Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Depressive Disorder and SLC6A15[original query] |
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A variant of the neuronal amino acid transporter SLC6A15 is associated with ACTH and cortisol responses and cognitive performance in unipolar depression. The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2013 Feb 16 (1): 83-90. Schuhmacher Anna, Lennertz Leonhard, Wagner Michael, Höfels Susanne, Pfeiffer Ute, Guttenthaler Vera, Maier Wolfgang, Zobel Astrid, Mössner Raina |
Functional coding variants in SLC6A15, a possible risk gene for major depression. PloS one 2013 8 (7): e68645. Quast Carina, Cuboni Serena, Bader Daniel, Altmann André, Weber Peter, Arloth Janine, Röh Simone, Brückl Tanja, Ising Marcus, Kopczak Anna, Erhardt Angelika, Hausch Felix, Lucae Susanne, Binder Elisabeth |
Effects of a Polymorphism of the Neuronal Amino Acid Transporter SLC6A15 Gene on Structural Integrity of White Matter Tracts in Major Depressive Disorder. PloS one 2016 11 (10): e0164301. Choi Sunyoung, Han Kyu-Man, Kang June, Won Eunsoo, Chang Hun Soo, Tae Woo Suk, Son Kyu Ri, Kim Su-Jin, Lee Min-Soo, Ham Byung-J |
A Combined Study of SLC6A15 Gene Polymorphism and the Resting-State Functional Magnetic Resonance Imaging in First-Episode Drug-Naive Major Depressive Disorder. Genetic testing and molecular biomarkers 2017 Sep 21 (9): 523-530. Wang Lijuan, Liu Zhifen, Cao Xiaohua, Li Jianying, Zhang Aixia, Sun Ning, Yang Chunxia, Zhang Kera |
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