Treffer 1 - 20 von 62 für Suche 'Ruth, Wayne K.', Suchdauer: 1,85s Treffer weiter einschränken
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    Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction von Darst, Burcu F., Sheng, Xin, Olama, Ali Amin Al, Dadaev, Tokhir, Brook, Mark N., Hoffmann, Thomas J., Matsuda, Koichi, Wan, Peggy, Tammela, Teuvo L. J., Giles, Graham G., MacInnis, Robert J., Cybulski, Cezary, Wokołorczyk, Dominika, Lubiński, Jan, Hamdy, Freddie C., Martin, Richard M., Nordestgaard, Børge G., Nielsen, Sune F., Weischer, Maren, Chambers, Suzanne, Horvath, Lisa, Gronberg, Henrik, Aly, Markus, Nordström, Tobias, Pashayan, Nora, Travis, Ruth C., Riboli, Elio, Lin, Hui-Yi, Mucci, Lorelei A., Penney, Kathryn L., Turman, Constance, Tangen, Catherine M., Fleshner, Neil E., Finelli, Antonio, Koutros, Stella, Freeman, Laura E. Beane, Wolk, Alicja, Håkansson, Niclas, Hoover, Robert N., Sørensen, Karina Dalsgaard, Blot, William J., Zhang, Hong-Wei, Feng, Ninghan, Mao, Xueying, Schaid, Daniel J., Burnet, Neil, Schnoeller, Thomas, Kibel, Adam S., Cussenot, Olivier, Cancel-Tassin, Géraldine, Menegaux, Florence, Koudou, Yves Akoli, Stern, Mariana C., Fachal, Laura, Rosenstein, Barry S., Ostrer, Harry, Paulo, Paula, Watya, Stephen, Lubwama, Alexander, Llorca, Javier, Multigner, Luc, Kaneva, Radka, Slavov, Chavdar, Mitev, Vanio, Brenner, Hermann, Saum, Kai-Uwe, Klein, Eric A., Hsing, Ann W., Kittles, Rick A., Murphy, Adam B., Logothetis, Christopher J., Kim, Jeri, Steele, Linda, Pandha, Hardev, De Ruyck, Kim, Ost, Piet, Xu, Jianfeng, Lim, Jasmine, Teo, Soo-Hwang, Newcomb, Lisa F., Lin, Daniel W., Neslund-Dudas, Christine, Rybicki, Benjamin A., Gamulin, Marija, Lessel, Davor, Singhal, Sandeep, Joniau, Steven, Van den Broeck, Thomas, Martinez, Maria Elena, Larkin, Samantha, Aukim-Hastie, Claire, Bush, William S., Aldrich, Melinda C., Crawford, Dana C., Petrovics, Gyorgy, Casey, Graham, Sanderson, Maureen, Van Den Eeden, Stephen K., Easton, Douglas F., Eeles, Rosalind A.

    Veröffentlicht in Nature genetics

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    Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease von Zhao, Wei, Rasheed, Asif, Tikkanen, Emmi, Lee, Jung-Jin, Butterworth, Adam S, Howson, Joanna M M, Assimes, Themistocles L, Chowdhury, Rajiv, Orho-Melander, Marju, Damrauer, Scott, Small, Aeron, Asma, Senay, Imamura, Minako, Yamauch, Toshimasa, Chambers, John C, Chen, Peng, Sapkota, Bishwa R, Shah, Nabi, Jabeen, Sehrish, Surendran, Praveen, Lu, Yingchang, Zhang, Weihua, Imran, Atif, Abbas, Shahid, Majeed, Faisal, Trindade, Kevin, Qamar, Nadeem, Mallick, Nadeem Hayyat, Yaqoob, Zia, Saghir, Tahir, Rizvi, Syed Nadeem Hasan, Memon, Anis, Rasheed, Syed Zahed, Memon, Fazal-ur-Rehman, Mehmood, Khalid, Ahmed, Naveeduddin, Qureshi, Irshad Hussain, Tanveer-us-Salam, Iqbal, Wasim, Malik, Uzma, Mehra, Narinder, Kuo, Jane Z, Sheu, Wayne H-H, Guo, Xiuqing, Hsiung, Chao A, Juang, Jyh-Ming J, Taylor, Kent D, Hung, Yi-Jen, Lee, Wen-Jane, Quertermous, Thomas, Lee, I-Te, Hsu, Chih-Cheng, Bottinger, Erwin P, Ralhan, Sarju, Teo, Yik Ying, Wang, Tzung-Dau, Alam, Dewan S, Di Angelantonio, Emanuele, Epstein, Steve, Nielsen, Sune F, Nordestgaard, Børge G, Tybjaerg-Hansen, Anne, Young, Robin, Benn, Marianne, Frikke-Schmidt, Ruth, Kamstrup, Pia R, Jukema, J Wouter, Sattar, Naveed, Smit, Roelof, Chung, Ren-Hua, Liang, Kae-Woei, Anand, Sonia, Sanghera, Dharambir K, Ripatti, Samuli, Loos, Ruth J F, Kooner, Jaspal S, Tai, E Shyong, Rotter, Jerome I, Chen, Yii-Der Ida, Frossard, Philippe, Maeda, Shiro, Kadowaki, Takashi, Reilly, Muredach, Pare, Guillaume, Melander, Olle, Salomaa, Veikko, Rader, Daniel J, Danesh, John, Voight, Benjamin F, Saleheen, Danish

    Veröffentlicht in Nature genetics

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    Association of Cardiometabolic Multimorbidity With Mortality von Di Angelantonio, Emanuele, Kaptoge, Stephen, Wormser, David, Willeit, Peter, Butterworth, Adam S, Bansal, Narinder, O’Keeffe, Linda M, Gao, Pei, Wood, Angela M, Burgess, Stephen, Freitag, Daniel F, Pennells, Lisa, Peters, Sanne A, Hart, Carole L, Håheim, Lise Lund, Gillum, Richard F, Nordestgaard, Børge G, Psaty, Bruce M, Yeap, Bu B, Knuiman, Matthew W, Nietert, Paul J, Kauhanen, Jussi, Salonen, Jukka T, Kuller, Lewis H, Simons, Leon A, van der Schouw, Yvonne T, Barrett-Connor, Elizabeth, Selmer, Randi, Crespo, Carlos J, Rodriguez, Beatriz, Verschuren, W. M. Monique, Salomaa, Veikko, Svärdsudd, Kurt, van der Harst, Pim, Björkelund, Cecilia, Wilhelmsen, Lars, Wallace, Robert B, Brenner, Hermann, Amouyel, Philippe, Barr, Elizabeth L. M, Iso, Hiroyasu, Onat, Altan, Trevisan, Maurizio, D'Agostino, Ralph B, Cooper, Cyrus, Kavousi, Maryam, Welin, Lennart, Roussel, Ronan, Hu, Frank B, Sato, Shinichi, Davidson, Karina W, Howard, Barbara V, Leening, Maarten J. G, Rosengren, Annika, Dörr, Marcus, Deeg, Dorly J. H, Kiechl, Stefan, Stehouwer, Coen D. A, Nissinen, Aulikki, Giampaoli, Simona, Donfrancesco, Chiara, Kromhout, Daan, Price, Jackie F, Peters, Annette, Meade, Tom W, Casiglia, Edoardo, Lawlor, Debbie A, Gallacher, John, Nagel, Dorothea, Franco, Oscar H, Assmann, Gerd, Dagenais, Gilles R, Jukema, J. Wouter, Sundström, Johan, Woodward, Mark, Brunner, Eric J, Khaw, Kay-Tee, Wareham, Nicholas J, Whitsel, Eric A, Njølstad, Inger, Hedblad, Bo, Wassertheil-Smoller, Sylvia, Engström, Gunnar, Rosamond, Wayne D, Selvin, Elizabeth, Sattar, Naveed, Thompson, Simon G, Danesh, John


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    Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections von Mis, Emily K., Brodsky, Nina N., Ionita, Cristian, Darbinyan, Armine, Drummond-Borg, Margaret, McGee, Elisabeth, Nugent, Kimberly, Ortega, Lucy, Goodkin, Howard P., Sapp, Katie, McKee, Shane, Rea, Gillian, Cooper, Nicola, O’Driscoll, Mary, Scurr, Ingrid, Abbs, Steve, Armstrong, Ruth, Raymond, Lucy, Green, Andrew, Cleary, Elaine, Lampe, Anne, Castle, Bruce, Loughlin, Sam, Izatt, Louise, Roworth, Wendy, Yau, Shu, Jewell, Rosalyn, Sarkar, Ajoy, Canham, Natalie, Burkitt-Wright, Emma, Jones, Elizabeth, Smith, Audrey, Wright, Ronnie, Henderson, Alex, Allen, Zoe, Bernhard, Birgitta, Busby, Louise, Clowes, Virginia, Blair, Edward, Stewart, Alison, Kamath, Arveen, Halai, D., Holman, J.E., Jackson, R., Lopez, F.J., Rogers, T., Savage, K., Sieghart, A., Thomas, E.R.A., Thompson, S.R., Tucci, A., Alejandro, Mercedes E., Amendola, Laura, Andrews, Ashley, Bademci, Guney, Baker, Eva, Baldridge, Dustin, Bamshad, Michael, Bayrak-Toydemir, Pinar, Botto, Lorenzo, Coakley, Terra R., Coggins, Matthew, Cooper, Cynthia M., Cunningham, Michael, Dai, Hongzheng, Duncan, Laura, Fieg, Elizabeth L., Forghani, Irman, Hahn, Sihoun, Hanchard, Neil A., Hayes, Nichole, High, Frances, Hisama, Fuki M., Holm, Ingrid A., Jamal, Fariha, Kennedy, Jennifer, LeBlanc, Kimberly, Macnamara, Ellen F., Maduro, Valerie V., Mak, Bryan, McCauley, Jacob, McGee, Elisabeth, Nickerson, Deborah, Nieves-Rodriguez, Shirley, Novacic, Donna, Pace, Laura, Potocki, Lorraine, Quinlan, Aaron, Raja, Archana N., Robertson, Amy K., Rodan, Lance H., Saporta, Mario, Schaechter, Judy, Signer, Rebecca, Solem, Emily, Solnica-Krezel, Lilianna, Sutton, Shirley, Velinder, Matt, Wheeler, Matthew T., Khokha, Mustafa K.

    Veröffentlicht in Genetics in medicine

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    Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility von Wessel, Jennifer, Chu, Audrey Y, Willems, Sara M, Dauriz, Marco, Raghavan, Sridharan, Hidalgo, Bertha, An, Ping, Lu, Yingchang, Ehm, Margaret G, Baldridge, Abigail S, Freitag, Daniel F, Garcia, Melissa E, Hara, Kazuo, Jakobsdottir, Johanna, Lange, Leslie A, Layton, Jill C, Li, Man, Morrison, Alanna C, Peters, Marjolein J, Southam, Lorraine, Stoiber, Marcus H, Strawbridge, Rona J, Varga, Tibor V, Barbieri, Caterina, Bombieri, Cristina, Bowden, Donald W, Burns, Sean M, Chen, Yuning, Chen, Yii-DerI, Cheng, Ching-Yu, Ehret, Georg B, Eiriksdottir, Gudny, Escher, Stefan A, Frånberg, Mattias, Gambaro, Giovanni, Goel, Anuj, Grove, Megan L, Karaleftheri, Maria, Kirkpatrick, Andrea, Kraja, Aldi T, Kuusisto, Johanna, Lange, Ethan M, Lee, I T, Lee, Wen-Jane, Leong, Aaron, Liao, Jiemin, Lindgren, Cecilia M, Malerba, Giovanni, Mamakou, Vasiliki, Maruthur, Nisa M, McLeod, Olga, Mohlke, Karen L, Muzny, Donna M, Renström, Frida, Rice, Ken, Sala, Cinzia F, Soranzo, Nicole, Speliotes, Elizabeth K, Stirrups, Kathleen, Thanopoulou, Anastasia, Traglia, Michela, Tsafantakis, Emmanouil, Javad, Sundas, Yanek, Lisa R, Becker, Diane M, Bis, Joshua C, Brown, James B, Ingelsson, Erik, Karter, Andrew J, Lorenzo, Carlos, Peloso, Gina M, Vaidya, Dhananjay, Varma, Rohit, Wagenknecht, Lynne E, Dedoussis, George, Deloukas, Panos, Franco, Oscar H, Gibbs, Richard A, Gudnason, Vilmundur, Hofman, Albert, Jansson, Jan-Håkan, Langenberg, Claudia, Launer, Lenore J, Levy, Daniel, Oostra, Ben A, Padmanabhan, Sandosh, Pankow, James S, Rudan, Igor, Schulze, Matthias B, Smith, Blair H, Walker, Mark, Wong, Tien Y, Laakso, Markku, Borecki, Ingrid B, van Duijn, Cornelia M, Waterworth, Dawn M, Loos, Ruth J.F., Meigs, James B, Scott, Robert A, Goodarzi, Mark O

    Veröffentlicht in Nature communications

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