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Publications

Multiple Sclerosis

Sawcer S, Ban M, Maranian M, Yeo TW, Compston A, Daly MJ, Kirby A, De Jager PL, Ivinson A, Walsh E, Lander ES, Rioux JD, Hafler DA, Rimmler J, Gregory SG, Schmidt S, Pericak-Vance MA, Åkesson E, Datta P, Ryder LP, Oturai A, Harbo HF, Spurkland A, Myhr KM, Laaksonen M, Hillert J, Booth D, Heard R, Stewart G, Lincoln R, Barcellos LF, Hauser SL, Oksenberg JR, Kenealy SJ, Haines JL for The International Multiple Sclerosis Genetics Consortium. A high density screen for linkage to multiple sclerosis. Am J Hum Genet. 2005 July 29; [Epub ahead of print].

Cree BA, Khan O, Bourdette D, Goodin DS, Cohen JA, Marrie RA, Glidden D, Weinstock-Guttman B, Reich D, Patterson N, Haines JL, Pericak-Vance M, DeLoa C, Oksenberg JR, Hauser SL. Clinical characteristics of African Americans vs Caucasian Americans with multiple sclerosis. Neurology 63(11):2039-45, 2004.Kenealy SJ, Babron MC, Bradford Y, Schnetz-Boutaud N, Haines JL, Rimmler JB, Schmidt S, Pericak-Vance MA, Barcellos LF, Lincoln RR, Oksenberg JR, Hauser SL, Clanet M, Brassat D, Edan G, Yaouanq J, Semana G, Cournu-Rebeix I, Lyon-Caen O, Fontaine B; American-French Multiple Sclerosis Genetics Group. A Second-Generation Genomic Screen for Multiple Sclerosis. Am. J. Hum. Genet., 75:1070-1078, 2004.

Barcellos LF, Begovich AB, Reynolds RL, Caillier SJ, Brassat D, Schmidt S, Grams SE, Walker K, Steiner LL, Cree BA, Stillman A, Lincoln RR, Pericak-Vance MA, Haines JL, Erlich HA, Hauser SL, Oksenberg JR. Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosis. Ann Neurol. 55(6):793-800, 2004.

Oksenberg JR, Barcellos LF, Cree BA, Baranzini SE, Bugawan TL, Khan O, Lincoln RR, Swerdlin A, Mignot E, Lin L, Goodin D, Erlich HA, Schmidt S, Thomson G, Reich DE, Pericak-Vance MA, Haines JL, Hauser SL. Mapping Multiple Sclerosis Susceptibility to the HLA-DR Locus in African Americans. Am J Hum Genet 74(1):160-7, 2004.

Haines JL, Bradford Y, Garcia ME, Reed AD, Neumeister E, Pericak-Vance MA, Rimmler JB, Menold MM, Martin ER, Oksenberg JR, Barcellos LF, Lincoln R, Hauser SL, for the Multiple Sclerosis Genetics Group. Multiple susceptibility loci for multiple sclerosis. Hum Mol Genet 11(19):2251-2256, 2002.

Barcellos LF, Oksenberg JR, Begovich AB, Martin ER, Schmidt S, Vittinghoff E, Goodin DS, Pelletier D, Lincoln RR, Bucher P, Swerdlin A, Pericak-Vance MA, Haines JL, Hauser SL; The Multiple Sclerosis Genetics Group. HLA-DR2 Dose Effect on Susceptibility to Multiple Sclerosis and Influence on Disease Course. Am J Hum Genet 72:710-6, 2003.

Caillier S, Barcellos LF, Baranzini SE, Swerdlin A, Lincoln RR, Steinman L, Martin E, Haines JL, Pericak-Vance M, Hauser SL, Okensenberg JR (The Multiple Sclerosis Genetics Group). Osteopontin polymorphisms and disease course in multiple sclerosis. Genes and Immunity 4(4):312-315, 2003.

Kenealy SJ, Pericak-Vance MA, Haines JL. The genetic epidemiology of multiple sclerosis. J Neuroimmunol 43(1-2):7-12, 2003.

Pericak-Vance MA, Rimmler JB, Haines JL, Garcia ME, Oksenberg JR, Barcellos LF, Lincoln R, Hauser SL, Cournu-Rebeix I, Azoulay-Cayla A, Lyon-Caen O, Fontaine B, Duhamel E, Coppin H, Brassat D, Roth MP, Clanet M, Alizadeh M, Yaouanq J, Quelvennec E, Semana G, Edan G, Babron MC, Genin E, Clerget-Darpoux F. Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study. Neurogenetics, Volume 5, Issue 1, Feb 2004, Pages 45 - 48.

Rimmler JB, Menold MM; Martin ER, Oksenberg JR, Barcellos LF, Lincoln R, Hauser SL. Multiple Sclerosis Genetics Group. Multiple susceptibility loci for multiple sclerosis. Human Molecular Genetics 11(19):2251-6, 2002.

Schmidt S, Barcellos LF, DeSombre K, Rimmler JB, Lincoln RR, Bucher P, Saunders AM, Lai E, Martin ER, Vance JM, Oksenberg JR, Hauser SL, Pericak-Vance MA, Haines JL. Association of polymorphisms in the APOE region with susceptibility to and progression of multiple sclerosis. Am J Hum Genet 70(3):708-717, 2002.

Barcellos LF, Oksenberg JR, Green AJ, Bucher P, Rimmler JB, Schmidt S, Garcia ME, Lincoln RR, Pericak-Vance MA, Haines JL, Hauser SL [The Multiple Sclerosis Genetics Group]. Genetic basis for clinical expression in multiple sclerosis. Brain 125(1):150-158, 2002.

The Transatlantic Multiple Sclerosis Genetics Cooperative (Pericak-Vance MA, Rimmler JB, Saunders Am, Martin ER, Haines JL, Garcia ME, Oksenberg JR, Barcellos LF, Lincoln R, Goodkin DE, Hauser SL, Cmompston DAS, Sawcer SJ, Clayton D, Jones JB, Walker N, Goodfellow PN, Bulman D, SadovnickD, Ebers G, Dyment D, Willer C. A meta-analysis of genomic screens in multiple sclerosis. Multiple Sclerosis 7(1):3-11, 2001.

Green AR, Barcellos LF, Rimmler JB, Garcia ME, Caillier S, Lincoln RR, Bucher P, Pericak-Vance MA, Haines JL, Hauser SL, Oksenberg JR. The Multiple Sclerosis Genetics Group. Sequence variation in the transforming growth factor-beta 1 (TGFB1) gene and multiple sclerosis susceptibility. J Neuroimmunogy 116(1):116-124, 2001.

Barcellos LF, Caillier S, Dragone L, Elder M, Vittinghoff E, Bucher P, Pericak-Vance MA, Haines JL, Weiss A, Hauser SL, Oksenberg JR. PTPRC (CD45) is not associated with the development of multiple sclerosis in U.S. Caucasian patients. Nature Genetics 29(1):23-24, 2001.

Pericak-Vance MA, Rimmler JB, Martin ER, Haines JL, Garcia ME, Oksenberg JR, Barcellos LF, Lincoln R, Goodkin DE, Hauser SL. Linkage and association analysis of chromosome 19q13 in multiple sclerosis. Neurogenetics 3: 195-201, 2001.

Barcellos LF, Schito AM, Rimmler JB, Vittinghoff E, Shih A, Lincoln R, Callier S, Elkins MK, Goodkin DE, Haines JL, Pericak-Vance MA, Hauser SL, and Oksenberg JR (The Multiple Sclerosis Genetics Group). CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis. Immunogenetics 51(4/5):281-288, 2000.

Haines JL, Pericak-Vance MA. Genetics of multiple sclerosis. Current Directions in Autoimmunity 1:273-88, 1999.

Fontaine B, Cournu I, Arnaud I, Babron MC, Eichenbaum-Voline S, Oksenberg JR, Pericak-Vance MA, Haines JL, Semama G, Liblau R, Lyon-Caen O, Clerget-Darpoux F, Clanet M, Hauser SL. Chromosome 17q22-q24 and multiple sclerosis genetic susceptibility. American-French Multiple Sclerosis Genetic Group. Genes & Immunity 1(2):149-50, 1999.

Seboun E, Oksenberg JR, Rombos A, Usuku K, Goodkin DE, Lincoln RR, Wong M, Pham-Dinh D, Boesplug-Tanguy O, Carsique R, Fitoussi R, Gartioux C, Reyes C, Ribierre F, Faure S, Fizames C, Gyapay G, Weissenbach J, Dautigny A, Rimmler JB, Garcia ME, Pericak-Vance MA, Haines JL, Hauser SL. Linkage analysis of candidate myelin genes in familial multiple sclerosis. Neurogenetics 2(3):155-62, 1999.

Haines JL, Terwedow HA, Burgess K, Pericak-Vance MA, Rimmler JB, Martin ER, Oksenberg JR, Lincoln R, Zhang DY, Banatao DR, Gatto N, Goodkin DE, Hauser SL. Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group. Human Molecular Genetics 7(8):1229-34, 1998.

Haines JL, Ter-Minassian M, Bazyk A, Gusella JF, Kim DJ, Terwedow H, Pericak-Vance MA, Rimmler JB, Haynes CS, Roses AD, Lee A, Shaner B, Menold M, Seboun E, Fitoussi RP, Gartioux C, Reyes C, Ribierre F, Gyapay G, Weissenbach J, Hauser SL, Goodkin DE, Lincoln R, Usuku K, Oksenberg JR. A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group. Nature Genetics 13(4):469-71, 1996.

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