Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: SLC39A13[original query] |
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Phenotypically distinct subtypes of psychosis accompany novel or rare variants in four different signaling genes. EBioMedicine 2016 Apr 6 206-14. Kranz Thorsten M, Berns Adam, Shields Jerry, Rothman Karen, Walsh-Messinger Julie, Goetz Raymond R, Chao Moses V, Malaspina Dolor |
Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts.
The American journal of psychiatry 2019 02 176 (2): 107-118. Sanchez-Roige Sandra, Palmer Abraham A, Fontanillas Pierre, Elson Sarah L, , Adams Mark J, Howard David M, Edenberg Howard J, Davies Gail, Crist Richard C, Deary Ian J, McIntosh Andrew M, Clarke Toni-K |
Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies.
The Lancet. Neurology 2021 (5): 351-361. Traylor Matthew, Persyn Elodie, Tomppo Liisa, Klasson Sofia, Abedi Vida, Bakker Mark K, Torres Nuria, Li Linxin, Bell Steven, Rutten-Jacobs Loes, Tozer Daniel J, Griessenauer Christoph J, Zhang Yanfei, Pedersen Annie, Sharma Pankaj, Jimenez-Conde Jordi, Rundek Tatjana, Grewal Raji P, Lindgren Arne, Meschia James F, Salomaa Veikko, Havulinna Aki, Kourkoulis Christina, Crawford Katherine, Marini Sandro, Mitchell Braxton D, Kittner Steven J, Rosand Jonathan, Dichgans Martin, Jern Christina, Strbian Daniel, Fernandez-Cadenas Israel, Zand Ramin, Ruigrok Ynte, Rost Natalia, Lemmens Robin, Rothwell Peter M, Anderson Christopher D, Wardlaw Joanna, Lewis Cathryn M, Markus Hugh S, , , , |
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