| 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 | 3608 | 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 | 2464 | 2003 |
| Chromosome fragile sites SG Durkin, TW Glover Annu. Rev. Genet. 41, 169-192, 2007 | 821 | 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 | 819 | 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 | 804 | 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 | 715 | 1984 |
| 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 | 692 | 2000 |
| ATR regulates fragile site stability AM Casper, P Nghiem, MF Arlt, TW Glover Cell 111 (6), 779-789, 2002 | 691 | 2002 |
| 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 | 565 | 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 | 472 | 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 | 379 | 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 | 327 | 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 | 310 | 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 | 293 | 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 | 285 | 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 | 277 | 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 | 268 | 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 | 243 | 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 | 235 | 2000 |
| Chromosome breakage and recombination at fragile sites. TW Glover, CK Stein American journal of human genetics 43 (3), 265, 1988 | 232 | 1988 |
