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| Assessment of microRNA-related SNP effects in the 3' untranslated region of the IL22RA2 risk locus in multiple sclerosis |
| Authors: Lill, Christina M.; Schilling, Marcel; Ansaloni, Sara; Schröder, Julia; Jaedicke, Marian; Luessi, Felix; Schjeide, Brit-Maren M.; Mashychev, Andriy; Graetz, Christiana; Akkad, Denis A.; Gerdes, Lisa-Ann; Kroner, Antje; Blaschke, Paul; Hoffjan, Sabine; Winkelmann, Alexander; Dörner, Thomas; Rieckmann, Peter; Steinhagen-Thiessen, Elisabeth; Lindenberger, Ulman; Chan, Andrew; Hartung, Hans-Peter; Aktas, Orhan; Lohse, Peter; Buttmann, Mathias; Kümpfel, Tania; Kubisch, Christian; Zettl, Uwe K.; Epplen, Joerg T.; Zipp, Frauke; Bertram, Lars | | Date of Publication (YYYY-MM-DD): 2014 | | Title of Journal: Neurogenetics | | Volume: 15 | | Issue / Number: 2 | | Start Page: 129 | | End Page: 134 | | Document Type: Article | | ID: 695790.0 |
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| MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis |
| Authors: Lill, Christina M.; Schjejde, Brit-Maren M.; Graetz, Christiane; Ban, Maria; Alcina, Antonio; Ortiz, Miguel A.; Pérez, Jennifer; Damotte, Vincent; Booth, David; Lopez de Lapuente, Aitzkoa; Broer, Linda; Schilling, Marcel; Akkad, Denis A.; Aktas, Orhan; Alloza, Iraide; Antigüedad, Alfredo; Arroyo, Rafa; Blaschke, Paul; Buttmann, Mathias; Chan, Andrew; Compston, Alastair; Cournu-Rebeix, Isabelle; Dörner, Thomas; Epplen, Joerg T.; Fernández, Óscar; Gerdes, Lisa-Ann; Guillot-Noël, Léna; Hartung, Hans-Peter; Hoffjan, Sabine; Izquierdo, Guillermo; Kemppinen, Anu; Kroner, Antje; Kubisch, Christian; Kümpfel, Tania; Li, Shu-Chen; Lindenberger, Ulman; Lohse, Peter; Lubetzki, Catherine; Luessi, Felix; Malhotra, Sunny; Mescheriakova, Julia; Montalban, Xavier; Papeix, Caroline; Paredes, Lidia F.; Rieckmann, Peter; Steinhagen-Thiessen, Elisabeth; Winkelmann, Alexander; Zettl, Uwe K.; Hintzen, Rogier; Vandenbroeck, Koen; Stewart, Graeme; Fontaine, Bertrand; Comabella, Manuel; Urcelay, Elena; Matesanz, Fuencisla; Sawcer, Stephen; Bertram, Lars; Zipp, Frauke; International Multiple Sclerosis Genetics Consortium | | Date of Publication (YYYY-MM-DD): 2013 | | Title of Journal: Brain | | Volume: 136 | | Issue / Number: 6 | | Start Page: 1778 | | End Page: 1782 | | Document Type: Article | | ID: 668049.0 |
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| Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk |
| Authors: Lill, Christina M.; Schjeide, Britt-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; Antigüedad, 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; Bertram, Lars | | Date of Publication (YYYY-MM-DD): 2013 | | Title of Journal: Journal of Medical Genetics | | Volume: 50 | | Issue / Number: 3 | | Start Page: 140 | | End Page: 143 | | Document Type: Article | | ID: 675458.0 |
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| Independent replication of STAT3 association with multiple sclerosis risk in a large German case-control sample |
| Authors: Lill, Christina M.; Schjejde, Brit-Maren M.; Akkad, Denis A.; Blaschke, Paul; Winkelmann, Alexander; Gerdes, Lisa-Ann; Hoffjan, Sabine; Luessi, Felix; Dörner, Thomas; Li, Shu-Chen; Steinhagen-Thiessen, Elisabeth; Lindenberger, Ulman; Chan, Andrew; Hartung, Hans-Peter; Aktas, Orhan; Lohse, Peter; Kümpfel, Tania; Kubisch, Christian; Epplen, Joerg T.; Zettl, Uwe K.; Bertram, Lars; Zipp, Frauke | | Date of Publication (YYYY-MM-DD): 2012 | | Title of Journal: Neurogenetics | | Volume: 13 | | Issue / Number: 1 | | Start Page: 83 | | End Page: 86 | | Document Type: Article | | ID: 610796.0 |
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| Severe mental retardation with breathing abnormalities (Pitt−Hopkins syndrome) is caused by haploinsufficiency of the neuronal bHLH transcription factor TCF4 |
| Authors: Brockschmidt, Antje; Todt, Unda; Ryu, Soojin; Hoischen, Alexander; Landwehr, Christina; Birnbaum, Stefanie; Frenck, Wilhelm; Radlwimmer, Bernhard; Lichter, Peter; Engels, Hartmut; Driever, Wolfgang; Kubisch, Christian; Weber, Ruthild G. | | Date of Publication (YYYY-MM-DD): 2007-06-15 | | Title of Journal: Hum. Mol. Genet. | | Volume: 16 | | Issue / Number: 12 | | Start Page: 1488 | | End Page: 1494 | | Document Type: Article | | ID: 569574.0 |
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| Rare Missense Variants in ATP1A2 in Families With Clustering of Common Forms of Migraine |
| Authors: Todt, Unda; Dichgans, Martin; Jurkat-Rott, Karin; Heinze, Axel; Zifarelli, Giovanni; Koenderink, Jan B.; Goebel, Ingrid; Zumbroich, Vera; Stiller, Anne; Ramirez, Alfredo; Friedrich, Thomas; Göbel, Hartmut; Kubisch, Christian | | Date of Publication (YYYY-MM-DD): 2005 | | Title of Journal: Human Mutation | | Volume: 26 | | Issue / Number: 4 | | Start Page: 315 | | End Page: 321 | | Document Type: Article | | ID: 262985.0 |
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| Identification of a novel mutation in the coding region of the grey-lethal gene OSTM1 in human malignant infantile osteopetrosis |
| Authors: Ramirez, Alfredo; Faupel, Julia; Goebel, Ingrid; Stiller, Anne; Beyer, Susanne; Stockle, Christina; Hasan, Carola; Bode, Udo; Kornak, Uwe; Kubisch, Christian | | Date of Publication (YYYY-MM-DD): 2004-05 | | Title of Journal: Human Mutation | | Volume: 23 | | Issue / Number: 5 | | Start Page: 471 | | End Page: 476 | | Document Type: Article | | ID: 228798.0 |
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