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Christopher M. Watson
Christopher M. Watson
The Leeds Teaching Hospitals NHS Trust & The University of Leeds
Verified email at leeds.ac.uk
Title
Cited by
Cited by
Year
Large‐scale analysis of association between GDF5 and FRZB variants and osteoarthritis of the hip, knee, and hand
E Evangelou, K Chapman, I Meulenbelt, FB Karassa, J Loughlin, A Carr, ...
Arthritis & Rheumatism: Official Journal of the American College of …, 2009
2232009
A meta-analysis of European and Asian cohorts reveals a global role of a functional SNP in the 5′ UTR of GDF5 with osteoarthritis susceptibility
K Chapman, A Takahashi, I Meulenbelt, C Watson, J Rodriguez-Lopez, ...
Human molecular genetics 17 (10), 1497-1504, 2008
2102008
CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation
R Hjeij, A Onoufriadis, CM Watson, CE Slagle, NT Klena, GW Dougherty, ...
The American Journal of Human Genetics 95 (3), 257-274, 2014
1582014
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
Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in Infancy
CP Diggle, SJS Rizzo, M Popiolek, R Hinttala, JP Schülke, MA Kurian, ...
The American Journal of Human Genetics 98 (4), 735-743, 2016
642016
Concordant Association of Insulin Degrading Enzyme Gene (IDE) Variants with IDE mRNA, Aß, and Alzheimer's Disease
MM Carrasquillo, O Belbin, F Zou, M Allen, N Ertekin-Taner, M Ansari, ...
PloS one 5 (1), e8764, 2010
632010
High prevalence of CCDC103 p. His154Pro mutation causing primary ciliary dyskinesia disrupts protein oligomerisation and is associated with normal diagnostic investigations
A Shoemark, E Moya, RA Hirst, MP Patel, EA Robson, J Hayward, J Scully, ...
Thorax 73 (2), 157-166, 2018
612018
Identification of a mutation in the ubiquitin-fold modifier1-specific peptidase 2 gene, UFSP2, in an extended South African family with Beukes hip dysplasia: research
CM Watson, LA Crinnion, L Gleghorn, WG Newman, R Ramesar, ...
South African Medical Journal 105 (7), 558-563, 2015
522015
Structure of ubiquitin-fold modifier 1-specific protease UfSP2
BH Ha, YJ Jeon, SC Shin, K Tatsumi, M Komatsu, K Tanaka, CM Watson, ...
Journal of Biological Chemistry 286 (12), 10248-10257, 2011
472011
Biallelic mutations in LRRC56, encoding a protein associated with intraflagellar transport, cause mucociliary clearance and laterality defects
S Bonnefoy, CM Watson, KD Kernohan, M Lemos, S Hutchinson, ...
The American Journal of Human Genetics 103 (5), 727-739, 2018
442018
Robust Diagnostic Genetic Testing Using Solution Capture Enrichment and a Novel Variant‐Filtering Interface
CM Watson, LA Crinnion, JE Morgan, SM Harrison, CP Diggle, J Adlard, ...
Human mutation 35 (4), 434-441, 2014
442014
Association between missense mutations in the BBS2 gene and nonsyndromic retinitis pigmentosa
E Shevach, M Ali, L Mizrahi-Meissonnier, M McKibbin, M El-Asrag, ...
JAMA ophthalmology 133 (3), 312-318, 2015
402015
Association between missense mutations in the BBS2 gene and nonsyndromic retinitis pigmentosa
E Shevach, M Ali, L Mizrahi-Meissonnier, M McKibbin, M El-Asrag, ...
JAMA ophthalmology 133 (3), 312-318, 2015
402015
Clinical utility of NGS diagnosis and disease stratification in a multiethnic primary ciliary dyskinesia cohort
MR Fassad, MP Patel, A Shoemark, T Cullup, J Hayward, M Dixon, ...
Journal of medical genetics 57 (5), 322-330, 2020
392020
Cas9-based enrichment and single-molecule sequencing for precise characterization of genomic duplications
CM Watson, LA Crinnion, S Hewitt, J Bates, R Robinson, IM Carr, ...
Laboratory Investigation 100 (1), 135-146, 2020
332020
Enhanced diagnostic yield in Meckel-Gruber and Joubert syndrome through exome sequencing supplemented with split-read mapping
CM Watson, LA Crinnion, IR Berry, SM Harrison, C Lascelles, ...
BMC medical genetics 17 (1), 1-9, 2016
302016
DNAAF1 links heart laterality with the AAA+ ATPase RUVBL1 and ciliary intraflagellar transport
VL Hartill, G van de Hoek, MP Patel, R Little, CM Watson, IR Berry, ...
Human molecular genetics 27 (3), 529-545, 2018
292018
m6aViewer: software for the detection, analysis, and visualization of N6-methyladenosine peaks from m6A-seq/ME-RIP sequencing data
A Antanaviciute, B Baquero-Perez, CM Watson, SM Harrison, C Lascelles, ...
RNA 23 (10), 1493-1501, 2017
282017
OVA: integrating molecular and physical phenotype data from multiple biomedical domain ontologies with variant filtering for enhanced variant prioritization
A Antanaviciute, CM Watson, SM Harrison, C Lascelles, L Crinnion, ...
Bioinformatics 31 (23), 3822-3829, 2015
282015
GeneTIER: prioritization of candidate disease genes using tissue-specific gene expression profiles
A Antanaviciute, C Daly, LA Crinnion, AF Markham, CM Watson, ...
Bioinformatics 31 (16), 2728-2735, 2015
272015
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Articles 1–20