Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Mental Retardation and FXR1[original query] |
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Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes. EMBO molecular medicine 2015 Nov . Stepniak Beata, Kästner Anne, Poggi Giulia, Mitjans Marina, Begemann Martin, Hartmann Annette, Van der Auwera Sandra, Sananbenesi Farahnaz, Krueger-Burg Dilja, Matuszko Gabriela, Brosi Cornelia, Homuth Georg, Völzke Henry, Benseler Fritz, Bagni Claudia, Fischer Utz, Dityatev Alexander, Grabe Hans-Jörgen, Rujescu Dan, Fischer Andre, Ehrenreich Hannelo |
Analyzing the Role of MicroRNAs in Schizophrenia in the Context of Common Genetic Risk Variants. JAMA psychiatry 2016 Mar . Hauberg Mads Engel, Roussos Panos, Grove Jakob, Børglum Anders Dupont, Mattheisen Manuel, |
Mental Illnesses-Associated Fxr1 and Its Negative Regulator Gsk3? Are Modulators of Anxiety and Glutamatergic Neurotransmission. Frontiers in molecular neuroscience 2018 11 119. Khlghatyan Jivan, Evstratova Alesya, Chamberland Simon, Marakhovskaia Aleksandra, Bahremand Arash, Toth Katalin, Beaulieu Jean-Mart |
Evidence of an interaction between FXR1 and GSK3? polymorphisms on levels of Negative Symptoms of Schizophrenia and their response to antipsychotics. European psychiatry : the journal of the Association of European Psychiatrists 2021 4 64 (1): e39. Rampino Antonio, Torretta Silvia, Gelao Barbara, Veneziani Federica, Iacoviello Matteo, Marakhovskaya Aleksandra, Masellis Rita, Andriola Ileana, Sportelli Leonardo, Pergola Giulio, Minelli Alessandra, Magri Chiara, Gennarelli Massimo, Vita Antonio, Beaulieu Jean Martin, Bertolino Alessandro, Blasi Giusep |
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