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170 results

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Evaluation of Endobronchial Ultrasound-Guided Transbronchial Needle Aspiration (EBUS-TBNA) Samples from Advanced Non-Small Cell Lung Cancer for Whole Genome, Whole Exome and Comprehensive Panel Sequencing.
Fielding D, Lakis V, Dalley AJ, Chittoory H, Newell F, Koufariotis LT, Patch AM, Kazakoff S, Bashirzadeh F, Son JH, Ryan K, Steinfort D, Williamson JP, Bint M, Pahoff C, Nguyen PT, Twaddell S, Arnold D, Grainge C, Pattison A, Fairbairn D, Gune S, Christie J, Holmes O, Leonard C, Wood S, Pearson JV, Lakhani SR, Waddell N, Simpson PT, Nones K. Fielding D, et al. Among authors: fairbairn d. Cancers (Basel). 2024 Feb 15;16(4):785. doi: 10.3390/cancers16040785. Cancers (Basel). 2024. PMID: 38398180 Free PMC article.
Evaluating Diff-Quik cytology smears for large-panel mutation testing in lung cancer-Predicting DNA content and success with low-malignant-cellularity samples.
Fielding DI, Dalley AJ, Singh M, Nandakumar L, Lakis V, Chittoory H, Fairbairn D, Patch AM, Kazakoff SH, Ferguson K, Bashirzadeh F, Bint M, Pahoff C, Son JH, Hodgson A, Sharma S, Waddell N, Lakhani SR, Hartel G, Nones K, Simpson PT. Fielding DI, et al. Among authors: fairbairn d. Cancer Cytopathol. 2023 Jun;131(6):373-382. doi: 10.1002/cncy.22690. Epub 2023 Mar 20. Cancer Cytopathol. 2023. PMID: 36938641 Free article.
Whole Genome Sequencing in Advanced Lung Cancer can be Performed Using Diff-Quik Cytology Smears Derived from Endobronchial Ultrasound, Transbronchial Needle Aspiration (EBUS TBNA).
Fielding D, Dalley AJ, Singh M, Nandakumar L, Lakis V, Chittoory H, Fairbairn D, Ferguson K, Bashirzadeh F, Bint M, Pahoff C, Son JH, Hodgson A, Pearson JV, Waddell N, Lakhani SR, Hartel G, Nones K, Simpson PT. Fielding D, et al. Among authors: fairbairn d. Lung. 2023 Aug;201(4):407-413. doi: 10.1007/s00408-023-00631-9. Epub 2023 Jul 5. Lung. 2023. PMID: 37405466 Free PMC article.
Discrepancies in tumor mutation burden reporting from sequential endobronchial ultrasound transbronchial needle aspiration samples within single lymph node stations - brief report.
Fielding D, Dalley AJ, Singh M, Nandakumar L, Lakis V, Chittoory H, Fairbairn D, Patch AM, Kazakoff SH, Ferguson K, Bashirzadeh F, Bint M, Pahoff C, Son JH, Ryan K, Hodgson A, Sharma S, Pearson JV, Waddell N, Lakhani SR, Hartel G, Simpson PT, Nones K. Fielding D, et al. Among authors: fairbairn d. Front Oncol. 2023 Oct 19;13:1259882. doi: 10.3389/fonc.2023.1259882. eCollection 2023. Front Oncol. 2023. PMID: 37927461 Free PMC article.
Guidelines for genetic testing in prostate cancer: a scoping review.
Tuffaha H, Edmunds K, Fairbairn D, Roberts MJ, Chambers S, Smith DP, Horvath L, Arora S, Scuffham P. Tuffaha H, et al. Among authors: fairbairn d. Prostate Cancer Prostatic Dis. 2024 Dec;27(4):594-603. doi: 10.1038/s41391-023-00676-0. Epub 2023 May 18. Prostate Cancer Prostatic Dis. 2024. PMID: 37202470 Free PMC article. Review.
Demonstration of a novel Xp22.2 microdeletion as the cause of familial extreme skewing of X-inactivation utilizing case-parent trio SNP microarray analysis.
Mason JA, Aung HT, Nandini A, Woods RG, Fairbairn DJ, Rowell JA, Young D, Susman RD, Brown SA, Hyland VJ, Robertson JD. Mason JA, et al. Among authors: fairbairn dj. Mol Genet Genomic Med. 2018 May;6(3):357-369. doi: 10.1002/mgg3.378. Epub 2018 Feb 28. Mol Genet Genomic Med. 2018. PMID: 29490426 Free PMC article.
170 results