Graham Taylor
Graham Taylor
Viapath, Guy's Hospital & King's College, London
Verified email at
Cited by
Cited by
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
PCR: a practical approach.
MJ McPherson, P Quirke, GR Taylor
MLPA and MAPH: new techniques for detection of gene deletions
LN Sellner, GR Taylor
Human mutation 23 (5), 413-419, 2004
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
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
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
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
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
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
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
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
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
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
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
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
Annie Besant, A Biography
A Taylor
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
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
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
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
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