Hello! I'm Varsha, a researcher and medical writer based in Helsinki. I work at the intersection of genetics, genomics and cancer biology, using both experimental and evidence-synthesis approaches to understand how genetic variation shapes disease and treatment response. Alongside my lab and research work, I love translating complex science into clear, accessible writing for patients, clinicians and the wider public.
Learn more about meMy research centres on genetics, genomics and cancer biology. Most recently, I worked on cisplatin resistance in cervical cancer as a project researcher at the Cancer Institute (WIA), using cell-line models to identify genes and pathways linked to chemotherapy response. I have also worked on rare genetic conditions and the psychosocial impact of genomic medicine, including newborn genomic screening and migraine genetics.
Explore my preprints, ongoing projects and research experience below.
Preprint research on identifying genes and pathways associated with chemoresistance in cervical cancer cell lines.
Explore some of my recent contributions to the Klarity Health Library, where I write evidence‑based articles on genetics, rare diseases and health.
An overview of the growth challenges faced by individuals with PURA syndrome and why early intervention matters.
Discussing the unique challenges and opportunities for adults living with Fragile X Syndrome.
Breaking down the role of neutrophils and inflammation in this painful skin disorder.
Exploring the genetic underpinnings of Barakat syndrome and its multi‑system impacts.
I also like to share reflections, ideas and research summaries on my personal blog. Here are some recent posts:
How I talk to friends when they ask me for help translating medicine.
Curious about my full background? You can download a PDF version of my complete CV directly.
Download CV