Human Genome Epidemiology Literature Finder
|
Records 1 - 24 (of 24 Records) |
| Query Trace: Myocardial Infarction and MS[original query] |
|---|
| The D-allele of the ACE polymorphism is related to increased QT dispersion in 609 patients after myocardial infarction. European heart journal 2001 Apr 22 (8): 663-8. Jeron A, Hengstenberg C, Engel S, Löwel H, Riegger GA, Schunkert H, Holmer S |
| Influence of a methionine synthase (D919G) polymorphism on plasma homocysteine and folate levels and relation to risk of myocardial infarction. Atherosclerosis 2001 Feb 154 (3): 667-72. Chen J, Stampfer M J, Ma J, Selhub J, Malinow M R, Hennekens C H, Hunter D |
| Gene polymorphisms of homocysteine metabolism-related enzymes in Chinese patients with occlusive coronary artery or cerebral vascular diseases. Thrombosis research 2001 Nov 104 (3): 187-95. Zhang G, Dai |
| [Correlation analysis between plasma homocysteine level and polymorphism of homocysteine metabolism related enzymes in ischemic cerebrovascular or cardiovascular diseases]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2002 Mar 23 (3): 126-9. Zhang Guangsen, Dai Chongw |
| [Study on homocysteine metabolism related enzymes gene mutations in Chinese patients with ischemic cardiovascular and cerebrovascular diseases]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2001 Sep 22 (9): 484-7. Dai C, Zhang |
| 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 |
| Association between the 2756A> G variant in the gene encoding methionine synthase and myocardial infarction in Tunisian patients. Clinical chemistry and laboratory medicine : CCLM / FESCC 2008 46 (10): 1364-8. Jemaa Riadh, Achouri Afef, Kallel Amani, Ben Ali Samir, Mourali Sami, Feki Moncef, Elasmi Monia, Taieb Samah Haj, Sanhaji Haïfa, Omar Souheil, Mechmeche Rachid, Kaabachi Nazi |
| Lack of association of the CIITA -168A?G promoter SNP with myasthenia gravis and its role in autoimmunity. BMC medical genetics 2010 11 (1): 147. Ramanujam Ryan, Zhao Yaofeng, Pirskanen Ritva, Hammarström Lenna |
| [Impact of cytochrome P450 2C19 polymorphisms on outcome of cardiovascular events in clopidogrel-treated Chinese patients after percutaneous coronary intervention]. Zhonghua xin xue guan bing za zhi 2011 Jul 39 (7): 617-20. Tang Xiao-Fang, He Chen, Yuan Jin-Qing, Meng Xian-Min, Yang Yue-Jin, Qin Xue-Wen, Qiao Shu-Bin, Liu Hai-Bo, Wu Yong-Jian, Yao Min, Chen Jue, You Shi-Jie, Wu Yuan, Li Jian-Jun, Dai Jun, Chen Ji-Lin, Gao Run-Lin, Chen Zai-J |
| KCNE5 polymorphism rs697829 is associated with QT interval and survival in acute coronary syndromes patients. Journal of cardiovascular electrophysiology 2012 Mar 23 (3): 319-24. Palmer Barry R, Frampton C M, Skelton Lorraine, Yandle Tim G, Doughty Rob N, Whalley Gillian A, Ellis Chris J, Troughton Richard W, Richards A M, Cameron Vicky |
| Plasma 25-hydroxyvitamin D and its genetic determinants in relation to incident myocardial infarction and stroke in the European prospective investigation into cancer and nutrition (EPIC)-Germany study. PloS one 2013 8 (7): e69080. Kühn Tilman, Kaaks Rudolf, Teucher Birgit, Hirche Frank, Dierkes Jutta, Weikert Cornelia, Katzke Verena, Boeing Heiner, Stangl Gabriele I, Buijsse Bri |
| P-Glycoprotein Polymorphism C3435T Is Associated with Dose-Adjusted Clopidogrel and 2-Oxo-Clopidogrel Concentration. Pharmacology 2015 Dec 97 (3-4): 101-106. Stokanovic Dragana, Nikolic Valentina N, Konstantinovic Sandra S, Zvezdanovic Jelena B, Lilic Jelena, Apostolovic Svetlana R, Pavlovic Milan, Zivkovic Vladimir S, Jevtovic-Stoimenov Tatjana, Jankovic Slobodan |
| [Relationship between ATP-binding cassette subfamily B member 1 and cytochrome P450 2C19 polymorphisms and the effect of clopidogrel post percutaneous coronary intervention in patients with acute coronary syndrome]. Zhonghua xin xue guan bing za zhi 2016 Apr 44 (4): 309-14. Zhou C F, Ren Y H, Song Y Q, Yi J, Han B S, Xue Q, Fu Z H, Li D |
| The Relationship between Angiotensin-II Type 1 Receptor Gene Polymorphism and Repolarization Parameters after a First Anterior Acute Myocardial Infarction. Korean circulation journal 2016 Nov 46 (6): 791-797. Ozturk Onder, Ozturk Unal, Nergiz Sebnem, Karahan M Zulk |
| Polymorphisms in MTHFR, MS and CBS genes and premature acute myocardial infarction in a Pakistani population. Pakistan journal of pharmaceutical sciences 2016 Nov 29 (6): 1901-1906. Iqbal Mohammad Perwaiz, Iqbal Khalida, Tareen Asal Khan, Parveen Siddiqa, Mehboobali Naseema, Haider Ghulam, Iqbal Saleem Perwa |
| Genetic Variants of CYP2R1 Are Key Regulators of Serum Vitamin D Levels and Incidence of Myocardial Infarction in Middle-Aged Egyptians. Current pharmaceutical biotechnology 2018 May . Sedky Nada K, Abdel Rahman Mohamed F, Hassanein Sally I, Gad Mohamed |
| Development and Validation of Apolipoprotein AI-Associated Lipoprotein Proteome Panel for the Prediction of Cholesterol Efflux Capacity and Coronary Artery Disease. Clinical chemistry 2018 11 65 (2): 282-290. Jin Zhicheng, Collier Timothy S, Dai Darlene L Y, Chen Virginia, Hollander Zsuzsanna, Ng Raymond T, McManus Bruce M, Balshaw Robert, Apostolidou Sophia, Penn Marc S, Bystrom Co |
| Vitamin D-binding protein (rs4588) T/T genotype is associated with anteroseptal myocardial infarction in coronary artery disease patients. Annals of translational medicine 2019 Aug 7 (16): 374. Perši? Viktor, Raljevi? Damir, Markova-Car Elitza, Cindri? Leon, Miškulin Rajko, Žuvi? Marta, Kraljevi? Paveli? Sand |
| New evidence from plasma ceramides links apoE polymorphism to greater risk of coronary artery disease in Finnish adults. Journal of lipid research 2019 7 60 (9): 1622-1629. Karjalainen Juho-Pekka, Mononen Nina, Hutri-Kähönen Nina, Lehtimäki Miikael, Hilvo Mika, Kauhanen Dimple, Juonala Markus, Viikari Jorma, Kähönen Mika, Raitakari Olli, Laaksonen Reijo, Lehtimäki Ter |
| Correlation between HCN4 gene polymorphisms and lone atrial fibrillation risk. Artificial cells, nanomedicine, and biotechnology 2019 7 47 (1): 2989-2993. Li Xiao-Hong, Hu Ya-Min, Yin Guang-Li, Wu Pi |
| Untargeted Mass Spectrometry Lipidomics identifies correlation between serum sphingomyelins and plasma cholesterol. Lipids in health and disease 2019 2 18 (1): 38. Zalloua Pierre, Kadar Hanane, Hariri Essa, Abi Farraj Layal, Brial Francois, Hedjazi Lyamine, Le Lay Aurelie, Colleu Alexandre, Dubus Justine, Touboul David, Matsuda Fumihiko, Lathrop Mark, Nicholson Jeremy K, Dumas Marc-Emmanuel, Gauguier Dominiq |
| SAA1 gene polymorphisms in osteoporosis patients. Bioscience reports 2019 Feb . Zhou Xindie, Li Jin, Jiang Lifeng, Zhou Dong, Wu Lidong, Huang Yong, Xu Nanw |
| A NOS1AP gene variant is associated with a paradoxical increase of the QT-interval shortening effect of digoxin. The pharmacogenomics journal 2021 Oct . Soroush Negin, Aarnoudse Albert-Jan, Kavousi Maryam, Kors Jan A, Ikram M Arfan, Newton-Cheh Christopher, Ahmadizar Fariba, Stricker Bruno |
| ATAD3B and SKIL polymorphisms associated with antipsychotic-induced QTc interval change in patients with schizophrenia: a genome-wide association study.
Translational psychiatry 2022 2 12 (1): 56. Lu Zhe, Zhang Yuyanan, Yan Hao, Su Yi, Guo Liangkun, Liao Yundan, Lu Tianlan, Yu Hao, Wang Lifang, Li Jun, Li Wenqiang, Yang Yongfeng, Xiao Xiao, Lv Luxian, Tan Yunlong, Zhang Dai, Yue Weih |
- Page last reviewed:Feb 1, 2024
- Content source:

