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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 1, 2023. (Total: 221588Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Syndrome and GRM5[original query]
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.
Molecular psychiatry 2010 Jun 15 (6): 637-46.
Elia J, Gai X, Xie H M, Perin J C, Geiger E, Glessner J T, D'arcy M, deBerardinis R, Frackelton E, Kim C, Lantieri F, Muganga B M, Wang L, Takeda T, Rappaport E F, Grant S F A, Berrettini W, Devoto M, Shaikh T H, Hakonarson H, White P
[Association of glutamate receptor metabotropic 5 polymorphisms with schizophrenia susceptibility in a Chinese Han population].
Zhonghua yi xue za zhi 2022 Jul 102 (27): 2108-2114.
Song M, Liu Y, Wang X J, Zhang L W, Liu Q, Chen T F, Su X, Li W W, Lyu L X, Yang Y
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development. GWAS Catalog
Ophthalmology 2022 1 129 (6): 626-636.
Simcoe Mark J, Shah Ameet, Fan Baojian, Choquet Hélène, Weisschuh Nicole, Waseem Naushin H, Jiang Chen, Melles Ronald B, Ritch Robert, Mahroo Omar A, Wissinger Bernd, Jorgenson Eric, Wiggs Janey L, Garway-Heath David F, Hysi Pirro G, Hammond Christopher
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