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Sumantra Chatterjee

9PUBLICATIONS

12CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Genome structure and regulationNeurogenetics

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Publications (9)

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|Apr 03, 2026

Whole Genome Sequencing Reveals a <i>RET</i> Enhancer Risk Haplotype Associated with Hirschsprung Disease in Mowat Wilson Syndrome.

Sydney Collins, Ibrahim Bah, Ryan Pysar

|Feb 09, 2026

<i>Sod1</i> trisomy causes ENS developmental defects and susceptibility to Hirschsprung disease via neuronal <i>Ret</i> suppression and glial remodeling.

Gabriel Grullon, Jarod Rollins, Lauren Wilkes

|Feb 03, 2025

Synergistic effects of <i>Ret</i> 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 <i>de novo</i> and Ultra-Rare Variants in Hirschsprung Disease (HSCR): Extended Gene Discovery for Risk Profiling of Patients.

Mingzhou Fu, Hanna E Berk-Rauch, Sumantra Chatterjee

|Oct 07, 2024

Variability in proliferative and migratory defects in Hirschsprung disease-associated <i>RET</i> pathogenic variants.

Lauren E Fries, Sree Dharma, Aravinda Chakravarti

|Nov 10, 2023

RET enhancer haplotype-dependent remodeling of the human fetal gut development program.

Sumantra Chatterjee, Lauren E Fries, Or Yaacov

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Frequent Collaborators

5 joint publications

Aravinda Chakravarti

3 joint publications

Lauren E Fries

3 joint publications

Hanna E Berk-Rauch

3 joint publications

Gabriel Grullon

1 joint publications

Jonas Bybjerg-Grauholm

1 joint publications

Bjarke Feenstra

1 joint publications

Or Yaacov

1 joint publications

Mingzhou Fu

1 joint publications

Jarod Rollins

1 joint publications

Sydney Collins

Frequent Collaborators

5 joint publications

Aravinda Chakravarti

3 joint publications

Lauren E Fries

3 joint publications

Hanna E Berk-Rauch

3 joint publications

Gabriel Grullon

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