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This blog explains how twin and family studies help researchers understand the role of genetics and environment in health and disease. It explores shared DNA, epigenetics, and why twins are especially valuable for studying complex conditions such as Parkinson’s disease and Alzheimer’s disease.

Learn how DNA is collected for research, from swabs to blood samples, why it matters for genetics and medicine, and the ethical rules that protect your data.

What would anyone want?

A participant’s take on the CCBP

Key points to understanding a new interpretation of an old hypothesis.

Unlocking the potential of 21st century genetics

Where does one begin and the other end?

How can we change what we cannot measure?