Home News About Us Contact Contributors Disclaimer Privacy Policy Help FAQ

Home
Search
Quick Search
Advanced
Fulltext
Browse
Collections
Persons
My eDoc
Session History
Login
Name:
Password:
Documentation
Help
Support Wiki
Direct access to
document ID:


          Display Documents


Institute:
Collection:
Print in Citation style Print version     Display:
Sort by: Display records with Fulltext only
Entries: 1-7  
 Basket 
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
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
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
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
Entries: 1-7  
The scope and number of records on eDoc is subject to the collection policies defined by each institute - see "info" button in the collection browse view.