Prostate cancer in BRCA2 germline mutation carriers is associated with poorer prognosis
Edwards, S M, Evans, D G R, Hope, Q, Norman, A R, Barbachano, Y, Bullock, S, Kote-Jarai, Z, Meitz, J, Falconer, A, Osin, P, Fisher, C, Guy, M, Jhavar, S G, Hall, A L, O'Brien, L T, Gehr-Swain, B N, Wilkinson, R A, Forrest, M S, Dearnaley, D P, Ardern-Jones, A T, Page, E C, Easton, D F, Eeles, R A
Published in British journal of cancer (07.09.2010)
Published in British journal of cancer (07.09.2010)
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Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3
Solomon, N M, Ross, S A, Morgan, T, Belsky, J L, Hol, F A, Karnes, P S, Hopwood, N J, Myers, S E, Tan, A S, Warne, G L, Forrest, S M, Thomas, P Q
Published in Journal of medical genetics (01.09.2004)
Published in Journal of medical genetics (01.09.2004)
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Friedreich ataxia: an overview
Delatycki, Martin B, Williamson, Robert, Forrest, Susan M
Published in Journal of medical genetics (01.01.2000)
Published in Journal of medical genetics (01.01.2000)
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Book Review
Mutations of the Flavin-Containing Monooxygenase Gene (FMO3) cause Trimethylaminuria, a Defect in Detoxication
Treacy, E. P., Akerman, B. R., Chow, L. M. L., Youil, R., Lin, C. Bibeau, J., Bruce, A. G., Knight, M., Danks, D. M., Cashman, J. R., Forrest, S. M.
Published in Human molecular genetics (01.05.1998)
Published in Human molecular genetics (01.05.1998)
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A new autosomal dominant pure cerebellar ataxia
Storey, E, Gardner, R J, Knight, M A, Kennerson, M L, Tuck, R R, Forrest, S M, Nicholson, G A
Published in Neurology (27.11.2001)
Published in Neurology (27.11.2001)
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Spinocerebellar ataxia type 20 is genetically distinct from spinocerebellar ataxia type 5
Lorenzo, D N, Forrest, S M, Ikeda, Y, Dick, K A, Ranum, L P W, Knight, M A
Published in Neurology (12.12.2006)
Published in Neurology (12.12.2006)
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Diagnostic accuracy of a prototype rapid chlamydia and gonorrhoea recombinase polymerase amplification assay: a multicentre cross-sectional preclinical evaluation
Harding-Esch, E.M., Fuller, S.S., Chow, S.-L.C., Nori, A.V., Harrison, M.A., Parker, M., Piepenburg, O., Forrest, M.S., Brooks, D.G., Patel, R., Hay, P.E., Fearnley, N., Pond, M.J., Dunbar, J.K., Butcher, P.D., Planche, T., Lowndes, C.M., Sadiq, S.T.
Published in Clinical microbiology and infection (01.03.2019)
Published in Clinical microbiology and infection (01.03.2019)
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Very mild muscular dystrophy associated with the deletion of 46% of dystrophin
England, S. B, Nicholson, L. V. B, Johnson, M. A, Forrest, S. M, Love, D. R, Zubrzycka-Gaarn, E. E, Bulman, D. E, Harris, J. B, Davies, K.E
Published in Nature (London) (11.01.1990)
Published in Nature (London) (11.01.1990)
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Journal Article
Association between hormonal genetic polymorphisms and early-onset prostate cancer
Forrest, M S, Edwards, S M, Houlston, R, Kote-Jarai, Z, Key, T, Allen, N, Knowles, M A, Turner, F, Ardern-Jones, A, Murkin, A, Williams, S, Oram, R, Bishop, D T, Eeles, R A
Published in Prostate cancer and prostatic diseases (01.03.2005)
Published in Prostate cancer and prostatic diseases (01.03.2005)
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Journal Article
Sperm DNA analysis in a Friedreich ataxia premutation carrier suggests both meiotic and mitotic expansion in the FRDA gene
Delatycki, M B, Paris, D, Gardner, R J, Forshaw, K, Nicholson, G A, Nassif, N, Williamson, R, Forrest, S M
Published in Journal of medical genetics (01.09.1998)
Published in Journal of medical genetics (01.09.1998)
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Journal Article
Early-onset Alzheimer's disease caused by a novel mutation at codon 219 of the presenilin-1 gene
Smith, M J, Gardner, R J, Knight, M A, Forrest, S M, Beyreuther, K, Storey, E, McLean, C A, Cotton, R G, Cappal, R, Masters, C L
Published in Neuroreport (25.02.1999)
Published in Neuroreport (25.02.1999)
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Preferential deletion of exons in Duchenne and Becker muscular dystrophies
Forrest, S M, Cross, G S, Speer, A, Gardner-Medwin, D, Burn, J, Davies, K E
Published in Nature (London) (15.10.1987)
Published in Nature (London) (15.10.1987)
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Journal Article
Segregation of mutations in arylsulphatase E and correlation with the clinical presentation of chondrodysplasia punctata
Sheffield, L J, Osborn, A H, Hutchison, W M, Sillence, D O, Forrest, S M, White, S J, Dahl, H H
Published in Journal of medical genetics (01.12.1998)
Published in Journal of medical genetics (01.12.1998)
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Journal Article
G130V, a common FRDA point mutation, appears to have arisen from a common founder
DELATYCKI, M. B, KNIGHT, M, KOENIG, M, COSSEE, M, WILLIAMSON, R, FORREST, S. M
Published in Human genetics (01.10.1999)
Published in Human genetics (01.10.1999)
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Journal Article
Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney disease
Ravine, D, Forrest, S.M, Sheffield, L.J, Danks, D.M, Walker, R.G, Kincaid-Smith, P, Gibson, R.N, Richards, R.I., Friend, K.
Published in The Lancet (British edition) (28.11.1992)
Published in The Lancet (British edition) (28.11.1992)
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Journal Article
X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26
LAGERSTRÖM-FERMER, M, SUNDVALL, M, JOHNSEN, E, WARNE, G. L, FORREST, S. M, ZAJAC, J. D, RICKARDS, A, RAVINE, D, LANDEGREN, U, PETTERSSON, U
Published in American journal of human genetics (01.04.1997)
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Published in American journal of human genetics (01.04.1997)
Journal Article
Clinical and genetic study of Friedreich ataxia in an Australian population
Delatycki, M B, Paris, D B, Gardner, R J, Nicholson, G A, Nassif, N, Storey, E, MacMillan, J C, Collins, V, Williamson, R, Forrest, S M
Published in American journal of medical genetics (19.11.1999)
Published in American journal of medical genetics (19.11.1999)
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The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA gene
Forrest, S M, Knight, M, Delatycki, M B, Paris, D, Williamson, R, King, J, Yeung, L, Nassif, N, Nicholson, G A
Published in Neurogenetics (01.08.1998)
Published in Neurogenetics (01.08.1998)
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