Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies
Sarwar, Nadeem, Butterworth, Adam S, Freitag, Daniel F, Gregson, John, Willeit, Peter, Gorman, Donal N, Gao, Pei, Saleheen, Danish, Rendon, Augusto, Nelson, Christopher P, Braund, Peter S, Hall, Alistair S, Chasman, Daniel I, Tybjærg-Hansen, Anne, Chambers, John C, Benjamin, Emelia J, Franks, Paul W, Clarke, Robert, Wilde, Arthur A M, Trip, Mieke D, Steri, Maristella, Witteman, Jacqueline C M, Qi, Lu, van der Schoot, C Ellen, de Faire, Ulf, Erdmann, Jeanette, Stringham, Heather M, Koenig, Wolfgang, Rader, Daniel J, Melzer, David, Reich, David, Psaty, Bruce M, Kleber, Marcus E, Panagiotakos, Demosthenes B, Willeit, Johann, Wennberg, Patrik, Woodward, Mark, Adamovic, Svetlana, Rimm, Eric B, Meade, Tom W, Gillum, Richard F, Shaffer, Jonathan A, Hofman, Albert, Onat, Altan, Sundström, Johan, Wassertheil-Smoller, Sylvia, Mellström, Dan, Gallacher, John, Cushman, Mary, Tracy, Russell P, Kauhanen, Jussi, Karlsson, Magnus, Salonen, Jukka T, Wilhelmsen, Lars, Amouyel, Philippe, Cantin, Bernard, Best, Lyle G, Ben-Shlomo, Yoav, Manson, JoAnn E, Davey-Smith, George, de Bakker, Paul I W, O'Donnell, Christopher J, Wilson, James F, Wilson, Anthony G, Assimes, Themistocles L, Jansson, John-Olov, Ohlsson, Claes, Tivesten, Åsa, Ljunggren, Östen, Reilly, Muredach P, Hamsten, Anders, Ingelsson, Erik, Cambien, Francois, Hung, Joseph, Thomas, G Neil, Boehnke, Michael, Schunkert, Heribert, Asselbergs, Folkert W, Kastelein, John J P, Gudnason, Vilmundur, Salomaa, Veikko, Harris, Tamara B, Kooner, Jaspal S, Allin, Kristine H, Nordestgaard, Børge G, Hopewell, Jemma C, Goodall, Alison H, Ridker, Paul M, Hólm, Hilma, Watkins, Hugh, Ouwehand, Willem H, Samani, Nilesh J, Kaptoge, Stephen, Di Angelantonio, Emanuele, Harari, Olivier, Danesh, John
Published in The Lancet (British edition) (2012)
Published in The Lancet (British edition) (2012)
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Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder
Jia, Xiaoming, Goes, Fernando S, Locke, Adam E, Palmer, Duncan, Wang, Weiqing, Cohen-Woods, Sarah, Genovese, Giulio, Jackson, Anne U, Jiang, Chen, Kvale, Mark, Mullins, Niamh, Nguyen, Hoang, Pirooznia, Mehdi, Rivera, Margarita, Ruderfer, Douglas M, Shen, Ling, Thai, Khanh, Zawistowski, Matthew, Zhuang, Yongwen, Abecasis, Gonçalo, Akil, Huda, Bergen, Sarah, Burmeister, Margit, Chapman, Sinéad, DelaBastide, Melissa, Juréus, Anders, Kang, Hyun Min, Kwok, Pui-Yan, Li, Jun Z, Levy, Shawn E, Monson, Eric T, Moran, Jennifer, Sobell, Janet, Watson, Stanley, Willour, Virginia, Zöllner, Sebastian, Adolfsson, Rolf, Blackwood, Douglas, Boehnke, Michael, Breen, Gerome, Corvin, Aiden, Craddock, Nick, DiFlorio, Arianna, Hultman, Christina M, Landen, Mikael, Lewis, Cathryn, McCarroll, Steven A, Richard McCombie, W, McGuffin, Peter, McIntosh, Andrew, McQuillin, Andrew, Morris, Derek, Myers, Richard M, O'Donovan, Michael, Ophoff, Roel, Boks, Marco, Kahn, Rene, Ouwehand, Willem, Owen, Michael, Pato, Carlos, Pato, Michele, Posthuma, Danielle, Potash, James B, Reif, Andreas, Sklar, Pamela, Smoller, Jordan, Sullivan, Patrick F, Vincent, John, Walters, James, Neale, Benjamin, Purcell, Shaun, Risch, Neil, Schaefer, Catherine, Stahl, Eli A, Zandi, Peter P, Scott, Laura J
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Published in Molecular psychiatry (01.09.2021)
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Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome
Collins, Francis S, Eriksson, Maria, Brown, W. Ted, Gordon, Leslie B, Glynn, Michael W, Singer, Joel, Scott, Laura, Erdos, Michael R, Robbins, Christiane M, Moses, Tracy Y, Berglund, Peter, Dutra, Amalia, Pak, Evgenia, Durkin, Sandra, Csoka, Antonei B, Boehnke, Michael, Glover, Thomas W
Published in Nature (London) (15.05.2003)
Published in Nature (London) (15.05.2003)
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Metabolic and cardiovascular traits: an abundance of recently identified common genetic variants
Mohlke, Karen L., Boehnke, Michael, Abecasis, Gonçalo R.
Published in Human molecular genetics (15.10.2008)
Published in Human molecular genetics (15.10.2008)
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role for coding functional variants in HNF4A in type 2 diabetes susceptibility
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Published in Diabetologia (01.01.2011)
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Improved Inference of Relationship for Pairs of Individuals
Epstein, Michael P., Duren, William L., Boehnke, Michael
Published in American journal of human genetics (01.11.2000)
Published in American journal of human genetics (01.11.2000)
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Toxic effects of indocyanine green, infracyanine green, and trypan blue on the human retinal pigmented epithelium
Kodjikian, L, Richter, T, Halberstadt, M, Beby, F, Flueckiger, F, Boehnke, M, Garweg, J G
Published in Graefe's archive for clinical and experimental ophthalmology (01.09.2005)
Published in Graefe's archive for clinical and experimental ophthalmology (01.09.2005)
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Variation in the resistin gene is associated with obesity and insulin-related phenotypes in Finnish subjects
CONNEELY, K. N, SILANDER, K, COLLINS, F. S, BOEHNKE, M, SCOTT, L. J, MOHLKE, K. L, LAZARIDIS, K. N, VALLE, T. T, TUOMILEBTO, J, BERGMAN, R. N, WATANABE, R. M, BUCHANAN, T. A
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Published in Diabetologia (01.10.2004)
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Autosomal Dominant Nanophthalmos ( NNO1) with High Hyperopia and Angle-Closure Glaucoma Maps to Chromosome 11
Othman, M.I., Sullivan, S.A., Skuta, G.L., Cockrell, D.A., Stringham, H.M., Downs, C.A., Fornés, A., Mick, A., Boehnke, M., Vollrath, D., Richards, J.E.
Published in American journal of human genetics (01.11.1998)
Published in American journal of human genetics (01.11.1998)
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Two-trait-locus linkage analysis : a powerful strategy for mapping complex genetic traits
SCHORK, N. J, BOEHNKE, M, TERWILLIGER, J. D, OTT, J
Published in American journal of human genetics (01.11.1993)
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Published in American journal of human genetics (01.11.1993)
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A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33-34
McDonald, M.T, Papenberg, K.A, Ghosh, S, Glatfelter, A.A, Biesecker, B.B, Helmbold, E.A, Markel, D.S, Zolotor, A, McKinnon, W.C, Vanderstoep, J.L, Jackson, C.E, Iannuzzi, M, Collins, F.S, Boehnke, M, Porteous, M.E, Guttmacher, A.E, Marchuk, D.A
Published in Nature genetics (01.02.1994)
Published in Nature genetics (01.02.1994)
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Large-scale association analyses identify host factors influencing human gut microbiome composition
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Published in Nature genetics (01.02.2021)
Published in Nature genetics (01.02.2021)
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Rare coding variants in ten genes confer substantial risk for schizophrenia
Poterba, Timothy, Curtis, David, Akil, Huda, Al Eissa, Mariam, Barchas, Jack D, Bigdeli, Tim B, Breen, Gerome, Buckley, Peter F, Bunney, William E, Bybjerg-Grauholm, Jonas, Chapman, Sinéad B, Chen, Wei J, Churchhouse, Claire, Craddock, Nicholas, Cusick, Caroline M, DeLisi, Lynn, Dodge, Sheila, Eskelinen, Saana, Fanous, Ayman H, Faraone, Stephen V, Fiorentino, Alessia, Francioli, Laurent, Gabriel, Stacey B, Gage, Diane, Gagliano Taliun, Sarah A, Ganna, Andrea, Genovese, Giulio, Glahn, David C, Grove, Jakob, Hall, Mei-Hua, Hämäläinen, Eija, Heyne, Henrike O, Holi, Matti, Hougaard, David M, Howrigan, Daniel P, Huang, Hailiang, Kahn, René S, Kang, Hyun Min, Karczewski, Konrad J, Kirov, George, Knowles, James A, Lee, Francis S, Lescai, Francesco, Malaspina, Dolores, Marder, Stephen R, McCarroll, Steven A, Medeiros, Helena, Milani, Lili, Morley, Christopher P, Morris, Derek W, Mortensen, Preben Bo, Myers, Richard M, Nordentoft, Merete, O'Brien, Niamh L, Olivares, Ana Maria, Ongur, Dost, Ouwehand, Willem H, Palmer, Duncan S, Paunio, Tiina, Quested, Digby, Rapaport, Mark H, Rees, Elliott, Rollins, Brandi, Satterstrom, F Kyle, Schatzberg, Alan, Scolnick, Edward, Scott, Laura J, Sharp, Sally I, Sklar, Pamela, Smoller, Jordan W, Sobell, Janet L, Solomonson, Matthew, Stahl, Eli A, Stevens, Christine R, Tiao, Grace, Watson, Stanley J, Watts, Nicholas A, Blackwood, Douglas H, Cohen, Bruce M, Corvin, Aiden P, Esko, Tõnu, Freimer, Nelson B, Glatt, Stephen J, Hultman, Christina M, McQuillin, Andrew, Palotie, Aarno, Pato, Carlos N, Pato, Michele T, Pulver, Ann E, St Clair, David, Tsuang, Ming T, Vawter, Marquis P, Walters, James T, Werge, Thomas M, Ophoff, Roel A, Sullivan, Patrick F, Owen, Michael J, O'Donovan, Michael C, Neale, Benjamin M, Daly, Mark J
Published in Nature (London) (21.04.2022)
Published in Nature (London) (21.04.2022)
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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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