Annapurna Poduri

44PUBLICATIONS
269CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)NeurogeneticsMedical infection agents (incl. prions)Developmental genetics (incl. sex determination)Autonomic nervous system
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Publications (44)

|Oct 24, 2026
CAMSAP3 loss of function models suggest causative role in generalized genetic epilepsy.

|Feb 13, 2026
Diagnostic Yield of Comprehensive Reanalysis After Nondiagnostic Short-Read Genome Sequencing in Infants With Unexplained Epilepsy.

Jimmy N H Nguyen, Maria Lachgar-Ruiz, Edward J Higginbotham

|Feb 11, 2026
Diverse Genetic Etiologies of Unilateral Polymicrogyria.

Abbe Lai, Jennifer E Neil, Shyam K Akula

|Dec 22, 2025
Early death and neuronal abnormalities in depdc5 loss-of-function mosaic zebrafish models.

Sneham Tiwari, Christopher M LaCoursiere, Hyun Yong Koh

|Dec 10, 2025
Characterization of the functional and clinical impacts of CACNA1A missense variants found in neurodevelopmental disorders.

Erkin Kurganov, Lei Cui, Nikita Budnik

|Nov 24, 2025
High-throughput imaging of GABA fluorescence as a functional assay for variants in the neurodevelopmental gene, SLC6A1.

Christopher Michael McGraw, Guoqi Zhang, Gillian Prinzing

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Frequent Collaborators

5 joint publications

Rikke Steensbjerre Møller

5 joint publications

Christopher Michael McGraw

5 joint publications

Heather Olson

4 joint publications

John Christodoulou