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Direk, Nese, Williams, Stephanie, Smith, Jennifer A, Ripke, Stephan, Air, Tracy, Amare, Azmeraw T, Amin, Najaf, Baune, Bernhard T, Bennett, David A, Blackwood, Douglas HR et al (show 92 more authors) , Boomsma, Dorret, Breen, Gerome, Buttenschon, Henriette N, Byrne, Enda M, Borglum, Anders D, Castelao, Enrique, Cichon, Sven, Clarke, Toni-Kim, Cornelis, Marilyn C, Dannlowski, Udo, De Jager, Philip L, Demirkan, Ayse, Domenici, Enrico, van Duijn, Cornelia M, Dunn, Erin C, Eriksson, Johan G, Esko, Tonu, Faul, Jessica D, Ferrucci, Luigi, Fornage, Myriam, de Geus, Eco, Gill, Michael, Gordon, Scott D, Grabe, Hans Joergen, van Grootheest, Gerard, Hamilton, Steven P, Hartman, Catharina A, Heath, Andrew C, Hek, Karin, Hofman, Albert, Homuth, Georg, Horn, Carsten, Hottenga, Jouke Jan, Kardia, Sharon LR, Kloiber, Stefan, Koenen, Karestan, Kutalik, Zoltan, Ladwig, Karl-Heinz, Lahti, Jari, Levinson, Douglas F, Lewis, Cathryn M, Lewis, Glyn, Li, Qingqin S, Llewellyn, David J, Lucae, Susanne, Lunetta, Kathryn L, MacIntyre, Donald J, Madden, Pamela, Martin, Nicholas G, McIntosh, Andrew M, Metspalu, Andres, Milaneschi, Yuri, Montgomery, Grant W, Mors, Ole, Mosley, Thomas H, Murabito, Joanne M, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Nothen, Markus M, Nyholt, Dale R, O'Donovan, Michael C, Penninx, Brenda W, Pergadia, Michele L, Perlis, Roy, Potash, James B, Preisig, Martin, Purcell, Shaun M, Quiroz, Jorge A, Raikkonen, Katri, Rice, John P, Rietschel, Marcella, Rivera, Margarita, Schulze, Thomas G, Shi, Jianxin, Shyn, Stanley, Sinnamon, Grant C, Smit, Johannes H, Smoller, Jordan W, Snieder, Harold, Tanaka, Toshiko, Tansey, Katherine E, Teumer, Alexander, Uher, Rudolf, Umbricht, Daniel, Van der Auwera, Sandra, Ware, Erin B, Weir, David R, Weissman, Myrna M, Willemsen, Gonneke, Yang, Jingyun, Zhao, Wei, Tiemeier, Henning and Sullivan, Patrick F
(2017)
An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype.
BIOLOGICAL PSYCHIATRY, 82 (5).
pp. 322-329.
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Amin, Najaf, Allebrandt, Karla V, van der Spek, Ashley, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Hek, Karin, Teder-Laving, Maris, Hayward, Caroline, Esko, Tonu, van Mill, Josine G, Mbarek, Hamdi et al (show 64 more authors) , Watson, Nathaniel F, Melville, Scott A, Del Greco, Fabiola M, Byrne, Enda M, Oole, Edwin, Kolcic, Ivana, Chen, Ting-hsu, Evans, Daniel S, Coresh, Josef, Vogelzangs, Nicole, Karjalainen, Juha, Willemsen, Gonneke, Gharib, Sina A, Zgaga, Lina, Mihailov, Evelin, Stone, Katie L, Campbell, Harry, Brouwer, Rutger Ww, Demirkan, Ayse, Isaacs, Aaron, Dogas, Zoran, Marciante, Kristin D, Campbell, Susan, Borovecki, Fran, Luik, Annemarie I, Li, Man, Hottenga, Jouke Jan, Huffman, Jennifer E, van den Hout, Mirjam CGN, Cummings, Steven R, Aulchenko, Yuru S, Gehrman, Philip R, Uitterlinden, Andre G, Wichmann, Heinz-Erich, Muller-Nurasyid, Martina, Fehrmann, Rudolf SN, Montgomery, Grant W, Hofman, Albert, Kao, Wen Hong Linda, Oostra, Ben A, Wright, Alan F, Vink, Jacqueline M, Wilson, James F, Pramstaller, Peter P, Hicks, Andrew A, Polasek, Ozren, Punjabi, Naresh M, Redline, Susan, Psaty, Bruce M, Heath, Andrew C, Merrow, Martha, Tranah, Gregory J, Gottlieb, Daniel J, Boomsma, Dorret I, Martin, Nicholas G, Rudan, Igor, Tiemeier, Henning, van IJcken, Wilfred FJ, Penninx, Brenda W, Metspalu, Andres, Meitinger, Thomas, Franke, Lude, Roenneberg, Till and van Duijn, Cornelia M
(2016)
Genetic variants in <i>RBFOX3</i> are associated with sleep latency.
EUROPEAN JOURNAL OF HUMAN GENETICS, 24 (10).
pp. 1488-1495.
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Mahajan, Anubha, Wessel, Jennifer, Willems, Sara M, Zhao, Wei, Robertson, Neil R, Chu, Audrey Y, Gan, Wei, Kitajima, Hidetoshi, Taliun, Daniel, Rayner, N William et al (show 233 more authors) , Guo, Xiuqing, Lu, Yingchang, Li, Man, Jensen, Richard A, Hu, Yao, Huo, Shaofeng, Lohman, Kurt K, Zhang, Weihua, Cook, James P, Prins, Bram Peter, Flannick, Jason, Grarup, Niels, Trubetskoy, Vassily Vladimirovich, Kravic, Jasmina, Kim, Young Jin, Rybin, Denis V, Yaghootkar, Hanieh, Mueller-Nurasyid, Martina, Meidtner, Karina, Li-Gao, Ruifang, Varga, Tibor V, Marten, Jonathan, Li, Jin, Smith, Albert Vernon, An, Ping, Ligthart, Symen, Gustafsson, Stefan, Malerba, Giovanni, Demirkan, Ayse, Tajes, Juan Fernandez, Steinthorsdottir, Valgerdur, Wuttke, Matthias, Lecoeur, Cecile, Preuss, Michael, Bielak, Lawrence F, Graff, Marielisa, Highland, Heather M, Justice, Anne E, Liu, Dajiang J, Marouli, Eirini, Peloso, Gina Marie, Warren, Helen R, Afaq, Saima, Afzal, Shoaib, Ahlqvist, Emma, Almgren, Peter, Amin, Najaf, Bang, Lia B, Bertoni, Alain G, Bombieri, Cristina, Bork-Jensen, Jette, Brandslund, Ivan, Brody, Jennifer A, Burtt, Noel P, Canouil, Mickael, Chen, Yii-Der Ida, Cho, Yoon Shin, Christensen, Cramer, Eastwood, Sophie V, Eckardt, Kai-Uwe, Fischer, Krista, Gambaro, Giovanni, Giedraitis, Vilmantas, Grove, Megan L, de Haan, Hugoline G, Hackinger, Sophie, Hai, Yang, Han, Sohee, Tybjaerg-Hansen, Anne, Hivert, Marie-France, Isomaa, Bo, Jager, Susanne, Jorgensen, Marit E, Jorgensen, Torben, Karajamaki, Annemari, Kim, Bong-Jo, Kim, Sung Soo, Koistinen, Heikki A, Kovacs, Peter, Kriebel, Jennifer, Kronenberg, Florian, Lall, Kristi, Lange, Leslie A, Lee, Jung-Jin, Lehne, Benjamin, Li, Huaixing, Lin, Keng-Hung, Linneberg, Allan, Liu, Ching-Ti, Liu, Jun, Loh, Marie, Magi, Reedik, Mamakou, Vasiliki, McKean-Cowdin, Roberta, Nadkarni, Girish, Neville, Matt, Nielsen, Sune F, Ntalla, Ioanna, Peyser, Patricia A, Rathmann, Wolfgang, Rice, Kenneth, Rich, Stephen S, Rode, Line, Rolandsson, Olov, Schonherr, Sebastian, Selvin, Elizabeth, Small, Kerrin S, Stancakova, Alena, Surendran, Praveen, Taylor, Kent D, Teslovich, Tanya M, Thorand, Barbara, Thorleifsson, Gudmar, Tin, Adrienne, Tonjes, Anke, Varbo, Anette, Witte, Daniel R, Wood, Andrew R, Yajnik, Pranav, Yao, Jie, Yengo, Loic, Young, Robin, Amouyel, Philippe, Boeing, Heiner, Boerwinkle, Eric, Bottinger, Erwin P, Chowdhury, Rajiv, Collins, Francis S, Dedoussis, George, Dehghan, Abbas, Deloukas, Panos, Ferrario, Marco M, Ferrieres, Jean, Florez, Jose C, Frossard, Philippe, Gudnason, Vilmundur, Harris, Tamara B, Heckbert, Susan R, Howson, Joanna MM, Ingelsson, Martin, Kathiresan, Sekar, Kee, Frank, Kuusisto, Johanna, Langenberg, Claudia, Launer, Lenore J, Lindgren, Cecilia M, Mannisto, Satu, Meitinger, Thomas, Melander, Olle, Mohlke, Karen L, Moitry, Marie, Morris, Andrew D, Murray, Alison D, de Mutsert, Renee, Orho-Melander, Marju, Owen, Katharine R, Perola, Markus, Peters, Annette, Province, Michael A, Rasheed, Asif, Ridker, Paul M, Rivadineira, Fernando, Rosendaal, Frits R, Rosengren, Anders H, Salomaa, Veikko, Sheu, Wayne H-H, Sladek, Rob, Smith, Blair H, Strauch, Konstantin, Uitterlinden, Andre G, Varma, Rohit, Willer, Cristen J, Bluher, Matthias, Butterworth, Adam S, Chambers, John Campbell, Chasman, Daniel I, Danesh, John, van Duijn, Cornelia, Dupuis, Josee, Franco, Oscar H, Franks, Paul W, Froguel, Philippe, Grallert, Harald, Groop, Leif, Han, Bok-Ghee, Hansen, Torben, Hattersley, Andrew T, Hayward, Caroline, Ingelsson, Erik, Kardia, Sharon LR, Karpe, Fredrik, Kooner, Jaspal Singh, Kottgen, Anna, Kuulasmaa, Kari, Laakso, Markku, Lin, Xu, Lind, Lars, Liu, Yongmei, Loos, Ruth JF, Marchini, Jonathan, Metspalu, Andres, Mook-Kanamori, Dennis, Nordestgaard, Borge G, Palmer, Colin NA, Pankow, James S, Pedersen, Oluf, Psaty, Bruce M, Rauramaa, Rainer, Sattar, Naveed, Schulze, Matthias B, Soranzo, Nicole, Spector, Timothy D, Stefansson, Kari, Stumvoll, Michael, Thorsteinsdottir, Unnur, Tuomi, Tiinamaija, Tuomilehto, Jaakko, Wareham, Nicholas J, Wilson, James G, Zeggini, Eleftheria, Scott, Robert A, Barroso, Ines, Frayling, Timothy M, Goodarzi, Mark O, Meigs, James B, Boehnke, Michael, Saleheen, Danish, Morris, Andrew P, Rotter, Jerome I, McCarthy, Mark I, Consortium, ExomeBP, Consortium, MAGIC and Consortium, GIANT
(2018)
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.
NATURE GENETICS, 50 (4).
559-571+.
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Wuttke, Matthias, Li, Yong, Li, Man, Sieber, Karsten B, Feitosa, Mary F, Gorski, Mathias, Tin, Adrienne, Wang, Lihua, Chu, Audrey Y, Hoppmann, Anselm et al (show 318 more authors) , Kirsten, Holger, Giri, Ayush, Chai, Jin-Fang, Sveinbjornsson, Gardar, Tayo, Bamidele O, Nutile, Teresa, Fuchsberger, Christian, Marten, Jonathan, Cocca, Massimiliano, Ghasemi, Sahar, Xu, Yizhe, Horn, Katrin, Noce, Damia, Van der Most, Peter J, Sedaghat, Sanaz, Yu, Zhi, Akiyama, Masato, Afaq, Saima, Ahluwalia, Tarunveer S, Almgren, Peter, Amin, Najaf, Arnlov, Johan, Bakker, Stephan JL, Bansal, Nisha, Baptista, Daniela, Bergmann, Sven, Biggs, Mary L, Biino, Ginevra, Boehnke, Michael, Boerwinkle, Eric, Boissel, Mathilde, Bottinger, Erwin P, Boutin, Thibaud S, Brenner, Hermann, Brumat, Marco, Burkhardt, Ralph, Butterworth, Adam S, Campana, Eric, Campbell, Archie, Campbell, Harry, Canouil, Mickael, Carroll, Robert J, Catamo, Eulalia, Chambers, John C, Chee, Miao-Ling, Chee, Miao-Li, Chen, Xu, Cheng, Ching-Yu, 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M, Edward, Digna R Velez, Verweij, Niek, Vogelezang, Suzanne, Volker, Uwe, Vollenweider, Peter, Waeber, Gerard, Waldenberger, Melanie, Wallentin, Lars, Wang, Ya Xing, Wang, Chaolong, Waterworth, Dawn M, Bin Wei, Wen, White, Harvey, Whitfield, John B, Wild, Sarah H, Wilson, James F, Wojczynski, Mary K, Wong, Charlene, Wong, Tien-Yin, Xu, Liang, Yang, Qiong, Yasuda, Masayuki, Yerges-Armstrong, Laura M, Zhang, Weihua, Zonderman, Alan B, Rotter, Jerome I, Bochud, Murielle, Psaty, Bruce M, Vitart, Veronique, Wilson, James G, Dehghan, Abbas, Parsa, Afshin, Chasman, Daniel I, Ho, Kevin, Morris, Andrew P, Devuyst, Olivier, Akilesh, Shreeram, Pendergrass, Sarah A, Sim, Xueling, Boger, Carsten A, Okada, Yukinori, Edwards, Todd L, Snieder, Harold, Stefansson, Kari, Hung, Adriana M, Heid, Iris M, Scholz, Markus, Teumer, Alexander, Kottgen, Anna and Pattaro, Cristian
(2019)
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
NATURE GENETICS, 51 (6).
957-+.