Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Schizophrenia and DGCR8[original query] |
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Evaluation of six SNPs of MicroRNA machinery genes and risk of schizophrenia. Journal of molecular neuroscience : MN 2013 Mar 49 (3): 594-9. Zhou Yi, Wang Jun, Lu Xiaojun, Song Xingbo, Ye Yuanxin, Zhou Juan, Ying Binwu, Wang Lanl |
Systematic association analysis of microRNA machinery genes with schizophrenia informs further study. Neuroscience letters 2012 Jun 520 (1): 47-50. Zhang Fuquan, Chen Yaguang, Liu Chenxing, Lu Tianlan, Yan Hao, Ruan Yanyan, Yue Weihua, Wang Lifang, Zhang D |
Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome. The Journal of biological chemistry 2015 Sep 290 (38): 23240-53. Napoli Eleonora, Tassone Flora, Wong Sarah, Angkustsiri Kathleen, Simon Tony J, Song Gyu, Giulivi Cecil |
Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017 Jan . Thompson Carlie A, Karelis Jason, Middleton Frank A, Gentile Karen, Coman Ioana L, Radoeva Petya D, Mehta Rashi, Fremont Wanda P, Antshel Kevin M, Faraone Stephen V, Kates Wendy |
Gene expression over the course of schizophrenia: from clinical high-risk for psychosis to chronic stages. NPJ schizophrenia 2019 Mar 5 (1): 5. Ota Vanessa Kiyomi, Moretti Patricia Natalia, Santoro Marcos Leite, Talarico Fernanda, Spindola Leticia Maria, Xavier Gabriela, Carvalho Carolina Muniz, Marques Diogo Ferri, Costa Giovany Oliveira, Pellegrino Renata, de Jong Simone, Cordeiro Quirino, Hakonarson Hakon, Breen Gerome, Noto Cristiano, Bressan Rodrigo Affonseca, Gadelha Ary, Jesus Mari Jair de, Belangero Sintia |
MicroRNAs in the Onset of Schizophrenia. Cells 2021 Oct 10 (10): . Thomas Kristen T, Zakharenko Stanislav |
Schizophrenia Risk Mediated by microRNA Target Genes Overlapped by Genome-Wide Rare Copy Number Variation in 22q11.2 Deletion Syndrome. Frontiers in genetics 2022 5 13 812183. Ying Shengjie, Heung Tracy, Zhang Zhaolei, Yuen Ryan K C, Bassett Anne |
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