Treffer 1 - 15 von 15 für Suche 'Lind, Nicholas Anton', Suchdauer: 0,65s Treffer weiter einschränken
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    Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies von Chauhan, Ganesh, Arnold, Corey R, Chu, Audrey Y, Reyahi, Azadeh, Bis, Joshua C, Havulinna, Aki S, Trompet, Stella, Manichaikul, Ani, Teumer, Alexander, Gustafsson, Stefan, Bartz, Traci M, Bellenguez, Céline, Vidal, Jean Sebastien, Kjartansson, Olafur, Satizabal, Claudia L, Xue, Flora, Liu, Yongmei, Bevan, Steve, Hopewell, Jemma C, Heckbert, Susan R, Rice, Kenneth, Smith, Nicholas L, Levi, Christopher, Sharma, Pankaj, Sudlow, Cathie LM, Cole, John W, Schmidt, Reinhold, Meschia, James, Thijs, Vincent, Melander, Olle, Grewal, Raji P, Sacco, Ralph L, Rundek, Tatjana, Rothwell, Peter M, Jern, Christina, Johnson, Julie A, Benavente, Oscar R, Lee, Jin-Moo, Wong, Quenna, Aparicio, Hugo J, Engelter, Stefan T, Kloss, Manja, Pezzini, Alessandro, Buring, Julie E, Ridker, Paul M, Berr, Claudine, Dartigues, Jean-François, Hamsten, Anders, Traylor, Matthew, Pedersen, Nancy L, Lannfelt, Lars, Morris, Andrew P, Jimenez-Conde, Jordi, Montaner, Joan, Slowik, Agnieszka, Woo, Daniel, Hofman, Albert, Koudstaal, Peter J, Portegies, Marileen L P, Uitterlinden, André G, Ford, Ian, Jukema, J Wouter, Stott, David J, Allen, Norrina B, Johnson, Andrew D, De Jager, Philip L, White, Charles C, Markus, Marcello Ricardo Paulista, Schminke, Ulf, Boncoraglio, Giorgio B, Clarke, Robert, Kamatani, Yoichiro, Dallongeville, Jean, Rotter, Jerome I, Nalls, Michael A, Griswold, Michael E, Knopman, David S, Windham, B Gwen, Beiser, Alexa, Vartiainen, Erkki, French, Curtis R, Pastinen, Tomi, Gudnason, Vilmundur, Kurth, Tobias, Harris, Tamara B, Rich, Stephen S, deStefano, Anita L, Rosand, Jonathan, Mosley, Thomas H, Ingelsson, Erik, van Duijn, Cornelia M, Tzourio, Christophe, Rexrode, Kathryn M, Lehmann, Ordan J, Launer, Lenore J, Carlsson, Peter, Chasman, Daniel I, Childs, Sarah J, Seshadri, Sudha, Debette, Stéphanie

    Veröffentlicht in Lancet neurology

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    Understanding the genetic complexity of puberty timing across the allele frequency spectrum von Kaisinger, Lena R, Vaudel, Marc, Mendes de Oliveira, Edson, Messina, Andrea, Helgason, Hannes, Thompson, Deborah J, Santoni, Federico, Zouaghi, Yassine, Gardner, Eugene J, Zhao, Yajie, Bradfield, Jonathan P, Broer, Linda, Campbell, Archie, Franceschini, Nora, Franke, Lude H, Girotto, Giorgia, Järvelin, Marjo-Riitta, Joshi, Peter K, Karlsson, Robert, Luan, Jian’an, Mangino, Massimo, Noordam, Raymond, Nutile, Teresa, Concas, Maria Pina, Polašek, Ozren, Sala, Cinzia, van der Most, Peter J, Willemsen, Gonneke, Anton-Culver, Hoda, Beckmann, Matthias W, Berrington de Gonzalez, Amy, Bojesen, Stig E, Canzian, Federico, Chang-Claude, Jenny, Couch, Fergus J, Czene, Kamila, Daly, Mary B, Demerath, Ellen W, De Vivo, Immaculata, Dunning, Alison M, Dwek, Miriam, Fasching, Peter A, Fernandez-Rhodes, Lindsay, García-Sáenz, José A, González-Neira, Anna, Haiman, Christopher A, Hamann, Ute, Hakonarson, Hakon, Hart, Roger J, Hooning, Maartje J, Hoppe, Reiner, Hottenga, Jouke-Jan, Hu, Frank B, Huebner, Hanna, Hunter, David J, Lind, Penelope A, Magnusson, Patrik K. E, Mannermaa, Arto, Michailidou, Kyriaki, Milne, Roger L, Nyholt, Dale R, Obi, Nadia, Ostrowski, Sisse R, Palotie, Aarno, Peters, Annette, Plaseska-Karanfilska, Dijana, Rennert, Gad, Rosendaal, Frits R, Saloustros, Emmanouil, Spedicati, Beatrice, Teras, Lauren R, Turman, Constance, Vachon, Celine M, Wang, Qin, Zemel, Babette S, Zheng, Wei, van Dijk, Ko W, Ciullo, Marina, Chenevix-Trench, Georgia, Cucca, Francesco, Grant, Struan F. A, Gudnason, Vilmundur, Kraft, Peter, Martin, Nicholas G, Pennell, Craig E, Ridker, Paul M, Robino, Antonietta, Stöckl, Doris, Sudlow, Cathie, Toniolo, Daniela, Uitterlinden, André, Pharoah, Paul D. P, Easton, Douglas F, Njølstad, Pål R, Murray, Anna, Manousaki, Despoina, Stefansson, Kari, Farooqi, I. Sadaf, Day, Felix R, Perry, John R. B

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    Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum von Kaisinger, Lena R, Vaudel, Marc, Mendes de Oliveira, Edson, Messina, Andrea, Helgason, Hannes, Thompson, Deborah J, Santoni, Federico, Zouaghi, Yassine, Gardner, Eugene J, Zhao, Yajie, Bradfield, Jonathan P, Broer, Linda, Campbell, Archie, Franceschini, Nora, Franke, Lude H, Girotto, Giorgia, Järvelin, Marjo-Riitta, Joshi, Peter K, Karlsson, Robert, Mangino, Massimo, Noordam, Raymond, Nutile, Teresa, Concas, Maria Pina, Polašek, Ozren, Sala, Cinzia, van der Most, Peter J, Willemsen, Gonneke, Andrulis, Irene L, Anton-Culver, Hoda, Barnes, Catriona LK, Beckmann, Matthias W, Berrington de Gonzalez, Amy, Bojesen, Stig E, Canzian, Federico, Chang-Claude, Jenny, Couch, Fergus J, Czene, Kamila, Daly, Mary B, Demerath, Ellen W, De Vivo, Immaculata, Dunning, Alison M, Dwek, Miriam, Fasching, Peter A, Fernandez-Rhodes, Lindsay, García-Sáenz, José A, González-Neira, Anna, Haiman, Christopher A, Hamann, Ute, Hakonarson, Hakon, Hart, Roger J, Hooning, Maartje J, Hoppe, Reiner, Hottenga, Jouke-Jan, Hu, Frank B, Huebner, Hanna, Hunter, David J, Launer, Lenore J, Mannermaa, Arto, McCarthy, Mark I, Menni, Cristina, Nyholt, Dale R, O'Brien, Katie M, Offit, Kenneth, Ostrowski, Sisse R, Pedersen, Ole B, Peters, Annette, Pianigiani, Giulia, Rennert, Gad, Rosendaal, Frits R, Saloustros, Emmanouil, Schipf, Sabine, Small, Kerrin, Stone, Jennifer, Tamimi, Rulla M, Teras, Lauren R, Vachon, Celine M, Wang, Qin, Zemel, Babette S, van Dijk, Ko W, Boerwinkle, Eric, Chenevix-Trench, Georgia, Cucca, Francesco, Grant, Struan FA, Kraft, Peter, Lawlor, Deborah A, Pedersen, Nancy L, Pennell, Craig E, Sudlow, Cathie, Uitterlinden, André, Wareham, Nicholas J, Lifelines Cohort Study, Easton, Douglas F, Sulem, Patrick, Murray, Anna, Juul, Anders, Erikstrup, Christian, Horikoshi, Momoko, Chen, Zhengming, Farooqi, I Sadaf, Pitteloud, Nelly

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