Treffer 1 - 20 von 51 für Suche 'William D. B. Loos', Suchdauer: 4,50s Treffer weiter einschränken
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    Common genetic determinants of vitamin D insufficiency: a genome-wide association study von Wang, Thomas J, MD, Zhang, Feng, PhD, Richards, J Brent, MD, Kestenbaum, Bryan, MD, van Meurs, Joyce B, PhD, Berry, Diane, MSc, Kiel, Douglas P, MD, Streeten, Elizabeth A, MD, Ohlsson, Claes, Prof, Koller, Daniel L, PhD, Peltonen, Leena, Prof, Cooper, Jason D, PhD, O'Reilly, Paul F, PhD, Houston, Denise K, PhD, Glazer, Nicole L, PhD, Vandenput, Liesbeth, PhD, Peacock, Munro, Prof, Shi, Julia, MSc, Rivadeneira, Fernando, PhD, McCarthy, Mark I, Prof, Anneli, Pouta, PhD, de Boer, Ian H, MD, Mangino, Massimo, PhD, Kato, Bernet, PhD, Smyth, Deborah J, BSc, Booth, Sarah L, Prof, Jacques, Paul F, ScD, Burke, Greg L, Prof, Goodarzi, Mark, Prof, Cheung, Ching-Lung, PhD, Wolf, Myles, MD, Rice, Kenneth, PhD, Goltzman, David, Prof, Hidiroglou, Nick, PhD, Ladouceur, Martin, PhD, Wareham, Nicholas J, Prof, Hocking, Lynne J, PhD, Hart, Deborah, PhD, Arden, Nigel K, Prof, Cooper, Cyrus, Prof, Malik, Suneil, PhD, Fraser, William D, Prof, Hartikainen, Anna-Liisa, Prof, Zhai, Guangju, PhD, Macdonald, Helen M, PhD, Forouhi, Nita G, FFPH, Loos, Ruth JF, PhD, Reid, David M, Prof, Hakim, Alan, MA, Dennison, Elaine, PhD, Liu, Yongmei, PhD, Power, Chris, Prof, Stevens, Helen E, HNC, Jaana, Laitinen, PhD, Vasan, Ramachandran S, Prof, Soranzo, Nicole, PhD, Bojunga, Jörg, MD, Psaty, Bruce M, Prof, Lorentzon, Mattias, PhD, Foroud, Tatiana, Prof, Harris, Tamara B, MD, Hofman, Albert, Prof, Jansson, John-Olov, Prof, Cauley, Jane A, PhD, Uitterlinden, Andre G, Prof, Gibson, Quince, MBA, Järvelin, Marjo-Riitta, Prof, Karasik, David, PhD, Siscovick, David S, Prof, Econs, Michael J, Prof, Kritchevsky, Stephen B, Prof, Florez, Jose C, PhD, Todd, John A, Prof, Dupuis, Josee, Prof, Hyppönen, Elina, PhD, Spector, Timothy D, Prof

    Veröffentlicht in The Lancet (British edition)

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    Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders von Tucker-Drob, Elliot M., Yu, Dongmei, Ge, Tian, Derks, Eske M., Keski-Rahkonen, Anna, Kirov, George, Asherson, Philip, Baldursson, Gísli, Bybjerg-Grauholm, Jonas, Churchhouse, Claire, Crosbie, Jennifer, Demontis, Ditte, Grove, Jakob, Martin, Joanna, McGough, James J., Pedersen, Carsten B., Poulsen, Jesper B., Rothenberger, Aribert, Schachar, Russell, Turley, Patrick, Arking, Dan E., Collins, Ryan L., Coon, Hilary, Delorme, Richard, Hope, Sigrun, Nyegaard, Mette, Pinto, Dalila, Qvist, Per, Talkowski, Michael E., Albani, Diego, Alda, Martin, Bass, Nicholas, Bauer, Michael, Cichon, Sven, Clarke, Toni-Kim, Czerski, Piotr M., Fischer, Sascha B., Frank, Josef, Goes, Fernando S., Holland, Dominic, Jones, Lisa A., Joachim, Oedegaard Ketil, Maaser, Anna, Malt, Ulrik F., McMahon, Francis J., Montgomery, Grant W., Myers, Richard M., Nöthen, Markus M., Perry, Amy, Vieta, Eduard, Aschauer, Harald, Bencko, Vladimir, Burghardt, Roland, Carlberg, Laura, Guo, Yiran, Klump, Kelly L., Le Hellard, Stephanie, Monteleone, Alessio Maria, Seitz, Jochen, Treasure, Janet, Wade, Tracey D., Wichmann, H-Erich, Woodside, D. Blake, Grabe, Hans J., Horn, Carsten, Penninx, Brenda WJH, Schulte, Eva C., Smith, Daniel J., Alexander, Madeline, Begemann, Martin, Campion, Dominique, Ehrenreich, Hannelore, Murphy, Kieran C., Riley, Brien, Sham, Pak C., van Os, Jim, Weiser, Mark, Brown, Lawrence W., Cheon, Keun-Ah, Denys, Damiaan, Gilbert, Donald L., Grados, Marco A., Ibanez-Gomez, Laura, King, Robert A., Leventhal, Bennett L., Okun, Michael S., Piras, Federica, Robertson, Mary, Samuels, Jack F., Spalletta, Gianfranco, Stein, Dan J., Stewart, S Evelyn, Storch, Eric A., Stranger, Barbara, Tübing, Jennifer, Visscher, Frank, Wagner, Michael, Santangelo, Susan L., Thornton, Laura M., Neale, Benjamin M.

    Veröffentlicht in Cell

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    Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms von Rusu, Victor, Hoch, Eitan, Mercader, Josep M., Tenen, Danielle E., Gymrek, Melissa, Hartigan, Christina R., DeRan, Michael, Guzman, Gaelen, Deik, Amy A., Pierce, Kerry A., Dennis, Courtney, Clish, Clary B., Carr, Steven A., Wagner, Bridget K., Chen, Brian H., Ng, Maggie C.Y., Chen, Brian H., Guo, Xiuqing, Liu, Jiankang, Bielinski, Suzette J., Nalls, Michael A., Rasmussen-Torvik, Laura J., Evans, Daniel S., Sun, Yan V., Patel, Sanjay R., Lu, Yingchang, Long, Jirong, Armstrong, Loren L., Yang, Lingyao, Snively, Beverly M., Palmer, Nicholette D., Mudgal, Poorva, Keene, Keith L., Freedman, Barry I., Goodarzi, Mark O., Correa, Adolfo, Sims, Mario, Couper, David, Pankow, James S., Boerwinkle, Eric, Adeyemo, Adebowale, Doumatey, Ayo, Vaidya, Dhananjay, Sedor, John R., Kabagambe, Edmond K., McKnight, Barbara, Rice, Kenneth, Bielak, Lawrence F., Gottesman, Omri, Cai, Qiuyin, Zheng, Wei, Blot, William J., Lowe, William L., Pacheco, Jennifer A., Crawford, Dana C., Rich, Stephen S., Shu, Xiao-Ou, Loos, Ruth J.F., Borecki, Ingrid B., Peyser, Patricia A., Fornage, Myriam, Evans, Michele K., Becker, Diane M., Kao, W.H. Linda, Wilson, James G., Sale, Michèle M., Liu, Simin, Rotimi, Charles N., Bowden, Donald W., Huerta-Chagoya, Alicia, Moreno-Macías, Hortensia, Manning, Alisa, Caulkins, Lizz, Burtt, Noël P., Flannick, Jason, Patterson, Nick, Tusié-Luna, Teresa, Altshuler, David, Florez, Jose C., Martínez-Hernández, Angélica, Centeno-Cruz, Federico, Zerrweck, Carlos, Contreras-Cubas, Cecilia, Córdova, Emilio, Soberón, Xavier, Orozco, Lorena, González-Villalpando, María Elena, Haiman, Christopher A., Le Marchand, Loic, Kolonel, Laurence, Rodríguez-Torres, Maribel, Segura-Kato, Yayoi, Rodríguez-Guillén, Rosario, Gómez, Donají, Alvirde, Ulices, Cortes, Maria L., Centeno-Cruz, Federico, Zerrweck, Carlos, Orozco, Lorena, Jacobs, Suzanne B.R.

    Veröffentlicht in Cell

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    Defining the role of common variation in the genomic and biological architecture of adult human height von Amin, Najaf, Croteau-Chonka, Damien C, Jackson, Anne U, Randall, Joshua C, Westra, Harm-Jan, Absher, Devin, Baron, Jeffrey, Feitosa, Mary F, Fischer, Krista, Kanoni, Stavroula, Leach, Irene Mateo, Palmer, Cameron D, Prokopenko, Inga, Ripke, Stephan, Stancáková, Alena, Sung, Yun Ju, Trompet, Stella, Blüher, Matthias, Bolton, Jennifer L, Claudi-Boehm, Simone, Cooper, Matthew, Daw, E Warwick, Dörr, Marcus, Folkersen, Lasse, Grönberg, Henrik, Hannemann, Anke, Helmer, Quinta, Hemani, Gibran, Hoffmann, Wolfgang, Holmen, Oddgeir, Kho, Abel N, Kratzer, Wolfgang, Magnusson, Patrik K E, McLaren, Paul J, Menni, Cristina, Merger, Sigrun, Milani, Lili, Nauck, Matthias, Oozageer, Laticia, Pilz, Stefan, Rayner, Nigel W, Renstrom, Frida, Scott, Robert A, Stringham, Heather M, Swertz, Morris A, Syvänen, Ann-Christine, van Dijk, Suzanne, Vonk, Judith M, Wennauer, Roman, Wilsgaard, Tom, Wong, Andrew, Wright, Alan F, Bergmann, Sven, Bornstein, Stefan R, Brambilla, Paolo, Brown, Morris J, Chakravarti, Aravinda, Danesh, John, de Faire, Ulf, Erbel, Raimund, Ferrières, Jean, Gejman, Pablo V, Heath, Andrew C, Hengstenberg, Christian, Hingorani, Aroon D, Kaprio, Jaakko, Madden, Pamela A F, Marette, André, Montgomery, Grant W, Nelis, Mari, Ong, Ken K, Peters, Annette, Qi, Lu, Rice, Treva K, Saramies, Jouko, Sebert, Sylvain, Steinthorsdottir, Valgerdur, Tardif, Jean-Claude, Tremblay, Angelo, Assimes, Themistocles L, Dedoussis, George, Franks, Paul W, Groop, Leif C, Hamsten, Anders, Kuh, Diana, Laakso, Markku, Munroe, Patricia B, Schlessinger, David, Slagboom, P Eline, Snieder, Harold, Spector, Tim D, Tuomilehto, Jaakko, Uusitupa, Matti, Walker, Mark, Thorsteinsdottir, Unnur, Barroso, Inês, Borecki, Ingrid B, McCarthy, Mark I, Visscher, Peter M, Frayling, Timothy M

    Veröffentlicht in Nature genetics

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    Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry von Chen, Fei, Madduri, Ravi K., Rodriguez, Alex A., Darst, Burcu F., Sheng, Xin, Wang, Anqi, Shen, Jiayi, Saunders, Edward J., Rhie, Suhn K., Bensen, Jeannette T., Ingles, Sue A., Kittles, Rick A., Strom, Sara S., Nemesure, Barbara, Isaacs, William B., Zheng, Wei, Sanderson, Maureen, Park, Jong Y., Xu, Jianfeng, Wang, Ying, Huff, Chad D., Tettey, Yao, Lachance, Joseph, Tang, Wei, Rentsch, Christopher T., Cho, Kelly, Mcmahon, Benjamin H., Biritwum, Richard B., Truelove, Ann, Niwa, Shelley, Sellers, Thomas A., Yamoah, Kosj, Murphy, Adam B., Crawford, Dana C., Patel, Alpa V., Bush, William S., Aldrich, Melinda C., Cussenot, Olivier, Cullen, Jennifer, Neslund-Dudas, Christine M., Stern, Mariana C., Kote-Jarai, Zsofia, Cook, Michael B., Chokkalingam, Anand P., Hsing, Ann W., Hoffmann, Thomas J., Drake, Bettina F., Hu, Jennifer J., Keaton, Jacob M., Clark, Peter E., Jalloh, Mohamed, Gueye, Serigne M., Niang, Lamine, Ogunbiyi, Olufemi, Idowu, Michael O., Popoola, Olufemi, Aisuodionoe-Shadrach, Oseremen I., Ajibola, Hafees O., Jamda, Mustapha A., Oluwole, Olabode P., Adusei, Ben, Mensah, James E., Diop, Halimatou, Van Den Eeden, Stephen K., Blanchet, Pascal, Fowke, Jay H., Casey, Graham, Hennis, Anselm J., Lubwama, Alexander, Thompson, Ian M., Leach, Robin, Easton, Douglas F., Preuss, Michael H., Loos, Ruth J., Gundell, Susan M., Wan, Peggy, Mohler, James L., Fontham, Elizabeth T., Smith, Gary J., Taylor, Jack A., Srivastava, Shiv, Eeles, Rosaline A., Multigner, Luc, Parent, Marie-Élise, Menegaux, Florence, Cancel-Tassin, Geraldine, Klein, Eric A., Andrews, Caroline, Rebbeck, Timothy R., Brureau, Laurent, Ambs, Stefan, Edwards, Todd L., Watya, Stephen, Chanock, Stephen J., Witte, John S., Blot, William J., Michael Gaziano, J., Justice, Amy C., Conti, David V., Haiman, Christopher A.

    Veröffentlicht in European urology

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    Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease von Gupta, Yask, Friedman, David J., McNulty, Michelle T., Khan, Atlas, Lane, Brandon, Wang, Chen, Ke, Juntao, Jin, Gina, Wooden, Benjamin, Knob, Andrea L., Lim, Tze Y., Appel, Gerald B., Huggins, Kinsie, Liu, Lili, Mitrotti, Adele, Stangl, Megan C., Bomback, Andrew, Westland, Rik, Bodria, Monica, Marasa, Maddalena, Shang, Ning, Cohen, David J., Crew, Russell J., Morello, William, Canetta, Pietro, Radhakrishnan, Jai, Martino, Jeremiah, Liu, Qingxue, Chung, Wendy K., Espinoza, Angelica, Luo, Yuan, Wei, Wei-Qi, Feng, Qiping, Weng, Chunhua, Fang, Yilu, Kullo, Iftikhar J., Naderian, Mohammadreza, Limdi, Nita, Irvin, Marguerite R., Tiwari, Hemant, Mohan, Sumit, Rao, Maya, Dube, Geoffrey K., Chaudhary, Ninad S., Gutiérrez, Orlando M., Judd, Suzanne E., Cushman, Mary, Lange, Leslie A., Lange, Ethan M., Bivona, Daniel L., Verbitsky, Miguel, Winkler, Cheryl A., Kopp, Jeffrey B., Santoriello, Dominick, Batal, Ibrahim, Pinheiro, Sérgio Veloso Brant, Oliveira, Eduardo Araújo, Simoes e Silva, Ana Cristina, Pisani, Isabella, Fiaccadori, Enrico, Lin, Fangming, Gesualdo, Loreto, Amoroso, Antonio, Ghiggeri, Gian Marco, D’Agati, Vivette D., Magistroni, Riccardo, Kenny, Eimear E., Loos, Ruth J. F., Montini, Giovanni, Hildebrandt, Friedhelm, Paul, Dirk S., Petrovski, Slavé, Goldstein, David B., Kretzler, Matthias, Gbadegesin, Rasheed, Gharavi, Ali G., Kiryluk, Krzysztof, Sampson, Matthew G., Pollak, Martin R., Sanna-Cherchi, Simone

    Veröffentlicht in Nature communications

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    Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma von Chambers, John C, Elliott, Paul, Kooner, Jaspal S, Sehmi, Joban, Li, Xinzhong, Wass, Mark N, Van der Harst, Pim, Holm, Hilma, Kavousi, Maryam, Deng, Guohong, Gieger, Christian, Heard-Costa, Nancy L, Hottenga, Jouke-Jan, Kühnel, Brigitte, Kumar, Vinod, Lagou, Vasiliki, Liang, Liming, Luan, Jian'an, Vidal, Pedro Marques, Leach, Irene Mateo, O'Reilly, Paul F, Peden, John F, Rahmioglu, Nilufer, Speliotes, Elizabeth K, Yuan, Xin, Alizadeh, Behrooz Z, Atwood, Larry D, Borecki, Ingrid B, Charoen, Pimphen, Cucca, Francesco, de Geus, Eco J C, Dixon, Anna L, Döring, Angela, Ehret, Georg, Forouhi, Nita G, Goessling, Wolfram, Gudbjartsson, Daniel F, Harris, Tamara B, Hartikainen, Anna-Liisa, Hirschfield, Gideon M, Homuth, Georg, Hyppönen, Elina, Janssen, Harry L A, Kangas, Antti J, Kema, Ido P, Kühn, Jens P, Lai, Sandra, Lathrop, Mark, Lerch, Markus M, Li, Yun, Liang, T Jake, Loos, Ruth J F, Martin, Nicholas G, Moffatt, Miriam F, Montgomery, Grant W, Munroe, Patricia B, Musunuru, Kiran, O'Donnell, Christopher J, Prokopenko, Inga, Ruokonen, Aimo, Savolainen, Markku J, Schlessinger, David, Seedorf, Udo, Sen-Chowdhry, Srijita, Siminovitch, Katherine A, Smit, Johannes H, Spector, Timothy D, Tan, Wenting, Teslovich, Tanya M, Tukiainen, Taru, Wallace, Chris, Wallaschofski, Henri, Wichmann, H-Erich, Willemsen, Gonneke, Würtz, Peter, Xu, Chun, Yerges-Armstrong, Laura M, Boomsma, Dorret I, Froguel, Philippe, Matsuda, Koichi, McCarthy, Mark I, Meisinger, Christa, Pietiläinen, Kirsi H, Schumann, Gunter, Snieder, Harold, Sternberg, Michael J E, Stolk, Ronald P, Thomas, Howard C, Thorsteinsdottir, Unnur, Wareham, Nicholas J, Waterworth, Dawn M, Watkins, Hugh, Whitfield, John B, Witteman, Jacqueline C M, Wolffenbuttel, Bruce H R, Fox, Caroline S, Ala-Korpela, Mika, Stefansson, Kari, Völzke, Henry, Järvelin, Marjo-Riitta

    Veröffentlicht in Nature genetics

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    Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline von Li, Yong, Wuttke, Matthias, Winkler, Thomas W., Chai, Jin-Fang, Chu, Audrey Y., Cocca, Massimiliano, Feitosa, Mary F., Hoppmann, Anselm, Horn, Katrin, Li, Man, Nutile, Teresa, Tin, Adrienne, Tayo, Bamidele O., Bakker, Stephan J.L., Banas, Bernhard, Biggs, Mary L., Bottinger, Erwin P., Brenner, Hermann, Chalmers, John, Chee, Miao-Ling, Degenhardt, Frauke, Eckardt, Kai-Uwe, Ghanbari, Mohsen, Gieger, Christian, Hofer, Edith, Xian Foo, Valencia Hui, Hutri-Kähönen, Nina, Ikram, M. Arfan, Kähönen, Mika, Khor, Chiea-Chuen, Koenig, Wolfgang, Kramer, Holly, Krämer, Bernhard K., Kühnel, Brigitte, Lange, Leslie A., Franke, Lude, van der Harst, Pim, Navis, Gerjan, Snieder, Harold, Swertz, Morris, Wolffenbuttel, Bruce H.R., Wijmenga, Cisca, Abecasis, Goncalo, Baras, Aris, Coppola, Giovanni, Economides, Aris, Lotta, Luca A., Overton, John D., Reid, Jeffrey G., Beechert, Christina, Forsythe, Caitlin, Gu, Zhenhua, Lattari, Michael, Padilla, Maria Sotiropoulos, Toledo, Karina, Pradhan, Manasi, Manoochehri, Kia, Ulloa, Ricardo H., Bai, Xiaodong, Barnard, Leland, Blumenfeld, Andrew, Habegger, Lukas, Hawes, Alicia, Khalid, Shareef, Maxwell, Evan K., Salerno, William, Mitnaul, Lyndon J., Loos, Ruth J.F., Meisinger, Christa, Meitinger, Thomas, Melander, Olle, Milaneschi, Yuri, Mishra, Pashupati P., Mychaleckyj, Josyf C., Nikus, Kjell, Nolte, Ilja M., O’Donoghue, Michelle L., Pendergrass, Sarah A., Penninx, Brenda W.J.H., Preuss, Michael H., Psaty, Bruce M., Raitakari, Olli T., Rettig, Rainer, Rheinberger, Myriam, Rice, Kenneth M., Rosenkranz, Alexander R., Rossing, Peter, Sedaghat, Sanaz, Taylor, Kent D., Tremblay, Johanne, Völker, Uwe, Wallentin, Lars, Waterworth, Dawn M., White, Harvey D., Wilson, James G., Wong, Tien-Yin, Snieder, Harold, Böger, Carsten A., Köttgen, Anna, Heid, Iris M.

    Veröffentlicht in Kidney international

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    Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes von Ng, Maggie C Y, Shriner, Daniel, Chen, Brian H, Li, Jiang, Chen, Wei-Min, Guo, Xiuqing, Liu, Jiankang, Bielinski, Suzette J, Yanek, Lisa R, Nalls, Michael A, Comeau, Mary E, Rasmussen-Torvik, Laura J, Jensen, Richard A, Evans, Daniel S, Sun, Yan V, An, Ping, Patel, Sanjay R, Lu, Yingchang, Long, Jirong, Armstrong, Loren L, Wagenknecht, Lynne, Yang, Lingyao, Snively, Beverly M, Palmer, Nicholette D, Mudgal, Poorva, Langefeld, Carl D, Keene, Keith L, Freedman, Barry I, Mychaleckyj, Josyf C, Nayak, Uma, Raffel, Leslie J, Goodarzi, Mark O, Chen, Y-D Ida, Taylor, Jr, Herman A, Correa, Adolfo, Sims, Mario, Couper, David, Pankow, James S, Boerwinkle, Eric, Adeyemo, Adebowale, Doumatey, Ayo, Chen, Guanjie, Mathias, Rasika A, Vaidya, Dhananjay, Singleton, Andrew B, Zonderman, Alan B, Igo, Jr, Robert P, Sedor, John R, Kabagambe, Edmond K, Siscovick, David S, McKnight, Barbara, Rice, Kenneth, Liu, Yongmei, Hsueh, Wen-Chi, Zhao, Wei, Bielak, Lawrence F, Kraja, Aldi, Province, Michael A, Bottinger, Erwin P, Gottesman, Omri, Cai, Qiuyin, Zheng, Wei, Blot, William J, Lowe, William L, Pacheco, Jennifer A, Crawford, Dana C, Grundberg, Elin, Rich, Stephen S, Hayes, M Geoffrey, Shu, Xiao-Ou, Loos, Ruth J F, Borecki, Ingrid B, Peyser, Patricia A, Cummings, Steven R, Psaty, Bruce M, Fornage, Myriam, Iyengar, Sudha K, Evans, Michele K, Becker, Diane M, Kao, W H Linda, Wilson, James G, Rotter, Jerome I, Sale, Michèle M, Liu, Simin, Rotimi, Charles N, Bowden, Donald W

    Veröffentlicht in PLoS genetics

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    Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits von Keaton, Jacob M., Kamali, Zoha, Xie, Tian, Vaez, Ahmad, Ani, Alireza, Hellwege, Jacklyn N., Yengo, Loic, Young, William J., Traylor, Matthew, Giri, Ayush, Zheng, Zhili, Zeng, Jian, Chasman, Daniel I., Morris, Andrew P., Caulfield, Mark J., Hwang, Shih-Jen, Kooner, Jaspal S., Conen, David, Attia, John R., Morrison, Alanna C., Loos, Ruth J. F., Hicks, Andrew A., Pramstaller, Peter P., Nelson, Christopher P., Melander, Olle, Riese, Harriette, Wilson, James F., Campbell, Harry, Rich, Stephen S., Psaty, Bruce M., Lu, Yingchang, Rotter, Jerome I., Guo, Xiuqing, Vollenweider, Peter, Langenberg, Claudia, Tuomilehto, Jaakko, Salomaa, Veikko, Girotto, Giorgia, Trompet, Stella, Jukema, J. Wouter, van der Harst, Pim, Ridker, Paul M., Vitart, Veronique, Goel, Anuj, Harris, Sarah E., Deary, Ian J., van der Most, Peter J., Oldehinkel, Albertine J., Campbell, Archie, Boehnke, Michael, Boutin, Thibaud, Mamasoula, Chrysovalanto, Knekt, Paul, Enroth, Stefan, Polašek, Ozren, Concas, Maria Pina, Catamo, Eulalia, Cocca, Massimiliano, Li-Gao, Ruifang, Hofer, Edith, Spedicati, Beatrice, Waldenberger, Melanie, Laan, Maris, Teumer, Alexander, Cook, James P., Ruggiero, Daniela, Kolcic, Ivana, Boerwinkle, Eric, Traglia, Michela, Lehtimäki, Terho, Raitakari, Olli T., Johnson, Andrew D., Newton-Cheh, Christopher, Dominiczak, Anna F., Sever, Peter J., Siscovick, David, Metspalu, Andres, Strawbridge, Rona J., Laakso, Markku, Hottenga, Jouke-Jan, Morris, Andrew D., Nolte, Ilja M., Milaneschi, Yuri, Marten, Jonathan, Wright, Alan, Zeggini, Eleftheria, Spector, Tim, Simonsick, Eleanor M., van Duijn, Cornelia M., Butterworth, Adam S., Danesh, John N., Khaw, Kay-Tee, Sun, Yan V., Wilson, Peter W. F., Cho, Kelly, Levy, Daniel, Edwards, Todd L., Munroe, Patricia B., Snieder, Harold, Warren, Helen R.

    Veröffentlicht in Nature genetics

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