Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: LRRTM1[original query] |
---|
Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry. Molecular autism 2010 1 (1): 7. Sousa Inês, Clark Taane G, Holt Richard, Pagnamenta Alistair T, Mulder Erik J, Minderaa Ruud B, Bailey Anthony J, Battaglia Agatino, Klauck Sabine M, Poustka Fritz, Monaco Anthony P, |
Family-based analysis of genetic variation underlying psychosis-inducing effects of cannabis: sibling analysis and proband follow-up. Archives of general psychiatry 2011 Feb 68 (2): 148-57. van Winkel Ruud, |
PCSK6 VNTR Polymorphism Is Associated with Degree of Handedness but Not Direction of Handedness. PloS one 2013 8 (6): e67251. Arning Larissa, Ocklenburg Sebastian, Schulz Stefanie, Ness Vanessa, Gerding Wanda M, Hengstler Jan G, Falkenstein Michael, Epplen Jörg T, Güntürkün Onur, Beste Christi |
The imprinted gene LRRTM1 mediates schizotypy and handedness in a nonclinical population. Journal of human genetics 2014 Jun 59 (6): 332-6. Leach Emma L, Prefontaine Gratien, Hurd Peter L, Crespi Bernard |
Cognitive Control Processes and Functional Cerebral Asymmetries: Association with Variation in the Handedness-Associated Gene LRRTM1. Molecular neurobiology 2017 Mar . Beste Christian, Arning Larissa, Gerding Wanda M, Epplen Jörg T, Mertins Alexandra, Röder Melanie C, Bless Josef J, Hugdahl Kenneth, Westerhausen René, Güntürkün Onur, Ocklenburg Sebasti |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: