Branched chain amino acids harbor distinct and often opposing effects on health and disease von Avery, Christy L., Howard, Annie Green, Lee, Harold H., Downie, Carolina G., Lee, Moa P., Koenigsberg, Sarah H., Ballou, Anna F., Preuss, Michael H., Raffield, Laura M., Yarosh, Rina A., North, Kari E., Gordon-Larsen, Penny, Graff, Mariaelisa

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Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps von Mahajan, Anubha, Taliun, Daniel, Thurner, Matthias, Robertson, Neil R., Torres, Jason M., Rayner, N. William, Payne, Anthony J., Steinthorsdottir, Valgerdur, Scott, Robert A., Grarup, Niels, Schmidt, Ellen M., Wuttke, Matthias, Sarnowski, Chloé, Mägi, Reedik, Nano, Jana, Gieger, Christian, Trompet, Stella, Lecoeur, Cécile, Preuss, Michael H., Prins, Bram Peter, Guo, Xiuqing, Bielak, Lawrence F., Below, Jennifer E., Bowden, Donald W., Kim, Young Jin, Petty, Lauren E., Sim, Xueling, Bennett, Amanda J., Bork-Jensen, Jette, Brummett, Chad M., Canouil, Mickaël, Ec kardt, Kai-Uwe, Fischer, Krista, Kardia, Sharon L. R., Kronenberg, Florian, Läll, Kristi, Luan, Jian’an, Ntalla, Ioanna, Nylander, Vibe, Schönherr, Sebastian, Schurmann, Claudia, Yengo, Loïc, Bottinger, Erwin P., Brandslund, Ivan, Christensen, Cramer, Dedoussis, George, Florez, Jose C., Ford, Ian, Franco, Oscar H., Frayling, Timothy M., Giedraitis, Vilmantas, Hackinger, Sophie, Hattersley, Andrew T., Herder, Christian, Ikram, M. Arfan, Jørgensen, Marit E., Jørgensen, Torben, Kriebel, Jennifer, Kuusisto, Johanna, Ligthart, Symen, Linneberg, Allan, Lyssenko, Valeriya, Mamakou, Vasiliki, Meitinger, Thomas, Morris, Andrew D., Nadkarni, Girish, Pankow, James S., Peters, Annette, Sattar, Naveed, Stančáková, Alena, Strauch, Konstantin, Taylor, Kent D., Thorand, Barbara, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Tuomilehto, Jaakko, Witte, Daniel R., Dupuis, Josée, Peyser, Patricia A., Zeggini, Eleftheria, Froguel, Philippe, Ingelsson, Erik, Lind, Lars, Laakso, Markku, Collins, Francis S., Jukema, J. Wouter, Grallert, Harald, Metspalu, Andres, Köttgen, Anna, Abecasis, Goncalo R., Meigs, James B., Rotter, Jerome I., Marchini, Jonathan, Hansen, Torben, Langenberg, Claudia, Wareham, Nicholas J., Stefansson, Kari, Morris, Andrew P., Boehnke, Michael, McCarthy, Mark I.

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Comments on: Association Study between Coronary Artery Disease and rs1333049 and rs10757274 Polymorphisms at 9p21 Locus in South-West Iran von Michael H, Preuß, Ziegler, Andreas

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1273-P: The Interplay between Polygenic and Rare HNF1A Variant Risk in Type 2 Diabetes von STALBOW, LAUREN, PREUSS, MICHAEL H., CHAMI, NATHALIE, SMIT, ROELOF A.J., LOOS, RUTH J.

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The contribution of functional HNF1A variants and polygenic susceptibility to risk of type 2 diabetes in ancestrally diverse populations von Stalbow, Lauren A., Preuss, Michael H., Smit, Roelof A. J., Chami, Nathalie, Bjørkhaug, Lise, Aukrust, Ingvild, Gloyn, Anna L., Loos, Ruth J. F.

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Host genetic effects in pneumonia von Chen, Hung-Hsin, Shaw, Douglas M., Petty, Lauren E., Graff, Misa, Bohlender, Ryan J., Polikowsky, Hannah G., Zhong, Xue, Kim, Daeeun, Buchanan, Victoria L., Preuss, Michael H., Shuey, Megan M., Loos, Ruth J.F., Huff, Chad D., Cox, Nancy J., Bastarache, Julie A., Bastarache, Lisa, North, Kari E., Below, Jennifer E.

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Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies von Sun, Quan, Graff, Misa, Rowland, Bryce, Wen, Jia, Huang, Le, Miller-Fleming, Tyne W, Haessler, Jeffrey, Preuss, Michael H, Chai, Jin-Fang, Lee, Moa P, Avery, Christy L, Cheng, Ching-Yu, Franceschini, Nora, Sim, Xueling, Cox, Nancy J, Kooperberg, Charles, North, Kari E, Li, Yun, Raffield, Laura M

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Rare variant contribution to the heritability of coronary artery disease von Rocheleau, Ghislain, Clarke, Shoa L., Auguste, Gaëlle, Hasbani, Natalie R., Morrison, Alanna C., Heath, Adam S., Bielak, Lawrence F., Iyer, Kruthika R., Young, Erica P., Stitziel, Nathan O., Jun, Goo, Laurie, Cecelia, Broome, Jai G., Khan, Alyna T., Arnett, Donna K., Becker, Lewis C., Bis, Joshua C., Boerwinkle, Eric, Bowden, Donald W., Carson, April P., Ellinor, Patrick T., Fornage, Myriam, Franceschini, Nora, Freedman, Barry I., Heard-Costa, Nancy L., Hou, Lifang, Chen, Yii-Der Ida, Kenny, Eimear E., Kooperberg, Charles, Kral, Brian G., Loos, Ruth J. F., Lutz, Sharon M., Manson, JoAnn E., Martin, Lisa W., Mitchell, Braxton D., Nassir, Rami, Palmer, Nicholette D., Post, Wendy S., Preuss, Michael H., Psaty, Bruce M., Raffield, Laura M., Regan, Elizabeth A., Rich, Stephen S., Smith, Jennifer A., Taylor, Kent D., Yanek, Lisa R., Young, Kendra A., Hilliard, Austin T., Tcheandjieu, Catherine, Peyser, Patricia A., Vasan, Ramachandran S., Rotter, Jerome I., Miller, Clint L., Assimes, Themistocles L., de Vries, Paul S., Do, Ron

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A common TCN1 loss-of-function variant is associated with lower vitamin B 12 concentration in African Americans von Hu, Yao, Raffield, Laura M, Polfus, Linda M, Moscati, Arden, Nadkarni, Girish, Preuss, Michael H, Zhong, Xue, Wei, Qiang, Rich, Stephen S, Li, Yun, Wilson, James G, Correa, Adolfo, Loos, Ruth J F, Li, Bingshan, Auer, Paul L, Reiner, Alex P

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Whole genome sequence association with E-selectin levels reveals loss-of-function variant in African Americans von Polfus, Linda M, Raffield, Laura M, Wheeler, Marsha M, Tracy, Russell P, Lange, Leslie A, Lettre, Guillaume, Miller, Amanda, Correa, Adolfo, Bowler, Russell P, Bis, Joshua C, Salimi, Shabnam, Jenny, Nancy Swords, Pankratz, Nathan, Wang, Biqi, Preuss, Michael H, Zhou, Lisheng, Moscati, Arden, Nadkarni, Girish N, Loos, Ruth J F, Zhong, Xue, Li, Bingshan, Johnsen, Jill M, Nickerson, Deborah A, Reiner, Alex P, Auer, Paul L

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A common TCN1 loss-of-function variant is associated with lower vitamin B12 concentration in African Americans von Hu, Yao, Raffield, Laura M., Polfus, Linda M., Moscati, Arden, Nadkarni, Girish, Preuss, Michael H., Zhong, Xue, Wei, Qiang, Rich, Stephen S., Li, Yun, Wilson, James G., Correa, Adolfo, Loos, Ruth J.F., Li, Bingshan, Auer, Paul L., Reiner, Alex P., the NHLBI Trans-Omics for Precision Medicine Consortium

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Ancestral diversity in lipoprotein(a) studies helps address evidence gaps von Lee, Moa P, Dimos, Sofia F, Raffield, Laura M, Wang, Zhe, Ballou, Anna F, Downie, Carolina G, Arehart, Christopher H, Correa, Adolfo, de Vries, Paul S, Du, Zhaohui, Gignoux, Christopher R, Gordon-Larsen, Penny, Guo, Xiuqing, Haessler, Jeffrey, Howard, Annie Green, Hu, Yao, Kassahun, Helina, Kent, Shia T, Lopez, J Antonio G, Monda, Keri L, North, Kari E, Peters, Ulrike, Preuss, Michael H, Rich, Stephen S, Rhodes, Shannon L, Yao, Jie, Yarosh, Rina, Tsai, Michael Y, Rotter, Jerome I, Kooperberg, Charles L, Loos, Ruth J F, Ballantyne, Christie, Avery, Christy L, Graff, Mariaelisa

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Genetic analyses of diverse populations improves discovery for complex traits von Wojcik, Genevieve L., Graff, Mariaelisa, Nishimura, Katherine K., Tao, Ran, Haessler, Jeffrey, Gignoux, Christopher R., Highland, Heather M., Patel, Yesha M., Sorokin, Elena P., Avery, Christy L., Belbin, Gillian M., Bien, Stephanie A., Cheng, Iona, Cullina, Sinead, Hodonsky, Chani J., Hu, Yao, Huckins, Laura M., Jeff, Janina, Justice, Anne E., Kocarnik, Jonathan M., Lim, Unhee, Lin, Bridget M., Lu, Yingchang, Nelson, Sarah C., Park, Sung-Shim L., Poisner, Hannah, Preuss, Michael H., Richard, Melissa A., Schurmann, Claudia, Setiawan, Veronica W., Sockell, Alexandra, Vahi, Karan, Verbanck, Marie, Vishnu, Abhishek, Walker, Ryan W., Young, Kristin L., Zubair, Niha, Acuña-Alonso, Victor, Ambite, Jose Luis, Barnes, Kathleen C., Boerwinkle, Eric, Bottinger, Erwin P., Bustamante, Carlos D., Caberto, Christian, Canizales-Quinteros, Samuel, Conomos, Matthew P., Deelman, Ewa, Do, Ron, Doheny, Kimberly, Fernández-Rhodes, Lindsay, Fornage, Myriam, Hailu, Benyam, Heiss, Gerardo, Henn, Brenna M., Hindorff, Lucia A., Jackson, Rebecca D., Laurie, Cecelia A., Laurie, Cathy C., Li, Yuqing, Lin, Dan-Yu, Moreno-Estrada, Andres, Nadkarni, Girish, Norman, Paul J., Pooler, Loreall C., Reiner, Alexander P., Romm, Jane, Sabatti, Chiara, Sandoval, Karla, Sheng, Xin, Stahl, Eli A., Stram, Daniel O., Thornton, Timothy A., Wassel, Christina L., Wilkens, Lynne R., Winkler, Cheryl A., Yoneyama, Sachi, Buyske, Steven, Haiman, Christopher A., Kooperberg, Charles, Le Marchand, Loic, Loos, Ruth J. F., Matise, Tara C., North, Kari E., Peters, Ulrike, Kenny, Eimear E., Carlson, Christopher S.

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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.

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The contribution of functional HNF1A variants and polygenic susceptibility to risk of type 2 diabetes in ancestrally diverse populations von Stalbow, Lauren, Preuss, Michael H., Smit, Roelof A.J., Chami, Nathalie, Bjørkhaug, Lise, Aukrust, Ingvild, Gloyn, Anna L, Loos, Ruth J.F.

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Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways von Isaacs, Aaron, Duong, ThuyVy, Foco, Luisa, Ahmed, Farah, Brody, Jennifer A., Salman, Reem, Noordam, Raymond, Benjamins, Jan-Walter, Repetto, Linda, Concas, Maria Pina, van den Berg, Marten E., Weiss, Stefan, Baldassari, Antoine R., Bartz, Traci M., Cook, James P., Evans, Daniel S., Freudling, Rebecca, Mei, Hao, Moscati, Arden, Müller-Nurasyid, Martina, Nursyifa, Casia, Ryan, Kathleen A., Tarazona-Santos, Eduardo, van Duijvenboden, Stefan, Yao, Jie, Andreasen, Laura, Bis, Joshua C., Cutler, Michael J., Ellervik, Christina, Ellinor, Patrick T., Felix, Stephan B., Graff, Mariaelisa, Guo, Xiuqing, Heckbert, Susan R., Huang, Paul L., Hutri-Kähönen, Nina, Ikram, M. Arfan, Jackson, Rebecca D., Junttila, Juhani, Kavousi, Maryam, Kors, Jan A., Leal, Thiago P., Lemaitre, Rozenn N., Lind, Lars, Liu, Simin, MacFarlane, Peter W., Mangino, Massimo, Meitinger, Thomas, Mezzavilla, Massimo, Mishra, Pashupati P., Montasser, May E., Navarro, Pau, Nikus, Kjell, Pare, Guillaume, Patton, Kristen K., Pelliccione, Giulia, Porteous, David J., Pramstaller, Peter P., Preuss, Michael H., Risch, Lorenz, Schurmann, Claudia, Sinner, Moritz F., Stoll, Monika, Tarasov, Kirill, Taylor, Kent D., Trompet, Stella, Uitterlinden, André, Völker, Uwe, Waldenberger, Melanie, Weng, Lu-Chen, Whitsel, Eric A., Wilson, James G., Avery, Christy L., Conen, David, Dörr, Marcus, Gharib, Sina A., Girotto, Giorgia, Grarup, Niels, Hayward, Caroline, Jamshidi, Yalda, Kähönen, Mika, Kanters, Jørgen K., Lima-Costa, Maria Fernanda, Liu, Yongmei, Loos, Ruth J. F., Mook-Kanamori, Dennis O., Morris, Andrew P., O’Connell, Jeffrey R., Olesen, Morten Salling, Orini, Michele, Pattaro, Cristian, Psaty, Bruce M., Rotter, Jerome I., Stricker, Bruno, van der Harst, Pim, van Duijn, Cornelia M., Arking, Dan E., Ramirez, Julia, Sotoodehnia, Nona, Munroe, Patricia B.

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Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease von Zhou, Wei, Tsuo, Kristin, Hirbo, Jibril B., Wang, Ying, Bhattacharya, Arjun, Zhao, Huiling, Surakka, Ida, Wolford, Brooke N., Lo Faro, Valeria, Lopera-Maya, Esteban A., Läll, Kristi, Favé, Marie-Julie, Chapman, Sinéad B., Karjalainen, Juha, Maasha, Mutaamba, Chavan, Sameer, Daya, Michelle, Ding, Yi, Feng, Yen-Chen A., Guare, Lindsay A., Gignoux, Christopher R., Graham, Sarah E., Ingold, Nathan, Ismail, Said I., Laisk, Triin, Lin, Kuang, Millwood, Iona Y., Moreno-Grau, Sonia, Nam, Kisung, Palta, Priit, Saad, Chadi, Setia-Verma, Shefali, Thorsteinsdottir, Unnur, Verma, Anurag, Zawistowski, Matthew, Afifi, Nahla, Al-Dabhani, Kawthar M., Campbell, Archie, Crooks, Kristy, Fritsche, Lars G., Fthenou, Eleni, Guo, Yu, Hunt, Karen A., Ioannidis, Alexander, Jansonius, Nomdo M., Konuma, Takahiro, Lee, Ming Ta Michael, Lopez-Pineda, Arturo, Matsuda, Yuta, Marioni, Riccardo E., Numakura, Kensuke, Patil, Snehal, Richmond, Anne, Rojas-Muñoz, Agustin, Shortt, Jonathan A., Tao, Ran, Vanderwerff, Brett, Vernekar, Manvi, Veturi, Yogasudha, Barnes, Kathleen C., Chen, Zhengming, Smith, George Davey, Finucane, Hilary K., Gamazon, Eric R., Gaunt, Tom R., Ge, Tian, Katsanis, Nicholas, Koskela, Jukka T., Law, Matthew H., Li, Liming, Loos, Ruth J.F., Matsuda, Koichi, Olsen, Catherine M., Shavit, Jordan A., Snieder, Harold, Takano, Tomohiro, Vonk, Judith M., Wicks, Stephen J., Wijmenga, Cisca, Wright, John, Zhou, Xiang, Awadalla, Philip, Boehnke, Michael, Bustamante, Carlos D., Fatumo, Segun, Hayward, Caroline, Hveem, Kristian, Kenny, Eimear E., Lee, Seunggeun, Mbarek, Hamdi, Mägi, Reedik, Martin, Hilary C., Medland, Sarah E., Palotie, Aarno V., Pasaniuc, Bogdan, Rader, Daniel J., Ritchie, Marylyn D., Smoller, Jordan W., Stefansson, Kari, Martin, Alicia R.

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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction von Ntalla, Ioanna, Cartwright, James H., Hall, Amelia Weber, Tucker, Nathan R., Choi, Seung Hoan, Barnes, Michael R., Warren, Helen R., Hayward, Caroline, Marten, Jonathan, Concas, Maria Pina, Boutin, Thibaud, Lima-Costa, Maria Fernanda, Souza, Renan P., Tarazona-Santos, Eduardo, Giedraitis, Vilmantas, Foco, Luisa, Gögele, Martin, Hicks, Andrew A., Cook, James P., Lindgren, Cecilia M., Riaz, Muhammad B., Sinagra, Gianfranco, Ulivi, Sheila, Kähönen, Mika, Mishra, Pashupati P., Nikus, Kjell, Padmanabhan, Sandosh, O’Connell, Jeff R., Aeschbacher, Stefanie, Risch, Lorenz, Thériault, Sébastien, Hutri-Kähönen, Nina, Lehtimäki, Terho, Barnes, Catriona L. K., Joshi, Peter K., Isaacs, Aaron, van Duijn, Cornelia M., Gudnason, Vilmundur, Harris, Tamara B., Nadkarni, Girish N., Correa, Adolfo, Mei, Hao, Wilson, James, Müller-Nurasyid, Martina, Waldenberger, Melanie, Mangino, Massimo, Kääb, Stefan, Schramm, Katharina, Strauch, Konstantin, Cutler, Michael J., Fatkin, Diane, Olesen, Morten, Roden, Dan M., Gustav Smith, J., Biggs, Mary L., Bis, Joshua C., Sotoodehnia, Nona, Pramstaller, Peter P., Ford, Ian, Wouter Jukema, J., Macfarlane, Peter W., Trompet, Stella, Dörr, Marcus, Felix, Stephan B., Weiss, Stefan, Havulinna, Aki S., Jula, Antti, Sääksjärvi, Katri, Rotter, Jerome I., Yao, Jie, Maan, Arie C., Mook-Kanamori, Dennis O., Cucca, Francesco, Lakatta, Edward G., Qian, Yong, Lin, Honghuang, Newton-Cheh, Christopher H., Lunetta, Kathryn L., Murray, Alison D., Stricker, Bruno H., Uitterlinden, André, van den Berg, Marten E., Haessler, Jeffrey, Kooperberg, Charles, Peters, Ulrike, Reiner, Alexander P., Arking, Dan E., Boerwinkle, Eric, Soliman, Elsayed Z., Gogarten, Stephanie M., Kerr, Kathleen F., Laurie, Cathy C., Abdullah Said, M., Yldau van der Ende, M., Ramirez, Julia, Van Duijvenboden, Stefan, Arnar, David O., Thorolfsdottir, Rosa B., Ellinor, Patrick T., Lubitz, Steven A.

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Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development von Nielsen, Jonas B., Fritsche, Lars G., Zhou, Wei, Teslovich, Tanya M., Holmen, Oddgeir L., Gustafsson, Stefan, Gabrielsen, Maiken E., Schmidt, Ellen M., Beaumont, Robin, Wolford, Brooke N., Lin, Maoxuan, Brummett, Chad M., Preuss, Michael H., Refsgaard, Lena, Bottinger, Erwin P., Graham, Sarah E., Surakka, Ida, Chu, Yunhan, Skogholt, Anne Heidi, Dalen, Håvard, Boyle, Alan P., Oral, Hakan, Herron, Todd J., Kitzman, Jacob, Jalife, José, Svendsen, Jesper H., Olesen, Morten S., Njølstad, Inger, Løchen, Maja-Lisa, Baras, Aris, Gottesman, Omri, Marcketta, Anthony, O’Dushlaine, Colm, Ritchie, Marylyn D., Wilsgaard, Tom, Loos, Ruth J.F., Frayling, Timothy M., Boehnke, Michael, Ingelsson, Erik, Carey, David J., Dewey, Frederick E., Kang, Hyun M., Abecasis, Gonçalo R., Hveem, Kristian, Willer, Cristen J.

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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.

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