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Evaluating a genetic counseling narrative group session for people who have tested positive for the Huntington's disease expansion: An interpretative phenomenological analysis

Journal of genetic counseling, 2020-12, Vol.29 (6), p.1015-1025

2020

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Pharmacogenetics to Avoid Loss of Hearing (PALOH) trial: a protocol for a prospective observational implementation trial

BMJ open, 2021-06, Vol.11 (6), p.e044457-e044457

2021

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The emotional effects of genetic diseases: Implications for clinical genetics

American journal of medical genetics. Part A, 2007-11, Vol.143A (22), p.2651-2661

2007

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Outcome Measurement in Clinical Genetics Services: A Systematic Review of Validated Measures

Value in health, 2008-05, Vol.11 (3), p.497-508

2008

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Receiving results of uncertain clinical relevance from population genetic screening: systematic review & meta-synthesis of qualitative research

European journal of human genetics : EJHG, 2022-05, Vol.30 (5), p.520-531

2022

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G07 Improving follow-up after predictive testing in huntington’s disease: evaluating a narrative group session in a genetic counselling clinic

Journal of neurology, neurosurgery and psychiatry, 2018-09, Vol.89 (Suppl 1), p.A68

2018

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Outcome measures for clinical genetics services: A comparison of genetics healthcare professionals and patients’ views

Health policy (Amsterdam), 2007-11, Vol.84 (1), p.112-122

2007

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The Process of Disclosure: Mothers’ Experiences of Communicating X-Linked Carrier Risk Information to At-Risk Daughters

Journal of genetic counseling, 2018-09, Vol.27 (5), p.1265-1274

2018

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Genetic testing for monogenic forms of motor neuron disease/amyotrophic lateral sclerosis in unaffected family members

European journal of human genetics : EJHG, 2024-11

2024

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Delivering effective genetic services for patients and families affected by cleft lip and/or palate

European journal of human genetics : EJHG, 2019-07, Vol.27 (7), p.1018-1025

2019

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Informed consent for whole genome sequencing in mainstream clinics: logistical constraints and possible solutions

European journal of human genetics : EJHG, 2024-03, Vol.32 (3), p.260-262

2024

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Improving Service Evaluation in Clinical Genetics: Identifying Effects of Genetic Diseases on Individuals and Families

Journal of genetic counseling, 2007-02, Vol.16 (1), p.71-83

2007

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A family systems approach to genetic counseling: Development of narrative interventions

Journal of genetic counseling, 2021-02, Vol.30 (1), p.22-29

2021

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Rapid Point-of-Care Genotyping to Avoid Aminoglycoside-Induced Ototoxicity in Neonatal Intensive Care

JAMA pediatrics, 2022-05, Vol.176 (5), p.486

2022

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Experiences of predictive testing in young people at risk of Huntington's disease, familial cardiomyopathy or hereditary breast and ovarian cancer

European journal of human genetics : EJHG, 2014-03, Vol.22 (3), p.396-401

2014

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The global status of genetic counselors in 2023: What has changed in the past 5 years?

Genetics in Medicine Open, 2024-08, p.101887, Article 101887

2024

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Exploring NICU nurses' views of a novel genetic point‐of‐care test identifying neonates at risk of antibiotic‐induced ototoxicity: A qualitative study

Journal of advanced nursing, 2024-08, Vol.80 (8), p.3359-3370

2024

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Improving follow up after predictive testing in Huntington’s disease: evaluating a genetic counselling narrative group session

Journal of community genetics, 2020-01, Vol.11 (1), p.47-58

2020

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The role of genetic counsellors in genomic healthcare in the United Kingdom: a statement by the Association of Genetic Nurses and Counsellors

European journal of human genetics : EJHG, 2017-03, Vol.25 (6), p.659-661

2017

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Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery

European journal of human genetics : EJHG, 2016-06, Vol.24 (6), p.794-802

2016

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Genetic Counselling and Narrative Practices: A Model of Support following a “Negative” Predictive Test for Huntington’s Disease

Journal of Huntington's disease, 2018-01, Vol.7 (2), p.175-183

2018

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A case-note review of continued pregnancies found to be at a high risk of Huntington's disease: considerations for clinical practice

European journal of human genetics : EJHG, 2019-08, Vol.27 (8), p.1215-1224

2019

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Patient Empowerment in Clinical Genetics Services

Journal of health psychology, 2008-10, Vol.13 (7), p.895-905

2008

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J2 Predictive testing for huntington’s disease (HD) on those under 18 years: the UK experience 1994–2015

Journal of neurology, neurosurgery and psychiatry, 2016-09, Vol.87 (Suppl 1), p.A76-A76

2016

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Training Genetic Counsellors to Deliver an Innovative Therapeutic Intervention: their Views and Experience of Facilitating Multi-Family Discussion Groups

Journal of genetic counseling, 2017-04, Vol.26 (2), p.199-214

2017

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Evaluating a genetic counseling narrative group session for people who have tested positive for the Huntington's disease expansion: An interpretative phenomenological analysis

Pharmacogenetics to Avoid Loss of Hearing (PALOH) trial: a protocol for a prospective observational implementation trial

The emotional effects of genetic diseases: Implications for clinical genetics

Outcome Measurement in Clinical Genetics Services: A Systematic Review of Validated Measures

Receiving results of uncertain clinical relevance from population genetic screening: systematic review & meta-synthesis of qualitative research

G07 Improving follow-up after predictive testing in huntington’s disease: evaluating a narrative group session in a genetic counselling clinic

Outcome measures for clinical genetics services: A comparison of genetics healthcare professionals and patients’ views

The Process of Disclosure: Mothers’ Experiences of Communicating X-Linked Carrier Risk Information to At-Risk Daughters

Genetic testing for monogenic forms of motor neuron disease/amyotrophic lateral sclerosis in unaffected family members

Delivering effective genetic services for patients and families affected by cleft lip and/or palate

Informed consent for whole genome sequencing in mainstream clinics: logistical constraints and possible solutions

Improving Service Evaluation in Clinical Genetics: Identifying Effects of Genetic Diseases on Individuals and Families

A family systems approach to genetic counseling: Development of narrative interventions

Rapid Point-of-Care Genotyping to Avoid Aminoglycoside-Induced Ototoxicity in Neonatal Intensive Care

Experiences of predictive testing in young people at risk of Huntington's disease, familial cardiomyopathy or hereditary breast and ovarian cancer

The global status of genetic counselors in 2023: What has changed in the past 5 years?

Exploring NICU nurses' views of a novel genetic point‐of‐care test identifying neonates at risk of antibiotic‐induced ototoxicity: A qualitative study

Improving follow up after predictive testing in Huntington’s disease: evaluating a genetic counselling narrative group session

The role of genetic counsellors in genomic healthcare in the United Kingdom: a statement by the Association of Genetic Nurses and Counsellors

Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery

Genetic Counselling and Narrative Practices: A Model of Support following a “Negative” Predictive Test for Huntington’s Disease

A case-note review of continued pregnancies found to be at a high risk of Huntington's disease: considerations for clinical practice

Patient Empowerment in Clinical Genetics Services

J2 Predictive testing for huntington’s disease (HD) on those under 18 years: the UK experience 1994–2015

Training Genetic Counsellors to Deliver an Innovative Therapeutic Intervention: their Views and Experience of Facilitating Multi-Family Discussion Groups

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