Jones HB - Search Results

1

HLA typing in the United Kingdom multiple sclerosis genome screen.

Coraddu F, Sawcer S, Feakes R, Chataway J, Broadley S, Jones HB, Clayton D, Gray J, Smith S, Taylor C, Goodfellow PN, Compston A. Coraddu F, et al. Among authors: jones hb. Neurogenetics. 1998 Dec;2(1):24-33. doi: 10.1007/s100480050048. Neurogenetics. 1998. PMID: 9933297

2

The genetics of multiple sclerosis: principles, background and updated results of the United Kingdom systematic genome screen.

Chataway J, Feakes R, Coraddu F, Gray J, Deans J, Fraser M, Robertson N, Broadley S, Jones H, Clayton D, Goodfellow P, Sawcer S, Compston A. Chataway J, et al. Brain. 1998 Oct;121 ( Pt 10):1869-87. doi: 10.1093/brain/121.10.1869. Brain. 1998. PMID: 9798743 Review.

3

A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22.

Sawcer S, Jones HB, Feakes R, Gray J, Smaldon N, Chataway J, Robertson N, Clayton D, Goodfellow PN, Compston A. Sawcer S, et al. Among authors: jones hb. Nat Genet. 1996 Aug;13(4):464-8. doi: 10.1038/ng0896-464. Nat Genet. 1996. PMID: 8696343

4

Exploring the dense mapping of a region of potential linkage in complex disease: an example in multiple sclerosis.

Feakes R, Sawcer S, Chataway J, Coraddu F, Broadley S, Gray J, Jones HB, Clayton D, Goodfellow PN, Compston A. Feakes R, et al. Among authors: jones hb. Genet Epidemiol. 1999;17(1):51-63. doi: 10.1002/(SICI)1098-2272(1999)17:1<51::AID-GEPI4>3.0.CO;2-V. Genet Epidemiol. 1999. PMID: 10323184

5

Evidence that allelic variants of the spinocerebellar ataxia type 2 gene influence susceptibility to multiple sclerosis.

Chataway J, Sawcer S, Coraddu F, Feakes R, Broadley S, Jones HB, Clayton D, Gray J, Goodfellow PN, Compston A. Chataway J, et al. Among authors: jones hb. Neurogenetics. 1999 Apr;2(2):91-6. doi: 10.1007/s100480050058. Neurogenetics. 1999. PMID: 10369884

6

A screen of candidates from peaks of linkage: evidence for the involvement of myeloperoxidase in multiple sclerosis.

Chataway J, Sawcer S, Feakes R, Coraddu F, Broadley S, Jones HB, Clayton D, Gray J, Goodfellow PN, Compston A. Chataway J, et al. Among authors: jones hb. J Neuroimmunol. 1999 Aug 3;98(2):208-13. doi: 10.1016/s0165-5728(99)00089-2. J Neuroimmunol. 1999. PMID: 10430054

7

No evidence for association of multiple sclerosis with the complement factors C6 and C7.

Chataway J, Sawcer S, Sherman D, Hobart M, Fernie B, Coraddu F, Feakes R, Broadley S, Gray J, Jones HB, Clayton D, Goodfellow PN, Compston A. Chataway J, et al. Among authors: jones hb. J Neuroimmunol. 1999 Sep 1;99(1):150-6. doi: 10.1016/s0165-5728(99)00054-5. J Neuroimmunol. 1999. PMID: 10496188

8

Transmission/disequilibrium tests for extended marker haplotypes.

Clayton D, Jones H. Clayton D, et al. Am J Hum Genet. 1999 Oct;65(4):1161-9. doi: 10.1086/302566. Am J Hum Genet. 1999. PMID: 10486335 Free PMC article.

9

Empirical genomewide significance levels established by whole genome simulations.

Sawcer S, Jones HB, Judge D, Visser F, Compston A, Goodfellow PN, Clayton D. Sawcer S, et al. Among authors: jones hb. Genet Epidemiol. 1997;14(3):223-9. doi: 10.1002/(SICI)1098-2272(1997)14:3<223::AID-GEPI1>3.0.CO;2-6. Genet Epidemiol. 1997. PMID: 9181352

10

Susceptibility to multiple sclerosis and the immunoglobulin heavy chain gene cluster.

Feakes R, Chataway J, Sawcer S, Jones HB, Clayton D, Goodfellow PN, Compston A. Feakes R, et al. Among authors: jones hb. Ann Neurol. 1998 Dec;44(6):984. doi: 10.1002/ana.410440622. Ann Neurol. 1998. PMID: 9851448 No abstract available.

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