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Genomics week in brief: Week ending 8th July

Check out the latest Genomics Week in Brief – full of intriguing news and research from the genomics space! Top […]

A Spotlight On: Genomics in Qatar – Said Ismail, Director of Qatar Genome

Said Ismail is the Director of Qatar Genome, a national programme trying to spearhead Qatar’s vision to become a pioneer […]

World of Genomics: Lithuania

Sometimes referred to as the Land of Nature, for this week’s World of Genomics we head over to Lithuania. Over […]

A Spotlight On: Polygenic Embryo Screening – Dr. Todd Lencz, Professor at the Feinstein Institutes for Medical Research

Dr Todd Lencz is a Professor at the Feinstein Institutes for Medical Research in Manhasset, New York. Lencz’s team were […]

Multi-omics: Exploring Inside Cells

Introduction Multi-omics is an emerging field. ‘Omics’ refers to the comprehensive collection of a set of biological molecules. Essentially, the […]

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 […]

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 […]

Researchers have generated the first complete model of the human embryo

Two research groups have now generated human blastocyst-like structures from cells in a dish. This valuable model provides hope of […]

Rare VEXAS syndrome is more common than originally thought

Researchers at the University of Leeds have found that a rare disease first discovered in 2020 – VEXAS syndrome – […]

The Rarest of the Rare

In Europe, a rare disease is defined rare when it affects fewer than 1 in 2,000 people. However, this definition […]