Human Genome Epidemiology Literature Finder
|
Records 1 - 3 (of 3 Records) |
| Query Trace: Disease and PSMD3[original query] |
|---|
| Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network.
Human genetics 2012 Apr 131 (4): 639-52. Crosslin David R, McDavid Andrew, Weston Noah, Nelson Sarah C, Zheng Xiuwen, Hart Eugene, de Andrade Mariza, Kullo Iftikhar J, McCarty Catherine A, Doheny Kimberly F, Pugh Elizabeth, Kho Abel, Hayes M Geoffrey, Pretel Stephanie, Saip Alexander, Ritchie Marylyn D, Crawford Dana C, Crane Paul K, Newton Katherine, Li Rongling, Mirel Daniel B, Crenshaw Andrew, Larson Eric B, Carlson Chris S, Jarvik Gail P, |
| Systematic protein-protein interaction and pathway analyses in the idiopathic inflammatory myopathies. Arthritis research & therapy 2016 18 (1): 156. Parkes Joanna E, Rothwell Simon, Day Philip J, McHugh Neil J, Betteridge Zoë E, Cooper Robert G, Ollier William E, Chinoy Hector, Lamb Janine A, |
| 2SNP heritability and effects of genetic variants for neutrophil-to-lymphocyte and platelet-to-lymphocyte ratio.
Journal of human genetics 2017 Nov 62 (11): 979-988. Lin Bochao Danae, Carnero-Montoro Elena, Bell Jordana T, Boomsma Dorret I, de Geus Eco J, Jansen Rick, Kluft Cornelis, Mangino Massimo, Penninx Brenda, Spector Tim D, Willemsen Gonneke, Hottenga Jouke-J |
- Page last reviewed:Feb 1, 2024
- Content source:

