William Evans

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University of Nottingham

United Kingdom

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Recent Grants

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NIHR In Practice Fello

Open Date: 2018-10-01

Close Date: 2021-04-01

Articles (16)

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Collaborators (6)

Jeremy Shearman

Honorary Associate Clinical Professor

University of Warwick

UNITED KINGDOM

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Frances Platt

Head of Department

University of Oxford

UNITED KINGDOM

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Lara Menzies

Honorary Associate Professor

University College London

UNITED KINGDOM

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Joe Kai

University of Nottingham

UNITED KINGDOM

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Julie Greenfield

Head of Research

UNITED KINGDOM

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Caroline Hastings

Professor of Pediatrics, Hematology Oncology

UCSF Benioff Children's Hospital

UNITED STATES

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William Evans

Research Interests

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Recent Grants

Articles (16)

Enhancing care coordination for neurofibromatosis type 1 in primary care: insights and applications for rare diseases

Opportunities and challenges for identifying undiagnosed Rare Disease patients through analysis of primary care records: long QT syndrome as a test case

Precision Medicine—Are We There Yet? A Narrative Review of Precision Medicine’s Applicability in Primary Care

Managing raised ferritin in primary care.

Antinuclear antibody (ANA) testing in primary care. The test is positive what now? A two-phase observational study of UK primary care

Educational needs in diagnosing rare diseases: A multinational, multispecialty clinician survey

Embedding genomics across the NHS: a primary care perspective

Collaboration between patient advocacy and industry to create a master protocol to investigate the novel therapy acetyl-L-leucine for three ultra-rare neurodegenerative diseases: Niemann-Pick type C, the GM2 gangliosides and ataxia-telangiectasia

N-acetyl-L-leucine for Niemann-Pick type C: a multinational double-blind randomized placebo-controlled crossover study

Is it possible to implement a rare disease case-finding tool in primary care? A UK-based pilot study

Identifying Patients with Bicuspid Aortic Valve Disease in UK Primary Care: A Case–Control Study and Prediction Model

International consensus on clinical severity scale use in evaluating Niemann–Pick disease Type C in paediatric and adult patients: results from a Delphi Study

The Mendelian and Modality NHS Partnership rare disease diagnosis program in the UK: an interview with Will Evans

A master protocol to investigate a novel therapy acetyl-L-leucine for three ultra-rare neurodegenerative diseases: Niemann-Pick type C, the GM2 gangliosidoses, and ataxia telangiectasia.

Identifying, managing and supporting patients with a rare disease

How genomic information is accessed in clinical practice: an electronic survey of UK general practitioners

Collaborators (6)

Jeremy Shearman

Frances Platt

Lara Menzies

Joe Kai

Julie Greenfield

Caroline Hastings

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