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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: trotman j. Neuropathol Appl Neurobiol. 2021 Oct;47(6):882-888. doi: 10.1111/nan.12701. Epub 2021 Feb 22. Neuropathol Appl Neurobiol. 2021. PMID: 33534137
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: trotman j. 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.
Embryonal tumor with multilayered rosettes: Overview of diagnosis and therapy.
Chadda KR, Solano-Páez P, Khan S, Llempén-López M, Phyu P, Horan G, Trotman J, Tarpey P, Erker C, Lindsay H, Addy D, Jacques TS, Allinson K, Pizer B, Huang A, Murray MJ. Chadda KR, et al. Among authors: trotman j. Neurooncol Adv. 2023 Apr 26;5(1):vdad052. doi: 10.1093/noajnl/vdad052. eCollection 2023 Jan-Dec. Neurooncol Adv. 2023. PMID: 37727849 Free PMC article. No abstract available.
Introduction and impact of routine whole genome sequencing in the diagnosis and management of sarcoma.
Watkins JA, Trotman J, Tadross JA, Harrington J, Hatcher H, Horan G, Prewett S, Wong HH, McDonald S, Tarpey P, Roberts T, Su J, Tischkowitz M, Armstrong R, Amary F, Sosinsky A. Watkins JA, et al. Among authors: trotman j. Br J Cancer. 2024 Sep;131(5):860-869. doi: 10.1038/s41416-024-02721-8. Epub 2024 Jul 12. Br J Cancer. 2024. PMID: 38997407 Free PMC article.
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. 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.
Benefits for children with suspected cancer from routine whole-genome sequencing.
Hodder A, Leiter SM, Kennedy J, Addy D, Ahmed M, Ajithkumar T, Allinson K, Ancliff P, Bailey S, Barnard G, Burke GAA, Burns C, Cano-Flanagan J, Chalker J, Coleman N, Cheng D, Clinch Y, Dryden C, Ghorashian S, Griffin B, Horan G, Hubank M, May P, McDerra J, Nagrecha R, Nicholson J, O'Connor D, Pavasovic V, Quaegebeur A, Rao A, Roberts T, Samarasinghe S, Stasevich I, Tadross JA, Trayers C, Trotman J, Vora A, Watkins J, Chitty LS, Bowdin S, Armstrong R, Murray MJ, Hook CE, Tarpey P, Vedi A, Bartram J, Behjati S. Hodder A, et al. Among authors: trotman j. Nat Med. 2024 Jul;30(7):1905-1912. doi: 10.1038/s41591-024-03056-w. Epub 2024 Jul 2. Nat Med. 2024. PMID: 38956197 Free PMC article.
Identification of novel pathogenic variants and features in patients with pseudohypoparathyroidism and acrodysostosis, subtypes of the newly classified inactivating PTH/PTHrP signaling disorders.
Truelove A, Mulay A, Prapa M, Casey RT, Adler AI, Offiah AC, Poole KES, Trotman J, Al Hasso N, Park SM. Truelove A, et al. Among authors: trotman j. Am J Med Genet A. 2019 Jul;179(7):1330-1337. doi: 10.1002/ajmg.a.61163. Epub 2019 May 1. Am J Med Genet A. 2019. PMID: 31041856 Free article.
193 results