Aravinda Chakravarti
10PUBLICATIONS
45CO-AUTHORS

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Publications (10)
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|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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Frequent Collaborators
5 joint publications
Sumantra Chatterjee
4 joint publications
Hanna E Berk-Rauch
2 joint publications
Gabriel Grullon
2 joint publications
Huda Zoghbi
2 joint publications
Kelsey Hennick
2 joint publications
Yang Sui
2 joint publications
Tomasz Nowakowski
2 joint publications
Fisher Cherry
2 joint publications
Tianyun Wang
2 joint publications
Lauren E Fries