Benjamin H Mullin
Dr Mullin is a postdoctoral genetic scientist with experience in both diagnostic and research settings. His research interests include the genetics of complex disease, particularly osteoporosis and polycystic ovary syndrome (PCOS). He has worked on several genome-wide association studies and recently played a leading role in the generation of a unique osteoclast-specific expression quantitative trait locus (eQTL) resource for study of the genetics of bone disease.
Abstracts this author is presenting: