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Martina Cornel
Martina Cornel
Professor of Community Genetics & Public Health Genomics, Amsterdam University Medical Centre
Verified email at amsterdamumc.nl
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Cited by
Cited by
Year
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
5222013
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
4592015
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
3332016
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
2702000
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
2241992
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
2132006
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
2102012
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
2082021
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
1761991
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
1692009
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
1582011
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
1482013
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
1442009
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
1332010
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
1292008
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
1222012
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
1212015
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
1182015
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
1162000
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
1142017
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