Sumantra Chatterjee

11PUBLICATIONS
13CO-AUTHORS
Major global burdens of diseaseNeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Genome structure and regulation
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Publications (11)

|Oct 08, 2026
Population Differences in the Epidemiology, Phenotype, and Genetics of Hirschsprung Disease in the United States.

|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.

|Apr 03, 2026
Whole Genome Sequencing Reveals a RET Enhancer Risk Haplotype Associated with Hirschsprung Disease in Mowat Wilson Syndrome.

Sydney Collins, Ibrahim Bah, Ryan Pysar

|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

|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

7 joint publications

Aravinda Chakravarti

5 joint publications

Hanna E Berk-Rauch

4 joint publications

Lauren E Fries

4 joint publications

Gabriel Grullon