Ong PY - Search Results

1

Whole-exome sequencing of BRCA-negative breast cancer patients and case-control analyses identify variants associated with breast cancer susceptibility.

Lee NY, Hum M, Amali AA, Lim WK, Wong M, Myint MK, Tay RJ, Ong PY, Samol J, Lim CW, Ang P, Tan MH, Lee SC, Lee ASG. Lee NY, et al. Among authors: ong py. Hum Genomics. 2022 Nov 23;16(1):61. doi: 10.1186/s40246-022-00435-7. Hum Genomics. 2022. PMID: 36424660 Free PMC article.

2

Clinical genetic testing outcome with multi-gene panel in Asian patients with multiple primary cancers.

Chan GHJ, Ong PY, Low JJH, Kong HL, Ow SGW, Tan DSP, Lim YW, Lim SE, Lee SC. Chan GHJ, et al. Among authors: ong py. Oncotarget. 2018 Jul 17;9(55):30649-30660. doi: 10.18632/oncotarget.25769. eCollection 2018 Jul 17. Oncotarget. 2018. PMID: 30093976 Free PMC article.

3

Discoveries beyond BRCA1/2: Multigene testing in an Asian multi-ethnic cohort suspected of hereditary breast cancer syndrome in the real world.

Ow SGW, Ong PY, Lee SC. Ow SGW, et al. Among authors: ong py. PLoS One. 2019 Mar 15;14(3):e0213746. doi: 10.1371/journal.pone.0213746. eCollection 2019. PLoS One. 2019. PMID: 30875412 Free PMC article.

4

Next Generation Sequencing Reveals Novel Mutations in Mismatch Repair Genes and Other Cancer Predisposition Genes in Asian Patients with Suspected Lynch Syndrome.

Ow SGW, Tan KT, Yang H, Yap HL, Sapari NSB, Ong PY, Soong R, Lee SC. Ow SGW, et al. Among authors: ong py. Clin Colorectal Cancer. 2019 Dec;18(4):e324-e334. doi: 10.1016/j.clcc.2019.05.007. Epub 2019 Jun 7. Clin Colorectal Cancer. 2019. PMID: 31350202

5

Using next-generation sequencing (NGS) platform to diagnose pathogenic germline BRCA1/2 mutations from archival tumor specimens.

Ong PY, Poon SL, Tan KT, Putti TC, Ow SGW, Chen SJ, Chen CH, Lee SC. Ong PY, et al. Gynecol Oncol. 2019 Nov;155(2):275-279. doi: 10.1016/j.ygyno.2019.08.027. Epub 2019 Aug 31. Gynecol Oncol. 2019. PMID: 31481248

6

Characteristics and genetic testing outcomes of patients with clinically suspected paraganglioma/pheochromocytoma (PGL/PCC) syndrome in Singapore.

Ting KR, Ong PY, Wei SOG, Parameswaran R, Khoo CM, Deepak DS, Lee SC. Ting KR, et al. Among authors: ong py. Hered Cancer Clin Pract. 2020 Dec 11;18(1):24. doi: 10.1186/s13053-020-00156-9. Hered Cancer Clin Pract. 2020. PMID: 33308260 Free PMC article.

7

Clinical characteristics and genetic testing outcome of suspected hereditary peripheral nerve sheath tumours in a tertiary cancer institution in Singapore.

Loh J, Ong PY, Goh DLM, Puhaindran ME, Vellayappan BA, Ow SGW, Chan G, Lee SC. Loh J, et al. Among authors: ong py. Hered Cancer Clin Pract. 2022 Jun 13;20(1):23. doi: 10.1186/s13053-022-00230-4. Hered Cancer Clin Pract. 2022. PMID: 35698239 Free PMC article.

8

Germline Variants Associated with Nasopharyngeal Carcinoma Predisposition Identified through Whole-Exome Sequencing.

Lee NY, Hum M, Ong PY, Myint MK, Ong EHW, Low KP, Li Z, Goh BC, Tay JK, Loh KS, Chua MLK, Lee SC, Khor CC, Lee ASG. Lee NY, et al. Among authors: ong py, ong ehw. Cancers (Basel). 2022 Jul 28;14(15):3680. doi: 10.3390/cancers14153680. Cancers (Basel). 2022. PMID: 35954343 Free PMC article.

9

Correction: Whole-exome sequencing of BRCA-negative breast cancer patients and case-control analyses identify variants associated with breast cancer susceptibility.

Lee NY, Hum M, Amali AA, Lim WK, Wong M, Myint MK, Tay RJ, Ong PY, Samol J, Lim CW, Ang P, Tan MH, Lee SC, Lee ASG. Lee NY, et al. Among authors: ong py. Hum Genomics. 2022 Dec 19;16(1):68. doi: 10.1186/s40246-022-00443-7. Hum Genomics. 2022. PMID: 36536425 Free PMC article. No abstract available.

10

Alleviating misclassified germline variants in underrepresented populations: A strategy using popmax.

Lee NY, Hum M, Wong M, Ong PY, Lee SC, Lee ASG. Lee NY, et al. Among authors: ong py. Genet Med. 2024 Jun;26(6):101124. doi: 10.1016/j.gim.2024.101124. Epub 2024 Mar 21. Genet Med. 2024. PMID: 38522067 Free article.

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