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Entries: 1-6  
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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
 
Full text / Content available
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
 
Full text / Content available
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
 
Full text / Content available
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
Three novel mutations in the ACTA2 gene in German patients with thoracic aortic aneurysms and dissections
Authors: Hoffjan, Sabine; Waldmüller, Stephan; Blankenfeldt, Wulf; Kötting, Judith; Gehle, Petra; Binner, Priska; Epplen, Joerg T.; Scheffold, Thomas
Date of Publication (YYYY-MM-DD): 2011
Title of Journal: European Journal of Human Genetics
Volume: 19
Issue / Number: 5
Start Page: 520
End Page: 524
Sequence Number of Article: 1
Document Type: Article
ID: 563643.0
Trinucleotide repeat expansions in the junctophilin-3 gene are not found in caucasian patients with a huntington's disease-like phenotype
Authors: Bauer, Ingrid; Gencik, Martin; Laccone, Franco; Peters, Hartmut; Weber, Bernhard H. F.; Holinski Feder, Elke; Weirich, Helga; Morris-Rosendahl, Deborah J.; Rolfs, Arndt; Gencikova, Alexandra; Bauer, Peter; Wenning, Gregor K.; Epplen, Jörg T.; Holmes, Susan E.; Margolis, Russell L.; Ross, Christopher A.; Riess, Olaf
Date of Publication (YYYY-MM-DD): 2002-04-23
Title of Journal: Annals of Neurology
Volume: 51
Issue / Number: 5
Start Page: 662
End Page: 662
Document Type: Article
ID: 24441.0
Entries: 1-6  
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