Miranda Durkie

Rare Disease Lead Consultant Clinical Scientist for North East Yorkshire (Ney) Glh @Neygenomics

Sheffield, GB
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WORK HISTORY

Feb 2025 — Present

Rare Disease Lead Consultant Clinical Scientist for North East Yorkshire (Ney) Glh @Neygenomics

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EDUCATION

1993 — 1996

The University of Sheffield

Bachelor of Science (BSc), Molecular Biology

2018 — 2019

Royal College of Pathology

FRCPath

1999 — 2000

The University of Sheffield

Master of Philosophy (MPhil), Molecular Genetics

2009 — 2010

Royal College of Pathology

Dip RC Path, Molecular Genetics

SKILLS

Molecular GeneticsGeneticsAssay DevelopmentManagementDiagnosticPcrLaboratory TechniquesHuman GeneticsClinical ResearchScienceLaboratoryCancerOncologyMolecular BiologyClinical TrialsDna Sequencing

ABOUT MIRANDA DURKIE

Consultant Clinical Scientist and Rare disease Lead Scientist for North East Yorkshire GLH. Clinical Scientist for NHS Rare and Inherited Disease Genomic Network of Excellence.Scientist co-lead of Cancer Variant Interpretation Group (CanVIG-UK), biocurator on Cystic VCEP, ClinGen Variant Classification Working Group member, expert for GENie HRR gene variant interpretation & GENie WES/WGS proportionate analysis EQAs. Co-author of ACGS rare disease variant interpretation guidelines 20••••25 in progress), EMQN HBOC genomic testing best practice guidelines 2024 and CanVIG guidelines. Publications:

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Miranda Durkie — Rare Disease Lead Consultant Clinical Scientist for North East Yorkshire (Ney) Glh at Neygenomics in Sheffield, GB | Unifers