Benjamin H Mullin
Dr Benjamin Mullin is a Research Fellow and Bioinformatician with the University of Western Australia. 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. This resource has successfully been used to identify multiple GWAS effector genes for osteoporosis, osteoarthritis and Paget’s disease of bone.
Abstracts this author is presenting: