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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 | 470 | 2015 |
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 | 342 | 2016 |
Teratogenic effects of antiepileptic drugs: use of an International Database on Malformations and Drug Exposure (MADRE) C Arpino, S Brescianini, E Robert, EE Castilla, G Cocchi, MC Cornel, ... Epilepsia 41 (11), 1436-1443, 2000 | 272 | 2000 |
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The interface between assisted reproductive technologies and genetics: technical, social, ethical and legal issues S Soini, D Ibarreta, V Anastasiadou, S Aymé, S Braga, M Cornel, ... European Journal of Human Genetics 14 (5), 588-645, 2006 | 218 | 2006 |
Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 1–From blood spot to screening result JG Loeber, P Burgard, MC Cornel, T Rigter, SS Weinreich, K Rupp, ... Journal of Inherited Metabolic Disease: Official Journal of the Society for …, 2012 | 213 | 2012 |
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Genetic testing in asymptomatic minors P Borry, G Evers-Kiebooms, MC Cornel, A Clarke, K Dierickx European Journal of Human Genetics 17 (6), 711-719, 2009 | 176 | 2009 |
Genetic educational needs and the role of genetics in primary care: a focus group study with multiple perspectives EJF Houwink, SJ van Luijk, L Henneman, C van der Vleuten, ... BMC family practice 12, 1-9, 2011 | 167 | 2011 |
Public attitudes towards genetic testing revisited: comparing opinions between 2002 and 2010 L Henneman, E Vermeulen, CG Van El, L Claassen, DRM Timmermans, ... European Journal of Human Genetics 21 (8), 793-799, 2013 | 150 | 2013 |
Population screening for genetic disorders in the 21st century: evidence, economics, and ethics SD Grosse, WH Rogowski, LF Ross, MC Cornel, WJ Dondorp, MJ Khoury Public health genomics 13 (2), 106-115, 2009 | 147 | 2009 |
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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 | 135 | 2010 |
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 | 123 | 2015 |
Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 2–From screening laboratory results to treatment, follow‐up and quality assurance P Burgard, K Rupp, M Lindner, G Haege, T Rigter, SS Weinreich, ... Journal of Inherited Metabolic Disease: Official Journal of the Society for …, 2012 | 123 | 2012 |
Towards a European consensus for reporting incidental findings during clinical NGS testing JY Hehir-Kwa, M Claustres, RJ Hastings, C van Ravenswaaij-Arts, ... European Journal of Human Genetics 23 (12), 1601-1606, 2015 | 122 | 2015 |
Recent developments in genetics and medically-assisted reproduction: from research to clinical applications JC Harper, K Aittomäki, P Borry, MC Cornel, G De Wert, W Dondorp, ... Human reproduction open 2017 (3), hox015, 2017 | 121 | 2017 |
Accuracy of family history of cancer: clinical genetic implications RH Sijmons, AE Boonstra, J Reefhuis, JM Hordijk-Hos, HEK de Walle, ... European Journal of Human Genetics 8 (3), 181-186, 2000 | 117 | 2000 |