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Evaluation of non-invasive prenatal testing (NIPT) for aneuploidy in an NHS setting: a reliable accurate prenatal non-invasive diagnosis (RAPID) protocol

BMC pregnancy and childbirth, 2014-07, Vol.14 (1), p.229-229, Article 229

2014

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Understanding polygenic models, their development and the potential application of polygenic scores in healthcare

Journal of medical genetics, 2020-11, Vol.57 (11), p.725-732

2020

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Uptake, outcomes, and costs of implementing non-invasive prenatal testing for Down's syndrome into NHS maternity care: prospective cohort study in eight diverse maternity units

BMJ (Online), 2016-07, Vol.354, p.i3426

2016

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Towards implementation of comprehensive breast cancer risk prediction tools in health care for personalised prevention

Preventive medicine, 2022-06, Vol.159, p.107075-107075, Article 107075

2022

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Evaluation of genetic tests for susceptibility to common complex diseases: why, when and how

Human genetics, 2010-02, Vol.127 (2), p.125-134

2010

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Realising the promise of non-invasive prenatal testing

BMJ (Online), 2015-04, Vol.350 (apr10 5), p.h1792-h1792

2015

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The PROPHET project paves the way for personalized prevention in the future healthcare

European journal of cancer prevention, 2024-09, Vol.33 (5), p.387-389

2024

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How can we address the uncertainties regarding the potential clinical utility of polygenic score-based tests?

Personalized medicine, 2022-05, Vol.19 (3), p.263-270

2022

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'Personalized medicine': what's in a name?

Personalized medicine, 2014-03, Vol.11 (2), p.197-210

2014

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How can the evaluation of genetic tests be enhanced? Lessons learned from the ACCE framework and evaluating genetic tests in the United Kingdom

Genetics in medicine, 2005-09, Vol.7 (7), p.495-500

2005

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Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness

European journal of human genetics : EJHG, 2015-06, Vol.23 (6), p.729-735

2015

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Risk stratification, genomic data and the law

Journal of community genetics, 2018-07, Vol.9 (3), p.195-199

2018

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Implications of using whole genome sequencing to test unselected populations for high risk breast cancer genes: a modelling study

Hereditary cancer in clinical practice, 2016-06, Vol.14 (1), p.12-12, Article 12

2016

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The evaluation of genetic tests

Journal of public health (Oxford, England), 2007-09, Vol.29 (3), p.246-250

2007

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Personalised medicine in the UK: challenges of implementation and impact on healthcare system

Genome medicine, 2014-04, Vol.6 (4), p.28-28, Article 28

2014

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Defining purpose: a key step in genetic test evaluation

Genetics in medicine, 2007-10, Vol.9 (10), p.675-681

2007

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Uptake, Outcomes, and Costs of Implementing Non-invasive Prenatal Testing for Down Syndrome Into NHS Maternity Care: Prospective Cohort Study in Eight Diverse Maternity Units

Obstetrical & gynecological survey, 2016-11, Vol.71 (11), p.637-639

2016

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Primary open angle glaucoma. The need for a consensus case definition

Journal of epidemiology and community health (1979), 2003-09, Vol.57 (9), p.752-754

2003

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Acknowledgment to reviewers of Journal of Translational Genetics and Genomics in 2022

Journal of Translational Genetics and Genomics, 2023, Vol.6 (4), p.443-444

2023

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How can genetic tests be evaluated for clinical use? Experience of the UK Genetic Testing Network

European journal of human genetics : EJHG, 2007-09, Vol.15 (9), p.917-921

2007

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A Framework for the Prioritization of Investment in the Provision of Genetic Tests

Public health genomics, 2010-01, Vol.13 (7/8), p.538-543

2010

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HER2 status in breast cancer--an example of pharmacogenetic testing

Journal of the Royal Society of Medicine, 2007-07, Vol.100 (7), p.326-329

2007

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Genetic tests and their evaluation: Can we answer the key questions?

Genetics in medicine, 2004-11, Vol.6 (6), p.475-480

2004

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Evaluation of non-invasive prenatal testing (NIPT) for aneuploidy in an NHS setting: a reliable accurate prenatal non-invasive diagnosis (RAPID) protocol

Optimising Exome Prenatal Sequencing Services (EXPRESS): a study protocol to evaluate rapid prenatal exome sequencing in the NHS Genomic Medicine Service [version 2; peer review: 2 approved]

Understanding polygenic models, their development and the potential application of polygenic scores in healthcare

Uptake, outcomes, and costs of implementing non-invasive prenatal testing for Down's syndrome into NHS maternity care: prospective cohort study in eight diverse maternity units

Towards implementation of comprehensive breast cancer risk prediction tools in health care for personalised prevention

Evaluation of genetic tests for susceptibility to common complex diseases: why, when and how

Realising the promise of non-invasive prenatal testing

The PROPHET project paves the way for personalized prevention in the future healthcare

How can we address the uncertainties regarding the potential clinical utility of polygenic score-based tests?

'Personalized medicine': what's in a name?

How can the evaluation of genetic tests be enhanced? Lessons learned from the ACCE framework and evaluating genetic tests in the United Kingdom

Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness

Risk stratification, genomic data and the law

Implications of using whole genome sequencing to test unselected populations for high risk breast cancer genes: a modelling study

The evaluation of genetic tests

Personalised medicine in the UK: challenges of implementation and impact on healthcare system

Defining purpose: a key step in genetic test evaluation

Uptake, Outcomes, and Costs of Implementing Non-invasive Prenatal Testing for Down Syndrome Into NHS Maternity Care: Prospective Cohort Study in Eight Diverse Maternity Units

Primary open angle glaucoma. The need for a consensus case definition

Optimising Exome Prenatal Sequencing Services (EXPRESS): a study protocol to evaluate rapid prenatal exome sequencing in the NHS Genomic Medicine Service

Acknowledgment to reviewers of Journal of Translational Genetics and Genomics in 2022

How can genetic tests be evaluated for clinical use? Experience of the UK Genetic Testing Network

A Framework for the Prioritization of Investment in the Provision of Genetic Tests

HER2 status in breast cancer--an example of pharmacogenetic testing

Genetic tests and their evaluation: Can we answer the key questions?

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