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Henry Wood
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Mutational signature in colorectal cancer caused by genotoxic pks+ E. coli
C Pleguezuelos-Manzano, J Puschhof, A Rosendahl Huber, A van Hoeck, ...
Nature 580 (7802), 269-273, 2020
3312020
A randomised trial of the effect of omega-3 polyunsaturated fatty acid supplements on the human intestinal microbiota
H Watson, S Mitra, FC Croden, M Taylor, HM Wood, SL Perry, JA Spencer, ...
Gut 67 (11), 1974-1983, 2018
2462018
Correcting for cancer genome size and tumour cell content enables better estimation of copy number alterations from next-generation sequence data
A Gusnanto, HM Wood, Y Pawitan, P Rabbitts, S Berri
Bioinformatics 28 (1), 40-47, 2012
1772012
HER2 overexpression and amplification as a potential therapeutic target in colorectal cancer: analysis of 3256 patients enrolled in the QUASAR, FOCUS and PICCOLO colorectal …
SD Richman, K Southward, P Chambers, D Cross, J Barrett, G Hemmings, ...
The Journal of pathology 238 (4), 562-570, 2016
1552016
Sequence differentiation in regions identified by a genome scan for local adaptation
HM Wood, JW Grahame, S Humphray, J Rogers, RK Butlin
Molecular Ecology 17 (13), 3123-3135, 2008
1412008
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
1322010
MicroRNAs and head and neck cancer: reviewing the first decade of research
N Sethi, A Wright, H Wood, P Rabbitts
European Journal of Cancer 50 (15), 2619-2635, 2014
772014
Diagnosis of copy number variation by Illumina next generation sequencing is comparable in performance to oligonucleotide array comparative genomic hybridisation
JL Hayes, A Tzika, H Thygesen, S Berri, HM Wood, S Hewitt, ...
Genomics 102 (3), 174-181, 2013
692013
Next-generation sequencing for simultaneous determination of human papillomavirus load, subtype, and associated genomic copy number changes in tumors
C Conway, R Chalkley, A High, K Maclennan, S Berri, P Chengot, ...
The Journal of Molecular Diagnostics 14 (2), 104-111, 2012
592012
The genomic road to invasion—examining the similarities and differences in the genomes of associated oral pre-cancer and cancer samples
HM Wood, C Daly, R Chalkley, B Senguven, L Ross, P Egan, P Chengot, ...
Genome medicine 9 (1), 1-14, 2017
292017
Next-generation sequencing analysis for detecting human papillomavirus in oral verrucous carcinoma
M Samman, H Wood, C Conway, S Berri, M Pentenero, S Gandolfo, ...
Oral surgery, oral medicine, oral pathology and oral radiology 118 (1), 117 …, 2014
272014
The clonal relationships between pre‐cancer and cancer revealed by ultra‐deep sequencing
HM Wood, C Conway, C Daly, R Chalkley, S Berri, B Senguven, L Stead, ...
The Journal of pathology 237 (3), 296-306, 2015
262015
Estimating optimal window size for analysis of low-coverage next-generation sequence data
A Gusnanto, CC Taylor, I Nafisah, HM Wood, P Rabbitts, S Berri
Bioinformatics 30 (13), 1823-1829, 2014
252014
Cloning of the CYP51 gene from the eyespot pathogen Tapesia yallundae indicates that resistance to the DMI fungicide prochloraz is not related to sequence …
HM Wood, MJ Dickinson, JA Lucas, PS Dyer
FEMS Microbiology Letters 196 (2), 183-187, 2001
252001
Clinical and genomic analysis of a randomised phase II study evaluating anastrozole and fulvestrant in postmenopausal patients treated for large operable or locally advanced …
N Quenel-Tueux, M Debled, J Rudewicz, G Macgrogan, M Pulido, ...
British journal of cancer 113 (4), 585-594, 2015
222015
IMSA: integrated metagenomic sequence analysis for identification of exogenous reads in a host genomic background
MT Dimon, HM Wood, PH Rabbitts, ST Arron
PloS one 8 (5), e64546, 2013
222013
Survival of head and neck cancer cells relies upon LZK kinase-mediated stabilization of mutant p53
ZC Edwards, EW Trotter, P Torres-Ayuso, P Chapman, HM Wood, ...
Cancer Research 77 (18), 4961-4972, 2017
202017
Diagnosis of fetal submicroscopic chromosomal abnormalities in failed array CGH samples: copy number by sequencing as an alternative to microarrays for invasive fetal testing
K Cohen, A Tzika, H Wood, S Berri, P Roberts, G Mason, E Sheridan
Ultrasound in Obstetrics & Gynecology 45 (4), 394-401, 2015
192015
A computational index derived from whole-genome copy number analysis is a novel tool for prognosis in early stage lung squamous cell carcinoma
O Belvedere, S Berri, R Chalkley, C Conway, F Barbone, F Pisa, ...
Genomics 99 (1), 18-24, 2012
192012
Examining the potential use and long-term stability of guaiac faecal occult blood test cards for microbial DNA 16S rRNA sequencing
M Taylor, HM Wood, SP Halloran, P Quirke
Journal of Clinical Pathology 70 (7), 600-606, 2017
182017
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Articles 1–20