Mutations in the p53 gene occur in diverse human tumour types JM Nigro, SJ Baker, AC Preisinger, JM Jessup, R Hosteller, K Cleary, ... Nature 342 (6250), 705-708, 1989 | 3620 | 1989 |
Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome M Eriksson, WT Brown, LB Gordon, MW Glynn, J Singer, L Scott, ... Nature 423 (6937), 293-298, 2003 | 2514 | 2003 |
Chromosome fragile sites SG Durkin, TW Glover Annu. Rev. Genet. 41 (1), 169-192, 2007 | 833 | 2007 |
Isolation of a partial candidate gene for Menkes disease by positional cloning JFB Mercer, J Livingston, B Hall, JA Paynter, C Begy, ... Nature genetics 3 (1), 20-25, 1993 | 824 | 1993 |
Aberrant regulation of ras proteins in malignant tumour cells from type 1 neurofibromatosis patients TN Basu, DH Gutmann, JA Fletcher, TW Glover, FS Collins, J Downward Nature 356 (6371), 713-715, 1992 | 807 | 1992 |
DNA polymerase α inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes TW Glover, C Berger, J Coyle, B Echo Human genetics 67 (2), 136-142, 1984 | 721 | 1984 |
ATR regulates fragile site stability AM Casper, P Nghiem, MF Arlt, TW Glover Cell 111 (6), 779-789, 2002 | 697 | 2002 |
Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome J Fang, SL Dagenais, RP Erickson, MF Arlt, MW Glynn, JL Gorski, ... The American Journal of Human Genetics 67 (6), 1382-1388, 2000 | 696 | 2000 |
A de novo Alu insertion results in neurofibromatosis type 1 MR Wallace, LB Andersen, AM Saulino, PE Gregory, TW Glover, ... Nature 353 (6347), 864-866, 1991 | 567 | 1991 |
Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis E Legius, DA Marchuk, FS Collins, TW Glover Nature genetics 3 (2), 122-126, 1993 | 473 | 1993 |
Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative RhoRac guanine nucleotide exchange factor NG Pasteris, A Cadle, LJ Logie, MEM Porteous, CE Schwartz, ... Cell 79 (4), 669-678, 1994 | 381 | 1994 |
The Fanconi anemia pathway is required for the DNA replication stress response and for the regulation of common fragile site stability NG Howlett, T Taniguchi, SG Durkin, AD D'Andrea, TW Glover Human molecular genetics 14 (5), 693-701, 2005 | 329 | 2005 |
FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: direct evidence for the coincidence of viral integration sites and fragile sites CM Wilke, BK Hall, A Hoge, W Paradee, DI Smith, TW Glover Human molecular genetics 5 (2), 187-195, 1996 | 309 | 1996 |
Incomplete processing of mutant lamin A in Hutchinson–Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition MW Glynn, TW Glover Human molecular genetics 14 (20), 2959-2969, 2005 | 298 | 2005 |
Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: implications for the mechanism of fragile site induction MM Le Beau, FV Rassool, ME Neilly, R Espinosa III, TW Glover, DI Smith, ... Human molecular genetics 7 (4), 755-761, 1998 | 283 | 1998 |
FUdR induction of the X chromosome fragile site: evidence for the mechanism of folic acid and thymidine inhibition. TW Glover American Journal of Human Genetics 33 (2), 234, 1981 | 274 | 1981 |
X‐linked mental retardation: A study of 7 families PA Jacobs, TW Glover, M Mayer, P Fox, JW Gerrard, HG Dunn, DS Herbst, ... American journal of medical genetics 7 (4), 471-489, 1980 | 270 | 1980 |
Common fragile sites as targets for chromosome rearrangements MF Arlt, SG Durkin, RL Ragland, TW Glover DNA repair 5 (9-10), 1126-1135, 2006 | 247 | 2006 |
Isolation of a murine copper transporter gene, tissue specific expression and functional complementation of a yeast copper transport mutant J Lee, JR Prohaska, SL Dagenais, TW Glover, DJ Thiele Gene 254 (1-2), 87-96, 2000 | 238 | 2000 |
Fragile sites in cancer: more than meets the eye TW Glover, TE Wilson, MF Arlt Nature Reviews Cancer 17 (8), 489-501, 2017 | 234 | 2017 |