Comparison of novel clinic-based approach (amblyopia school) Vs. home-based occlusion for amblyopia therapy - A retrospective study von Bhattacharya, Subhajit, Subhedar, Ketaki, Bhadauria, Madhu, Shukla, Ranjana, Manaktala, Ruchita, Kumar, Abhinav, Wilson, Ayush

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Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program von Hellwege, Jacklyn N., Velez Edwards, Digna R., Giri, Ayush, Qiu, Chengxiang, Park, Jihwan, Torstenson, Eric S., Keaton, Jacob M., Wilson, O. D., Robinson-Cohen, Cassianne, Chung, Cecilia P., Roumie, Christianne L., Klarin, Derek, Damrauer, Scott M., DuVall, Scott L., Siew, Edward, Akwo, Elvis A., Wuttke, Matthias, Gorski, Mathias, Li, Man, Li, Yong, Gaziano, J. Michael, Wilson, Peter W. F., Tsao, Philip S., O’Donnell, Christopher J., Kovesdy, Csaba P., Pattaro, Cristian, Köttgen, Anna, Susztak, Katalin, Edwards, Todd L., Hung, Adriana M.

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Trans-ethnic association study of blood pressure determinants in over 750,000 individuals von Giri, Ayush, Hellwege, Jacklyn N., Keaton, Jacob M., Park, Jihwan, Qiu, Chengxiang, Warren, Helen R., Torstenson, Eric S., Kovesdy, Csaba P., Sun, Yan V., Wilson, Otis D., Robinson-Cohen, Cassianne, Roumie, Christianne L., Chung, Cecilia P., Birdwell, Kelly A., Damrauer, Scott M., DuVall, Scott L., Klarin, Derek, Cho, Kelly, Wang, Yu, Evangelou, Evangelos, Cabrera, Claudia P., Wain, Louise V., Shrestha, Rojesh, Mautz, Brian S., Akwo, Elvis A., Sargurupremraj, Muralidharan, Debette, Stéphanie, Boehnke, Michael, Scott, Laura J., Luan, Jian’an, Zhao, Jing-Hua, Willems, Sara M., Thériault, Sébastien, Shah, Nabi, Oldmeadow, Christopher, Almgren, Peter, Li-Gao, Ruifang, Verweij, Niek, Boutin, Thibaud S., Mangino, Massimo, Ntalla, Ioanna, Feofanova, Elena, Surendran, Praveen, Cook, James P., Karthikeyan, Savita, Lahrouchi, Najim, Liu, Chunyu, Sepúlveda, Nuno, Richardson, Tom G., Kraja, Aldi, Amouyel, Philippe, Farrall, Martin, Poulter, Neil R., Laakso, Markku, Zeggini, Eleftheria, Sever, Peter, Scott, Robert A., Langenberg, Claudia, Wareham, Nicholas J., Conen, David, Palmer, Colin Neil Alexander, Attia, John, Chasman, Daniel I., Ridker, Paul M., Melander, Olle, Mook-Kanamori, Dennis Owen, Harst, Pim van der, Cucca, Francesco, Schlessinger, David, Hayward, Caroline, Spector, Tim D., Jarvelin, Marjo-Riitta, Hennig, Branwen J., Timpson, Nicholas J., Wei, Wei-Qi, Smith, Joshua C., Xu, Yaomin, Matheny, Michael E., Siew, Edward E., Lindgren, Cecilia, Herzig, Karl-Heinz, Dedoussis, George, Denny, Joshua C., Psaty, Bruce M., Howson, Joanna M. M., Munroe, Patricia B., Newton-Cheh, Christopher, Caulfield, Mark J., Elliott, Paul, Gaziano, J. Michael, Concato, John, Wilson, Peter W. F., Tsao, Philip S., Velez Edwards, Digna R., Susztak, Katalin, O’Donnell, Christopher J., Hung, Adriana M., Edwards, Todd L.

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Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals von Ntalla, Ioanna, Karthikeyan, Savita, Mifsud, Borbala, Kraja, Aldi T., Cartwright, James H., Hellwege, Jacklyn N., Giri, Ayush, Tragante, Vinicius, Prins, Bram P., Cabrera, Claudia P., Eales, James M., Akbarov, Artur, Bielak, Lawrence F., Brody, Jennifer A., Drenos, Fotios, Nielsen, Sune Fallgaard, Faul, Jessica D., Franceschini, Nora, Gao, He, Giulianini, Franco, Hwang, Shih-Jen, Kanoni, Stavroula, Lindström, Jaana, Luan, Jian’an, Mahajan, Anubha, Malerba, Giovanni, Perola, Markus, Richard, Melissa, Richardson, Tom G., Sepúlveda, Nuno, Thériault, Sébastien, Trompet, Stella, Varga, Tibor V., Velez Edwards, Digna R., Veronesi, Giovanni, Weiss, Stefan, Willems, Sara M., Young, Robin, Zhang, Weihua, Zhao, Wei, Evangelou, Evangelos, Aeschbacher, Stefanie, Asllanaj, Eralda, Mutsert, Renée de, Dörr, Marcus, Gaziano, J. Michael, Have, Christian T., Kajantie, Eero, Kamat, Mihir, Karpe, Fredrik, Koistinen, Heikki A., Moitry, Marie, Peters, James, Rossouw, Jacques, Sever, Peter S., Sigurdsson, Emil L., Skaaby, Tea, Sun, Yan V., Trabetti, Elisabetta, Vaartjes, Ilonca, Buring, Julie E., Chowdhury, Rajiv, Correa, Adolfo, Deary, Ian J., Deloukas, Panos, Ferrières, Jean, Fornage, Myriam, Gaunt, Tom R., Harris, Tamara B., Järvelin, Marjo-Riitta, Kooperberg, Charles, Launer, Lenore J., Majumder, Abdulla al Shafi, Laakso, Markku, Melander, Olle, Mohlke, Karen L., Orho-Melander, Marju, Palmas, Walter, Polasek, Ozren, Province, Michael A., Rolandsson, Olov, Rosendaal, Frits R., Rotter, Jerome I., Samani, Nilesh J., Soranzo, Nicole, Spector, Timothy D., Starr, John M., van der Harst, Pim, van der Meer, Peter, Verweij, Niek, Virtamo, Jarmo, Wareham, Nicholas J., Langenberg, Claudia, Liu, Chunyu, Manning, Alisa K., Morrison, Alanna C., O’Donnell, Christopher J., Saleheen, Danish, Boerwinkle, Eric, Chasman, Daniel I.

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SMART INDIA App: A cost-effective novel solution for real-time telestroke care in India von Antil, Yamini, Vinny, Pulikottil Wilson, Vishnu, V.Y., Sharma, Sakshi, Mukherjee, Aprajita, Kuthiala, Neha, Bhasin, Ashu, Agarwal, Ayush, Padma Srivastava, M.V.

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Large-scale genome-wide association study of coronary artery disease in genetically diverse populations von Tcheandjieu, Catherine, Zhu, Xiang, Hilliard, Austin T., Clarke, Shoa L., Napolioni, Valerio, Ma, Shining, Lee, Kyung Min, Fang, Huaying, Chen, Fei, Lu, Yingchang, Tsao, Noah L., Raghavan, Sridharan, Koyama, Satoshi, Gorman, Bryan R., Vujkovic, Marijana, Klarin, Derek, Levin, Michael G., Sinnott-Armstrong, Nasa, Wojcik, Genevieve L., Plomondon, Mary E., Maddox, Thomas M., Waldo, Stephen W., Bick, Alexander G., Pyarajan, Saiju, Huang, Jie, Song, Rebecca, Ho, Yuk-Lam, Buyske, Steven, Kooperberg, Charles, Haessler, Jeffrey, Loos, Ruth J. F., Do, Ron, Verbanck, Marie, Chaudhary, Kumardeep, North, Kari E., Avery, Christy L., Graff, Mariaelisa, Haiman, Christopher A., Le Marchand, Loïc, Wilkens, Lynne R., Bis, Joshua C., Leonard, Hampton, Shen, Botong, Lange, Leslie A., Giri, Ayush, Dikilitas, Ozan, Kullo, Iftikhar J., Stanaway, Ian B., Jarvik, Gail P., Gordon, Adam S., Hebbring, Scott, Namjou, Bahram, Kaufman, Kenneth M., Ito, Kaoru, Ishigaki, Kazuyoshi, Kamatani, Yoichiro, Verma, Shefali S., Ritchie, Marylyn D., Kember, Rachel L., Baras, Aris, Lotta, Luca A., Kathiresan, Sekar, Hauser, Elizabeth R., Miller, Donald R., Lee, Jennifer S., Saleheen, Danish, Reaven, Peter D., Cho, Kelly, Gaziano, J. Michael, Natarajan, Pradeep, Huffman, Jennifer E., Voight, Benjamin F., Rader, Daniel J., Chang, Kyong-Mi, Lynch, Julie A., Damrauer, Scott M., Wilson, Peter W. F., Tang, Hua, Sun, Yan V., Tsao, Philip S., O’Donnell, Christopher J., Assimes, Themistocles L.

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A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation von Vujkovic, Marijana, Ramdas, Shweta, Lorenz, Kim M., Guo, Xiuqing, Darlay, Rebecca, Cordell, Heather J., He, Jing, Gindin, Yevgeniy, Chung, Chuhan, Myers, Robert P., Schneider, Carolin V., Park, Joseph, Lee, Kyung Min, Serper, Marina, Carr, Rotonya M., Kaplan, David E., Haas, Mary E., MacLean, Matthew T., Witschey, Walter R., Zhu, Xiang, Tcheandjieu, Catherine, Kember, Rachel L., Kranzler, Henry R., Verma, Anurag, Giri, Ayush, Klarin, Derek M., Sun, Yan V., Huang, Jie, Huffman, Jennifer E., Creasy, Kate Townsend, Hand, Nicholas J., Liu, Ching-Ti, Long, Michelle T., Yao, Jie, Budoff, Matthew, Tan, Jingyi, Li, Xiaohui, Lin, Henry J., Chen, Yii-Der Ida, Taylor, Kent D., Chang, Ruey-Kang, Krauss, Ronald M., Vilarinho, Silvia, Brancale, Joseph, Nielsen, Jonas B., Locke, Adam E., Jones, Marcus B., Verweij, Niek, Baras, Aris, Reddy, K. Rajender, Neuschwander-Tetri, Brent A., Schwimmer, Jeffrey B., Sanyal, Arun J., Chalasani, Naga, Ryan, Kathleen A., Mitchell, Braxton D., Gill, Dipender, Wells, Andrew D., Manduchi, Elisabetta, Saiman, Yedidya, Mahmud, Nadim, Miller, Donald R., Reaven, Peter D., Phillips, Lawrence S., Muralidhar, Sumitra, DuVall, Scott L., Lee, Jennifer S., Assimes, Themistocles L., Pyarajan, Saiju, Cho, Kelly, Edwards, Todd L., Damrauer, Scott M., Wilson, Peter W., Gaziano, J. Michael, O’Donnell, Christopher J., Khera, Amit V., Grant, Struan F. A., Brown, Christopher D., Tsao, Philip S., Saleheen, Danish, Lotta, Luca A., Bastarache, Lisa, Anstee, Quentin M., Daly, Ann K., Meigs, James B., Rotter, Jerome I., Lynch, Julie A., Rader, Daniel J., Voight, Benjamin F., Chang, Kyong-Mi

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Comparative genomics of Alexander Fleming’s original Penicillium isolate (IMI 15378) reveals sequence divergence of penicillin synthesis genes von Pathak, Ayush, Nowell, Reuben W., Wilson, Christopher G., Ryan, Matthew J., Barraclough, Timothy G.

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Enhancer reprogramming in PRC2-deficient malignant peripheral nerve sheath tumors induces a targetable de-differentiated state von Kochat, Veena, Raman, Ayush T., Landers, Sharon M., Tang, Ming, Schulz, Jonathan, Terranova, Christopher, Landry, Jace P., Bhalla, Angela D., Beird, Hannah C., Wu, Chia-Chin, Jiang, Yingda, Mao, Xizeng, Lazcano, Rossana, Gite, Swati, Ingram, Davis R., Yi, Min, Zhang, Jianhua, Keung, Emily Z., Scally, Christopher P., Roland, Christina L., Hunt, Kelly K., Feig, Barry W., Futreal, P. Andrew, Hwu, Patrick, Wang, Wei-Lien, Lazar, Alexander J., Slopis, John M., Wilson-Robles, Heather, Wiener, Dominique J., McCutcheon, Ian E., Wustefeld-Janssens, Brandan, Rai, Kunal, Torres, Keila E.

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1333-P: A Mutation Causing Glucose-6-Phosphate Dehydrogenase Deficiency Increases the Risk of Diabetes Complications in Men with African Ancestry von Breeyear, Joseph H, Hellwege, Jacklyn, House, John S, Mitchell, Sabrina L, Charest, Brian, Basnet, Til B, Reaven, Peter, Meigs, James B, Rhee, Mary K, Sun, Yang, Wilson, Otis, Hung, Adriana M, Iyengar, Sudha K, Rotroff, Daniel M, Buse, John B, Leong, Aaron, Mercader, Josep M, Brantley, Milam, Peachey, Neal S, Motsinger-Reif, Alison, Wilson, Peter W, Sun, Yan, Giri, Ayush, Phillips, Lawrence S, Edwards, Todd L

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Automated real-world data integration improves cancer outcome prediction von Jee, Justin, Fong, Christopher, Pichotta, Karl, Tran, Thinh Ngoc, Luthra, Anisha, Waters, Michele, Fu, Chenlian, Altoe, Mirella, Liu, Si-Yang, Maron, Steven B., Ahmed, Mehnaj, Kim, Susie, Pirun, Mono, Chatila, Walid K., de Bruijn, Ino, Pasha, Arfath, Kundra, Ritika, Gross, Benjamin, Mastrogiacomo, Brooke, Aprati, Tyler J., Liu, David, Gao, JianJiong, Capelletti, Marzia, Pekala, Kelly, Loudon, Lisa, Perry, Maria, Bandlamudi, Chaitanya, Donoghue, Mark, Satravada, Baby Anusha, Martin, Axel, Shen, Ronglai, Chen, Yuan, Brannon, A. Rose, Chang, Jason, Braunstein, Lior, Li, Anyi, Safonov, Anton, Stonestrom, Aaron, Sanchez-Vela, Pablo, Wilhelm, Clare, Robson, Mark, Scher, Howard, Ladanyi, Marc, Reis-Filho, Jorge S., Solit, David B., Jones, David R., Gomez, Daniel, Yu, Helena, Chakravarty, Debyani, Yaeger, Rona, Abida, Wassim, Park, Wungki, O’Reilly, Eileen M., Garcia-Aguilar, Julio, Socci, Nicholas, Sanchez-Vega, Francisco, Carrot-Zhang, Jian, Stetson, Peter D., Levine, Ross, Rudin, Charles M., Berger, Michael F., Shah, Sohrab P., Schrag, Deborah, Razavi, Pedram, Kehl, Kenneth L., Li, Bob T., Riely, Gregory J., Schultz, Nikolaus

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Adaptive selection at G6PD and disparities in diabetes complications von Breeyear, Joseph H., Hellwege, Jacklyn N., Schroeder, Philip H., House, John S., Poisner, Hannah M., Mitchell, Sabrina L., Charest, Brian, Khakharia, Anjali, Basnet, Til B., Halladay, Christopher W., Reaven, Peter D., Meigs, James B., Rhee, Mary K., Sun, Yang, Lynch, Mary G., Bick, Alexander G., Wilson, Otis D., Hung, Adriana M., Nealon, Cari L., Iyengar, Sudha K., Rotroff, Daniel M., Buse, John B., Leong, Aaron, Mercader, Josep M., Sobrin, Lucia, Brantley, Milam A., Peachey, Neal S., Motsinger-Reif, Alison A., Wilson, Peter W., Sun, Yan V., Giri, Ayush, Phillips, Lawrence S., Edwards, Todd L.

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Development of electronic health record based algorithms to identify individuals with diabetic retinopathy von Breeyear, Joseph H, Mitchell, Sabrina L, Nealon, Cari L, Hellwege, Jacklyn N, Charest, Brian, Khakharia, Anjali, Halladay, Christopher W, Yang, Janine, Garriga, Gustavo A, Wilson, Otis D, Basnet, Til B, Hung, Adriana M, Reaven, Peter D, Meigs, James B, Rhee, Mary K, Sun, Yang, Lynch, Mary G, Sobrin, Lucia, Brantley, Milam A, Sun, Yan V, Wilson, Peter W, Iyengar, Sudha K, Peachey, Neal S, Phillips, Lawrence S, Edwards, Todd L, Giri, Ayush

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Genome analysis of the platypus reveals unique signatures of evolution von WARREN, Wesley C, HILLIER, Ladeana W, YANG, Shiaw-Pyng, HEGER, Andreas, LOCKE, Devin P, MIETHKE, Pat, WATERS, Paul D, VEYRUNES, Frédéric, FULTON, Lucinda, FULTON, Bob, GRAVES, Tina, WALLIS, John, MARSHALL GRAVES, Jennifer A, PUENTE, Xose S, LOPEZ-OTIN, Carlos, ORDONEZ, Gonzalo R, EICHLER, Evan E, LIN CHEN, ZE CHENG, DEAKIN, Janine E, ALSOP, Amber, THOMPSON, Katherine, KIRBY, Patrick, BIRNEY, Ewan, PAPENFUSS, Anthony T, WAKEFIELD, Matthew J, OLENDER, Tsviya, LANCET, Doron, HUTTLEY, Gavin A, SMIT, Arian F. A, PASK, Andrew, TEMPLE-SMITH, Peter, BATZER, Mark A, WALKER, Jerilyn A, PONTING, Chris P, KONKEL, Miriam K, HARRIS, Robert S, WHITTINGTON, Camilla M, WONG, Emily S. W, GEMMELL, Neil J, BUSCHIAZZO, Emmanuel, VARGAS JENTZSCH, Iris M, MERKEL, Angelika, SCHMITZ, Juergen, ZEMANN, Anja, GRUTZNER, Frank, CHURAKOV, Gennady, KRIEGS, Jan Ole, BROSIUS, Juergen, MURCHISON, Elizabeth P, SACHIDANANDAM, Ravi, SMITH, Carly, HANNON, Gregory J, TSEND-AYUSH, Enkhjargal, MCMILLAN, Daniel, ATTENBOROUGH, Rosalind, BELOV, Katherine, MILLER, Webb, CLARKE, Laura, CHINWALLA, Asif T

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Association of APOL1 Risk Alleles With Cardiovascular Disease in Blacks in the Million Veteran Program von Bick, Alexander G, Akwo, Elvis, Robinson-Cohen, Cassianne, Lee, Kyung, Lynch, Julie, Assimes, Themistocles L, DuVall, Scott, Edwards, Todd, Fang, Huaying, Freiberg, S Matthew, Giri, Ayush, Huffman, Jennifer E, Huang, Jie, Hull, Leland, Kember, Rachel L, Klarin, Derek, Lee, Jennifer S, Levin, Michael, Miller, Donald R, Natarajan, Pradeep, Saleheen, Danish, Shao, Qing, Sun, Yan V, Tang, Hua, Wilson, Otis, Chang, Kyong-Mi, Cho, Kelly, Concato, John, Gaziano, J Michael, Kathiresan, Sekar, O'Donnell, Christopher J, Rader, Daniel J, Tsao, Philip S, Wilson, Peter W, Hung, Adriana M, Damrauer, Scott M

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Pharmacological restoration of NAD+/NADH prevents chronic neurodegeneration and neuropsychiatric impairment after whole-brain radiotherapy von Vázquez-Rosa, Edwin, Shin, Min-Kyoo, Chaubey, Kalyani, Barker, Sarah, Tripathi, Sunil, Chakraborty, Suwarna, Lindley, Kate, Vyas, Ayush, Miller, Emiko, Koh, Yeojung, Yu, Youngmin, Bud, Zea, Cintrón-Pérez, Coral J., Dhar, Matasha, Mapuskar, Kranti, Schoenfeld, Joshua, Fujioka, Hisashi, Dashora, Himanshu, Yu, Jennifer, Wilson, Brigid, Paul, Bindu, Spitz, Doug, Allen, Bryan, Pieper, Andrew

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Monkeypox‐Associated Central Nervous System Disease: A Case Series and Review von Money, Kelli M., Barnett, T. Allen, Rapaka, Samuel, Osborn, Rebecca, Kitani, Takashi, Fuguet, Daniel, Amjad, Faria, Clark, Jeffrey R., Chakravarty, Debanjana, Copeland, Matthew J., Honce, Justin M., Kumar, Princy N., Kumar, Rebecca N., Mousa‐Ibrahim, Fady, Sirdar, Bilaal, Sobota, Rafal, Tang, Mengxuan, Bolon, Maureen K., Russell, Eric J., Wilson, Michael, Tornatore, Carlo, Batra, Ayush, Tyler, Kenneth L., Pastula, Daniel M.

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Association of Apparent Treatment-Resistant Hypertension With Differential Risk of End-Stage Kidney Disease Across Racial Groups in the Million Veteran Program von Akwo, Elvis A., Robinson-Cohen, Cassianne, Chung, Cecilia P., Shah, Shailja C., Brown, Nancy J., Ikizler, T. Alp, Wilson, Otis D., Rowan, Bryce X., Shuey, Megan M., Siew, Edward D., Luther, James M., Giri, Ayush, Hellwege, Jacklyn N., Velez Edwards, Digna R., Roumie, Christianne L., Tao, Ran, Tsao, Phil S., Gaziano, J. Michael, Wilson, Peter W.F., O’Donnell, Christopher J., Edwards, Todd L., Kovesdy, Csaba P., Hung, Adriana M.

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Association of Apparent Treatment-Resistant Hypertension With Differential Risk of End-Stage Kidney Disease Across Racial Groups in the Million Veteran Program von Akwo, Elvis A., Robinson-Cohen, Cassianne, Chung, Cecilia P., Shah, Shailja C., Brown, Nancy J., Ikizler, T. Alp, Wilson, Otis D., Rowan, Bryce X., Shuey, Megan M., Siew, Edward D., Luther, James M., Giri, Ayush, Hellwege, Jacklyn N., Velez Edwards, Digna R., Roumie, Christianne L., Tao, Ran, Tsao, Phil S., Gaziano, J. Michael, Wilson, Peter W.F., O’Donnell, Christopher J., Edwards, Todd L., Kovesdy, Csaba P., Hung, Adriana M.

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Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals von Eicher, John D., Kacprowski, Tim, Nomura, Akihiro, Chen, Ming-Huei, Yanek, Lisa R., Tajuddin, Salman M., Slater, Andrew J., Polfus, Linda, Schurmann, Claudia, Brody, Jennifer A., Manichaikul, Ani, Hill, W. David, Pazoki, Raha, Elliot, Paul, Evangelou, Evangelos, Tzoulaki, Ioanna, Gao, He, Vergnaud, Anne-Claire, Mathias, Rasika A., Becker, Diane M., Becker, Lewis C., Burt, Amber, Crosslin, David R., Lyytikäinen, Leo-Pekka, Nikus, Kjell, Hernesniemi, Jussi, Kähönen, Mika, Raitoharju, Emma, Mononen, Nina, Raitakari, Olli T., Lehtimäki, Terho, Cushman, Mary, Zakai, Neil A., Nickerson, Deborah A., Raffield, Laura M., Quarells, Rakale, Willer, Cristen J., Peloso, Gina M., Abecasis, Goncalo R., Liu, Dajiang J., Deloukas, Panos, Samani, Nilesh J., Schunkert, Heribert, Erdmann, Jeanette, Fornage, Myriam, Richard, Melissa, Tardif, Jean-Claude, Rioux, John D., Dube, Marie-Pierre, de Denus, Simon, Bottinger, Erwin P., Loos, Ruth J.F., Smith, Albert Vernon, Harris, Tamara B., Launer, Lenore J., Gudnason, Vilmundur, Velez Edwards, Digna R., Torstenson, Eric S., Liu, Yongmei, Tracy, Russell P., Rotter, Jerome I., Rich, Stephen S., Highland, Heather M., Li, Jin, Lange, Ethan, Wilson, James G., Mihailov, Evelin, Hirschhorn, Joel, Metspalu, Andres, Esko, Tõnu, Vacchi-Suzzi, Caterina, Zonderman, Alan B., Evans, Michele K., Engström, Gunnar, Orho-Melander, Marju, Melander, Olle, O’Donoghue, Michelle L., Waterworth, Dawn M., Floyd, James S., Rice, Kenneth M., Psaty, Bruce M., Starr, J.M., Liewald, David C.M., Hayward, Caroline, Deary, Ian J., Greinacher, Andreas, Völker, Uwe, Thiele, Thomas, Völzke, Henry, van Rooij, Frank J.A., Uitterlinden, André G., Franco, Oscar H., Dehghan, Abbas, Edwards, Todd L., Ganesh, Santhi K., Kathiresan, Sekar, Faraday, Nauder, Reiner, Alex P., Lettre, Guillaume, Johnson, Andrew D.

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