Mariam Mathew

Mariam Mathew's work focuses on identifying and characterizing genetic causes of rare and inherited diseases, including hereditary cancer syndromes and neurodevelopmental disorders. Her research often involves detailed case studies that link specific gene variants to disease features, contributing to the broader understanding of how genetic mutations lead to conditions like kidney cancer syndromes and developmental disorders. This work is typically done in collaboration with a small, consistent group of co-authors.

Publication activity began around 2020 and has remained steady to slightly increasing since then, averaging about 3 papers per year over the last five years.

Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026