Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: WDR12[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 |
Large scale association analysis identifies three susceptibility loci for coronary artery disease. PloS one 2011 6 (12): e29427. Saade Stephanie, Cazier Jean-Baptiste, Ghassibe-Sabbagh Michella, Youhanna Sonia, Badro Danielle A, Kamatani Yoichiro, Hager Jörg, Yeretzian Joumana S, El-Khazen Georges, Haber Marc, Salloum Angelique K, Douaihy Bouchra, Othman Raed, Shasha Nabil, Kabbani Samer, Bayeh Hamid El, Chammas Elie, Farrall Martin, Gauguier Dominique, Platt Daniel E, Zalloua Pierre A, |
Association Between Coronary Artery Disease Genetic Variants and Subclinical Atherosclerosis: An Association Study and Meta-analysis. Revista espanola de cardiologia (English ed.) 2015 Oct 68 (10): 869-877. Zabalza Michel, Subirana Isaac, Lluis-Ganella Carla, Sayols-Baixeras Sergi, de Groot Eric, Arnold Roman, Cenarro Ana, Ramos Rafel, Marrugat Jaume, Elosua Rober |
Analysis of rs6725887 in the WD Repeat Protein 12 in Association with Coronary Artery Disease in Iranian Patients. International journal of molecular and cellular medicine 2015 4 (3): 160-166. Piryaei Mohammad, Ghaderian Sayyed Mohammad Hossein, Vakili Hossein, Zaimkohan Hooshang, Mohammadi Ghahhari Nastaran, Mafi Golchin Mary |
Influence of coronary artery disease and subclinical atherosclerosis related polymorphisms on the risk of atherosclerosis in rheumatoid arthritis. Scientific reports 2017 Jan 7 40303. López-Mejías Raquel, Corrales Alfonso, Vicente Esther, Robustillo-Villarino Montserrat, González-Juanatey Carlos, Llorca Javier, Genre Fernanda, Remuzgo-Martínez Sara, Dierssen-Sotos Trinidad, Miranda-Filloy José A, Huaranga Marco A Ramírez, Pina Trinitario, Blanco Ricardo, Alegre-Sancho Juan J, Raya Enrique, Mijares Verónica, Ubilla Begoña, Ferraz-Amaro Iván, Gómez-Vaquero Carmen, Balsa Alejandro, López-Longo Francisco J, Carreira Patricia, González-Álvaro Isidoro, Ocejo-Vinyals J Gonzalo, Rodríguez-Rodríguez Luis, Fernández-Gutiérrez Benjamín, Castañeda Santos, Martín Javier, González-Gay Miguel |
Elevated ambulatory systolic-diastolic pressure regression index is genetically determined in hypertensive patients with coronary heart disease. Blood pressure 2017 Jan 1-10. Wirtwein Marcin, Melander Olle, Sj?gren Marketa, Hoffmann Michal, Narkiewicz Krzysztof, Gruchala Marcin, Sobiczewski Wojcie |
Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance Imaging.
Stroke 2018 Jul . Jian Xueqiu, Satizabal Claudia L, Smith Albert V, Wittfeld Katharina, Bis Joshua C, Smith Jennifer A, Hsu Fang-Chi, Nho Kwangsik, Hofer Edith, Hagenaars Saskia P, Nyquist Paul A, Mishra Aniket, Adams Hieab H H, Li Shuo, Teumer Alexander, Zhao Wei, Freedman Barry I, Saba Yasaman, Yanek Lisa R, Chauhan Ganesh, van Buchem Mark A, Cushman Mary, Royle Natalie A, Bryan R Nick, Niessen Wiro J, Windham Beverly G, DeStefano Anita L, Habes Mohamad, Heckbert Susan R, Palmer Nicholette D, Lewis Cora E, Eiriksdottir Gudny, Maillard Pauline, Mathias Rasika A, Homuth Georg, Valdés-Hernández Maria Del C, Divers Jasmin, Beiser Alexa S, Langner Sönke, Rice Kenneth M, Bastin Mark E, Yang Qiong, Maldjian Joseph A, Starr John M, Sidney Stephen, Risacher Shannon L, Uitterlinden André G, Gudnason Vilmundur G, Nauck Matthias, Rotter Jerome I, Schreiner Pamela J, Boerwinkle Eric, van Duijn Cornelia M, Mazoyer Bernard, von Sarnowski Bettina, Gottesman Rebecca F, Levy Daniel, Sigurdsson Sigurdur, Vernooij Meike W, Turner Stephen T, Schmidt Reinhold, Wardlaw Joanna M, Psaty Bruce M, Mosley Thomas H, DeCarli Charles S, Saykin Andrew J, Bowden Donald W, Becker Diane M, Deary Ian J, Schmidt Helena, Kardia Sharon L R, Ikram M Arfan, Debette Stéphanie, Grabe Hans J, Longstreth W T, Seshadri Sudha, Launer Lenore J, Fornage Myriam, |
Genome-wide association study of cerebral small vessel disease reveals established and novel loci.
Brain : a journal of neurology 2019 Oct 142 (10): 3176-3189. Chung Jaeyoon, Marini Sandro, Pera Joanna, Norrving Bo, Jimenez-Conde Jordi, Roquer Jaume, Fernandez-Cadenas Israel, Tirschwell David L, Selim Magdy, Brown Devin L, Silliman Scott L, Worrall Bradford B, Meschia James F, Demel Stacie, Greenberg Steven M, Slowik Agnieszka, Lindgren Arne, Schmidt Reinhold, Traylor Matthew, Sargurupremraj Muralidharan, Tiedt Steffen, Malik Rainer, Debette Stéphanie, Dichgans Martin, Langefeld Carl D, Woo Daniel, Rosand Jonathan, Anderson Christopher |
Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies.
The Lancet. Neurology 2021 (5): 351-361. Traylor Matthew, Persyn Elodie, Tomppo Liisa, Klasson Sofia, Abedi Vida, Bakker Mark K, Torres Nuria, Li Linxin, Bell Steven, Rutten-Jacobs Loes, Tozer Daniel J, Griessenauer Christoph J, Zhang Yanfei, Pedersen Annie, Sharma Pankaj, Jimenez-Conde Jordi, Rundek Tatjana, Grewal Raji P, Lindgren Arne, Meschia James F, Salomaa Veikko, Havulinna Aki, Kourkoulis Christina, Crawford Katherine, Marini Sandro, Mitchell Braxton D, Kittner Steven J, Rosand Jonathan, Dichgans Martin, Jern Christina, Strbian Daniel, Fernandez-Cadenas Israel, Zand Ramin, Ruigrok Ynte, Rost Natalia, Lemmens Robin, Rothwell Peter M, Anderson Christopher D, Wardlaw Joanna, Lewis Cathryn M, Markus Hugh S, , , , |
Impact of PCSK9, WDR12, CDKN2A, and CXCL12 Polymorphisms in Jordanian Cardiovascular Patients on Warfarin Responsiveness and Sensitivity. International journal of general medicine 2021 14 103-118. Ibdah Rasheed K, Al-Eitan Laith N, Alrabadi Nasr N, Almasri Ayah Y, Alnaamneh Adan H, Khasawneh Rame H, Alghamdi Mansour |
Analysis of 61 SNPs from the CAD specific genomic loci reveals unique set of SNPs as significant markers in the Southern Indian population of Hyderabad. BMC cardiovascular disorders 2022 4 22 (1): 148. Gorre Manjula, Rayabarapu Pranavchand, Battini Sriteja Reddy, Irgam Kumuda, Battini Mohan Red |
Genetic overlap for ten cardiovascular diseases: A comprehensive gene-centric pleiotropic association analysis and Mendelian randomization study. iScience 2023 11 26 (11): 108150. Zeye Liu, Jing Xu, Jiangshan Tan, Xiaofei Li, Fengwen Zhang, Wenbin Ouyang, Shouzheng Wang, Yuan Huang, Shoujun Li, Xiangbin P |
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