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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Disease and GRIK5[original query]
Association study of polymorphisms in the GluR7, KA1 and KA2 kainate receptor genes (GRIK3, GRIK4, GRIK5) with schizophrenia.
Psychiatry research 2006 Jan 141 (1): 39-51.
Shibata Hiroki, Aramaki Toshihiro, Sakai Mayumi, Ninomiya Hideaki, Tashiro Nobutada, Iwata Nakao, Ozaki Norio, Fukumaki Yasuyu
Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non-synonymous SNPs of 306 genes involved in neurotransmission and neurodevelopment.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009 Sep 150B (6): 808-16.
Gratacòs Mònica, Costas Javier, de Cid Rafael, Bayés Mònica, González Juan R, Baca-García Enrique, de Diego Yolanda, Fernández-Aranda Fernando, Fernández-Piqueras José, Guitart Miriam, Martín-Santos Rocío, Martorell Lourdes, Menchón José M, Roca Miquel, Sáiz-Ruiz Jerónimo, Sanjuán Julio, Torrens Marta, Urretavizcaya Mikel, Valero Joaquín, Vilella Elisabet, Estivill Xavier, Carracedo Angel,
Association analysis of the glutamic acid decarboxylase 2 and the glutamine synthetase genes (GAD2, GLUL) with schizophrenia.
Psychiatric genetics 2009 Feb 19 (1): 6-13.
Arai Shinsaku, Shibata Hiroki, Sakai Mayumi, Ninomiya Hideaki, Iwata Nakao, Ozaki Norio, Fukumaki Yasuyu
[Polymorphic Variants of Glutamate Receptor (GRIK5, GRIN2B) and Serotonin Receptor (HTR2A) Genes Are Associated with Chronic Obstructive Pulmonary Disease].
Molekuliarnaia biologiia 0 51 (4): 603-614.
Korytina G F, Akhmadishina L Z, Kochetova O V, Aznabaeva Y G, Zagidullin Sh Z, Victorova T
GRIK5 Genetically Regulated Expression Associated with Eye and Vascular Phenomes: Discovery through Iteration among Biobanks, Electronic Health Records, and Zebrafish.
American journal of human genetics 2019 3 104 (3): 503-519.
Unlu Gokhan, Gamazon Eric R, Qi Xinzi, Levic Daniel S, Bastarache Lisa, Denny Joshua C, Roden Dan M, Mayzus Ilya, Breyer Max, Zhong Xue, Konkashbaev Anuar I, Rzhetsky Andrey, Knapik Ela W, Cox Nancy
Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders.
Journal of neurodevelopmental disorders 2019 2 11 (1): 3.
Costain Gregory, Walker Susan, Argiropoulos Bob, Baribeau Danielle A, Bassett Anne S, Boot Erik, Devriendt Koen, Kellam Barbara, Marshall Christian R, Prasad Aparna, Serrano Moises A, Stavropoulos D James, Twede Hope, Vermeesch Joris R, Vorstman Jacob A S, Scherer Stephen
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