Zachary T. Sentell

Central Parkway
Newcastle Upon Tyne, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 10 publications

Ethical, legal, and policy dimensions and contentions for reanalysis and reinterpretation of clinical genetic testing results.

Ethical, legal, and policy dimensions and contentions for reanalysis and reinterpretation of clinical genetic testing results.

Journal: Frontiers in genetics

Published: August 14, 2025

Biallelic TMEM126B Variants as a Novel Cause of Kidney Failure-Implications for Mitochondrial Genetic Testing in Nephrology.

Biallelic TMEM126B Variants as a Novel Cause of Kidney Failure-Implications for Mitochondrial Genetic Testing in Nephrology.

Journal: Clinical genetics

Published: August 11, 2025

Nephrotic syndrome genomic discovery in the Mass General Brigham Biobank identifies monoallelic MEFV variants as a risk factor for focal segmental glomerulosclerosis.

Nephrotic syndrome genomic discovery in the Mass General Brigham Biobank identifies monoallelic MEFV variants as a risk factor for focal segmental glomerulosclerosis.

Journal: Kidney international

Published: July 09, 2025

Nephrotic syndrome genomic discovery in the Mass General Brigham Biobank identifies monoallelic MEFV variants as a risk factor for focal segmental glomerulosclerosis.

Nephrotic syndrome genomic discovery in the Mass General Brigham Biobank identifies monoallelic MEFV variants as a risk factor for focal segmental glomerulosclerosis.

Journal: Kidney international

Published: July 09, 2025

Urinary renal epithelial cells can be used for NPHP1 phenotyping and a personalized therapeutic strategy.

Urinary renal epithelial cells can be used for NPHP1 phenotyping and a personalized therapeutic strategy.

Journal: Journal of cell science

Published: May 10, 2025

Urine-derived renal epithelial cells for deep phenotyping and transcriptomic response to therapy in Fabry disease.

Urine-derived renal epithelial cells for deep phenotyping and transcriptomic response to therapy in Fabry disease.

Journal: Clinical science (London, England : 1979)

Published: January 22, 2025

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

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

Journal: Human molecular genetics

Published: August 13, 2024

Phenotypic Discordance among Siblings with Autosomal Recessive Polycystic Kidney Disease: Case Report and Review of the Literature.

Phenotypic Discordance among Siblings with Autosomal Recessive Polycystic Kidney Disease: Case Report and Review of the Literature.

Journal: Nephron

Published: November 25, 2023

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

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

Journal: European journal of human genetics : EJHG

Published: November 01, 2023

Primary cilia and actin regulatory pathways in renal ciliopathies.

Primary cilia and actin regulatory pathways in renal ciliopathies.

Journal: Frontiers in nephrology

Published: November 01, 2023

Showing 1-10 of 10

Last Updated: 09/26/2026