Barcellos LF - Search Results

1

Osteopontin polymorphisms and disease course in multiple sclerosis.

Caillier S, Barcellos LF, Baranzini SE, Swerdlin A, Lincoln RR, Steinman L, Martin E, Haines JL, Pericak-Vance M, Hauser SL, Oksenberg JR; Multiple Sclerosis Genetics Group. Caillier S, et al. Among authors: barcellos lf. Genes Immun. 2003 Jun;4(4):312-5. doi: 10.1038/sj.gene.6363952. Genes Immun. 2003. PMID: 12761568

2

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

3

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

4

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.

5

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.

6

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

7

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

8

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

9

Linkage and association analysis of chromosome 19q13 in multiple sclerosis.

Pericak-Vance MA, Rimmler JB, Martin ER, Haines JL, Garcia ME, Oksenberg JR, Barcellos LF, Lincoln R, Goodkin DE, Hauser SL. Pericak-Vance MA, et al. Among authors: barcellos lf. Neurogenetics. 2001 Oct;3(4):195-201. doi: 10.1007/s100480100119. Neurogenetics. 2001. PMID: 11714099

10

Genetic basis for clinical expression in multiple sclerosis.

Barcellos LF, Oksenberg JR, Green AJ, Bucher P, Rimmler JB, Schmidt S, Garcia ME, Lincoln RR, Pericak-Vance MA, Haines JL, Hauser SL; Multiple Sclerosis Genetics Group. Barcellos LF, et al. Brain. 2002 Jan;125(Pt 1):150-8. doi: 10.1093/brain/awf009. Brain. 2002. PMID: 11834600

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