HuGE Literature Finder
Records 1-9
Analyzing and validating the prognostic value and mechanism of colon cancer immune microenvironment.
Journal of translational medicine 2020 Aug 18 (1): 324. Wang Xinyi, Duanmu Jinzhong, Fu Xiaorui, Li Taiyuan, Jiang Qungua |
Genetic variants associated with vein graft stenosis after coronary artery bypass grafting.
![]() The heart surgery forum 2015 18 (1): E1-5. Shah Asad A, Haynes Carol, Craig Damian M, Sebek Jacqueline, Grass Elizabeth, Abramson Karen, Hauser Elizabeth, Gregory Simon G, Kraus William E, Smith Peter K, Shah Svati |
Association of polymorphisms in GCKR and TRIB1 with nonalcoholic fatty liver disease and metabolic syndrome traits.
Endocrine journal 2014 61 (7): 683-9. Kitamoto Aya, Kitamoto Takuya, Nakamura Takahiro, Ogawa Yuji, Yoneda Masato, Hyogo Hideyuki, Ochi Hidenori, Mizusawa Seiho, Ueno Takato, Nakao Kazuwa, Sekine Akihiro, Chayama Kazuaki, Nakajima Atsushi, Hotta Kiku |
Polymorphism of the palladin gene and cardiovascular outcome in patients with atherosclerosis.
European journal of clinical investigation 2011 Apr 41 (4): 365-71. Hoke Matthias, Schillinger Martin, Dick Petra, Exner Markus, Koppensteiner Renate, Minar Erich, Mlekusch Wolfgang, Schlager Oliver, Wagner Oswald, Mannhalter Christi |
Variations of specific non-candidate genes and risk of myocardial infarction: a replication study.
International journal of cardiology 2011 Feb 147 (1): 38-41. Koch Werner, Hoppmann Petra, Schömig Albert, Kastrati Adn |
Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia.
![]() Molecular psychiatry 2009 Nov 14 (11): 1024-31. Volpi S, Heaton C, Mack K, Hamilton J B, Lannan R, Wolfgang C D, Licamele L, Polymeropoulos M H, Lavedan |
Absence of deleterious palladin mutations in patients with familial pancreatic cancer.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2009 Apr 18 (4): 1328-30. Klein Alison P, Borges Michael, Griffith Margaret, Brune Kieran, Hong Seung-Mo, Omura Noriyuki, Hruban Ralph H, Goggins Micha |
Five common gene variants identify elevated genetic risk for coronary heart disease.
Genetics in medicine : official journal of the American College of Medical Genetics 2007 Oct 9 (10): 682-9. Bare Lance A, Morrison Alanna C, Rowland Charles M, Shiffman Dov, Luke May M, Iakoubova Olga A, Kane John P, Malloy Mary J, Ellis Stephen G, Pankow James S, Willerson James T, Devlin James J, Boerwinkle Er |
A genome-wide scan in forty large pedigrees with multiple sclerosis.
Journal of human genetics 2007 52 (12): 955-62. Willer Cristen J, Dyment David A, Cherny Stacey, Ramagopalan Sreeram V, Herrera Blanca M, Morrison Katie M E, Sadovnick A Dessa, Risch Neil J, Ebers George |
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- Page last updated:Feb 24, 2021
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