Shrinivas Radder

OverviewAI-generated summary

Shrinivas Radder's research focuses on the application of advanced medical imaging techniques for the characterization and diagnosis of pediatric neurological and ophthalmological conditions. His work involves the fusion of different imaging modalities, such as PET-CT and MRI, to achieve enhanced diagnostic accuracy. Publications highlight his investigations into rare genetic disorders, including Poretti-Boltshauser syndrome and Joubert syndrome, detailing novel neuroimaging features and clinical presentations in affected children.

Radder also studies congenital anomalies, such as persistent hyperplastic primary vitreous and Morning Glory disc anomaly, examining their imaging characteristics and clinical implications. His research extends to conditions like Leigh syndrome and craniosynostosis, correlating imaging findings with genetic mutations and surgical management strategies. He has a significant number of shared publications with Nivedita Radder, indicating a collaborative research network within the University of Arkansas for Medical Sciences.

Metrics

• h-index: 1
• Publications: 14
• Citations: 3