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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 4
2021
Smith, Rebecca G.; Pishva, Ehsan; Shireby, Gemma; Smith, Adam R.; Roubroeks, Janou A. Y.; Hannon, Eilis; Wheildon, Gregory; Mastroeni, Diego; Gasparoni, Gilles; Riemenschneider, Matthias; Giese, Armin; Sharp, Andrew J.; Schalkwyk, Leonard; Haroutunian, Vahram; Viechtbauer, Wolfgang; Hove, Daniel L. A. van den; Weedon, Michael; Brokaw, Danielle; Francis, Paul T.; Thomas, Alan J.; Love, Seth; Morgan, Kevin; Walter, Joern; Coleman, Paul D.; Bennett, David A.; Jager, Philip L. de; Mill, Jonathan und Lunnon, Katie
(2021):
A meta-analysis of epigenome-wide association studies in Alzheimer's disease highlights novel differentially methylated loci across cortex.
In: Nature Communications, Bd. 12, Nr. 1, 3517
2018
Wray, Naomi R.; Ripke, Stephan; Mattheisen, Manuel; Trzaskowski, Maciej; Byrne, Enda M.; Abdellaoui, Abdel; Adams, Mark J.; Agerbo, Esben; Air, Tracy M.; Andlauer, Till M. F.; Bacanu, Silviu-Alin; Baekvad-Hansen, Marie; Beekman, Aartjan F. T.; Bigdeli, Tim B.; Binder, Elisabeth B.; Blackwood, Douglas R. H.; Bryois, Julien; Buttenschon, Henriette N.; Bybjerg-Grauholm, Jonas; Cai, Na; Castelao, Enrique; Christensen, Jane Hvarregaard; Clarke, Toni-Kim; Coleman, Jonathan I. R.; Colodro-Conde, Lucia; Couvy-Duchesne, Baptiste; Craddock, Nick; Crawford, Gregory E.; Crowley, Cheynna A.; Dashti, Hassan S.; Davies, Gail; Deary, Ian J.; Degenhardt, Franziska; Derks, Eske M.; Direk, Nese; Dolan, Conor V.; Dunn, Erin C.; Eley, Thalia C.; Eriksson, Nicholas; Escott-Price, Valentina; Kiadeh, Farnush Hassan Farhadi; Finucane, Hilary K.; Forstner, Andreas J.; Frank, Josef; Gaspar, Helena A.; Gill, Michael; Giusti-Rodriguez, Paola; Goes, Fernando S.; Gordon, Scott D.; Grove, Jakob; Hall, Lynsey S.; Hannon, Eilis; Hansen, Christine Soholm; Hansen, Thomas F.; Herms, Stefan; Hickie, Ian B.; Hoffmann, Per; Homuth, Georg; Horn, Carsten; Hottenga, Jouke-Jan; Hougaard, David M.; Hu, Ming; Hyde, Craig L.; Ising, Marcus; Jansen, Rick; Jin, Fulai; Jorgenson, Eric; Knowles, James A.; Kohane, Isaac S.; Kraft, Julia; Kretzschmar, Warren W.; Krogh, Jesper; Kutalik, Zoltan; Lane, Jacqueline M.; Li, Yihan; Li, Yun; Lind, Penelope A.; Liu, Xiaoxiao; Lu, Leina; MacIntyre, Donald J.; MacKinnon, Dean F.; Maier, Robert M.; Maier, Wolfgang; Marchini, Jonathan; Mbarek, Hamdi; McGrath, Patrick; McGuffin, Peter; Medland, Sarah E.; Mehta, Divya; Middeldorp, Christel M.; Mihailov, Evelin; Milaneschi, Yuri; Milani, Lili; Mill, Jonathan; Mondimore, Francis M.; Montgomery, Grant W.; Mostafavi, Sara; Mullins, Niamh; Nauck, Matthias; Ng, Bernard; Nivard, Michel G.; Nyholt, Dale R.; O'Reilly, Paul F.; Oskarsson, Hogni; Owen, Michael J.; Painter, Jodie N.; Pedersen, Carsten Bocker; Pedersen, Marianne Giortz; Peterson, Roseann E.; Pettersson, Erik; Peyrot, Wouter J.; Pistis, Giorgio; Posthuma, Danielle; Purcell, Shaun M.; Quiroz, Jorge A.; Qvist, Per; Rice, John P.; Riley, Brien P.; Rivera, Margarita; Mirza, Saira Saeed; Saxena, Richa; Schövers, Robert; Schulte, Eva C.; Shen, Ling; Shi, Jianxin; Shyn, Stanley I.; Sigurdsson, Engilbert; Sinnamon, Grant B. C.; Smit, Johannes H.; Smith, Daniel J.; Stefansson, Hreinn; Steinberg, Stacy; Stockmeier, Craig A.; Streit, Fabian; Strohmaier, Jana; Tansey, Katherine E.; Teismann, Henning; Teumer, Alexander; Thompson, Wesley; Thomson, Pippa A.; Thorgeirsson, Thorgeir E.; Tian, Chao; Traylor, Matthew; Treutlein, Jens; Trubetskoy, Vassily; Uitterlinden, Andre G.; Umbricht, Daniel; Auwera, Sandra van der; Hemert, Albert M. van; Viktorin, Alexander; Visscher, Peter M.; Wang, Yunpeng; Webb, Bradley T.; Weinsheimer, Shantel Marie; Wellmann, Juegen; Willemsen, Gonneke; Witt, Stephanie H.; Wu, Yang; Xi, Hualin S.; Yang, Jian; Zhang, Futao; Arolt, Volker; Baune, Bernhard T.; Berger, Klaus; Boomsma, Dorret I.; Cichon, Sven; Dannlowski, Udo; Geus, E. C. J. de; DePaulo, J. Raymond; Domenici, Enrico; Domschke, Katharina; Esko, Tonu; Grabe, Hans J.; Hamilton, Steven P.; Hayward, Caroline; Heath, Andrew C.; Hinds, David A.; Kendler, Kenneth S.; Kloiber, Stefan; Lewis, Glyn; Li, Qingqin S.; Lucae, Susanne; Madden, Pamela F. A.; Magnusson, Patrik K.; Martin, Nicholas G.; McIntosh, Andrew M.; Metspalu, Andres; Mors, Ole; Mortensen, Preben Bo; Müller-Myhsok, Bertram; Nordentoft, Merete; Nöthen, Markus M.; O'Donovan, Michael C.; Paciga, Sara A.; Pedersen, Nancy L.; Penninx, Brenda W. J. H.; Perlis, Roy H.; Porteous, David J.; Potash, James B.; Preisig, Martin; Rietschel, Marcella; Schaefer, Catherine; Schulze, Thomas G.; Smoller, Jordan W.; Stefansson, Kari; Tiemeier, Henning; Uher, Rudolf; Völzke, Henry; Weissman, Myrna M.; Werge, Thomas; Winslow, Ashley R.; Lewis, Cathryn M.; Levinson, Douglas F.; Breen, Gerome; Borglum, Anders D. und Sullivan, Patrick F.
(2018):
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
In: Nature Genetics, Bd. 50, Nr. 5: S. 668-681
Luijk, Rene; Wu, Haoyu; Ward-Caviness, Cavin K.; Hannon, Eilis; Carnero-Montoro, Elena; Min, Josine L.; Mandaviya, Pooja; Müller-Nurasyid, Martina; Mei, Hailiang; Maarel, Silvere M. van der; Relton, Caroline; Mill, Jonathan; Waldenberger, Melanie; Bell, Jordana T.; Jansen, Rick; Zhernakova, Alexandra; Franke, Lude; Hoen, Peter A. C. 't; Boomsma, Dorret I.; Duijn, Cornelia M. van; Greevenbroek, Marleen M. J. van 
ORCID: https://orcid.org/0000-0002-2989-1631; Veldink, Jan H.; Wijmenga, Cisca; Meurs, Joyce van; Daxinger, Lucia; Slagboom, P. Eline; Zwet, Erik W. van und Heijmans, Bastiaan T.
(2018):
Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation.
In: Nature Communications, Bd. 9, 3738
[PDF, 988kB]
ORCID: https://orcid.org/0000-0002-2989-1631; Veldink, Jan H.; Wijmenga, Cisca; Meurs, Joyce van; Daxinger, Lucia; Slagboom, P. Eline; Zwet, Erik W. van und Heijmans, Bastiaan T.
(2018):
Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation.
In: Nature Communications, Bd. 9, 3738
[PDF, 988kB]
2017
Traylor, Matthew; Malik, Rainer; Nalls, Mike A.; Cotlarciuc, Ioana; Radmanesh, Farid; Thorleifsson, Gudmar; Hanscombe, Ken B.; Langefeld, Carl; Saleheen, Danish; Rost, Natalia S.; Yet, Idil; Spector, Tim D.; Bell, Jordana T.; Hannon, Eilis; Mill, Jonathan; Chauhan, Ganesh; Debette, Stephanie; Bis, Joshua C.; Longstreth, W. T.; Ikram, M. Arfan; Launer, Lenore J.; Seshadri, Sudha; Hamilton-Bruce, Monica Anne; Jimenez-Conde, Jordi; Cole, John W.; Schmidt, Reinhold; Slowik, Agnieszka; Lemmens, Robin; Lindgren, Arne; Melander, Olle; Grewal, Raji P.; Sacco, Ralph L.; Rundek, Tatjana; Rexrode, Kathryn; Arnett, Donna K.; Johnson, Julie A.; Benavente, Oscar R.; Wasssertheil-Smoller, Sylvia; Lee, Jin-Moo; Pulit, Sara L.; Wong, Quenna; Rich, Stephen S.; Bakker, Paul I. W. de; McArdle, Patrick F.; Woo, Daniel; Anderson, Christopher D.; Xu, Huichun; Heitsch, Laura; Fornage, Myriam; Jern, Christina; Stefansson, Kari; Thorsteinsdottir, Unnur; Gretarsdottir, Solveig; Lewis, Cathryn M.; Sharma, Pankaj; Sudlow, Cathie L. M.; Rothwell, Peter M.; Boncoraglio, Giorgio B.; Thijs, Vincent; Levi, Chris; Meschia, James F.; Rosand, Jonathan; Kittner, Steven J.; Mitchell, Braxton D.; Dichgans, Martin; Worrall, Bradford B. und Markus, Hugh S.
(2017):
Genetic Variation at 16q24.2 Is Associated With Small Vessel Stroke.
In: Annals of Neurology, Bd. 81, Nr. 3: S. 383-394
[PDF, 532kB]