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List of works by Felicity K. Boardman

"I didn't take it too seriously because I'd just never heard of it": Experiential knowledge and genetic screening for thalassaemia in the UK

scientific article published on 24 December 2018

Accessing the field: Disability and the research process.

scientific article published on 23 October 2010

Becoming pregnant: exploring the perspectives of women living with diabetes

scientific article

Experience as knowledge: Disability, distillation and (reprogenetic) decision-making.

scientific article published on 8 September 2017

How do genetically disabled adults view selective reproduction? Impairment, identity, and genetic screening

scientific article published on 09 September 2018

Human genome editing and the identity politics of genetic disability

scientific article published on 06 September 2019

Improving the content validity of the mixed methods appraisal tool: a modified e-Delphi study

scientific article published on 22 March 2019

Knowledge is power? The role of experiential knowledge in genetically 'risky' reproductive decisions.

scientific article

Letter to the editor. Gene editing and disabled people: a response to Iñigo de Miguel Beriain

scientific article published on 30 April 2020

Newborn genetic screening for spinal muscular atrophy in the UK: The views of the general population

scientific article published on 23 November 2017

Newborn screening for haemophilia: The views of families and adults living with haemophilia in the UK

scientific article published on 28 February 2019

Newborn screening for spinal muscular atrophy: The views of affected families and adults.

scientific article

Population screening for spinal muscular atrophy: A mixed methods study of the views of affected families

scientific article published on 28 October 2016

Preventing lives affected by hemophilia: A mixed methods study of the views of adults with hemophilia and their families toward genetic screening

scientific article published on 05 March 2019

Resilience as a response to the stigma of depression: a mixed methods analysis

scientific article

Responsibility, identity, and genomic sequencing: A comparison of published recommendations and patient perspectives on accepting or declining incidental findings

scientific article published on 28 October 2018

Social and cultural influences on genetic screening programme acceptability: A mixed-methods study of the views of adults, carriers, and family members living with thalassemia in the UK

scientific article published on 01 March 2020

Social networks--the future for health care delivery

scientific article published on September 2012

The Warwick Patient Experiences Framework: patient-based evidence in clinical guidelines.

scientific article published on 20 February 2014

The effect of strategies of personal resilience on depression recovery in an Australian cohort: a mixed methods study

scientific article

The expressivist objection to prenatal testing: the experiences of families living with genetic disease.

scientific article published on 14 February 2014

The role of experiential knowledge within attitudes towards genetic carrier screening: A comparison of people with and without experience of spinal muscular atrophy.

scientific article

Whose life is worth preserving? Disabled people and the expressivist objection to neonatology

scientific article published on 02 May 2020

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