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Dr. Susanna Sorrentino, MD, FACMG, FAAP
Dr. Susanna Sorrentino, MD, FACMG, FAAP
Founder and Expert Witness, Medical Genetics of Nevada LLC (Henderson, NV)
Bachelor of Science, Brooklyn College
Dr. Susanna Sorrentino has specialized experience in the fields of Clinical Genetics (M.D.), Pediatrics, and Pediatric Medical Genetics. They earned their BS in Psychology from Brooklyn College and their MD from Ross University School of Medicine. After completing their residency in Pediatrics at New York University School of Medicine at Winthrop, they went on to complete a fellowship in Genetics and Genomics at Icahn School of Medicine at Mount Sinai. Today, the expert holds certifications in Clinical Genetics and Genomics and Pediatrics. Previously, they held roles as a Director at Valley Children's Healthcare and Chief and Assistant Professor at Kirk Kerkorian School of Medicine at the University of Nevada, Las Vegas. Currently, they work as a Clinical Geneticist, Pediatrician and Medical Director at Keck School of Medicine at the University of Southern California and Founder and Expert Witness at Medical Genetics of Nevada LLC.
m*********@g*****.com
(702) ***-****
Henderson, Nevada
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Radar Metrics At A Glance
Expert Witness Activity
Plaintiff Cases
Defense Cases
Expert Challenges
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Publications
Media & News
35
Social Media Mentions
31
Expert Witness Activity
Case Name | Role | Filed Date |
|---|---|---|
Nathaniel Neuser v. The State of Texas | Examining Physician | 2024-09-27 |
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Litigation Analytics
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Education
Institution | Degree Type |
|---|---|
Brooklyn College | Bachelor of Science |
Ross University School of Medicine | Doctor of Medicine |
Hofstra University | Coursework (Non-Degree) |
Work History
Title | Employer |
|---|---|
Founder and Expert Witness | Medical Genetics of Nevada LLC (Henderson, NV) |
Physician | Culinary Health Center (Las Vegas, NV) |
Medical Director | Keck School of Medicine at the University of Southern California (Los Angeles, CA) |
Clinical Geneticist and Pediatrician | Keck School of Medicine at the University of Southern California (Los Angeles, CA) |
Publications
Title | Type |
|---|---|
De novo variants in EBF3 are associated with hypotonia, developmental delay, intellectual disability, and autism | Journal Article |
Compound heterozygous variants in the LARP7 gene as a cause of Alazami syndrome in a Caucasian female with significant failure to thrive, short stature, and developmental disability | Journal Article |
OTX2 mutations contribute to the otocephaly-dysgnathia complex | Journal Article |
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