Whole-genome sequencing in health care CG Van El, MC Cornel, P Borry, RJ Hastings, F Fellmann, SV Hodgson, ... European Journal of Human Genetics 21 (6), 580-584, 2013 | 554 | 2013 |
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 | 483 | 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 | 356 | 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 | 275 | 2000 |
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 | 264 | 2021 |
Spectrum of neural-tube defects in 34 infants prenatally exposed to antiepileptic drugs. D Lindhout, JGE Omtzigt, MC Cornel Neurology 42 (4 Suppl 5), 111-118, 1992 | 226 | 1992 |
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 | 220 | 2012 |
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 | 219 | 2006 |
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 | 178 | 2009 |
Prevalence of neural tube defects in 20 regions of Europe and the impact of prenatal diagnosis, 1980-1986 EUROCAT Working Group Journal of Epidemiology and Community Health (1979-), 52-58, 1991 | 178 | 1991 |
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 | 172 | 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 | 158 | 2013 |
Orphanet: a European database for rare diseases SS Weinreich, R Mangon, JJ Sikkens, MEE Teeuw, MC Cornel Nederlands tijdschrift voor geneeskunde 152 (9), 518-519, 2008 | 152 | 2008 |
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 | 151 | 2009 |
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 | 139 | 2020 |
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 | 137 | 2010 |
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 | 131 | 2021 |
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 | 128 | 2015 |
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 | 124 | 2015 |
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 | 123 | 2017 |