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Martina Cornel
Martina Cornel
Professor of Community Genetics & Public Health Genomics, Amsterdam University Medical Centre
在 amsterdamumc.nl 的电子邮件经过验证
标题
引用次数
引用次数
年份
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
4812013
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
4322015
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
3082016
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
2642000
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
2201992
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
2042006
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
1972012
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
1711991
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
1612009
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
1552021
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
1542011
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
1422009
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
1362013
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
1282010
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
1162012
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
1132000
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
1122015
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
1102008
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
1092015
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
1072017
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