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AleksandarRajkovicAleksandar Rajkovic
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
NIH/NICHDR01HD094373
Role: Co-Principal Investigator

Aug 8, 2018 - Jul 31, 2020

Med12 mechanisms of uterine leiomyoma formation
NIH/NICHDR01HD088629
Role: Principal Investigator

Jul 1, 2017 - Jun 30, 2022

Genomic integrity of the X chromosome &Ovary-Specific Autosomal Genes
NIH/NICHDR21HD074278
Role: Principal Investigator

May 1, 2014 - Apr 30, 2016

Genomic Basis of Premature Ovarian Insufficiency
NIH/NICHDR01HD070647
Role: Principal Investigator

Apr 1, 2012 - Jan 31, 2017

LIM Homeodomain Regulated Genetic Pathways in Oogenesis and Ovarian Failure
NIH/NICHDR01HD056351

Role: Principal Investigator

Sep 30, 2009 - Aug 31, 2012

THE ROLE OF HORMAD1 IN GERM CELL DEVELOPMENT AND MEIOSIS
NIH/NICHDR03HD054829
Role: Principal Investigator

Sep 4, 2009 - Jul 31, 2011

Genetics of Human Ovarian Failure
NIH/NICHDR21HD058125
Role: Principal Investigator

Apr 11, 2008 - Mar 31, 2011

The role of Obox in mammalian oogenesis
NIH/NICHDR03HD047514
Role: Principal Investigator

Aug 1, 2004 - Jul 31, 2006

Transcriptional Regulation of Early Folliculogenesis
NIH/NICHDR01HD044858
Role: Principal Investigator

Sep 25, 2003 - Jun 30, 2018

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