Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis

David R. Booth, Robert N. Heard, Graeme J. Stewart, Mathew Cox, Rodney J. Scott, Jeannette Lechner-Scott, An Goris, Rita Dobosi, Bénédicte Dubois, Janna Saarela, Virpi Leppä, Leena Peltonen, Tuula Pirttila, Isabelle Cournu-Rebeix, Bertrand Fontaine, Laura Bergamaschi, Sandra D'Alfonso, Maurizio Leone, Aslaug R. Lorentzen, Hanne F. HarboElisabeth G. Celius, Anne Spurkland, Jenny Link, Ingrid Kockum, Tomas Olsson, Jan Hillert, Maria Ban, Amie Baker, Anu Kemppinen, Stephen Sawcer, Alastair Compston, Neil P. Robertson, Philip L. De Jager, David A. Hafler, Lisa F. Barcellos, Adrian J. Ivinson, Jacob L McCauley, Margaret A Pericak-Vance, Jorge R. Oksenberg, Stephen L. Hauser, David Sexton, Jonathan Haines

Research output: Contribution to journalArticle

21 Citations (Scopus)
Original languageEnglish
Pages (from-to)469-470
Number of pages2
JournalNature Genetics
Volume42
Issue number6
DOIs
StatePublished - Jun 1 2010

ASJC Scopus subject areas

  • Genetics

Cite this

Booth, D. R., Heard, R. N., Stewart, G. J., Cox, M., Scott, R. J., Lechner-Scott, J., ... Haines, J. (2010). Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis. Nature Genetics, 42(6), 469-470. https://doi.org/10.1038/ng0610-469

Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis. / Booth, David R.; Heard, Robert N.; Stewart, Graeme J.; Cox, Mathew; Scott, Rodney J.; Lechner-Scott, Jeannette; Goris, An; Dobosi, Rita; Dubois, Bénédicte; Saarela, Janna; Leppä, Virpi; Peltonen, Leena; Pirttila, Tuula; Cournu-Rebeix, Isabelle; Fontaine, Bertrand; Bergamaschi, Laura; D'Alfonso, Sandra; Leone, Maurizio; Lorentzen, Aslaug R.; Harbo, Hanne F.; Celius, Elisabeth G.; Spurkland, Anne; Link, Jenny; Kockum, Ingrid; Olsson, Tomas; Hillert, Jan; Ban, Maria; Baker, Amie; Kemppinen, Anu; Sawcer, Stephen; Compston, Alastair; Robertson, Neil P.; De Jager, Philip L.; Hafler, David A.; Barcellos, Lisa F.; Ivinson, Adrian J.; McCauley, Jacob L; Pericak-Vance, Margaret A; Oksenberg, Jorge R.; Hauser, Stephen L.; Sexton, David; Haines, Jonathan.

In: Nature Genetics, Vol. 42, No. 6, 01.06.2010, p. 469-470.

Research output: Contribution to journalArticle

Booth, DR, Heard, RN, Stewart, GJ, Cox, M, Scott, RJ, Lechner-Scott, J, Goris, A, Dobosi, R, Dubois, B, Saarela, J, Leppä, V, Peltonen, L, Pirttila, T, Cournu-Rebeix, I, Fontaine, B, Bergamaschi, L, D'Alfonso, S, Leone, M, Lorentzen, AR, Harbo, HF, Celius, EG, Spurkland, A, Link, J, Kockum, I, Olsson, T, Hillert, J, Ban, M, Baker, A, Kemppinen, A, Sawcer, S, Compston, A, Robertson, NP, De Jager, PL, Hafler, DA, Barcellos, LF, Ivinson, AJ, McCauley, JL, Pericak-Vance, MA, Oksenberg, JR, Hauser, SL, Sexton, D & Haines, J 2010, 'Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis', Nature Genetics, vol. 42, no. 6, pp. 469-470. https://doi.org/10.1038/ng0610-469
Booth DR, Heard RN, Stewart GJ, Cox M, Scott RJ, Lechner-Scott J et al. Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis. Nature Genetics. 2010 Jun 1;42(6):469-470. https://doi.org/10.1038/ng0610-469
Booth, David R. ; Heard, Robert N. ; Stewart, Graeme J. ; Cox, Mathew ; Scott, Rodney J. ; Lechner-Scott, Jeannette ; Goris, An ; Dobosi, Rita ; Dubois, Bénédicte ; Saarela, Janna ; Leppä, Virpi ; Peltonen, Leena ; Pirttila, Tuula ; Cournu-Rebeix, Isabelle ; Fontaine, Bertrand ; Bergamaschi, Laura ; D'Alfonso, Sandra ; Leone, Maurizio ; Lorentzen, Aslaug R. ; Harbo, Hanne F. ; Celius, Elisabeth G. ; Spurkland, Anne ; Link, Jenny ; Kockum, Ingrid ; Olsson, Tomas ; Hillert, Jan ; Ban, Maria ; Baker, Amie ; Kemppinen, Anu ; Sawcer, Stephen ; Compston, Alastair ; Robertson, Neil P. ; De Jager, Philip L. ; Hafler, David A. ; Barcellos, Lisa F. ; Ivinson, Adrian J. ; McCauley, Jacob L ; Pericak-Vance, Margaret A ; Oksenberg, Jorge R. ; Hauser, Stephen L. ; Sexton, David ; Haines, Jonathan. / Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis. In: Nature Genetics. 2010 ; Vol. 42, No. 6. pp. 469-470.
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