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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 63
2024
Qu, Kang; Li, Ming-xi; Yu, Peng; Palotie, Aarno; Pressman, Alice; Belin, Andrea C.; Bjornsdottir, Anna; Maagdenberg, Arn M. J. M. van den; Harder, Aster V. E.; Winsvold, Bendik S.; Müller-Myhsok, Bertram; Cormand, Bru; Ran, Caroline; Northover, Carrie; Kubisch, Christian; Duijn, Cornelia van; Nyholt, Dale R.; Chasman, Daniel I.; Posthuma, Danielle; Lessel, Davor; Boomsma, Dorret I.; Hämäläinen, Eija; Kristoffersen, Espen S.; Cuenca-Leon, Ester; Davey-Smith, George; Terwindt, Gisela M.; Sigurdardottir, Gudrun R.; Bjornsdottir, Gyda; Hautakangas, Heidi; Stefansson, Hreinn; de Boer, Irene; Kaprio, Jaakko; Olesen, Jes; Zwart, John-Anker; Stefansson, Kari; Ligthart, Lannie; Launer, Lenore; Pedersen, Linda M.; Kogelman, Lisette J. A.; Griffiths, Lyn R.; Ikram, M. Arfan; Wessman, Maija; Kaunisto, Mari; Hrafnsdottir, Maria G.; Hiekkala, Marjo; Järvelin, Marjo-Riitta; Dichgans, Martin; Pirinen, Matti; Kallela, Mikko; Kurki, Mitja; Chalmer, Mona A.; Pedersen, Nancy; Sveinsson, Olafur A.; Raitakari, Olli; Gormley, Padhraig; Pozo-Rosich, Patricia; Palta, Priit; Malik, Rainer; Kajanne, Risto; Børte, Sigrid; Magnusson, Sigurdur H.; Lehtimäki, Terho; Hansen, Thomas F.; Thorgeirsson, Thorgeir E.; Freilinger, Tobias; Kurth, Tobias; Esko, Tonu; Anttila, Verneri; Artto, Ville; Wu, Bai-hua; Shi, Miao und Dong, Ming
(2024):
HMG-CoA reductase is a potential therapeutic target for migraine: a mendelian randomization study.
In: Scientific Reports, Bd. 14, Nr. 1, 12094
[PDF, 3MB]
2023
Zhao, Lei; Zhao, Wenhui; Anttila, Verneri; Artto, Ville; Belin, Andrea C.; Bjornsdottir, Anna; Bjornsdottir, Gyda; Boomsma, Dorret I.; Børte, Sigrid; Chalmer, Mona A.; Chasman, Daniel I.; Cormand, Bru; Cuenca-Leon, Ester; Davey-Smith, George; de Boer, Irene; Dichgans, Martin 
ORCID: https://orcid.org/0000-0002-0654-387X; Esko, Tonu; Freilinger, Tobias; Gormley, Padhraig; Griffiths, Lyn R.; Hämäläinen, Eija; Hansen, Thomas F.; Harder, Aster V. E.; Hautakangas, Heidi; Hiekkala, Marjo; Hrafnsdottir, Maria G.; Ikram, M. Arfan; Järvelin, Marjo-Riitta; Kajanne, Risto; Kallela, Mikko; Kaprio, Jaakko; Kaunisto, Mari; Kogelman, Lisette J. A.; Kristoffersen, Espen S.; Kubisch, Christian; Kurki, Mitja; Kurth, Tobias; Launer, Lenore; Lehtimäki, Terho; Lessel, Davor; Ligthart, Lannie; Magnusson, Sigurdur H.; Malik, Rainer; Müller-Myhsok, Bertram; Northover, Carrie; Nyholt, Dale R.; Olesen, Jes; Palotie, Aarno; Palta, Priit; Pedersen, Linda M.; Pedersen, Nancy; Pirinen, Matti; Posthuma, Danielle; Pozo-Rosich, Patricia; Pressman, Alice; Raitakari, Olli; Ran, Caroline; Sigurdardottir, Gudrun R.; Stefansson, Hreinn; Stefansson, Kari; Sveinsson, Olafur A.; Terwindt, Gisela M.; Thorgeirsson, Thorgeir E.; van den Maagdenberg, Arn M. J. M.; van Duijn, Cornelia; Wessman, Maija; Winsvold, Bendik S.; Zwart, John-Anker; Cao, Jin und Tu, Yiheng
(2023):
Causal relationships between migraine and microstructural white matter: a Mendelian randomization study.
In: Journal of Headache and Pain, Bd. 24, Nr. 1
[PDF, 4MB]
ORCID: https://orcid.org/0000-0002-0654-387X; Esko, Tonu; Freilinger, Tobias; Gormley, Padhraig; Griffiths, Lyn R.; Hämäläinen, Eija; Hansen, Thomas F.; Harder, Aster V. E.; Hautakangas, Heidi; Hiekkala, Marjo; Hrafnsdottir, Maria G.; Ikram, M. Arfan; Järvelin, Marjo-Riitta; Kajanne, Risto; Kallela, Mikko; Kaprio, Jaakko; Kaunisto, Mari; Kogelman, Lisette J. A.; Kristoffersen, Espen S.; Kubisch, Christian; Kurki, Mitja; Kurth, Tobias; Launer, Lenore; Lehtimäki, Terho; Lessel, Davor; Ligthart, Lannie; Magnusson, Sigurdur H.; Malik, Rainer; Müller-Myhsok, Bertram; Northover, Carrie; Nyholt, Dale R.; Olesen, Jes; Palotie, Aarno; Palta, Priit; Pedersen, Linda M.; Pedersen, Nancy; Pirinen, Matti; Posthuma, Danielle; Pozo-Rosich, Patricia; Pressman, Alice; Raitakari, Olli; Ran, Caroline; Sigurdardottir, Gudrun R.; Stefansson, Hreinn; Stefansson, Kari; Sveinsson, Olafur A.; Terwindt, Gisela M.; Thorgeirsson, Thorgeir E.; van den Maagdenberg, Arn M. J. M.; van Duijn, Cornelia; Wessman, Maija; Winsvold, Bendik S.; Zwart, John-Anker; Cao, Jin und Tu, Yiheng
(2023):
Causal relationships between migraine and microstructural white matter: a Mendelian randomization study.
In: Journal of Headache and Pain, Bd. 24, Nr. 1
[PDF, 4MB]
Zhang, Wenqiang; Zhang, Li; Yang, Luo; Xiao, Chenghan; Wu, Xueyao; Yan, Peijing; Cui, Huijie; Yang, Chao; Zhu, Jingwei; Wu, Xuan; Tang, Mingshuang; Wang, Yutong; Chen, Lin; Liu, Yunjie; Zou, Yanqiu; Zhang, Ling; Yang, Chunxia; Yao, Yuqin; Li, Jiayuan; Liu, Zhenmi; Zhang, Ben ORCID: https://orcid.org/0000-0002-4972-5171; Jiang, Xia; Anttila, Verneri; Artto, Ville; Belin, Andrea C.; Bjornsdottir, Anna; Bjornsdottir, Gyda; Boomsma, Dorret I.; Børte, Sigrid; Chalmer, Mona A.; Chasman, Daniel I.; Cormand, Bru; Cuenca-Leon, Ester; Davey-Smith, George; de Boer, Irene; Dichgans, Martin ORCID: https://orcid.org/0000-0002-0654-387X; Esko, Tonu; Freilinger, Tobias; Gormley, Padhraig; Griffiths, Lyn R.; Hämäläinen, Eija; Hansen, Thomas F.; Harder, Aster V. E.; Hautakangas, Heidi; Hiekkala, Marjo; Hrafnsdottir, Maria G.; Ikram, M. Arfan; Järvelin, Marjo-Riitta; Kajanne, Risto; Kallela, Mikko; Kaprio, Jaakko; Kaunisto, Mari; Kogelman, Lisette J. A.; Kristoffersen, Espen S.; Kubisch, Christian; Kurki, Mitja; Kurth, Tobias; Launer, Lenore; Lehtimäki, Terho; Lessel, Davor; Ligthart, Lannie; Magnusson, Sigurdur H.; Malik, Rainer; Müller-Myhsok, Bertram; Northover, Carrie; Nyholt, Dale R.; Olesen, Jes; Palotie, Aarno; Palta, Priit; Pedersen, Linda M.; Pedersen, Nancy; Pirinen, Matti; Posthuma, Danielle; Pozo-Rosich, Patricia; Pressman, Alice; Raitakari, Olli; Ran, Caroline; Sigurdardottir, Gudrun R.; Stefansson, Hreinn; Stefansson, Kari; Sveinsson, Olafur A.; Terwindt, Gisela M.; Thorgeirsson, Thorgeir E.; van den Maagdenberg, Arn M. J. M.; van Duijn, Cornelia; Wessman, Maija; Winsvold, Bendik S. und Zwart, John-Anker
(2023):
Migraine, chronic kidney disease and kidney function: observational and genetic analyses.
In: Human Genetics, Bd. 142, Nr. 8: S. 1185-1200
[PDF, 1MB]
ORCID: https://orcid.org/0000-0002-4972-5171; Jiang, Xia; Anttila, Verneri; Artto, Ville; Belin, Andrea C.; Bjornsdottir, Anna; Bjornsdottir, Gyda; Boomsma, Dorret I.; Børte, Sigrid; Chalmer, Mona A.; Chasman, Daniel I.; Cormand, Bru; Cuenca-Leon, Ester; Davey-Smith, George; de Boer, Irene; Dichgans, Martin ORCID: https://orcid.org/0000-0002-0654-387X; Esko, Tonu; Freilinger, Tobias; Gormley, Padhraig; Griffiths, Lyn R.; Hämäläinen, Eija; Hansen, Thomas F.; Harder, Aster V. E.; Hautakangas, Heidi; Hiekkala, Marjo; Hrafnsdottir, Maria G.; Ikram, M. Arfan; Järvelin, Marjo-Riitta; Kajanne, Risto; Kallela, Mikko; Kaprio, Jaakko; Kaunisto, Mari; Kogelman, Lisette J. A.; Kristoffersen, Espen S.; Kubisch, Christian; Kurki, Mitja; Kurth, Tobias; Launer, Lenore; Lehtimäki, Terho; Lessel, Davor; Ligthart, Lannie; Magnusson, Sigurdur H.; Malik, Rainer; Müller-Myhsok, Bertram; Northover, Carrie; Nyholt, Dale R.; Olesen, Jes; Palotie, Aarno; Palta, Priit; Pedersen, Linda M.; Pedersen, Nancy; Pirinen, Matti; Posthuma, Danielle; Pozo-Rosich, Patricia; Pressman, Alice; Raitakari, Olli; Ran, Caroline; Sigurdardottir, Gudrun R.; Stefansson, Hreinn; Stefansson, Kari; Sveinsson, Olafur A.; Terwindt, Gisela M.; Thorgeirsson, Thorgeir E.; van den Maagdenberg, Arn M. J. M.; van Duijn, Cornelia; Wessman, Maija; Winsvold, Bendik S. und Zwart, John-Anker
(2023):
Migraine, chronic kidney disease and kidney function: observational and genetic analyses.
In: Human Genetics, Bd. 142, Nr. 8: S. 1185-1200
[PDF, 1MB]
He, Qiang; Wang, Wenjing; Xiong, Yang; Tao, Chuanyuan; Ma, Lu; Ma, Junpeng; You, Chao; Anttila, Verneri; Artto, Ville; Belin, Andrea C.; Bjornsdottir, Anna; Bjornsdottir, Gyda; Boomsma, Dorret I.; Børte, Sigrid; Chalmer, Mona A.; Chasman, Daniel I.; Cormand, Bru; Cuenca-Leon, Ester; Davey-Smith, George; Boer, Irene de; Dichgans, Martin ORCID: https://orcid.org/0000-0002-0654-387X; Esko, Tonu; Freilinger, Tobias; Gormley, Padhraig; Griffiths, Lyn R.; Hämäläinen, Eija; Hansen, Thomas F.; Harder, Aster V. E.; Hautakangas, Heidi; Hiekkala, Marjo; Hrafnsdottir, Maria G.; Ikram, M. Arfan; Järvelin, Marjo-Riitta; Kajanne, Risto; Kallela, Mikko; Kaprio, Jaakko; Kaunisto, Mari; Kogelman, Lisette J. A.; Kristoffersen, Espen S.; Kubisch, Christian; Kurki, Mitja; Kurth, Tobias; Launer, Lenore; Lehtimäki, Terho; Lessel, Davor; Ligthart, Lannie; Magnusson, Sigurdur H.; Malik, Rainer; Müller-Myhsok, Bertram; Northover, Carrie; Nyholt, Dale R.; Olesen, Jes; Palotie, Aarno; Palta, Priit; Pedersen, Linda M.; Pedersen, Nancy; Pirinen, Matti; Posthuma, Danielle; Pozo-Rosich, Patricia; Pressman, Alice; Raitakari, Olli; Ran, Caroline; Sigurdardottir, Gudrun R.; Stefansson, Hreinn; Stefansson, Kari; Sveinsson, Olafur A.; Terwindt, Gisela M.; Thorgeirsson, Thorgeir E.; Maagdenberg, Arn M. J. M. van den; Duijn, Cornelia van; Wessman, Maija; Winsvold, Bendik S. und Zwart, John-Anker
(2023):
A causal effects of gut microbiota in the development of migraine.
In: Journal of Headache and Pain, Bd. 24, 90
[PDF, 7MB]
ORCID: https://orcid.org/0000-0002-0654-387X; Esko, Tonu; Freilinger, Tobias; Gormley, Padhraig; Griffiths, Lyn R.; Hämäläinen, Eija; Hansen, Thomas F.; Harder, Aster V. E.; Hautakangas, Heidi; Hiekkala, Marjo; Hrafnsdottir, Maria G.; Ikram, M. Arfan; Järvelin, Marjo-Riitta; Kajanne, Risto; Kallela, Mikko; Kaprio, Jaakko; Kaunisto, Mari; Kogelman, Lisette J. A.; Kristoffersen, Espen S.; Kubisch, Christian; Kurki, Mitja; Kurth, Tobias; Launer, Lenore; Lehtimäki, Terho; Lessel, Davor; Ligthart, Lannie; Magnusson, Sigurdur H.; Malik, Rainer; Müller-Myhsok, Bertram; Northover, Carrie; Nyholt, Dale R.; Olesen, Jes; Palotie, Aarno; Palta, Priit; Pedersen, Linda M.; Pedersen, Nancy; Pirinen, Matti; Posthuma, Danielle; Pozo-Rosich, Patricia; Pressman, Alice; Raitakari, Olli; Ran, Caroline; Sigurdardottir, Gudrun R.; Stefansson, Hreinn; Stefansson, Kari; Sveinsson, Olafur A.; Terwindt, Gisela M.; Thorgeirsson, Thorgeir E.; Maagdenberg, Arn M. J. M. van den; Duijn, Cornelia van; Wessman, Maija; Winsvold, Bendik S. und Zwart, John-Anker
(2023):
A causal effects of gut microbiota in the development of migraine.
In: Journal of Headache and Pain, Bd. 24, 90
[PDF, 7MB]
2022
Nenadić, Igor ORCID: https://orcid.org/0000-0002-0749-7473; Meller, Tina; Schmitt, Simon; Stein, Frederike; Brosch, Katharina; Mosebach, Johannes; Ettinger, Ulrich; Grant, Phillip; Meinert, Susanne; Opel, Nils; Lemke, Hannah; Fingas, Stella; Förster, Katharina; Hahn, Tim; Jansen, Andreas; Andlauer, Till F. M.; Forstner, Andreas J.; Heilmann-Heimbach, Stefanie; Hall, Alisha S. M.; Awasthi, Swapnil; Ripke, Stephan; Witt, Stephanie H.; Rietschel, Marcella; Müller-Myhsok, Bertram; Nöthen, Markus M.; Dannlowski, Udo; Krug, Axel; Streit, Fabian und Kircher, Tilo
(2022):
Polygenic risk for schizophrenia and schizotypal traits in non-clinical subjects.
In: Psychological Medicine, Bd. 52, Nr. 6: S. 1069-1079
ORCID: https://orcid.org/0000-0002-0749-7473; Meller, Tina; Schmitt, Simon; Stein, Frederike; Brosch, Katharina; Mosebach, Johannes; Ettinger, Ulrich; Grant, Phillip; Meinert, Susanne; Opel, Nils; Lemke, Hannah; Fingas, Stella; Förster, Katharina; Hahn, Tim; Jansen, Andreas; Andlauer, Till F. M.; Forstner, Andreas J.; Heilmann-Heimbach, Stefanie; Hall, Alisha S. M.; Awasthi, Swapnil; Ripke, Stephan; Witt, Stephanie H.; Rietschel, Marcella; Müller-Myhsok, Bertram; Nöthen, Markus M.; Dannlowski, Udo; Krug, Axel; Streit, Fabian und Kircher, Tilo
(2022):
Polygenic risk for schizophrenia and schizotypal traits in non-clinical subjects.
In: Psychological Medicine, Bd. 52, Nr. 6: S. 1069-1079
Tilch, Erik; Schormair, Barbara ORCID: https://orcid.org/0000-0003-0942-5243; Zhao, Chen; Högl, Birgit; Stefani, Ambra; Berger, Klaus; Trenkwalder, Claudia; Bachmann, Cornelius G.; Hornyak, Magdolna; Fietze, Ingo; Müller-Nurasyid, Martina ORCID: https://orcid.org/0000-0003-3793-5910; Peters, Annette; Herms, Stefan; Nöthen, Markus M.; Müller-Myhsok, Bertram; Oexle, Konrad und Winkelmann, Juliane
(2022):
ExomeChip-based rare variant association study in restless legs syndrome.
In: Sleep Medicine, Bd. 94: S. 26-30
[PDF, 598kB]
ORCID: https://orcid.org/0000-0003-0942-5243; Zhao, Chen; Högl, Birgit; Stefani, Ambra; Berger, Klaus; Trenkwalder, Claudia; Bachmann, Cornelius G.; Hornyak, Magdolna; Fietze, Ingo; Müller-Nurasyid, Martina ORCID: https://orcid.org/0000-0003-3793-5910; Peters, Annette; Herms, Stefan; Nöthen, Markus M.; Müller-Myhsok, Bertram; Oexle, Konrad und Winkelmann, Juliane
(2022):
ExomeChip-based rare variant association study in restless legs syndrome.
In: Sleep Medicine, Bd. 94: S. 26-30
[PDF, 598kB]
Eising, Else; Mirza-Schreiber, Nazanin; de Zeeuw, Eveline L.; Wang, Carol A.; Truong, Dongnhu T.; Allegrini, Andrea G.; Shapland, Chin Yang; Zhu, Gu; Wigg, Karen G.; Gerritse, Margot L.; Molz, Barbara; Alagoz, Gokberk; Gialluisi, Alessandro; Abbondanza, Filippo; Rimfeld, Kaili; Donkelaar, Marjolein van; Liao, Zhijie; Jansen, Philip R.; Andlauer, Till F. M.; Bates, Timothy C.; Bernard, Manon; Blokland, Kirsten; Bonte, Milene; Borglum, Anders D.; Bourgeron, Thomas; Brandeis, Daniel; Ceronihh, Fabiola; Csepe, Valeria; Dale, Philip S.; Jong, Peter F. de; DeFries, John C.; Demonet, Jean-Francois; Demontis, Ditte; Feng, Yu; Gordon, Scott D.; Guger, Sharon L.; Hayiou-Thomas, Marianna E.; Hernandez-Cabrera, Juan A.; Hottenga, Jouke-Jan; Hulme, Charles; Kere, Juha; Kerr, Elizabeth N.; Koomar, Tanner; Landerl, Karin; Leonard, Gabriel T.; Lovett, Maureen W.; Lyytinen, Heikki; Martin, Nicholas G.; Martinelli, Angela; Maurer, Urs; Michaelson, Jacob J.; Moll, Kristina; Monaco, Anthony P.; Morgan, Angela T.; Nothen, Markus M.; Pausova, Zdenka; Pennell, Craig E.; Pennington, Bruce F.; Price, Kaitlyn M.; Rajagopal, Veera M.; Ramus, Franck; Richer, Louis; Simpson, Nuala H.; Smith, Shelley D.; Snowling, Margaret J.; Stein, John; Struguuu, Lisa J.; Talcott, Joel B.; Tiemeier, Henning; Schroeff, Marc P. van der; Verhoef, Ellen; Watkins, Kate E.; Wilkinson, Margaret; Wright, Margaret J.; Barr, Cathy L.; Boomsma, Dorret I.; Carreiras, Manuel; Franken, Marie-Christine J.; Gruen, Jeffrey R.; Luciano, Michelle; Müller-Myhsok, Bertram; Newbury, Dianne F.; Olson, Richard K.; Paracchini, Silvia; Paus, Tomas; Plomin, Robert; Reilly, Sheena; Schulte-Körne, Gerd; Tomblin, J. Bruce; Bergen, Elsjevan; Whitehouse, Andrew J. O.; Willcutt, Erik G.; St Pourcain, Beate; Francks, Clyde und Fisher, Simon E.
(2022):
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.
In: Proceedings of the National Academy of Sciences of the United States of America, Bd. 119, Nr. 35, e2202764119
Trubetskoy, Vassily; Pardinas, Antonio F.; Qi, Ting; Panagiotaropoulou, Georgia; Awasthi, Swapnil; Bigdeli, Tim B.; Bryois, Julien; Chen, Chia-Yen; Dennison, Charlotte A.; Hall, Lynsey S.; Lam, Max; Watanabe, Kyoko; Frei, Oleksandr; Ge, Tian; Harwood, Janet C.; Koopmans, Frank; Magnusson, Sigurdur; Richards, Alexander L.; Sidorenko, Julia; Wu, Yang; Zeng, Jian; Grove, Jakob; Kim, Minsoo; Li, Zhiqiang; Voloudakis, Georgios; Zhang, Wen; Adams, Mark; Agartz, Ingrid; Atkinson, Elizabeth G.; Agerbo, Esben; Al Eissa, Mariam; Albus, Margot; Alexander, Madeline; Alizadeh, Behrooz Z.; Alptekin, Koksal; Als, Thomas D.; Amin, Farooq; Arolt, Volker; Arrojo, Manuel; Athanasiu, Lavinia; Azevedo, Maria Helena; Bacanu, Silviu A.; Bass, Nicholas J.; Begemann, Martin; Belliveau, Richard A.; Bene, Judit; Benyamin, Beben; Bergen, Sarah E.; Blasi, Giuseppe; Bobes, Julio; Bonassi, Stefano; Braun, Alice; Bressan, Rodrigo Affonseca; Bromet, Evelyn J.; Bruggeman, Richard; Buckley, Peter F.; Buckner, Randy L.; Bybjerg-Grauholm, Jonas; Cahn, Wiepke; Cairns, Murray J.; Calkins, Monica E.; Carr, Vaughan J.; Castle, David; Catts, Stanley V.; Chambert, Kimberley D.; Chan, Raymond C. K.; Chaumette, Boris; Cheng, Wei; Cheung, Eric F. C.; Chong, Siow Ann; Cohen, David; Consoli, Angele; Cordeiro, Quirino; Costas, Javier; Curtis, Charles; Davidson, Michael; Davis, Kenneth L.; Haan, Lieuwe de; Degenhardt, Franziska; DeLisi, Lynn E.; Demontis, Ditte; Dickerson, Faith; Dikeos, Dimitris; Dinan, Timothy; Djurovic, Srdjan; Duan, Jubao; Ducci, Giuseppe; Dudbridge, Frank; Eriksson, Johan G.; Fananas, Lourdes; Faraone, Stephen V.; Fiorentino, Alessia; Forstner, Andreas; Frank, Josef; Freimer, Nelson B.; Fromer, Menachem; Frustaci, Alessandra; Gadelha, Ary; Genovese, Giulio; Gershon, Elliot S.; Giannitelli, Marianna; Giegling, Ina; Giusti-Rodriguez, Paola; Godard, Stephanie; Goldstein, Jacqueline I.; Penas, Javier Gonzalez; Gonzalez-Pinto, Ana; Gopal, Srihari; Gratten, Jacob; Green, Michael F.; Greenwood, Tiffany A.; Guillin, Olivier; Guloksuz, Sinan; Gur, Raquel E.; Gur, Ruben C.; Gutierrez, Blanca; Hahn, Eric; Hakonarson, Hakon; Haroutunian, Vahram; Hartmann, Annette M.; Harvey, Carol; Hayward, Caroline; Henskens, Frans A.; Herms, Stefan; Hoffmann, Per; Howrigan, Daniel P.; Ikeda, Masashi; Iyegbe, Conrad; Joa, Inge; Julia, Antonio; Kahler, Anna K.; Kam-Thong, Tony; Kamatani, Yoichiro; Karachanak-Yankova, Sena; Kebir, Oussama; Keller, Matthew C.; Kelly, Brian J.; Khrunin, Andrey; Kim, Sung-Wan; Klovins, Janis; Kondratiev, Nikolay; Konte, Bettina; Kraft, Julia; Kubo, Michiaki; Kucinskas, Vaidutis; Kucinskiene, Zita Ausrele; Kusumawardhani, Agung; Kuzelova-Ptackova, Hana; Landi, Stefano; Lazzeroni, Laura C.; Lee, Phil H.; Legge, Sophie E.; Lehrer, Douglas S.; Lencer, Rebecca; Lerer, Bernard; Li, Miaoxin; Lieberman, Jeffrey; Light, Gregory A.; Limborska, Svetlana; Liu, Chih-Min; Lonnqvist, Jouko; Loughland, Carmel M.; Lubinski, Jan; Luykx, Jurjen J.; Lynham, Amy; Macek, Milan; Mackinnon, Andrew; Magnusson, Patrik K. E.; Maher, Brion S.; Maier, Wolfgang; Malaspina, Dolores; Mallet, Jacques; Marder, Stephen R.; Marsal, Sara; Martin, Alicia R.; Martorell, Lourdes; Mattheisen, Manuel; McCarley, Robert W.; McDonald, Colm; McGrath, John J.; Medeiros, Helena; Meier, Sandra; Melegh, Bela; Melle, Ingrid; Mesholam-Gately, Raquelle I.; Metspalu, Andres; Michie, Patricia T.; Milani, Lili; Milanova, Vihra; Mitjans, Marina; Molden, Espen; Molina, Esther; Molto, Maria Dolores; Mondelli, Valeria; Moreno, Carmen; Morley, Christopher P.; Muntane, Gerard; Murphy, Kieran C.; Myin-Germeys, Inez; Nenadic, Igor; Nestadt, Gerald; Nikitina-Zake, Liene; Noto, Cristiano; Nuechterlein, Keith H.; O'Brien, Niamh Louise; O'Neill, F. Anthony; Oh, Sang-Yun; Olincy, Ann; Ota, Vanessa Kiyomi; Pantelis, Christos; Papadimitriou, George N.; Parellada, Mara; Paunio, Tiina; Pellegrino, Renata; Periyasamy, Sathish; Perkins, Diana O.; Pfuhlmann, Bruno; Pietilainen, Olli; Pimm, Jonathan; Porteous, David; Powell, John; Quattrone, Diego; Quested, Digby; Radant, Allen D.; Rampino, Antonio; Rapaport, Mark H.; Rautanen, Anna; Reichenberg, Abraham; Roe, Cheryl; Roffman, Joshua L.; Roth, Julian; Rothermundt, Matthias; Rutten, Bart P. F.; Saker-Delye, Safaa; Salomaa, Veikko; Sanjuan, Julio; Santoro, Marcos Leite; Savitz, Adam; Schall, Ulrich; Scott, Rodney J.; Seidman, Larry J.; Sharp, Sally Isabel; Shi, Jianxin; Siever, Larry J.; Sigurdsson, Engilbert; Sim, Kang; Skarabis, Nora; Slominsky, Petr; So, Hon-Cheong; Sobell, Janet L.; Soderman, Erik; Stain, Helen J.; Steen, Nils Eiel; Steixner-Kumar, Agnes A.; Stogmann, Elisabeth; Stone, William S.; Straub, Richard E.; Streit, Fabian; Strengman, Eric; Stroup, T. Scott; Subramaniam, Mythily; Sugar, Catherine A.; Suvisaari, Jaana; Svrakic, Dragan M.; Swerdlow, Neal R.; Szatkiewicz, Jin P.; Thi Minh, Tam Ta; Takahashi, Atsushi; Terao, Chikashi; Thibaut, Florence; Toncheva, Draga; Tooney, Paul A.; Torretta, Silvia; Tosato, Sarah; Tura, Gian Battista; Turetsky, Bruce I.; Ucok, Alp; Vaaler, Arne; Amelsvoort, Therese van; Winkel, Ruud van; Veijola, Juha; Waddington, John; Walter, Henrik; Waterreus, Anna; Webb, Bradley T.; Weiser, Mark; Williams, Nigel M.; Witt, Stephanie H.; Wormley, Brandon K.; Wu, Jing Qin; Xu, Zhida; Yolken, Robert; Zai, Clement C.; Zhou, Wei; Zhu, Feng; Zimprich, Fritz; Ayub, Muhammad; Benner, Christian; Bertolino, Alessandro; Black, Donald W.; Bray, Nicholas J.; Breen, Gerome; Buccola, Nancy G.; Byerley, William F.; Chen, Wei J.; Cloninger, C. 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Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities.
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2021
Miranda, Lucas; Paul, Riya; Pütz, Benno; Koutsouleris, Nikolaos und Müller-Myhsok, Bertram
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Systematic Review of Functional MRI Applications for Psychiatric Disease Subtyping.
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[PDF, 735kB]
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(2021):
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.
In: Biological Psychiatry, Bd. 91, Nr. 1: S. 102-117
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(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
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(2021):
Characterisation of age and polarity at onset in bipolar disorder.
In: British Journal of Psychiatry, Bd. 219, Nr. 6, PII S0007125021001021: S. 659-669
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(2021):
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.
In: Nature Genetics, Bd. 53, Nr. 6: S. 817-829
[PDF, 1MB]
Ostkamp, Patrick; Salmen, Anke; Pignolet, Beatrice; Görlich, Dennis; Andlauer, Till F. M.; Schulte-Mecklenbeck, Andreas; Gonzalez-Escamilla, Gabriel; Bucciarelli, Florence; Gennero, Isabelle; Breuer, Johanna; Antony, Gisela; Schneider-Hohendorf, Tilman; Mykicki, Nadine; Bayas, Antonios; Bergh, Florian Then; Bittner, Stefan; Hartung, Hans-Peter; Friese, Manuel A.; Linker, Ralf A.; Luessi, Felix; Lehmann-Horn, Klaus; Mühlau, Mark; Paul, Friedemann; Stangel, Martin; Tackenberg, Björn; Tumani, Hayrettin; Warnke, Clemens; Weber, Frank; Wildemann, Brigitte; Zettl, Uwe K.; Ziemann, Ulf; Müller-Myhsok, Bertram; Kümpfel, Tania; Klotz, Luisa; Meuth, Sven G.; Zipp, Frauke; Hemmer, Bernhard; Hohlfeld, Reinhard; Brassat, David; Gold, Ralf; Gross, Catharina C.; Lukas, Carsten; Groppa, Sergiu; Loser, Karin; Wiendl, Heinz und Schwab, Nicholas
(2021):
Sunlight exposure exerts immunomodulatory effects to reduce multiple sclerosis severity.
In: Proceedings of the National Academy of Sciences of the United States of America, Bd. 118, Nr. 1, e2018457118
[PDF, 2MB]
Kalman, Janos L.; Olde Loohuis, Loes M.; Smoller, Jordan W.; Biernacka, Joanna M.; McMahon, Francis J.; Alda, Martin; Müller-Myhsok, Bertram; Koutsouleris, Nikolaos; Falkai, Peter; Freimer, Nelson B.; Andlauer, Till F. M.; Schulze, Thomas G. und Ophoff, Roel A.
(2021):
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In: British journal of psychiatry : the journal of mental science, Bd. 219, Nr. 6: S. 659-669
[PDF, 992kB]
2020
Gola, Damian; Erdmann, Jeanette ORCID: https://orcid.org/0000-0002-4486-6231; Läll, Kristi; Mägi, Reedik ORCID: https://orcid.org/0000-0002-2964-6011; Müller-Myhsok, Bertram; Schunkert, Heribert ORCID: https://orcid.org/0000-0001-6428-3001 und König, Inke R. ORCID: https://orcid.org/0000-0003-0504-6465
(2020):
Population Bias in Polygenic Risk Prediction Models for Coronary Artery Disease.
In: Circulation: Genomic and Precision Medicine, Bd. 13, Nr. 6
ORCID: https://orcid.org/0000-0002-4486-6231; Läll, Kristi; Mägi, Reedik ORCID: https://orcid.org/0000-0002-2964-6011; Müller-Myhsok, Bertram; Schunkert, Heribert ORCID: https://orcid.org/0000-0001-6428-3001 und König, Inke R. ORCID: https://orcid.org/0000-0003-0504-6465
(2020):
Population Bias in Polygenic Risk Prediction Models for Coronary Artery Disease.
In: Circulation: Genomic and Precision Medicine, Bd. 13, Nr. 6
Coleman, Jonathan R. I.; Peyrot, Wouter J.; Purves, Kirstin L.; Davis, Katrina A. S.; Rayner, Christopher; Choi, Shing Wan; Hubel, Christopher; Gaspar, Helena A.; Kan, Carol; Auwera, Sandra van der; Adams, Mark James; Lyall, Donald M.; Choi, Karmel W.; Dunn, Erin C.; Vassos, Evangelos; Danese, Andrea; Maughan, Barbara; Grabe, Hans J.; Lewis, Cathryn M.; O'Reilly, Paul F.; McIntosh, Andrew M.; Smith, Daniel J.; Wray, Naomi R.; Hotopf, Matthew; Eley, Thalia C.; 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.; 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.; Foo, Jerome C.; Forstner, Andreas J.; Frank, Josef; Gaspar, Helena A.; Gill, Michael; Goes, Fernando S.; Gordon, Scott D.; Grove, Jakob; Hall, Lynsey S.; Hansen, Christine Soholm; Hansen, Thomas F.; Herms, Stefan; Hickie, Ian B.; Hoffmann, Per; Homuth, Georg; Horn, Carsten; Hottenga, Jouke-Jan; Hougaard, David M.; Howard, David M.; Ising, Marcus; Jansen, Rick; Jones, Ian; Jones, Lisa A.; Jorgenson, Eric; Knowles, James A.; Kohane, Isaac S.; Kraft, Julia; Kretzschmar, Warren W.; 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.; 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; Quiroz, Jorge A.; Qvist, Per; Rice, John P.; Riley, Brien P.; Rivera, Margarita; Mirza, Saira Saeed; Schoevers, Robert; Schulte, Eva C.; Shen, Ling; Shi, Jianxin; Shyn, Stanley I.; 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, Andres 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, Jurgen; 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; de Geus, E. J. C.; 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; Noethen, 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; Volzke, Henry; Weissman, Myrna M.; Werge, Thomas; Lewis, Cathryn M.; Levinson, Douglas F.; Breen, Gerome; Borglum, Anders D. und Sullivan, Patrick F.
(2020):
Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank.
In: Molecular Psychiatry, Bd. 25, Nr. 7: S. 1430-1446
[PDF, 650kB]
Grimm, Tiemo; Garshasbi, Masoud; Puettmann, Lucia; Chen, Wei; Ullmann, Reinhard; Müller-Myhsok, Bertram; Klopocki, Eva; Herbst, Lina; Haug, Janina; Jensen, Lars R.; Fischer, Christine; Nöthen, Markus; Ludwig, Kerstin; Warnke, Andreas; Ott, Jürg; Schulte-Körne, Gerd; Ropers, Hans-Hilger und Kuss, Andreas W.
(2020):
A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q.
In: Zeitschrift für Kinder-und Jugendpsychiatrie und Psychotherapie, Bd. 48, Nr. 6: S. 478-489
Glanville, Kylie P.; Coleman, Jonathan R.; Hanscombe, Ken B.; Euesden, Jack; Choi, Shing Wan; Purves, Kirstin L.; Breen, Gerome; Air, Tracy M.; Andlauer, Till F. M.; Baune, Bernhard T.; Binder, Elisabeth B.; Blackwood, Douglas H. R.; Boomsma, Dorret; Buttenschon, Henriette N.; Colodro-Conde, Lucia; Dannlowski, Udo; Direk, Nese; Dunn, Erin C.; Forstner, Andreas J.; de Geus, Eco J. C.; Grabe, Hans J.; Hamilton, Steven P.; Jones, Ian; Jones, Lisa A.; Knowles, James A.; Kutalik, Zoltan; Levinson, Douglas F.; Lewis, Glyn; Lind, Penelope A.; Lucae, Susanne; Magnusson, Patrik K.; McGuffin, Peter; McIntosh, Andrew M.; Milaneschi, Yuri; Mors, Ole; Mostafavi, Sara; Müller-Myhsok, Bertram; Pedersen, Nancy L.; Penninx, Brenda W. J. H.; Potash, James B.; Preisig, Martin; Ripke, Stephan; Shi, Jianxin; Shyn, Stanley; Smoller, Jordan W.; Streit, Fabian; Sullivan, Patrick F.; Tiemeier, Henning; Uher, Rudolf; Auwera, Sandra van der; Weissman, Myrna M.; O'Reilly, Paul F.; Lewis, Cathryn M.; Wray, Naomi R.; Mattheisen, Manuel; Trzaskowski, Maciej; Byrne, Enda M.; Abdellaoui, Abdel; Adams, Mark J.; Agerbo, Esben; Bacanu, Silviu-Alin; Baekvad-Hansen, Marie; Beekman, Aartjan T. F.; Bigdeli, Tim B.; Bryois, Julien; Bybjerg-Grauholm, Jonas; Cai, Na; Castelao, Enrique; Christensen, Jane Hvarregaard; Clarke, Toni-Kim; Couvy-Duchesne, Baptiste; Craddock, Nick; Crawford, Gregory E.; Davies, Gail; Deary, Ian J.; Degenhardt, Franziska; Derks, Eske M.; Dolan, Conor; Eley, Thalia C.; Escott-Price, Valentina; Kiadeh, Farnush Farhadi Hassan; Finucane, Hilary K.; Foo, Jerome C.; Frank, Josef; Gaspar, Helena A.; Gill, Michael; Goes, Fernando S.; Gordon, Scott D.; Grove, Jakob; Hall, Lynsey S.; Hansen, Christine Soholm; Hansen, Thomas F.; Herms, Stefan; Hickie, Ian B.; Hoffmann, Per; Homuth, Georg; Horn, Carsten; Hottenga, Jouke-Jan; Hougaard, David M.; Howard, David M.; Ising, Marcus; Jansen, Rick; Jorgenson, Eric; Kohane, Isaac S.; Kraft, Julia; Kretzschmar, Warren W.; Li, Yihan; MacIntyre, Donald J.; MacKinnon, Dean F.; Maier, Robert M.; Maier, Wolfgang; Marchini, Jonathan; Mbarek, Hamdi; McGrath, Patrick; Medland, Sarah E.; Mehta, Divya; Middeldorp, Christel M.; Mihailov, Evelin; Milani, Lili; Mondimore, Francis M.; Montgomery, Grant W.; 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; Schoevers, Robert; Schulte, Eva C.; Shen, Ling; Sigurdsson, Engilbert; Sinnamon, Grant C. B.; Smit, Johannes H.; Smith, Daniel J.; Stefansson, Hreinn; Steinberg, Stacy; Strohmaier, Jana; Tansey, Katherine E.; Teismann, Henning; Teumer, Alexander; Thompson, Wesley; Thomson, Pippa A.; Thorgeirsson, Thorgeir E.; Traylor, Matthew; Treutlein, Jens; Trubetskoy, Vassily; Uitterlinden, Andres G.; Umbricht, Daniel; 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; Berger, Klaus; Cichon, Sven; de Geus, E. J. C.; DePaulo, J. Raymond; Domenici, Enrico; Domschke, Katharina; Esko, Tonu; Hayward, Caroline; Heath, Andrew C.; Kendler, Kenneth S.; Kloiber, Stefan; Li, Qingqin S.; Madden, Pamela A. F.; Martin, Nicholas G.; Metspalu, Andres; Mortensen, Preben Bo; Müller-Myhsok, Bertram; Nordentoft, Merete; Noethen, Markus M.; O'Donovan, Michael C.; Paciga, Sara A.; Perlis, Roy H.; Porteous, David J.; Rietschel, Marcella; Schaefer, Catherine; Schulze, Thomas G.; Stefansson, Kari; Voelzke, Henry; Werge, Thomas und Borglum, Anders D.
(2020):
Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression.
In: Biological Psychiatry, Bd. 87, Nr. 5: S. 419-430
[PDF, 843kB]
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]
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(2020):
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.
In: Addiction Biology, Bd. 26, Nr. 1, e12880
Shen, Xueyi ORCID: https://orcid.org/0000-0002-0538-4774; Howard, David M. ORCID: https://orcid.org/0000-0002-6005-1972; Adams, Mark J. ORCID: https://orcid.org/0000-0002-3599-6018; Hill, W. David; Clarke, Toni-Kim; Adams, Mark J.; Clarke, Toni-Kim; McIntosh, Andrew M.; Deary, Ian J.; Wray, Naomi R.; Ripke, Stephan; Mattheisen, Manuel; Trzaskowski, Maciej; Byrne, Enda M.; Abdellaoui, Abdel; Agerbo, Esben; Air, Tracy M.; Andlauer, Till F. M.; Bacanu, Silviu-Alin; Bækvad-Hansen, Marie; Beekman, Aartjan T. F.; Bigdeli, Tim B.; Binder, Elisabeth B.; Bryois, Julien; Buttenschøn, Henriette N.; Bybjerg-Grauholm, Jonas; Cai, Na; Castelao, Enrique; Christensen, Jane Hvarregaard; Coleman, Jonathan R. I.; Colodro-Conde, Lucía; Couvy-Duchesne, Baptiste; Craddock, Nick; Crawford, Gregory E.; Davies, Gail; 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.; Foo, Jerome C.; Forstner, Andreas J.; Frank, Josef; Gaspar, Héléna A.; Gill, Michael; Goes, Fernando S.; Gordon, Scott D.; Grove, Jakob; Hall, Lynsey S.; Hansen, Christine Søholm; Hansen, Thomas F.; Herms, Stefan; Hickie, Ian B.; Hoffmann, Per; Homuth, Georg; Horn, Carsten; Hottenga, Jouke-Jan; Hougaard, David M.; Howard, David M.; Ising, Marcus; Jansen, Rick; Jones, Ian; Jones, Lisa A.; Jorgenson, Eric; Knowles, James A.; Kohane, Isaac S.; Kraft, Julia; Kretzschmar, Warren W.; Kutalik, Zoltán; 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.; O’Reilly, Paul F.; Oskarsson, Hogni; Owen, Michael J.; Painter, Jodie N.; Pedersen, Carsten Bøcker; Pedersen, Marianne Giørtz; 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; Schoevers, Robert; Schulte, Eva C.; Shen, Ling; Shi, Jianxin; Shyn, Stanley I.; 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, Andrés G.; Umbricht, Daniel; Auwera, Sandra Van der; van Hemert, Albert M.; 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 I.; Cichon, Sven; Dannlowski, Udo; de Geus, E. J. C.; DePaulo, J. Raymond; Domenici, Enrico; Domschke, Katharina; Esko, Tõnu; 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.; 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.; Breen, Gerome; Børglum, Anders D.; Sullivan, Patrick F.; Deary, Ian J.; Whalley, Heather C. ORCID: https://orcid.org/0000-0002-4505-8869 und McIntosh, Andrew M. ORCID: https://orcid.org/0000-0002-0198-4588
(2020):
A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank.
In: Nature Communications, Bd. 11, Nr. 1, 2301
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(2019):
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(2019):
Identification of common genetic risk variants for autism spectrum disorder.
In: Nature Genetics, Bd. 51, Nr. 3
[PDF, 1MB]
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(2019):
Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns.
In: Nature Communications, Bd. 10, 2548
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(2019):
Association of Polygenic Liabilities for Major Depression, Bipolar Disorder, and Schizophrenia With Risk for Depression in the Danish Population.
In: Jama Psychiatry, Bd. 76, Nr. 5: S. 516-525
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(2019):
GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.
In: American Journal of Psychiatry, Bd. 176, Nr. 8: S. 651-660
[PDF, 766kB]
Foo, Jerome C.; Streit, Fabian; Frank, Josef; Witt, Stephanie H.; Treutlein, Jens; Baune, Bernhard T.; Moebus, Susanne; Joeckel, Karl-Heinz; Forstner, Andreas J.; Noethen, Markus M.; Rietschel, Marcella; Sartorius, Alexander; Kranaster, Laura; 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.; Gaspar, Helena A.; Gill, Michael; Goes, Fernando S.; Gordon, Scott D.; Grove, Jakob; Hall, Lynsey S.; 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.; Jörgenson, 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.; 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; Quiroz, Jörge A.; Qvist, Per; Rice, John P.; Riley, Brien P.; Rivera, Margarita; Mirza, Saira Saeed; Schoevers, Robert; Schulte, Eva C.; Shen, Ling; Shi, Jianxin; Shyn, Stanley I.; Sigurdsson, Engilbert; Sinnamon, Grant C. B.; Smit, Johannes H.; Smith, Daniel J.; Stefansson, Hreinn; Steinberg, Stacy; Strohmaier, Jana; Tansey, Katherine E.; Teismann, Henning; Teumer, Alexander; Thompson, Wesley; Thomson, Pippa A.; Thorgeirsson, Thorgeir E.; Traylor, Matthew; Trubetskoy, Vassily; Uitterlinden, Andre G.; Umbricht, Daniel; Van der Auwera, Sandra; van Hemert, Albert M.; Viktorin, Alexander; Visscher, Peter M.; Wang, Yunpeng; Webb, Bradley T.; Weinsheimer, Shantel Marie; Wellmann, Jurgen; Willemsen, Gonneke; Wu, Yang; Xi, Hualin S.; Yang, Jian; Zhang, Futao; Arolt, Volker; Berger, Klaus; Boomsma, Dorret I.; Cichon, Sven; Dannlowski, Udo; de Geus, E. J. C.; 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; 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; Schäfer, Catherine; Schulze, Thomas G.; Smoller, Jordan W.; Stefansson, Kari; Tiemeier, Henning; Uher, Rudolf; Voelzke, Henry; Weissman, Myrna M.; Werge, Thomas; Lewis, Cathryn M.; Levinson, Douglas F.; Breen, Gerome; Borglum, Anders D. und Sullivan, Patrick F.
(2019):
Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy.
In: American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, Bd. 180, Nr. 1: S. 35-45
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]
Gasperi, Christiane; Salmen, Anke; Antony, Gisela; Bayas, Antonios; Heesen, Christoph; Kuempfel, Tania; Linker, Ralf A.; Paul, Friedemann; Stangel, Martin; Tackenberg, Björn; Bergh, Florian Then; Warnke, Clemens; Weber, Frank; Wiendl, Heinz; Wildemann, Brigitte; Zettl, Uwe K.; Ziemann, Ulf; Zipp, Frauke; Tumani, Hayrettin; Gold, Ralf; Hemmer, Bernhard; Aktas, Orhan; Antony, Gisela; Ayzenberg, Ilya; Gold, Ralf; Hellwig, Kerstin; Salmen, Anke; Lukas, Carsten; Bahn, Erik; Brueck, Wolfgang; Fluegel, Alexander; Friede, Tim; Lodygin, Dmitri; Meissner, Tina; Berger, Klaus; Buck, Dorothea; Hemmer, Bernhard; Muehlau, Mark; Korn, Thomas; Friese, Manuel; Heesen, Christoph; Stellmann, Jan-Patrick; Groppa, Sergiu; Luessi, Felix; Zipp, Frauke; Gross, Catharina; Klotz, Luisa; Meuth, Sven; Ruck, Tobias; Wiendl, Heinz; Haas, Jürgen; Wildemann, Brigitte; Hohlfeld, Reinhard; Kerschensteiner, Martin; Kuempfel, Tania; Meinl, Edgar; Hohlfeld, Reinhard; Kerschensteiner, Martin; Korn, Thomas; Hemmer, Bernhard; König, Inke; Kowarik, Markus; Ziemann, Ulf; Krishnamoorthy, Gurumoorthy; Müller-Myhsok, Bertram; Nischwitz, Sandra; Müller-Myhsok, Bertram; Prinz, Marco; Salmen, Anke; Stangel, Martin; Trebst, Corinna; Tumani, Hayrettin; Bayas, Antonios; Hartung, Hans-Peter; Linker, Ralf; Nischwitz, Sandra; Paul, Friedemann; Tackenberg, Björn; Bergh, Florian Then und Zettl, Uwe
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Association of Intrathecal Immunoglobulin G Synthesis With Disability Worsening in Multiple Sclerosis.
In: Jama Neurology, Bd. 76, Nr. 7: S. 841-849
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2018
Foo, Jerome C.; Streit, Fabian; Treutlein, Jens; Ripke, Stephan; Witt, Stephanie H.; Strohmaier, Jana; Degenhardt, Franziska; Forstner, Andreas J.; Hoffmann, Per; Soyka, Michael; Dahmen, Norbert; Scherbaum, Norbert; Wodarz, Norbert; Heilmann-Heimbach, Stefanie; Herms, Stefan; Cichon, Sven; Preuss, Ulrich W.; Gäbel, Wolfgang; Ridinger, Monika; Hoffmann, Sabine; Schulze, Thomas G.; Maier, Wolfgang; Zill, Peter; Müller-Myhsok, Bertram; Ising, Marcus; Lucae, Susanne; Nöthen, Markus M.; Mann, Karl; Kiefer, Falk; Rietschel, Marcella und Frank, Josef
(2018):
Shared genetic etiology between alcohol dependence and major depressive disorder.
In: Psychiatric Genetics, Bd. 28, Nr. 4: S. 66-70
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Renzi, Chiara; Provencal, Nadine; Bassil, Katherine C.; Evers, Kathinka; Kihlbom, Ulrik; Radford, Elizabeth J.; Koupil, Ilona; Müller-Myhsok, Bertram; Hansson, Mats G. und Rutten, Bart P. F.
(2018):
From Epigenetic Associations to Biological and Psychosocial Explanations in Mental Health.
In: Neuroepigenetics and Mental Illness, Bd. 158: S. 299-323
Salminen, Aaro V.; Schormair, Barbara; Flachskamm, Cornelia; Torres, Miguel; Müller-Myhsok, Bertram; Kimura, Mayumi und Winkelmann, Juliane
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Sleep disturbance by pramipexole is modified by Meis1 in mice.
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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]
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
Mühleisen, Thomas W.; Reinbold, Celine S.; Forstner, Andreas J.; Abramova, Lilia I.; Alda, Martin; Babadjanova, Gulja; Bauer, Michael; Brennan, Paul; Chuchalin, Alexander; Cruceanu, Cristiana; Czerski, Piotr M.; Degenhardt, Franziska; Fischer, Sascha B.; Fullerton, Janice M.; Gordon, Scott D.; Grigoroiu-Serbanescu, Maria; Grof, Paul; Hauser, Joanna; Hautzinger, Martin; Herms, Stefan; Hoffmann, Per; Kammerer-Ciernioch, Jutta; Khusnutdinova, Elza; Kogevinas, Manolis; Krasnova, Valery; Lacour, Andre; Laprise, Catherine; Leber, Markus; Lissowska, Jolanta; Lucae, Susanne; Maaser, Anna; Maier, Wolfgang; Martin, Nicholas G.; Mattheisen, Manuel; Mayoral, Fermin; McKay, James D.; Medland, Sarah E.; Mitchell, Philip B.; Moebus, Susanne; Montgomery, Grant W.; Müller-Myhsok, Bertram; Oruc, Lilijana; Pantelejeva, Galina; Pfennig, Andrea; Pojskic, Lejla; Polonikov, Alexey; Reif, Andreas; Rivas, Fabio; Rouleau, Guy A.; Schenk, Lorena M.; Schofield, Peter R.; Schwarz, Markus; Streit, Fabian; Strohmaier, Jana; Szeszenia-Dabrowska, Neonila; Tiganov, Alexander S.; Treutlein, Jens; Turecki, Gustavo; Vedder, Helmut; Witt, Stephanie H.; Schulze, Thomas G.; Rietschel, Marcella; Nöthen, Markus M. und Cichon, Sven
(2018):
Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder.
In: Journal of Affective Disorders, Bd. 228: S. 20-25
2017
Chang, Hong; Li, Lingyi; Peng, Tao; Grigoroiu-Serbanescu, Maria; Bergen, Sarah E.; Landen, Mikael; Hultman, Christina M.; Forstner, Andreas J.; Strohmaier, Jana; Hecker, Julian; Schulze, Thomas G.; Müller-Myhsok, Bertram; Reif, Andreas; Mitchell, Philip B.; Martin, Nicholas G.; Cichon, Sven; Nöthen, Markus M.; Jamain, Stephane; Leboyer, Marion; Bellivier, Frank; Etain, Bruno; Kahn, Jean-Pierre; Henry, Chantal; Rietschel, Marcella; Xiao, Xiao und Li, Ming
(2017):
Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1.
In: Molecular Neurobiology, Bd. 54, Nr. 7: S. 5166-5176
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
Anderson-Schmidt, Heike; Papiol, Sergi; Andlauer, Till F. M.; Heilbronner, Urs; Budde, Monika; Kalman, Janos; Degenhardt, Franziska; Nöthen, Markus; Strohmaier, Jana; Frank, Josef; Witt, Stephanie; Müller-Myhsok, Bertram; Falkai, Peter ORCID: https://orcid.org/0000-0003-2873-8667; Rietschel, Marcella und Schulze, Thomas G.
(2017):
Using Polygenic Scores Based On Schneiderian First Rank Symptoms To Characterize Disease Trajectories In Severe Mental Illnesses.
In: European Neuropsychopharmacology, Bd. 27:
S395-S396
ORCID: https://orcid.org/0000-0003-2873-8667; Rietschel, Marcella und Schulze, Thomas G.
(2017):
Using Polygenic Scores Based On Schneiderian First Rank Symptoms To Characterize Disease Trajectories In Severe Mental Illnesses.
In: European Neuropsychopharmacology, Bd. 27:
S395-S396
Heilbronner, Urs; Andlauer, Till F. M.; Papiol, Sergi; Budde, Monika; Strohmaier, Jana; Streit, Fabian; Frank, Josef; Amelang, Manfred; Stürmer, Til; Müller-Myhsok, Bertram; Rietschel, Marcella und Schulze, Thomas G.
(2017):
Common Genetic Variants Associated With Personality Dimensions In The Heidelberg Cohort Study Of The Elderly (Heide).
In: European Neuropsychopharmacology, Bd. 27:
S381-S382
Zeng, Yanni; Navarro, Pau; Shirali, Masoud; Howard, David M.; Adams, Mark J.; Hall, Lynsey S.; Clarke, Toni-Kim; Thomson, Pippa A.; Smith, Blair H.; Murray, Alison; Padmanabhan, Sandosh; Hayward, Caroline; Boutin, Thibaud; MacIntyre, Donald J.; Lewis, Cathryn M.; Wray, Naomi R.; Mehta, Divya; Penninx, Brenda W. J. H.; Milaneschi, Yuri; Baune, Bernhard T.; Air, Tracy; Hottenga, Jouke-Jan; Mbarek, Hamdi; Castelao, Enrique; Pistis, Giorgio; Schulze, Thomas G.; Streit, Fabian; Forstner, Andreas J.; Byrne, Enda M.; Martin, Nicholas G.; Breen, Gerome; Müller-Myhsok, Bertram; Lucae, Susanne; Kloiber, Stefan; Domenici, Enrico; Deary, Ian J.; Porteous, David J.; Haley, Chris S. und McIntosh, Andrew M.
(2017):
Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder.
In: Biological Psychiatry, Bd. 82, Nr. 5: S. 312-321
Direk, Nese; Williams, Stephanie; Smith, Jennifer A.; Ripke, Stephan; Air, Tracy; Amare, Azmeraw T.; Amin, Najaf; Baune, Bernhard T.; Bennett, David A.; Blackwood, Douglas H. R.; Boomsma, Dorret; Breen, Gerome; Buttenschon, Henriette N.; Byrne, Enda M.; Borglum, Anders D.; Castelao, Enrique; Cichon, Sven; Clarke, Toni-Kim; Cornelis, Marilyn C.; Dannlowski, Udo; Jager, Philip L. de; Demirkan, Ayse; Domenici, Enrico; Duijn, Cornelia M. van; Dunn, Erin C.; Eriksson, Johan G.; Esko, Tonu; Faul, Jessica D.; Ferrucci, Luigi; Fornage, Myriam; Geus, Eco de; Gill, Michael; Gordon, Scott D.; Grabe, Hans Jörgen; Grootheest, Gerard van; Hamilton, Steven P.; Hartman, Catharina A.; Heath, Andrew C.; Hek, Karin; Hofman, Albert; Homuth, Georg; Horn, Carsten; Hottenga, Jouke Jan; Kardia, Sharon L. R.; Kloiber, Stefan; Koenen, Karestan; Kutalik, Zoltan; Ladwig, Karl-Heinz; Lahti, Jari; Levinson, Douglas F.; Lewis, Cathryn M.; Lewis, Glyn; Li, Qingqin S.; Llewellyn, David J.; Lucae, Susanne; Lunetta, Kathryn L.; MacIntyre, Donald J.; Madden, Pamela; Martin, Nicholas G.; McIntosh, Andrew M.; Metspalu, Andres; Milaneschi, Yuri; Montgomery, Grant W.; Mors, Ole; Mosley, Thomas H.; Murabito, Joanne M.; Müller-Myhsok, Bertram; Nöthen, Markus M.; Nyholt, Dale R.; O'Donovan, Michael C.; Penninx, Brenda W.; Pergadia, Michele L.; Perlis, Roy; Potash, James B.; Preisig, Martin; Purcell, Shaun M.; Quiroz, Jörge A.; Räikkönen, Katri; Rice, John P.; Rietschel, Marcella; Rivera, Margarita; Schulze, Thomas G.; Shi, Jianxin; Shyn, Stanley; Sinnamon, Grant C.; Smit, Johannes H.; Smoller, Jordan W.; Snieder, Harold; Tanaka, Toshiko; Tansey, Katherine E.; Teumer, Alexander; Uher, Rudolf; Umbricht, Daniel; Auwera, Sandra van der; Ware, Erin B.; Weir, David R.; Weissman, Myrna M.; Willemsen, Gonneke; Yang, Jingyun; Zhao, Wei; Tiemeier, Henning und Sullivan, Patrick F.
(2017):
An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype.
In: Biological Psychiatry, Bd. 82, Nr. 5: S. 322-329
Treutlein, Jens; Frank, Josef; Streit, Fabian; Reinbold, Celine S.; Juraeva, Dilafruz; Degenhardt, Franziska; Rietschel, Liz; Witt, Stephanie H.; Forstner, Andreas J.; Ridinger, Monika; Strohmaier, Jana; Wodarz, Norbert; Dukal, Helene; Foo, Jerome C.; Hoffmann, Per; Herms, Stefan; Heilmann-Heimbach, Stefanie; Soyka, Michael; Maier, Wolfgang; Gäbel, Wolfgang; Dahmen, Norbert; Scherbaum, Norbert; Müller-Myhsok, Bertram; Lucae, Susanne; Ising, Marcus; Stickel, Felix; Berg, Thomas; Roggenbuck, Ulla; Jöckel, Karl-Heinz; Scholz, Henrike; Zimmermann, Ulrich S.; Buch, Stephan; Sommer, Wolfgang H.; Spanagel, Rainer; Brors, Benedikt; Cichon, Sven; Mann, Karl; Kiefer, Falk; Hampe, Jochen; Rosendahl, Jonas; Nöthen, Markus M. und Rietschel, Marcella
(2017):
Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis.
In: Genes, Bd. 8, Nr. 7, 183
[PDF, 277kB]
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]
2016
Zhao, Huiying; Eising, Else; Vries, Boukje de; Vijfhuizen, Lisanne S.; Anttila, Verneri; Winsvold, Bendik S.; Kurth, Tobias; Stefansson, Hreinn; Kallela, Mikko; Malik, Rainer; Stam, Anine H.; Ikram, M. Arfan; Ligthart, Lannie; Freilinger, Tobias; Alexander, Michael; Müller-Myhsok, Bertram; Schreiber, Stefan; Meitinger, Thomas; Aromas, Arpo; Eriksson, Johan G.; Boomsma, Dorret I.; Duijn, Cornelia M. van; Zwart, John-Anker; Quaye, Lydia; Kubisch, Christian; Dichgans, Martin; Wessman, Maija; Stefansson, Kari; Chasman, Daniel I.; Palotie, Aarno; Martin, Nicholas G.; Montgomery, Grant W.; Ferrari, Michel D.; Terwindt, Gisela M.; Maagdenberg, Arn M. J. M. van den und Nyholt, Dale R.
(2016):
Gene-based pleiotropy across migraine with aura and migraine without aura patient groups.
In: Cephalalgia, Bd. 36, Nr. 7: S. 648-657
[PDF, 179kB]
Amin, Najaf; Allebrandt, Karla V.; Spek, Ashley van der; Müller-Myhsok, Bertram; Hek, Karin; Teder-Laving, Maris; Hayward, Caroline; Esko, Tõnu; Mill, Josine G. van; Mbarek, Hamdi; Watson, Nathaniel F.; Melville, Scott A.; Del Greco, Fabiola M.; Byrne, Enda M.; Oole, Edwin; Kolcic, Ivana; Chen, Ting-hsu; Evans, Daniel S.; Coresh, Josef; Vogelzangs, Nicole; Karjalainen, Juha; Willemsen, Gonneke; Gharib, Sina A.; Zgaga, Lina; Mihailov, Evelin; Stone, Katie L.; Campbell, Harry; Brouwer, Rutger Ww; Demirkan, Ayse; Isaacs, Aaron; Dogas, Zoran; Marciante, Kristin D.; Campbell, Susan; Borovecki, Fran; Luik, Annemarie I.; Li, Man; Hottenga, Jouke Jan; Huffman, Jennifer E.; Hout, Mirjam C. G. N. van den; Cummings, Steven R.; Aulchenko, Yuru S.; Gehrman, Philip R.; Uitterlinden, Andre G.; Wichmann, Heinz-Erich; Müller-Nurasyid, Martina; Fehrmann, Rudolf S. N.; Montgomery, Grant W.; Hofman, Albert; Kao, Wen Hong Linda; Oostra, Ben A.; Wright, Alan F.; Vink, Jacqueline M.; Wilson, James F.; Pramstaller, Peter P.; Hicks, Andrew A.; Polasek, Ozren; Punjabi, Naresh M.; Redline, Susan; Psaty, Bruce M.; Heath, Andrew C.; Merrow, Martha; Tranah, Gregory J.; Gottlieb, Daniel J.; Boomsma, Dorret I.; Martin, Nicholas G.; Rudan, Igor; Tiemeier, Henning; IJcken, Wilfred F. J. van; Penninx, Brenda W.; Metspalu, Andres; Meitinger, Thomas; Franke, Lude; Roenneberg, Till ORCID: https://orcid.org/0000-0003-2939-0332 und Duijn, Cornelia M. van
(2016):
Genetic variants in RBFOX3 are associated with sleep latency.
In: European Journal of Human Genetics, Bd. 24, Nr. 10: S. 1488-1495
ORCID: https://orcid.org/0000-0003-2939-0332 und Duijn, Cornelia M. van
(2016):
Genetic variants in RBFOX3 are associated with sleep latency.
In: European Journal of Human Genetics, Bd. 24, Nr. 10: S. 1488-1495
Li, Ming; Huang, Liang; Grigoroiu-Serbanescu, Maria; Bergen, Sarah E.; Landén, Mikael; Hultman, Christina M.; Forstner, Andreas J.; Strohmaier, Jana; Hecker, Julian; Schulze, Thomas G.; Müller-Myhsok, Bertram; Reif, Andreas; Mitchell, Philip B.; Martin, Nicholas G.; Cichon, Sven; Nöthen, Markus M.; Alkelai, Anna; Lerer, Bernard; Jamain, Stéphane; Leboyer, Marion; Bellivier, Frank; Etain, Bruno; Kahn, Jean-Pierre; Henry, Chantal und Rietschel, Marcella
(2016):
Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis.
In: Molecular Neurobiology, Bd. 53, Nr. 10: S. 6608-6619
Gormley, Padhraig; Anttila, Verneri; Winsvold, Bendik S.; Palta, Priit; Esko, Tonu; Pers, Tune H.; Farh, Kai-How; Cuenca-Leon, Ester; Muona, Mikko; Furlotte, Nicholas A.; Kurth, Tobias; Ingason, Andres; McMahon, George; Ligthart, Lannie; Terwindt, Gisela M.; Kallela, Mikko; Freilinger, Tobias M.; Ran, Caroline; Gordon, Scott G.; Stam, Anine H.; Steinberg, Stacy; Borck, Guntram; Koiranen, Markku; Quaye, Lydia; Adams, Hieab H. H.; Lehtimäki, Terho; Sarin, Antti-Pekka; Wedenoja, Juho; Hinds, David A.; Buring, Julie E.; Schürks, Markus; Ridker, Paul M.; Hrafnsdottir, Maria Gudlaug; Stefansson, Hreinn; Ring, Susan M.; Hottenga, Jouke-Jan; Penninx, Brenda W. J. H.; Färkkilä, Markus; Artto, Ville; Kaunisto, Mari; Vepsäläinen, Salli; Malik, Rainer; Heath, Andrew C.; Madden, Pamela A. F.; Martin, Nicholas G.; Montgomery, Grant W.; Kurki, Mitja I.; Kals, Mart; Mägi, Reedik; Pärn, Kalle; Hämäläinen, Eija; Huang, Hailiang; Byrnes, Andrea E.; Franke, Lude; Huang, Jie; Stergiakouli, Evie; Lee, Phil H.; Sandor, Cynthia; Webber, Caleb; Cader, Zameel; Müller-Myhsok, Bertram; Schreiber, Stefan; Meitinger, Thomas; Eriksson, Johan G.; Salomaa, Veikko; Heikkila, Kauko; Loehrer, Elizabeth; Uitterlinden, Andre G.; Hofman, Albert; Duijn, Cornelia M. van; Cherkas, Lynn; Pedersen, Linda M.; Stubhaug, Audun; Nielsen, Christopher S.; Männikkö, Minna; Mihailov, Evelin; Milani, Lili; Göbel, Hartmut; Esserlind, Ann-Louise; Christensen, Anne Francke; Hansen, Thomas Folkmann; Werge, Thomas; Kaprio, Jaakko; Aromaa, Arpo J.; Raitakari, Olli; Ikram, M. Arfan; Spector, Tim; Järvelin, Marjo-Riitta; Metspalu, Andres; Kubisch, Christian; Strachan, David P.; Ferrari, Michel D.; Belin, Andrea C.; Dichgans, Martin; Wessman, Maija; Maagdenberg, Arn M. J. M. van den; Zwart, John-Anker; Boomsma, Dorret I.; Smith, George Davey; Stefansson, Kari; Eriksson, Nicholas; Daly, Mark J.; Neale, Benjamin M.; Olesen, Jes; Chasman, Daniel I.; Nyholt, Dale R. und Palotie, Aarno
(2016):
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.
In: Nature Genetics, Bd. 48, Nr. 8: S. 856-866
Andlauer, Till F. M.; Buck, Dorothea; Antony, Gisela; Bayas, Antonios; Bechmann, Lukas; Berthele, Achim; Chan, Andrew; Gasperi, Christiane; Gold, Ralf; Graetz, Christiane; Haas, Jürgen; Hecker, Michael; Infante-Duarte, Carmen; Knop, Matthias; Kümpfel, Tania; Limmroth, Volker; Linker, Ralf A.; Loleit, Verena; Luessi, Felix; Meuth, Sven G.; Mühlau, Mark; Nischwitz, Sandra; Paul, Friedemann; Pütz, Michael; Ruck, Tobias; Salmen, Anke; Stangel, Martin; Stellmann, Jan-Patrick; Stürner, Klarissa H.; Tackenberg, Björn; Bergh, Florian Then; Tumani, Hayrettin; Warnke, Clemens; Weber, Frank; Wiendl, Heinz; Wildemann, Brigitte; Zettl, Uwe K.; Ziemann, Ulf; Zipp, Frauke; Arloth, Janine; Weber, Peter; Radivojkov-Blagojevic, Milena; Scheinhardt, Markus O.; Dankowski, Theresa; Bettecken, Thomas; Lichtner, Peter; Czamara, Darina; Carrillo-Roa, Tania; Binder, Elisabeth B.; Berger, Klaus; Bertram, Lars; Franke, Andre; Gieger, Christian; Herms, Stefan; Homuth, Georg; Ising, Marcus; Jöckel, Karl-Heinz; Kacprowski, Tim; Kloiber, Stefan; Laudes, Matthias; Lieb, Wolfgang; Lill, Christina M.; Lucae, Susanne; Meitinger, Thomas; Moebus, Susanne; Müller-Nurasyid, Martina; Nöthen, Markus M.; Petersmann, Astrid; Rawal, Rajesh; Schminke, Ulf; Strauch, Konstantin; Völzke, Henry; Waldenberger, Melanie; Wellmann, Jürgen; Porcu, Eleonora; Mulas, Antonella; Pitzalis, Maristella; Sidore, Carlo; Zara, Ilenia; Cucca, Francesco; Zoledziewska, Magdalena; Ziegler, Andreas; Hemmer, Bernhard und Müller-Myhsok, Bertram
(2016):
Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation.
In: Science Advances, Bd. 2, Nr. 6, e1501678
[PDF, 678kB]
2015
Nyholt, Dale R.; Anttila, Verneri; Winsvold, Bendik S.; Kurth, Tobias; Stefansson, Hreinn; Kallela, Mikko; Malik, Rainer; Vries, Boukje de; Terwindt, Gisela M.; Arfan Ikram, M.; Stam, Anine H.; Ligthart, Lannie; Freilinger, Tobias; Alexander, Michael; Müller-Myhsok, Bertram; Schreiber, Stefan; Meitinger, Thomas; Aromaa, Arpo J.; Eriksson, Johan G.; Kaprio, Jaakko; Boomsma, Dorret I.; Duijn, Cornelia van; Raitakari, Olli; Jarvelin, Marjo-Riitta; Zwart, John-Anker; Quaye, Lydia; Strachan, David P.; Kubisch, Christian; Ferrari, Michel D.; Maagdenberg, Arn M. J. M. van den; Dichgans, Martin; Wessman, Maija; Smith, George Davey; Stefansson, Kari; Chasman, Daniel I. und Palotie, Aarno
(Mai 2015):
Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies.
In: Cephalalgia, Bd. 35, Nr. 6: S. 489-499
[PDF, 178kB]
2012
Neuhoff, Nina; Bruder, Jennifer; Bartling, Jürgen; Warnke, Andreas; Remschmidt, Helmut; Müller-Myhsok, Bertram und Schulte-Körne, Gerd
(2012):
Evidence for the late MMN as a neurophysiological endophenotype for dyslexia.
In: PLOS ONE 7(5), e34909 [PDF, 415kB]
In: PLOS ONE 7(5), e34909 [PDF, 415kB]
Glas, Jürgen; Seiderer, Julia; Czamara, Darina; Pasciuto, Giulia; Diegelmann, Julia; Wetzke, Martin; Olszak, Torsten; Wolf, Christiane; Müller-Myhsok, Bertram; Balschun, Tobias; Achkar, Jean-Paul; Kamboh, M. Ilyas; Franke, Andre; Duerr, Richard H. und Brand, Stephan
(2012):
PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-κB and XBP1 binding sites.
In: PLOS ONE 7(12), e52873 [PDF, 206kB]
In: PLOS ONE 7(12), e52873 [PDF, 206kB]
2011
Schormair, Barbara; Plag, Jens; Kaffe, Maria; Gross, Nadine; Czamara, Darina; Samtleben, Walter; Lichtner, Peter; Ströhle, Andreas; Stefanidis, Ioannis; Vainas, Andreas; Dardiotis, Efthimios; Sakkas, George K.; Gieger, Christian; Müller-Myhsok, Bertram; Meitinger, Thomas; Heemann, Uwe; Hadjigeorgiou, Georgios M.; Oexle, Konrad und Winkelmann, Juliane
(Juli 2011):
MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease.
In: Journal of medical genetics, Bd. 48, Nr. 7: S. 462-466
[PDF, 131kB]
Glas, Jürgen; Seiderer, Julia; Fries, Christoph; Tillack, Cornelia; Pfennig, Simone; Weidinger, Maria; Beigel, Florian; Olszak, Torsten; Lass, Ulrich; Göke, Burkhard; Ochsenkühn, Thomas; Wolf, Christiane; Lohse, Peter; Müller-Myhsok, Bertram; Diegelmann, Julia; Czamara, Darina und Brand, Stephan
(2011):
CEACAM6 gene variants in inflammatory bowel disease.
In: PLOS ONE 6(4), e19319 [PDF, 214kB]
In: PLOS ONE 6(4), e19319 [PDF, 214kB]
2010
Glas, Jürgen; Seiderer, Julia; Nagy, Melinda; Fries, Christoph; Beigel, Florian; Weidinger, Maria; Pfennig, Simone; Klein, Wolfram; Epplen, Jörg T.; Lohse, Peter; Folwaczny, Matthias; Göke, Burkhard; Ochsenkühn, Thomas; Diegelmann, Julia; Müller-Myhsok, Bertram; Roeske, Darina und Brand, Stephan
(2010):
Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset.
In: PLOS ONE 5(4), e10373 [PDF, 128kB]
In: PLOS ONE 5(4), e10373 [PDF, 128kB]
Glas, Jürgen; Seiderer, Julia; Tillack, Cornelia; Pfennig, Simone; Beigel, Florian; Jürgens, Matthias; Olszak, Torsten; Laubender, Rüdiger P.; Weidinger, Maria; Müller-Myhsok, Bertram; Göke, Burkhard; Ochsenkühn, Thomas; Lohse, Peter; Diegelmann, Julia; Czamara, Darina und Brand, Stephan
(2010):
The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants.
In: PLOS ONE 5(12), e14466 [PDF, 125kB]
In: PLOS ONE 5(12), e14466 [PDF, 125kB]
2008
Browning, B.L.; Annese, V.; Barclay, M.L.; Bingham, S.A.; Brand, Stefan; Büning, C.; Castro, M.; Cucchiara, S.; Dallapiccola, B.; Drummond, H.; Ferguson, L.R.; Ferraris, A.; Fisher, S.A.; Gearry, R.B.; Glas, Jürgen; Henckaerts, L.; Huebner, C.; Knafelz, D.; Lakatos, L.; Lakatos, P.L.; Latiano, A.; Liu, X.; Mathew, C.; Müller-Myhsok, Bertram; Newman, W.G.; Nimmo, E.R.; Noble, C.L.; Palmieri, O.; Parkes, M.; Petermann, I.; Rutgeerts, P.; Satsangi, J.; Shelling, A.N.; Siminovitch, K.A.; Török, H.-P.; Tremelling, M.; Vermeire, S.; Valvano, M.R. und Witt, H.
(2008):
Gender-stratified analysis of DLG5 R30Q in 4707 patients with Crohn disease and 4973 controls from 12 Caucasian cohorts.
In: Journal of Medical Genetics, Bd. 45: S. 36-42
[PDF, 322kB]
2007
Glas, Jürgen; Seiderer, Julia; Wetzke, Martin; Konrad, Astrid; Török, Helga-Paula; Schmechel, Silke; Tonenchi, Laurian; Grassl, Christine; Dambacher, Julia; Pfennig, Simone; Maier, Kerstin; Griga, Thomas; Klein, Wolfram; Epplen, Jörg T.; Schiemann, Uwe; Folwaczny, Christian; Lohse, Peter; Göke, Burkhard; Ochsenkühn, Thomas; Müller-Myhsok, Bertram; Folwaczny, Matthias; Mussack, Thomas und Brand, Stephan
(2007):
rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants.
In: PLOS ONE (9), e819 [PDF, 133kB]
In: PLOS ONE (9), e819 [PDF, 133kB]