Human Genome Epidemiology Literature Finder
|
Records 1 - 7 (of 7 Records) |
| Query Trace: Psychopathology and CACNA1C[original query] |
|---|
| Brain function in carriers of a genome-wide supported bipolar disorder variant. Archives of general psychiatry 2010 Aug 67 (8): 803-11. Erk Susanne, Meyer-Lindenberg Andreas, Schnell Knut, Opitz von Boberfeld Carola, Esslinger Christine, Kirsch Peter, Grimm Oliver, Arnold Claudia, Haddad Leila, Witt Stephanie H, Cichon Sven, Nöthen Markus M, Rietschel Marcella, Walter Henr |
| Variations in FKBP5 and BDNF genes are suggestively associated with depression in a Swedish population-based cohort. Journal of affective disorders 2010 Sep 125 (1-3): 249-55. Lavebratt Catharina, Aberg Elin, Sjöholm Louise K, Forsell Yvon |
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
Lancet (London, England) 2013 Apr 381 (9875): 1371-9. Authors are not available |
| Epistatic interaction of genetic depression risk variants in the human subgenual cingulate cortex during memory encoding. Translational psychiatry 2014 4 e372. Schott B H, Assmann A, Schmierer P, Soch J, Erk S, Garbusow M, Mohnke S, Pöhland L, Romanczuk-Seiferth N, Barman A, Wüstenberg T, Haddad L, Grimm O, Witt S, Richter S, Klein M, Schütze H, Mühleisen T W, Cichon S, Rietschel M, Noethen M M, Tost H, Gundelfinger E D, Düzel E, Heinz A, Meyer-Lindenberg A, Seidenbecher C I, Walter |
| Variation in CACNA1C is Associated with Amygdala Structure and Function in Adolescents. Journal of child and adolescent psychopharmacology 2015 Sep . Sumner Jennifer A, Sheridan Margaret A, Drury Stacy S, Esteves Kyle C, Walsh Kate, Koenen Karestan C, McLaughlin Katie |
| Role of CACNA1C gene polymorphisms and protein expressions in the pathogenesis of schizophrenia: a case-control study in a Chinese population. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2017 Jun . Zhang Sheng-Yu, Hu Qiang, Tang Tao, Liu Chao, Li Cheng-Chong, Yang Xiao-Guang, Zang Yin-Yin, Cai Wei-Xio |
| Psychiatric manifestations of rare variation in medically actionable genes: a PheWAS approach. BMC genomics 2022 May 23 (1): 385. Feng Yen-Chen A, Stanaway Ian B, Connolly John J, Denny Joshua C, Luo Yuan, Weng Chunhua, Wei Wei-Qi, Weiss Scott T, Karlson Elizabeth W, Smoller Jordan |
- Page last reviewed:Feb 1, 2024
- Content source: