Aravinda Chakravarti

10PUBLICATIONS
45CO-AUTHORS
Developmental genetics (incl. sex determination)Gene mappingGenome structure and regulationNeurogeneticsEpigenetics (incl. genome methylation and epigenomics)
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Publications (10)

|Feb 09, 2026
Sod1 trisomy causes ENS developmental defects and susceptibility to Hirschsprung disease via neuronal Ret suppression and glial remodeling.

Gabriel Grullon, Jarod Rollins, Lauren Wilkes

|Jan 23, 2026
Using the linear references from the pangenome to discover missing autism variants.

Yang Sui, Jiadong Lin, Michelle D Noyes

|Oct 21, 2025
Joint disruption of Ret and Ednrb transcription shifts cell fate trajectories in the enteric nervous system in Hirschsprung disease.

Ryan D Fine, Rebecca Chubaryov, Mingzhou Fu

|Feb 03, 2025
Synergistic effects of Ret coding and enhancer loss-of-function alleles cause progressive loss of inhibitory motor neurons in the enteric nervous system.

Lauren E Fries, Gabriel Grullon, Lauren Wilkes

|Jan 20, 2025
The Role of de novo and Ultra-Rare Variants in Hirschsprung Disease (HSCR): Extended Gene Discovery for Risk Profiling of Patients.

Mingzhou Fu, Hanna E Berk-Rauch, Sumantra Chatterjee

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