Human Genome Epidemiology Literature Finder
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Records 1 - 3 (of 3 Records) |
| Query Trace: Disease and SERPINA12[original query] |
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| Novel common and rare genetic determinants of paraoxonase activity: FTO, SERPINA12, and ITGAL. Journal of lipid research 2012 Nov . Kim DS, Burt AA, Crosslin DR, Robertson PD, Ranchalis JE, Boyko EJ, Nickerson DA, Furlong CE, Jarvik GP |
| Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12. Thorax 2016 Feb . Jackson Victoria E, Ntalla Ioanna, Sayers Ian, Morris Richard, Whincup Peter, Casas Juan-Pablo, Amuzu Antoinette, Choi Minkyoung, Dale Caroline, Kumari Meena, Engmann Jorgen, Kalsheker Noor, Chappell Sally, Guetta-Baranes Tamar, McKeever Tricia M, Palmer Colin N A, Tavendale Roger, Holloway John W, Sayer Avan A, Dennison Elaine M, Cooper Cyrus, Bafadhel Mona, Barker Bethan, Brightling Chris, Bolton Charlotte E, John Michelle E, Parker Stuart G, Moffat Miriam F, Wardlaw Andrew J, Connolly Martin J, Porteous David J, Smith Blair H, Padmanabhan Sandosh, Hocking Lynne, Stirrups Kathleen E, Deloukas Panos, Strachan David P, Hall Ian P, Tobin Martin D, Wain Louise |
Exome-Wide Association Study Reveals Host Genetic Variants Likely Associated with the Severity of COVID-19 in Patients of European Ancestry.
Life (Basel, Switzerland) 2022 Aug 12 (9): . Upadhyai Priyanka, Shenoy Pooja U, Banjan Bhavya, Albeshr Mohammed F, Mahboob Shahid, Manzoor Irfan, Das Ranaj |
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