Clayton D - Search Results

1

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: clayton d. Nat Genet. 1996 Aug;13(4):464-8. doi: 10.1038/ng0896-464. Nat Genet. 1996. PMID: 8696343

2

A whole genome screen for linkage disequilibrium in multiple sclerosis confirms disease associations with regions previously linked to susceptibility.

Sawcer S, Maranian M, Setakis E, Curwen V, Akesson E, Hensiek A, Coraddu F, Roxburgh R, Sawcer D, Gray J, Deans J, Goodfellow PN, Walker N, Clayton D, Compston A. Sawcer S, et al. Among authors: clayton d. Brain. 2002 Jun;125(Pt 6):1337-47. doi: 10.1093/brain/awf143. Brain. 2002. PMID: 12023322

3

Susceptibility to multiple sclerosis and the immunoglobulin heavy chain variable region.

Wood NW, Sawcer SJ, Kellar-Wood HF, Holmans P, Clayton D, Robertson N, Compston DA. Wood NW, et al. Among authors: clayton d. J Neurol. 1995 Oct;242(10):677-82. doi: 10.1007/BF00866919. J Neurol. 1995. PMID: 8568530

4

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: clayton d. 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

5

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. Among authors: clayton d. Brain. 1998 Oct;121 ( Pt 10):1869-87. doi: 10.1093/brain/121.10.1869. Brain. 1998. PMID: 9798743 Review.

6

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: clayton d. Neurogenetics. 1998 Dec;2(1):24-33. doi: 10.1007/s100480050048. Neurogenetics. 1998. PMID: 9933297

7

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: clayton d. 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

8

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: clayton d. Neurogenetics. 1999 Apr;2(2):91-6. doi: 10.1007/s100480050058. Neurogenetics. 1999. PMID: 10369884

9

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: clayton d. J Neuroimmunol. 1999 Aug 3;98(2):208-13. doi: 10.1016/s0165-5728(99)00089-2. J Neuroimmunol. 1999. PMID: 10430054

10

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.

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