Human Genome Epidemiology Literature Finder
|
Records 1 - 3 (of 3 Records) |
| Query Trace: Disease and ACP2[original query] |
|---|
| Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms. American journal of human genetics 2007 Apr 80 (4): 769-78. Melquist Stacey, Craig David W, Huentelman Matthew J, Crook Richard, Pearson John V, Baker Matt, Zismann Victoria L, Gass Jennifer, Adamson Jennifer, Szelinger Szabolcs, Corneveaux Jason, Cannon Ashley, Coon Keith D, Lincoln Sarah, Adler Charles, Tuite Paul, Calne Donald B, Bigio Eileen H, Uitti Ryan J, Wszolek Zbigniew K, Golbe Lawrence I, Caselli Richard J, Graff-Radford Neill, Litvan Irene, Farrer Matthew J, Dickson Dennis W, Hutton Mike, Stephan Dietrich |
| Genetic diversity and functional effect of common polymorphisms in genes involved in the first heterodimeric complex of the Nucleotide Excision Repair pathway. DNA repair 2019 Dec 86 102770. Hamdi Yosr, Jerbi Manel, Romdhane Lilia, Ben Rekaya Mariem, El Benna Houda, Chouchane Lotfi, Boubaker Mohamed Samir, Abdelhak Sonia, Yacoub-Youssef Hou |
| Co-existence of multiple functional variants and genes underlie genetic risk locus 11p11.2 of Alzheimer's disease. Biological psychiatry 2023 6 . Min Xu, Qianjin Liu, Rui Bi, Yu Li, Hongli Li, Wei-Bo Kang, Zhongjiang Yan, Quanzhen Zheng, Chunli Sun, Maosen Ye, Bo-Lin Xiang, Xiong-Jian Luo, Ming Li, Deng-Feng Zhang, Yong-Gang Y |
- Page last reviewed:Feb 1, 2024
- Content source:

