Shaw T - Search Results

1

Early-onset breast cancer in a woman with a germline mobile element insertion resulting in BRCA2 disruption: a case report.

Deuitch N, Li ST, Courtney E, Shaw T, Dent R, Tan V, Yackowski L, Torene R, Berkofsky-Fessler W, Ngeow J. Deuitch N, et al. Among authors: shaw t. Hum Genome Var. 2020 Aug 25;7:24. doi: 10.1038/s41439-020-00111-z. eCollection 2020. Hum Genome Var. 2020. PMID: 32884827 Free PMC article.

2

Evaluation of the relative effectiveness of the 2017 updated Manchester scoring system for predicting BRCA1/2 mutations in a Southeast Asian country.

Chew W, Moorakonda RB, Courtney E, Soh H, Li ST, Chen Y, Shaw T, Allen JC, Evans DGR, Ngeow J. Chew W, et al. Among authors: shaw t. J Med Genet. 2018 May;55(5):344-350. doi: 10.1136/jmedgenet-2017-105073. Epub 2017 Dec 23. J Med Genet. 2018. PMID: 29275357

3

Predictors of next-generation sequencing panel selection using a shared decision-making approach.

Courtney E, Li ST, Shaw T, Chen Y, Allen JC Jr, Ngeow J. Courtney E, et al. Among authors: shaw t. NPJ Genom Med. 2018 Apr 27;3:11. doi: 10.1038/s41525-018-0050-y. eCollection 2018. NPJ Genom Med. 2018. PMID: 29736259 Free PMC article.

4

Impact of Appointment Waiting Time on Attendance Rates at a Clinical Cancer Genetics Service.

Shaw T, Metras J, Ting ZAL, Courtney E, Li ST, Ngeow J. Shaw T, et al. J Genet Couns. 2018 Dec;27(6):1473-1481. doi: 10.1007/s10897-018-0259-z. Epub 2018 May 24. J Genet Couns. 2018. PMID: 29799102

5

The influence of Malay cultural beliefs on breast cancer screening and genetic testing: A focus group study.

Shaw T, Ishak D, Lie D, Menon S, Courtney E, Li ST, Ngeow J. Shaw T, et al. Psychooncology. 2018 Dec;27(12):2855-2861. doi: 10.1002/pon.4902. Epub 2018 Oct 16. Psychooncology. 2018. PMID: 30264524 Review.

6

Clinical relevance of screening checklists for detecting cancer predisposition syndromes in Asian childhood tumours.

Chan SH, Chew W, Ishak NDB, Lim WK, Li ST, Tan SH, Teo JX, Shaw T, Chang K, Chen Y, Iyer P, Tan EEK, Seng MS, Chan MY, Tan AM, Low SYY, Soh SY, Loh AHP, Ngeow J. Chan SH, et al. Among authors: shaw t. NPJ Genom Med. 2018 Nov 15;3:30. doi: 10.1038/s41525-018-0070-7. eCollection 2018. NPJ Genom Med. 2018. PMID: 30455982 Free PMC article.

7

Impact of free cancer predisposition cascade genetic testing on uptake in Singapore.

Courtney E, Chok AK, Ting Ang ZL, Shaw T, Li ST, Yuen J, Ngeow J. Courtney E, et al. Among authors: shaw t. NPJ Genom Med. 2019 Sep 13;4:22. doi: 10.1038/s41525-019-0096-5. eCollection 2019. NPJ Genom Med. 2019. PMID: 31531230 Free PMC article.

8

Use of telephone intake for family history taking at a cancer genetics service in Asia.

Chin XW, Ang ZLT, Tan RYC, Courtney E, Shaw T, Chen Y, Li ST, Ngeow JYY. Chin XW, et al. Among authors: shaw t. J Genet Couns. 2020 Dec;29(6):1192-1199. doi: 10.1002/jgc4.1286. Epub 2020 May 5. J Genet Couns. 2020. PMID: 32368849

9

Biallelic NF1 inactivation in high grade serous ovarian cancers from patients with neurofibromatosis type 1.

Courtney E, Chan SH, Li ST, Ishak D, Merchant K, Shaw T, Chay WY, Chin FHX, Wong WL, Wong A, Ngeow J. Courtney E, et al. Among authors: shaw t. Fam Cancer. 2020 Oct;19(4):353-358. doi: 10.1007/s10689-020-00184-3. Fam Cancer. 2020. PMID: 32405727

10

Investigation into the origins of an ancient BRCA1 founder mutation identified among Chinese families in Singapore.

Shaw T, Chan SH, Teo JX, Chong ST, Li ST, Courtney E, Ishak D, Sankar H, Ang ZLT, Chiang J, Loh M, Zhou L, Lee SC, Yeh HY, Kolinjivadi AM, Lim WK, Ngeow J. Shaw T, et al. Int J Cancer. 2021 Feb 1;148(3):637-645. doi: 10.1002/ijc.33241. Epub 2020 Aug 21. Int J Cancer. 2021. PMID: 32745242

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