Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and meta-analysis and NOS1[original query] |
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| Functional variants in NOS1 and NOS2A are not associated with progressive hearing loss in Ménière's disease in a European Caucasian population. DNA and cell biology 2011 Sep 30 (9): 699-708. Gazquez Irene, Lopez-Escamez Jose A, Moreno Antonia, Campbell Colleen A, Meyer Nicole C, Carey John P, Minor Lloyd B, Gantz Bruce J, Hansen Marlan R, Della Santina Charles C, Aran Ismael, Soto-Varela Andres, Santos Sofia, Batuecas Angel, Perez-Garrigues Herminio, Lopez-Nevot Alicia, Smith Richard J H, Lopez-Nevot Miguel |
| The genetic contribution of the NO system at the glutamatergic post-synapse to schizophrenia: further evidence and meta-analysis. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2014 Jan 24 (1): 65-85. Weber H, Klamer D, Freudenberg F, Kittel-Schneider S, Rivero O, Scholz C-J, Volkert J, Kopf J, Heupel J, Herterich S, Adolfsson R, Alttoa A, Post A, Grußendorf H, Kramer A, Gessner A, Schmidt B, Hempel S, Jacob C P, Sanjuán J, Moltó M D, Lesch K-P, Freitag C M, Kent L, Reif |
| On the role of NOS1 ex1f-VNTR in ADHD-allelic, subgroup, and meta-analysis. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Jun . Weber Heike, Kittel-Schneider Sarah, Heupel Julia, Weißflog Lena, Kent Lindsey, Freudenberg Florian, Alttoa Aet, Post Antonia, Herterich Sabine, Haavik Jan, Halmøy Anne, Fasmer Ole B, Landaas Elisabeth T, Johansson Stefan, Cormand Bru, Ribasés Marta, Sánchez-Mora Cristina, Ramos-Quiroga Josep Antoni, Franke Barbara, Lesch Klaus-Peter, Reif Andre |
| Genetic association of NOS1 exon18, NOS1 exon29, ABCB1 1236C/T, and ABCB1 3435C/T polymorphisms with the risk of Parkinson's disease: A meta-analysis. Medicine 2016 Oct 95 (40): e4982. Huang Hongbin, Peng Cong, Liu Yong, Liu Xu, Chen Qicong, Huang Zunn |
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