Barcellos LF - Search Results

1

Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosis.

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. Barcellos LF, et al. Ann Neurol. 2004 Jun;55(6):793-800. doi: 10.1002/ana.20092. Ann Neurol. 2004. PMID: 15174013

2

Chromosome 19 single-locus and multilocus haplotype associations with multiple sclerosis. Evidence of a new susceptibility locus in Caucasian and Chinese patients.

Barcellos LF, Thomson G, Carrington M, Schafer J, Begovich AB, Lin P, Xu XH, Min BQ, Marti D, Klitz W. Barcellos LF, et al. JAMA. 1997 Oct 15;278(15):1256-61. JAMA. 1997. PMID: 9333267

3

Evidence for the genetic role of human leukocyte antigens in low frequency DRB1*1501 multiple sclerosis patients in Israel.

Karni A, Kohn Y, Safirman C, Abramsky O, Barcellos L, Oksenberg JR, Kahana E, Karussis D, Chapman J, Brautbar C. Karni A, et al. Mult Scler. 1999 Dec;5(6):410-5. doi: 10.1177/135245859900500i607. Mult Scler. 1999. PMID: 10618697

4

CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis. Multiple Sclerosis Genetics Group.

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, Oksenberg JR. Barcellos LF, et al. Immunogenetics. 2000 Apr;51(4-5):281-8. doi: 10.1007/s002510050621. Immunogenetics. 2000. PMID: 10803840

5

The complex genetic aetiology of multiple sclerosis.

Oksenberg JR, Barcellos LF. Oksenberg JR, et al. Among authors: barcellos lf. J Neurovirol. 2000 May;6 Suppl 2:S10-4. J Neurovirol. 2000. PMID: 10871777 Review.

6

Multiple sclerosis: genomic rewards.

Oksenberg JR, Baranzini SE, Barcellos LF, Hauser SL. Oksenberg JR, et al. Among authors: barcellos lf. J Neuroimmunol. 2001 Feb 15;113(2):171-84. doi: 10.1016/s0165-5728(00)00444-6. J Neuroimmunol. 2001. PMID: 11164900 Review.

7

Sequence variation in the transforming growth factor-beta1 (TGFB1) gene and multiple sclerosis susceptibility.

Green AJ, Barcellos LF, Rimmler JB, Garcia ME, Caillier S, Lincoln RR, Bucher P, Pericak-Vance MA, Haines JL, Hauser SL, Oksenberg JR; Multiple Sclerosis Genetics Group. Green AJ, et al. Among authors: barcellos lf. J Neuroimmunol. 2001 May 1;116(1):116-24. doi: 10.1016/s0165-5728(01)00283-1. J Neuroimmunol. 2001. PMID: 11311337

8

Evolution of the CCR5 Delta32 mutation based on haplotype variation in Jewish and Northern European population samples.

Klitz W, Brautbar C, Schito AM, Barcellos LF, Oksenberg JR. Klitz W, et al. Among authors: barcellos lf. Hum Immunol. 2001 May;62(5):530-8. doi: 10.1016/s0198-8859(01)00239-7. Hum Immunol. 2001. PMID: 11334678

9

PTPRC (CD45) is not associated with the development of multiple sclerosis in U.S. patients.

Barcellos LF, Caillier S, Dragone L, Elder M, Vittinghoff E, Bucher P, Lincoln RR, Pericak-Vance M, Haines JL, Weiss A, Hauser SL, Oksenberg JR. Barcellos LF, et al. Nat Genet. 2001 Sep;29(1):23-4. doi: 10.1038/ng722. Nat Genet. 2001. PMID: 11528386

10

Genetic variability and linkage disequilibrium within the HLA-DP region: analysis of 15 different populations.

Begovich AB, Moonsamy PV, Mack SJ, Barcellos LF, Steiner LL, Grams S, Suraj-Baker V, Hollenbach J, Trachtenberg E, Louie L, Zimmerman P, Hill AV, Stoneking M, Sasazuki T, Konenkov VI, Sartakova ML, Titanji VP, Rickards O, Klitz W. Begovich AB, et al. Among authors: barcellos lf. Tissue Antigens. 2001 May;57(5):424-39. doi: 10.1034/j.1399-0039.2001.057005424.x. Tissue Antigens. 2001. PMID: 11556967

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