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Graham Taylor
Graham Taylor
Viapath, Guy's Hospital & King's College, London
Verified email at kcl.ac.uk
Title
Cited by
Cited by
Year
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
6782009
PCR: a practical approach.
MJ McPherson, P Quirke, GR Taylor
5971991
MLPA and MAPH: new techniques for detection of gene deletions
LN Sellner, GR Taylor
Human mutation 23 (5), 413-419, 2004
3852004
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
3511991
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
3491990
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
3221993
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
2742001
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
2482011
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
2411993
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
2092012
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
1992020
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
1952017
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
1932003
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
1892009
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
1812006
Annie Besant, A Biography
A Taylor
1661994
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
1622002
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
1482005
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
1372010
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
1332009
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