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Recent developments in genetic/genomic medicine

Clinical science (1979), 2019-03, Vol.133 (5), p.697

2019

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Interventions to support patients with sharing genetic test results with at-risk relatives: a synthesis without meta-analysis (SWiM)

European journal of human genetics : EJHG, 2023-09, Vol.31 (9), p.988-1002

2023

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Beyond regulatory approaches to ethics: making space for ethical preparedness in healthcare research

Journal of medical ethics, 2023-05, Vol.49 (5), p.352

2023

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What is the meaning of a 'genomic result' in the context of pregnancy?

European journal of human genetics : EJHG, 2021-02, Vol.29 (2), p.225-230

2021

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Exploring broad consent in the context of the 100,000 Genomes Project: a mixed methods study

European journal of human genetics : EJHG, 2020-06, Vol.28 (6), p.732-741

2020

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Old consent and new developments: health professionals should ask and not presume

Journal of medical ethics, 2020-06, Vol.46 (6), p.412

2020

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Familial genetic risks: how can we better navigate patient confidentiality and appropriate risk disclosure to relatives?

Journal of medical ethics, 2019-08, Vol.45 (8), p.504

2019

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Genome sequencing in healthcare: understanding the UK general public's views and implications for clinical practice

European journal of human genetics : EJHG, 2020-02, Vol.28 (2), p.155-164

2020

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Responsible implementation of expanded carrier screening

European journal of human genetics : EJHG, 2016-06, Vol.24 (6), p.e1-e12

2016

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Towards a national genomics medicine service: the challenges facing clinical-research hybrid practices and the case of the 100 000 genomes project

Journal of medical ethics, 2018-06, Vol.44 (6), p.397

2018

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The environmental impact of data-driven precision medicine initiatives

Cambridge prisms. Precision medicine, 2023, Vol.1, p.e1-e1, Article e1

2023

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"A very big challenge": a qualitative study to explore the early barriers and enablers to implementing a national genomic medicine service in England

Frontiers in genetics, 2024-01, Vol.14, p.1282034-1282034

2024

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Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

European journal of human genetics : EJHG, 2015-03, Vol.23 (11), p.1438-1450

2015

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Ethical issues raised by new genomic technologies: the case study of newborn genome screening

Cambridge prisms. Precision medicine, 2023, Vol.1, p.e2-16

2023

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Is there a duty to recontact in light of new genetic technologies? A systematic review of the literature

Genetics in medicine, 2015-08, Vol.17 (8), p.668-678

2015

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Using a biomarker acutely to identify babies at risk of serious adverse effects from antibiotics: where is the 'Terrible Moral and Medical Dilemma'?

Journal of medical ethics, 2021-02, Vol.47 (2), p.117

2021

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Is it acceptable to contact an anonymous egg donor to facilitate diagnostic genetic testing for the donor-conceived child?

Journal of medical ethics, 2019-06, Vol.45 (6), p.357

2019

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Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics

European journal of human genetics : EJHG, 2019-02, Vol.27 (2), p.169-182

2019

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Defining and managing incidental findings in genetic and genomic practice

Journal of Medical Genetics, 2014-11, Vol.51 (11), p.715-723

2014

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Population-based preconception carrier screening: how potential users from the general population view a test for 50 serious diseases

European journal of human genetics : EJHG, 2016-10, Vol.24 (10), p.1417-1423

2016

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Feasibility of couple-based expanded carrier screening offered by general practitioners

European journal of human genetics : EJHG, 2019-05, Vol.27 (5), p.691-700

2019

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Genetic testing of children for adult-onset conditions: opinions of the British adult population and implications for clinical practice

European journal of human genetics : EJHG, 2015-10, Vol.23 (10), p.1281-1285

2015

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Mitochondrial DNA variants in genomic data: diagnostic uplifts and predictive implications

Nature reviews. Genetics, 2021-09, Vol.22 (9), p.547

2021

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Systematic reanalysis of genomic data by diagnostic laboratories: a scoping review of ethical, economic, legal and (psycho)social implications

European journal of human genetics : EJHG, 2024-03

2024

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Healthcare professionals' and patients' perspectives on consent to clinical genetic testing: moving towards a more relational approach

BMC medical ethics, 2017-08, Vol.18 (1), p.47-47, Article 47

2017

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Recent developments in genetic/genomic medicine

Interventions to support patients with sharing genetic test results with at-risk relatives: a synthesis without meta-analysis (SWiM)

Beyond regulatory approaches to ethics: making space for ethical preparedness in healthcare research

What is the meaning of a 'genomic result' in the context of pregnancy?

Exploring broad consent in the context of the 100,000 Genomes Project: a mixed methods study

Old consent and new developments: health professionals should ask and not presume

Familial genetic risks: how can we better navigate patient confidentiality and appropriate risk disclosure to relatives?

Genome sequencing in healthcare: understanding the UK general public's views and implications for clinical practice

Responsible implementation of expanded carrier screening

Towards a national genomics medicine service: the challenges facing clinical-research hybrid practices and the case of the 100 000 genomes project

The environmental impact of data-driven precision medicine initiatives

"A very big challenge": a qualitative study to explore the early barriers and enablers to implementing a national genomic medicine service in England

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

Ethical issues raised by new genomic technologies: the case study of newborn genome screening

Is there a duty to recontact in light of new genetic technologies? A systematic review of the literature

Using a biomarker acutely to identify babies at risk of serious adverse effects from antibiotics: where is the 'Terrible Moral and Medical Dilemma'?

Is it acceptable to contact an anonymous egg donor to facilitate diagnostic genetic testing for the donor-conceived child?

Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics

Defining and managing incidental findings in genetic and genomic practice

Population-based preconception carrier screening: how potential users from the general population view a test for 50 serious diseases

Feasibility of couple-based expanded carrier screening offered by general practitioners

Genetic testing of children for adult-onset conditions: opinions of the British adult population and implications for clinical practice

Mitochondrial DNA variants in genomic data: diagnostic uplifts and predictive implications

Systematic reanalysis of genomic data by diagnostic laboratories: a scoping review of ethical, economic, legal and (psycho)social implications

Healthcare professionals' and patients' perspectives on consent to clinical genetic testing: moving towards a more relational approach

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