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Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk

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Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk. / 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; 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.

In: J MED GENET, Vol. 50, No. 3, 01.03.2013, p. 140-3.

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Harvard

Lill, CM, Schjeide, B-MM, Graetz, C, Liu, T, Damotte, V, Akkad, DA, Blaschke, P, Gerdes, L-A, Kroner, A, Luessi, F, Cournu-Rebeix, I, Hoffjan, S, Winkelmann, A, Touze, E, Pico, F, Corcia, P, Otaegui, D, Antigüedad, A, Alcina, A, Comabella, M, Montalban, X, Olascoaga, J, Matesanz, F, Dörner, T, Li, S-C, Steinhagen-Thiessen, E, Lindenberger, U, Chan, A, Rieckmann, P, Hartung, H-P, Aktas, O, Lohse, P, Buttmann, M, Kümpfel, T, Kubisch, C, Zettl, UK, Epplen, JT, Fontaine, B, Zipp, F, Vandenbroeck, K & Bertram, L 2013, 'Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk', J MED GENET, vol. 50, no. 3, pp. 140-3. https://doi.org/10.1136/jmedgenet-2012-101411

APA

Lill, C. M., Schjeide, B-M. M., Graetz, C., Liu, T., Damotte, V., Akkad, D. A., Blaschke, P., Gerdes, L-A., Kroner, A., Luessi, F., Cournu-Rebeix, I., Hoffjan, S., Winkelmann, A., Touze, E., Pico, F., Corcia, P., Otaegui, D., Antigüedad, A., Alcina, A., ... Bertram, L. (2013). Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk. J MED GENET, 50(3), 140-3. https://doi.org/10.1136/jmedgenet-2012-101411

Vancouver

Lill CM, Schjeide B-MM, Graetz C, Liu T, Damotte V, Akkad DA et al. Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk. J MED GENET. 2013 Mar 1;50(3):140-3. https://doi.org/10.1136/jmedgenet-2012-101411

Bibtex

@article{c89bf795936a41b39e4f1c4210d3c41d,
title = "Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk",
keywords = "Adult, Ankyrin Repeat, Carrier Proteins, Case-Control Studies, Databases, Genetic, European Continental Ancestry Group, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Male, Middle Aged, Multiple Sclerosis, Polymorphism, Single Nucleotide",
author = "Lill, {Christina M} and Schjeide, {Brit-Maren M} and Christiane Graetz and Tian Liu and Vincent Damotte and Akkad, {Denis A} and Paul Blaschke and Lisa-Ann Gerdes and Antje Kroner and Felix Luessi and Isabelle Cournu-Rebeix and Sabine Hoffjan and Alexander Winkelmann and Emmanuel Touze and Fernando Pico and Philippe Corcia and David Otaegui and Alfredo Antig{\"u}edad and Antonio Alcina and Manuel Comabella and Xavier Montalban and Javier Olascoaga and Fuencisla Matesanz and Thomas D{\"o}rner and Shu-Chen Li and Elisabeth Steinhagen-Thiessen and Ulman Lindenberger and Andrew Chan and Peter Rieckmann and Hans-Peter Hartung and Orhan Aktas and Peter Lohse and Mathias Buttmann and Tania K{\"u}mpfel and Christian Kubisch and Zettl, {Uwe K} and Epplen, {Joerg T} and Bertrand Fontaine and Frauke Zipp and Koen Vandenbroeck and Lars Bertram",
year = "2013",
month = mar,
day = "1",
doi = "10.1136/jmedgenet-2012-101411",
language = "English",
volume = "50",
pages = "140--3",
journal = "J MED GENET",
issn = "0022-2593",
publisher = "BMJ PUBLISHING GROUP",
number = "3",

}

RIS

TY - JOUR

T1 - Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk

AU - Lill, Christina M

AU - Schjeide, Brit-Maren M

AU - Graetz, Christiane

AU - Liu, Tian

AU - Damotte, Vincent

AU - Akkad, Denis A

AU - Blaschke, Paul

AU - Gerdes, Lisa-Ann

AU - Kroner, Antje

AU - Luessi, Felix

AU - Cournu-Rebeix, Isabelle

AU - Hoffjan, Sabine

AU - Winkelmann, Alexander

AU - Touze, Emmanuel

AU - Pico, Fernando

AU - Corcia, Philippe

AU - Otaegui, David

AU - Antigüedad, Alfredo

AU - Alcina, Antonio

AU - Comabella, Manuel

AU - Montalban, Xavier

AU - Olascoaga, Javier

AU - Matesanz, Fuencisla

AU - Dörner, Thomas

AU - Li, Shu-Chen

AU - Steinhagen-Thiessen, Elisabeth

AU - Lindenberger, Ulman

AU - Chan, Andrew

AU - Rieckmann, Peter

AU - Hartung, Hans-Peter

AU - Aktas, Orhan

AU - Lohse, Peter

AU - Buttmann, Mathias

AU - Kümpfel, Tania

AU - Kubisch, Christian

AU - Zettl, Uwe K

AU - Epplen, Joerg T

AU - Fontaine, Bertrand

AU - Zipp, Frauke

AU - Vandenbroeck, Koen

AU - Bertram, Lars

PY - 2013/3/1

Y1 - 2013/3/1

KW - Adult

KW - Ankyrin Repeat

KW - Carrier Proteins

KW - Case-Control Studies

KW - Databases, Genetic

KW - European Continental Ancestry Group

KW - Female

KW - Genetic Predisposition to Disease

KW - Genome-Wide Association Study

KW - Humans

KW - Male

KW - Middle Aged

KW - Multiple Sclerosis

KW - Polymorphism, Single Nucleotide

U2 - 10.1136/jmedgenet-2012-101411

DO - 10.1136/jmedgenet-2012-101411

M3 - SCORING: Journal article

C2 - 23315543

VL - 50

SP - 140

EP - 143

JO - J MED GENET

JF - J MED GENET

SN - 0022-2593

IS - 3

ER -