Matthew Edwards

Publication Activity (10 Years)

Years Active: 2023-2024
Publications (10 Years): 3

Top Topics

Quality Control

Cystic Fibrosis

Top Venues

European journal of human genetics : EJHG

This page only lists publications with an associated author ORCID identifier.

Publications

Andrew Fleming, Miranda Galey, Lizi Briggs, Matthew Edwards, Claire Hogg, Shibu John, Sam Wilkinson, Ellie Quinn, Ranjit Rai, Tom Burgoyne, Andy Rogers, Mitali P Patel, Paul Griffin, Steven Muller, Siobhán B Carr, Michael R Loebinger, Jane S A Lucas, Anand Shah, Ricardo Jose, Hannah M Mitchison, Amelia Shoemark, Danny E Miller, Deborah J Morris-Rosendahl
Combined approaches, including long-read sequencing, address the diagnostic challenge of HYDIN in primary ciliary dyskinesia. European journal of human genetics : EJHG 32 (9) (2024)
Andrew Fleming, Miranda Galey, Lizi Briggs, Matthew Edwards, Claire Hogg, Shibu John, Sam Wilkinson, Ellie Quinn, Ranjit Rai, Tom Burgoyne, Andy Rogers, Mitali P Patel, Paul Griffin, Steven Muller, Siobhán B Carr, Michael R Loebinger, Jane S A Lucas, Anand Shah, Ricardo Jose, Hannah M Mitchison, Amelia Shoemark, Danny E Miller, Deborah J Morris-Rosendahl
Combined approaches, including long-read sequencing, address the diagnostic challenge of HYDIN in primary ciliary dyskinesia. European journal of human genetics : EJHG (2024)
Jesse B G Hayesmoore, Zahurul A Bhuiyan, Domenico A Coviello, Desirée du Sart, Matthew Edwards, Maria Iascone, Deborah J Morris-Rosendahl, Katie Sheils, Marjon van Slegtenhorst, Kate L Thomson
EMQN: Recommendations for genetic testing in inherited cardiomyopathies and arrhythmias. European journal of human genetics : EJHG (2023)