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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 5, 2023. (Total: 217663Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Neoplasms and SNCA[original query]
A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2.
Neurology 2010 Sep 75 (13): 1189-94.
Kay D M, Stevens C F, Hamza T H, Montimurro J S, Zabetian C P, Factor S A, Samii A, Griffith A, Roberts J W, Molho E S, Higgins D S, Gancher S, Moses L, Zareparsi S, Poorkaj P, Bird T, Nutt J, Schellenberg G D, Payami
A population scale analysis of rare SNCA variation in the UK Biobank.
Neurobiology of disease 2020 Dec 105182.
Blauwendraat Cornelis, Makarious Mary B, Leonard Hampton L, Bandres-Ciga Sara, Iwaki Hirotaka, Nalls Mike A, Noyce Alastair J, Singleton Andrew
Subthalamic deep brain stimulation in Parkinson's disease with SNCA mutations: Based on the follow-up to 10 years.
Brain and behavior 2022 1 12 (2): e2503.
Youn Jinyoung, Oyama Genko, Hattori Nobutaka, Shimo Yasushi, Kuusimäki Tomi, Kaasinen Valtteri, Antonini Angelo, Kim Dongyeop, Lee Jung-Il, Cho Kyung Rae, Cho Jin Wh
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