Impact Case Study | June 18, 2018

The fourth culprit for Larsen Syndrome

Saudi scientists identify a new gene implicated in the complex musculo-skeletal and eye condition known as Larsen syndrome.

Impact Case Study | September 12, 2018

Uncovering autism genetics in Arabs

Saudi Human Genome Project discovers mutations linked to autism in Saudi families.

Impact Case Study | September 20, 2018

Uncovering the elusive causes of fetal death

Molecular autopsy reveals gene variants not previously associated with pregnancy loss and diseases. 

Impact Case Study | February 26, 2019

Unlocking the origin of a severe neurological disorder

Gene sequencing brings the origin of a fatal neurological genetic disease to light.

Impact Case Study | April 17, 2019

Genetic study uncovers Ehlers-Danlos syndrome mutation

Scientists find links between a rare connective tissue disorder and mutations in a wound-healing gene called AEBP1.