The genetic architecture of Parkinson's disease von Blauwendraat, Cornelis, Nalls, Mike A, Singleton, Andrew B

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Genome-wide CRISPRi/a screens in human neurons link lysosomal failure to ferroptosis von Tian, Ruilin, Abarientos, Anthony, Hong, Jason, Hashemi, Sayed Hadi, Yan, Rui, Dräger, Nina, Leng, Kun, Nalls, Mike A., Singleton, Andrew B., Xu, Ke, Faghri, Faraz, Kampmann, Martin

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Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies von Vallerga, Costanza L, Tan, Manuela, Kia, Demis A, Xue, Angli, Young, Emily, Sharma, Manu, Krohn, Lynne, Siitonen, Ari, Iwaki, Hirotaka, Leonard, Hampton, Botia, Juan A, Martinez, Maria, Jankovic, Joseph, Sutherland, Margaret, Majamaa, Kari, Andreassen, Ole A, Gan-Or, Ziv, Gasser, Thomas, Heutink, Peter, Gratten, Jacob, Alvarez, Ignacio, Alvarez, Victoria, Bandres-Ciga, Sara, Bergareche Yarza, Jesús Alberto, Billingsley, Kimberley, Bonilla-Toribio, Marta, Botía, Juan A, Boungiorno, María Teresa, Bras, Jose, Bubb, Vivien, Buiza-Rueda, Dolores, Cerdan, Debora, Chelban, Viorica, Corvol, Jean-Christophe, Craig, David W, Danjou, Fabrice, Diez-Fairen, Monica, Escott-Price, Valentina, Ezquerra, Mario, Fernández, Manel, Fernández-Santiago, Rubén, Gan-Or, Ziv, Garcia, Ciara, García-Ruiz, Pedro, Hernandez, Dena G, Hoenicka, Janet, Infante, Jon, Jesús, Silvia, Kaiyrzhanov, Rauan, Kia, Demis A, Leonard, Hampton L, Lewis, Patrick, Lopez-Sendon, Jose Luis, Lovering, Ruth, Lubbe, Steven, Majamaa, Kari, Manzoni, Claudia, Marti, Maria Jose, Méndez-del-Barrio, Carlota, Middlehurst, Ben, Mínguez, Adolfo, Muñoz, Esteban, Pagola, Ana Gorostidi, Pastor, Pau, Perez Errazquin, Francisco, Periñán-Tocino, Teresa, Reed, Xylena, Rezola, Elisabet Mondragon, Rodriguez, Antonio Sanchez, Ruiz-Martínez, Javier, Sadykova, Dinara, Shashkin, Chingiz, Sierra, María, Simón-Sánchez, Javier, Singleton, Andrew B, Suarez-Sanmartin, Esther, Tabernero, Cesar, Tolosa, Eduard, van Hilten, Jacobus J, Vargas-González, Laura, Wood, Nicholas W, Zimprich, Alexander, Reich, Stephen, Savitt, Joseph, Bryc, Katarzyna, Hicks, Barry, Jiang, Yunxuan, McCreight, Jennifer C., McIntyre, Matthew H., Noblin, Elizabeth S., Sathirapongsasuti, J. Fah, Tung, Joyce, Anderson, Tim, Bentley, Steven, Kennedy, Martin, Mellick, George, Sidorenko, Julia, Silburn, Peter A., Visscher, Peter M., Yang, Jian

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A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci von Chang, Diana, Nalls, Mike A, Hallgrímsdóttir, Ingileif B, Hunkapiller, Julie, van der Brug, Marcel, Cai, Fang, Kerchner, Geoffrey A, Ayalon, Gai, Bingol, Baris, Sheng, Morgan, Hinds, David, Behrens, Timothy W, Singleton, Andrew B, Bhangale, Tushar R, Graham, Robert R

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MUC5B Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease von Juge, Pierre-Antoine, Lee, Joyce S, Ebstein, Esther, Furukawa, Hiroshi, Dobrinskikh, Evgenia, Gazal, Steven, Kannengiesser, Caroline, Ottaviani, Sébastien, Oka, Shomi, Tohma, Shigeto, Tsuchiya, Naoyuki, Rojas-Serrano, Jorge, González-Pérez, Montserrat I, Mejía, Mayra, Buendía-Roldán, Ivette, Falfán-Valencia, Ramcés, Ambrocio-Ortiz, Enrique, Manali, Effrosyni, Papiris, Spyros A, Karageorgas, Theofanis, Boumpas, Dimitrios, Antoniou, Katarina, van Moorsel, Coline H.M, van der Vis, Joanne, de Man, Yaël A, Grutters, Jan C, Wang, Yaping, Borie, Raphaël, Wemeau-Stervinou, Lidwine, Wallaert, Benoît, Flipo, René-Marc, Nunes, Hilario, Valeyre, Dominique, Saidenberg-Kermanac’h, Nathalie, Boissier, Marie-Christophe, Marchand-Adam, Sylvain, Frazier, Aline, Richette, Pascal, Allanore, Yannick, Sibilia, Jean, Dromer, Claire, Richez, Christophe, Schaeverbeke, Thierry, Lioté, Huguette, Thabut, Gabriel, Nathan, Nadia, Amselem, Serge, Soubrier, Martin, Cottin, Vincent, Clément, Annick, Deane, Kevin, Walts, Avram D, Fingerlin, Tasha, Fischer, Aryeh, Ryu, Jay H, Matteson, Eric L, Niewold, Timothy B, Assayag, Deborah, Gross, Andrew, Wolters, Paul, Schwarz, Marvin I, Holers, Michael, Solomon, Joshua J, Doyle, Tracy, Rosas, Ivan O, Blauwendraat, Cornelis, Nalls, Mike A, Debray, Marie-Pierre, Boileau, Catherine, Crestani, Bruno, Schwartz, David A, Dieudé, Philippe

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Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease von Nalls, Mike A, Pankratz, Nathan, Lill, Christina M, Do, Chuong B, Hernandez, Dena G, Saad, Mohamad, DeStefano, Anita L, Kara, Eleanna, Bras, Jose, Sharma, Manu, Schulte, Claudia, Keller, Margaux F, Arepalli, Sampath, Letson, Christopher, Edsall, Connor, Stefansson, Hreinn, Liu, Xinmin, Pliner, Hannah, Lee, Joseph H, Cheng, Rong, Ikram, M Arfan, Ioannidis, John P A, Hadjigeorgiou, Georgios M, Bis, Joshua C, Martinez, Maria, Perlmutter, Joel S, Goate, Alison, Marder, Karen, Fiske, Brian, Sutherland, Margaret, Xiromerisiou, Georgia, Myers, Richard H, Clark, Lorraine N, Stefansson, Kari, Hardy, John A, Heutink, Peter, Chen, Honglei, Wood, Nicholas W, Houlden, Henry, Payami, Haydeh, Brice, Alexis, Scott, William K, Gasser, Thomas, Bertram, Lars, Eriksson, Nicholas, Foroud, Tatiana, Singleton, Andrew B

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A CRISPRi/a platform in human iPSC-derived microglia uncovers regulators of disease states von Dräger, Nina M., Sattler, Sydney M., Huang, Cindy Tzu-Ling, Teter, Olivia M., Leng, Kun, Hashemi, Sayed Hadi, Hong, Jason, Aviles, Giovanni, Clelland, Claire D., Zhan, Lihong, Udeochu, Joe C., Kodama, Lay, Singleton, Andrew B., Nalls, Mike A., Ichida, Justin, Ward, Michael E., Faghri, Faraz, Gan, Li, Kampmann, Martin

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Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study von Noyce, Alastair J, Kia, Demis A, Hemani, Gibran, Nicolas, Aude, Price, T Ryan, De Pablo-Fernandez, Eduardo, Haycock, Philip C, Lewis, Patrick A, Foltynie, Thomas, Davey Smith, George, Schrag, Anette, Lees, Andrew J, Hardy, John, Singleton, Andrew, Nalls, Mike A, Pearce, Neil, Lawlor, Debbie A, Wood, Nicholas W

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Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis von Noyce, Alastair J., Hemani, Gibran, Mora, Gabriele, Bartolomei, Ilaria, Benigni, Michele, Borghero, Giuseppe, Brunetti, Maura, Calvo, Andrea, Cammarosano, Stefania, Cannas, Antonino, Caponnetto, Claudia, Casale, Federico, Cavallaro, Sebastiano, Chiò, Adriano, Colletti, Tiziana, Conforti, Francesca L., Conte, Amelia, Corrado, Lucia, Costantino, Emanuela, D'Alfonso, Sandra, Femiano, Cinzia, Ferrarese, Carlo, Fini, Nicola, Floris, Gianluca, Grassano, Maurizio, Lattante, Serena, Logroscino, Giancarlo, Loi, Daniela, Mancardi, Gianluigi, Mandich, Paola, Manera, Umberto, Marinou, Kalliopi, Marrali, Giuseppe, Marrosu, Maria Giovanna, Mazzini, Letizia, Melis, Maurizio, Messina, Sonia, Mora, Gabriele, Occhineri, Patrizia, Origone, Paola, Pani, Carla, Petrucci, Antonio, Pirisi, Angelo, Restagno, Gabriella, Ricci, Claudia, Riva, Nilo, Sabatelli, Mario, Santarelli, Marialuisa, Spataro, Rossella, Tanel, Raffaella, Tremolizzo, Lucio, Volanti, Paolo, Zollino, Marcella, Arepalli, Sampath, Bowser, Robert, Broach, James, Camu, William, Chia, Ruth, Chiò, Adriano, Ding, Jinhui, Dunckley, Travis L., Eicher, John D., Faghri, Faraz, Feldman, Eva, Fratta, Pietro, Geiger, Joshua T., Gerhard, Glenn, Hardy, John, Harms, Matthew B., Heiman‐Patterson, Terry D., Kamel, Freya, MacGowan, Daniel J.L., Maragakis, Nicholas J., Murphy, Natalie A., Myllykangas, Liisa, Nalls, Mike A., Nicolas, Aude, Orrell, Richard W., Pamphlett, Roger, Pickering‐Brown, Stuart, Pioro, Erik, Pliner, Hannah A., Pulst, Stefan M., Ravits, John M., Rothstein, Jeffrey D., Salvi, Erika, Sendtner, Michael, Simmons, Zachary, Stone, David C., Sulkava, Raimo, Troncoso, Juan C., Van Damme, Philip, Van Deerlin, Vivianna M., Van Den Bosch, Ludo, Zinman, Lorne, Tienari, Pentti J., Stone, David J., Nalls, Mike A., Singleton, Andrew B., Traynor, Bryan J.

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Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease von Beilina, Alexandria, Rudenko, Iakov N., Kaganovich, Alice, Civiero, Laura, Chau, Hien, Kalia, Suneil K., Kalia, Lorraine V., Lobbestael, Evy, Chia, Ruth, Ndukwe, Kelechi, Ding, Jinhui, Nalls, Mike A., Olszewski, Maciej, Hauser, David N., Kumaran, Ravindran, Lozano, Andres M., Baekelandt, Veerle, Greene, Lois E., Taymans, Jean-Marc, Greggio, Elisa, Cookson, Mark R.

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Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease von Blauwendraat, Cornelis, Reed, Xylena, Kia, Demis A, Gan-Or, Ziv, Lesage, Suzanne, Pihlstrøm, Lasse, Guerreiro, Rita, Gibbs, J. Raphael, Sabir, Marya, Ahmed, Sarah, Ding, Jinhui, Alcalay, Roy N, Hassin-Baer, Sharon, Pittman, Alan M, Brooks, Janet, Edsall, Connor, Hernandez, Dena G, Chung, Sun Ju, Goldwurm, Stefano, Toft, Mathias, Schulte, Claudia, Bras, Jose, Wood, Nicholas W, Brice, Alexis, Morris, Huw R, Scholz, Sonja W, Nalls, Mike A, Singleton, Andrew B, Cookson, Mark R

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Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies von Traylor, Matthew, MSc, Farrall, Martin, FRCPath, Holliday, Elizabeth G, PhD, Sudlow, Cathie, FRCP, Hopewell, Jemma C, PhD, Cheng, Yu-Ching, PhD, Fornage, Myriam, PhD, Ikram, M Arfan, MD, Malik, Rainer, PhD, Bevan, Steve, PhD, Thorsteinsdottir, Unnur, PhD, Nalls, Mike A, PhD, Longstreth, WT, MD, Wiggins, Kerri L, MS, Yadav, Sunaina, MSc, Parati, Eugenio A, MD, DeStefano, Anita L, PhD, Worrall, Bradford B, MD, Kittner, Steven J, MD, Khan, Muhammad Saleem, MSc, Reiner, Alex P, MD, Helgadottir, Anna, MD, Achterberg, Sefanja, PhD, Fernandez-Cadenas, Israel, PhD, Abboud, Sherine, MD, Schmidt, Reinhold, MD, Walters, Matthew, MD, Chen, Wei-Min, PhD, Ringelstein, E Bernd, MD, O'Donnell, Martin, MD, Ho, Weang Kee, PhD, Pera, Joanna, MD, Lemmens, Robin, MD, Norrving, Bo, MD, Higgins, Peter, MRCP, Benn, Marianne, MD, Sale, Michele, PhD, Kuhlenbäumer, Gregor, MD, Doney, Alexander S F, PhD, Vicente, Astrid M, PhD, Delavaran, Hossein, MD, Algra, Ale, MD, Davies, Gail, PhD, Oliveira, Sofia A, PhD, Palmer, Colin N A, PhD, Deary, Ian, PhD, Schmidt, Helena, MD, Pandolfo, Massimo, MD, Montaner, Joan, MD, Carty, Cara, PhD, de Bakker, Paul I W, PhD, Kostulas, Konstantinos, MD, Ferro, Jose M, MD, van Zuydam, Natalie R, MSc, Valdimarsson, Einar, MD, Nordestgaard, Børge G, MD, Lindgren, Arne, MD, Thijs, Vincent, MD, Slowik, Agnieszka, MD, Saleheen, Danish, MD, Paré, Guillaume, MD, Berger, Klaus, MD, Thorleifsson, Gudmar, PhD, Hofman, Albert, MD, Mosley, Thomas H, PhD, Mitchell, Braxton D, PhD, Furie, Karen, MD, Clarke, Robert, FRCP, Levi, Christopher, MD, Seshadri, Sudha, MD, Gschwendtner, Andreas, MD, Boncoraglio, Giorgio B, MD, Sharma, Pankaj, PhD, Bis, Joshua C, PhD, Gretarsdottir, Solveig, PhD, Psaty, Bruce M, Rothwell, Peter M, FMedSci, Rosand, Jonathan, MD, Meschia, James F, MD, Stefansson, Kari, MD, Dichgans, Martin, MD, Markus, Hugh S, Dr

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Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data von Mok, Kin Y, FRCP, Sheerin, Una, MRCP, Simón-Sánchez, Javier, PhD, Salaka, Afnan, PhD, Chester, Lucy, MPharm, Escott-Price, Valentina, PhD, Mantripragada, Kiran, PhD, Doherty, Karen M, MD, Noyce, Alastair J, MRCP, Mencacci, Niccolo E, MD, Lubbe, Steven J, PhD, Williams-Gray, Caroline H, PhD, Barker, Roger A, Prof, van Dijk, Karin D, MD, Berendse, Henk W, Prof, Heutink, Peter, Prof, Corvol, Jean-Christophe, Prof, Cormier, Florence, MD, Lesage, Suzanne, PhD, Brice, Alexis, Prof, Brockmann, Kathrin, MD, Schulte, Claudia, PhD, Gasser, Thomas, Prof, Foltynie, Thomas, PhD, Limousin, Patricia, Prof, Morrison, Karen E, Prof, Clarke, Carl E, Prof, Sawcer, Stephen, Prof, Warner, Tom T, Prof, Lees, Andrew J, Prof, Morris, Huw R, Prof, Nalls, Mike A, PhD, Singleton, Andrew B, PhD, Hardy, John, Prof, Abramov, Andrey Y, Prof, Plagnol, Vincent, PhD, Williams, Nigel M, Dr, Wood, Nicholas W, Prof

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Open science in precision medicine for neurodegenerative diseases von Leonard, Hampton L., Nalls, Mike A., Day-Williams, Aaron, Esmaeeli, Sahar, Jarreau, Paige, Bandres-Ciga, Sara, Heutink, Peter, Sardi, S. Pablo, Singleton, Andrew B.

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Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis von Johnson, Janel O, Glynn, Shannon M, Gibbs, J Raphael, Nalls, Mike A, Sabatelli, Mario, Restagno, Gabriella, Drory, Vivian E, Chiò, Adriano, Rogaeva, Ekaterina, Traynor, Bryan J

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Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study von Nalls, Mike A, PhD, McLean, Cory Y, PhD, Rick, Jacqueline, PhD, Eberly, Shirley, MS, Hutten, Samantha J, PhD, Gwinn, Katrina, MD, Sutherland, Margaret, PhD, Martinez, Maria, PhD, Heutink, Peter, PhD, Williams, Nigel M, PhD, Hardy, John, PhD, Gasser, Thomas, MD, Brice, Alexis, MD, Price, T Ryan, MS, Nicolas, Aude, PhD, Keller, Margaux F, PhD, Molony, Cliona, PhD, Gibbs, J Raphael, MS, Chen-Plotkin, Alice, MD, Suh, Eunran, PhD, Letson, Christopher, BS, Fiandaca, Massimo S, MD, Mapstone, Mark, PhD, Federoff, Howard J, MD, Noyce, Alastair J, MRCP, Morris, Huw, MD, Van Deerlin, Vivianna M, MD, Weintraub, Daniel, MD, Zabetian, Cyrus, MD, Hernandez, Dena G, MS, Lesage, Suzanne, PhD, Mullins, Meghan, BA, Conley, Emily Drabant, PhD, Northover, Carrie A M, PhD, Frasier, Mark, PhD, Marek, Ken, MD, Day-Williams, Aaron G, PhD, Stone, David J, PhD, Ioannidis, John P A, Prof, Singleton, Andrew B, Dr

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Sequential screening nominates the Parkinson's disease associated kinase LRRK2 as a regulator of Clathrin-mediated endocytosis von Heaton, George R., Landeck, Natalie, Mamais, Adamantios, Nalls, Mike A., Nixon-Abell, Jonathon, Kumaran, Ravindran, Beilina, Alexandra, Pellegrini, Laura, Li, Yan, Harvey, Kirsten, Cookson, Mark R.

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Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels von Carli, Jayne F. Martin, Sun, Qi, Kriebel, Jennifer, Feitosa, Mary F, Hedman, Åsa K., Pers, Tune H., Trompet, Stella, Mangino, Massimo, Kristiansson, Kati, Beekman, Marian, Lyytikäinen, Leo-Pekka, Henneman, Peter, Tanaka, Toshiko, Luan, Jian’an, Pasko, Dorota, Renström, Frida, Willems, Sara M., Mahajan, Anubha, Rose, Lynda M., Liu, Yongmei, Pérusse, Louis, Ju Sung, Yun, Ramos, Yolande F., Amuzu, Antoinette, Barroso, Inês, Blangero, John, Buckley, Brendan M., Böhringer, Stefan, Crosslin, David R., Dale, Caroline E., Dastani, Zari, Deelen, Joris, Delgado, Graciela E., Demirkan, Ayse, Finucane, Francis M., Gieger, Christian, Gustafsson, Stefan, Herder, Christian, Ingelsson, Erik, Ioan-Facsinay, Andreea, Jansson, John-Olov, Jenny, Nancy S., Jørgensen, Torben, Koenig, Wolfgang, Kraft, Peter, Kwekkeboom, Joanneke, Laatikainen, Tiina, Lu, Yingchang, Meisinger, Christa, Morris, Andrew P., Männistö, Satu, Paternoster, Lavinia, Rankinen, Tuomo, Rathmann, Wolfgang, Brent Richards, J, Timpson, Nicholas J., van Heemst, Diana, Uh, Hae-Won, Vohl, Marie-Claude, Walker, Mark, Wichmann, Heinz-Erich, Wood, Andrew R., Zeller, Tanja, Zhang, Yiying, Sørensen, Thorkild I. A., Rao, D. C., Jousilahti, Pekka, Hofman, Albert, Osmond, Clive, Palotie, Aarno, Knekt, Paul B., Perola, Markus, Huupponen, Risto K., Kähönen, Mika, Lehtimäki, Terho, Lorentzon, Mattias, Casas, Juan P., Bandinelli, Stefanie, März, Winfried, Isaacs, Aaron, van Dijk, Ko W., Harris, Tamara B., Allison, Matthew A., Chasman, Daniel I., Ohlsson, Claes, Lind, Lars, Langenberg, Claudia, Ferrucci, Luigi, Frayling, Timothy M., Borecki, Ingrid B., Bergmann, Sven, Vollenweider, Peter, Hansen, Torben, Eline Slagboom, P, Grallert, Harald, Spector, Tim D., Jukema, J.W., Klein, Robert J., Franks, Paul W., Lindgren, Cecilia M.

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Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects von Krohn, Lynne, Heilbron, Karl, Blauwendraat, Cornelis, Reynolds, Regina H., Yu, Eric, Senkevich, Konstantin, Rudakou, Uladzislau, Estiar, Mehrdad A., Gustavsson, Emil K., Brolin, Kajsa, Ruskey, Jennifer A., Freeman, Kathryn, Asayesh, Farnaz, Chia, Ruth, Arnulf, Isabelle, Hu, Michele T. M., Montplaisir, Jacques Y., Gagnon, Jean-François, Desautels, Alex, Dauvilliers, Yves, Gigli, Gian Luigi, Valente, Mariarosaria, Janes, Francesco, Bernardini, Andrea, Högl, Birgit, Stefani, Ambra, Ibrahim, Abubaker, Šonka, Karel, Kemlink, David, Oertel, Wolfgang, Janzen, Annette, Plazzi, Giuseppe, Biscarini, Francesco, Antelmi, Elena, Figorilli, Michela, Puligheddu, Monica, Mollenhauer, Brit, Trenkwalder, Claudia, Sixel-Döring, Friederike, Cochen De Cock, Valérie, Monaca, Christelle Charley, Heidbreder, Anna, Ferini-Strambi, Luigi, Dijkstra, Femke, Viaene, Mineke, Abril, Beatriz, Boeve, Bradley F., Scholz, Sonja W., Ryten, Mina, Bandres-Ciga, Sara, Noyce, Alastair, Cannon, Paul, Pihlstrøm, Lasse, Nalls, Mike A., Singleton, Andrew B., Rouleau, Guy A., Postuma, Ronald B., Gan-Or, Ziv

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Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration von Noordam, Raymond, Wang, Heming, Bentley, Amy R., de Vries, Paul S., Sung, Yun Ju, Schwander, Karen, Richard, Melissa, Aslibekyan, Stella, Feitosa, Mary, Horimoto, Andrea R., Ilkov, Marjan, Kho, Minjung, Kraja, Aldi, Li, Changwei, Liu, Yongmei, Mook-Kanamori, Dennis O., Tajuddin, Salman M., van der Spek, Ashley, Laville, Vincent, Alver, Maris, Evangelou, Evangelos, Graff, Maria E., He, Meian, Kühnel, Brigitte, Lyytikäinen, Leo-Pekka, Marques-Vidal, Pedro, Palmer, Nicholette D., Rauramaa, Rainer, Shu, Xiao-Ou, Wen, Wanqing, Adolfo, Correa, Ballantyne, Christie, Bielak, Larry, Dimou, Niki, Eiriksdottir, Gudny, Gao, Chuan, Gharib, Sina A., Gottlieb, Daniel J., Haba-Rubio, José, Harris, Tamara B., Heikkinen, Sami, Heinzer, Raphaël, Hixson, James E., Homuth, Georg, Krieger, Jose E., Lohman, Kurt K., Luik, Annemarie I., Martin, Lisa W., Nalls, Mike A., O’Connell, Jeff, Raitakari, Olli T., Reiner, Alex P., Rensen, Patrick C. N., Rich, Stephen S., Roenneberg, Till, Schreiner, Pamela J., Shikany, James, Sidney, Stephen S., Sitlani, Colleen M., Strauch, Konstantin, Swertz, Morris A., Uitterlinden, André G., van Duijn, Cornelia M., Völzke, Henry, Waldenberger, Melanie, Wallance, Robert B., van Dijk, Ko Willems, Yu, Caizheng, Zonderman, Alan B., Becker, Diane M., Elliott, Paul, Esko, Tõnu, Gieger, Christian, Grabe, Hans J., Lakka, Timo A., North, Kari E., Penninx, Brenda W. J. H., Vollenweider, Peter, Wagenknecht, Lynne E., Wu, Tangchun, Arnett, Donna K., Bouchard, Claude, Evans, Michele K., Gudnason, Vilmundur, Kelly, Tanika N., Loos, Ruth J. F., Pereira, Alexandre C., Province, Mike, Psaty, Bruce M., Rotimi, Charles, Zhu, Xiaofeng, Amin, Najaf, Cupples, L. Adrienne, Fornage, Myriam, Fox, Ervin F., Guo, Xiuqing, Gauderman, W. James, Liu, Ching-Ti, Rao, Dabeeru C., Redline, Susan

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