Omri Teltsh

Dublin, L, Ireland

Last Updated: 09/26/2026

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Found 17 publications

Long-Read Sequencing of the MUC1 VNTR: Genomic Variation, Mutational Landscape, and Its Impact on ADTKD Diagnosis and Progression.

Long-Read Sequencing of the MUC1 VNTR: Genomic Variation, Mutational Landscape, and Its Impact on ADTKD Diagnosis and Progression.

Journal: bioRxiv : the preprint server for biology

Published: September 26, 2025

Single-Molecule Real-Time Sequencing for MUC1 VNTR Variation to Improve Autosomal Dominant Tubulointerstitial Kidney Disease Diagnosis.

Single-Molecule Real-Time Sequencing for MUC1 VNTR Variation to Improve Autosomal Dominant Tubulointerstitial Kidney Disease Diagnosis.

Journal: Journal of the American Society of Nephrology : JASN

Published: August 27, 2025

Single-Molecule Real-Time Sequencing for MUC1 Variable Number of Tandem Repeat Variation to Improve Autosomal Dominant Tubulointerstitial Kidney Disease Diagnosis.

Single-Molecule Real-Time Sequencing for MUC1 Variable Number of Tandem Repeat Variation to Improve Autosomal Dominant Tubulointerstitial Kidney Disease Diagnosis.

Journal: Journal of the American Society of Nephrology : JASN

Published: August 27, 2025

An NGS-based investigation of copy number variants in the diagnosis and severity of adult polycystic kidney disease.

An NGS-based investigation of copy number variants in the diagnosis and severity of adult polycystic kidney disease.

Journal: European journal of human genetics : EJHG

Published: July 07, 2025

Characterization of Monogenic Kidney Disease in Older Patients With CKD.

Characterization of Monogenic Kidney Disease in Older Patients With CKD.

Journal: Kidney international reports

Published: November 11, 2024

Phenotypic outcomes of PKD1 compared with non-PKD1 genetically confirmed autosomal dominant polycystic kidney disease.

Phenotypic outcomes of PKD1 compared with non-PKD1 genetically confirmed autosomal dominant polycystic kidney disease.

Journal: Journal of nephrology

Published: August 29, 2024

Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data.

Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data.

Journal: medRxiv : the preprint server for health sciences

Published: January 10, 2024

Rare disease gene association discovery in the 100,000 Genomes Project.

Rare disease gene association discovery in the 100,000 Genomes Project.

Journal: Nature

Published: December 19, 2023

Familial Variability of Disease Severity in Adult Patients With ADPKD.

Familial Variability of Disease Severity in Adult Patients With ADPKD.

Journal: Kidney international reports

Published: June 06, 2023

Optimizing prediction of response to antidepressant medications using machine learning and integrated genetic, clinical, and demographic data.

Optimizing prediction of response to antidepressant medications using machine learning and integrated genetic, clinical, and demographic data.

Journal: Translational psychiatry

Published: January 10, 2021

The transcription factor CUX1 negatively regulates invasion in castrate resistant prostate cancer.

The transcription factor CUX1 negatively regulates invasion in castrate resistant prostate cancer.

Journal: Oncotarget

Published: August 06, 2019

NKp44 and NKp30 splice variant profiles in decidua and tumor tissues: a comparative viewpoint.

NKp44 and NKp30 splice variant profiles in decidua and tumor tissues: a comparative viewpoint.

Journal: Oncotarget

Published: August 04, 2016

Showing 1-12 of 17

Last Updated: 09/26/2026