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Dr. Sorrentino is a graduate of Ross University School of Medicine. She completed her residency in pediatrics at New York University Winthrop Hospital in Mineola, NY and her fellowship in clinical genetics at Mount Sinai Medical Center in New York, NY. Dr. Sorrentino is board certified in both clinical genetics and pediatrics.

Education & Training


MD, Ross University School of Medicine


Residency, Pediatrics, New York University  Winthrop Hospital


Fellowship, Clinical Genetics, Mount Sinai Medical Center


Chassaing, N*, Sorrentino, S* ET. Al “OTX2 Mutations Contribute to the Otocephaly-Dysgnathia Complex”, J Med Genet. 2012 Jun; 49(6):373-9. PMID: 22577225 *co first authors

Tanaka AJ, Cho MT, Willaert R Retterer K, Zarate YA, Bosanko K,Stefans V, Oishi K, Williamson A, Wilson GN, Basinger A, Barbaro-Dieber

T, Ortega L, Sorrentino S, Gabriel MK, Anderson IJ, Sacoto MJG, Schnur RE, Chung WK , “De novo variants in EBF3 are associated with hypotonia, developmental delay, intellectual disability, and autism.” Cold Spring Harb Mol Case Stud. 2017 Nov 21; 3(6). PMID: 29162653

Ling, T and Sorrentino, S. “Compound Heterozygous Variants in the LARP7 Gene as a Cause of Alazami Syndrome in a Caucasian Female with Primordial Dwarfism and Developmental Disability” Am J Med GenetA. 2016 Jan; 170(1): 217-9. Epub 2015 Sep 16. PMID: 26374271



Super Doctors (Pediatrics), Los Angeles Magazine


Rising Star (Genetic Medicine), Pasadena Magazine


Dean's Fellow Program, University of Nevada Las Vegas School of Medicine


Advisory Board Member, Mountain States Regional Genetics Network 


Board Member, Rare Disease Advisory Council of Nevada

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