Practical Neurology.

Por SAWCER, S.
Publicado em 1997

The complex genetics of multiple sclerosis: pitfalls and prospects

Por Sawcer, Stephen
Publicado em 2008

The genetic aspects of multiple sclerosis

Por Sawcer, Stephen
Publicado em 2009

Bayes factors in complex genetics

Por Sawcer, Stephen
Publicado em 2010

Detecting genes in complex disease: does phenotype accuracy limit the horizon?

Por Lee, Koon, Sawcer, Stephen
Publicado em 2010

The genetic basis of Parkinson's disease

Por Foltynie, T, Sawcer, S, Brayne, C, Barker, R
Publicado em 2002

Comment on: Month of birth and risk of multiple sclerosis: confounding and adjustments

Por Fiddes, Barnaby, Wason, James, Sawcer, Stephen
Publicado em 2014

Confounding in association studies: month of birth and multiple sclerosis

Por Fiddes, Barnaby, Wason, James, Sawcer, Stephen
Publicado em 2014

What role for genetics in the prediction of multiple sclerosis?

Por Sawcer, Stephen, Ban, Maria, Wason, James, Dudbridge, Frank
Publicado em 2010

Crohn's associated NOD2 gene variants are not involved in determining susceptibility to multiple sclerosis

Por Sawcer, S, Maranian, M, Hensiek, A, Roxburgh, R, Gray, J, Compston, A
Publicado em 2003

Confounding Underlies the Apparent Month of Birth Effect in Multiple Sclerosis

Por Fiddes, Barnaby, Wason, James, Kemppinen, Anu, Ban, Maria, Compston, Alastair, Sawcer, Stephen
Publicado em 2013

No evidence of association of the rare nsSNP rs35667974 in IFIH1 with Multiple Sclerosis

Por Bergamaschi, Laura, Ban, Maria, Leone, Maurizio A., Sawcer, Stephen J., D'Alfonso, Sandra
Publicado em 2010

Investigation of the role of mitochondrial DNA in multiple sclerosis susceptibility.

Por Maria Ban, Joanna Elson, Amie Walton, Douglas Turnbull, Alastair Compston, Patrick Chinnery, Stephen Sawcer
Publicado em 2008-08-01

No evidence for the involvement of interleukin 2 or the immunoglobulin heavy chain gene cluster in determining genetic susceptibility to multiple sclerosis

Por FEAKES, R., SAWCER, S., SMILLIE, B., CHATAWAY, J., BROADLEY, S., COMPSTON, A., CLAYTON, D., COMPSTON, A.
Publicado em 2000

Investigation of the Role of Mitochondrial DNA in Multiple Sclerosis Susceptibility

Por Ban, Maria, Elson, Joanna, Walton, Amie, Turnbull, Douglas, Compston, Alastair, Chinnery, Patrick, Sawcer, Stephen
Publicado em 2008

Mechanism of Human Dermal Fibroblast Migration Driven by Type I Collagen and Platelet-derived Growth Factor-BB

Por Li, Wei, Fan, Jianhua, Chen, Mei, Guan, Shengxi, Sawcer, David, Bokoch, Gary M., Woodley, David T.
Publicado em 2004

No Evidence for Association with Parkinson Disease for 13 Single-Nucleotide Polymorphisms Identified by Whole-Genome Association Screening

Por Goris, A., Williams-Gray, C. H., Foltynie, T., Compston, D. A. S., Barker, R. A., Sawcer, S. J.
Publicado em 2006

No association between multiple sclerosis and the Notch3 gene responsible for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

Por Broadley, S, Sawcer, S, Chataway, S, Coraddu, F, Coles, A, Gray, J, Roxburgh, R, Clayton, D, Compston, D
Publicado em 2001

Novel Olig1‐coding variants and susceptibility to multiple sclerosis

Por Goris, A, Yeo, T W, Maranian, M, Walton, A, Ban, M, Gray, J, Compston, A, Sawcer, S
Publicado em 2006

Multiple sclerosis in sibling pairs: an analysis of 250 families

Por Chataway, J, Mander, A, Robertson, N, Sawcer, S, Deans, J, Fraser, M, Broadley, S, Clayton, D, Compston, A
Publicado em 2001