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The 100 000 Genomes Project: bringing whole genome sequencing to the NHS

BMJ (Online), 2018-04, Vol.361, p.k1687

2018

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

Prenatal diagnosis, 2013-06, Vol.33 (6), p.532-541

2013

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Towards equitable and trustworthy genomics research

EBioMedicine, 2022-02, Vol.76, p.103879-103879, Article 103879

2022

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Professional duties are now considered legal duties of care within genomic medicine

European journal of human genetics : EJHG, 2020-10, Vol.28 (10), p.1301-1304

2020

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Return of individual research results from genomic research: A systematic review of stakeholder perspectives

PloS one, 2021-11, Vol.16 (11), p.e0258646-e0258646

2021

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"It didn't mean anything" - moving within a landscape of knowledge to interpret genetics and genetic test results within familial cancer concerns

New genetics and society, 2021-10, Vol.40 (4), p.570-598

2021

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Genetic counselling in the era of genomic medicine

British medical bulletin, 2018-06, Vol.126 (1), p.27-36

2018

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Developing a National Newborn Genomes Program: An Approach Driven by Ethics, Engagement and Co-design

Frontiers in genetics, 2022-05, Vol.13, p.866168-866168

2022

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Use of Antihypertensive Medications and Mortality of Patients With Autosomal Dominant Polycystic Kidney Disease: A Population-Based Study

American journal of kidney diseases, 2011-06, Vol.57 (6), p.856-862

2011

Volltextzugriff (PDF)

Current State of Genomics in Nursing: A Scoping Review of Healthcare Provider Oriented (Clinical and Educational) Outcomes (2012-2022)

Genes, 2023-10, Vol.14 (11), p.2013

2023

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Communication about genetic testing with breast and ovarian cancer patients: a scoping review

European journal of human genetics : EJHG, 2019-04, Vol.27 (4), p.511-524

2019

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Study of the relationship between Black men, culture and prostate cancer beliefs

Cogent medicine, 2018-01, Vol.5 (1), p.1442636

2018

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Ethical Challenges Associated with Pathogen and Host Genetics in Infectious Disease

The new bioethics, 2023-01, Vol.29 (1), p.24-36

2023

Volltextzugriff (PDF)

Point of View: An evolution from genetic counselling to genomic counselling

European journal of medical genetics, 2019-05, Vol.62 (5), p.288-289

2019

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Public engagement with genomics

Wellcome open research, 2023, Vol.8, p.310

2023

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Potential for diagnosis of infectious disease from the 100,000 Genomes Project Metagenomic Dataset: Recommendations for reporting results

Wellcome open research, 2019, Vol.4, p.155-155

2019

Volltextzugriff (PDF)

Living a normal life in an extraordinary way: A systematic review investigating experiences of families of young people's transition into adulthood when affected by a genetic and chronic childhood condition

International journal of nursing studies, 2016-10, Vol.62, p.44-59

2016

Volltextzugriff (PDF)

Should doctors have a legal duty to warn relatives of their genetic risks?

The Lancet (British edition), 2019-12, Vol.394 (10215), p.2133-2135

2019

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Second World Congress on Genetic Counseling: An introduction to the special issue

Journal of genetic counseling, 2021-02, Vol.30 (1), p.5-6

2021

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The family transition experience when living with childhood neuromuscular disease: A grounded theory study

Journal of advanced nursing, 2021-04, Vol.77 (4), p.1921-1933

2021

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Black and Minority Ethnic women's decision-making for risk reduction strategies after BRCA testing: Use of context and knowledge

European journal of medical genetics, 2019-05, Vol.62 (5), p.376-384

2019

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Managing expectations, rights, and duties in large-scale genomics initiatives: a European comparison

European journal of human genetics : EJHG, 2023-02, Vol.31 (2), p.142-147

2023

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The genetic counsellor role in the United Kingdom : Position on behalf of the Association of Genetic Nurses and Counsellors (AGNC), Endorsed by the Genetic Counsellor Registration Board (GCRB) and Academy for Healthcare Science (AHCS)

European journal of human genetics : EJHG, 2023-01, Vol.31 (1), p.13-15

2023

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World congress on genetic counselling

European journal of medical genetics, 2019-05, Vol.62 (5), p.287-287

2019

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The 100 000 Genomes Project: bringing whole genome sequencing to the NHS

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

Towards equitable and trustworthy genomics research

Professional duties are now considered legal duties of care within genomic medicine

Return of individual research results from genomic research: A systematic review of stakeholder perspectives

"It didn't mean anything" - moving within a landscape of knowledge to interpret genetics and genetic test results within familial cancer concerns

Genetic counselling in the era of genomic medicine

Developing a National Newborn Genomes Program: An Approach Driven by Ethics, Engagement and Co-design

Use of Antihypertensive Medications and Mortality of Patients With Autosomal Dominant Polycystic Kidney Disease: A Population-Based Study

Current State of Genomics in Nursing: A Scoping Review of Healthcare Provider Oriented (Clinical and Educational) Outcomes (2012-2022)

Communication about genetic testing with breast and ovarian cancer patients: a scoping review

Study of the relationship between Black men, culture and prostate cancer beliefs

Ethical Challenges Associated with Pathogen and Host Genetics in Infectious Disease

Point of View: An evolution from genetic counselling to genomic counselling

Public engagement with genomics

Engaged genomic science produces better and fairer outcomes: an engagement framework for engaging and involving participants, patients and publics in genomics research and healthcare implementation

Potential for diagnosis of infectious disease from the 100,000 Genomes Project Metagenomic Dataset: Recommendations for reporting results

Living a normal life in an extraordinary way: A systematic review investigating experiences of families of young people's transition into adulthood when affected by a genetic and chronic childhood condition

Should doctors have a legal duty to warn relatives of their genetic risks?

Second World Congress on Genetic Counseling: An introduction to the special issue

The family transition experience when living with childhood neuromuscular disease: A grounded theory study

Black and Minority Ethnic women's decision-making for risk reduction strategies after BRCA testing: Use of context and knowledge

Managing expectations, rights, and duties in large-scale genomics initiatives: a European comparison

The genetic counsellor role in the United Kingdom : Position on behalf of the Association of Genetic Nurses and Counsellors (AGNC), Endorsed by the Genetic Counsellor Registration Board (GCRB) and Academy for Healthcare Science (AHCS)

World congress on genetic counselling

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