Awards
- ACCEA Silver Award, Advisory Committee on Clinical Excellence Awards - GOV.UK, 2018
- ACCEA Bronze Award, Advisory Committee on Clinical Excellence Awards - GOV.UK, 2013
- Achievement Award in Rare Pulmonary Diseases, European Respiratory Society, 2012
- Presidential Lecturer, American Society of Hematology, 1999
- Award for Best Emerging Medical Researcher in the UK, BUPA Foundation, 1997
- Glaxo Wellcome Young Investigator Medal, Medical Research Society, 1997
- Young Investigator Award, Gordon Conference on Angiogenesis, 1995
- >10 Early Career Prizes to Dr Shovlin, from, 1980
- A former Presidential Lecturer for the American Society of Hematology (New Orleans 1999), and recipient of the European Respiratory Society 2012 Rare Pulmonary Disease Achievement Award for her work on adult onset ADA deficiency (1992-1994); and HHT/PAVMs (1992 to date), Dr Shovlin is Chair of the VASCERN HHT Working Group; British Thoracic Society PAVM Clinical Statement Group; is the Clinical Champion for Mainstreaming Genomics in Respiratory Medicine, and also chairs the West London NHS Genomic Medicine Centre Rare Disease MDT for the 100,000 Genomes Project.
- Dr Shovlin, 2017:, A former Presidential Lecturer for the American Society of Hematology (New Orleans 1999), and recipient of the European Respiratory Society 2012 Rare Pulmonary Disease Achievement Award for her work on adult onset ADA deficiency (1992-1994); and HHT/PAVMs (1992 to date), Dr Shovlin is Chair of the VASCern HHT Working Group (HHT Working Group. ); British Thoracic Society PAVM Clinical Statement Group; is the Clinical Champion for Mainstreaming Genomics in Respiratory Medicine, and also chairs the West London NHS Genomic Medicine Centre Rare Disease MDT for the 100,000 Genomes Project.
- Multiple awards to Dr Shovlin's students
External Positions
- British Thoracic Society Representative, Pharmacogenomics in the NHS (Working Party), Royal College of Physicians and Royal Pharmaceutical Society, 2020
- Chair, NHS Hereditary Haemorrhagic Telangiectasia Rare Disease Collaborative Network (Chair), National Health Service (NHS), 2020
- Chair, Genomics England Clinical Interpretation Partnership (GeCIP) for Respiratory Medicine (Chair), 2019
- Member, International HHT Guidelines Committee, 2019
- Chair, European Reference Network for Rare Vascular Diseases (VASCERN) HHT (Chair), European Commission, 2016 - 2020
- Chair and Founder, Genomics England Clinical Interpretation Partnership (GeCIP) subdomains for HHT and PAVMs (Chair), 2016
- Chair, Pulmonary AVM Clinical Statement Group (Chair), British Thoracic Society, 2016
- Chair and Founder, West London Genomics Medicine Centre Rare Disease MDT/MDT Board (Chair), West London Genomics Medicine Centre, 2016 - 2020
Membership of Professional Bodies
- NHS GMS Research Collaborative Steering Committee, 2022
- North Thames Genomic Medicine Service Alliance (GMSA) Research Director, 2022
Links with Other Academic Bodies
- Principal External Examiner, 2nd BM Examinations, University of Oxford, 2018