Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Disease and COL18A1[original query] |
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| A high risk of occurrence of sporadic breast cancer in individuals with the 104NN polymorphism of the COL18A1 gene. Breast cancer research and treatment 2006 Dec 100 (3): 335-8. Lourenço Gustavo J, Cardoso-Filho Cassio, Gonçales Neiva S L, Shinzato Julia Y, Zeferino Luis C, Nascimento Helvia, Costa Fernando F, Gurgel Maria S C, Lima Carmen S |
| Genetic risk factors for hepatopulmonary syndrome in patients with advanced liver disease. Gastroenterology 2010 Jul 139 (1): 130-9.e24. Roberts Kari E, Kawut Steven M, Krowka Michael J, Brown Robert S, Trotter James F, Shah Vijay, Peter Inga, Tighiouart Hocine, Mitra Nandita, Handorf Elizabeth, Knowles James A, Zacks Steven, Fallon Michael B, |
| A DNA pooling-based case-control study of myopia candidate genes COL11A1, COL18A1, FBN1, and PLOD1 in a Chinese population. Molecular vision 2011 17 810-21. Yip Shea Ping, Leung Kim Hung, Fung Wai Yan, Ng Po Wah, Sham Pak Chung, Yap Maurice K |
| Vascular endothelial growth factor pathway polymorphisms as prognostic and pharmacogenetic factors in cancer: a systematic review and meta-analysis. Clinical cancer research : an official journal of the American Association for Cancer Research 2012 Sep 18 (17): 4526-37. Eng Lawson, Azad Abul Kalam, Habbous Steven, Pang Vincent, Xu Wei, Maitland-van der Zee Anke H, Savas Sevtap, Mackay Helen J, Amir Eitan, Liu Geoffr |
| A 3' UTR SNP in COL18A1 is associated with susceptibility to HBV related hepatocellular carcinoma in Chinese: three independent case-control studies. PloS one 2012 7 (3): 3. Wu X, Wu J, Xin Z, Wang H, Zhu X, Pan L, Li Z, Li H, Liu Y |
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.
American journal of human genetics 2014 Feb 94 (2): 223-32. Peloso Gina M, Auer Paul L, Bis Joshua C, Voorman Arend, Morrison Alanna C, Stitziel Nathan O, Brody Jennifer A, Khetarpal Sumeet A, Crosby Jacy R, Fornage Myriam, Isaacs Aaron, Jakobsdottir Johanna, Feitosa Mary F, Davies Gail, Huffman Jennifer E, Manichaikul Ani, Davis Brian, Lohman Kurt, Joon Aron Y, Smith Albert V, Grove Megan L, Zanoni Paolo, Redon Valeska, Demissie Serkalem, Lawson Kim, Peters Ulrike, Carlson Christopher, Jackson Rebecca D, Ryckman Kelli K, Mackey Rachel H, Robinson Jennifer G, Siscovick David S, Schreiner Pamela J, Mychaleckyj Josyf C, Pankow James S, Hofman Albert, Uitterlinden Andre G, Harris Tamara B, Taylor Kent D, Stafford Jeanette M, Reynolds Lindsay M, Marioni Riccardo E, Dehghan Abbas, Franco Oscar H, Patel Aniruddh P, Lu Yingchang, Hindy George, Gottesman Omri, Bottinger Erwin P, Melander Olle, Orho-Melander Marju, Loos Ruth J F, Duga Stefano, Merlini Piera Angelica, Farrall Martin, Goel Anuj, Asselta Rosanna, Girelli Domenico, Martinelli Nicola, Shah Svati H, Kraus William E, Li Mingyao, Rader Daniel J, Reilly Muredach P, McPherson Ruth, Watkins Hugh, Ardissino Diego, , Zhang Qunyuan, Wang Judy, Tsai Michael Y, Taylor Herman A, Correa Adolfo, Griswold Michael E, Lange Leslie A, Starr John M, Rudan Igor, Eiriksdottir Gudny, Launer Lenore J, Ordovas Jose M, Levy Daniel, Chen Y-D Ida, Reiner Alexander P, Hayward Caroline, Polasek Ozren, Deary Ian J, Borecki Ingrid B, Liu Yongmei, Gudnason Vilmundur, Wilson James G, van Duijn Cornelia M, Kooperberg Charles, Rich Stephen S, Psaty Bruce M, Rotter Jerome I, O'Donnell Christopher J, Rice Kenneth, Boerwinkle Eric, Kathiresan Sekar, Cupples L Adrien |
| The rs3957357C>T SNP in GSTA1 Is Associated with a Higher Risk of Occurrence of Hepatocellular Carcinoma in European Individuals. PloS one 2016 11 (12): e0167543. Akhdar Hanane, El Shamieh Said, Musso Orlando, Désert Romain, Joumaa Wissam, Guyader Dominique, Aninat Caroline, Corlu Anne, Morel Fabri |
| Knobloch syndrome caused by homozygous frameshift mutation of the COL18A1 gene in a Chinese pedigree. International journal of ophthalmology 2018 7 11 (6): 918-922. Zhang Lu-Si, Li Hai-Bo, Zeng Jun, Yang Yan, Ding Ch |
| Knobloch Syndrome Associated with Novel COL18A1 Variants in Chinese Population. Genes 2021 10 12 (10): . Li Songshan, Wang You, Sun Limei, Yan Wenjia, Huang Li, Zhang Zhaotian, Zhang Ting, Ding Xiaoy |
| Fetal and neonatal outcomes of posterior fossa anomalies: a retrospective cohort study. Scientific reports 2024 4 14 (1): 8411. Hanan Alsehli, Saeed Mastour Alshahrani, Shatha Alzahrani, Farouq Ababneh, Nawal Mashni Alharbi, Nassebah Alarfaj, Duaa Baarm |
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