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538 results

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Page 1
A rare case of paediatric astroblastoma with concomitant MN1-GTSE1 and EWSR1-PATZ1 gene fusions altering management.
Chadda KR, Holland K, Scoffings D, Dean A, Pickles JC, Behjati S, Jacques TS, Trotman J, Tarpey P, Allinson K, Murray MJ; Genomics England Research Consortium. Chadda KR, et al. Among authors: murray mj. Neuropathol Appl Neurobiol. 2021 Oct;47(6):882-888. doi: 10.1111/nan.12701. Epub 2021 Feb 22. Neuropathol Appl Neurobiol. 2021. PMID: 33534137
A rare case of bone marrow infiltration by medulloblastoma in a child.
Santarsieri A, Dickens E, Hook CE, Allinson K, Matys T, Murray MJ. Santarsieri A, et al. Among authors: murray mj. Br J Haematol. 2019 Jun;185(6):1015. doi: 10.1111/bjh.16041. Br J Haematol. 2019. PMID: 31172519 Free article. No abstract available.
Clonal hematopoiesis and therapy-related myeloid neoplasms following neuroblastoma treatment.
Coorens THH, Collord G, Lu W, Mitchell E, Ijaz J, Roberts T, Oliver TRW, Burke GAA, Gattens M, Dickens E, Nangalia J, Tischkowitz M, Anderson J, Shlien A, Godfrey AL, Murray MJ, Behjati S. Coorens THH, et al. Among authors: murray mj. Blood. 2021 May 27;137(21):2992-2997. doi: 10.1182/blood.2020010150. Blood. 2021. PMID: 33598691 Free PMC article. No abstract available.
The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancer.
Trotman J, Armstrong R, Firth H, Trayers C, Watkins J, Allinson K, Jacques TS, Nicholson JC, Burke GAA; Genomics England Research Consortium; Behjati S, Murray MJ, Hook CE, Tarpey P. Trotman J, et al. Among authors: murray mj. Br J Cancer. 2022 Jul;127(1):137-144. doi: 10.1038/s41416-022-01788-5. Epub 2022 Apr 22. Br J Cancer. 2022. PMID: 35449451 Free PMC article.
Clonal diversification and histogenesis of malignant germ cell tumours.
Oliver TRW, Chappell L, Sanghvi R, Deighton L, Ansari-Pour N, Dentro SC, Young MD, Coorens THH, Jung H, Butler T, Neville MDC, Leongamornlert D, Sanders MA, Hooks Y, Cagan A, Mitchell TJ, Cortes-Ciriano I, Warren AY, Wedge DC, Heer R, Coleman N, Murray MJ, Campbell PJ, Rahbari R, Behjati S. Oliver TRW, et al. Among authors: murray mj. Nat Commun. 2022 Aug 11;13(1):4272. doi: 10.1038/s41467-022-31375-4. Nat Commun. 2022. PMID: 35953478 Free PMC article.
Recurrent posterior fossa group A (PFA) ependymoma in a young child with constitutional mismatch repair deficiency (CMMRD).
Briggs M, Das A, Firth H, Levine A, Sánchez-Ramírez S, Negm L, Ercan AB, Chung J, Bianchi V, Jalloh I, Phyu P, Thorp N, Grundy RG, Hawkins C, Trotman J, Tarpey P, Tabori U, Allinson K, Murray MJ; Genomics England Research Consortium. Briggs M, et al. Among authors: murray mj. Neuropathol Appl Neurobiol. 2023 Feb;49(1):e12862. doi: 10.1111/nan.12862. Epub 2022 Nov 18. Neuropathol Appl Neurobiol. 2023. PMID: 36341503 Free PMC article. No abstract available.
Recurrent FOSL1 rearrangements in desmoplastic fibroblastoma.
De Noon S, Piggott R, Trotman J, Tadross JA, Fittall M, Hughes D, Ye H, Munasinghe E, Murray M, Tirabosco R, Amary F, Coleman N, Watkins J, Hubank M, Tarpey P, Behjati S, Flanagan AM. De Noon S, et al. J Pathol. 2023 Feb;259(2):119-124. doi: 10.1002/path.6038. Epub 2023 Jan 3. J Pathol. 2023. PMID: 36426824 Free PMC article.
538 results