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33 results for Kroese,+Mark

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ArticlesPeer ReviewedFull Text
Evaluation of non-invasive prenatal testing (NIPT) for aneuploidy in an NHS setting: a reliable accurate prenatal non-invasive diagnosis (RAPID) protocol
Author / Creator:Hill, Melissa ; Wright, David ; Daley, Rebecca ; Lewis, Celine ; McKay, Fiona ; Mason, Sarah ; Lench, Nicholas ; Howarth, Abigail ; Boustred, Christopher ; Lo, Kitty ; Plagnol, Vincent ; Spencer, Kevin ; Fisher, Jane ; Kroese, Mark ; Morris, Stephen ; Chitty, Lyn S
Publisher:England: BioMed Central
Journal title:BMC pregnancy and childbirth, 2014-07, Vol.14 (1), p.229-229, Article 229
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Newsletter articlesFull Text
Pure Networks' Port Magic User Base Tops Half Million Mark; Strong Consumer Demand Fuels Need for Products that Make the Digital Home Easy to Manage and Operate
Publisher:New York: Business Wire
Journal title:Business Wire, 2004, p.1
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ArticlesPeer ReviewedFull Text
Understanding polygenic models, their development and the potential application of polygenic scores in healthcare
Author / Creator:Babb de Villiers, Chantal ; Kroese, Mark ; Moorthie, Sowmiya
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2020-11, Vol.57 (11), p.725-732
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ArticlesPeer ReviewedFull Text
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
Author / Creator:Chitty, Lyn S ; Wright, David ; Hill, Melissa ; Verhoef, Talitha I ; Daley, Rebecca ; Lewis, Celine ; Mason, Sarah ; McKay, Fiona ; Jenkins, Lucy ; Howarth, Abigail ; Cameron, Louise ; McEwan, Alec ; Fisher, Jane ; Kroese, Mark ; Morris, Stephen
Publisher:England: BMJ Publishing Group LTD
Journal title:BMJ (Online), 2016-07, Vol.354 (8065), p.i3426-i3426
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Microsoft Won't Bundle MSN Desktop Search with Windows
Publisher:QuinStreet Enterprise
Journal title:eWeek (New York, N.Y.), 2005-01
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ArticlesPeer ReviewedFull Text
A scoping review of the assessment reports of genetic or genomic tests reveals inconsistent consideration of key dimensions of clinical utility
Author / Creator:Pezzullo, Angelo Maria ; Valz Gris, Angelica ; Scarsi, Nicolò ; Tona, Diego Maria ; Porcelli, Martina ; Di Pumpo, Matteo ; Piko, Peter ; Adany, Roza ; Kannan, Pragathy ; Perola, Markus ; Cardoso, Maria Luis ; Costa, Alexandra ; Vicente, Astrid M ; Reigo, Anu ; Vaht, Mariliis ; Metspalu, Andres ; Kroese, Mark ; Pastorino, Roberta ; Boccia, Stefania
Publisher:United States: Elsevier Inc
Journal title:Journal of clinical epidemiology, 2025-05, Vol.181, p.111729-111729, Article 111729
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ArticlesPeer ReviewedFull Text
Evaluation of genetic tests for susceptibility to common complex diseases: why, when and how
Author / Creator:Wright, Caroline Fiona ; Kroese, Mark
Publisher:Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag
Journal title:Human genetics, 2010-02, Vol.127 (2), p.125-134
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ArticlesPeer ReviewedFull Text
'Personalized medicine': what's in a name?
Author / Creator:Pokorska-Bocci, Anna ; Stewart, Alison ; Sagoo, Gurdeep S ; Hall, Alison ; Kroese, Mark ; Burton, Hilary
Publisher:England: Future Medicine Ltd
Journal title:Personalized medicine, 2014-03, Vol.11 (2), p.197-210
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ArticlesPeer ReviewedFull Text
Realising the promise of non-invasive prenatal testing
Author / Creator:Chitty, Lyn S ; Kroese, Mark
Publisher:England: British Medical Journal Publishing Group
Journal title:BMJ (Online), 2015-04, Vol.350 (apr10 5), p.h1792-h1792
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ArticlesPeer ReviewedFull Text
Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness
Author / Creator:Severin, Franziska ; Borry, Pascal ; Cornel, Martina C ; Daniels, Norman ; Fellmann, Florence ; Victoria Hodgson, Shirley ; Howard, Heidi C ; John, Jürgen ; Kääriäinen, Helena ; Kayserili, Hülya ; Kent, Alastair ; Koerber, Florian ; Kristoffersson, Ulf ; Kroese, Mark ; Lewis, Celine ; Marckmann, Georg ; Meyer, Peter ; Pfeufer, Arne ; Schmidtke, Jörg ; Skirton, Heather ; Tranebjærg, Lisbeth ; Rogowski, Wolf H
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2015-06, Vol.23 (6), p.729-735
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ArticlesPeer ReviewedFull Text
Implications of using whole genome sequencing to test unselected populations for high risk breast cancer genes: a modelling study
Author / Creator:Warren-Gash, Charlotte ; Kroese, Mark ; Burton, Hilary ; Pharoah, Paul
Publisher:Poland: BioMed Central Ltd
Journal title:Hereditary cancer in clinical practice, 2016-06, Vol.14 (1), p.12-12, Article 12
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ArticlesPeer ReviewedFull Text
How can the evaluation of genetic tests be enhanced? Lessons learned from the ACCE framework and evaluating genetic tests in the United Kingdom
Author / Creator:Sanderson, Simon ; Zimmern, Ron ; Kroese, Mark ; Higgins, Julian ; Patch, Christine ; Emery, Jon
Publisher:United States: Elsevier Inc
Journal title:Genetics in medicine, 2005-09, Vol.7 (7), p.495-500
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ArticlesPeer ReviewedFull Text
Personalised medicine in the UK: challenges of implementation and impact on healthcare system
Author / Creator:Pokorska-Bocci, Anna ; Kroese, Mark ; Sagoo, Gurdeep S ; Hall, Alison ; Burton, Hilary
Publisher:England: BioMed Central Ltd
Journal title:Genome medicine, 2014-04, Vol.6 (4), p.28-28, Article 28
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ArticlesPeer ReviewedFull Text
The evaluation of genetic tests
Author / Creator:Zimmern, Ron L. ; Kroese, Mark
Publisher:England: Oxford University Press
Journal title:Journal of public health (Oxford, England), 2007-09, Vol.29 (3), p.246-250
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ArticlesPeer ReviewedFull Text
How can genetic tests be evaluated for clinical use? Experience of the UK Genetic Testing Network
Author / Creator:Kroese, Mark ; Zimmern, Ron L ; Farndon, Peter ; Stewart, Fiona ; Whittaker, Joanne
Publisher:Cham: Springer International Publishing
Journal title:European journal of human genetics : EJHG, 2007-09, Vol.15 (9), p.917-921
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ArticlesPeer ReviewedFull Text
A Framework for the Prioritization of Investment in the Provision of Genetic Tests
Author / Creator:Kroese, Mark ; Burton, Hilary ; Whittaker, Joanne ; Lakshman, Rajalakshmi ; Alberg, Corinna
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Community genetics, 2010-01, Vol.13 (7/8), p.538-543
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ArticlesPeer ReviewedFull Text
Primary open angle glaucoma. The need for a consensus case definition
Author / Creator:Kroese, M ; Burton, H
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of epidemiology and community health (1979), 2003-09, Vol.57 (9), p.752-754
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ArticlesPeer ReviewedFull Text
Genetic tests and their evaluation: Can we answer the key questions?
Author / Creator:Kroese, Mark ; Zimmern, Ron L. ; Sanderson, Simon
Publisher:United States: Elsevier Inc
Journal title:Genetics in medicine, 2004-11, Vol.6 (6), p.475-480
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ArticlesPeer ReviewedFull Text
The evaluation of genetic tests
Author / Creator:Zimmern, Ron L ; Kroese, Mark
Journal title:Journal of public health medicine, 2007-01, Vol.29 (3), p.246-250
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ArticlesPeer ReviewedFull Text
Prevalence of primary open angle glaucoma in general ophthalmic practice in the United Kingdom
Author / Creator:Kroese, M ; Burton, H ; Vardy, S ; Rimmer, T ; McCarter, D
Publisher:BMA House, Tavistock Square, London, WC1H 9JR: BMJ Publishing Group Ltd
Journal title:British journal of ophthalmology, 2002-09, Vol.86 (9), p.978-980
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Showing 1 to 20 of 33 results

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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

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Pure Networks' Port Magic User Base Tops Half Million Mark; Strong Consumer Demand Fuels Need for Products that Make the Digital Home Easy to Manage and Operate

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

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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

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Microsoft Won't Bundle MSN Desktop Search with Windows

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A scoping review of the assessment reports of genetic or genomic tests reveals inconsistent consideration of key dimensions of clinical utility

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

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

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Realising the promise of non-invasive prenatal testing

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

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

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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

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

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The evaluation of genetic tests

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

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

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

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

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The evaluation of genetic tests

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Prevalence of primary open angle glaucoma in general ophthalmic practice in the United Kingdom

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