Lista de obras - Felicity K. Boardman - Dominio Público Uruguay

"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.

artículo científico publicado en 2010

Becoming pregnant: exploring the perspectives of women living with diabetes

artículo científico publicado en 2008

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

artículo científico publicado en 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

artículo científico publicado en 2019

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

artículo científico publicado en 2019

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

artículo científico publicado en 2013

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

artículo científico publicado en 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.

artículo científico publicado en 2017

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

artículo científico publicado en 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

artículo científico publicado en 2011

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

artículo científico publicado en 2020

Social networks--the future for health care delivery

artículo científico publicado en 2012

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

artículo científico publicado en 2014

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

artículo científico publicado en 2014

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

artículo científico publicado en 2014

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

artículo científico publicado en 2017

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

artículo científico publicado en 2020

Lista de obras de 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

Accessing the field: Disability and the research process.

Becoming pregnant: exploring the perspectives of women living with diabetes

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

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

Human genome editing and the identity politics of genetic disability

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

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

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

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

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

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

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

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

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

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

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

Social networks--the future for health care delivery

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

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

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

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

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