Science inspired by life: An interview with Dennis Lo#
Professor Dennis Lo MAE reflects on the discovery of cell-free fetal DNA, the global impact of non-invasive prenatal testing, and how everyday inspiration drives advances in diagnostic medicine.
About Dennis Lo MAE#
Professor Dennis Lo MAE is a world‑renowned molecular biologist, celebrated as the “Father of Non‑Invasive Prenatal Testing.” In 1997, he discovered cell‑free fetal DNA in maternal blood- a breakthrough sparked by watching instant noodles cook, which led him to extract fetal DNA from plasma and revolutionise prenatal diagnostics for Down syndrome, with over 100 million tests being utilised globally in more than 100 countries.
Since January 2025, he has served as the 9th Vice‑Chancellor and President of The Chinese University of Hong Kong
(CUHK), where he champions a holistic, interdisciplinary education rooted in both the sciences and the humanities. He is also the Li Ka Shing Professor of Medicine at CUHK and currently serves as President of the Hong Kong Academy of Sciences
.
His pioneering work has been honoured with prestigious awards, including the Future Science Prize in Life Science (2016), Breakthrough Prize in Life Sciences (2021), Lasker–DeBakey Clinical Medical Research Award (2022), and the Jiménez Díaz Lecture Award (2024). He is a founding Member of the Hong Kong Academy of Sciences, a Fellow of the Royal Society
, a Member of the Chinese Academy of Sciences
, an International Member of the US National Academy of Sciences
and was elected to Academia Europaea in 2025.
Professor Lo will deliver a plenary lecture at Academia Europaea’s Building Bridges 2025 conference in Barcelona. His presentation, Non‑invasive prenatal testing and cancer detection: From dream to reality will explore how prenatal diagnostics are now guiding groundbreaking approaches in cancer screening.
Read the interview#
Your discovery of cell‑free fetal DNA in maternal blood revolutionised prenatal care. How has this insight transformed how we understand pregnancy and prenatal testing overall?
That’s the biological foundation. On the diagnostic side, it means we can take a simple blood sample from the mother and gain a wealth of information about the baby, starting with chromosomal abnormalities. We can go further to identify individual gene mutations and even sequence the entire genome of the fetus. And beyond DNA, we can now examine RNA, giving us insights into the baby’s gene expression profile.”
Non-invasive prenatal testing is now available in over 100 countries. What do you see as the global social impact of making this technology so widely accessible?
All this changed with non-invasive prenatal testing, which lets us gather that information as early as 10 weeks in a non-invasive way. It’s more accessible and reduces anxiety for expecting parents. Its implementation in numerous countries gives expectant families worldwide safer, earlier access to important genetic information.”
As a plenary speaker at Building Bridges 2025, how do you see collaboration across biology, engineering, ethics, and other disciplines shaping the future of diagnostic medicine?
Increasingly, the devices used in diagnostics generate large volumes of data- what we often refer to as big data. To handle and interpret that data, we need data scientists, computer scientists, and people with expertise in artificial intelligence.
Finally, the development and use of technology must also consider broader societal, legal, and ethical dimensions. That is why it’s important to engage ethicists, legal experts, and review bodies to assess the ethics and desirability of introducing new technologies.”
Looking ahead, what frontier excites you most in the future of cell‑free DNA? Beyond prenatal and cancer testing, where do you think its potential lies?
Another key area is other chronic disorders, such as neurological conditions like Alzheimer’s and strokes. Cardiovascular diseases also pose a significant concern. This raises the question: could liquid biopsy analysis be applied to these conditions as well?
In some chronic cases, treatment may involve transplantation. I discovered that after an organ transplant, DNA from the transplanted organ enters the recipient’s bloodstream. By measuring this donor-derived DNA, we can detect signs of organ rejection, because elevated levels indicate that the body is rejecting the graft. This provides a non-invasive way to monitor transplant health.
Finally, we can apply liquid biopsy to infectious diseases. We can detect microbial DNA (whether from bacteria or viruses) in the blood and derive useful health insights from it.”
Your breakthroughs have come from unexpected moments. For example, the way instant noodles separated while cooking led you to wonder whether fetal DNA might be hidden in plasma. Could you share another moment from daily life that inspired you?
, resulting in a potential test for cancer detection.
.For further information please contact AECardiffHub@cardiff.ac.uk
.



