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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 - 4 (of 4 Records)

Query Trace: Disease and PDE10A[original query]
Confirmed rare copy number variants implicate novel genes in schizophrenia.
Biochemical Society transactions 2010 Apr 38 (2): 445-51.
Tam Gloria W C, van de Lagemaat Louie N, Redon Richard, Strathdee Karen E, Croning Mike D R, Malloy Mary P, Muir Walter J, Pickard Ben S, Deary Ian J, Blackwood Douglas H R, Carter Nigel P, Grant Seth G
Linkage and association analysis of hyperthyrotropinaemia in an Alpine population reveal two novel loci on chromosomes 3q28-29 and 6q26-27.
Journal of medical genetics 2011 Jun .
Volpato CB, De Grandi A, Gögele M, Taliun D, Fuchsberger C, Facheris MF, Minelli C, Pattaro C, Pramstaller PP, Hicks AA
A Pooling Genome-Wide Association Study Combining a Pathway Analysis for Typical Sporadic Parkinson's Disease in the Han Population of Chinese Mainland. GWAS Catalog
Molecular neurobiology 2015 Jul .
Hu Yakun, Deng Libing, Zhang Jie, Fang Xin, Mei Puming, Cao Xuebing, Lin Jiari, Wei Yi, Zhang Xiong, Xu Rens
Common genetic variants associated with thyroid function may be risk alleles for Hashimoto's disease and Graves' disease.
Clinical endocrinology 2015 Feb .
Campbell Purdey, Brix Thomas H, Wilson Scott G, Ward Lynley C, Hui Jennie, Beilby John P, Hegedüs Laszlo, Walsh John
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