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Recent developments in genetic/genomic medicine

Clinical science (1979), 2019-03, Vol.133 (5), p.697-708

2019

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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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"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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The environmental impact of data-driven precision medicine initiatives

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

2023

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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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Ethical preparedness and developments in genomic healthcare

Journal of medical ethics, 2023-06, p.jme-2022-108528

2023

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The Need for Machine-Processable Agreements in Health Data Management

Algorithms, 2020-04, Vol.13 (4), p.87

2020

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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.352-356

2023

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Genomic variant sharing: a position statement

Wellcome open research, 2019, Vol.4, p.22-22

2019

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Screening for Familial Ovarian Cancer: Failure of Current Protocols to Detect Ovarian Cancer at an Early Stage According to the International Federation of Gynecology and Obstetrics System

Journal of clinical oncology, 2005-08, Vol.23 (24), p.5588-5596

2005

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Ethical preparedness in genomic medicine: how NHS clinical scientists navigate ethical issues

Journal of medical ethics, 2024-08, Vol.50 (8), p.517-522

2024

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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.504-507

2019

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Focusing attention on physicians’ climate-related duties may risk missing the bigger picture: towards a systems approach to health and climate

Journal of medical ethics, 2024-06, Vol.50 (6), p.380-381

2024

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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.412-413

2020

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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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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.397-403

2018

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The moral argument for heritable genome editing requires an inappropriately deterministic view of genetics

Journal of medical ethics, 2019-08, Vol.45 (8), p.526-527

2019

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Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol [version 1; peer review: 2 approved, 2 approved with reservations]

NIHR open research, 2021-11, Vol.1, p.23-23

2021

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Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

American journal of human genetics, 2016-03, Vol.98 (3), p.592-592

2016

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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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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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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.357-360

2019

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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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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, 2024-05, Vol.32 (5), p.489-497

2024

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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.117-118

2021

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Recent developments in genetic/genomic medicine

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

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

The environmental impact of data-driven precision medicine initiatives

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

Ethical preparedness and developments in genomic healthcare

The Need for Machine-Processable Agreements in Health Data Management

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

Genomic variant sharing: a position statement

Screening for Familial Ovarian Cancer: Failure of Current Protocols to Detect Ovarian Cancer at an Early Stage According to the International Federation of Gynecology and Obstetrics System

Ethical preparedness in genomic medicine: how NHS clinical scientists navigate ethical issues

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

Focusing attention on physicians’ climate-related duties may risk missing the bigger picture: towards a systems approach to health and climate

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

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

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

The moral argument for heritable genome editing requires an inappropriately deterministic view of genetics

Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol [version 1; peer review: 2 approved, 2 approved with reservations]

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

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

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

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

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

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

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

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