| Issue Date | Title | Author(s) |
| 2008 | Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease | Sugiana, C; Pagliarini, DJ; McKenzie, M; Kirby, DM; Salemi, R; Abu-Amero, KK; Dahl, HH; Hutchison, WM; Vascotto, KA; Newbold, RF |
| 2004 | There is no correlation between c-Myc mRNA expression and telomerase activity in human breast cancer | Kirkpatrick, KL; Newbold, RF; Mokbel, K |
| 2004 | The mRNA expression of hTERT in human breast carcinomas correlates with VEGF expression | Kirkpatrick, KL; Newbold, RF; Mokbel, K |
| 2003 | Transfer of chromosome 8 into two breast cancer cell lines: Total exclusion of three regions indicates location of putative in vitro growth suppressor genes | Newbold, RF; Wilson, PJ; Cuthbert, AP; March, A; Arnold, J; Mulford, C; Trott, D; Baker, E; Purdie, D; Chevenix-Trench, G |
| 2005 | Evidence for a tumour suppressive function of APRG1 in breast cancer | Newbold, RF; Leris, AC; Jiang, WG; Roberts, TR; Mikbel, K |
| 2007 | Contribution of BRCA1 and BRCA2 germline mutations to the incidence of early-onset breast cancer in Cyprus | Newbold, RF; Hadjisavvas, A; Loizidou, M; Marcou, Y; Anastasiadou, V; Kyriacou, K |
| 2008 | Evidence of a tumour suppressive function E2F1 gene in human breast cancer | Newbold, RF; Worku, D; Jouhra, F; Jiang, GW; Patani, N; Mokbel, K |
| 2001 | A novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13 | Seyda, A; Newbold, RF; Hudson, TJ; Verner, A; MacKay, N; Winter, S; Feigenbaum, A; Malaney, S; Gonzalez-Halphen, D; Cuthbert, AP |
| 2001 | Telomere length abnormalities in mammalian radiosensitive cells | McIllrath, J; Bouffler, SD; Samper, E; Cuthbert, AP; Wojcik, A; Szumiel, I; Bryant, PE; Riches, AC; Slijepcevic, P; Newbold, RF |
| 2002 | A mortality gene(s) for the human adenocarcinoma line HeLa maps to a 130-kb region of human chromosome 4q22-q23 | Bryce, SD; Morrison, V; Craig, NJ; Forsyth, NR; Fitzsimmons, SA; Ireland, H; Cuthbert, AP; Newbold, RF; Parkinson, EK |
