
USA
Professor, Pathology
School of Medicine
University of California, San Francisco
Education and Training
Johns Hopkins University, Baltimore, Maryland |
BS |
1985 |
Chemistry |
Case Western Reserve University, Cleveland, Ohio |
MD/PhD |
1992 |
Medicine/Molecular Biology |
Metrohealth Medical Center, Cleveland, Ohio |
Internship, General Medicine |
1993 |
Internal Medicine |
Metrohealth Medical Center, Cleveland, Ohio |
Residency |
1997 |
Obstetrics and Gynecology |
Metrohealth Medical Cente, Cleveland, Ohio |
Fellowship |
1997 |
Maternal Fetal Medicine |
Baylor College of Medicine, Houston, Texas |
Medical Genetic Residency |
1999 |
Medical Genetics |
Aleksandar Rajkovic, MD, PhD serves as the first Chief Genomics Officer (CGO) of UCSF Health. His appointment, which follows a national search, is effective May 1, 2018. In this role, Rajkovic, previously of the University of Pittsburgh Medical Center, will direct the activities of UCSF’s existing clinical genomics laboratories and work together with campus leadership to organize the clinical genetics and genomics services across the health system. The CGO’s first priorities will include understanding the needs of various departments and patient populations for genomic services across the system, particularly as they relate to genetic testing services.
Dr. Aleksandar Rajkovic comes to UCSF from University of Pittsburgh where he is was a Professor and Marcus Allen Hogge Chair in Reproductive Sciences, Division Chief of Medical Genetics and Medical Director for the Pittsburgh Cytogenomic and Genetic Laboratories in the Department of Obstetrics, Gynecology and Reproductive Sciences. His research interests lie in the area of gonadal development, with emphasis on germ cell differentiation. The finite pool of primordial follicles is activated continuously with each menstrual cycle to give rise to mature eggs, and the rate of primordial follicle activation determines reproductive life span. Dr. Rajkovic's laboratory has utilized mouse transgenic models to discover novel germ cell–specific transcriptional regulators that play an important role in primordial follicle activation, ovarian failure, and oocyte differentiation. These germ cell–specific transcriptional regulators Nobox, Sohlh1, Sohlh2, and Lhx8 coordinate unique oocyte-specific pathways that determine reproductive life span and ovarian aging. Moreover, his laboratory has discovered a major checkpoint in mammalian meiosis, Hormad1, and has shown that early oocyte loss is independent of meiosis. His current studies focus on mechanisms behind primordial follicle activation, pathways that lead to oocyte differentiation, and the relevance of these pathways to human ovarian failure.
Research Activities and Funding
Small molecule GPR10 antagonists for the treatment of uterine fibroids |
Aug 8, 2018 - Jul 31, 2020 |
Med12 mechanisms of uterine leiomyoma formation |
Jul 1, 2017 - Jun 30, 2022 |
Genomic integrity of the X chromosome &Ovary-Specific Autosomal Genes |
May 1, 2014 - Apr 30, 2016 |
Genomic Basis of Premature Ovarian Insufficiency |
Apr 1, 2012 - Jan 31, 2017 |
LIM Homeodomain Regulated Genetic Pathways in Oogenesis and Ovarian Failure Role: Principal Investigator |
Sep 30, 2009 - Aug 31, 2012 |
THE ROLE OF HORMAD1 IN GERM CELL DEVELOPMENT AND MEIOSIS |
Sep 4, 2009 - Jul 31, 2011 |
Genetics of Human Ovarian Failure |
Apr 11, 2008 - Mar 31, 2011 |
The role of Obox in mammalian oogenesis |
Aug 1, 2004 - Jul 31, 2006 |
Transcriptional Regulation of Early Folliculogenesis |
Sep 25, 2003 - Jun 30, 2018 |