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Nick Telford

Large deletions at the t(9;22) breakpoint are common and may identify a poor-prognosis subgroup of patients with chronic myeloid leukemia
2000 · P. B. Sinclair, E. P. Nacheva, et al. · Blood · 310
Constitutional and somatic rearrangement of chromosome 21 in acute lymphoblastic leukaemia
2014 · Yilong Li, Claire Schwab, et al. · Nature · 280
The t(8;9)(p22;p24) Is a Recurrent Abnormality in Chronic and Acute Leukemia that Fuses PCM1 to JAK2
2005 · Andreas Reiter, Christoph Walz, et al. · Cancer Research · 269
European recommendations and quality assurance for cytogenomic analysis of haematological neoplasms
2019 · K. A. Rack, E. van den Berg, et al. · Leukemia · 141
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Multiple mechanisms underlie HLA dysregulation in cervical cancer
2000 · C.S. Brady, J.S. Bartholomew, et al. · Tissue Antigens · 128
Identification of a novel fusion gene involving hTAFII68 and CHN from a t(9;17)(q22;q11.2) translocation in an extraskeletal myxoid chondrosarcoma
1999 · C Attwooll, M Tariq, et al. · Oncogene · 112
Response of ETV6-FLT3–positive myeloid/lymphoid neoplasm with eosinophilia to inhibitors of FMS-like tyrosine kinase 3
2011 · Christoph Walz, Philipp Erben, et al. · Blood · 88
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A novel translocation, t(14;19)(q32;p13), involving IGH@ and the cytokine receptor for erythropoietin
2008 · L J Russell, D G De Castro, et al. · Leukemia · 65
Extraskeletal Myxoid Chondrosarcoma With Neuroendocrine Differentiation
2000 · M. Harris, J. Coyne, et al. · The American Journal of Surgical Pathology · 64
MLL amplification in acute leukaemia: a United Kingdom Cancer Cytogenetics Group (UKCCG) study
2000 · G Cuthbert, K Thompson, et al. · Leukemia · 56
FISHing Tips: What Every Clinician Should Know About 1p19q Analysis in Gliomas Using Fluorescence in situ Hybridisation
2015 · M.B. Pinkham, N. Telford, et al. · Clinical Oncology · 41
Myeloid- and lymphoid-specific breakpoint cluster regions in chromosome band 13q14 in acute leukemia
1999 · Lionel J.A. Coignet, Carmen S.P. Lima, et al. · Genes Chromosomes and Cancer · 30
Myeloproliferative neoplasm with eosinophilia and T-lymphoblastic lymphoma with ETV6–LYN gene fusion
2016 · N Telford, S Alexander, et al. · Blood Cancer Journal · 28
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A report of a child with a deletion (9)(q34.3): a recognisable phenotype?
1997 · H Ayyash, R Mueller, et al. · Journal of Medical Genetics · 27
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Terminal deletion (14)(q32.3): a new case.
1990 · N Telford, D A Thomson, et al. · Journal of Medical Genetics · 24
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Microfluidic channel‐assisted screening of hematopoietic malignancies
2013 · Farah Mughal, Sara J. Baldock, et al. · Genes Chromosomes and Cancer · 18
Characterisation of the differential response of normal and CML haemopoietic progenitor cells to macrophage inflammatory protein-1α
1999 · J Dürig, NG Testa, et al. · Leukemia · 17
European recommendations and quality assurance for cytogenomic analysis of haematological neoplasms: reponse to the comments from the Francophone Group of Hematological Cytogenetics (GFCH)
2020 · K. A. Rack, E. van den Berg, et al. · Leukemia · 16
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Fanconi anemia with sun-sensitivity caused by a Xeroderma pigmentosum-associated missense mutation in XPF
2018 · Isabell Popp, Maqsood Punekar, et al. · BMC Medical Genetics · 14
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Deletions of the derivative chromosome 9 do not account for the poor prognosis associated with Philadelphia-positive acute lymphoblastic leukemia
2002 · Alistair G. Reid, Brian J. P. Huntly, et al. · Blood · 12
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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A mild phenotype associated with der(9)t(3;9) (p25;p23).
1996 · R J McClure, N Telford, et al. · Journal of Medical Genetics · 9
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Genomic profiling of acute myeloid leukaemia associated with ataxia telangiectasia identifies a complex karyotype with wild‐type TP53 and mutant KRAS, G3BP1 and IL7R
2020 · Mae A. Goldgraben, Eleanor Fewings, et al. · Pediatric Blood & Cancer · 5
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Deletion of chromosome arm 15q and hitherto unreported duplication of del(15q) in myeloid disorders
2004 · K. Saunders, Y. Williams, et al. · Cancer Genetics and Cytogenetics · 5
Extensive deletion at the t(9;22) break-point occurs in a minority of patients with Philadelphia-positive acute lymphoblastic leukaemia.
2001 · Reid, AG, Huntly, BJP, et al. · UCL Discovery (University College London) · 3
Works count: 44
Citation count: 1,778
H-index: 17
I10-index: 20
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