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
5922009
PCR: a practical approach
MJ McPherson, P Quirke, GR Taylor
IRL Press at Oxford University Press, 1991
5311991
Electron reconstruction and identification in the ATLAS experiment using the 2015 and 2016 LHC proton–proton collision data at s= 13 TeV
M Aaboud, G Aad, B Abbott, DC Abbott, B Abeloos, DK Abhayasinghe, ...
The European Physical Journal C 79 (8), 1-40, 2019
4312019
MLPA and MAPH: new techniques for detection of gene deletions
LN Sellner, GR Taylor
Human mutation 23 (5), 413-419, 2004
3622004
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
3341990
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
3241991
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
2971993
Search for resonances in diphoton events at s = 13 TeV with the ATLAS detector
M Aaboud, G Aad, B Abbott, J Abdallah, B Abeloos, R Aben, OS AbouZeid, ...
Journal of High Energy Physics 2016 (9), 1-50, 2016
2652016
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
2312001
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
2281993
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
1972011
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
1852003
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
1702006
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
1642009
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, 2012
1612012
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
1522002
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
1292010
A comparison of fluorescent SSCP and denaturing HPLC for high throughput mutation scanning
LA Ellis, CF Taylor, GR Taylor
Human mutation 15 (6), 556-564, 2000
1262000
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
1252005
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
1212009
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