brison Nathalie, Devriendt Koenraad, Peeters Hil
Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four Cohorts.
Biological psychiatry 2019 Mar .
Zhang Xianglong, Abdellaoui Abdel, Rucker James, de Jong Simone, Potash James B, Weissman Myrna M, Shi Jianxin, Knowles James A, Pato Carlos, Pato Michele, Sobell Janet, Smit Johannes H, Hottenga Jouke-Jan, de Geus Eco J C, Lewis Cathryn M, Buttenschøn Henriette N, Craddock Nick, Jones Ian, Jones Lisa, McGuffin Peter, Mors Ole, Owen Michael J, Preisig Martin, Rietschel Marcella, Rice John P, Rivera Margarita, Uher Rudolf, Gejman Pablo V, Sanders Alan R, Boomsma Dorret, Penninx Brenda W J H, Breen Gerome, Levinson Douglas
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