Sally Cottrell

Base-excision repair of oxidative DNA damage

The telomeric 60 kb of chromosome arm 4p is homologous to telomeric regions on 13p, 15p, 21p, and 22p

A large fraction of unclassified variants of the mismatch repair genesMLH1andMSH2is associated with splicing defects

WNT signalling pathways as therapeutic targets in cancer

?-Catenin mutation and expression analysis in ovarian cancer: Exon 3 mutations and nuclear translocation in 16% of endometrioid tumours

A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 ( SMAD4)

The genetics of FAP and FAP-like syndromes

Inflammation and Colon Cancer

Classification and diagnostic prediction of cancers using gene expression profiling and artificial neural networks

‘Mendelian randomization’: can genetic epidemiology contribute to understanding environmental determinants of disease?*

Human Splicing Finder: an online bioinformatics tool to predict splicing signals

The genetics of hereditary colon cancer

Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15

β-Catenin Expression Pattern in Stage I and II Ovarian Carcinomas

Hamartomatous Polyposis Syndromes

Polymorphisms and colorectal tumor risk

GSTM1, GSTT1, GSTP1, GSTA1 and colorectal cancer risk: A comprehensive meta-analysis

DNA methylation and human disease

Epidemiology of colorectal cancer: incidence, mortality, survival, and risk factors

Diagnosis of Ewing's sarcoma and peripheral neuroectodermal tumour based on the detection of t(11;22) using fluorescence in situ hybridisation

Colorectal cancer screening and surveillance: Clinical guidelines and rationale?Update based on new evidence

Alpha 2-chimerin, an SH2-containing GTPase-activating protein for the ras-related protein p21rac derived by alternate splicing of the human n-chimerin gene, is selectively expressed in brain regions and testes.

The Lymphatic System: Integral Roles in Immunity

Wnt signaling and cancer

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes

Impaired lymphatic function accelerates cancer growth

Sertoli-Sertoli and Sertoli-Germ Cell Interactions and Their Significance in Germ Cell Movement in the Seminiferous Epithelium during Spermatogenesis

A survey of phenotypic features in juvenile polyposis.

Intron splice acceptor site sequence variation in the hereditary non-polyposis colorectal cancer gene hMSH2

A 28-kb Deletion Spanning D15S63 (PW71) in Five Families: A Rare Neutral Variant?

Fine Mapping of Probes in the Adenomatous Polyposis Coli Region of Chromosome 5 by In Situ Hybridization

Loss of heterozygosity on chromosome 5 in sporadic ovarian carcinoma is a late event and is not associated with mutations in APC at 5q21-22

Genetic mapping of hereditary mixed polyposis syndrome to chromosome 6q.

FLT4/VEGFR3and Milroy Disease: Novel Mutations, a Review of Published Variants and Database Update