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Globally Rare BRCA2 Variants With Founder Haplotypes in the South African Population: Implications for Point-of-Care Testing Based on a Single-Institution BRCA1/2 Next-Generation Sequencing Study.
Oosthuizen J, Kotze MJ, Van Der Merwe N, Myburgh EJ, Bester P, van der Merwe NC. Oosthuizen J, et al. Among authors: van der merwe nc. Front Oncol. 2021 Feb 12;10:619469. doi: 10.3389/fonc.2020.619469. eCollection 2020. Front Oncol. 2021. PMID: 33643918 Free PMC article.
Pioneering BRCA1/2 Point-Of-Care Testing for Integration of Germline and Tumor Genetics in Breast Cancer Risk Management: A Vision for the Future of Translational Pharmacogenomics.
Mampunye L, van der Merwe NC, Grant KA, Peeters AV, Torrorey-Sawe R, French DJ, Moremi KE, Kidd M, van Eeden PC, Pienaar FM, Kotze MJ. Mampunye L, et al. Among authors: van der merwe nc. Front Oncol. 2021 Sep 29;11:619817. doi: 10.3389/fonc.2021.619817. eCollection 2021. Front Oncol. 2021. PMID: 34660253 Free PMC article.
Pathology-supported genetic testing for the application of breast cancer pharmacodiagnostics: family counselling, lifestyle adjustments and change of medication.
Okunola AO, Baatjes KJ, Zemlin AE, Torrorey-Sawe R, Conradie M, Kidd M, Erasmus RT, van der Merwe NC, Kotze MJ. Okunola AO, et al. Among authors: van der merwe nc. Expert Rev Mol Diagn. 2023 May;23(5):431-443. doi: 10.1080/14737159.2023.2203815. Epub 2023 Apr 20. Expert Rev Mol Diagn. 2023. PMID: 37060281
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