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Anna Middleton

University of Cambridge · GB
Area of research
Genetics · Public Health, Environmental and Occupational Health
Research interest
Research interests include BRCA gene mutations in cancer, Genomics and Rare Diseases, Ethics in Clinical Research, and Hearing Impairment and Communication.
h-index
45
citations
7,991
works
226
NIH funding
primary concept
email

Recent publications

Standards for the care of people with cystic fibrosis; establishing and maintaining health
Journal of Cystic Fibrosis 2023cited by 79position: middledoi
Web-based physical activity promotion in young people with CF: a randomised controlled trial
Thorax 2022cited by 16position: middledoi
Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries
Genome Medicine 2021cited by 78position: lastdoi
Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?
The American Journal of Human Genetics 2020cited by 145position: firstdoi
Willingness to donate genomic and other medical data: results from Germany
European Journal of Human Genetics 2020cited by 49position: middledoi
Trust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia
Human Genetics 2019cited by 130position: lastdoi
Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data
European Journal of Human Genetics 2019cited by 51position: middledoi
The Global State of the Genetic Counseling Profession
European Journal of Human Genetics 2018cited by 368position: middledoi
Genetic counseling globally: Where are we now?
American Journal of Medical Genetics Part C Seminars in Medical Genetics 2018cited by 175position: lastdoi
Genetic counselling in the era of genomic medicine
British Medical Bulletin 2018cited by 149position: lastdoi
Attitudes of publics who are unwilling to donate DNA data for research
European Journal of Medical Genetics 2018cited by 91position: firstdoi
APPLaUD: access for patients and participants to individual level uninterpreted genomic data
Human Genomics 2018cited by 49position: middledoi
Human Germline Genome Editing
The American Journal of Human Genetics 2017cited by 242position: middledoi
The role of genetic counsellors in genomic healthcare in the United Kingdom: a statement by the Association of Genetic Nurses and Counsellors
European Journal of Human Genetics 2017cited by 44position: firstdoi
Physiotherapy for cystic fibrosis in Australia and New Zealand: A clinical practice guideline
Respirology 2016cited by 163position: middledoi
Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research
European Journal of Human Genetics 2015cited by 203position: middledoi
Potential research participants support the return of raw sequence data
Journal of Medical Genetics 2015cited by 37position: firstdoi
Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data
The Lancet 2014cited by 789position: middledoi
Genetic counselors and Genomic Counseling in the United Kingdom
Molecular Genetics & Genomic Medicine 2014cited by 34position: firstdoi

Grants

No grants ingested yet.

Frequent collaborators

Katherine I. Morley · RAND Europe5 papers (2015–2019)Erika Kleiderman · McGill University Health Centre4 papers (2018–2019)Heidi Howard · University of Southampton4 papers (2018–2020)Adrian Thorogood · Terry Fox Research Institute4 papers (2018–2019)Emilia Niemiec · Lund University4 papers (2018–2020)James Smith · Wellcome Sanger Institute3 papers (2018–2019) · 3 papers (2018–2019)Paul Bevan · Columbia University3 papers (2018–2019)Christine Patch · Queen Mary University of London3 papers (2014–2018)Danya F. Vears · KU Leuven3 papers (2018–2019) · 2 papers (2019–2019)Erick R. Scott · Seattle University2 papers (2018–2019)Helen V. Firth · Cambridge University Hospitals NHS Foundation Trust2 papers (2015–2015)Caroline F. Wright · University of Exeter2 papers (2015–2015)Eugene Bragin · Quest Diagnostics (United Kingdom)2 papers (2015–2015)Peter Goodhand · McGill University2 papers (2019–2019)Jason Bobe · Directorate-General for Interpretation2 papers (2018–2019)Matthew E. Hurles · Wellcome Sanger Institute2 papers (2015–2015)Georgina Hall · Princeton University2 papers (2014–2017)Lauren Farley · University of South Florida2 papers (2018–2019)