Zachary T Sentell

6PUBLICATIONS
23CO-AUTHORS
Infant and child healthMedical molecular engineering of nucleic acids and proteinsNeurology and neuromuscular diseasesLiquid biopsiesMolecular targets
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Publications (6)

|Oct 05, 2026
Expanding the Phenotypic Spectrum of TXNDC15-Related Ciliopathies to Include Joubert Syndrome.

|Sep 19, 2025
Biallelic TMEM126B Variants as a Novel Cause of Kidney Failure-Implications for Mitochondrial Genetic Testing in Nephrology.

Zachary T Sentell, Anthony C T Cheung, Felicia Russo

|Aug 08, 2025
Urinary renal epithelial cells can be used for NPHP1 phenotyping and a personalized therapeutic strategy.

Praveen Dhondurao Sudhindar, Eric Olinger, Zachary T Sentell

|Jul 17, 2025
Urine-derived renal epithelial cells for deep phenotyping and transcriptomic response to therapy in Fabry disease.

Praveen Dhondurao Sudhindar, Sarah E Orr, Eve Miller-Hodges

|Dec 18, 2024
Use of patient-derived cell models for characterization of compound heterozygous hypomorphic C2CD3 variants in a patient with isolated nephronophthisis.

Zachary T Sentell, Lina Mougharbel, Zachary W Nurcombe

|Jul 10, 2024
Expanding the phenotypic spectrum of CC2D2A-related ciliopathies: a rare homozygous nonsense variant in a patient with suspected nephronophthisis.

Zachary T Sentell, Zachary W Nurcombe, Lina Mougharbel

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Frequent Collaborators

3 joint publications

John Sayer

3 joint publications

Thomas M Kitzler

2 joint publications

Praveen Sudhindar

2 joint publications

Juliana E Arcila-Galvis