| KRAS and BRAF Mutations in Advanced Colorectal Cancer Are Associated With Poor Prognosis but Do Not Preclude Benefit From Oxaliplatin or Irinotecan … SD Richman, MT Seymour, P Chambers, F Elliott, CL Daly, AM Meade, ... Journal of Clinical Oncology 27 (35), 5931-5937, 2009 | 676 | 2009 |
| PCR: a practical approach. MJ McPherson, P Quirke, GR Taylor | 601 | 1991 |
| MLPA and MAPH: new techniques for detection of gene deletions LN Sellner, GR Taylor Human mutation 23 (5), 413-419, 2004 | 387 | 2004 |
| Tissue extraction of DNA and RNA and analysis by the polymerase chain reaction. DP Jackson, FA Lewis, GR Taylor, AW Boylston, P Quirke Journal of Clinical Pathology 43 (6), 499-504, 1990 | 351 | 1990 |
| Direct polymerase chain reaction test for detection of Helicobacter pylori in humans and animals SA Ho, JA Hoyle, FA Lewis, AD Secker, D Cross, NP Mapstone, MF Dixon, ... Journal of clinical microbiology 29 (11), 2543-2549, 1991 | 349 | 1991 |
| Prognostic value of p53 overexpression and c-Ki-ras gene mutations in colorectal cancer SM Bell, N Scott, D Cross, P Sagar, FA Lewis, GE Blair, GR Taylor, ... Gastroenterology 104 (1), 57-64, 1993 | 320 | 1993 |
| A common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment L Van Laer, P Coucke, RF Mueller, G Caethoven, K Flothmann, ... Journal of medical genetics 38 (8), 515-518, 2001 | 275 | 2001 |
| Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte DA Parry, CV Logan, BE Hayward, M Shires, H Landolsi, C Diggle, I Carr, ... The American Journal of Human Genetics 89 (3), 451-458, 2011 | 246 | 2011 |
| Rapid detection of allele loss in colorectal tumours using microsatellites and fluorescent DNA technology L Cawkwell, SM Bell, FA Lewis, MF Dixon, GR Taylor, P Quirke British journal of cancer 67 (6), 1262-1267, 1993 | 244 | 1993 |
| Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration RK Koenekoop, H Wang, J Majewski, X Wang, I Lopez, H Ren, Y Chen, ... Nature genetics 44 (9), 1035-1039, 2012 | 207 | 2012 |
| Circulating tumour cells from patients with colorectal cancer have cancer stem cell hallmarks in ex vivo culture F Grillet, E Bayet, O Villeronce, L Zappia, EL Lagerqvist, S Lunke, ... Gut 66 (10), 1802-1810, 2017 | 193 | 2017 |
| Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non‐polyposis colorectal cancer: Identification of novel and recurrent deletions by MLPA CF Taylor, RS Charlton, J Burn, E Sheridan, GR Taylor Human mutation 22 (6), 428-433, 2003 | 192 | 2003 |
| Mutation of the variant α-tubulin TUBA8 results in polymicrogyria with optic nerve hypoplasia MR Abdollahi, E Morrison, T Sirey, Z Molnar, BE Hayward, IM Carr, ... The American Journal of Human Genetics 85 (5), 737-744, 2009 | 187 | 2009 |
| Cytosponge-trefoil factor 3 versus usual care to identify Barrett's oesophagus in a primary care setting: a multicentre, pragmatic, randomised controlled trial RC Fitzgerald, M di Pietro, M O'Donovan, R Maroni, B Muldrew, ... The Lancet 396 (10247), 333-344, 2020 | 182 | 2020 |
| Interactive visual analysis of SNP data for rapid autozygosity mapping in consanguineous families IM Carr, KJ Flintoff, GR Taylor, AF Markham, DT Bonthron Human mutation 27 (10), 1041-1046, 2006 | 180 | 2006 |
| The detection of large deletions or duplications in genomic DNA JAL Armour, DE Barton, DJ Cockburn, GR Taylor Human Mutation 20 (5), 325-337, 2002 | 164 | 2002 |
| Annie Besant, A Biography A Taylor | 158 | 1994 |
| Assessment of the genetic causes of recessive childhood non‐syndromic deafness in the UK–implications for genetic testing T Hutchin, NN Coy, H Conlon, E Telford, K Bromelow, D Blaydon, ... Clinical genetics 68 (6), 506-512, 2005 | 147 | 2005 |
| Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens HM Wood, O Belvedere, C Conway, C Daly, R Chalkley, M Bickerdike, ... Nucleic acids research 38 (14), e151-e151, 2010 | 137 | 2010 |
| Genetic and epigenetic analysis of recurrent hydatidiform mole BE Hayward, M De Vos, N Talati, MR Abdollahi, GR Taylor, E Meyer, ... Human mutation 30 (5), E629-E639, 2009 | 133 | 2009 |
