Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Myocardial Infarction and LRP1[original query] |
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| The LDL receptor-related protein (LRP1/A2MR) and coronary atherosclerosis--novel genomic variants and functional consequences. Human mutation 2002 Nov 20 (5): 404. Schulz Susanne, Schagdarsurengin Undraga, Greiser Petra, Birkenmeier Gerd, Müller-Werdan Ursula, Hagemann Monika, Riemann Dagmar, Werdan Karl, Gläser Christia |
| Genetic variability within the cholesterol lowering pathway and the effectiveness of statins in reducing the risk of MI. Atherosclerosis 2011 Aug 217 (2): 458-64. Peters Bas J M, Pett Helmi, Klungel Olaf H, Stricker Bruno H Ch, Psaty Bruce M, Glazer Nicole L, Wiggins Kerri L, Bis Josh C, de Boer Anthonius, Maitland-van der Zee Anke-Hil |
| Lack of association of common polymorphism of LRP1 gene with myocardial infarction in a Chinese Han population. Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban 2011 Jun 31 (3): 295-300. Ren Honggang, Guo Tao, Wang Huafang, Sun Chunyan, Zhang Xiaoping, Mei Heng, Hu |
| Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction.
Nature communications 2020 09 11 (1): 4432. Saw Jacqueline, Yang Min-Lee, Trinder Mark, Tcheandjieu Catherine, Xu Chang, Starovoytov Andrew, Birt Isabelle, Mathis Michael R, Hunker Kristina L, Schmidt Ellen M, Jackson Linda, Fendrikova-Mahlay Natalia, Zawistowski Matthew, Brummett Chad M, Zoellner Sebastian, Katz Alexander, Coleman Dawn M, Swan Kirby, O'Donnell Christopher J, , Zhou Xiang, Li Jun Z, Gornik Heather L, Assimes Themistocles L, Stanley James C, Brunham Liam R, Ganesh Santhi |
| Identification of Susceptibility Loci for Spontaneous Coronary Artery Dissection.
JAMA cardiology 2020 May . Turley Tamiel N, O'Byrne Megan M, Kosel Matthew L, de Andrade Mariza, Gulati Rajiv, Hayes Sharonne N, Tweet Marysia S, Olson Timothy |
| Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases.
Nature communications 2021 10 12 (1): 6031. Georges Adrien, Yang Min-Lee, Berrandou Takiy-Eddine, Bakker Mark K, Dikilitas Ozan, Kiando Soto Romuald, Ma Lijiang, Satterfield Benjamin A, Sengupta Sebanti, Yu Mengyao, Deleuze Jean-François, Dupré Delia, Hunker Kristina L, Kyryachenko Sergiy, Liu Lu, Sayoud-Sadeg Ines, Amar Laurence, Brummett Chad M, Coleman Dawn M, d'Escamard Valentina, de Leeuw Peter, Fendrikova-Mahlay Natalia, Kadian-Dodov Daniella, Li Jun Z, Lorthioir Aurélien, Pappaccogli Marco, Prejbisz Aleksander, Smigielski Witold, Stanley James C, Zawistowski Matthew, Zhou Xiang, Zöllner Sebastian, , , , Amouyel Philippe, De Buyzere Marc L, Debette Stéphanie, Dobrowolski Piotr, Drygas Wojciech, Gornik Heather L, Olin Jeffrey W, Piwonski Jerzy, Rietzschel Ernst R, Ruigrok Ynte M, Vikkula Miikka, Warchol Celinska Ewa, Januszewicz Andrzej, Kullo Iftikhar J, Azizi Michel, , Jeunemaitre Xavier, Persu Alexandre, Kovacic Jason C, Ganesh Santhi K, Bouatia-Naji Nabi |
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