Wren D - Search Results

1

Comprehensive translocation and clonality detection in lymphoproliferative disorders by next-generation sequencing.

Wren D, Walker BA, Brüggemann M, Catherwood MA, Pott C, Stamatopoulos K, Langerak AW, Gonzalez D; EuroClonality-NGS consortium. Wren D, et al. Haematologica. 2017 Feb;102(2):e57-e60. doi: 10.3324/haematol.2016.155424. Epub 2016 Oct 20. Haematologica. 2017. PMID: 27846615 Free PMC article. No abstract available.

2

CLLU1 expression has prognostic value in chronic lymphocytic leukemia after first-line therapy in younger patients and in those with mutated IGHV genes.

Gonzalez D, Else M, Wren D, Usai M, Buhl AM, Parker A, Oscier D, Morgan G, Catovsky D. Gonzalez D, et al. Among authors: wren d. Haematologica. 2013 Feb;98(2):274-8. doi: 10.3324/haematol.2012.070201. Epub 2012 Aug 16. Haematologica. 2013. PMID: 22899580 Free PMC article.

3

Angiomatoid fibrous histiocytoma: comparison of fluorescence in situ hybridization and reverse transcription polymerase chain reaction as adjunct diagnostic modalities.

Thway K, Gonzalez D, Wren D, Dainton M, Swansbury J, Fisher C. Thway K, et al. Among authors: wren d. Ann Diagn Pathol. 2015 Jun;19(3):137-42. doi: 10.1016/j.anndiagpath.2015.03.004. Epub 2015 Mar 14. Ann Diagn Pathol. 2015. PMID: 25804255

4

The comparative utility of fluorescence in situ hybridization and reverse transcription-polymerase chain reaction in the diagnosis of alveolar rhabdomyosarcoma.

Thway K, Wang J, Wren D, Dainton M, Gonzalez D, Swansbury J, Fisher C. Thway K, et al. Among authors: wren d. Virchows Arch. 2015 Aug;467(2):217-24. doi: 10.1007/s00428-015-1777-9. Epub 2015 Apr 26. Virchows Arch. 2015. PMID: 25912319

5

Ancillary molecular analysis in the diagnosis of soft tissue tumours: reassessment of its utility at a specialist centre.

Vroobel K, Gonzalez D, Wren D, Thompson L, Swansbury J, Fisher C, Thway K. Vroobel K, et al. Among authors: wren d. J Clin Pathol. 2016 Jun;69(6):505-10. doi: 10.1136/jclinpath-2015-203380. Epub 2015 Nov 19. J Clin Pathol. 2016. PMID: 26584594

6

Evaluation of the optimal provision of formalin-fixed, paraffin-embedded material for reverse transcription-PCR in soft-tissue tumour diagnosis.

Thway K, Wren D, Lee J, Thompson L, Fisher C, Gonzalez D. Thway K, et al. Among authors: wren d. J Clin Pathol. 2017 Jan;70(1):20-24. doi: 10.1136/jclinpath-2016-203691. Epub 2016 May 20. J Clin Pathol. 2017. PMID: 27207012

7

Desmoplastic small round cell tumor: evaluation of reverse transcription-polymerase chain reaction and fluorescence in situ hybridization as ancillary molecular diagnostic techniques.

Mohamed M, Gonzalez D, Fritchie KJ, Swansbury J, Wren D, Benson C, Jones RL, Fisher C, Thway K. Mohamed M, et al. Among authors: wren d. Virchows Arch. 2017 Nov;471(5):631-640. doi: 10.1007/s00428-017-2207-y. Epub 2017 Jul 26. Virchows Arch. 2017. PMID: 28748349

8

Validation of the EuroClonality-NGS DNA capture panel as an integrated genomic tool for lymphoproliferative disorders.

Stewart JP, Gazdova J, Darzentas N, Wren D, Proszek P, Fazio G, Songia S, Alcoceba M, Sarasquete ME, Villarese P, van der Klift MY, Heezen KC, McCafferty N, Pal K, Catherwood M, Kim CS, Srivastava S, Kroeze LI, Hodges E, Stamatopoulos K, Klapper W, Genuardi E, Ferrero S, van den Brand M, Cazzaniga G, Davi F, Sutton LA, Garcia-Sanz R, Groenen PJTA, Macintyre EA, Brüggemann M, Pott C, Langerak AW, Gonzalez D; EuroClonality-NGS Working Group. Stewart JP, et al. Among authors: wren d. Blood Adv. 2021 Aug 24;5(16):3188-3198. doi: 10.1182/bloodadvances.2020004056. Blood Adv. 2021. PMID: 34424321 Free PMC article.

9

TP53 Mutations Identified Using NGS Comprise the Overwhelming Majority of TP53 Disruptions in CLL: Results From a Multicentre Study.

Catherwood MA, Wren D, Chiecchio L, Cavalieri D, Donaldson D, Lawless S, ElHassadi E, Hayat A, Cahill MR, O'Shea D, Sargent J, Stewart P, Maurya M, Quinn J, Murphy P, de Castro DG, Mills K, Cross NCP, Forconi F, Iyengar S, Schuh A, Thornton P. Catherwood MA, et al. Among authors: wren d. Front Oncol. 2022 Jun 28;12:909615. doi: 10.3389/fonc.2022.909615. eCollection 2022. Front Oncol. 2022. PMID: 35837095 Free PMC article.

10

Extent of investigation and management of cases of 'unexplained' mismatch repair deficiency (u-dMMR): a UK Cancer Genetics Group consensus.

McVeigh TP, Monahan KJ, Christopher J, West N, Scott M, Murray J, Hanson H; UKCGG dMMR Consensus Meeting Attendees. McVeigh TP, et al. J Med Genet. 2024 Apr 6:jmg-2024-109886. doi: 10.1136/jmg-2024-109886. Online ahead of print. J Med Genet. 2024. PMID: 38531626 Free article.

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