Anna Middleton
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Most Influential Person Now
Social scientist
Anna Middleton's AcademicInfluence.com Rankings
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Sociology
Anna Middleton's Degrees
- Masters Sociology University of Oxford
- Bachelors Sociology University of Oxford
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Why Is Anna Middleton Influential?
(Suggest an Edit or Addition)According to Wikipedia, Anna Middleton is a social scientist and genetic counsellor. She is Head of the Society and Ethics Research group, part of Wellcome Connecting Science, based on the Wellcome Genome Campus. She is also a Professor/Affiliate Lecturer at the Faculty of Education at the University of Cambridge.
Anna Middleton's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Large-scale discovery of novel genetic causes of developmental disorders (2014) (908)
- Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene. (1997) (631)
- Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data (2015) (627)
- Prevalence and architecture of de novo mutations in developmental disorders (2017) (405)
- Attitudes of deaf adults toward genetic testing for hereditary deafness. (1998) (174)
- The Global State of the Genetic Counseling Profession (2018) (168)
- Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research (2015) (161)
- Human Germline Genome Editing. (2017) (156)
- A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse. (2006) (111)
- Genetic counseling globally: Where are we now? (2018) (84)
- Prenatal Diagnosis for Inherited Deafness—What is the Potential Demand? (2001) (84)
- GA4GH: International policies and standards for data sharing across genomic research and healthcare (2021) (62)
- Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations--molecular and audiological findings. (1999) (61)
- Genetic counselling in the era of genomic medicine (2018) (57)
- Trust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia (2019) (56)
- Policy challenges of clinical genome sequencing (2013) (53)
- Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study (2016) (49)
- Direct-to-consumer genetic testing: where and how does genetic counseling fit? (2017) (44)
- Attitudes of publics who are unwilling to donate DNA data for research (2019) (43)
- Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data? (2020) (43)
- APPLaUD: access for patients and participants to individual level uninterpreted genomic data (2018) (42)
- The Global Landscape of Nursing and Genomics (2018) (42)
- Potential research participants support the return of raw sequence data (2015) (34)
- The role of genetic counsellors in genomic healthcare in the United Kingdom: a statement by the Association of Genetic Nurses and Counsellors (2017) (29)
- Genetic counselors and Genomic Counseling in the United Kingdom (2014) (28)
- Position statement on opportunistic genomic screening from the Association of Genetic Nurses and Counsellors (UK and Ireland) (2014) (27)
- Society and personal genome data (2018) (26)
- 'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methods. (2018) (25)
- Finding people who will tell you their thoughts on genomics—recruitment strategies for social sciences research (2014) (24)
- Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries (2021) (23)
- Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data (2019) (22)
- No expectation to share incidental findings in genomic research (2015) (22)
- Online questionnaire development: Using film to engage participants and then gather attitudes towards the sharing of genomic data☆ (2014) (22)
- Views, Knowledge, and Beliefs about Genetics and Genetic Counseling among Deaf People (2010) (21)
- Stakeholders in psychiatry and their attitudes toward receiving pertinent and incident findings in genomic research (2017) (20)
- Increasing nursing capacity in genomics: Overview of existing global genomics resources. (2018) (20)
- Reflections on the Experience of Counseling Supervision by a Team of Genetic Counselors from the UK (2007) (19)
- Willingness to donate genomic and other medical data: results from Germany (2020) (19)
- Report from the UK and Eire Association of Genetic Nurses and Counsellors (AGNC) Supervision Working Group on Genetic Counselling Supervision (2007) (19)
- Empirical research on the ethics of genomic research (2013) (18)
- Genomic variant sharing: a position statement (2019) (17)
- CHD 3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (2019) (16)
- Towards equitable and trustworthy genomics research (2022) (16)
- Whose Deaf Genes Are They Anyway?: The Deaf Community’s Challenge to Legislation on Embryo Selection (2010) (16)
- A Roadmap for Global Acceleration of Genomics Integration Across Nursing (2020) (15)
- Returning genome sequences to research participants: Policy and practice (2017) (15)
- Your DNA, Your Say (2017) (14)
- Annotation of the Human Genome by High-Throughput Sequence Analysis of Naturally Occurring Proteins (2004) (14)
- Australians' perspectives on support around use of personal genomic testing: Findings from the Genioz study. (2019) (13)
- Australians’ views and experience of personal genomic testing: survey findings from the Genioz study (2019) (13)
- Providing a Transcultural Genetic Counseling Service in the UK (2007) (12)
- From Expectations to Experiences: Consumer Autonomy and Choice in Personal Genomic Testing (2019) (12)
- Australians’ views on personal genomic testing: focus group findings from the Genioz study (2018) (12)
- Genetics in the 21st Century: Implications for patients, consumers and citizens. (2017) (12)
- Getting the message across : communication with diverse populations in clinical genetics (2013) (10)
- Point of View: An evolution from genetic counselling to genomic counselling. (2019) (10)
- Popular culture and genetics; friend, foe or something more complex? (2019) (10)
- Genetics in the 21st Century: Implications for patients, consumers and citizens (2018) (10)
- A Maturity Matrix for Nurse Leaders to Facilitate and Benchmark Progress in Genomic Healthcare Policy, Infrastructure, Education, and Delivery (2020) (9)
- The preferences of potential stakeholders in psychiatric genomic research regarding consent procedures and information delivery (2019) (9)
- Communication about DTC Testing: Commentary on a ‘Family Experience of Personal Genomics’ (2012) (8)
- Should doctors have a legal duty to warn relatives of their genetic risks? (2019) (7)
- Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data (2019) (7)
- The genetic counsellor role in the United Kingdom (2022) (6)
- Editorial on Supervision (2007) (5)
- Genomic variant sharing: a position statement. (2019) (4)
- The relative contribution of mutations in the DFNB loci to congenital/early childhood non-syndromal sensorineural hearing impairment/deafness (2001) (4)
- Deaf Community and Genetics (2013) (3)
- Engaged genomic science produces better and fairer outcomes: an engagement framework for engaging and involving participants, patients and publics in genomics research and healthcare implementation (2021) (3)
- Optimising diagnostic yield in highly penetrant genomic disease (2022) (3)
- Return of genomic results does not motivate intent to participate in research for all: Perspectives across 22 countries. (2022) (3)
- Genetic counselling and the d/Deaf community (2006) (3)
- A pilot study of attitudes of deaf and hearing parents towards issues surrounding genetic testing for deafness. (1997) (2)
- Culture, Kinship and Genes: Towards Cross-Cultural Genetics (1998) (2)
- Attitudes of Costa Rican individuals towards donation of personal genetic data for research (2021) (2)
- Attitudes of deaf people and their families towards issues surrounding genetics (2007) (2)
- Public trust and genomic medicine in Canada and the UK. (2021) (1)
- World congress on genetic counselling. (2019) (1)
- Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (2019) (1)
- Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data (2019) (1)
- Attitudes of adults with otosclerosis towards issues surrounding genetics and the impact of hearing loss (2006) (1)
- Australians’ views and experience of personal genomic testing: survey findings from the Genioz study (2019) (1)
- Australians’ views on personal genomic testing: focus group findings from the Genioz study (2018) (1)
- Ethical, Legal, and Social Issues in Clinical Genomics (2014) (1)
- Scope of professional roles for genetic counsellors and clinical geneticists in the United Kingdom (2022) (1)
- THE CHOICE TO HAVE A DISABLED CHILD. AUTHORS' REPLY (1999) (1)
- Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (2019) (0)
- 2018-1105 CHD 3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (2019) (0)
- Empirical Research on the Ethics of Genomic (2013) (0)
- Public trust and genomic medicine in Canada and the UK (2021) (0)
- A heartfelt "thank you" to all the reviewers of the Journal of Community Genetics in 2010 (2011) (0)
- 61. HOW DOES THE PUBLIC IN LATIN AMERICAN COUNTRIES VIEW GENETIC AND GENOMIC DATA DONATION FOR RESEARCH? (2022) (0)
- Finding people who will tell you their thoughts on genomics—recruitment strategies for social sciences research (2014) (0)
- The expectations and realities of nutrigenomic testing in australia: A qualitative study (2021) (0)
- CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (2018) (0)
- 12 ‘Recreational’ consumer genomics: no such thing as a non-medical test (2019) (0)
- Willingness to donate genomic and other medical data: results from Germany (2020) (0)
- Working with the public: engaging with consumers about the ethics of and decision to pursue personal genomic testing (2019) (0)
- Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries (2021) (0)
- ASHG POSITION STATEMENT Human Germline Genome Editing (2017) (0)
- Opportunities for poaching: using the public's enjoyment of popular culture to foster dialogues around genetics (2022) (0)
- The choice to have a disabled child [5] (multiple letters) (1999) (0)
- The Global State of the Genetic Counseling Profession (2018) (0)
- APPLaUD: access for patients and participants to individual level uninterpreted genomic data (2018) (0)
- Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (2019) (0)
- Genetic Counsellor Registration Mentoring Framework (2010) (0)
- Sharing genomic research data: launch of an international ethics study (2012) (0)
- Consumer Health Informatics Aspects of Direct-to-Consumer Personal Genomic Testing (2017) (0)
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