Exome Sequencing in a Family with Luminal-Type Breast Cancer Underpinned by Variation in the Methylation Pathway

by Nicole van der Merwe, Armand V. Peeters, Fredrieka M. Pienaar, Juanita Bezuidenhout, Susan J. van Rensburg, Maritha J. Kotze
Published 2017-02-01

Identification of an iron-responsive subtype in two children diagnosed with relapsing-remitting multiple sclerosis using whole exome sequencing

by Susan J. van Rensburg, Armand V. Peeters, Ronald van Toorn, Johan Schoeman, Kelebogile E. Moremi, Carel J. van Heerden, Maritha J. Kotze
Published 2019-06-01

A 3-basepair deletion in repeat 1 of the LDL receptor promoter reduces transcriptional activity in a South African Pedi

by Armand V. Peeters, Maritha J. Kotze, Charlotte L. Scholtz, Linda F. De Waal, David C. Rubinsztein, Gerhard A. Coetzee, Giovanni Zuliani, Raphael Streiff, Jingwen Liu, Deneys R. van der Westhuyzen
Published 1998-05-01

Human whole genome sequencing in South Africa

by Brigitte Glanzmann, Tracey Jooste, Samira Ghoor, Richard Gordon, Rizwana Mia, Jun Mao, Hao Li, Patrick Charls, Craig Douman, Maritha J. Kotze, Armand V. Peeters, Glaudina Loots, Monika Esser, Caroline T. Tiemessen, Robert J. Wilkinson, Johan Louw, Glenda Gray, Robin M. Warren, Marlo Möller, Craig Kinnear
Published 2021-01-01

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

by Lwando Mampunye, Lwando Mampunye, Nerina C. van der Merwe, Nerina C. van der Merwe, Kathleen A. Grant, Armand V. Peeters, Rispah Torrorey-Sawe, Rispah Torrorey-Sawe, David J. French, Kelebogile E. Moremi, Martin Kidd, Petrus C. van Eeden, Fredrieka M. Pienaar, Maritha J. Kotze, Maritha J. Kotze
Published 2021-09-01