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Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

by Henry, Albert, Roselli, Carolina, Sveinbjörnsson, Garðar, Fatemifar, Ghazaleh, Hedman, Åsa K., Morley, Michael P., Helgadottir, Anna, Verweij, Niek, Dehghan, Abbas, Almgren, Peter, Andersson, Charlotte, Backman, Joshua D., Biggs, Mary L., Brandimarto, Jeffrey, Buckbinder, Leonard, Carey, David J., Chasman, Daniel I., Chen, Xu, Chung, Jonathan, Cook, James P., Delgado, Graciela E., Denaxas, Spiros, Dörr, Marcus, Dudley, Samuel C., Esko, Tõnu, Finan, Chris, Gottdiener, John S., Gross, Stefan, Guðbjartsson, Daníel F., Gutmann, Rebecca, Haggerty, Christopher M., Hyde, Craig L., Ingelsson, Erik, Jukema, J. Wouter, Kavousi, Maryam, Khaw, Kay-Tee, Kleber, Marcus E., Køber, Lars, Koekemoer, Andrea, Langenberg, Claudia, Lind, Lars, Lotta, Luca A., Luan, Jian’an, März, Winfried, Melander, Olle, Mordi, Ify R., Morgan, Thomas, Morris, Andrew D., Morris, Andrew P., Morrison, Alanna C., Nelson, Christopher P., Niessner, Alexander, Niiranen, Teemu, O’Donoghue, Michelle L., Owens, Anjali T., Parry, Helen M., Perola, Markus, Rice, Kenneth M., Ridker, Paul M., Rotter, Jerome I., Salo, Perttu, Salomaa, Veikko, Smelser, Diane T., Stender, Steen, Stott, David J., Tammesoo, Mari-Liis, Taylor, Kent D., Teder-Laving, Maris, Thorsteinsdottir, Unnur, Torp-Pedersen, Christian, Trompet, Stella, Tyl, Benoit, Uitterlinden, Andre G., Veluchamy, Abirami, Völker, Uwe, Voors, Adriaan A., Wareham, Nicholas J., Waterworth, Dawn, Weiss, Raul, Wiggins, Kerri L., Yerges-Armstrong, Laura M., Yu, Bing, Zannad, Faiez, Zhao, Jing Hua, Hemingway, Harry, McMurray, John J. V., Yang, Jian, Visscher, Peter M., Malarstig, Anders, Holm, Hilma, Sattar, Naveed, Holmes, Michael V., Cappola, Thomas P., Hingorani, Aroon D., Kuchenbaecker, Karoline, Ellinor, Patrick T., Smith, J. Gustav, Vasan, Ramachandran S., Swerdlow, Daniel I., Lumbers, R. Thomas
Published in Nature communications (2020)

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Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

by Aragam, Krishna G., Jiang, Tao, Goel, Anuj, Kanoni, Stavroula, Wolford, Brooke N., Atri, Deepak S., Weeks, Elle M., Wang, Minxian, Hindy, George, Zhou, Wei, Grace, Christopher, Roselli, Carolina, Marston, Nicholas A., Kamanu, Frederick K., Surakka, Ida, Venegas, Loreto Muñoz, Sherliker, Paul, Koyama, Satoshi, Ishigaki, Kazuyoshi, Åsvold, Bjørn O., Brown, Michael R., Brumpton, Ben, de Vries, Paul S., Giannakopoulou, Olga, Giardoglou, Panagiota, Gudbjartsson, Daniel F., Güldener, Ulrich, Haider, Syed M. Ijlal, Helgadottir, Anna, Ibrahim, Maysson, Kastrati, Adnan, Kessler, Thorsten, Kyriakou, Theodosios, Konopka, Tomasz, Li, Ling, Ma, Lijiang, Meitinger, Thomas, Mucha, Sören, Munz, Matthias, Murgia, Federico, Nielsen, Jonas B., Nöthen, Markus M., Pang, Shichao, Reinberger, Tobias, Schnitzler, Gavin, Smedley, Damian, Thorleifsson, Gudmar, von Scheidt, Moritz, Ulirsch, Jacob C., Arnar, David O., Burtt, Noël P., Costanzo, Maria C., Flannick, Jason, Ito, Kaoru, Jang, Dong-Keun, Kamatani, Yoichiro, Khera, Amit V., Komuro, Issei, Kullo, Iftikhar J., Lotta, Luca A., Nelson, Christopher P., Roberts, Robert, Thorgeirsson, Gudmundur, Thorsteinsdottir, Unnur, Webb, Thomas R., Baras, Aris, Björkegren, Johan L. M., Boerwinkle, Eric, Dedoussis, George, Holm, Hilma, Hveem, Kristian, Melander, Olle, Morrison, Alanna C., Orho-Melander, Marju, Rallidis, Loukianos S., Ruusalepp, Arno, Sabatine, Marc S., Stefansson, Kari, Zalloua, Pierre, Ellinor, Patrick T., Farrall, Martin, Danesh, John, Ruff, Christian T., Finucane, Hilary K., Hopewell, Jemma C., Clarke, Robert, Gupta, Rajat M., Erdmann, Jeanette, Samani, Nilesh J., Schunkert, Heribert, Watkins, Hugh, Willer, Cristen J., Deloukas, Panos, Kathiresan, Sekar, Butterworth, Adam S.
Published in Nature genetics (2022)

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Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

by Steinthorsdottir, Valgerdur, McGinnis, Ralph, Williams, Nicholas O., Stefansdottir, Lilja, Thorleifsson, Gudmar, Shooter, Scott, Fadista, João, Sigurdsson, Jon K., Auro, Kirsi M., Berezina, Galina, Borges, Maria-Carolina, Bumpstead, Suzannah, Bybjerg-Grauholm, Jonas, Colgiu, Irina, Dolby, Vivien A., Dudbridge, Frank, Engel, Stephanie M., Franklin, Christopher S., Frigge, Michael L., Frisbaek, Yr, Geirsson, Reynir T., Geller, Frank, Gretarsdottir, Solveig, Gudbjartsson, Daniel F., Harmon, Quaker, Hougaard, David Michael, Hegay, Tatyana, Helgadottir, Anna, Hjartardottir, Sigrun, Jääskeläinen, Tiina, Johannsdottir, Hrefna, Jonsdottir, Ingileif, Juliusdottir, Thorhildur, Kalsheker, Noor, Kasimov, Abdumadjit, Kemp, John P., Kivinen, Katja, Klungsøyr, Kari, Lee, Wai K., Melbye, Mads, Miedzybrodska, Zosia, Moffett, Ashley, Najmutdinova, Dilbar, Nishanova, Firuza, Olafsdottir, Thorunn, Perola, Markus, Pipkin, Fiona Broughton, Poston, Lucilla, Prescott, Gordon, Saevarsdottir, Saedis, Salimbayeva, Damilya, Scaife, Paula Juliet, Skotte, Line, Staines-Urias, Eleonora, Stefansson, Olafur A., Sørensen, Karina Meden, Thomsen, Liv Cecilie Vestrheim, Tragante, Vinicius, Trogstad, Lill, Simpson, Nigel A. B., Aripova, Tamara, Casas, Juan P., Dominiczak, Anna F., Walker, James J., Thorsteinsdottir, Unnur, Iversen, Ann-Charlotte, Feenstra, Bjarke, Lawlor, Deborah A., Boyd, Heather Allison, Magnus, Per, Laivuori, Hannele, Zakhidova, Nodira, Svyatova, Gulnara, Stefansson, Kari, Morgan, Linda
Published in Nature communications (25.11.2020)

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Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies

by Traylor, Matthew, MSc, Farrall, Martin, FRCPath, Holliday, Elizabeth G, PhD, Sudlow, Cathie, FRCP, Hopewell, Jemma C, PhD, Cheng, Yu-Ching, PhD, Fornage, Myriam, PhD, Ikram, M Arfan, MD, Malik, Rainer, PhD, Bevan, Steve, PhD, Thorsteinsdottir, Unnur, PhD, Nalls, Mike A, PhD, Longstreth, WT, MD, Wiggins, Kerri L, MS, Yadav, Sunaina, MSc, Parati, Eugenio A, MD, DeStefano, Anita L, PhD, Worrall, Bradford B, MD, Kittner, Steven J, MD, Khan, Muhammad Saleem, MSc, Reiner, Alex P, MD, Helgadottir, Anna, MD, Achterberg, Sefanja, PhD, Fernandez-Cadenas, Israel, PhD, Abboud, Sherine, MD, Schmidt, Reinhold, MD, Walters, Matthew, MD, Chen, Wei-Min, PhD, Ringelstein, E Bernd, MD, O'Donnell, Martin, MD, Ho, Weang Kee, PhD, Pera, Joanna, MD, Lemmens, Robin, MD, Norrving, Bo, MD, Higgins, Peter, MRCP, Benn, Marianne, MD, Sale, Michele, PhD, Kuhlenbäumer, Gregor, MD, Doney, Alexander S F, PhD, Vicente, Astrid M, PhD, Delavaran, Hossein, MD, Algra, Ale, MD, Davies, Gail, PhD, Oliveira, Sofia A, PhD, Palmer, Colin N A, PhD, Deary, Ian, PhD, Schmidt, Helena, MD, Pandolfo, Massimo, MD, Montaner, Joan, MD, Carty, Cara, PhD, de Bakker, Paul I W, PhD, Kostulas, Konstantinos, MD, Ferro, Jose M, MD, van Zuydam, Natalie R, MSc, Valdimarsson, Einar, MD, Nordestgaard, Børge G, MD, Lindgren, Arne, MD, Thijs, Vincent, MD, Slowik, Agnieszka, MD, Saleheen, Danish, MD, Paré, Guillaume, MD, Berger, Klaus, MD, Thorleifsson, Gudmar, PhD, Hofman, Albert, MD, Mosley, Thomas H, PhD, Mitchell, Braxton D, PhD, Furie, Karen, MD, Clarke, Robert, FRCP, Levi, Christopher, MD, Seshadri, Sudha, MD, Gschwendtner, Andreas, MD, Boncoraglio, Giorgio B, MD, Sharma, Pankaj, PhD, Bis, Joshua C, PhD, Gretarsdottir, Solveig, PhD, Psaty, Bruce M, Rothwell, Peter M, FMedSci, Rosand, Jonathan, MD, Meschia, James F, MD, Stefansson, Kari, MD, Dichgans, Martin, MD, Markus, Hugh S, Dr
Published in Lancet neurology (01.11.2012)

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