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Genetics Unzipped podcast: Back to the beginning – exploring the origins of life

In the latest episode of Genetics Unzipped, presenter Dr Kat Arney takes a trip back in a virtual time machine, […]

Patient Perspectives: Vaila Morrison – Architect, Mother and Rare Disease Advocate (KAT6A syndrome)

Vaila Morrison is an architect focused on sustainable and inclusive design as well as a mother to a child with […]

Patient Perspectives: Maddie Stoodley – Gaucher’s Association Ambassador and UK Board Member

Maddie Stoodley is a rare disease patient and Gaucher’s Association Ambassador and UK board member. Stoodley was diagnosed at 16 […]

Patient Perspectives: Jared Griffin – Founder and CEO, Annabelle’s Challenge

Jared Griffin is the Founder and CEO of Anabelle’s Challenge, the UK’s leading charity for Vascular Ehlers-Danlos Syndrome (EDS). In […]

Patient Perspectives: Nina Knight – Mother, Advocate and Chair of Acrodysostosis Support & Research

Nina Knight is a mother, advocate and Chair of the Acrodysostosis Support & Research Charity. Knight’s daughter, Lily, was diagnosed […]

A Spotlight On: Gene Therapy – Carolyn Chapman

Carolyn Riley Chapman is a Bioethicist and Faculty Affiliate with the Division of Medical Ethics at NYU Grossman School of […]

Down the Rabbit Hole: Genetics and Obesity – Giles Yeo

Giles Yeo is a Principal Research Associate at MRC Metabolic Diseases Unit and the Scientific Director of the Genomics/Transcriptomics Core […]

World of Genomics: The United Kingdom

Being a UK based company in the genomics field, we know the space here better than in any other country […]

Precision medicine in early life may improve adult health outcomes

Researchers have shown that optimising early life nutrition can reduce the risk of adult cardiometabolic disease in genetically predisposed infants, […]

Parental genome unification is error-prone

A new study has found that the process of combining maternal and paternal genetic information is surprisingly highly error-prone. Parental […]