Human Genome Epidemiology Literature Finder
|
Records 1 - 5 (of 5 Records) |
| Query Trace: Schizophrenia and MYT1L[original query] |
|---|
| Recurrent CNVs disrupt three candidate genes in schizophrenia patients. American journal of human genetics 2008 Oct 83 (4): 504-10. Vrijenhoek Terry, Buizer-Voskamp Jacobine E, van der Stelt Inge, Strengman Eric, , Sabatti Chiara, Geurts van Kessel Ad, Brunner Han G, Ophoff Roel A, Veltman Joris |
| Replication of association between schizophrenia and ZNF804A in the Irish Case-Control Study of Schizophrenia sample. Molecular psychiatry 2010 Jan 15 (1): 29-37. Riley B, Thiselton D, Maher B S, Bigdeli T, Wormley B, McMichael G O, Fanous A H, Vladimirov V, O'Neill F A, Walsh D, Kendler K |
| Association study of myelin transcription factor 1-like polymorphisms with schizophrenia in Han Chinese population. Genes, brain, and behavior 2012 Feb 11 (1): 87-93. Li W, Wang X, Zhao J, Lin J, Song X-Q, Yang Y, Jiang C, Xiao B, Yang G, Zhang H-X, Lv L |
| Genetic variants in Nogo receptor signaling pathways may be associated with early life adversity in schizophrenia susceptibility. BBA clinical 2015 Jun 3 36-43. Andrews Jessica L, Fernandez-Enright Frances |
| Fibromyalgia: A Review of Related Polymorphisms and Clinical Relevance. Anais da Academia Brasileira de Ciencias 2021 11 93 (suppl 4): e20210618. Janssen Luísa P, Medeiros Liciane F, Souza Andressa DE, Silva Juliana |
- Page last reviewed:Feb 1, 2024
- Content source: