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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 […]

The potential of Middle Eastern Genomics

New findings in Middle Eastern genomics show huge promise towards further understanding the human genome.  The Middle East is a […]

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 […]

A Spotlight On: Science Communication – Jonathan Roberts

Jonathan Roberts is a Registered Genetic Counsellor at Addenbrooke’s Hospital in Cambridge and a Researcher at the Society and Ethics […]

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 […]

Genome Giants – Janet Thornton – Senior Scientist and Director Emeritus at EBI

Dame Janet Thornton is a Senior Scientist and Emeritus Director of EMBL-EBI. Thornton is a pioneer in structural bioinformatics, having […]

World of Genomics: Canada

For the latest in the World of Genomics series, we head over to the Great White North and home of […]

No, testosterone does not determine your chances of success

With genetic causal inference methods, researchers showed that testosterone does not affect socioeconomic status or health in men, countering prior […]

Considerations for starting a FAIR data library

The FAIR principles have been defined to enable data producers and publishers to make their data findable, accessible, interoperable and […]