Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: NRSN1[original query] |
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Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study.
Translational psychiatry 2017 Oct 7 (10): e1249. Lencer R, Mills L J, Alliey-Rodriguez N, Shafee R, Lee A M, Reilly J L, Sprenger A, McDowell J E, McCarroll S A, Keshavan M S, Pearlson G D, Tamminga C A, Clementz B A, Gershon E S, Sweeney J A, Bishop J |
Common genetic variants in GAL, GAP43 and NRSN1 and interaction networks confer susceptibility to Hirschsprung disease. Journal of cellular and molecular medicine 2018 Apr . Wang Yang, Yan Weihui, Wang Jun, Zhou Ying, Chen Jie, Gu Beilin, Cai W |
Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease. Aging 2020 3 12 (5): 4379-4393. Wang Yang, Jiang Qian, Cai Hao, Xu Ze, Wu Wenjie, Gu Beilin, Li Long, Cai W |
Developmental dyslexia susceptibility genes DNAAF4, DCDC2, and NRSN1 are associated with brain function in fluently reading adolescents and young adults. Cerebral cortex (New York, N.Y. : 1991) 2024 4 34 (4): . Nea Rinne, Patrik Wikman, Elisa Sahari, Juha Salmi, Elisabet Einarsdóttir, Juha Kere, Kimmo Al |
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