Albert C. M. Ong

University of Sheffield Medical School

United Kingdom

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Articles (20)

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Collaborators (16)

Peter Harris

Professor

Mayo Clinic Rochester

UNITED STATES

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Sarah Flanagan

Associate Professor of Genomic Medicine and Sir Henry Dale Fellow

University of Exeter

UNITED KINGDOM

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Julius Jacobsen

Queen Mary University of London

UNITED KINGDOM

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Ronald D. Perrone

Tufts University School of Medicine

UNITED STATES

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Detlef Bockenhauer

Professor of Paediatric Nephrology

KU Leuven

BELGIUM

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Klemens Budde

Charité - Universitätsmedizin Berlin

GERMANY

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Roser Torra

Profesor titular

University of Barcelona

SPAIN

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Miranda Durkie

Deputy head of rare disease

UNITED KINGDOM

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Maria Vanessa Perez-Gomez

Universidad Autónoma de Madrid

SPAIN

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Claire Smith

Lecturer in Biomineralisation in Oral Health

University of Leeds

UNITED KINGDOM

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Joaquim Calado

Universidade de Aveiro

PORTUGAL

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Li Chan

Professor of Molecular Endocrinology and Metabolism/Honorary Consultant in Paediatric Endocrinology

UNITED KINGDOM

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Neil Turner

Professor of Nephrology

University of Edinburgh

UNITED KINGDOM

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Juan David Gonzalez Rodriguez

SPAIN

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Maria Szczepanska

Prof.

Medical University of Silesia Faculty of Medical Sciences in Zabrze

POLAND

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Joanna Kenny

University College London

UNITED KINGDOM

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Albert C. M. Ong

Research Interests

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Articles (20)

KDIGO 2025 Clinical Practice Guideline for the Evaluation, Management, and Treatment of Autosomal Dominant Polycystic Kidney Disease (ADPKD)

Drug and siRNA screens identify ROCK2 as a therapeutic target for ciliopathies

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

Insights from ADPedKD, ERKReg and RaDaR registries provide a multi-national perspective on the presentation of childhood autosomal dominant polycystic kidney disease in high- and middle-income countries

Monoallelic IFT140 Variants Causing Childhood-Onset Autosomal Dominant Polycystic Kidney Disease.

A conceptual model of factors potentially influencing prescribing decisions for chronic conditions: an overview of systematic reviews

The diagnostic accuracy of ultrasound and genomic tests for the diagnosis of autosomal-dominant polycystic kidney disease: a systematic mapping review

Quantifying association of early proteinuria and estimated glomerular filtration rate changes with long-term kidney failure in C3 glomerulopathy and immune-complex membranous proliferative glomerulonephritis using the United Kingdom RaDaR Registry

ANKHD1 promotes pathogenic proliferation in Autosomal Dominant Polycystic Kidney Disease via the Cyclin D1/CDK4 pathway

Commentary: Tolvaptan for Autosomal Dominant Polycystic Kidney Disease (ADPKD) - an update

The Common PKD1 p.(Ile3167Phe) Variant Is Hypomorphic and Associated with Very Early Onset, Biallelic Polycystic Kidney Disease

Chronic kidney disease as cardiovascular risk factor in routine clinical practice: a position statement by the Council of the European Renal Association.

OVERTURE: A Worldwide, Prospective, Observational Study of Disease Characteristics in Patients With ADPKD

Barriers and facilitators to the implementation of guidelines in rare diseases: a systematic review

Hypertension in young adults with autosomal dominant polycystic kidney disease: a case for early screening?

Patient Perspectives on ADPKD

A founderUMODvariant is a common cause of hereditary nephropathy in the British population

The association of urinary epidermal growth factors with ADPKD disease severity and progression

Diet and Polycystic Kidney Disease: Nutrients, Foods, Dietary Patterns, and Implications for Practice

WCN23-0391 THE CLINICAL CHARACTERISTICS AND KIDNEY OUTCOME IN CHINESE PATIENTS WITH TYPICAL AND ATYPICAL POLYCYSTIC KIDNEY DISEASE

Collaborators (16)

Peter Harris

Sarah Flanagan

Julius Jacobsen

Ronald D. Perrone

Detlef Bockenhauer

Klemens Budde

Roser Torra

Miranda Durkie

Maria Vanessa Perez-Gomez

Claire Smith

Joaquim Calado

Li Chan

Neil Turner

Juan David Gonzalez Rodriguez

Maria Szczepanska

Joanna Kenny

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