Exome Array GWAS in 10,000 Germans Identifies Association between MUC22 and 
Multiple Sclerosis

Dankowski, T.; Buck, D.; Andlauer, T. F.; Antony, G.; Bayas, A.; Bechmann, L.; Berthele, A.; Bettecken, Thomas; Chan, A.; Franke, A.; Gold, R.; Graetz, C.; Haas, J.; Hecker, M.; Herms, S.; Hohlfeld, R.; Infante-Duarte, C.; Joeckel, K. -H.; Kieseier, B. C.; Knier, B.; Knop, M.; Lichtner, P.; Lieb, W.; Lill, C. M.; Limmroth, V.; Linker, R. A.; Loleit, V.; Meuth, S.; Moebus, S.; Müller-Myhsok, B.; Nischwitz, S.; Noethen, M. M.; Friedemann, P.; Pütz, B.; Ruck, T.; Salmen, A.; Stangel, M.; Stellmann, J. -P.; Strauch, K.; Stuerner, K. H.; Tackenberg, B.; Bergh, F. Then; Tumani, H.; Waldenberger, M.; Weber, F.; Wiend, H.; Wildemann, B.; Zettl, U. K.; Ziemann, U.; Zipp, F.; Hemmer, B.; Ziegler, A.

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Exome Array GWAS in 10,000 Germans Identifies Association between MUC22 and Multiple Sclerosis

Dankowski, T., Buck, D., Andlauer, T. F., Antony, G., Bayas, A., Bechmann, L., et al. (2015). Exome Array GWAS in 10,000 Germans Identifies Association between MUC22 and Multiple Sclerosis. HUMAN HEREDITY, 79(1), 32-33.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0029-0AB5-8 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0029-0AE0-6

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Creators:
Dankowski, T.¹, Author
Buck, D.¹, Author
Andlauer, T. F.², Author
Antony, G.¹, Author
Bayas, A.¹, Author
Bechmann, L.¹, Author
Berthele, A.¹, Author
Bettecken, Thomas², Author
Chan, A.¹, Author
Franke, A.¹, Author
Gold, R.¹, Author
Graetz, C.¹, Author
Haas, J.¹, Author
Hecker, M.¹, Author
Herms, S.¹, Author
Hohlfeld, R.¹, Author
Infante-Duarte, C.¹, Author
Joeckel, K. -H.¹, Author
Kieseier, B. C.¹, Author
Knier, B.¹, Author
Knop, M.¹, AuthorLichtner, P.¹, AuthorLieb, W.¹, AuthorLill, C. M.¹, AuthorLimmroth, V.¹, AuthorLinker, R. A.¹, AuthorLoleit, V.¹, AuthorMeuth, S.¹, AuthorMoebus, S.¹, AuthorMüller-Myhsok, B.², Author         Nischwitz, S.², Author         Noethen, M. M.¹, AuthorFriedemann, P.¹, AuthorPütz, B.², Author         Ruck, T.¹, AuthorSalmen, A.¹, AuthorStangel, M.¹, AuthorStellmann, J. -P.¹, AuthorStrauch, K.¹, AuthorStuerner, K. H.¹, AuthorTackenberg, B.¹, AuthorBergh, F. Then¹, AuthorTumani, H.¹, AuthorWaldenberger, M.¹, AuthorWeber, F.², Author         Wiend, H.¹, AuthorWildemann, B.¹, AuthorZettl, U. K.¹, AuthorZiemann, U.¹, AuthorZipp, F.¹, AuthorHemmer, B.¹, AuthorZiegler, A.¹, Author more..

Affiliations:
1external, ou_persistent22
2Max Planck Institute of Psychiatry, Max Planck Society, ou_1607137

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Language(s): eng - English

Dates: Date issued: 2015

Publication Status: Issued

Pages: -

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Rev. Type: -

Identifiers: ISI: 000351881300015

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Title: 43rd European Mathematical Genetics Meeting (EMGM)

Place of Event: Brest, France

Start-/End Date: 2015-04-16 - 2015-04-17

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Title: HUMAN HEREDITY

Source Genre: Journal

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Publ. Info: Basel, CH : Karger

Pages: - Volume / Issue: 79 (1) Sequence Number: - Start / End Page: 32 - 33 Identifier: ISSN: 0001-5652