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

Clinical genetics, 2012-09, Vol.82 (3), p.210-218

2012

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How do parents perceive and utilize knowledge of their infant’s mental health? A systematic review

Journal of child health care, 2019-06, Vol.23 (2), p.242-255

2019

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Electronically ascertained extended pedigrees in breast cancer genetic counseling

Familial cancer, 2019-04, Vol.18 (2), p.153-160

2019

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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

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-07, Vol.18 (4), p.575-583

2012

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

Journal of community genetics, 2016-04, Vol.7 (2), p.107-118

2016

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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

Journal of genetic counseling, 2015-08, Vol.24 (4), p.616-625

2015

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Direct to Consumer Genetic Testing: A Systematic Review of Position Statements, Policies and Recommendations

Obstetrical & gynecological survey, 2013-01, Vol.68 (1), p.20-22

2013

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

Midwifery, 2010-06, Vol.26 (3), p.357-366

2010

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Educational gaming in the health sciences: systematic review

Journal of advanced nursing, 2009-02, Vol.65 (2), p.259-269

2009

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

European journal of human genetics : EJHG, 2016-03, Vol.24 (3), p.350-355

2016

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

Midwifery, 2010-12, Vol.26 (6), p.596-602

2010

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

Haemophilia : the official journal of the World Federation of Hemophilia, 2005-03, Vol.11 (2), p.145-163

2005

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

Human reproduction (Oxford), 2014-08, Vol.29 (8), p.1603-1609

2014

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

Journal of advanced nursing, 2006-07, Vol.55 (2), p.151-158

Skirton, Heather

2006

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Living without a diagnosis: the parental experience

Genetic testing and molecular biomarkers, 2010-12, Vol.14 (6), p.807

2010

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

Family practice, 2014-06, Vol.31 (3), p.341-348

2014

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Informed consent to healthcare interventions in people with learning disabilities - an integrative review

Journal of advanced nursing, 2008-12, Vol.64 (6), p.549-563

2008

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The Client's Perspective of Genetic Counseling—A Grounded Theory Study

Journal of genetic counseling, 2001-08, Vol.10 (4), p.311-329

Skirton, Heather

2001

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Parental experience of a pediatric genetic referral

MCN, the American journal of maternal child nursing, 2006-05, Vol.31 (3), p.178

Skirton, Heather

2006

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

Nursing & health sciences, 2010-03, Vol.12 (1), p.27-32

2010

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Genetic nurses and counsellors: Preparation for practice with families at risk of familial cancer

Disease markers, 1999-10, Vol.15 (1-3), p.145-147

SKIRTON, H

1999

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The emotional experiences of family carers in Huntington disease

Journal of advanced nursing, 2009-04, Vol.65 (4), p.789-798

2009

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Quality assessment of genetic counseling process in the context of presymptomatic testing for late-onset disorders: a thematic analysis of three review articles

Genetic testing and molecular biomarkers, 2012-01, Vol.16 (1), p.36

2012

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The role and practice of the genetic nurse: report of the AGNC Working Party

Journal of medical genetics, 1997-02, Vol.34 (2), p.141-147

1997

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Huntington disease: families' experiences of healthcare services

Journal of advanced nursing, 2010-03, Vol.66 (3), p.500-510

2010

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

How do parents perceive and utilize knowledge of their infant’s mental health? A systematic review

Electronically ascertained extended pedigrees in breast cancer genetic counseling

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

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

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

Direct to Consumer Genetic Testing: A Systematic Review of Position Statements, Policies and Recommendations

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

Educational gaming in the health sciences: systematic review

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

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

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

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

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

Living without a diagnosis: the parental experience

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

Informed consent to healthcare interventions in people with learning disabilities - an integrative review

The Client's Perspective of Genetic Counseling—A Grounded Theory Study

Parental experience of a pediatric genetic referral

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

Genetic nurses and counsellors: Preparation for practice with families at risk of familial cancer

The emotional experiences of family carers in Huntington disease

Quality assessment of genetic counseling process in the context of presymptomatic testing for late-onset disorders: a thematic analysis of three review articles

The role and practice of the genetic nurse: report of the AGNC Working Party

Huntington disease: families' experiences of healthcare services

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