A full time NHS consultant and paediatric clinical geneticist, Dr Shehla Mohammed has 24 years’ experience predominantly in rare genetic disorders and the care of children and families with life-limiting disorders. Until 2017, Shehla had been Head of Service of the Guy’s Regional Genetics Service for 20 years. She represents the genetics speciality on local, regional and national committees working on national policy developments and research.
Shehla has expertise in paediatric dysmorphology and DNA repair disorders and a special interest in translational research, the implementation of robust technology platforms and their rapid translation to deliver patient-focused, integrated genetics services
As an associate of the PHG Foundation, Dr Shehla Mohammed is contributing her clinical genetics and genomic medicine expertise to our work.
