Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 5 (of 5 Records)

Query Trace: Disease and PARL[original query]
Association of PARL rs3732581 genetic variant with insulin levels, metabolic syndrome and coronary artery disease.
Human genetics 2008 Oct 124 (3): 263-70.
Powell Brenda L, Wiltshire Steven, Arscott Gillian, McCaskie Pamela A, Hung Joseph, McQuillan Brendan M, Thompson Peter L, Carter Kim W, Palmer Lyle J, Beilby John
ABCC5 transporter is a novel type 2 diabetes susceptibility gene in European and African American populations.
Annals of human genetics 2014 Sep 78 (5): 333-44.
Direk Kenan, Lau Winston, Small Kerrin S, Maniatis Nikolas, Andrew To
Common variants in the PARL and PINK1 genes increase the risk to leprosy in Han Chinese from South China.
Scientific reports 2016 Nov 6 37086.
Wang Dong, Zhang Deng-Feng, Feng Jia-Qi, Li Guo-Dong, Li Xiao-An, Yu Xiu-Feng, Long Heng, Li Yu-Ye, Yao Yong-Ga
Mutation analyses and association studies to assess the role of the presenilin-associated rhomboid-like gene in Parkinson's disease.
Neurobiology of aging 2015 Dec .
Wüst Richard, Maurer Brigitte, Hauser Kathrin, Woitalla Dirk, Sharma Manu, Krüger Rej
Genetic Association of the PARL-ABCC5-HTR3D-HTR3C Locus With Primary Angle-Closure Glaucoma in Chinese.
Investigative ophthalmology & visual science 2017 Aug 58 (10): 4104-4109.
Tang Fang Yao, Ma Li, Tam Pancy O S, Pang Chi Pui, Tham Clement C, Chen Li J
TOP