Artigos com autorizações de acesso público - Martina CornelSaiba mais
1 artigo não disponível publicamente
2 Genomic medicine in 2025–
MC Cornel, GJ van Ommen
Ethical, Social and Psychological Impacts of Genomic Risk Communication, 2, 2020
Autorizações: US National Institutes of Health
64 artigos disponíveis publicamente
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening
W Dondorp, G De Wert, Y Bombard, DW Bianchi, C Bergmann, P Borry, ...
European Journal of Human Genetics 23 (11), 1438-1450, 2015
Autorizações: National Institute for Health Research, UK, Netherlands Organisation for …
Responsible implementation of expanded carrier screening
L Henneman, P Borry, D Chokoshvili, MC Cornel, CG van El, F Forzano, ...
European journal of human genetics 24 (6), e1-e12, 2016
Autorizações: National Health and Medical Research Council, Australia, Netherlands …
2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families
MK Stiles, AAM Wilde, DJ Abrams, MJ Ackerman, CM Albert, ER Behr, ...
Heart rhythm 18 (1), e1-e50, 2021
Autorizações: US National Institutes of Health, British Heart Foundation
The use of PROMs and shared decision‐making in medical encounters with patients: an opportunity to deliver value‐based health care to patients
OC Damman, A Jani, BA de Jong, A Becker, MJ Metz, MC de Bruijne, ...
Journal of evaluation in clinical practice 26 (2), 524-540, 2020
Autorizações: European Commission
Where are you going, where have you been: a recent history of the direct-to-consumer genetic testing market
P Borry, MC Cornel, HC Howard
Journal of Community Genetics 1, 101-106, 2010
Autorizações: Research Foundation (Flanders)
Opportunistic genomic screening. Recommendations of the European society of human genetics
G de Wert, W Dondorp, A Clarke, EMC Dequeker, C Cordier, Z Deans, ...
European Journal of Human Genetics 29 (3), 365-377, 2021
Autorizações: Netherlands Organisation for Health Research and Development
Whole-genome sequencing in newborn screening? A statement on the continued importance of targeted approaches in newborn screening programmes
HC Howard, BM Knoppers, MC Cornel, E Wright Clayton, K Sénécal, ...
European journal of human genetics 23 (12), 1593-1600, 2015
Autorizações: US National Institutes of Health
Genomic newborn screening: public health policy considerations and recommendations
JM Friedman, MC Cornel, AJ Goldenberg, KJ Lister, K Sénécal, DF Vears
BMC medical genomics 10, 1-13, 2017
Autorizações: US National Institutes of Health, Genome Canada
European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death
F Fellmann, CG Van El, P Charron, K Michaud, HC Howard, SN Boers, ...
European Journal of Human Genetics 27 (12), 1763-1773, 2019
Autorizações: Genome Canada, National Institute of Health and Medical Research, France
Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics
D Carrieri, HC Howard, C Benjamin, AJ Clarke, S Dheensa, S Doheny, ...
European Journal of Human Genetics 27 (2), 169-182, 2019
Autorizações: UK Economic and Social Research Council
One small edit for humans, one giant edit for humankind? Points and questions to consider for a responsible way forward for gene editing in humans
HC Howard, CG van El, F Forzano, D Radojkovic, E Rial-Sebbag, ...
European Journal of Human Genetics 26 (1), 1-11, 2018
Autorizações: European Commission
Developing a policy for paediatric biobanks: principles for good practice
K Hens, CE Van El, P Borry, A Cambon-Thomsen, MC Cornel, F Forzano, ...
European Journal of Human Genetics 21 (1), 2-7, 2013
Autorizações: Research Foundation (Flanders)
Preconceptional genetic carrier testing and the commercial offer directly-to-consumers
P Borry, L Henneman, P Lakeman, LP ten Kate, MC Cornel, HC Howard
Human Reproduction 26 (5), 972-977, 2011
Autorizações: Research Foundation (Flanders)
Implementing non-invasive prenatal testing for aneuploidy in a national healthcare system: global challenges and national solutions
RV Van Schendel, CG Van El, E Pajkrt, L Henneman, MC Cornel
BMC health services research 17, 1-10, 2017
Autorizações: Netherlands Organisation for Health Research and Development
The challenges of the expanded availability of genomic information: an agenda-setting paper
P Borry, HB Bentzen, I Budin-Ljøsne, MC Cornel, HC Howard, O Feeney, ...
Journal of community genetics 9, 103-116, 2018
Autorizações: Fundação para a Ciência e a Tecnologia, Portugal, European Commission …
What do parents of children with Down syndrome think about non-invasive prenatal testing (NIPT)?
RV Van Schendel, A Kater-Kuipers, EH van Vliet-Lachotzki, WJ Dondorp, ...
Journal of Genetic Counseling 26, 522-531, 2017
Autorizações: Netherlands Organisation for Health Research and Development
Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy
J Harper, J Geraedts, P Borry, MC Cornel, WJ Dondorp, L Gianaroli, ...
Human Reproduction 29 (8), 1603-1609, 2014
Autorizações: Fundação para a Ciência e a Tecnologia, Portugal
Prevention of congenital malformations and other adverse pregnancy outcomes with 4.0 mg of folic acid: community-based randomized clinical trial in Italy and the Netherlands
R Bortolus, F Blom, F Filippini, MNM van Poppel, E Leoncini, DJ de Smit, ...
BMC pregnancy and childbirth 14, 1-15, 2014
Autorizações: Netherlands Organisation for Health Research and Development, Government of …
Common elements in rare kidney diseases: conclusions from a kidney disease: improving global outcomes (KDIGO) controversies conference
S Aymé, D Bockenhauer, S Day, O Devuyst, LM Guay-Woodford, ...
Kidney international 92 (4), 796-808, 2017
Autorizações: US Department of Defense, US National Institutes of Health, National Health …
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