Henry Wood
Title
Cited by
Cited by
Year
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
1652012
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
1632018
Mutational signature in colorectal cancer caused by genotoxic pks+ E. coli
C Pleguezuelos-Manzano, J Puschhof, AR Huber, A van Hoeck, ...
Nature 580 (7802), 269-273, 2020
1482020
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
1382008
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
1272010
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
1162016
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
702014
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
652013
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
542012
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
232015
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
232014
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
232001
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
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
202015
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
192014
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
182012
Development of apothecia of the eyespot pathogen Tapesia on cereal crop stubble residue in England
PS Dyer, GL Bateman, HM Wood
Plant pathology 50 (3), 356-362, 2001
172001
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
162015
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
152017
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
142017
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Articles 1–20