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Anzahl der Publikationen: 18

Zeitschriftenartikel

Gomez-Fernandez, Paloma; de Lapuente Portilla, Aitzkoa Lopez; Astobiza, Ianire; Mena, Jorge; Urtasun, Andoni; Altmann, Vivian; Matesanz, Fuencisla; Otaegui, David; Urcelay, Elena; Antiguedad, Alfredo; Malhotra, Sunny; Montalban, Xavier; Castillo-Trivino, Tamara; Espino-Paisan, Laura; Aktas, Orhan; Buttmann, Mathias; Chan, Andrew; Fontaine, Bertrand; Gourraud, Pierre-Antoine; Hecker, Michael; Hoffjan, Sabine; Kubisch, Christian; Kuempfel, Tania; Luessi, Felix; Zettl, Uwe K.; Zipp, Frauke; Alloza, Iraide; Comabella, Manuel; Lill, Christina M. und Vandenbroeck, Koen (2020): The Rare IL22RA2 Signal Peptide Coding Variant rs28385692 Decreases Secretion of IL-22BP Isoform-1,-2 and-3 and Is Associated with Risk for Multiple Sclerosis. In: Cells, Bd. 9, Nr. 1, 175

Weber-Lassalle, Nana; Borde, Julika; Weber-Lassalle, Konstantin; Horvath, Judit; Niederacher, Dieter; Arnold, Norbert; Kaulfuss, Silke; Ernst, Corinna; Paul, Victoria G.; Honisch, Ellen; Klaschik, Kristina; Volk, Alexander E.; Kubisch, Christian; Rapp, Steffen; Lichey, Nadine; Altmüller, Janine; Lepkes, Louisa; Pohl-Rescigno, Esther; Thiele, Holger; Nuernberg, Peter; Larsen, Mirjam; Richters, Lisa; Rhiem, Kerstin; Wappenschmidt, Barbara; Engel, Christoph; Meindl, Alfons; Schmutzler, Rita K.; Hahnen, Eric und Hauke, Jan (2019): Germline loss-of-function variants in the BARD1 gene are associated with early-onset familial breast cancer but not ovarian cancer. In: Breast Cancer Research, Bd. 21, 55

Kogelman, Lisette J. A.; Esserlind, Ann-Louise; Christensen, Anne Francke; Awasthi, Swapnil; Ripke, Stephan; Ingason, Andres; Davidsson, Olafur B.; Erikstrup, Christian; Hjalgrim, Henrik; Ullum, Henrik; Olesen, Jes; Hansen, Thomas Folkmann; Gudbjartsson, Daniel; Gastafsson, Omar; Stefansson, Kari; Stefansson, Hreinn; Porsteinsdottir, Unnur; Andersen, Steffen; Banasik, Karina; Brunak, Soren; Buil, Alfonso; Burgdorf, Kristoffer; Gregor, Jemec; Jennum, Poul; Nielsen, Kasper Rene; Nyegaard, Mette; Paarup, Helene Mariana; Pedersen, Ole Birger; Sorensen, Erik; Werge, Thomas; Anttila, Verneri; Artto, Ville; Belin, Andrea Carmine; de Boer, Irene; Boomsma, Dorret; Borte, Sigrid; Chasman, Daniel; Cherkas, Lynn; Cormand, Bru; Cuenca-Leon, Ester; Davey-Smith, George; Dichgans, Martin; van Duijn, Cornelia; Esko, Tonu; Ferrari, Michel; Frants, Rune R.; Freilinger, Tobias; Furlotte, Nick; Gormley, Padhraig; Griffiths, Lyn; Hamalainen, Eija; Hiekkala, Marjo; Ikram, M. Arfan; Jarvelin, Marjo-Riitta; Kajanne, Risto; Kallela, Mikko; Kaprio, Jaakko; Kaunisto, Mari; Kubisch, Christian; Kurki, Mitja; Kurth, Tobias; Launer, Lenore; Lehtimaki, Terho; Lessel, Davor; Ligthart, Lannie; Litterman, Nadia; van den Maagdenberg, Arn; Macaya, Alfons; Malik, Rainer; Mangino, Massimo; McMahon, George; Muller-Myhsok, Bertram; Neale, Benjamin M.; Northover, Carrie; Nyholt, Dale R.; Palotie, Aarno; Palta, Priit; Pedersen, Linda; Pedersen, Nancy; Posthuma, Danielle; Pozo-Rosich, Patricia; Pressman, Alice; Raitakari, Olli; Schurks, Markus; Sintas, Celia; Steinberg, Stacy; Strachan, David; Terwindt, Gisela; Vila-Pueyo, Marta; Wessman, Maija; Winsvold, Bendik S.; Zhao, Huiying und Zwart, John-Anker (2019): Migraine polygenic risk score associates with efficacy of migraine-specific drugs. In: Neurology-Genetics, Bd. 5, Nr. 6, e364

Yang, Yuanhao; Zhao, Huiying; Boomsma, Dorret I.; Ligthart, Lannie; Belin, Andrea C.; Smith, George Davey; Esko, Tonu; Freilinger, Tobias M.; Hansen, Thomas Folkmann; Ikram, M. Arfan; Kallela, Mikko; Kubisch, Christian; Paraskevi, Christofidou; Strachan, David P.; Wessman, Maija; Maagdenberg, Arn M. J. M. van den; Terwindt, Gisela M. und Nyholt, Dale R. (2018): Molecular genetic overlap between migraine and major depressive disorder. In: European Journal of Human Genetics, Bd. 26, Nr. 8: S. 1202-1216

Hauke, Jan; Horvath, Judit; Gross, Eva; Gehrig, Andrea; Honisch, Ellen; Hackmann, Karl; Schmidt, Gunnar; Arnold, Norbert; Faust, Ulrike; Sutter, Christian; Hentschel, Julia; Wang-Gohrke, Shan; Smogavec, Mateja; Weber, Bernhard H. F.; Weber-Lassalle, Nana; Weber-Lassalle, Konstantin; Borde, Julika; Ernst, Corinna; Altmüller, Janine; Volk, Alexander E.; Thiele, Holger; Huebbel, Verena; Nuernberg, Peter; Keupp, Katharina; Versmold, Beatrix; Pohl, Esther; Kubisch, Christian; Grill, Sabine; Paul, Victoria; Herold, Natalie; Lichey, Nadine; Rhiem, Kerstin; Ditsch, Nina; Ruckert, Christian; Wappenschmidt, Barbara; Auber, Bernd; Rump, Andreas; Niederacher, Dieter; Haaf, Thomas; Ramser, Juliane; Dworniczak, Bernd; Engel, Christoph; Meindl, Alfons; Schmutzler, Rita K. und Hahnen, Eric (2018): Gene panel testing of 5589 BRCA1/2-negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Breast and Ovarian Cancer. In: Cancer Medicine, Bd. 7, Nr. 4: S. 1349-1358

Müller, Kathrin; Brenner, David; Weydt, Patrick; Meyer, Thomas; Grehl, Torsten; Petri, Susanne; Grosskreutz, Julian; Schuster, Joachim; Volk, Alexander E.; Borck, Guntram; Kubisch, Christian; Klopstock, Thomas; Zeller, Daniel; Jablonka, Sibylle; Sendtner, Michael; Klebe, Stephan; Knehr, Antje; Günther, Kornelia; Weis, Joachim; Claeys, Kristl G.; Schrank, Berthold; Sperfeld, Anne-Dorte; Hübers, Annemarie; Otto, Markus; Dorst, Johannes; Meitinger, Thomas; Strom, Tim M.; Andersen, Peter M.; Ludolph, Albert C. und Weishaupt, Jochen H. (2018): Comprehensive analysis of the mutation spectrum in 301 German ALS families. In: Journal of Neurology Neurosurgery and Psychiatry, Bd. 89, Nr. 8: S. 817-827 [PDF, 637kB]

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]

Eising, Else; Leeuw, Christiaan de; Min, Josine L.; Anttila, Verneri; Verheijen, Mark H. G.; Terwindt, Gisela M.; Dichgans, Martin; Freilinger, Tobias; Kubisch, Christian; Ferrari, Michel D.; Smit, August B.; Vries, Boukje de; Palotie, Aarno; Maagdenberg, Arn M. J. M. van den und Posthuma, Danielle (2016): Involvement of astrocyte and oligodendrocyte gene sets in migraine. In: Cephalalgia, Bd. 36, Nr. 7: S. 640-647 [PDF, 166kB]

Vries, Boukje de; Anttila, Verneri; Freilinger, Tobias; Wessman, Maija; Kaunisto, Mari A.; Kallela, Mikko; Artto, Ville; Vijfhuizen, Lisanne S.; Göbel, Hartmut; Dichgans, Martin; Kubisch, Christian; Ferrari, Michel D.; Palotie, Aarno; Terwindt, Gisela M. und Maagdenberg, Arn M. J. M. van den (2016): Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set. In: Cephalalgia, Bd. 36, Nr. 7: S. 604-614 [PDF, 438kB]

Eising, Else; Huisman, Sjoerd M. H.; Mahfouz, Ahmed; Vijfhuizen, Lisanne S.; Anttila, Verneri; Winsvold, Bendik S.; Kurth, Tobias; Ikram, M. Arfan; Freilinger, Tobias; Kaprio, Jaakko; Boomsma, Dorret I.; Duijn, Cornelia M. van; Järvelin, Marjo-Riitta R.; Zwart, John-Anker; Quaye, Lydia; Strachan, David P.; Kubisch, Christian; Dichgans, Martin; Smith, George Davey; Stefansson, Kari; Palotie, Aarno; Chasman, Daniel I.; Ferrari, Michel D.; Terwindt, Gisela M.; Vries, Boukje de; Nyholt, Dale R.; Lelieveldt, Boudewijn P. F.; Maagdenberg, Arn M. J. M. van den und Reinders, Marcel J. T. (2016): Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas. In: Human Genetics, Bd. 135, Nr. 4: S. 425-439

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

Sadovnick, A. Dessa; Traboulsee, Anthony L.; Bernales, Cecily Q.; Ross, Jay P.; Forwell, Amanda L.; Yee, Irene M.; Guillot-Noel, Lena; Fontaine, Bertrand; Cournu-Rebeix, Isabelle; Alcina, Antonio; Fedetz, Maria; Izquierdo, Guillermo; Matesanz, Fuencisla; Hilven, Kelly; Dubois, Benedicte; Goris, An; Astobiza, Ianire; Alloza, Iraide; Antigüedad, Alfredo; Vandenbroeck, Koen; Akkad, Denis A.; Aktas, Orhan; Blaschke, Paul; Buttmann, Mathias; Chan, Andrew; Epplen, Joerg T.; Gerdes, Lisa-Ann; Kroner, Antje; Kubisch, Christian; Kümpfel, Tania; Lohse, Peter; Rieckmann, Peter; Zettl, Uwe K.; Zipp, Frauke; Bertram, Lars; Lill, Christina M.; Fernandez, Oscar; Urbaneja, Patricia; Leyva, Laura; Carlos Alvarez-Cermeno, Jose; Arroyo, Rafael; Garagorri, Aroa M.; Garcia-Martinez, Angel; Villar, Luisa M.; Urcelay, Elena; Malhotra, Sunny; Montalban, Xavier; Comabella, Manuel; Berger, Thomas; Fazekas, Franz; Reindl, Markus; Schmied, Mascha C.; Zimprich, Alexander und Vilarino-Güell, Carles (2016): Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients. In: G3 - Genes Genomes Genetics, Bd. 6, Nr. 7: S. 2073-2079 [PDF, 1MB]

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]

Lill, Christina M.; Luessi, Felix; Alcina, Antonio; Sokolova, Ekaterina A.; Ugidos, Nerea; La Hera, Belen de; Guillot-Noel, Lena; Malhotra, Sunny; Reinthaler, Eva; Schjeide, Brit-Maren M.; Mescheriakova, Julia Y.; Mashychev, Andriy; Wohlers, Inken; Akkad, Denis A.; Aktas, Orhan; Alloza, Iraide; Antigüedad, Alfredo; Arroyo, Rafa; Astobiza, Ianire; Blaschke, Paul; Boyko, Alexei N.; Buttmann, Mathias; Chan, Andrew; Dörner, Thomas; Epplen, Joerg T.; Favorova, Olga O.; Fedetz, Maria; Fernandez, Oscar; Garcia-Martinez, Angel; Gerdes, Lisa-Ann; Graetz, Christiane; Hartung, Hans-Peter; Hoffjan, Sabine; Izquierdo, Guillermo; Korobko, Denis S.; Kroner, Antje; Kubisch, Christian; Kümpfel, Tania; Leyva, Laura; Lohse, Peter; Malkova, Nadezhda A.; Montalban, Xavier; Popova, Ekaterina V.; Rieckmann, Peter; Rozhdestvenskii, Alexei S.; Schmied, Christiane; Smagina, Inna V.; Tsareva, Ekaterina Y.; Winkelmann, Alexander; Zettl, Uwe K.; Binder, Harald; Cournu-Rebeix, Isabelle; Hintzen, Rogier; Zimprich, Alexander; Comabella, Manuel; Fontaine, Bertrand; Urcelay, Elena; Vandenbroeck, Koen; Filipenko, Maxim; Matesanz, Fuencisla; Zipp, Frauke und Bertram, Lars (2015): Genome-wide significant association with seven novel multiple sclerosis risk loci. In: Journal of medical genetics, Bd. 52, Nr. 12: S. 848-855 [PDF, 524kB]

Wildhardt, Gabriele; Zirn, Birgit; Graul-Neumann, Luitgard M.; Wechtenbruch, Juliane; Suckfuell, Markus; Buske, Annegret; Bohring, Axel; Kubisch, Christian; Vogt, Stefanie; Strobl-Wildemann, Gertrud; Greally, Marie; Bartsch, Oliver und Steinberger, Daniela (18. März 2013): Spectrum of novel mutations found in Waardenburg syndrome types 1 and 2: implications for molecular genetic diagnostics. In: BMJ Open, Bd. 3, Nr. 3, e001917 [PDF, 946kB]

Lill, Christina M.; Schjeide, Brit-Maren M.; Graetz, Christiane; Liu, Tian; Damotte, Vincent; Akkad, Denis A.; Blaschke, Paul; Gerdes, Lisa-Ann; Kroner, Antje; Luessi, Felix; Cournu-Rebeix, Isabelle; Hoffjan, Sabine; Winkelmann, Alexander; Touze, Emmanuel; Pico, Fernando; Corcia, Philippe; Otaegui, David; Antigueedad, Alfredo; Alcina, Antonio; Comabella, Manuel; Montalban, Xavier; Olascoaga, Javier; Matesanz, Fuencisla; Dörner, Thomas; Li, Shu-Chen; Steinhagen-Thiessen, Elisabeth; Lindenberger, Ulman; Chan, Andrew; Rieckmann, Peter; Hartung, Hans-Peter; Aktas, Orhan; Lohse, Peter; Buttmann, Mathias; Kümpfel, Tania; Kubisch, Christian; Zettl, Uwe K.; Epplen, Joerg T.; Fontaine, Bertrand; Zipp, Frauke; Vandenbroeck, Koen und Bertram, Lars (März 2013): Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk. In: Journal of Medical Genetics, Bd. 50, Nr. 3: S. 140-143 [PDF, 127kB]

de Vries, Boukje; Freilinger, Tobias; Anttila, Verneri; Malik, Rainer; Kallela, Mikko; Terwindt, Gisela M.; Pozo-Rosich, Patricia; Winsvold, Bendik; Nyholt, Dale R.; van Oosterhout, Willebrordus P. J.; Artto, Ville; Todt, Unda; Hamalainen, Eija; Fernandez-Morales, Jessica; Louter, Mark A.; Kaunisto, Mari A.; Schoenen, Jean; Raitakari, Olli; Lehtimaki, Terho; Vila-Pueyo, Marta; Goebel, Hartmut; Wichmann, Erich; Sintas, Celia; Uitterlinden, Andre G.; Hofman, Albert; Rivadeneira, Fernando; Heinze, Axel; Tronvik, Erling; Van Duijn, Cornelia M.; Kaprio, Jaakko; Cormand, Bru; Wessman, Maija; Frants, Rune R.; Meitinger, Thomas; Mueller-Myhsok, Bertram; Zwart, John-Anker; Farkkila, Markus; Macaya, Alfons; Ferrari, Michel D.; Kubisch, Christian; Palotie, Aarno; Dichgans, Martin und van den Maagdenberg, Arn M. J. M. (2013): Migraine without aura: genome-wide association analysis identifies several novel susceptibility. In: The Journal of Headache and Pain, Bd. 14, P18 [PDF, 134kB]

Lill, Christina M.; Liu, Tian; Schjeide, Brit-Maren M.; Roehr, Johannes T.; Akkad, Denis A.; Damotte, Vincent; Alcina, Antonio; Ortiz, Miguel A.; Arroyo, Rafa; Lopez de Lapuente, Aitzkoa; Blaschke, Paul; Winkelmann, Alexander; Gerdes, Lisa-Ann; Luessi, Felix; Fernadez, Oscar; Izquierdo, Guillermo; Antigüedad, Alfredo; Hoffjan, Sabine; Cournu-Rebeix, Isabelle; Gromöller, Silvana; Faber, Hans; Liebsch, Maria; Meissner, Esther; Chanvillard, Coralie; Touze, Emmanuel; Pico, Fernando; Corcia, Philippe; Dörner, Thomas; Steinhagen-Thiessen, Elisabeth; Baeckman, Lars; Heekeren, Hauke R.; Li, Shu-Chen; Lindenberger, Ulman; Chan, Andrew; Hartung, Hans-Peter; Aktas, Orhan; Lohse, Peter; Kümpfel, Tania; Kubisch, Christian; Epplen, Jörg T.; Zettl, Uwe K.; Fontaine, Bertrand; Vandenbroeck, Koen; Matesanz, Fuencisla; Urcelay, Elena; Bertram, Lars und Zipp, Frauke (September 2012): Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects. In: Journal of medical genetics, Bd. 49, Nr. 9: S. 558-562 [PDF, 217kB]

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