The human genome is a rich, complex record of migration, encounters, and inheritance written over thousands of millennia.

The human genome is a rich, complex record of migration, encounters, and inheritance written over thousands of millennia.

Geneticists have a better understanding of how prehistoric pairings unfolded, with new research suggesting they were mostly between male Neanderthals and female humans.

“From Brown to Evergreen: How Eye Colors Evolved” Your eyes may seem ordinary when you catch your reflection each morn ...

A rare inherited disorder affecting brain development and muscle strength has been officially named after an Abu Dhabi-based specialist at Burjeel Medical City, marking a significant scientific ...

For more than a century, Mendelian genetics has shaped how we think about inheritance: one gene, one trait. It is a model that still echoes through textbooks—and one that is increasingly reaching its ...

Background Monogenic disorders are a major cause of fetal structural anomalies. Most genetic diagnoses involve de novo, biallelic or X linked variants; however, inherited variants in autosomal ...

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 ...

Ninety-nine pediatric patients with DD or ID underwent CMA or WES. Of these, 82 received SNP array analysis, while 17 had WES. CNV pathogenicity was assessed using established databases and ACMG ...