Treffer 1 - 20 von 51 für Suche 'Augustine, Annette', Suchdauer: 1,57s Treffer weiter einschränken
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    Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk von Ehret, Georg B, Munroe, Patricia B, Rice, Kenneth M, Bochud, Murielle, Johnson, Andrew D, Chasman, Daniel I, Smith, Albert V, Tobin, Martin D, Verwoert, Germaine C, Hwang, Shih-Jen, Pihur, Vasyl, Vollenweider, Peter, O'Reilly, Paul F, Amin, Najaf, Bragg-Gresham, Jennifer L, Teumer, Alexander, Glazer, Nicole L, Launer, Lenore, Zhao, Jing Hua, Aulchenko, Yurii, Heath, Simon, Sõber, Siim, Parsa, Afshin, Luan, Jian'an, Arora, Pankaj, Dehghan, Abbas, Zhang, Feng, Lucas, Gavin, Hicks, Andrew A, Jackson, Anne U, Peden, John F, Tanaka, Toshiko, Wild, Sarah H, Rudan, Igor, Igl, Wilmar, Milaneschi, Yuri, Parker, Alex N, Fava, Cristiano, Chambers, John C, Fox, Ervin R, Kumari, Meena, Go, Min Jin, van der Harst, Pim, Kao, Wen Hong Linda, Sjögren, Marketa, Vinay, D G, Alexander, Myriam, Tabara, Yasuharu, Shaw-Hawkins, Sue, Whincup, Peter H, Liu, Yongmei, Shi, Gang, Kuusisto, Johanna, Tayo, Bamidele, Seielstad, Mark, Sim, Xueling, Nguyen, Khanh-Dung Hoang, Lehtimäki, Terho, Matullo, Giuseppe, Wu, Ying, Gaunt, Tom R, Onland-Moret, N Charlotte, Cooper, Matthew N, Platou, Carl G P, Org, Elin, Hardy, Rebecca, Dahgam, Santosh, Palmen, Jutta, Vitart, Veronique, Braund, Peter S, Kuznetsova, Tatiana, Uiterwaal, Cuno S P M, Adeyemo, Adebowale, Palmas, Walter, Campbell, Harry, Ludwig, Barbara, Tomaszewski, Maciej, Tzoulaki, Ioanna, Palmer, Nicholette D, Aspelund, Thor, Garcia, Melissa, Chang, Yen-Pei C, O'Connell, Jeffrey R, Steinle, Nanette I, Grobbee, Diederick E, Arking, Dan E, Kardia, Sharon L, Morrison, Alanna C, Hernandez, Dena, Najjar, Samer, McArdle, Wendy L, Hadley, David, Brown, Morris J, Connell, John M, Hingorani, Aroon D, Day, Ian N M, Lawlor, Debbie A, Beilby, John P, Lawrence, Robert W, Clarke, Robert

    Veröffentlicht in Nature (London)

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    Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility von Below, Jennifer E, Horikoshi, Momoko, Johnson, Andrew D, Ng, Maggie C Y, Abecasis, Goncalo R, Been, Latonya F, Caulfield, Mark, Chang, Li-Ching, Chang, Tien-Jyun, Chang, Yi-Cheng, Chen, Chien-Hsiun, Chen, Han, Chidambaram, Manickam, Cho, Young Min, Collins, Francis S, Das, Debashish, Dedoussis, George, Dimas, Antigone S, Doney, Alex S F, Dorkhan, Mozhgan, Edkins, Sarah, Erbel, Raimund, Fontanillas, Pierre, Fox, Caroline, Froguel, Philippe, Gao, Yutang, Gieger, Christian, Gigante, Bruna, Grallert, Harald, Guiducci, Candace, Hamsten, Anders, Hattersley, Andrew T, Hayward, Caroline, Herder, Christian, Hofman, Albert, Holmen, Oddgeir L, Humphries, Steve E, Hydrie, Zafar I, Jackson, Anne U, Jia, Weiping, Kato, Norihiro, Kelly, Ann M, Khan, Hassan, Kim, Hyung-Lae, Kong, Augustine, Korpi-Hyövälti, Eeva, Kumar, Ashish, Laakso, Markku, Langenberg, Claudia, Li, Man, Li, Xinzhong, Li, Yun, Liang, Junbin, Liju, Samuel, Lind, Lars, Lindgren, Cecilia M, Lobbens, Stéphane, Lu, Wei, Luan, Jian'an, Lyssenko, Valeriya, Männistö, Satu, Meigs, James B, Meyer, Julia, Mohlke, Karen L, Musk, Bill, Nakamura, Jiro, Park, Kyong Soo, Rallidis, Loukianos, Rasheed, Asif, Rehnberg, Emil, Rudan, Igor, Rybin, Denis, Saaristo, Timo E, Sanghera, Dharambir K, Saramies, Jouko, Scott, Robert A, Shah, Nabi, Sim, Xueling, Sivapalaratnam, Suthesh, Stančáková, Alena, Steinthorsdottir, Valgerdur, Stirrups, Kathleen, Strawbridge, Rona J, Takeuchi, Fumihiko, Thorsteinsdottir, Unnur, Trip, Mieke D, Valladares-Salgado, Adan, Wang, Congrong, Wickremasinghe, Ananda R, Wu, Ying, Yamamoto, Ken, Yang, Mingyu, Young, Robin, Zhang, Fan, Zhang, Rong, Altshuler, David, Cho, Yoon Shin, Lee, Jong-Young, Teo, Yik Ying, Boehnke, Michael

    Veröffentlicht in Nature genetics

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    Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease von Schunkert, Heribert, Kathiresan, Sekar, Stewart, Alexandre F R, Barbalic, Maja, Absher, Devin, Aherrahrou, Zouhair, Allayee, Hooman, Anand, Sonia S, Anderson, Jeffrey L, Ardissino, Diego, Balmforth, Anthony J, Boerwinkle, Eric, Braund, Peter S, Brown, Morris J, Burnett, Mary Susan, Buysschaert, Ian, Carlquist, John F, Chen, Li, Cichon, Sven, Davies, Robert W, Dehghan, Abbas, Demissie, Serkalem, Do, Ron, Eifert, Sandra, Mokhtari, Nour Eddine El, Elosua, Roberto, Engert, James C, Epstein, Stephen E, Fischer, Marcus, Folsom, Aaron R, Freyer, Jennifer, Halperin, Eran, Hammond, Naomi, Hazen, Stanley L, Horne, Benjamin D, Illig, Thomas, Iribarren, Carlos, Kaiser, Michael A, Kaplan, Lee M, Kastelein, John J P, Laaksonen, Reijo, Leander, Karin, Lettre, Guillaume, Li, Mingyao, Loley, Christina, Lotery, Andrew J, Mannucci, Pier M, Maouche, Seraya, Martinelli, Nicola, Meisinger, Christa, Melander, Olle, Mooser, Vincent, Mühleisen, Thomas W, Münzel, Thomas, Musunuru, Kiran, Nelson, Christopher P, Nöthen, Markus M, Olivieri, Oliviero, Patel, Riyaz S, Patterson, Chris C, Peters, Annette, Peyvandi, Flora, Quyyumi, Arshed A, Rallidis, Loukianos S, Rice, Catherine, Rosendaal, Frits R, Salomaa, Veikko, Sampietro, M Lourdes, Schäfer, Arne, Schillert, Arne, Schreiber, Stefan, Schrezenmeir, Jürgen, Schwartz, Stephen M, Sivananthan, Mohan, Smith, Albert, Smith, Tamara B, Snoep, Jaapjan D, Soranzo, Nicole, Spertus, John A, Stark, Klaus, Stirrups, Kathy, Stoll, Monika, Tang, W H Wilson, Thorgeirsson, Gudmundur, Thorleifsson, Gudmar, van Rij, Andre M, Wells, George A, Wichmann, H-Erich, Wild, Philipp S, Willenborg, Christina, Zeller, Tanja, Ziegler, Andreas, Cambien, Francois, Hengstenberg, Christian, Blankenberg, Stefan, Ouwehand, Willem H, Hall, Alistair S, Thompson, John R, McPherson, Ruth, Erdmann, Jeanette

    Veröffentlicht in Nature genetics

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    Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci von Reschen, Michael E, Mahajan, Anubha, William Rayner, N, Scott, Laura J, Yengo, Loic, Wahl, Simone, Kestler, Hans, Chheda, Himanshu, Eisele, Lewin, Steinthorsdottir, Valgerdur, Chen, Han, Fuchsberger, Christian, Kwan, Phoenix, Thomsen, Soren K, Rundle, Jana K, van de Bunt, Martijn, Voight, Benjamin F, Abecasis, Gonçalo R, Baldassarre, Damiano, Carey, Jason, Chines, Peter S, Crenshaw, Andrew T, Edkins, Sarah, Eury, Elodie, Fontanillas, Pierre, Franks, Paul W, Gertow, Karl, Groves, Christopher J, Hassinen, Maija, Herder, Christian, Hreidarsson, Astradur B, Jackson, Anne U, Jonsson, Anna, Jørgensen, Marit E, Jørgensen, Torben, Kao, Wen-Hong L, Kerrison, Nicola D, Kinnunen, Leena, Kravic, Jasmina, Langford, Cordelia, Lichtner, Peter, Lindholm, Eero, Lobbens, Stéphane, Luan, Jian'an, Meyer, Julia, Mihailov, Evelin, Mühleisen, Thomas W, Navarro, Carmen, Oskolkov, Nikolay N, Pechlivanis, Sonali, Platou, Carl G P, Rybin, Denis, van der Schouw, Yvonne T, Sennblad, Bengt, Steinbach, Gerald, Storm, Petter, Sun, Qi, Thorand, Barbara, Tikkanen, Emmi, Trakalo, Joseph, Tremoli, Elena, Wood, Andrew R, Zeggini, Eleftheria, Birney, Ewan, Pasquali, Lorenzo, Pankow, James S, van Duijn, Cornelia, Sijbrands, Eric, Hu, Frank B, Thorsteinsdottir, Unnur, Stefansson, Kari, Lakka, Timo A, Rauramaa, Rainer, Stumvoll, Michael, Korpi-Hyövälti, Eeva, Kuusisto, Johanna, Metspalu, Andres, Jöcke, Karl-Heinz, Moebus, Susanne, Bergman, Richard N, Collins, Francis S, Mohlke, Karen L, Koistinen, Heikki, Tuomilehto, Jaakko, Deloukas, Panagiotis, Donnelly, Peter J, Frayling, Timothy M, Sladek, Rob, Froguel, Philippe, Hansen, Torben, Kathiresan, Sekar, Barroso, Inês, Langenberg, Claudia, Wareham, Nicholas J, O'Callaghan, Christopher A, Gloyn, Anna L, Altshuler, David, Boehnke, Michael, Teslovich, Tanya M, Morris, Andrew P

    Veröffentlicht in Nature genetics

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    Common variants conferring risk of schizophrenia von Stefansson, Hreinn, Ophoff, Roel A., Steinberg, Stacy, Andreassen, Ole A., Cichon, Sven, Rujescu, Dan, Werge, Thomas, Pietiläinen, Olli P. H., Mors, Ole, Mortensen, Preben B., Sigurdsson, Engilbert, Gustafsson, Omar, Nyegaard, Mette, Tuulio-Henriksson, Annamari, Ingason, Andres, Hansen, Thomas, Suvisaari, Jaana, Lonnqvist, Jouko, Paunio, Tiina, Børglum, Anders D., Hartmann, Annette, Fink-Jensen, Anders, Nordentoft, Merete, Hougaard, David, Norgaard-Pedersen, Bent, Böttcher, Yvonne, Olesen, Jes, Breuer, René, Möller, Hans-Jürgen, Giegling, Ina, Rasmussen, Henrik B., Timm, Sally, Mattheisen, Manuel, Bitter, István, Réthelyi, János M., Magnusdottir, Brynja B., Sigmundsson, Thordur, Olason, Pall, Masson, Gisli, Gulcher, Jeffrey R., Haraldsson, Magnus, Fossdal, Ragnheidur, Thorgeirsson, Thorgeir E., Thorsteinsdottir, Unnur, Ruggeri, Mirella, Tosato, Sarah, Franke, Barbara, Strengman, Eric, Kiemeney, Lambertus A., Melle, Ingrid, Djurovic, Srdjan, Abramova, Lilia, Kaleda, Vasily, Sanjuan, Julio, de Frutos, Rosa, Bramon, Elvira, Vassos, Evangelos, Fraser, Gillian, Ettinger, Ulrich, Picchioni, Marco, Walker, Nicholas, Toulopoulou, Timi, Need, Anna C., Ge, Dongliang, Lim Yoon, Joeng, Shianna, Kevin V., Freimer, Nelson B., Cantor, Rita M., Murray, Robin, Kong, Augustine, Golimbet, Vera, Carracedo, Angel, Arango, Celso, Costas, Javier, Jönsson, Erik G., Terenius, Lars, Agartz, Ingrid, Petursson, Hannes, Nöthen, Markus M., Rietschel, Marcella, Matthews, Paul M., Muglia, Pierandrea, Peltonen, Leena, St Clair, David, Goldstein, David B., Stefansson, Kari, Collier, David A.

    Veröffentlicht in Nature (London)

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    Neonatal and Early Childhood Outcomes of Twin and Singleton Infants Born Preterm von Melamed, Nir, Weitzner, Omer, Church, Paige, Barrett, Jon, Piedboeuf, Bruno, Sherlock, Rebecca, Mehrem, Ayman Abou, Toye, Jennifer, Ting, Joseph, Fajardo, Carlos, Bodani, Jaya, Strueby, Lannae, Louis, Deepak, Alvaro, Ruben, Mukerji, Amit, Lee, Kyong-Soon, Ng, Eugene, Lemyre, Brigitte, Daboval, Thierry, Khurshid, Faiza, Bizgu, Victoria, Barrington, Keith, Lapointe, Anie, Ethier, Guillaume, Piedboeuf, Bruno, Claveau, Martine, Bertelle, Valerie, Masse, Edith, Mehdizadeh-Hakak, Hamid, Hudson, Jo-Anna, Lee, Shoo K., Abenhaim, Haim, Afifi, Jehier, Aziz, Khalid, Barrett, Jon, Blais, Lucie, Bocking, Alan, Burrows, Jason, Butt, Kimberly, Canning, Roderick, Carson, George, Cieslak, Zenon, Crane, Joan, de Cabo, Cecilia, Dow, Kimberly, Dunn, Michael, Helou, Salhab el, Foster, Jonathan, Gagnon, Robert, Gratton, Rob, Harrison, Adele, Helewa, Michael, Joseph, K.S., Kajetanowicz, Andrzej, Lacaze-Masmonteil, Thierry, Lodha, Abhay, Luu, Thuy Mai, Ly, Linh, Marc, Isabelle, McDonald, Sarah D., McMillan, Doug, Melamed, Nir, Moddemann, Diane, Murphy, Lynn, Murphy, Kellie, O'Brien, Karel, Ouellet, Annie, Pasquier, Jean-Charles, Pechlivanoglou, Petros, Pelausa, Ermelinda, Portales-Casamar, Elodie, Premji, Shahirose, Puligandla, Pramod, Pullenayegum, Eleanor, Robson, Kate, Schneider, Carol, Shah, Vibhuti, Skarsgard, Erik, Smith, Graeme, Thériault, Katherine, Ubhi, Jagdeep, Vincer, Michael, Whittle, Wendy, Wilson, Doug, Wood, Stephen, Ye, Philip, Yee, Wendy, Pillay, Thevanisha, Zwicker, Jill, Anson, Shelagh, Moodley, Anitha, Moddemann, Diane, McKnight, Sarah, Kelly, Edmond, Raghuram, Kamini, Thomas, Karen, Nguyen, Kim-Anh, Luu, Thuy Mai, Morin, Alyssa, Bélanger, Sylvie

    Veröffentlicht in The Journal of pediatrics

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