Holly Mabillard

6PUBLICATIONS
26CO-AUTHORS
Cardiology (incl. cardiovascular diseases)Neurology and neuromuscular diseasesNeonatologyMedical devicesGene expression (incl. microarray and other genome-wide approaches)
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Publications (6)

|Sep 23, 2026
Renal and systemic complications in autosomal dominant hypocalcemia type 1: a case series from North East England.

|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

|Nov 27, 2024
ANKS6 Variants Underlie Polycystic Kidneys in Prenatal and Neonatal Cases.

Lama S Almohlesy, Faiqa Imtiaz, Maha Tulbah

|May 19, 2023
Genetic analysis and outcomes of Omani children with steroid-resistant nephrotic syndrome.

Mohamed S Al Riyami, Intisar Al Alawi, Badria Al Gaithi

|Aug 10, 2022
An intermediate-effect size variant in UMOD confers risk for chronic kidney disease.

Eric Olinger, Céline Schaeffer, Kendrah Kidd

|Mar 15, 2022
Biallelic variants in TTC21B as a rare cause of early-onset arterial hypertension and tubuloglomerular kidney disease.

Eric Olinger, Pran Phakdeekitcharoen, Yasar Caliskan

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Frequent Collaborators

6 joint publications

John A Sayer

3 joint publications

Eric Olinger

1 joint publications

Yasar Caliskan

1 joint publications

Yincent Tse