New insights into the genetic etiology of Alzheimer's disease and related dementias
Bellenguez, Céline, Grenier-Boley, Benjamin, Holmans, Peter A, Kuulasmaa, Teemu, Yang, Qiong, Yaqub, Amber, Alarcón-Martín, Emilio, Alvarez, Ignacio, Tsolaki, Anthoula, Banaj, Nerisa, Beiser, Alexa, Pastor, Ana Belén, Besse, Céline, Boada, Mercè, Boerwinkle, Eric, Bûrger, Katharina, Burholt, Vanessa, Calero, Miguel, Chung, Jaeyoon, Cuccaro, Michael L, Carracedo, Ángel, Chillotti, Caterina, Clark, Christopher, Conti, Elisa, Custodero, Carlo, Daian, Delphine, Daniele, Antonio, de Witte, Lot D, Debette, Stéphanie, Del Ser, Teodoro, Denning, Nicola, DeStefano, Anita, Rossi, Paolo Dionigi, Dufouil, Carole, Foroud, Tatiana M, Fostinelli, Silvia, Frank-García, Ana, Froelich, Lutz, Fulton-Howard, Brian, García-González, Pablo, Giegling, Ina, Gomez-Fonseca, Duber, González-Pérez, Antonio, Green, Emma, Hadjigeorgiou, Georgios, Hamilton-Nelson, Kara L, Holstege, Henne, Jun, Gyungah R, Kehoe, Patrick G, Kornhuber, Johannes, Kunkle, Brian W, Kuzma, Amanda B, Laukka, Erika J, Lleó, Alberto, de Munain, Adolfo Lopez, Luckcuck, Lauren, Spallazzi, Marco, Marquié, Marta, Mecocci, Patrizia, Menéndez-González, Manuel, Molina-Porcel, Laura, Morelli, Laura, Nöthen, Markus M, Mukherjee, Shubhabrata, Nicolas, Gael, Nordestgaard, Børge G, Orellana, Adelina, Orsini, Michela, Pasquier, Florence, Pastor, Pau, Peloso, Gina, Pericard, Pierre, Pineda, Juan A, Rainero, Innocenzo, Real, Luis M, Reitz, Christiane, Rongve, Arvid, Allende, Irene Rosas, Rujescu, Dan, Sakka, Paraskevi, Juan, Pascual Sánchez, Scherbaum, Norbert, Sha, Jin, Song, Yeunjoo, Stordal, Eystein, Thalamuthu, Anbupalam, Traykov, Latchezar, Tybjærg-Hansen, Anne, Uitterlinden, Andre, van der Lugt, Aad, van Rooij, Jeroen, Vogelgsang, Jonathan, Weinhold, Leonie, Windle, Gill, Zare, Habil, Hort, Jakub, Clarimon, Jordi, Deleuze, Jean-François, Seshadri, Sudha, Ruiz, Agustín
Published in Nature genetics (2022)
Published in Nature genetics (2022)
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A cross-population atlas of genetic associations for 220 human phenotypes
Sakaue, Saori, Kanai, Masahiro, Tanigawa, Yosuke, Karjalainen, Juha, Kurki, Mitja, Koshiba, Seizo, Narita, Akira, Konuma, Takahiro, Yamamoto, Kenichi, Akiyama, Masato, Ishigaki, Kazuyoshi, Suzuki, Akari, Suzuki, Ken, Obara, Wataru, Yamaji, Ken, Takahashi, Kazuhisa, Asai, Satoshi, Takahashi, Yasuo, Suzuki, Takao, Shinozaki, Nobuaki, Yamaguchi, Hiroki, Minami, Shiro, Murayama, Shigeo, Yoshimori, Kozo, Nagayama, Satoshi, Obata, Daisuke, Higashiyama, Masahiko, Masumoto, Akihide, Koretsune, Yukihiro, Ito, Kaoru, Terao, Chikashi, Yamauchi, Toshimasa, Komuro, Issei, Kadowaki, Takashi, Tamiya, Gen, Yamamoto, Masayuki, Nakamura, Yusuke, Kubo, Michiaki, Murakami, Yoshinori, Yamamoto, Kazuhiko, Kamatani, Yoichiro, Palotie, Aarno, Rivas, Manuel A, Daly, Mark J, Matsuda, Koichi, Okada, Yukinori
Published in Nature genetics (01.10.2021)
Published in Nature genetics (01.10.2021)
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Large-scale association analyses identify host factors influencing human gut microbiome composition
Kurilshikov, Alexander, Medina-Gomez, Carolina, Bacigalupe, Rodrigo, Wang, Jun, Demirkan, Ayse, Le Roy, Caroline I, Raygoza Garay, Juan Antonio, Finnicum, Casey T, Liu, Xingrong, Zhernakova, Daria V, Bonder, Marc Jan, Hansen, Tue H, Frost, Fabian, Rühlemann, Malte C, Turpin, Williams, Moon, Jee-Young, Kim, Han-Na, Lüll, Kreete, Barkan, Elad, Shah, Shiraz A, Szopinska-Tokov, Joanna, Wallen, Zachary D, Borisevich, Dmitrii, Andreasson, Anna, Bang, Corinna, Bedrani, Larbi, Bisgaard, Hans, Boehnke, Michael, Boomsma, Dorret I, Burk, Robert D, Claringbould, Annique, Croitoru, Kenneth, Davies, Gareth E, van Duijn, Cornelia M, Duijts, Liesbeth, Falony, Gwen, Fu, Jingyuan, van der Graaf, Adriaan, Hansen, Torben, Homuth, Georg, Hughes, David A, Ijzerman, Richard G, Jackson, Matthew A, Jaddoe, Vincent W V, Joossens, Marie, Jørgensen, Torben, Keszthelyi, Daniel, Knight, Rob, Laakso, Markku, Laudes, Matthias, Launer, Lenore J, Lieb, Wolfgang, Lusis, Aldons J, Masclee, Ad A M, Moll, Henriette A, Mujagic, Zlatan, Qibin, Qi, Rothschild, Daphna, Shin, Hocheol, Sørensen, Søren J, Steves, Claire J, Thorsen, Jonathan, Timpson, Nicholas J, Tito, Raul Y, Vieira-Silva, Sara, Völker, Uwe, Völzke, Henry, Võsa, Urmo, Wade, Kaitlin H, Walter, Susanna, Watanabe, Kyoko, Weiss, Stefan, Weiss, Frank U, Weissbrod, Omer, Westra, Harm-Jan, Willemsen, Gonneke, Payami, Haydeh, Jonkers, Daisy M A E, Arias Vasquez, Alejandro, de Geus, Eco J C, Meyer, Katie A, Stokholm, Jakob, Segal, Eran, Org, Elin, Wijmenga, Cisca, Kim, Hyung-Lae, Kaplan, Robert C, Spector, Tim D, Uitterlinden, Andre G, Rivadeneira, Fernando, Franke, Andre, Lerch, Markus M, Franke, Lude, Sanna, Serena, D'Amato, Mauro, Pedersen, Oluf, Paterson, Andrew D, Kraaij, Robert, Raes, Jeroen, Zhernakova, Alexandra
Published in Nature genetics (01.02.2021)
Published in Nature genetics (01.02.2021)
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Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
Võsa, Urmo, Claringbould, Annique, Bonder, Marc Jan, Deelen, Patrick, Zeng, Biao, Kirsten, Holger, Saha, Ashis, Yazar, Seyhan, Brugge, Harm, Oelen, Roy, van der Wijst, Monique G P, Kasela, Silva, Pervjakova, Natalia, Alves, Isabel, Favé, Marie-Julie, Agbessi, Mawussé, Christiansen, Mark W, Jansen, Rick, Seppälä, Ilkka, Tong, Lin, Teumer, Alexander, Schramm, Katharina, Verlouw, Joost, Yaghootkar, Hanieh, Sönmez Flitman, Reyhan, Brown, Andrew, Kukushkina, Viktorija, Kalnapenkis, Anette, Rüeger, Sina, Porcu, Eleonora, Kronberg, Jaanika, Kettunen, Johannes, Lee, Bernett, Zhang, Futao, Qi, Ting, Hernandez, Jose Alquicira, Arindrarto, Wibowo, Beutner, Frank, Dmitrieva, Julia, Elansary, Mahmoud, Fairfax, Benjamin P, Georges, Michel, Heijmans, Bastiaan T, Hewitt, Alex W, Kähönen, Mika, Kim, Yungil, Knight, Julian C, Kovacs, Peter, Krohn, Knut, Li, Shuang, Loeffler, Markus, Marigorta, Urko M, Mei, Hailang, Momozawa, Yukihide, Müller-Nurasyid, Martina, Nauck, Matthias, Nivard, Michel G, Penninx, Brenda W J H, Pritchard, Jonathan K, Raitakari, Olli T, Rotzschke, Olaf, Slagboom, Eline P, Stehouwer, Coen D A, Stumvoll, Michael, Sullivan, Patrick, 't Hoen, Peter A C, Thiery, Joachim, Tönjes, Anke, van Dongen, Jenny, van Iterson, Maarten, Völker, Uwe, Warmerdam, Robert, Wijmenga, Cisca, Swertz, Morris, Andiappan, Anand, Montgomery, Grant W, Ripatti, Samuli, Perola, Markus, Kutalik, Zoltan, Dermitzakis, Emmanouil, Bergmann, Sven, Frayling, Timothy, van Meurs, Joyce, Prokisch, Holger, Ahsan, Habibul, Pierce, Brandon L, Lehtimäki, Terho, Psaty, Bruce M, Gharib, Sina A, Awadalla, Philip, Milani, Lili, Ouwehand, Willem H, Downes, Kate, Battle, Alexis, Yang, Jian, Scholz, Markus, Powell, Joseph, Gibson, Greg, Esko, Tõnu, Franke, Lude
Published in Nature genetics (01.09.2021)
Published in Nature genetics (01.09.2021)
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Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
Mullins, Niamh, Forstner, Andreas J, Coleman, Jonathan R I, Qiao, Zhen, Kim, Minsoo, Panagiotaropoulou, Georgia, Trubetskoy, Vassily, Won, Hong-Hee, Alliey-Rodriguez, Ney, Antilla, Verneri, Awasthi, Swapnil, Bækvad-Hansen, Marie, Bauer, Michael, Beins, Eva C, Bergen, Sarah E, Bøcker Pedersen, Carsten, Bosch, Rosa, Budde, Monika, Byerley, William, Casas, Miquel, Cruceanu, Cristiana, Czerski, Piotr M, Degenhardt, Franziska, Douzenis, Athanassios, Elvsåshagen, Torbjørn, Escott-Price, Valentina, Frisén, Louise, Gizer, Ian R, Gordon-Smith, Katherine, Grove, Jakob, Hautzinger, Martin, Huckins, Laura, Johnson, Jessica S, Koromina, Maria, Kranz, Thorsten M, Kranzler, Henry R, Kubo, Michiaki, Lee, Phil H, Lewis, Catrin, Liao, Calwing, Lundberg, Martin, Maihofer, Adam, Martinsson, Lina, McGregor, Nathaniel W, Medeiros, Helena, Moran, Jennifer L, O'Brien, Niamh, Oruc, Lilijana, Quested, Digby, Raj, Towfique, Rapaport, Mark H, DePaulo, J Raymond, Rivas, Fabio, Senner, Fanny, Sharp, Sally, Søholm Hansen, Christine, Soler Artigas, Maria, Stein, Dan J, Terao, Chikashi, Toma, Claudio, Tooney, Paul, Witt, Stephanie H, Yang, Jessica Mei Kay, Alda, Martin, Babadjanova, Gulja, Baune, Bernhard T, Boehnke, Michael, Carr, Vaughan J, Dannlowski, Udo, Dikeos, Dimitris, Fullerton, Janice M, Gawlik, Micha, Green, Melissa J, Hauser, Joanna, Hong, Kyung Sue, Jones, Ian, Jones, Lisa A, Kelsoe, John R, Landén, Mikael, Lewis, Cathryn M, Loughland, Carmel, Martin, Nicholas G, Melle, Ingrid, Mowry, Bryan, Nordentoft, Merete, Olsson, Tomas, Schalling, Martin, Schofield, Peter R, Serretti, Alessandro, Shannon Weickert, Cynthia, Smoller, Jordan W, Stefansson, Hreinn, Streit, Fabian, Turecki, Gustavo, Vieta, Eduard, Werge, Thomas, Biernacka, Joanna M, Stahl, Eli A, Di Florio, Arianna, Ophoff, Roel A
Published in Nature genetics (01.06.2021)
Published in Nature genetics (01.06.2021)
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A single-cell and spatially resolved atlas of human breast cancers
Wu, Sunny Z, Al-Eryani, Ghamdan, Roden, Daniel Lee, Junankar, Simon, Harvey, Kate, Andersson, Alma, Thennavan, Aatish, Wang, Chenfei, Torpy, James R, Bartonicek, Nenad, Wang, Taopeng, Larsson, Ludvig, Kaczorowski, Dominik, Weisenfeld, Neil I, Uytingco, Cedric R, Chew, Jennifer G, Bent, Zachary W, Chan, Chia-Ling, Gnanasambandapillai, Vikkitharan, Dutertre, Charles-Antoine, Gluch, Laurence, Hui, Mun N, Beith, Jane, Parker, Andrew, Robbins, Elizabeth, Segara, Davendra, Cooper, Caroline, Mak, Cindy, Chan, Belinda, Warrier, Sanjay, Ginhoux, Florent, Millar, Ewan, Powell, Joseph E, Williams, Stephen R, Liu, X Shirley, O'Toole, Sandra, Lim, Elgene, Lundeberg, Joakim, Perou, Charles M, Swarbrick, Alexander
Published in Nature genetics (01.09.2021)
Published in Nature genetics (01.09.2021)
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Tumor mutational load predicts survival after immunotherapy across multiple cancer types
Samstein, Robert M, Lee, Chung-Han, Shoushtari, Alexander N, Hellmann, Matthew D, Shen, Ronglai, Janjigian, Yelena Y, Barron, David A, Zehir, Ahmet, Jordan, Emmet J, Omuro, Antonio, Kaley, Thomas J, Kendall, Sviatoslav M, Motzer, Robert J, Hakimi, A Ari, Voss, Martin H, Russo, Paul, Rosenberg, Jonathan, Iyer, Gopa, Bochner, Bernard H, Bajorin, Dean F, Al-Ahmadie, Hikmat A, Chaft, Jamie E, Rudin, Charles M, Riely, Gregory J, Baxi, Shrujal, Ho, Alan L, Wong, Richard J, Pfister, David G, Wolchok, Jedd D, Barker, Christopher A, Gutin, Philip H, Brennan, Cameron W, Tabar, Viviane, Mellinghoff, Ingo K, DeAngelis, Lisa M, Ariyan, Charlotte E, Lee, Nancy, Tap, William D, Gounder, Mrinal M, D'Angelo, Sandra P, Saltz, Leonard, Stadler, Zsofia K, Scher, Howard I, Baselga, Jose, Razavi, Pedram, Klebanoff, Christopher A, Yaeger, Rona, Segal, Neil H, Ku, Geoffrey Y, DeMatteo, Ronald P, Ladanyi, Marc, Rizvi, Naiyer A, Berger, Michael F, Riaz, Nadeem, Solit, David B, Chan, Timothy A, Morris, Luc G T
Published in Nature genetics (01.02.2019)
Published in Nature genetics (01.02.2019)
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Clinical use of current polygenic risk scores may exacerbate health disparities
Martin, Alicia R, Kanai, Masahiro, Kamatani, Yoichiro, Okada, Yukinori, Neale, Benjamin M, Daly, Mark J
Published in Nature genetics (01.04.2019)
Published in Nature genetics (01.04.2019)
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A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease
Wightman, Douglas P, Jansen, Iris E, Savage, Jeanne E, Shadrin, Alexey A, Bahrami, Shahram, Holland, Dominic, Rongve, Arvid, Børte, Sigrid, Winsvold, Bendik S, Drange, Ole Kristian, Martinsen, Amy E, Skogholt, Anne Heidi, Willer, Cristen, Bråthen, Geir, Bosnes, Ingunn, Nielsen, Jonas Bille, Fritsche, Lars G, Thomas, Laurent F, Pedersen, Linda M, Gabrielsen, Maiken E, Johnsen, Marianne Bakke, Meisingset, Tore Wergeland, Zhou, Wei, Proitsi, Petroula, Hodges, Angela, Dobson, Richard, Velayudhan, Latha, Heilbron, Karl, Auton, Adam, Sealock, Julia M, Davis, Lea K, Pedersen, Nancy L, Reynolds, Chandra A, Karlsson, Ida K, Magnusson, Sigurdur, Stefansson, Hreinn, Thordardottir, Steinunn, Jonsson, Palmi V, Snaedal, Jon, Zettergren, Anna, Skoog, Ingmar, Kern, Silke, Waern, Margda, Zetterberg, Henrik, Blennow, Kaj, Stordal, Eystein, Hveem, Kristian, Zwart, John-Anker, Athanasiu, Lavinia, Selnes, Per, Saltvedt, Ingvild, Sando, Sigrid B, Ulstein, Ingun, Djurovic, Srdjan, Fladby, Tormod, Aarsland, Dag, Selbæk, Geir, Ripke, Stephan, Stefansson, Kari, Andreassen, Ole A, Posthuma, Danielle
Published in Nature genetics (01.09.2021)
Published in Nature genetics (01.09.2021)
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Computationally efficient whole-genome regression for quantitative and binary traits
Mbatchou, Joelle, Barnard, Leland, Backman, Joshua, Marcketta, Anthony, Kosmicki, Jack A, Ziyatdinov, Andrey, Benner, Christian, O'Dushlaine, Colm, Barber, Mathew, Boutkov, Boris, Habegger, Lukas, Ferreira, Manuel, Baras, Aris, Reid, Jeffrey, Abecasis, Goncalo, Maxwell, Evan, Marchini, Jonathan
Published in Nature genetics (01.07.2021)
Published in Nature genetics (01.07.2021)
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Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk
Jansen, Iris E, Savage, Jeanne E, Watanabe, Kyoko, Bryois, Julien, Williams, Dylan M, Steinberg, Stacy, Sealock, Julia, Karlsson, Ida K, Hägg, Sara, Athanasiu, Lavinia, Voyle, Nicola, Proitsi, Petroula, Witoelar, Aree, Stringer, Sven, Aarsland, Dag, Almdahl, Ina S, Andersen, Fred, Bergh, Sverre, Bettella, Francesco, Bjornsson, Sigurbjorn, Brækhus, Anne, Bråthen, Geir, de Leeuw, Christiaan, Desikan, Rahul S, Djurovic, Srdjan, Dumitrescu, Logan, Fladby, Tormod, Hohman, Timothy J, Jonsson, Palmi V, Kiddle, Steven J, Rongve, Arvid, Saltvedt, Ingvild, Sando, Sigrid B, Selbæk, Geir, Shoai, Maryam, Skene, Nathan G, Snaedal, Jon, Stordal, Eystein, Ulstein, Ingun D, Wang, Yunpeng, White, Linda R, Hardy, John, Hjerling-Leffler, Jens, Sullivan, Patrick F, van der Flier, Wiesje M, Dobson, Richard, Davis, Lea K, Stefansson, Hreinn, Stefansson, Kari, Pedersen, Nancy L, Ripke, Stephan, Andreassen, Ole A, Posthuma, Danielle
Published in Nature genetics (01.03.2019)
Published in Nature genetics (01.03.2019)
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Identification of common genetic risk variants for autism spectrum disorder
Grove, Jakob, Ripke, Stephan, Als, Thomas D, Mattheisen, Manuel, Walters, Raymond K, Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A, Anney, Richard, Awashti, Swapnil, Belliveau, Rich, Bettella, Francesco, Buxbaum, Joseph D, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Christensen, Jane H, Churchhouse, Claire, Dellenvall, Karin, Demontis, Ditte, De Rubeis, Silvia, Devlin, Bernie, Djurovic, Srdjan, Dumont, Ashley L, Goldstein, Jacqueline I, Hansen, Christine S, Hauberg, Mads Engel, Hollegaard, Mads V, Hope, Sigrun, Howrigan, Daniel P, Huang, Hailiang, Hultman, Christina M, Klei, Lambertus, Maller, Julian, Martin, Joanna, Martin, Alicia R, Moran, Jennifer L, Nyegaard, Mette, Nærland, Terje, Palmer, Duncan S, Palotie, Aarno, Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, dPoterba, Timothy, Poulsen, Jesper Buchhave, Pourcain, Beate St, Qvist, Per, Rehnström, Karola, Reichenberg, Abraham, Reichert, Jennifer, Robinson, Elise B, Roeder, Kathryn, Roussos, Panos, Saemundsen, Evald, Sandin, Sven, Satterstrom, F Kyle, Davey Smith, George, Stefansson, Hreinn, Steinberg, Stacy, Stevens, Christine R, Sullivan, Patrick F, Turley, Patrick, Walters, G Bragi, Xu, Xinyi, Stefansson, Kari, Geschwind, Daniel H, Nordentoft, Merete, Hougaard, David M, Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Neale, Benjamin M, Daly, Mark J, Børglum, Anders D
Published in Nature genetics (01.03.2019)
Published in Nature genetics (01.03.2019)
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Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations
Khera, Amit V, Chaffin, Mark, Aragam, Krishna G, Haas, Mary E, Roselli, Carolina, Choi, Seung Hoan, Natarajan, Pradeep, Lander, Eric S, Lubitz, Steven A, Ellinor, Patrick T, Kathiresan, Sekar
Published in Nature genetics (01.09.2018)
Published in Nature genetics (01.09.2018)
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Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
Demontis, Ditte, Walters, Raymond K, Martin, Joanna, Mattheisen, Manuel, Als, Thomas D, Agerbo, Esben, Baldursson, Gísli, Belliveau, Rich, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Eriksson, Nicholas, Gandal, Michael, Goldstein, Jacqueline I, Grasby, Katrina L, Grove, Jakob, Gudmundsson, Olafur O, Hansen, Christine S, Hauberg, Mads Engel, Hollegaard, Mads V, Howrigan, Daniel P, Huang, Hailiang, Maller, Julian B, Martin, Alicia R, Martin, Nicholas G, Moran, Jennifer, Pallesen, Jonatan, Palmer, Duncan S, Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, Poterba, Timothy, Poulsen, Jesper Buchhave, Ripke, Stephan, Robinson, Elise B, Satterstrom, F Kyle, Stefansson, Hreinn, Stevens, Christine, Turley, Patrick, Walters, G Bragi, Won, Hyejung, Wright, Margaret J, Andreassen, Ole A, Asherson, Philip, Burton, Christie L, Boomsma, Dorret I, Cormand, Bru, Dalsgaard, Søren, Franke, Barbara, Gelernter, Joel, Geschwind, Daniel, Hakonarson, Hakon, Haavik, Jan, Kranzler, Henry R, Kuntsi, Jonna, Langley, Kate, Lesch, Klaus-Peter, Middeldorp, Christel, Reif, Andreas, Rohde, Luis Augusto, Roussos, Panos, Schachar, Russell, Sklar, Pamela, Sonuga-Barke, Edmund J S, Sullivan, Patrick F, Thapar, Anita, Tung, Joyce Y, Waldman, Irwin D, Medland, Sarah E, Stefansson, Kari, Nordentoft, Merete, Hougaard, David M, Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Daly, Mark J, Faraone, Stephen V, Børglum, Anders D, Neale, Benjamin M
Published in Nature genetics (01.01.2019)
Published in Nature genetics (01.01.2019)
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Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
Liu, Mengzhen, Jiang, Yu, Wedow, Robbee, Li, Yue, Chen, Fang, Datta, Gargi, Davila-Velderrain, Jose, McGuire, Daniel, Zhan, Xiaowei, Choquet, Hélène, Docherty, Anna R, Faul, Jessica D, Foerster, Johanna R, Gabrielsen, Maiken Elvestad, Gordon, Scott D, Haessler, Jeffrey, Hottenga, Jouke-Jan, Huang, Hongyan, Jang, Seon-Kyeong, Jansen, Philip R, Mägi, Reedik, McMahon, George, Mulas, Antonella, Orrù, Valeria, Palviainen, Teemu, Pandit, Anita, Reginsson, Gunnar W, Skogholt, Anne Heidi, Smith, Jennifer A, Taylor, Amy E, Turman, Constance, Willemsen, Gonneke, Young, Hannah, Zajac, Gregory J M, Zhao, Wei, Zhou, Wei, Bjornsdottir, Gyda, Boardman, Jason D, Boehnke, Michael, Boomsma, Dorret I, Cucca, Francesco, Davies, Gareth E, Eaton, Charles B, Ehringer, Marissa A, Esko, Tõnu, Fiorillo, Edoardo, Haller, Toomas, Harris, Kathleen Mullan, Heath, Andrew C, Hewitt, John K, Hickie, Ian B, Hokanson, John E, Hopfer, Christian J, Hunter, David J, Iacono, William G, Johnson, Eric O, Kamatani, Yoichiro, Kardia, Sharon L R, Kellis, Manolis, Kooperberg, Charles, Kraft, Peter, Krauter, Kenneth S, Laakso, Markku, Lind, Penelope A, Loukola, Anu, Lutz, Sharon M, Madden, Pamela A F, Martin, Nicholas G, McQueen, Matthew B, Medland, Sarah E, Mohlke, Karen L, Nielsen, Jonas B, Okada, Yukinori, Peters, Ulrike, Polderman, Tinca J C, Posthuma, Danielle, Reiner, Alexander P, Rice, John P, Rimm, Eric, Rose, Richard J, Runarsdottir, Valgerdur, Stallings, Michael C, Stančáková, Alena, Stefansson, Hreinn, Thai, Khanh K, Weir, David R, Weisner, Constance, Whitfield, John B, Hveem, Kristian, Lee, James J, Munafò, Marcus R, Saccone, Nancy L, Cornelis, Marilyn C, Hinds, David A, Jorgenson, Eric, Kaprio, Jaakko, Stitzel, Jerry A, Stefansson, Kari, Liu, Dajiang J, Vrieze, Scott
Published in Nature genetics (01.02.2019)
Published in Nature genetics (01.02.2019)
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Journal Article
Genome-wide association study identifies 30 loci associated with bipolar disorder
Stahl, Eli A, Forstner, Andreas J, McQuillin, Andrew, Coleman, Jonathan R I, de Leeuw, Christiaan A, Steinberg, Stacy, Pavlides, Jennifer M Whitehead, Richards, Alexander L, Akil, Huda, Als, Thomas D, Awasthi, Swapnil, Barchas, Jack D, Boks, Marco P, Byerley, William, Casas, Miquel, Cerrato, Felecia, Craig, David W, Czerski, Piotr M, Dale, Anders M, de Jong, Simone, Degenhardt, Franziska, Djurovic, Srdjan, Fan, Chun Chieh, Forty, Liz, Frank, Josef, Fraser, Christine, Freimer, Nelson B, Gade, Katrin, Garnham, Julie, Goldstein, Jaqueline, Greenwood, Tiffany A, Hautzinger, Martin, Heilbronner, Urs, Herms, Stefan, Hoffmann, Per, Holland, Dominic, Huckins, Laura, Jamain, Stéphane, Johnson, Jessica S, Kandaswamy, Radhika, Lavebratt, Catharina, Levy, Shawn E, MacIntyre, Donald J, Martinsson, Lina, McInnis, Melvin G, McKay, James D, Montgomery, Grant W, Adolfsson, Annelie Nordin, Ori, Anil P S, Pfennig, Andrea, Regeer, Eline J, Reif, Andreas, Rivas, Fabio, Scheftner, William A, Shilling, Paul D, Slaney, Claire, Søholm Hansen, Christine, Spijker, Anne T, Streit, Fabian, Vedder, Helmut, Weickert, Thomas W, Xi, Simon, Xu, Wei, Zhang, Peng, Alda, Martin, Backlund, Lena, Baune, Bernhard T, Berrettini, Wade H, Blackwood, Douglas H R, Boehnke, Michael, Craddock, Nicholas, Esko, Tõnu, Etain, Bruno, Frye, Mark, Fullerton, Janice M, Gershon, Elliot S, Goes, Fernando, Hauser, Joanna, Hougaard, David M, Hultman, Christina M, Kahn, René S, Kirov, George, Leboyer, Marion, Mitchell, Philip B, Mors, Ole, Nöthen, Markus M, Oedegaard, Ketil J, Owen, Michael J, Paciga, Sara A, Pato, Carlos, Ramos-Quiroga, Josep Antoni, Schofield, Peter R, Serretti, Alessandro, Smoller, Jordan W, Vaaler, Arne E, Vieta, Eduard, Nurnberger, John I, Ophoff, Roel A, Andreassen, Ole A, Kelsoe, John
Published in Nature genetics (01.05.2019)
Published in Nature genetics (01.05.2019)
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Large-scale integration of the plasma proteome with genetics and disease
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Published in Nature genetics (01.12.2021)
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Published in Nature genetics (01.08.2018)
Published in Nature genetics (01.08.2018)
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