Closing the case of APOE in multiple sclerosis: No association with disease risk in over 29 000 subjects

C.M. Lill, T. Liu, B.M. Schjeide, J.T. Roehr, D.A. Akkad, V. Damotte, A. Alcina, M.A. Ortiz, R. Arroyo, A.L. De Lapuente, P. Blaschke, A. Winkelmann, L.-A. Gerdes, F. Luessi, O. Fernadez, G. Izquierdo, A. Antigüedad, S. Hoffjan, I. Cournu-Rebeix, S. Gromöller & 29 others H. Faber, M. Liebsch, E. Meissner, C. Chanvillard, E. Touze, F. Pico, P. Corcia, T. Dörner, Allan Anzgene Consortium, Bill Anzgene Consortium, E. Steinhagen-Thiessen, L. Baeckman, H.R. Heekeren, S.-C. Li, U. Lindenberger, H.-P. Hartung, O. Aktas, P. Lohse, T. Kümpfel, C. Kubisch, J.T. Epplen, U.K. Zettl, B. Fontaine, K. Vandenbroeck, F. Matesanz, E. Urcelay, L. Bertram, F. Zipp, A. Chan

Research output: Contribution to journalArticle

18 Citations (Scopus)
Original languageEnglish
Pages (from-to)558-562
JournalJournal of Medical Genetics
Volume49
Issue number9
DOIs
Publication statusPublished - 2012

Cite this

Lill, C. M., Liu, T., Schjeide, B. M., Roehr, J. T., Akkad, D. A., Damotte, V., ... Chan, A. (2012). Closing the case of APOE in multiple sclerosis: No association with disease risk in over 29 000 subjects. Journal of Medical Genetics, 49(9), 558-562. https://doi.org/10.1136/Jmedgenet-2012-101175
Lill, C.M. ; Liu, T. ; Schjeide, B.M. ; Roehr, J.T. ; Akkad, D.A. ; Damotte, V. ; Alcina, A. ; Ortiz, M.A. ; Arroyo, R. ; De Lapuente, A.L. ; Blaschke, P. ; Winkelmann, A. ; Gerdes, L.-A. ; Luessi, F. ; Fernadez, O. ; Izquierdo, G. ; Antigüedad, A. ; Hoffjan, S. ; Cournu-Rebeix, I. ; Gromöller, S. ; Faber, H. ; Liebsch, M. ; Meissner, E. ; Chanvillard, C. ; Touze, E. ; Pico, F. ; Corcia, P. ; Dörner, T. ; Anzgene Consortium, Allan ; Anzgene Consortium, Bill ; Steinhagen-Thiessen, E. ; Baeckman, L. ; Heekeren, H.R. ; Li, S.-C. ; Lindenberger, U. ; Hartung, H.-P. ; Aktas, O. ; Lohse, P. ; Kümpfel, T. ; Kubisch, C. ; Epplen, J.T. ; Zettl, U.K. ; Fontaine, B. ; Vandenbroeck, K. ; Matesanz, F. ; Urcelay, E. ; Bertram, L. ; Zipp, F. ; Chan, A. / Closing the case of APOE in multiple sclerosis: No association with disease risk in over 29 000 subjects. In: Journal of Medical Genetics. 2012 ; Vol. 49, No. 9. pp. 558-562.
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title = "Closing the case of APOE in multiple sclerosis: No association with disease risk in over 29 000 subjects",
author = "C.M. Lill and T. Liu and B.M. Schjeide and J.T. Roehr and D.A. Akkad and V. Damotte and A. Alcina and M.A. Ortiz and R. Arroyo and {De Lapuente}, A.L. and P. Blaschke and A. Winkelmann and L.-A. Gerdes and F. Luessi and O. Fernadez and G. Izquierdo and A. Antig{\"u}edad and S. Hoffjan and I. Cournu-Rebeix and S. Grom{\"o}ller and H. Faber and M. Liebsch and E. Meissner and C. Chanvillard and E. Touze and F. Pico and P. Corcia and T. D{\"o}rner and {Anzgene Consortium}, Allan and {Anzgene Consortium}, Bill and E. Steinhagen-Thiessen and L. Baeckman and H.R. Heekeren and S.-C. Li and U. Lindenberger and H.-P. Hartung and O. Aktas and P. Lohse and T. K{\"u}mpfel and C. Kubisch and J.T. Epplen and U.K. Zettl and B. Fontaine and K. Vandenbroeck and F. Matesanz and E. Urcelay and L. Bertram and F. Zipp and A. Chan",
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Lill, CM, Liu, T, Schjeide, BM, Roehr, JT, Akkad, DA, Damotte, V, Alcina, A, Ortiz, MA, Arroyo, R, De Lapuente, AL, Blaschke, P, Winkelmann, A, Gerdes, L-A, Luessi, F, Fernadez, O, Izquierdo, G, Antigüedad, A, Hoffjan, S, Cournu-Rebeix, I, Gromöller, S, Faber, H, Liebsch, M, Meissner, E, Chanvillard, C, Touze, E, Pico, F, Corcia, P, Dörner, T, Anzgene Consortium, A, Anzgene Consortium, B, Steinhagen-Thiessen, E, Baeckman, L, Heekeren, HR, Li, S-C, Lindenberger, U, Hartung, H-P, Aktas, O, Lohse, P, Kümpfel, T, Kubisch, C, Epplen, JT, Zettl, UK, Fontaine, B, Vandenbroeck, K, Matesanz, F, Urcelay, E, Bertram, L, Zipp, F & Chan, A 2012, 'Closing the case of APOE in multiple sclerosis: No association with disease risk in over 29 000 subjects' Journal of Medical Genetics, vol. 49, no. 9, pp. 558-562. https://doi.org/10.1136/Jmedgenet-2012-101175

Closing the case of APOE in multiple sclerosis: No association with disease risk in over 29 000 subjects. / Lill, C.M.; Liu, T.; Schjeide, B.M.; Roehr, J.T.; Akkad, D.A.; Damotte, V.; Alcina, A.; Ortiz, M.A.; Arroyo, R.; De Lapuente, A.L.; Blaschke, P.; Winkelmann, A.; Gerdes, L.-A.; Luessi, F.; Fernadez, O.; Izquierdo, G.; Antigüedad, A.; Hoffjan, S.; Cournu-Rebeix, I.; Gromöller, S.; Faber, H.; Liebsch, M.; Meissner, E.; Chanvillard, C.; Touze, E.; Pico, F.; Corcia, P.; Dörner, T.; Anzgene Consortium, Allan; Anzgene Consortium, Bill; Steinhagen-Thiessen, E.; Baeckman, L.; Heekeren, H.R.; Li, S.-C.; Lindenberger, U.; Hartung, H.-P.; Aktas, O.; Lohse, P.; Kümpfel, T.; Kubisch, C.; Epplen, J.T.; Zettl, U.K.; Fontaine, B.; Vandenbroeck, K.; Matesanz, F.; Urcelay, E.; Bertram, L.; Zipp, F.; Chan, A.

In: Journal of Medical Genetics, Vol. 49, No. 9, 2012, p. 558-562.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Closing the case of APOE in multiple sclerosis: No association with disease risk in over 29 000 subjects

AU - Lill, C.M.

AU - Liu, T.

AU - Schjeide, B.M.

AU - Roehr, J.T.

AU - Akkad, D.A.

AU - Damotte, V.

AU - Alcina, A.

AU - Ortiz, M.A.

AU - Arroyo, R.

AU - De Lapuente, A.L.

AU - Blaschke, P.

AU - Winkelmann, A.

AU - Gerdes, L.-A.

AU - Luessi, F.

AU - Fernadez, O.

AU - Izquierdo, G.

AU - Antigüedad, A.

AU - Hoffjan, S.

AU - Cournu-Rebeix, I.

AU - Gromöller, S.

AU - Faber, H.

AU - Liebsch, M.

AU - Meissner, E.

AU - Chanvillard, C.

AU - Touze, E.

AU - Pico, F.

AU - Corcia, P.

AU - Dörner, T.

AU - Anzgene Consortium, Allan

AU - Anzgene Consortium, Bill

AU - Steinhagen-Thiessen, E.

AU - Baeckman, L.

AU - Heekeren, H.R.

AU - Li, S.-C.

AU - Lindenberger, U.

AU - Hartung, H.-P.

AU - Aktas, O.

AU - Lohse, P.

AU - Kümpfel, T.

AU - Kubisch, C.

AU - Epplen, J.T.

AU - Zettl, U.K.

AU - Fontaine, B.

AU - Vandenbroeck, K.

AU - Matesanz, F.

AU - Urcelay, E.

AU - Bertram, L.

AU - Zipp, F.

AU - Chan, A.

PY - 2012

Y1 - 2012

U2 - 10.1136/Jmedgenet-2012-101175

DO - 10.1136/Jmedgenet-2012-101175

M3 - Article

VL - 49

SP - 558

EP - 562

JO - Journal of Medical Genetics

JF - Journal of Medical Genetics

SN - 0022-2593

IS - 9

ER -