Sawcer S - Search Results

1

Evaluating the role of the 620W allele of protein tyrosine phosphatase PTPN22 in Crohn's disease and multiple sclerosis.

De Jager PL, Sawcer S, Waliszewska A, Farwell L, Wild G, Cohen A, Langelier D, Bitton A, Compston A, Hafler DA, Rioux JD. De Jager PL, et al. Among authors: sawcer s. Eur J Hum Genet. 2006 Mar;14(3):317-21. doi: 10.1038/sj.ejhg.5201548. Eur J Hum Genet. 2006. PMID: 16391555

2

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

3

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. 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

4

The genetic analysis of multiple sclerosis.

Sawcer S, Goodfellow PN, Compston A. Sawcer S, et al. Trends Genet. 1997 Jun;13(6):234-9. doi: 10.1016/S0168-9525(97)01140-2. Trends Genet. 1997. PMID: 9196329 Review.

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: sawcer s. Brain. 1998 Oct;121 ( Pt 10):1869-87. doi: 10.1093/brain/121.10.1869. Brain. 1998. PMID: 9798743 Review.

6

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: sawcer s. Ann Neurol. 1998 Dec;44(6):984. doi: 10.1002/ana.410440622. Ann Neurol. 1998. PMID: 9851448 No abstract available.

7

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

8

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: sawcer s. 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

9

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

10

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

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