Dr Stojanov has over 26 years of experience in diverse aspects of the health, biotechnology and agriculture sectors from the perspective of scientific research, operational management and technology commercialization.
Dr Schmidt has over 15 years of R&D and technology commercialization experience in cell biology, stem cells, drug discovery and screening. He co-authored over 20 peer-reviewed scientific publications and is an inventor of 10 patent/application families. Dr Schmidt is now an executive of Genea Limited and as General Manager of Genea Biocells shapes the company’s scientific direction and business strategy. Prior to joining Genea in 2007, he founded a company for novel GPCR drug screening technologies and was the scientific founder of a European diagnostics/drug delivery company.
Dr Arjomand has 13 years of pharmaceutical and biotechnology experience and co-authored 8 scientific publications. He joined Genea Biocells in 2013 and established a pipeline of leads for contract research services and successfully set up multiple strategic partnerships to facilitate Genea Biocells’ long term goals. Previously, Dr Arjomand was the Director of Basic Research at High Q Foundation/CHDI Management (USA) a not-for-profit foundation dedicated to Huntington’s disease (HD) therapeutics. He designed and managed a complex portfolio comprising of academic, clinical and industry driven projects in support of Foundation drug discovery efforts.
Dr Kiselyov has over 20 years of Pharma/Biotech and Foundation experience in drug discovery and preclinical development. He oversees all chemistry aspects of Genea Biocells’ drug discovery program as well as chemical genomics, biophysics, structural biology, target ID/validation and systems biology relevant to pluripotency, differentiation and proliferation of stem cells. Previously, Dr Kiselyov has authored and directly contributed to over 10 clinical programs across multiple therapeutic areas including oncology (Motesanib™ for the treatment of renal carcinoma, Phase III), cardiovascular disease (Veliflapon™ for the treatment of acute CV events associated with coronary arthery disease, Phase III; DG041 and DG051 for the treatment of artherial thrombosis and atherosclerosis, respectively, Phase IIb); dementias and cognitive disorders (DG071, Phase Ib); Spinal Muscular Atrophy (SMA, RG3039 Phase Ib) and others.
Dr Colman has over 40 years of R&D experience in both academic and industry laboratories. His illustrious career as a scientist started by training under Nobel laureate Prof John Gurdon. His early work focused on human protein secretion from frog eggs and in the milk of transgenic animals and culminated with his involvement in making the Dolly the Sheep in 1996. With the emergence of human pluripotent stem cell technologies, Dr Colman focused on differentiation, disease modeling and regenerative medicine. Dr Colman has co-authored over 150 scientific publications.
Dr. Loring is a prominent stem cell scientist whose laboratory focuses on the genomics and epigenetics of human pluripotent stem cells. Her research group is developing stem cell-based therapies for Parkinson’s disease, multiple sclerosis, and Fragile X syndrome/autism. The group is also working with the San Diego Zoo to generate stem cells from endangered species, in an effort to rescue animals from the brink of extinction. Dr Loring is also recognized for her public involvement in bioethics, stem cell patenting, and regulation of stem cell therapies (“stem cell tourism”).