Barcellos LF - Search Results

1

A second-generation genomic screen for multiple sclerosis.

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. Kenealy SJ, et al. Among authors: barcellos lf. Am J Hum Genet. 2004 Dec;75(6):1070-8. doi: 10.1086/426459. Epub 2004 Oct 19. Am J Hum Genet. 2004. PMID: 15494893 Free PMC 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

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

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

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