Research priorities for autosomal dominant polycystic kidney disease: a UK priority setting partnership

• Tess Harris,
• Albert Ong,
• Paul J D Winyard,
• Richard N Sandford,
• Maryrose Tarpey,
• Hannah R Bridges,
• Wendy D Brown,
• Natasha L O’Brien,
• Ann C Daly,
• Bharat K Jindal,
• Gillian S Mundy,
• Albert J Power,
• John Sayer,
• Roslyn J Simms,
• Patricia D Wilson

Affiliations

Tess Harris

Population Health Research Institute, St George’s University of London, London, UK

Albert Ong

Academic Nephrology Unit, The Henry Wellcome Laboratories for Medical Research, University of Sheffield Medical School, Sheffield, UK

Paul J D Winyard

1Institute of Child Health, University College London, London, UK

Richard N Sandford

6 Department of Medical Genetics, University of Cambridge, Cambridge, UK

Maryrose Tarpey

5 James Lind Alliance, University of Southampton, Southampton, UK

Hannah R Bridges

HB Health Comms Ltd, Orpington, UK

Wendy D Brown

London Kidney Network, London, UK

Natasha L O’Brien

ADPKD patient representative, Reading, UK

Ann C Daly

Birmingham Women’s and Children’s Hospitals NHS Foundation Trust, Birmingham, UK

Bharat K Jindal

Royal College of General Practitioners Yorkshire Faculty, Huddersfield, UK

Gillian S Mundy

ADPKD Patient Representative, Newcastle, UK

Albert J Power

North Bristol NHS Trust, Bristol, UK

John Sayer

University of Newcastle upon Tyne, Newcastle upon Tyne, UK

Roslyn J Simms

Northern General, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK

Patricia D Wilson

Department of Renal Medicine, Royal Free NHS Foundation Trust, University College London, London, UK