Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: MIA3[original query] |
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Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
Nature genetics 2009 Mar 41 (3): 334-41. , Kathiresan Sekar, Voight Benjamin F, Purcell Shaun, Musunuru Kiran, Ardissino Diego, Mannucci Pier M, Anand Sonia, Engert James C, Samani Nilesh J, Schunkert Heribert, Erdmann Jeanette, Reilly Muredach P, Rader Daniel J, Morgan Thomas, Spertus John A, Stoll Monika, Girelli Domenico, McKeown Pascal P, Patterson Chris C, Siscovick David S, O'Donnell Christopher J, Elosua Roberto, Peltonen Leena, Salomaa Veikko, Schwartz Stephen M, Melander Olle, Altshuler David, Ardissino Diego, Merlini Pier Angelica, Berzuini Carlo, Bernardinelli Luisa, Peyvandi Flora, Tubaro Marco, Celli Patrizia, Ferrario Maurizio, Fetiveau Raffaela, Marziliano Nicola, Casari Giorgio, Galli Michele, Ribichini Flavio, Rossi Marco, Bernardi Francesco, Zonzin Pietro, Piazza Alberto, Mannucci Pier M, Schwartz Stephen M, Siscovick David S, Yee Jean, Friedlander Yechiel, Elosua Roberto, Marrugat Jaume, Lucas Gavin, Subirana Isaac, Sala Joan, Ramos Rafael, Kathiresan Sekar, Meigs James B, Williams Gordon, Nathan David M, MacRae Calum A, O'Donnell Christopher J, Salomaa Veikko, Havulinna Aki S, Peltonen Leena, Melander Olle, Berglund Goran, Voight Benjamin F, Kathiresan Sekar, Hirschhorn Joel N, Asselta Rosanna, Duga Stefano, Spreafico Marta, Musunuru Kiran, Daly Mark J, Purcell Shaun, Voight Benjamin F, Purcell Shaun, Nemesh James, Korn Joshua M, McCarroll Steven A, Schwartz Stephen M, Yee Jean, Kathiresan Sekar, Lucas Gavin, Subirana Isaac, Elosua Roberto, Surti Aarti, Guiducci Candace, Gianniny Lauren, Mirel Daniel, Parkin Melissa, Burtt Noel, Gabriel Stacey B, Samani Nilesh J, Thompson John R, Braund Peter S, Wright Benjamin J, Balmforth Anthony J, Ball Stephen G, Hall Alistair S, , Schunkert Heribert, Erdmann Jeanette, Linsel-Nitschke Patrick, Lieb Wolfgang, Ziegler Andreas, König Inke, Hengstenberg Christian, Fischer Marcus, Stark Klaus, Grosshennig Anika, Preuss Michael, Wichmann H-Erich, Schreiber Stefan, Schunkert Heribert, Samani Nilesh J, Erdmann Jeanette, Ouwehand Willem, Hengstenberg Christian, Deloukas Panos, Scholz Michael, Cambien Francois, Reilly Muredach P, Li Mingyao, Chen Zhen, Wilensky Robert, Matthai William, Qasim Atif, Hakonarson Hakon H, Devaney Joe, Burnett Mary-Susan, Pichard Augusto D, Kent Kenneth M, Satler Lowell, Lindsay Joseph M, Waksman Ron, Knouff Christopher W, Waterworth Dawn M, Walker Max C, Mooser Vincent, Epstein Stephen E, Rader Daniel J, Scheffold Thomas, Berger Klaus, Stoll Monika, Huge Andreas, Girelli Domenico, Martinelli Nicola, Olivieri Oliviero, Corrocher Roberto, Morgan Thomas, Spertus John A, McKeown Pascal, Patterson Chris C, Schunkert Heribert, Erdmann Erdmann, Linsel-Nitschke Patrick, Lieb Wolfgang, Ziegler Andreas, König Inke R, Hengstenberg Christian, Fischer Marcus, Stark Klaus, Grosshennig Anika, Preuss Michael, Wichmann H-Erich, Schreiber Stefan, Hólm Hilma, Thorleifsson Gudmar, Thorsteinsdottir Unnur, Stefansson Kari, Engert James C, Do Ron, Xie Changchun, Anand Sonia, Kathiresan Sekar, Ardissino Diego, Mannucci Pier M, Siscovick David, O'Donnell Christopher J, Samani Nilesh J, Melander Olle, Elosua Roberto, Peltonen Leena, Salomaa Veikko, Schwartz Stephen M, Altshuler Dav |
Common genetic polymorphisms in moyamoya and atherosclerotic disease in Europeans. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 2011 Feb 27 (2): 245-52. Roder Constantin, Peters Vera, Kasuya Hidetoshi, Nishizawa Tsutomu, Takehara Yayoi, Berg Daniela, Schulte Claudia, Khan Nadia, Tatagiba Marcos, Krischek Bor |
Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration. European heart journal 2012 Feb 33 (3): 393-407. Angelakopoulou Aspasia, Shah Tina, Sofat Reecha, Shah Sonia, Berry Diane J, Cooper Jackie, Palmen Jutta, Tzoulaki Ioanna, Wong Andrew, Jefferis Barbara J, Maniatis Nikolas, Drenos Fotios, Gigante Bruna, Hardy Rebecca, Laxton Ross C, Leander Karin, Motterle Anna, Simpson Iain A, Smeeth Liam, Thomson Andy, Verzilli Claudio, Kuh Diana, Ireland Helen, Deanfield John, Caulfield Mark, Wallace Chris, Samani Nilesh, Munroe Patricia B, Lathrop Mark, Fowkes F Gerry R, Marmot Michael, Whincup Peter H, Whittaker John C, de Faire Ulf, Kivimaki Mika, Kumari Meena, Hypponen Elina, Power Chris, Humphries Steve E, Talmud Philippa J, Price Jackie, Morris Richard W, Ye Shu, Casas Juan P, Hingorani Aroon |
Association of SNP rs17465637 on chromosome 1q41 and rs599839 on 1p13.3 with myocardial infarction in an American caucasian population. Annals of human genetics 2011 Jul 75 (4): 475-82. Wang Annabel Z, Li Lin, Zhang Bin, Shen Gong-Qing, Wang Qing Kenne |
Extended evidence for association between the melanoma inhibitory activity 3 gene and myocardial infarction. Thrombosis and haemostasis 2011 Apr 105 (4): 670-5. Koch Werner, Schatke Anna, Wolferstetter Hannah, Mueller Jakob C, Schömig Albert, Kastrati Adn |
Association study of MIA3 rs17465637 polymorphism with cardiovascular disease in rheumatoid arthritis patients. DNA and cell biology 2012 Aug 31 (8): 1412-7. García-Bermúdez Mercedes, López-Mejías Raquel, González-Juanatey Carlos, Corrales Alfonso, Castañeda Santos, Miranda-Filloy José A, Gómez-Vaquero Carmen, Fernández-Gutiérrez Benjamín, Balsa Alejandro, Pascual-Salcedo Dora, Blanco Ricardo, González-Álvaro Isidoro, Llorca Javier, Martín Javier, González-Gay Miguel |
Meta-analysis identifies robust association between SNP rs17465637 in MIA3 on chromosome 1q41 and coronary artery disease. Atherosclerosis 2013 Nov 231 (1): 136-40. Li Xiuchun, Huang Yufeng, Yin Dan, Wang Dan, Xu Chengqi, Wang Fan, Yang Qin, Wang Xiaojing, Li Sisi, Chen Shanshan, Xiong Xin, Huang Yuan, Zhao Yuanyuan, Wang Li, Zhu Xuan, Su Zhenhong, Zhou Bisheng, Zhang Yuting, Wang Longfei, Chang Le, Xu Chaoping, Li Hui, Ke Tie, Ren Xiang, Cheng Xiang, Yang Yanzong, Liao Yuhua, Tu Xin, Wang Qing |
The Relationship Between Gene Polymorphisms and Dipping Profile in Patients With Coronary Heart Disease. American journal of hypertension 2016 09 29 (9): 1094-102. Wirtwein Marcin, Melander Olle, Sjogren Marketa, Hoffmann Michal, Narkiewicz Krzysztof, Gruchala Marcin, Sobiczewski Wojcie |
Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia. British journal of cancer 2017 Jul . Schubert Stephanie A, Ruano Dina, Elsayed Fadwa A, Boot Arnoud, Crobach Stijn, Sarasqueta Arantza Farina, Wolffenbuttel Bruce, van der Klauw Melanie M, Oosting Jan, Tops Carli M, van Eijk Ronald, Vasen Hans Fa, Vossen Rolf Ham, Nielsen Maartje, Castellví-Bel Sergi, Ruiz-Ponte Clara, Tomlinson Ian, Dunlop Malcolm G, Vodicka Pavel, Wijnen Juul T, Hes Frederik J, Morreau Hans, de Miranda Noel Fcc, Sijmons Rolf H, van Wezel T |
Genetic variants of increased waist circumference in psychosis. Psychiatric genetics 2017 12 27 (6): 210-218. Hukic Dzana S, Ösby Urban, Olsson Eric, Hilding Agneta, Östenson Claes-Göran, Gu Harvest F, Ehrenborg Ewa, Edman Gunnar, Schalling Martin, Lavebratt Catharina, Frisén Loui |
Effect of Coronary Artery Disease risk SNPs on serum cytokine levels and cytokine imbalance in Premature Coronary Artery Disease. Cytokine 2017 Jul . Ansari Wafa M, Humphries Steve E, Naveed Abdul K, Khan Omer J, Khan Dilshad A, Khattak Ejaz Hass |
Genetic risk analysis of coronary artery disease in Pakistani subjects using a genetic risk score of 21 variants. Atherosclerosis 2017 Jan 258 1-7. Shahid Saleem Ullah, Shabana , Cooper Jackie A, Beaney Katherine E, Li Kawah, Rehman Abdul, Humphries Steve |
The Relationship Between Coronary Artery Disease and Genetic Polymorphisms of Melanoma Inhibitory Activity 3. Iranian Red Crescent medical journal 2016 Sep 18 (9): e31146. Zaimkohan Hooshang, Keramatipour Mohammad, Mirhafez Seyed Reza, Tavakkoly-Bazzaz Javad, Tahooni Azadeh, Piryaei Mohammad, Ghayour-Mobarhan Majid, Ghaderian Seyed Mohammad Hosse |
GWAS implicated risk variants in different genes contribute additively to increase the risk of coronary artery disease (CAD) in the Pakistani subjects. Lipids in health and disease 2018 Apr 17 (1): 89. Shahid Saleem Ullah, Shabana N A, Rehman Abdul, Humphries Ste |
The Mediterranean diet reduces the genetic risk of chromosome 9p21 for myocardial infarction in an Asian population community cohort. Scientific reports 2019 Dec 9 (1): 18405. Leu Hsin-Bang, Chung Chia-Min, Chen Jaw-Wen, Pan Wen-Ha |
Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle Cells.
Circulation research 2020 10 127 (12): 1552-1565. Aherrahrou Redouane, Guo Liang, Nagraj V Peter, Aguhob Aaron, Hinkle Jameson, Chen Lisa, Yuhl Soh Joon, Lue Dillon, Alencar Gabriel F, Boltjes Arjan, van der Laan Sander W, Farber Emily, Fuller Daniela, Anane-Wae Rita, Akingbesote Ngozi, Manichaikul Ani W, Ma Lijiang, Kaikkonen Minna U, Björkegren Johan L M, Önengüt-Gümü?cü Suna, Pasterkamp Gerard, Miller Clint L, Owens Gary K, Finn Aloke, Navab Mohamad, Fogelman Alan M, Berliner Judith A, Civelek Me |
Low HDL concentration in rs2048327-G carriers can predispose men to develop coronary heart disease: Tehran Cardiometabolic genetic study (TCGS). Gene 2021 Feb 145485. Najd Hassan Bonab Leila, Moazzam-Jazi Maryam, Miri Moosavi Reyhaneh-Sadat, Fallah Mohammad-Sadegh, Lanjanian Hossein, Masjoudi Sajedeh, Daneshpour Maryam |
Association study between polymorphisms in MIA3, SELE, SMAD3 and CETP genes and coronary artery disease in an Iranian population. BMC cardiovascular disorders 2022 6 22 (1): 298. Rayat Sima, Ramezanidoraki Nasim, Kazemi Nima, Modarressi Mohammad H, Falah Masoumeh, Zardadi Safoura, Morovvati Sae |
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