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Christopher Wragg

Effect of remote ischaemic conditioning on clinical outcomes in patients with acute myocardial infarction (CONDI-2/ERIC-PPCI): a single-blind randomised controlled trial
2019 · Derek J Hausenloy, Rajesh K Kharbanda, et al. · The Lancet · 347
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Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders
2017 · Víctor Faundes, William G. Newman, et al. · The American Journal of Human Genetics · 282
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Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia
2016 · Esther Meyer, Deciphering Developmental Disorders Study, et al. · Nature Genetics · 245
Not all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype
2017 · Lynette G. Sadleir, Emily I. Mountier, et al. · Neurology · 134
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EBF1-PDGFRB fusion in pediatric B-cell precursor acute lymphoblastic leukemia (BCP-ALL): genetic profile and clinical implications
2016 · Claire Schwab, Sarra L. Ryan, et al. · Blood · 129
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CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
2018 · Lot Snijders Blok, Justine Rousseau, et al. · Nature Communications · 123
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MGMT promoter methylation testing to predict overall survival in people with glioblastoma treated with temozolomide: a comprehensive meta-analysis based on a Cochrane Systematic Review
2021 · Sebastian Brandner, Alexandra McAleenan, et al. · Neuro-Oncology · 102
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Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy
2019 · Anne H. O’Donnell-Luria, Lynn S. Pais, et al. · The American Journal of Human Genetics · 96
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Next generation sequencing of chromosomal rearrangements in patients with split-hand/split-foot malformation provides evidence for DYNC1I1 exonic enhancers of DLX5/6 expression in humans
2014 · Hana Lango Allen, Richard Caswell, et al. · Journal of Medical Genetics · 81
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BRAF Fusion Analysis in Pilocytic Astrocytomas: KIAA1549-BRAF 15-9 Fusions Are More Frequent in the Midline Than Within the Cerebellum
2015 · Claire Faulkner, Hayley Patricia Ellis, et al. · Journal of Neuropathology & Experimental Neurology · 75
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EGFR and EGFRvIII analysis in glioblastoma as therapeutic biomarkers
2014 · Claire Faulkner, Abigail Palmer, et al. · British Journal of Neurosurgery · 74
Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia
2019 · Kathleen M. Gorman, Esther Meyer, et al. · The American Journal of Human Genetics · 67
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Prognostic value of test(s) for O6-methylguanine–DNA methyltransferase (MGMT) promoter methylation for predicting overall survival in people with glioblastoma treated with temozolomide
2021 · Alexandra McAleenan, Claire Kelly, et al. · Cochrane Database of Systematic Reviews · 54
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Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study
2016 · Jeremy F McRae, Stephen Clayton, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 40
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Diagnostic accuracy of 1p/19q codeletion tests in oligodendroglioma: A comprehensive meta‐analysis based on a Cochrane systematic review
2021 · Sebastian Brandner, Alexandra McAleenan, et al. · Neuropathology and Applied Neurobiology · 28
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Germline predisposition to haematological malignancies: Best practice consensus guidelines from the UK Cancer Genetics Group ( UKCGG) , CanGene‐CanVar and the NHS England Haematological Oncology Working Group
2023 · Beverley Speight, Helen Hanson, et al. · British Journal of Haematology · 27
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Diagnostic test accuracy and cost-effectiveness of tests for codeletion of chromosomal arms 1p and 19q in people with glioma
2022 · Alexandra McAleenan, Hayley E Jones, et al. · Cochrane Database of Systematic Reviews · 19
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Diagnostic test accuracy and cost-effectiveness of tests for codeletion of chromosomal arms 1p and 19q in people with glioma
2019 · Alexandra McAleenan, Hayley E Jones, et al. · Cochrane Database of Systematic Reviews · 12
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Association for Clinical Genomic Science (ACGS) guidelines for the classification of oncogenicity of somatic variants in cancer: recommendations by the UK somatic variant interpretation group (SVIG-UK)
2025 · George J Burghel, Joanne Mason, et al. · Journal of Medical Genetics · 10
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Recommendations for laboratory testing of UK patients with acute myeloid leukaemia
2022 · Priyanka Mehta, Nick Telford, et al. · British Journal of Haematology · 9
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Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data
2019 · Stuart Aitken, Helen V. Firth, et al. · The American Journal of Human Genetics · 9
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Clinically Actionable Insights into Initial and Matched Recurrent Glioblastomas to Inform Novel Treatment Approaches
2019 · H. P. Ellis, C. E. McInerney, et al. · Journal of Oncology · 8
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Erratum: Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia
2017 · Esther Meyer, Deciphering Developmental Disorders Study, et al. · Nature Genetics · 6
Quantifying evidence for phenotypic specificity (PP4) for syndromic phenotypes: Large-scale integration of rare germline FH variants from diagnostic laboratory testing for HLRCC and renal cancer
2025 · Sophie Allen, Charlie F. Rowlands, et al. · Genetics in Medicine · 3
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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
2019 · Lot Snijders Blok, Justine Rousseau, et al. · Nature Communications · 3
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Works count: 39
Citation count: 1,990
H-index: 17
I10-index: 19
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