Refining genetic associations in multiple sclerosis

The IMSGC contributors

doi:10.1016/S1474-4422(08)70122-4

Refining genetic associations in multiple sclerosis

The IMSGC contributors

Hussman Institute for Human Genomics

Research output: Contribution to journal › Letter › peer-review

83 Scopus citations

Original language	English (US)
Pages (from-to)	567-569
Number of pages	3
Journal	The Lancet Neurology
Volume	7
Issue number	7
DOIs	https://doi.org/10.1016/S1474-4422(08)70122-4
State	Published - Jul 1 2008

ASJC Scopus subject areas

Clinical Neurology

Access to Document

10.1016/S1474-4422(08)70122-4

Cite this

@article{2852b0dfa60f455daaa6b948b4110683,

title = "Refining genetic associations in multiple sclerosis",

author = "{The IMSGC contributors} and Stephen Sawcer and David Booth and Robert Heard and Graeme Stewart and An Goris and Rita Dobosi and Benedicte Dubois and Annette Oturai and Soendergaard, {Helle B.} and Finn Sellebjerg and Janna Saarela and Virpi Leppy{\"a} and Aarno Palotie and Leena Peltonen and Bertrand Fontaine and Isabelle Cournu-Rebeix and Francoise Clerget-Darpoux and Babron, {Marie Claude} and Frank Weber and Florian Holsboer and Bertram M{\"u}ller-Myhsok and Peter Rieckmann and Antje Kroner and Colin Graham and Koen Vandenbroeck and Stanley Hawkins and Sandra D'Alfonso and Laura Bergamaschi and Paola Naldi and Guerini, {Franca R.} and Marco Salvetti and Daniela Galimberti and Rogier Hintzen and {van Duijn}, Cornelia and Lorentzen, {{\AA}slaug R.} and Celius, {Elisabeth G.} and Harbo, {Hanne F.} and Anne Spurkland and Francesco Cucca and {Giovanna Marrosu}, Maria and Manuel Comabella and Xavier Montalban and Pablo Villoslada and Tomas Olsson and Ingrid Kockum and Jan Hillert and Maria Ban and Amie Walton and Margaret Pericak-Vance and Jacob McCauley",

note = "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. ",

year = "2008",

month = jul,

day = "1",

doi = "10.1016/S1474-4422(08)70122-4",

language = "English (US)",

volume = "7",

pages = "567--569",

journal = "The Lancet Neurology",

issn = "1474-4422",

publisher = "Lancet Publishing Group",

number = "7",

}

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 -