Thomas W. Glover

Mutations in the p53 gene occur in diverse human tumour types

Janice Nigro, Suzanne J. Baker, Antonette C. Preisinger et al. · Nature · 1989 · 2.8K citations · Full text

Tumor Biology, Somatic Variant, Tumor Heterogeneity +7

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

Maria Eriksson, W. Ted Brown, Leslie B. Gordon et al. · Nature · 2003 · 2.2K citations · Full text

Point Mutations, Genetic Disorder, Genetics +5

Isolation of a partial candidate gene for Menkes disease by positional cloning

Julian F. B. Mercer, Janie Livingston, Bryan Hall et al. · Nature Genetics · 1993 · 696 citations

Mendelian Disorder, Menkes Disease, Genetic Disorder +11

Aberrant regulation of ras proteins in malignant tumour cells from type 1 neurofibromatosis patients

Tanya Basu, David H. Gutmann, Jonathan A. Fletcher et al. · Nature · 1992 · 662 citations · Full text

Tumor Biology, Neuro-oncology, Type 1 +8

Mutations in FOXC2 (MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome

Jianming Fang, Susan L. Dagenais, Robert P. Erickson et al. · The American Journal of Human Genetics · 2000 · 609 citations · Full text

Mendelian Disorder, Genetic Disorder, Are Responsible +7