June 07 Jun 07
2023
12:00 PM - 01:00 PM
Wednesday Wed
ZOOM [PST]
Event

Advancements in Pediatric Patholology & Laboratory Medicine: “VMA4Kids: A Highly Sensitive Next Generation Sequencing Panel for Patients with Vascular Anomalies and Somatic Mosaic Disorders”

Avinash V. Dharmadhikari, MS, PhD, DABMGG, FACMG, NYCQ
Assistant Professor of Clinical Pathology at the Keck School of Medicine of USC. Assistant Director in the Center for Personalized Medicine at Children’s Hospital Los Angeles

This Lecture is available via Zoom meeting.

The lecture series Advancements in Pediatric Pathology & Laboratory Medicine is open to those affiliated with Stanford University Medical Center and invited guests only. The objective is to increase knowledge in the field of Pediatric Pathology. There is no commercial support received for this course unless otherwise specified. Contact Audra Jones at audraj@stanford.edu for more information.

 

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About the Speaker

Avinash V. Dharmadhikari, MS, PhD, DABMGG, FACMG, NYCQ

Assistant Professor of Clinical Pathology at the Keck School of Medicine of USC. Assistant Director in the Center for Personalized Medicine at Children’s Hospital Los Angeles

Dr. Avinash V. Dharmadhikari is board certified in Laboratory Genetics and Genomics (LGG) by the American Board of Medical Genetics and Genomics (ABMGG) and serves as an Assistant Director in the Center for Personalized Medicine at Children's Hospital Los Angeles and as Assistant Professor of Clinical Pathology at the Keck School of Medicine of USC. He has expertise with interpreting complex molecular and cytogenomic data for patient care and is a member of the ClinGen Intellectual disability/ Autism Spectrum Disorder gene curation expert panel, the Cancer Genomics Consortium (CGC) Early Career Committee and serves on the editorial board of the Journal of Molecular Diagnostics (JMD). His major areas of research interests include the identification of clinically relevant structural and molecular variants causative of genetically heterogeneous neurodevelopmental disorders, and the utility of next generation sequencing technologies in detection of the genetic causes of vascular anomalies and mosaic disorders.