Lista de obras - Heather Skirton - Dominio Público Uruguay

A Delphi study to determine the European core curriculum for Master programmes in genetic counselling

artículo científico publicado en 2013

A framework for genetic service provision for haemophilia and other inherited bleeding disorders

artículo científico publicado en 2005

A historical comparison of the development of specialist genetic nursing in the United Kingdom and Japan

artículo científico publicado en 2006

A legacy for the children--attitudes of older adults in the United Kingdom to genetic testing.

artículo científico publicado en 2006

A profile of the genetic counsellor and genetic nurse profession in European countries.

artículo científico publicado en 2011

A report of two linked studies of knowledge and attitudes to prenatal screening and testing in adults of reproductive age in Japan and the UK.

artículo científico publicado en 2007

A review assessing the current treatment strategies for postnatal psychological morbidity with a focus on post-traumatic stress disorder.

artículo científico publicado en 2012

A systematic review of factors influencing uptake of invasive fetal genetic testing by pregnant women of advanced maternal age.

artículo científico publicado en 2013

A systematic review of factors that act as barriers to patient referral to genetic services

artículo científico publicado en 2014

A systematic review of the impact of foreign postings on accompanying spouses of military personnel.

artículo científico publicado en 2012

A systematic review of variability and reliability of manual and automated blood pressure readings.

artículo científico publicado en 2011

Adaption and adjustment of military spouses to overseas postings: an online forum study.

artículo científico publicado en 2014

Addressing the issue of e-learning and online genetics for health professionals.

artículo científico publicado en 2007

An assessment of written patient information provided at the genetic clinic and relating to genetic testing in seven European countries

scientific article published on 13 June 2007

An easy test but a hard decision: ethical issues concerning non-invasive prenatal testing for autosomal recessive disorders

artículo científico publicado en 2014

Antenatal screening and informed choice: a cross-sectional survey of parents and professionals

artículo científico publicado en 2009

Are health professionals ready for direct-to-consumer genetic and genomic testing?

article

Assessing the need for certainty in users of a clinical genetic health service

artículo científico publicado en 2006

Building the genetic counsellor profession in the United Kingdom: two decades of growth and development

artículo científico publicado en 2013

Can I get a retweet please? Health research recruitment and the Twittersphere

artículo científico publicado en 2013

Can we make assumptions about the psychosocial impact of living as a carrier, based on studies assessing the effects of carrier testing?

artículo científico publicado en 2010

Components of genetic counsellor education: A systematic review of the peer-reviewed literature

artículo científico publicado en 2016

Costs and difficulties of recruiting patients to provide e-health support: pilot study in one primary care trust.

artículo científico publicado en 2012

Counseling Adolescents and the Challenges for Genetic Counselors

scientific article published on 03 December 2011

Critical care outreach--a meaningful evaluation

artículo científico publicado en 2006

Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy

article

Determination of foetal sex in pregnancies at risk of haemophilia: a qualitative study exploring the clinical practices and attitudes of health professionals in the United Kingdom.

artículo científico publicado en 2011

Development and validation of a measure of informed choice for women undergoing non-invasive prenatal testing for aneuploidy

artículo científico publicado en 2015

Development of a registration system for genetic counsellors and nurses in health-care services in Europe.

artículo científico publicado en 2015

Development of an audit tool for genetic services

article

Development of an evidence-based information booklet to support parents of children without a diagnosis.

artículo científico publicado en 2012

Direct to consumer genetic testing: a systematic review of position statements, policies and recommendations.

artículo científico

Direct-to-consumer genomic testing from the perspective of the health professional: a systematic review of the literature.

artículo científico publicado en 2013

Direct-to-consumer genomic testing: systematic review of the literature on user perspectives.

artículo científico publicado en 2012

Educational gaming in the health sciences: systematic review

artículo científico publicado en 2008

Effects of knowledge, education, and experience on acceptance of first trimester screening for chromosomal anomalies

artículo científico publicado en 2010

Ethics, policy, and educational issues in genetic testing

artículo científico publicado en 2006

EuroGentest patient information leaflets: a free resource available in over 20 languages

artículo científico publicado en 2009

Experiences of UK patients with hepatitis C virus infection accessing phlebotomy: A qualitative analysis.

artículo científico publicado en 2014

Experiences regarding maternal age-specific risks and prenatal testing of women of advanced maternal age in Japan.

artículo científico publicado en 2015

Factors affecting the clinical use of non-invasive prenatal testing: a mixed methods systematic review

artículo científico

Factors influencing the sustainability of volunteer peer support for breast-feeding mothers within a hospital environment: An exploratory qualitative study.

artículo científico publicado en 2015

Fair allocation of health-care resources: finding a model that does not disenfranchise users of genetic services. A commentary on Rogowski et al....

artículo científico publicado en 2013

Family carer personal concerns in Huntington disease

artículo científico publicado en 2011

Family communication about cystic fibrosis from the mother's perspective: an exploratory study

scholarly article by Nicola Coates et al published November 2007 in Journal of Research in Nursing

Feasibility of combining e-health for patients with e-learning for students using synchronous technologies

artículo científico publicado en 2006

Fetal sex determination using cell-free fetal DNA: service users' experiences of and preferences for service delivery

artículo científico publicado en 2012

Genetic Counsellors: A Registration System to Assure Competence in Practice in the United Kingdom

article

Genetic competence of midwives in the UK and Japan.

artículo científico publicado en 2010

Genetic counseling: a survey to explore knowledge and attitudes of Italian nurses and midwives

artículo científico publicado en 2012

Genetic counsellors in Sweden: their role and added value in the clinical setting

artículo científico publicado en 2015

Genetic education and the challenge of genomic medicine: development of core competences to support preparation of health professionals in Europe

artículo científico publicado en 2010

Genetics Health Professionals' Views on Quality of Genetic Counseling Service Provision for Presymptomatic Testing in Late-Onset Neurological Diseases in Portugal: Core Components, Specific Challenges and the Need for Assessment Tools

artículo científico publicado en 2014

Genetics and nursing: A whole new ball game or back to basics?

artículo científico publicado en 2017

Genomics in nursing education

artículo científico publicado en 2005

Guidance for patients considering direct-to-consumer genetic testing and health professionals involved in their care: development of a practical decision tool.

artículo científico publicado en 2014

Huntington disease: families' experiences of healthcare services

artículo científico publicado en 2010

Impact of fetal or child loss on parents' perceptions of non-invasive prenatal diagnosis for autosomal recessive conditions

artículo científico

Impact of presymptomatic genetic testing on young adults: a systematic review

artículo científico publicado en 2015

Implications for educating the next generation of nurses on genetics and genomics in the 21st century

artículo científico publicado en 2011

Incidental findings in genetic research and clinical diagnostic tests: a systematic review

article

Informed consent for blood tests in people with a learning disability

artículo científico publicado en 2012

Informed decision making regarding antenatal screening for fetal abnormality in the United Kingdom: a qualitative study of parents and professionals

artículo científico publicado en 2013

Integrative review of cervical cancer screening in Western Asian and Middle Eastern Arab countries

artículo científico publicado en 2017

Knowledge of genetics and the role of the nurse in genetic health care: a survey of Italian nurses

artículo científico publicado en 2012

Living with genetic test results for hereditary breast and ovarian cancer

artículo científico publicado en 2009

Living without a diagnosis: the parental experience.

artículo científico

Non-invasive prenatal diagnosis for fetal sex determination: benefits and disadvantages from the service users' perspective

artículo científico publicado en 2012

Non-invasive prenatal testing for aneuploidy: a systematic review of Internet advertising to potential users by commercial companies and private health providers

artículo científico

Nurses' competence in genetics: a mixed method systematic review.

artículo científico publicado en 2012

Nurses' knowledge and educational needs regarding genetics.

artículo científico publicado en 2014

Offering prenatal diagnostic tests: European guidelines for clinical practice [corrected].

artículo científico publicado en 2013

Palliative day care: a qualitative study of service users' experiences in the United Kingdom

artículo científico publicado en 2011

Parental experience of a pediatric genetic referral

artículo científico publicado en 2006

Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness

artículo científico publicado en 2014

Predictive or not predictive: understanding the mixed messages from the patient's DNA sequence

artículo científico publicado en 2015

Preparedness of newly qualified midwives to deliver clinical care: An evaluation of pre-registration midwifery education through an analysis of key events ⬇️

artículo científico publicado el 25 de septiembre de 2011

Psychological factors that impact on women's experiences of first-time motherhood: a qualitative study of the transition

artículo científico publicado en 2008

Quality Assessment of Genetic Counseling Process in the Context of Presymptomatic Testing for Late-Onset Disorders: A Thematic Analysis of Three Review Articles ⬇️

artículo científico publicado el 5 de agosto de 2011

Quality in genetic counselling for presymptomatic testing--clinical guidelines for practice across the range of genetic conditions

artículo científico publicado en 2012

Quality issues concerning genetic counselling for presymptomatic testing: a European Delphi study

artículo científico publicado en 2015

Quality of patient information leaflets for Down syndrome screening: A comparison between the UK and Thailand

artículo científico publicado en 2015

Relevance of genomics to healthcare and nursing practice

artículo científico publicado en 2013

Reproductive empowerment: the main motivator and outcome of carrier testing

artículo científico publicado en 2011

Social support within a mother and child group: An ethnographic study situated in the UK.

artículo científico publicado en 2013

Storytellers as partners in developing a genetics education resource for health professionals

artículo científico publicado en 2011

The emotional experiences of family carers in Huntington disease

artículo científico publicado en 2009

The evidence base regarding the experiences of and attitudes to preimplantation genetic diagnosis in prospective parents

artículo científico publicado en 2014

The need to develop an evidence base for genetic counselling in Europe.

artículo científico publicado en 2015

The role of the genetic counsellor: a systematic review of research evidence

artículo científico publicado en 2014

The use of genealogy databases for risk assessment in genetic health service: a systematic review

artículo científico publicado en 2013

Use of educational games in the health professions: a mixed-methods study of educators' perspectives in the UK.

artículo científico publicado en 2010

Using a community of practice to develop standards of practice and education for genetic counsellors in Europe ⬇️

artículo científico publicado en 2010

Value of a confidant relationship in psychosocial care of people with multiple sclerosis

artículo científico publicado en 2012

What counts as effective genetic counselling for presymptomatic testing in late-onset disorders? A study of the consultand's perspective.

artículo científico publicado en 2013

Lista de obras de Heather Skirton

A Delphi study to determine the European core curriculum for Master programmes in genetic counselling

A framework for genetic service provision for haemophilia and other inherited bleeding disorders

A historical comparison of the development of specialist genetic nursing in the United Kingdom and Japan

A legacy for the children--attitudes of older adults in the United Kingdom to genetic testing.

A profile of the genetic counsellor and genetic nurse profession in European countries.

A report of two linked studies of knowledge and attitudes to prenatal screening and testing in adults of reproductive age in Japan and the UK.

A review assessing the current treatment strategies for postnatal psychological morbidity with a focus on post-traumatic stress disorder.

A systematic review of factors influencing uptake of invasive fetal genetic testing by pregnant women of advanced maternal age.

A systematic review of factors that act as barriers to patient referral to genetic services

A systematic review of the impact of foreign postings on accompanying spouses of military personnel.

A systematic review of variability and reliability of manual and automated blood pressure readings.

Adaption and adjustment of military spouses to overseas postings: an online forum study.

Addressing the issue of e-learning and online genetics for health professionals.

An assessment of written patient information provided at the genetic clinic and relating to genetic testing in seven European countries

An easy test but a hard decision: ethical issues concerning non-invasive prenatal testing for autosomal recessive disorders

Antenatal screening and informed choice: a cross-sectional survey of parents and professionals

Are health professionals ready for direct-to-consumer genetic and genomic testing?

Assessing the need for certainty in users of a clinical genetic health service

Building the genetic counsellor profession in the United Kingdom: two decades of growth and development

Can I get a retweet please? Health research recruitment and the Twittersphere

Can we make assumptions about the psychosocial impact of living as a carrier, based on studies assessing the effects of carrier testing?

Components of genetic counsellor education: A systematic review of the peer-reviewed literature

Costs and difficulties of recruiting patients to provide e-health support: pilot study in one primary care trust.

Counseling Adolescents and the Challenges for Genetic Counselors

Critical care outreach--a meaningful evaluation

Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy

Determination of foetal sex in pregnancies at risk of haemophilia: a qualitative study exploring the clinical practices and attitudes of health professionals in the United Kingdom.

Development and validation of a measure of informed choice for women undergoing non-invasive prenatal testing for aneuploidy

Development of a registration system for genetic counsellors and nurses in health-care services in Europe.

Development of an audit tool for genetic services

Development of an evidence-based information booklet to support parents of children without a diagnosis.

Direct to consumer genetic testing: a systematic review of position statements, policies and recommendations.

Direct-to-consumer genomic testing from the perspective of the health professional: a systematic review of the literature.

Direct-to-consumer genomic testing: systematic review of the literature on user perspectives.

Educational gaming in the health sciences: systematic review

Effects of knowledge, education, and experience on acceptance of first trimester screening for chromosomal anomalies

Ethics, policy, and educational issues in genetic testing

EuroGentest patient information leaflets: a free resource available in over 20 languages

Experiences of UK patients with hepatitis C virus infection accessing phlebotomy: A qualitative analysis.

Experiences regarding maternal age-specific risks and prenatal testing of women of advanced maternal age in Japan.

Factors affecting the clinical use of non-invasive prenatal testing: a mixed methods systematic review

Factors influencing the sustainability of volunteer peer support for breast-feeding mothers within a hospital environment: An exploratory qualitative study.

Fair allocation of health-care resources: finding a model that does not disenfranchise users of genetic services. A commentary on Rogowski et al....

Family carer personal concerns in Huntington disease

Family communication about cystic fibrosis from the mother's perspective: an exploratory study

Feasibility of combining e-health for patients with e-learning for students using synchronous technologies

Fetal sex determination using cell-free fetal DNA: service users' experiences of and preferences for service delivery

Genetic Counsellors: A Registration System to Assure Competence in Practice in the United Kingdom

Genetic competence of midwives in the UK and Japan.

Genetic counseling: a survey to explore knowledge and attitudes of Italian nurses and midwives

Genetic counsellors in Sweden: their role and added value in the clinical setting

Genetic education and the challenge of genomic medicine: development of core competences to support preparation of health professionals in Europe

Genetics Health Professionals' Views on Quality of Genetic Counseling Service Provision for Presymptomatic Testing in Late-Onset Neurological Diseases in Portugal: Core Components, Specific Challenges and the Need for Assessment Tools

Genetics and nursing: A whole new ball game or back to basics?

Genomics in nursing education

Guidance for patients considering direct-to-consumer genetic testing and health professionals involved in their care: development of a practical decision tool.

Huntington disease: families' experiences of healthcare services

Impact of fetal or child loss on parents' perceptions of non-invasive prenatal diagnosis for autosomal recessive conditions

Impact of presymptomatic genetic testing on young adults: a systematic review

Implications for educating the next generation of nurses on genetics and genomics in the 21st century

Incidental findings in genetic research and clinical diagnostic tests: a systematic review

Informed consent for blood tests in people with a learning disability

Informed decision making regarding antenatal screening for fetal abnormality in the United Kingdom: a qualitative study of parents and professionals

Integrative review of cervical cancer screening in Western Asian and Middle Eastern Arab countries

Knowledge of genetics and the role of the nurse in genetic health care: a survey of Italian nurses

Living with genetic test results for hereditary breast and ovarian cancer

Living without a diagnosis: the parental experience.

Non-invasive prenatal diagnosis for fetal sex determination: benefits and disadvantages from the service users' perspective

Non-invasive prenatal testing for aneuploidy: a systematic review of Internet advertising to potential users by commercial companies and private health providers

Nurses' competence in genetics: a mixed method systematic review.

Nurses' knowledge and educational needs regarding genetics.

Offering prenatal diagnostic tests: European guidelines for clinical practice [corrected].

Palliative day care: a qualitative study of service users' experiences in the United Kingdom

Parental experience of a pediatric genetic referral

Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness

Predictive or not predictive: understanding the mixed messages from the patient's DNA sequence

Preparedness of newly qualified midwives to deliver clinical care: An evaluation of pre-registration midwifery education through an analysis of key events ⬇️

Psychological factors that impact on women's experiences of first-time motherhood: a qualitative study of the transition

Quality Assessment of Genetic Counseling Process in the Context of Presymptomatic Testing for Late-Onset Disorders: A Thematic Analysis of Three Review Articles ⬇️