People often remark that allergies run in their family, but the genetic causes have remained unclear. Previous food allergy ...

A 10-year study shows that a multipronged approach using whole exome sequencing can improve diagnostic yield in patients with ...

Expecting Growth in 2026 Families are not just receiving results - they are gaining the confidence and capability to ...

In India, rare diseases are not so rare. It is estimated that around 70 million Indians live with one of more than 7,000 rare ...

SickKids is providing the C-GUIDE™ tool evaluation of iHope's genomic testing for the diagnosis, care, and well-being ...

Integration of HiFi Long-Read Whole-Genome Sequencing Expands the Collective Capabilities of iHope’s Global Rare Disease ...

Segun Fatumo discusses how he is working towards a true global genomics framework and strengthening African research capacity ...

Hypermobile Ehlers–Danlos syndrome (hEDS) is one of the most common heritable connective tissue disorders. Early estimates have reported that this genetic disorder affects at least one in 5,000 ...

A new study links telomere length genetics to IPF risk, showing how rare variants and polygenic scores may guide future screening and precision care.

By Tarun Sai Lomte A new AI-driven diagnostic framework combines clinical, genetic, and phenotypic data to help shorten the ...