Dr. Lindiwe Lamola

Lindiwe Lamola is a South African researcher specializing in medical genetics and molecular oncology, with a focus on paediatric cancers in underrepresented populations. Her work centers on the application of next-generation sequencing technologies to uncover germline variants associated with inherited cancer predisposition. Through collaborations reflected in peer-reviewed clinical and oncology journals, she contributes to advancing genomic medicine within the African context.

Her research explores mutation profiling in paediatric solid tumours, emphasizing candidate gene panels tailored to inherited cancer syndromes. A notable contribution includes the identification of novel pathogenic variants in South African children, highlighting the genetic diversity of understudied populations. She has also reported the first documented African case of Takenouchi–Kosaki syndrome, expanding global understanding of rare genetic disorders.

Based on the limited publications currently available, her scholarly work demonstrates strengths in clinical genomics, variant interpretation, and translational research. Her contributions support improved diagnostic precision and promote equitable representation of African patients in genetic research.