Original language | English (US) |
---|---|
Pages (from-to) | 567-569 |
Number of pages | 3 |
Journal | The Lancet Neurology |
Volume | 7 |
Issue number | 7 |
DOIs | |
State | Published - Jul 1 2008 |
ASJC Scopus subject areas
- Clinical Neurology
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Refining genetic associations in multiple sclerosis. / The IMSGC contributors.
In: The Lancet Neurology, Vol. 7, No. 7, 01.07.2008, p. 567-569.Research output: Contribution to journal › Letter › peer-review
}
TY - JOUR
T1 - Refining genetic associations in multiple sclerosis
AU - The IMSGC contributors
AU - Sawcer, Stephen
AU - Booth, David
AU - Heard, Robert
AU - Stewart, Graeme
AU - Goris, An
AU - Dobosi, Rita
AU - Dubois, Benedicte
AU - Oturai, Annette
AU - Soendergaard, Helle B.
AU - Sellebjerg, Finn
AU - Saarela, Janna
AU - Leppyä, Virpi
AU - Palotie, Aarno
AU - Peltonen, Leena
AU - Fontaine, Bertrand
AU - Cournu-Rebeix, Isabelle
AU - Clerget-Darpoux, Francoise
AU - Babron, Marie Claude
AU - Weber, Frank
AU - Holsboer, Florian
AU - Müller-Myhsok, Bertram
AU - Rieckmann, Peter
AU - Kroner, Antje
AU - Graham, Colin
AU - Vandenbroeck, Koen
AU - Hawkins, Stanley
AU - D'Alfonso, Sandra
AU - Bergamaschi, Laura
AU - Naldi, Paola
AU - Guerini, Franca R.
AU - Salvetti, Marco
AU - Galimberti, Daniela
AU - Hintzen, Rogier
AU - van Duijn, Cornelia
AU - Lorentzen, Åslaug R.
AU - Celius, Elisabeth G.
AU - Harbo, Hanne F.
AU - Spurkland, Anne
AU - Cucca, Francesco
AU - Giovanna Marrosu, Maria
AU - Comabella, Manuel
AU - Montalban, Xavier
AU - Villoslada, Pablo
AU - Olsson, Tomas
AU - Kockum, Ingrid
AU - Hillert, Jan
AU - Ban, Maria
AU - Walton, Amie
AU - Pericak-Vance, Margaret
AU - McCauley, Jacob
N1 - Funding Information: None of the IMSGC has any conflict of interest to declare. This work was supported by the National Multiple Sclerosis Society (AP 3758-A-16, RG 2899, FG-1718-A1), grants from the NINDS (NS049477, NS032830, NS26799), AI067152, the NIAID (P01 AI039671), an NMSS Collaborative Research Award (CA 1001-A-14), and the Penates Foundation. This study makes use of data generated by the Wellcome Trust Case Control Consortium. Funding for the project was provided by the Wellcome Trust under award 076113. We thank the National Institutes of Mental Health for generously allowing the use of their genotype data. Work in Finland was supported by Neuropromise EU project grant LSHM-CT-2005-018637 and NIH grant NS43559. Work of the French network REFGENSEP was supported by grants from AFM, ARSEP, and INSERM. The Italian work was supported by the Italian Foundation for Multiple Sclerosis (FISM grants, 2002/R/40 and 2005/R/10); Regione Piemonte (grants 2003 and 2004). The Norwegian Bone Marrow Donor Registry is acknowledged for collaboration in establishment of the Norwegian control material. We also thank the many study participants and their families.
PY - 2008/7/1
Y1 - 2008/7/1
UR - http://www.scopus.com/inward/record.url?scp=49849091315&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=49849091315&partnerID=8YFLogxK
U2 - 10.1016/S1474-4422(08)70122-4
DO - 10.1016/S1474-4422(08)70122-4
M3 - Letter
C2 - 18565446
AN - SCOPUS:49849091315
VL - 7
SP - 567
EP - 569
JO - The Lancet Neurology
JF - The Lancet Neurology
SN - 1474-4422
IS - 7
ER -