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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Nov 8, 2024. (Total: 233355Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Syndrome and ATG16L1[original query]
NOD2 mutations are associated with the development of intestinal failure in the absence of Crohn's disease.
Clinical nutrition (Edinburgh, Scotland) 2013 Dec 32 (6): 1029-35.
Schäffler Holger, Schneider Nina, Hsieh Chih-Jen, Reiner Johannes, Nadalin Silvio, Witte Maria, Königsrainer Alfred, Blumenstock Gunnar, Lamprecht Geo
Detection of Mycobacterium avium subspecies paratuberculosis in patients with Crohn's disease is unrelated to the presence of single nucleotide polymorphisms rs2241880 (ATG16L1) and rs10045431 (IL12B).
Medical microbiology and immunology 2014 Jun 203 (3): 195-205.
Dalton James P, Desmond Alan, Shanahan Fergus, Hill Col
Genetic determinants of quantitative traits associated with cardiovascular disease risk.
Mutation research 2015 Aug 778 18-25.
Smolková Božena, Bonassi Stefano, Buociková Verona, Dušinská Mária, Horská Alexandra, Kuba Daniel, Džupinková Zuzana, Rašlová Katarína, Gašparovi? Juraj, Slíž Ivan, Ceppi Marcello, Vohnout Branislav, Wsólová Ladislava, Volkovová Katarí
Association of ATG5 Gene Polymorphisms With Behçet's Disease and ATG10 Gene Polymorphisms With VKH Syndrome in a Chinese Han Population.
Investigative ophthalmology & visual science 2015 Dec 56 (13): 8280-7.
Zheng Minming, Yu Hongsong, Zhang Lijun, Li Hua, Liu Yunjia, Kijlstra Aize, Yang Peize
A large-scale genome-wide cross-trait analysis reveals shared genetic architecture between Alzheimer's disease and gastrointestinal tract disorders. GWAS Catalog
Communications biology 2022 7 5 (1): 691.
Adewuyi Emmanuel O, O'Brien Eleanor K, Nyholt Dale R, Porter Tenielle, Laws Simon
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