Rodrigo Mendez, MD is a Medical Geneticist with a passion for using genomic science to improve patient care.

With a solid commitment to diagnosing prenatal, pediatric, and adult patients with birth defects and rare/ultra-rare genetic disorders, Hector has developed expertise in interpreting the clinical significance of genetic variants, including chromosomal and structural variation, monogenic and complex genetic disorders.

His dream is to drive progress in curing rare diseases, particularly among critically sick infants.

With extensive experience in conducting cutting-edge research, analyzing large genomic datasets, and collaborating internationally to advance research worldwide, Hector is dedicated to advancing the field of human genetics.