![[höher]](/style/images/multi_up.png)
Eine Ebene höherGruppiert nach:
Dokumententyp
| Veröffentlichungsdatum
Springe zu: Zeitschriftenartikel
Anzahl der Publikationen: 15
Zeitschriftenartikel
Gehlen, Jan; Giel, Ann-Sophie; Koellges, Ricarda; Haas, Stephan L.; Zhang, Rong; Trcka, Jiri; Sungur, Ayse O.; Renziehausen, Florian; Bornholdt, Dorothea; Jung, Daphne; Hoyer, Paul D.; Nordenskjold, Agneta; Tibboel, Dick; Vlot, John; Spaander, Manon C. W.; Smigiel, Robert; Patkowski, Dariusz; Roeleveld, Nel; Rooij, Iris A. L. M. van; Blaauw, Ivo de; Hoelscher, Alice; Pauly, Marcus; Leutner, Andreas; Fuchs, Joerg; Niethammer, Joel; Melissari, Maria-Theodora; Jenetzky, Ekkehart; Zwink, Nadine; Thiele, Holger; Hilger, Alina Christine; Hess, Timo; Trautmann, Jessica; Marks, Matthias; Baumgarten, Martin; Blaess, Gaby; Landen, Mikael; Fundin, Bengt; Bulik, Cynthia M.; Pennimpede, Tracie; Ludwig, Michael; Ludwig, Kerstin U.; Mangold, Elisabeth; Heilmann-Heimbach, Stefanie; Moebus, Susanne; Herrmann, Bernhard G.; Alsabeah, Kristina; Burgos, Carmen M.; Lilja, Helene E.; Azodi, Sahar; Stenstrom, Pernilla; Arnbjornsson, Einar; Frybova, Barbora; Lebensztejn, Dariusz M.; Debek, Wojciech; Kolodziejczyk, Elwira; Kozera, Katarzyna; Kierkus, Jaroslaw; Kalicinski, Piotr; Stefanowicz, Marek; Socha-Banasiak, Anna; Kolejwa, Michal; Piaseczna-Piotrowska, Anna; Czkwianianc, Elzbieta; Noethen, Markus M.; Grote, Phillip; Rygl, Michal; Reinshagen, Konrad; Spychalski, Nicole; Ludwikowski, Barbara; Hubertus, Jochen; Heydweiller, Andreas; Ure, Benno; Muensterer, Oliver J.; Aubert, Ophelia; Gosemann, Jan-Hendrik; Lacher, Martin; Degenhardt, Petra; Boemers, Thomas M.; Mokrowiecka, Anna; Malecka-Panas, Ewa; Woehr, Markus; Knapp, Michael; Seitz, Guido; de Klein, Annelies; Oracz, Grzegorz; Brosens, Erwin; Reutter, Heiko und Schumacher, Johannes
(2022):
First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B.
In: Human Genetics and Genomics Advances, Bd. 3, Nr. 2, 100093
Brandt, Margot; Kim-Hellmuth, Sarah; Ziosi, Marcello; Gokden, Alper; Wolman, Aaron; Lam, Nora; Recinos, Yocelyn; Daniloski, Zharko; Morris, John A.; Hornung, Veit; Schumacher, Johannes und Lappalainen, Tuuli
(2021):
An autoimmune disease risk variant: A trans master regulatory effect mediated by IRF1 under immune stimulation?
In: PLOS Genetics 17(7), e1009684
In: PLOS Genetics 17(7), e1009684
Forstner, Andreas J.; Awasthi, Swapnil; Wolf, Christiane; Maron, Eduard; Erhardt, Angelika; Czamara, Darina; Eriksson, Elias; Lavebratt, Catharina; Allgulander, Christer; Friedrich, Nina; Becker, Jessica; Hecker, Julian; Rambau, Stefanie; Conrad, Rupert; Geiser, Franziska; McMahon, Francis J.; Moebus, Susanne; Hess, Timo; Buerfent, Benedikt C.; Hoffmann, Per; Herms, Stefan; Heilmann-Heimbach, Stefanie; Kockum, Ingrid; Olsson, Tomas; Alfredsson, Lars; Weber, Heike; Alpers, Georg W.; Arolt, Volker; Fehm, Lydia; Fydrich, Thomas; Gerlach, Alexander L.; Hamm, Alfons; Kircher, Tilo; Pane-Farre, Christiane A.; Pauli, Paul; Rief, Winfried; Ströhle, Andreas; Plag, Jens; Lang, Thomas; Wittchen, Hans-Ulrich; Mattheisen, Manuel; Meier, Sandra; Metspalu, Andres; Domschke, Katharina; Reif, Andreas; Hovatta, Iiris; Lindefors, Nils; Andersson, Evelyn; Schalling, Martin; Mbarek, Hamdi; Milaneschi, Yuri; Geus, Eco J. C. de; Boomsma, Dorret I.; Penninx, Brenda W. J. H.; Thorgeirsson, Thorgeir E.; Steinberg, Stacy; Stefansson, Kari; Stefansson, Hreinn; Müller-Myhsok, Bertram; Hansen, Thomas Folkmann; Borglum, Anders D.; Werge, Thomas; Mortensen, Preben Bo; Nordentoft, Merete; Hougaard, David M.; Hultman, Christina M.; Sullivan, Patrick F.; Nöthen, Markus M.; Woldbye, David P. D.; Mors, Ole; Binder, Elisabeth B.; Rueck, Christian; Ripke, Stephan; Deckert, Jürgen und Schumacher, Johannes
(2021):
Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression.
In: Molecular Psychiatry, Bd. 26, Nr. 8: S. 4179-4190
Franck, Caspar; Zimmermann, Nadja; Goni, Elisabetta; Lippert, Hans; Ridwelski, Karsten; Kruschewski, Martin; Kreuser, Nicole; Lingohr, Philipp; Schildberg, Claus; Vassos, Nikolaos; Waidmann, Oliver; Peitz, Ulrich; Lang, Hauke; Grmminger, Peter P.; Bruns, Christiane; Veits, Lothar; Vieth, Michael; Moehler, Markus; Lordick, Florian; Gockel, Ines; Schumacher, Johannes; Malfertheiner, Peter und Venerito, Marino
(2021):
Different Prevalence of Alarm, Dyspeptic and Reflux Symptoms in Patients with Cardia and Non-cardia Gastric Cancer.
In: Journal of Gastrointestinal and Liver Diseases, Bd. 30, Nr. 4: S. 431-437
Gialluisi, Alessandro; Andlauer, Till F. M.; Mirza-Schreiber, Nazanin; Moll, Kristina; Becker, Jessica; Hoffmann, Per; Ludwig, Kerstin U.; Czamara, Darina; Pourcain, Beate St; Honbolygó, Ferenc; Tóth, Dénes; Csépe, Valéria; Huguet, Guillaume; Chaix, Yves; Iannuzzi, Stephanie; Demonet, Jean-Francois; Morris, Andrew P.; Hulslander, Jacqueline; Willcutt, Erik G.; DeFries, John C.; Olson, Richard K.; Smith, Shelley D.; Pennington, Bruce F.; Vaessen, Anniek; Maurer, Urs; Lyytinen, Heikki; Peyrard-Janvid, Myriam; Leppänen, Paavo H. T.; Brandeis, Daniel; Bonte, Milene; Stein, John F.; Talcott, Joel B.; Fauchereau, Fabien; Wilcke, Arndt; Kirsten, Holger; Müller, Bent; Francks, Clyde; Bourgeron, Thomas; Monaco, Anthony P.; Ramus, Franck; Landerl, Karin; Kere, Juha; Scerri, Thomas S.; Paracchini, Silvia; Fisher, Simon E.; Schumacher, Johannes; Nöthen, Markus M.; Müller-Myhsok, Bertram und Schulte-Körne, Gerd
(2020):
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia.
In: Molecular psychiatry
[PDF, 2MB]
Zhang, Rong; Gehlen, Jan; Kawalia, Amit; Melissari, Maria-Theodora; Dakal, Tikam Chand; Menon, Athira M.; Hoefele, Julia; Riedhammer, Korbinian; Waffenschmidt, Lea; Fabian, Julia; Breuer, Katinka; Kalanithy, Jeshurun; Hilger, Alina Christine; Sharma, Amit; Hoelscher, Alice; Boemers, Thomas M.; Pauly, Markus; Leutner, Andreas; Fuchs, Jörg; Seitz, Guido; Ludwikowski, Barbara M.; Gomez, Barbara; Hubertus, Jochen; Heydweiller, Andreas; Kurz, Ralf; Leonhardt, Johannes; Kosch, Ferdinand; Holland-Cunz, Stefan; Muensterer, Oliver; Ure, Beno; Schmiedeke, Eberhard; Neser, Jörg; Degenhardt, Petra; Maerzheuser, Stefanie; Kleine, Katharina; Schaefer, Mattias; Spychalski, Nicole; Deffaa, Oliver J.; Gosemann, Jan-Hendrik; Lacher, Martin; Heilmann-Heimbach, Stefanie; Zwink, Nadine; Jenetzky, Ekkehart; Ludwig, Michael; Grote, Phillip; Schumacher, Johannes; Thiele, Holger und Reutter, Heiko
(2020):
Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia.
In: PLOS One 15(6), e0234246 [PDF, 1MB]
In: PLOS One 15(6), e0234246 [PDF, 1MB]
Weise, Friederike; Vieth, Michael; Reinhold, Dirk; Haybaeck, Johannes; Goni, Elisabetta; Lippert, Hans; Ridwelski, Karsten; Lingohr, Philipp; Schildberg, Claus; Vassos, Nikolaos; Kruschewski, Martin; Krasniuk, Iurii; Grimminger, Peter P.; Waidmann, Oliver; Peitz, Ulrich; Veits, Lothar; Kreuser, Nicole; Lang, Hauke; Bruns, Christiane; Moehler, Markus; Lordick, Florian; Gockel, Ines; Schumacher, Johannes; Malfertheiner, Peter und Venerito, Marino
(2019):
Gastric cancer in autoimmune gastritis: A case-control study from the German centers of the staR project on gastric cancer research.
In: United European Gastroenterology Journal, Bd. 8, Nr. 2, UNSP 2050640619891580: S. 175-184
Gialluisi, Alessandro; Andlauer, Till F. M.; Mirza-Schreiber, Nazanin; Moll, Kristina; Becker, Jessica; Hoffmann, Per; Ludwig, Kerstin U.; Czamara, Darina; St Pourcain, Beate; Brandler, William; Honbolygo, Ferenc; Toth, Denes; Csepe, Valeria; Huguet, Guillaume; Morris, Andrew P.; Hulslander, Jacqueline; Willcutt, Erik G.; DeFries, John C.; Olson, Richard K.; Smith, Shelley D.; Pennington, Bruce F.; Vaessen, Anniek; Maurer, Urs; Lyytinen, Heikki; Peyrard-Janvid, Myriam; Leppanen, Paavo H. T.; Brandeis, Daniel; Bonte, Milene; Stein, John F.; Talcott, Joel B.; Fauchereau, Fabien; Wilcke, Arndt; Francks, Clyde; Bourgeron, Thomas; Monaco, Anthony P.; Ramus, Franck; Landerl, Karin; Kere, Juha; Scerri, Thomas S.; Paracchini, Silvia; Fisher, Simon E.; Schumacher, Johannes; Noethen, Markus M.; Müller-Myhsok, Bertram und Schulte-Koerne, Gerd
(2019):
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.
In: Translational Psychiatry, Bd. 9, 77
[PDF, 1MB]
Jong, Simone de; Abdalla Diniz, Mateus Jose; Saloma, Andiara; Gadelha, Ary; Santoro, Marcos L.; Ota, Vanessa K.; Noto, Cristiano; Curtis, Charlesg; Newhouse, Stephen J.; Patel, Hamel; Hall, Lynsey S.; O'Reilly, Paul F.; Belangero, Sintia I.; Bressan, Rodrigo A.; Breen, Gerome; Wray, Naomi R.; Ripke, Stephan; Mattheisen, Manuel; Trzaskowski, Maciej; Byrne, Enda M.; Abdellaoui, Abdel; Adams, Mark J.; Agerbo, Esben; Air, Tracy M.; Andlauer, Till F. M.; Bacanu, Silviu-Alin; Baekvad-Hansen, Marie; Beekman, Aartjan T. F.; Bigdeli, Tim B.; Binder, Elisabeth B.; Blackwood, Douglas H. R.; Bryois, Julien; Buttenschon, Henriette N.; Bybjerg-Grauholm, Jonas; Cai, Na; Castelao, Enrique; Christensen, Jane Hvarregaard; Clarke, Toni-Kim; Coleman, Jonathan R. I.; Colodro-Conde, Lucia; Couvy-Duchesne, Baptiste; Craddock, Nick; Crawford, Gregory E.; Davies, Gail; Deary, Ian J.; Degenhardt, Franziska; Derks, Eske M.; Direk, Nese; Dolan, Conor V.; Dunn, Erin C.; Eley, Thalia C.; Escott-Price, Valentina; Kiadeh, Farnush Farhadi Hassan; Finucane, Hilary K.; Forstner, Andreas J.; Frank, Josef; Gaspar, Helena A.; Gill, Michael; Goes, Fernando S.; Gordon, Scott D.; Grove, Jakob; Hansen, Christine Soholm; Hansen, Thomas F.; Herms, Stefan; Hickie, Ian B.; Hoffmann, Per; Homuth, Georg; Horn, Carsten; Hottenga, Jouke-Jan; Hougaard, David M.; Ising, Marcus; Jansen, Rick; Jones, Ian; Jones, Lisa A.; Jorgenson, Eric; Knowles, James A.; Kohane, Isaac S.; Kraft, Julia; Kretzschmar, Warren W.; Krogh, Jesper; Kutalik, Zoltan; Li, Yihan; Lind, Penelope A.; 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; Mondimore, Francis M.; Montgomery, Grant W.; Mostafavi, Sara; Mullins, Niamh; Nauck, Matthias; Ng, Bernard; Nivard, Michel G.; Nyholt, Dale R.; 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; Quiroz, Jorge A.; Qvist, Per; Rice, John P.; Riley, Brien P.; Rivera, Margarita; Mirza, Saira Saeed; Schövers, Robert; Schulte, Eva C.; Shen, Ling; Shyn, Stanley; Sigurdsson, Engilbert; Sinnamon, Grant C. B.; Smit, Johannes H.; Smith, Daniel J.; Stefansson, Hreinn; Steinberg, Stacy; Streit, Fabian; Strohmaier, Jana; Tansey, Katherine E.; Teismann, Henning; Teumer, Alexander; Thompson, Wesley; Thomson, Pippa A.; Thorgeirsson, Thorgeir E.; 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, Jürgen; Willemsen, Gonneke; Witt, Stephanie H.; Wu, Yang; Xi, Hualin S.; Yang, Jian; Zhang, Futao; Arolt, Volker; Baune, Bernhard T.; Berger, Klaus; Boomsma, Dorret; Cichon, Sven; Dannlowski, Udo; Geus, E. J. C. de; DePaulo, J. Raymond; Domenici, Enrico; Domschke, Katharina; Esko, Tonu; Grabe, Hans J.; Hamilton, Steven P.; Hayward, Caroline; Heath, Andrew C.; Kendler, Kenneth S.; Kloiber, Stefan; Lewis, Glyn; Li, Qingqin S.; Lucae, Susanne; Madden, Pamela A. F.; 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; Lewis, Cathryn M.; Levinson, Douglas F.; Borglum, Anders D.; Sullivan, Patrick F.; Meier, Sandra; Strauss, John; Xu, Wei; Vincent, John B.; Matthews, Keith; Ferreira, Manuel; O'Dushlaine, Colm; Purcell, Shaun; Raychaudhuri, Soumya; Ruderfer, Douglas M.; Sklar, Pamela; Scott, Laura J.; Flickinger, Matthew; Burmeister, Margit; Li, Jun; Guan, Weihua; Absher, Devin; Thompson, Robert C.; Meng, Fan Guo; Schatzberg, Alan F.; Bunney, William E.; Barchas, Jack D.; Watson, Stanley J.; Myers, Richard M.; Akil, Huda; Böhnke, Michael; Chambert, Kimberly; Moran, Jennifer; Scolnick, Edward; Djurovic, Srdjan; Melle, Ingrid; Morken, Gunnar; Corvin, Aiden; Anjorin, Adebayo; Kandaswamy, Radhika; Lawrence, Jacob; McLean, Alan W.; Pickard, Benjamin S.; Bergen, Sarah E.; Nimgaonkar, Vishwajit; Landen, Mikael; Schalling, Martin; Osby, Urban; Backlund, Lena; Frisen, Louise; Langstrom, Niklas; Stahl, Eli; Dobbyn, Amanda; Jamain, Stephane; Etain, Bruno; Bellivier, Frank; Leber, Markus; Maaser, Anna; Fischer, Sascha B.; Reinbold, Celine S.; Kittel-Schneider, Sarah; Fullerton, Janice M.; Oruc, Lilijana; Para, Jose G.; Mayoral, Fermin; Rivas, Fabio; Czerski, Piotr M.; Kammerer-Ciernioch, Jutta; Vedder, Helmut; Borrmann-Hassenbach, Margitta; Pfennig, Andrea; Brennan, Paul; McKay, James D.; Kogevinas, Manolis; Schwarz, Markus; Schofield, Peter R.; Mühleisen, Thomas W.; Schumacher, Johannes; Bauer, Michael; Wright, Adam; Mitchell, Philip B.; Hautzinger, Martin; Kelsoe, John R.; Greenwood, Tiffany A.; Nievergelt, Caroline M.; Shilling, Paul D.; Smith, Erin N.; Bloss, Cinnamon S.; Edenberg, Howard J.; Koller, Daniel L.; Gershon, Elliot S.; Liu, Chunyu; Badner, Judith A.; Scheftner, William A.; Lawson, William B.; Nwulia, Evaristus A.; Hipolito, Maria; Coryell, William; Rice, John; Byerley, William; McMahon, Francis J.; Lohoff, Falk W.; Zandi, Peter P.; Mahon, Pamela B.; McInnis, Melvin G.; Zollner, Sebastian; Zhang, Peng; Szelinger, Szabolcs; St Clair, David; Caesar, Sian; Gordon-Smith, Katherine; Fraser, Christine; Green, Elaine K.; Grozeva, Detelina; Hamshere, Marian L.; Kirov, George; Nikolov, Ivan; Collier, David A.; Elkin, Amanda; Williamson, Richard; Young, Allan H.; Ferrier, I. Nicol; Milanova, Vihra; Alda, Martin; Cervantes, Pablo; Cruceanu, Cristiana; Rouleau, Guy A.; Turecki, Gustavo; Paciga, Sara; Winslow, Ashley R.; Grigoroiu-Serbanescu, Maria; Ophoff, Roel; Adolfsson, Rolf; Adolfsson, Annelie Nordin; Del-Favero, Jurgen; Pato, Carlos; Biernacka, Joanna M.; Frye, Mark A.; Morris, Derek; Schork, Nicholas J.; Reif, Andreas; Lissowska, Jolanta; Hauser, Joanna; Szeszenia-Dabrowska, Neonila; McGhee, Kevin; Quinn, Emma; Moskvina, Valentina; Holmans, Peter A.; Farmer, Anne; Kennedy, James L.; Andreassen, Ole A.; Mattingsdal, Morten; Bass, Nicholas J.; Gurling, Hugh; McQuillin, Andrew; Breuer, Rene; Hultman, Christina; Lichtenstein, Paul; Huckins, Laura M.; Leboyer, Marion; Lathrop, Mark; Nurnberger, John; Steffens, Michael; Foroud, Tatiana M.; Berrettini, Wade H.; Craig, David W. und Shi, Jianxin
(2018):
Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder.
In: Communications Biology, Bd. 1, 163
[PDF, 697kB]
Karbalai, Nazanin; Czamara, Darina; Moll, Kristina; Ramus, Franck; Malik, Rainer; Scerri, Thomas S.; Schumacher, Johannes; Morris, Andrew P.; Bourgeron, Thomas; Monaco, Anthony P.; Paracchini, Silvia; Fisher, Simon E.; Nöthen, Markus M.; Schulte-Körne, Gerd und Müller-Myhsok, Bertram
(2017):
Identification of genetic interactions involved in dyslexia pathogenesis.
In: European Neuropsychopharmacology, Bd. 27, Nr. Suppl. 2:
S183-S184
Harbeck, Nadia; Gluz, Oleg; Christgen, Matthias; Kates, Ronald Ernest; Braun, Michael; Küemmel, Sherko; Schumacher, Claudia; Potenberg, Jochem; Krämer, Stefan; Kleine-Tebbe, Anke; Augustin, Doris; Aktas, Bahriye; Forstbauer, Helmut; Tio, Joke; Schumann, Raquel von; Liedtke, Cornelia; Grischke, Eva-Maria; Schumacher, Johannes; Würstlein, Rachel; Kreipe, Hans Heinrich und Nitz, Ulrike Anneliese
(2017):
De-Escalation Strategies in Human Epidermal Growth Factor Receptor 2 (HER2)-Positive Early Breast Cancer (BC): Final Analysis of the West German Study Group Adjuvant Dynamic Marker-Adjusted Personalized Therapy Trial Optimizing Risk Assessment and Therapy Response Prediction in Early BC HER2-and Hormone Receptor-Positive Phase II Randomized Trial-Efficacy, Safety, and Predictive Markers for 12 Weeks of Neoadjuvant Trastuzumab Emtansine With or Without Endocrine Therapy (ET) Versus Trastuzumab Plus ET.
In: Journal of Clinical Oncology, Bd. 35, Nr. 26: S. 3046-3056
Kim-Hellmuth, Sarah; Bechheim, Matthias; Pütz, Benno; Mohammadi, Pejman; Nedelec, Yohann; Giangreco, Nicholas; Becker, Jessica; Kaiser, Vera; Fricker, Nadine; Beier, Esther; Boor, Peter; Castel, Stephane E.; Nöthen, Markus M.; Barreiro, Luis B.; Pickrell, Joseph K.; Müller-Myhsok, Bertram; Lappalainen, Tuuli; Schumacher, Johannes und Hornung, Veit
(2017):
Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations.
In: Nature Communications, Bd. 8
[PDF, 1MB]
Forstner, Andreas J.; Hecker, Julian; Hofmann, Andrea; Maaser, Anna; Reinbold, Céline S.; Mühleisen, Thomas W.; Leber, Markus; Strohmaier, Jana; Degenhardt, Franziska; Treutlein, Jens; Mattheisen, Manuel; Schumacher, Johannes; Streit, Fabian; Meier, Sandra; Herms, Stefan; Hoffmann, Per; Lacour, André; Witt, Stephanie H.; Reif, Andreas; Müller-Myhsok, Bertram; Lucae, Susanne; Maier, Wolfgang; Schwarz, Markus; Vedder, Helmut; Kammerer-Ciernioch, Jutta; Pfennig, Andrea; Bauer, Michael; Hautzinger, Martin; Moebus, Susanne; Schenk, Lorena M.; Fischer, Sascha B.; Sivalingam, Sugirthan; Czerski, Piotr M.; Hauser, Joanna; Lissowska, Jolanta; Szeszenia-Dabrowska, Neonila; Brennan, Paul; McKay, James D.; Wright, Adam; Mitchell, Philip B.; Fullerton, Janice M.; Schofield, Peter R.; Montgomery, Grant W.; Medland, Sarah E.; Gordon, Scott D.; Martin, Nicholas G.; Krasnov, Valery; Chuchalin, Alexander; Babadjanova, Gulja; Pantelejeva, Galina; Abramova, Lilia I.; Tiganov, Alexander S.; Polonikov, Alexey; Khusnutdinova, Elza; Alda, Martin; Cruceanu, Cristiana; Rouleau, Guy A.; Turecki, Gustavo; Laprise, Catherine; Rivas, Fabio; Mayoral, Fermin; Kogevinas, Manolis; Grigoroiu-Serbanescu, Maria; Becker, Tim; Schulze, Thomas G.; Rietschel, Marcella; Cichon, Sven; Fier, Heide und Nöthen, Markus M.
(2017):
Identification of shared risk loci and pathways for bipolar disorder and schizophrenia.
In: PLOS One 12(2), e0171595 [PDF, 1MB]
In: PLOS One 12(2), e0171595 [PDF, 1MB]
Hou, Liping; Bergen, Sarah E.; Akula, Nirmala; Song, Jie; Hultman, Christina M.; Landén, Mikael; Adli, Mazda; Alda, Martin; Ardau, Raffaella; Arias, Bárbara; Aubry, Jean-Michel; Backlund, Lena; Badner, Judith A.; Barrett, Thomas B.; Bauer, Michael; Baune, Bernhard T.; Bellivier, Frank; Benabarre, Antonio; Bengesser, Susanne; Berrettini, Wade H.; Bhattacharjee, Abesh Kumar; Biernacka, Joanna M.; Birner, Armin; Bloss, Cinnamon S.; Brichant-Petitjean, Clara; Bui, Elise T.; Byerley, William; Cervantes, Pablo; Chillotti, Caterina; Cichon, Sven; Colom, Francesc; Coryell, William; Craig, David W.; Cruceanu, Cristiana; Czerski, Piotr M.; Davis, Tony; Dayer, Alexandre; Degenhardt, Franziska; Del Zompo, Maria; DePaulo, J. Raymond; Edenberg, Howard J.; Étain, Bruno; Falkai, Peter 
ORCID: https://orcid.org/0000-0003-2873-8667; Foroud, Tatiana; Forstner, Andreas J.; Frisen, Louise; Frye, Mark A.; Fullerton, Janice M.; Gard, Sébastien; Garnham, Julie S.; Gershon, Elliot S.; Goes, Fernando S.; Greenwood, Tiffany A.; Grigoroiu-Serbanescu, Maria; Hauser, Joanna; Heilbronner, Urs; Heilmann-Heimbach, Stefanie; Herms, Stefan; Hipolito, Maria; Hitturlingappa, Shashi; Hoffmann, Per; Hofmann, Andrea; Jamain, Stephane; Jiménez, Esther; Kahn, Jean-Pierre; Kassem, Layla; Kelsoe, John R.; Kittel-Schneider, Sarah; Kliwicki, Sebastian; Koller, Daniel L.; König, Barbara; Lackner, Nina; Laje, Gonzalo; Lang, Maren; Lavebratt, Catharina; Lawson, William B.; Leboyer, Marion; Leckband, Susan G.; Liu, Chunyu; Maaser, Anna; Mahon, Pamela B.; Maier, Wolfgang; Maj, Mario; Manchia, Mirko; Martinsson, Lina; McCarthy, Michael J.; McElroy, Susan L.; McInnis, Melvin G.; McKinney, Rebecca; Mitchell, Philip B.; Mitjans, Marina; Mondimore, Francis M.; Monteleone, Palmiero; Mühleisen, Thomas W.; Nievergelt, Caroline M.; Nöthen, Markus M.; Novak, Tomas; Nurnberger, John I.; Nwulia, Evaristus A.; Ösby, Urban; Pfennig, Andrea; Potash, James B.; Propping, Peter; Reif, Andreas; Reininghaus, Eva; Rice, John; Rietschel, Marcella; Rouleau, Guy A.; Rybakowski, Janusz K.; Schalling, Martin; Scheftner, William A.; Schofield, Peter R.; Schork, Nicholas J.; Schulze, Thomas G.; Schumacher, Johannes; Schweizer, Barbara W.; Severino, Giovanni; Shekhtman, Tatyana; Shilling, Paul D.; Simhandl, Christian; Slaney, Claire M.; Smith, Erin N.; Squassina, Alessio; Stamm, Thomas; Stopkova, Pavla; Streit, Fabian; Strohmaier, Jana; Szelinger, Szabolcs; Tighe, Sarah K.; Tortorella, Alfonso; Turecki, Gustavo; Vieta, Eduard; Volkert, Julia; Witt, Stephanie H.; Wright, Adam; Zandi, Peter P.; Zhang, Peng; Zollner, Sebastian und McMahon, Francis J.
(2016):
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.
In: Human Molecular Genetics, Bd. 25, Nr. 15: S. 3383-3394
ORCID: https://orcid.org/0000-0003-2873-8667; Foroud, Tatiana; Forstner, Andreas J.; Frisen, Louise; Frye, Mark A.; Fullerton, Janice M.; Gard, Sébastien; Garnham, Julie S.; Gershon, Elliot S.; Goes, Fernando S.; Greenwood, Tiffany A.; Grigoroiu-Serbanescu, Maria; Hauser, Joanna; Heilbronner, Urs; Heilmann-Heimbach, Stefanie; Herms, Stefan; Hipolito, Maria; Hitturlingappa, Shashi; Hoffmann, Per; Hofmann, Andrea; Jamain, Stephane; Jiménez, Esther; Kahn, Jean-Pierre; Kassem, Layla; Kelsoe, John R.; Kittel-Schneider, Sarah; Kliwicki, Sebastian; Koller, Daniel L.; König, Barbara; Lackner, Nina; Laje, Gonzalo; Lang, Maren; Lavebratt, Catharina; Lawson, William B.; Leboyer, Marion; Leckband, Susan G.; Liu, Chunyu; Maaser, Anna; Mahon, Pamela B.; Maier, Wolfgang; Maj, Mario; Manchia, Mirko; Martinsson, Lina; McCarthy, Michael J.; McElroy, Susan L.; McInnis, Melvin G.; McKinney, Rebecca; Mitchell, Philip B.; Mitjans, Marina; Mondimore, Francis M.; Monteleone, Palmiero; Mühleisen, Thomas W.; Nievergelt, Caroline M.; Nöthen, Markus M.; Novak, Tomas; Nurnberger, John I.; Nwulia, Evaristus A.; Ösby, Urban; Pfennig, Andrea; Potash, James B.; Propping, Peter; Reif, Andreas; Reininghaus, Eva; Rice, John; Rietschel, Marcella; Rouleau, Guy A.; Rybakowski, Janusz K.; Schalling, Martin; Scheftner, William A.; Schofield, Peter R.; Schork, Nicholas J.; Schulze, Thomas G.; Schumacher, Johannes; Schweizer, Barbara W.; Severino, Giovanni; Shekhtman, Tatyana; Shilling, Paul D.; Simhandl, Christian; Slaney, Claire M.; Smith, Erin N.; Squassina, Alessio; Stamm, Thomas; Stopkova, Pavla; Streit, Fabian; Strohmaier, Jana; Szelinger, Szabolcs; Tighe, Sarah K.; Tortorella, Alfonso; Turecki, Gustavo; Vieta, Eduard; Volkert, Julia; Witt, Stephanie H.; Wright, Adam; Zandi, Peter P.; Zhang, Peng; Zollner, Sebastian und McMahon, Francis J.
(2016):
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.
In: Human Molecular Genetics, Bd. 25, Nr. 15: S. 3383-3394
Schumacher, Johannes; Hoffmann, Per; Schmäl, Christine; Schulte-Körne, Gerd und Nöthen, Markus M.
(2007):
Genetics of dyslexia: the evolving landscape.
In: Journal of Medical Genetics, Bd. 44: S. 289-297
[PDF, 192kB]