Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Disease and CTRB1[original query] |
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| Connecting SNPs in Diabetes: A Spatial Analysis of Meta-GWAS Loci. Frontiers in endocrinology 2015 6 102. Schierding William, O'Sullivan Justin |
| Protective coding variants in CFH and PELI3 and a variant near CTRB1 are associated with age-related macular degeneration†. Human molecular genetics 2016 Dec . Yu Yi, Wagner Erin K, Souied Eric H, Seitsonen Sanna, Immonen Ilkka J, Häppölä Paavo, Raychaudhuri Soumya, Daly Mark J, Seddon Johanna |
| The CTRB1-CTRB2 risk allele for chronic pancreatitis discovered in European populations does not contribute to disease risk variation in the Chinese population due to near allele fixation. Gut 2017 9 67 (7): 1368-1369. Tang Xin-Ying, Zou Wen-Bin, Masson Emmanuelle, Hu Liang-Hao, Ferec Claude, Chen Jian-Min, Li Zhao-Shen, Liao Zhu |
| Genome-wide analysis of disease progression in age-related macular degeneration.
Human molecular genetics 2018 Mar 27 (5): 929-940. Yan Qi, Ding Ying, Liu Yi, Sun Tao, Fritsche Lars G, Clemons Traci, Ratnapriya Rinki, Klein Michael L, Cook Richard J, Liu Yu, Fan Ruzong, Wei Lai, Abecasis Gonçalo R, Swaroop Anand, Chew Emily Y, , Weeks Daniel E, Chen W |
| Analysis of overlapping genetic association in type 1 and type 2 diabetes.
Diabetologia 2021 (6): 1342-1347. Inshaw Jamie R J, Sidore Carlo, Cucca Francesco, Stefana M Irina, Crouch Daniel J M, McCarthy Mark I, Mahajan Anubha, Todd John |
- Page last reviewed:Feb 1, 2024
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