Items where Author is "Mort, M"

COOPER, D.N., CHEN, J.M., BALL, E.V., HOWELLS, K., MORT, M., PHILLIPS, A.D., CHUZHANOVA, N., KEHRER-SAWATZKI, H. and STEPHENS, M., 2010. Genes, mutations and human inherited disease at the dawn of the 100K mutome era. Human Mutation, 31, pp. 631-655.

COOPER, D.N., MORT, M., STENSON, P.D., BALL, E.V. and CHUZHANOVA, N.A., 2010. Methylation-mediated deamination of 5-methylcytosine appears to give rise to mutations causing human inherited disease in CpNpG trinucleotides as well as in CpG dinucleotides. Human Genomics, 4, pp. 406-410.

MORT, M., IVANOV, D., COOPER, D.N. and CHUZHANOVA, N.A., 2008. A meta-analysis of nonsense mutations causing human genetic disease. Human Mutation, 29 (8), pp. 1037-1047. ISSN 1059-7794

KHAN, I., MORT, M., BUCKLAND, P.R., COOPER, D.N., O'DONAVAN, M.C. and CHUZHANOVA, N.A., 2006. In silico discrimination of single nucleotide polymorphisms and pathological mutations in human gene promoter regions by means of local DNA sequence context and regularity. In Silico Biology, 6, pp. 23-34.