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
1472012
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
1302008
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
1222010
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
892016
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
782018
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
622014
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
562013
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
482012
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
242001
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
222014
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
192015
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), 2013
192013
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
182015
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
172012
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
152001
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
142014
The transcriptional consequences of somatic amplifications, deletions, and rearrangements in a human lung squamous cell carcinoma
LF Stead, S Berri, HM Wood, P Egan, C Conway, C Daly, ...
Neoplasia 14 (11), 1075-IN16, 2012
122012
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
112015
Nonreciprocal chromosomal translocations in renal cancer involve multiple DSBs and NHEJ associated with breakpoint inversion but not necessarily with transcription
H Ali, A Daser, P Dear, H Wood, P Rabbitts, T Rabbitts
Genes, Chromosomes and Cancer 52 (4), 402-409, 2013
112013
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), 53, 2017
102017
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Articles 1–20