GlobalView
Ripke, Stephan

Your search on Stephan Chalup produced these results.

Showing items 1 - 9 of 9.

Add to Quick Collection   All 9 Results

  • First
  • Previous
  • 1
  • Next
  • Last
Sort:
 Add All Items to Quick Collection
Date: 2015
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.13/1317269
Description: Polygenic risk scores have shown great promise in predicting complex disease risk and will become more accurate as training sample sizes increase. The standard approach for calculating risk scores inv... More
Reviewed: Reviewed
Date: 2015
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.13/1332788
Description: Objective: IBS shows genetic predisposition, but adequately powered gene-hunting efforts have been scarce so far. We sought to identify true IBS genetic risk factors by means of genome-wide associatio... More
Reviewed: Reviewed
Date: 2015
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.13/1339677
Description: Both polygenicity (many small genetic effects) and confounding biases, such as cryptic relatedness and population stratification, can yield an inflated distribution of test statistics in genome-wide a... More
Reviewed: Reviewed
Date: 2014
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.13/1301958
Description: Regulatory and coding variants are known to be enriched with associations identified by genome-wide association studies (GWASs) of complex disease, but their contributions to trait heritability are cu... More
Reviewed: Reviewed
Date: 2013
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.13/1305393
Description: Background: Thousands of common single nucleotide polymorphisms (SNPs) are weakly associated with schizophrenia. It is likely that subsets of disease-associated SNPs are associated with distinct herit... More
Reviewed: Reviewed
Date: 2016
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.13/1345438
Description: Genome-wide association studies (GWAS) of schizophrenia have yielded more than 100 common susceptibility variants, and strongly support a substantial polygenic contribution of a large number of small ... More
Reviewed: Reviewed
Creators: Ripke, Stephan | Neale, Benjamin M. | Pers, Tune H. | Julià, Antonio | Kahn, René S. | Kalaydjieva, Luba | Karachanak-Yankova, Sena | Karjalainen, Juha | Kavanagh, David | Keller, Matthew C. | Kennedy, James L. | Khrunin, Audrey | Kim, Yunjung | Agartz, Iingrid | Klovins, Janis | Knowles, James A. | Konte, Bettina | Kucinskas, Vaidutis | Ausrele Kucinskiene, Zita | Kuzelova-Ptackova, Hana | Kähler, Anna K. | Laurent, Claudine | Lee Chee Keong, Jimmy | Hong Lee, S. | Agerbo, Esben | Legge, Sophie E. | Lerer, Bernard | Li, Miaoxin | Li, Tao | Liang, Kung-Yee | Lieberman, Jeffrey | Limborska, Svetlana | Loughland, Carmel M. | Lubinski, Jan | Lönnqvist, Jouko | Albus, Margot | Macek Jr, Milan | Magnusson, Patrik K. E. | Maher, Brion S. | Maier, Wolfgang | Mallet, Jacques | Marsal, Sara | Mattheisen, Manuel | Mattingsdal, Morten | McCarley, Robert W. | McDonald, Colm | Alexander, Madeline | McIntosh, Andrew M. | Meier, Sandra | Meijer, Carin J. | Melegh, Bela | Melle, Iingrid | Mesholam-Gately, Raquelle I. | Metspalu, Andres | Michie, Patricia T. | Milani, Lili | Milanova, Virha | Amin, Farooq | Mokrab, Younes | Morris, Derek W. | Mors, Ole | Murphy, Kieran C. | Murray, Robin M. | Myin-Germeys, Inez | Müller-Myhsok, Bertram | Nelis, Mari | Nenadic, Igor | Nertney, Deborah A. | Bacanu, Silviu A. | Nestadt, Gerald | Nicodemus, Kristin K. | Nikitina-Zake, Liene | Nisenbaum, Laura | Nordin, Annelie | O'Callaghan, Eadbhard | O'Dushlaine, Colm | O'Neill, F. Anthony | Oh, Sang-Yun | Olincy, Ann | Begemann, Martin | Olsen, Line | Van Os, Jim | Psychosis Endophenotypes International Consortium | Pantelis, Christos | Papadimitriou, George N. | Papiol, Sergi | Parkhomenko, Elena | Pato, Michele T. | Paunio, Tiina | Pejovic-Milovancevic, Milica | Belliveau Jr, Richard A. | Perkins, Diana O. | Pietiläinen, Olli | Pimm, Jonathan | Pocklington, Andrew J. | Powell, John | Price, Alkes | Pulver, Ann E. | Purcell, Shaun M. | Quested, Digby | Rasmussen, Henrik B. | Bene, Judit | Reichenberg, Abraham | Reimers, Mark A. | Richards, Alexander L. | Roffman, Joshua L. | Roussos, Panos | Ruderfer, Douglas M. | Salomaa, Veikko | Sanders, Alan R. | Schall, Ulrich | Schubert, Christian R. | Corvin, Aiden | Bergen, Sarah E. | Schulze, Thomas G. | Schwab, Sibylle G. | Scolnick, Edward M. | Scott, Rodney J. | Seidman, Larry J. | Shi, Jianxin | Sigurdsson, Engilbert | Silagadze, Teimuraz | Silverman, Jeremy M. | Sim, Kang | Bevilacqua, Elizabeth | Slominsky, Petr | Smoller, Jordan W. | So, Hon-Cheong | Spencer, Chris C. A. | Stahl, Eli A. | Stefansson, Hreinn | Steinberg, Stacy | Stogmann, Elisabeth | Straub, Richard E. | Strengman, Eric | Bigdeli, Tim B. | Strohmaier, Jana | Scott Stroup, T. | Subramaniam, Mythily | Suvisaari, Jaana | Svrakic, Dragan M. | Szatkiewicz, Jin P. | Söderman, Erik | Thirumalai, Srinivas | Toncheva, Draga | Tosato, Sarah | Black, Donald W. | Veijola, Juha | Waddington, John | Walsh, Dermot | Wang, Dai | Wang, Qiang | Webb, Bradley T. | Weiser, Mark | Wildenauer, Dieter B. | Williams, Nigel M. | Williams, Stephanie | Bruggeman, Richard | Witt, Stephanie H. | Wolen, Aaron R. | Wong, Emily H. M. | Wormley, Brandon K. | Simon Xi, Hualin | Zai, Clement C. | Zheng, Xuebin | Zimprich, Fritz | Wray, Naomi R. | Stefansson, Kari | Buccola, Nancy G. | Visscher, Peter M. | Welcome Trust Case-Control Consortium, | Adolfsson, Rolf | Andreassen, Ole A. | Blackwood, Douglas H. R. | Bramon, Elvira | Buxbaum, Joseph D. | Børglum, Anders D. | Cichon, Sven | Darvasi, Ariel | Buckner, Randy L. | Domenici, Enrico | Ehrenreich, Hannelore | Esko, Tõnu | Gejman, Pablo V. | Gill, Michael | Gurling, Hugh | Hultman, Christina M. | Iwata, Nakao | Jablensky, Assen V. | Jönsson, Erik G. | Byerley, William | Kendler, Kenneth S. | Kirov, George | Knight, Jo | Lencz, Todd | Levinson, Douglas F. | Li, Qingqin S. | Liu, Jianjun | Malhotra, Anil K. | McCarroll, Steven A. | McQuillin, Andrew | Cahn, Wiepke | Moran, Jennifer L. | Mortensen, Preben B. | Mowry, Bryan J. | Nöthen, Markus M. | Ophoff, Roel A. | Owen, Michael J. | Palotie, Aarno | Pato, Carlos N. | Petryshen, Tracey L. | Posthuma, Danielle | Cai, Guiqing | Rietschel, Marcella | Riley, Brien P. | Rujescu, Dan | Sham, Pak C. | Sklar, Pamela | St Clair, David | Weinberger, David R. | Wendland, Jens R. | Werge, Thomas | Daly, Mark J. | Walters, James T. R. | Campion, Dominique | Sullivan, Patrick F. | O'Donovan, Michael C. | Cantor, Rita M. | Carr, Vaughan J. | Carrera, Noa | Catts, Stanley V. | Chambert, Kimberly D. | Chan, Raymond C. K. | Chen, Ronald Y. L. | Chen, Eric Y. H. | Cheng, Wei | Farh, Kai-How | Cheung, Eric F. C. | Ann Chong, Siow | Robert Cloninger, C. | Cohen, David | Cohen, Nadine | Cormican, Paul | Craddock, Nick | Crowley, James J. | Curtis, David | Davidson, Michael | Holmans, Peter A. | Davis, Kenneth L. | Degenhardt, Franziska | Del Favero, Jurgen | Demontis, Ditte | Dikeos, Dimitris | Dinan, Timothy | Djurovic, Srdjan | Donohoe, Gary | Drapeau, Elodie | Duan, Jubao | Lee, Phil | Dudbridge, Frank | Durmishi, Naser | Eichhammer, Peter | Eriksson, Johan | Escott-Price, Valentina | Essioux, Laurent | Fanous, Ayman H. | Farrell, Martilias S. | Frank, Josef | Franke, Lude | Bulik-Sullivan, Brendan | Freedman, Robert | Freimer, Nelson B. | Friedl, Marion | Friedman, Joseph I. | Fromer, Menachem | Genovese, Giulio | Georgieva, Lyudmila | Giegling, Ina | Giusti-Rodríguez, Paola | Godard, Stephanie | Collier, David A. | Goldstein, Jacqueline I. | Golimbet, Vera | Gopal, Srihari | Gratten, Jacob | de Haan, Lieuwe | Hammer, Christian | Hamshere, Marian L. | Hansen, Mark | Hansen, Thomas | Haroutunian, Vahram | Huang, Hailiang | Hartmann, Annette M. | Henskens, Frans A. | Herms, Stefan | Hirschhorn, Joel N. | Hoffmann, Per | Hofman, Andrea | Hollegaard, Mads V. | Hougaard, David M. | Ikeda, Masashi | Joa, Inge
Date: 2014
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.13/1307580
Description: Schizophrenia is a highly heritable disorder. Genetic risk is conferred by a large number of alleles, including common alleles of small effect that might be detected by genome-wide association studies... More
Reviewed: Reviewed
  • First
  • Previous
  • 1
  • Next
  • Last