Clancy T - Search Results

1

Informed consent for whole genome sequencing in mainstream clinics: logistical constraints and possible solutions.

Chaouch A, Ulph F, Alder J, Hamdalla H, Ealing J, Clancy T, Macleod R, Clarke AJ. Chaouch A, et al. Among authors: clancy t. Eur J Hum Genet. 2024 Mar;32(3):260-262. doi: 10.1038/s41431-023-01520-8. Epub 2024 Jan 4. Eur J Hum Genet. 2024. PMID: 38177407 Free PMC article. No abstract available.

2

Exploring the role of Islam on the lived experience of patients with Long QT Syndrome in Saudi Arabia.

Bakur KH, Al-Aama JY, Alhassnan ZN, Brooks H, Clancy T, Manea W, Takroni SA, Ulph F. Bakur KH, et al. Among authors: clancy t. J Genet Couns. 2022 Aug;31(4):922-936. doi: 10.1002/jgc4.1562. Epub 2022 Feb 22. J Genet Couns. 2022. PMID: 35194886

3

Uptake of risk-reducing salpingo-oophorectomy in women carrying a BRCA1 or BRCA2 mutation: evidence for lower uptake in women affected by breast cancer and older women.

Sidon L, Ingham S, Clancy T, Clayton R, Clarke A, Jones EA, Lalloo F, Evans DG. Sidon L, et al. Among authors: clancy t. Br J Cancer. 2012 Feb 14;106(4):775-9. doi: 10.1038/bjc.2011.573. Epub 2011 Dec 20. Br J Cancer. 2012. PMID: 22187038 Free PMC article.

4

30 year experience of index case identification and outcomes of cascade testing in high-risk breast and colorectal cancer predisposition genes.

Woodward ER, Green K, Burghel GJ, Bulman M, Clancy T, Lalloo F, Schlecht H, Wallace AJ, Evans DG. Woodward ER, et al. Among authors: clancy t. Eur J Hum Genet. 2022 Apr;30(4):413-419. doi: 10.1038/s41431-021-01011-8. Epub 2021 Dec 6. Eur J Hum Genet. 2022. PMID: 34866136 Free PMC article.

5

Mainstreaming germline BRCA1/2 testing in non-mucinous epithelial ovarian cancer in the North West of England.

Flaum N, Morgan RD, Burghel GJ, Bulman M, Clamp AR, Hasan J, Mitchell CL, Badea D, Moon S, Hogg M, Hadjiyiannakis D, Clancy T, Schlecht H, Woodward ER, Crosbie EJ, Edmondson RJ, Wallace AJ, Jayson GC, Lalloo FI, Harkness EF, Evans DGR. Flaum N, et al. Among authors: clancy t. Eur J Hum Genet. 2020 Nov;28(11):1541-1547. doi: 10.1038/s41431-020-0692-y. Epub 2020 Jul 10. Eur J Hum Genet. 2020. PMID: 32651552 Free PMC article.

6

Assessment of mismatch repair deficiency in ovarian cancer.

Crosbie EJ, Ryan NAJ, McVey RJ, Lalloo F, Bowers N, Green K, Woodward ER, Clancy T, Bolton J, Wallace AJ, McMahon RF, Evans DG. Crosbie EJ, et al. Among authors: clancy t. J Med Genet. 2021 Oct;58(10):687-691. doi: 10.1136/jmedgenet-2020-107270. Epub 2020 Sep 11. J Med Genet. 2021. PMID: 32917768 Free PMC article.

7

Severe Gardner syndrome in families with mutations restricted to a specific region of the APC gene.

Davies DR, Armstrong JG, Thakker N, Horner K, Guy SP, Clancy T, Sloan P, Blair V, Dodd C, Warnes TW, et al. Davies DR, et al. Among authors: clancy t. Am J Hum Genet. 1995 Nov;57(5):1151-8. Am J Hum Genet. 1995. PMID: 7485167 Free PMC article.

8

Lynch syndrome caused by MLH1 mutations is associated with an increased risk of breast cancer: a cohort study.

Harkness EF, Barrow E, Newton K, Green K, Clancy T, Lalloo F, Hill J, Evans DG. Harkness EF, et al. Among authors: clancy t. J Med Genet. 2015 Aug;52(8):553-6. doi: 10.1136/jmedgenet-2015-103216. Epub 2015 Jun 22. J Med Genet. 2015. PMID: 26101330

9

Advances in genetic technologies result in improved diagnosis of mismatch repair deficiency in colorectal and endometrial cancers.

Evans DG, Lalloo F, Ryan NA, Bowers N, Green K, Woodward ER, Clancy T, Bolton J, McVey RJ, Wallace AJ, Newton K, Hill J, McMahon R, Crosbie EJ. Evans DG, et al. Among authors: clancy t. J Med Genet. 2022 Apr;59(4):328-334. doi: 10.1136/jmedgenet-2020-107542. Epub 2021 Jan 15. J Med Genet. 2022. PMID: 33452216 Free PMC article.

10

Pathology update to the Manchester Scoring System based on testing in over 4000 families.

Evans DG, Harkness EF, Plaskocinska I, Wallace AJ, Clancy T, Woodward ER, Howell TA, Tischkowitz M, Lalloo F. Evans DG, et al. Among authors: clancy t. J Med Genet. 2017 Oct;54(10):674-681. doi: 10.1136/jmedgenet-2017-104584. Epub 2017 May 10. J Med Genet. 2017. PMID: 28490612

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