A. Middleton

A. Middleton, C. Patch, K. Calzone, 2020, Journal of nursing scholarship : an official publication of Sigma Theta Tau International Honor Society of Nursing.

The preferences of potential stakeholders in psychiatric genomic research regarding consent procedures and information delivery

H. Ullum, K. Burgdorf, O. Mors, 2019, European Psychiatry.

Direct-to-consumer genetic testing: where and how does genetic counseling fit?

A. Middleton, H. Howard, Á. Mendes, 2017, Personalized medicine.

The Global Landscape of Nursing and Genomics

A. Middleton, K. Calzone, E. Tonkin, 2018, Journal of nursing scholarship : an official publication of Sigma Theta Tau International Honor Society of Nursing.

Providing a Transcultural Genetic Counseling Service in the UK

A. Middleton, F. Robson, Mushtaq Ahmed, 2007, Journal of Genetic Counseling.

Australians' perspectives on support around use of personal genomic testing: Findings from the Genioz study.

K. Gray, A. Middleton, S. Metcalfe, 2019, European journal of medical genetics.

A Maturity Matrix for Nurse Leaders to Facilitate and Benchmark Progress in Genomic Healthcare Policy, Infrastructure, Education, and Delivery

A. Middleton, C. Patch, K. Calzone, 2020, Journal of nursing scholarship : an official publication of Sigma Theta Tau International Honor Society of Nursing.

Should doctors have a legal duty to warn relatives of their genetic risks?

Richard Milne, A. Middleton, C. Patch, 2019, The Lancet.

World congress on genetic counselling.

A. Middleton, C. Patch, B. Biesecker, 2019, European journal of medical genetics.

Point of View: An evolution from genetic counselling to genomic counselling.

A. Middleton, C. Patch, 2019, European journal of medical genetics.

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

A. Duncanson, Kazuto Kato, M. Doerr, 2021, Wellcome open research.

Deaf Community and Genetics

Steven D. Emery, A. Middleton, C. Palmer, 2013 .

Human Germline Genome Editing.

D. Shriner, K. Ormond, Y. Bombard, 2017, American journal of human genetics.

Prevalence and architecture of de novo mutations in developmental disorders

Joan, Caroline, Rajan, 2017, Nature.

Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study

Joshua C Randall, Tomas W. Fitzgerald, G. J. Swaminathan, 2016, bioRxiv.

CHD 3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Joshua C Randall, G. J. Swaminathan, A. Green, 2019 .

GA4GH: International policies and standards for data sharing across genomic research and healthcare

Grant M. Wood, James A. Eddy, Julius O. B. Jacobsen, 2021, Cell genomics.

Policy challenges of clinical genome sequencing

E. Birney, S. Humphries, H. Firth, 2013, BMJ.

Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data

Erick R. Scott, Jason R. Bobe, Richard Milne, 2019, European Journal of Human Genetics.

APPLaUD: access for patients and participants to individual level uninterpreted genomic data

Erick R. Scott, Jason R. Bobe, A. Middleton, 2018, Human Genomics.

Returning genome sequences to research participants: Policy and practice

Matthew E Hurles, Caroline F Wright, Anna Middleton, 2017, Wellcome open research.

Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research

M. Hurles, H. Firth, A. Middleton, 2015, European Journal of Human Genetics.

Potential research participants support the return of raw sequence data

M. Hurles, H. Firth, A. Middleton, 2015, Journal of Medical Genetics.

Getting the message across : communication with diverse populations in clinical genetics

A. Middleton, J. Wiggins, 2013 .

Genomic variant sharing: a position statement

Sian Ellard, Caroline F. Wright, Helen V. Firth, 2019, Wellcome Open Research.

Genomic variant sharing: a position statement

Nazneen Rahman, Caroline F Wright, James S Ware, 2019, Wellcome open research.

Genetic counselling in the era of genomic medicine

A. Middleton, C. Patch, 2018, British medical bulletin.

Position statement on opportunistic genomic screening from the Association of Genetic Nurses and Counsellors (UK and Ireland)

A. Middleton, Anita Bruce, C. Patch, 2014, European Journal of Human Genetics.

Prenatal Diagnosis for Inherited Deafness—What is the Potential Demand?

A. Middleton, J. Hewison, R. Mueller, 2001, Journal of Genetic Counseling.

Attitudes of deaf adults toward genetic testing for hereditary deafness.

A. Middleton, J. Hewison, R. Mueller, 1998, American journal of human genetics.

The Global State of the Genetic Counseling Profession

A. Obregon-Tito, K. Ormond, R. Moldovan, 2018, European Journal of Human Genetics.

Australians’ views and experience of personal genomic testing: survey findings from the Genioz study

K. Gray, A. Middleton, S. Metcalfe, 2019, European Journal of Human Genetics.

Attitudes of deaf people and their families towards issues surrounding genetics

A. Middleton, 2007 .

Genetic counseling globally: Where are we now?

K. Ormond, A. Middleton, K. Barlow-Stewart, 2018, American journal of medical genetics. Part C, Seminars in medical genetics.

Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries

Richard Milne, A. Middleton, C. Patch, 2021, Genome medicine.

Empirical research on the ethics of genomic research

M. Hurles, M. Parker, A. Middleton, 2013, American journal of medical genetics. Part A.

Report from the UK and Eire Association of Genetic Nurses and Counsellors (AGNC) Supervision Working Group on Genetic Counselling Supervision

A. Clarke, A. Middleton, R. Macleod, 2007, Journal of Genetic Counseling.

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Joshua C Randall, Tomas W. Fitzgerald, G. J. Swaminathan, 2018, Nature Communications.

Trust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia

Richard Milne, A. Middleton, K. Morley, 2019, Human Genetics.

Views, Knowledge, and Beliefs about Genetics and Genetic Counseling among Deaf People

Steven D. Emery, A. Middleton, G. Turner, 2010 .

Reflections on the Experience of Counseling Supervision by a Team of Genetic Counselors from the UK

A. Middleton, A. Kershaw, S. Everest, 2007, Journal of Genetic Counseling.

Towards equitable and trustworthy genomics research

Richard Milne, A. Middleton, C. Patch, 2022, EBioMedicine.

Return of genomic results does not motivate intent to participate in research for all: Perspectives across 22 countries.

Richard Milne, A. Middleton, C. Patch, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methods.

Erick R. Scott, Jason R. Bobe, A. Middleton, 2018, Personalized medicine.

Stakeholders in psychiatry and their attitudes toward receiving pertinent and incident findings in genomic research

H. Ullum, K. Burgdorf, O. Mors, 2017, American journal of medical genetics. Part A.

Your DNA, Your Say

A. Middleton, 2017, The New bioethics : a multidisciplinary journal of biotechnology and the body.

No expectation to share incidental findings in genomic research

M. Hurles, H. Firth, A. Middleton, 2015, The Lancet.

Finding people who will tell you their thoughts on genomics—recruitment strategies for social sciences research

A. Middleton, M. Parker, E. Bragin, 2014, Journal of Community Genetics.

Increasing nursing capacity in genomics: Overview of existing global genomics resources.

A. Middleton, K. Calzone, E. Tonkin, 2018, Nurse education today.

J. DeWitt, L. Archer, A. Middleton, 2019, European journal of medical genetics.

The genetic counsellor role in the United Kingdom

A. Middleton, C. Patch, Roberta Rizzo, 2022, European Journal of Human Genetics.

Genetic counselors and Genomic Counseling in the United Kingdom

A. Middleton, G. Hall, C. Patch, 2014, Molecular genetics & genomic medicine.

From Expectations to Experiences: Consumer Autonomy and Choice in Personal Genomic Testing

Clara Gaff, Ainsley J Newson, Anna Middleton, 2019, AJOB empirical bioethics.

Australians’ views on personal genomic testing: focus group findings from the Genioz study

K. Gray, A. Middleton, S. Metcalfe, 2018, European Journal of Human Genetics.

The expectations and realities of nutrigenomic testing in australia: A qualitative study

A. Middleton, S. Metcalfe, B. McClaren, 2021, Health expectations : an international journal of public participation in health care and health policy.

Australians’ views on personal genomic testing: focus group findings from the Genioz study

K. Gray, A. Middleton, S. Metcalfe, 2018, European Journal of Human Genetics.

Attitudes of Costa Rican individuals towards donation of personal genetic data for research

H. Raventós, A. Middleton, L. Robarts, 2021, Personalized medicine.

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene.

C. Petit, M. Mustapha, D. Weil, 1997, Human molecular genetics.

Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders.

Joshua C Randall, Tomas W. Fitzgerald, G. J. Swaminathan, 2018, American journal of human genetics.

Governance, access, and harms: perspectives of the Irish public on the use of their genetic data for research

Richard Milne, A. Middleton, C. Staunton, 2023, Wellcome Open Research.

Public engagement with genomics

Richard Milne, A. Middleton, C. Patch, 2023, Wellcome open research.