Aravinda Chakravarti

12PUBLICATIONS
48CO-AUTHORS
NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Gene mappingGenome structure and regulation
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Publications (12)

|Sep 16, 2026
Combined effects of Ret coding and enhancer loss-of-function alleles cause progressive loss of inhibitory motor neurons in the enteric nervous system.

|Sep 03, 2026
Partitioned blood pressure polygenic risk reveals differential genetic effects of tissue-specific enhancers and their interactions on cardiovascular disease.

|May 18, 2026
A massively parallel reporter assay of MECP2 cis-regulatory elements reveals genetic candidates for male-biased autism.

|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

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Frequent Collaborators

6 joint publications

Sumantra Chatterjee

5 joint publications

Hanna E Berk-Rauch

3 joint publications

Gabriel Grullon

3 joint publications

Lauren E Fries