Summary
Stephan Sanders is a genomic medicine leader with eight years of experience translating high-throughput sequencing and bioinformatics into discoveries about childhood neurodevelopmental disorders. He holds a PhD in Genetics from Yale and combines academic leadership as Professor of Paediatric Neurogenetics at Oxford with directorship of the MRC CoRE Therapeutic Genomics program and ongoing faculty roles at UCSF. His work spans genome sequencing, copy number and microarray analysis to elucidate autism risk, sex bias, and heritability, and he has a track record of building research programs that move from variant discovery to clinical insight. Trained as a clinician and expedition doctor, he brings rare operational experience in pediatrics and high-altitude medicine that informs pragmatic, field-ready approaches to complex genetics problems.
8 years of coding experience
4 years of employment as a software developer
Medicine, Medicine, Medicine, Medicine at University of Nottingham
PhD, Genetics, PhD, Genetics at Yale University
Diploma in Mountain Medicine, Expedition Medicine, Diploma in Mountain Medicine, Expedition Medicine at University of Leeds