Barcellos LF - Search Results

1

Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis.

Barcellos LF, Sawcer S, Ramsay PP, Baranzini SE, Thomson G, Briggs F, Cree BC, Begovich AB, Villoslada P, Montalban X, Uccelli A, Savettieri G, Lincoln RR, DeLoa C, Haines JL, Pericak-Vance MA, Compston A, Hauser SL, Oksenberg JR. Barcellos LF, et al. Hum Mol Genet. 2006 Sep 15;15(18):2813-24. doi: 10.1093/hmg/ddl223. Epub 2006 Aug 11. Hum Mol Genet. 2006. PMID: 16905561 Free article.

2

Association mapping of disease loci, by use of a pooled DNA genomic screen.

Barcellos LF, Klitz W, Field LL, Tobias R, Bowcock AM, Wilson R, Nelson MP, Nagatomi J, Thomson G. Barcellos LF, et al. Am J Hum Genet. 1997 Sep;61(3):734-47. doi: 10.1086/515512. Am J Hum Genet. 1997. PMID: 9326338 Free PMC article.

3

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

4

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

5

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

6

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.

7

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.

8

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

9

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

10

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

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