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Publications

Articles:

Goodarzi B, Holten L, Van El C, De Vries R, Franx A & Houwaart E, Risk and the politics of boundary work: preserving autonomous midwifery in the Netherlands. Health, Risk & Society 2018;20:379-407.

Van El CG, Baccolini V, Piko P, Cornel MC. Stakeholder Views on Active Cascade Screening for Familial Hypercholesterolemia. Healthcare 2018;6:108.

Carrieri D, Howard HC, Benjamin C, Clarke AJ, Dheensa S, Doheny S, Hawkins N, Halbersma-Konings TF, Jackson L, Kayserili H, Kelly SE, Lucassen AM, Mendes Á, Rial-Sebbag E, Stefánsdóttir V, Turnpenny PD, van El CG, van Langen IM, Cornel MC, Forzano F; European Society of Human Genetics.Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics. Eur J Hum Genet. 2018 Oct 11. doi: 10.1038/s41431-018-0285-1. [Epub ahead of print]

Samuel G, Howard HC, Cornel M, van El C, Hall A, Forzano F, Prainsack B. A response to the forensic genetics policy initiative's report "Establishing Best Practice for Forensic DNA Databases". Forensic Sci Int Genet. 2018 Sep;36:e19-e21. doi: 10.1016/j.fsigen.2018.07.002. Epub 2018 Jul 5.

Sirchia F, Carrieri D, Dheensa S, Benjamin C, Kayserili H, Cordier C, van El CG, Turnpenny PD, Melegh B, Mendes Á, Halbersma-Konings TF, van Langen IM, Lucassen AM, Clarke AJ, Forzano F, Kelly SE. Recontacting or not recontacting? A survey of current practices in clinical genetics centres in Europe. Eur J Hum Genet. 2018 Jul;26(7):946-954. doi: 10.1038/s41431-018-0131-5. Epub 2018 Apr 23.

de Wert G, Pennings G, Clarke A, Eichenlaub-Ritter U, van El CG, Forzano F, Goddijn M, Heindryckx B, Howard HC, Radojkovic D, Rial-Sebbag E, Tarlatzis BC, Cornel MC; European Society of Human Genetics and the European Society of Human Reproduction and Embryology. Human germline gene editing: Recommendations of ESHG and ESHRE. Eur J Hum Genet. 2018 Jan 12. doi: 10.1038/s41431-017-0076-0. [Epub ahead of print]

De Wert G, Heindryckx B, Pennings G, Clarke A, Eichenlaub-Ritter U, van El CG, Forzano F, Goddijn M, Howard HC, Radojkovic D, Rial-Sebbag E, Dondorp W, Tarlatzis BC, Cornel MC; Responsible innovation in human germline gene editing: Background document to the recommendations of ESHG and ESHRE. European Society of Human Genetics and the European Society of Human Reproduction and Embryology. Eur J Hum Genet. 2018 Jan 12. doi: 10.1038/s41431-017-0077-z. [Epub ahead of print]

Howard HC, van El CG, Forzano F, Radojkovic D, Rial-Sebbag E, de Wert G, Borry P, Cornel MC; Public and Professional Policy Committee of the European Society of Human Genetics. 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. Eur J Hum Genet. 2018 Jan;26(1):1-11. doi: 10.1038/s41431-017-0024-z. Epub 2017 Nov 30

Van Schendel RV, van El CG, Pajkrt E, Henneman L, Cornel MC.Implementing non-invasive prenatal testing for aneuploidy in a national healthcare system: global challenges and national solutions. BMC Health Serv Res. 2017 Sep 19;17(1):670. doi: 10.1186/s12913-017-2618-0

Cornel MC, van El CG. Barriers and Facilitating Factors for Implementation of Genetic Services: A Public Health Perspective. Frontiers in Public Health 2017;5:195.PDF

Aalfs CM, Westermann AM, van El CG.[Making better use of the clinical geneticist's expertise; treating physician could request a DNA test for most cancer patients].Ned Tijdschr Geneeskd. 2017;161(0):D1525. (article in Dutch).

Henneman L, Borry P, Chokoshvili D, Cornel MC, van El CG, Forzano F, Hall A, Howard H, Janssens S, Kayserili H, Lakeman P, Lucassen A, Metcalfe SA, Vidmar L, de Wert G, Dondorp WJ, Peterlin B on behalf of the European Society of Human Genetics (ESHG). Responsible implementation of expanded carrier screening. Eur J Hum Genet 2016; doi:10.1038/ejhg.2015.271. PDF

Ter Harmsel JF, Molendijk TM, van El CG, M’Charek A, Kempes M, Rinne T, Pieters T. Rapportages pro Justitia van het Nederlands Instituut voor Forensische Psychiatrie en Psychologie in retrospectief; toepassingen van genetische en neurowetenschappelijke inzichten, in 2000 en 2009. [Forensic assessments from the Netherlands Institute of Forensic Psychiatry and Psychology in retrospect; applications of genetics and neuroscience, in 2000 and 2009].Tijdschrift voor Psychiatrie 2016;58:20-29 (article in Dutch).
http://www.tijdschriftvoorpsychiatrie.nl/assets/articles/58-2016-1-artikel-terharmsel.pdf

van Teeffelen SR, Douglas DMW, Van El CG, Weinreich SS, Henneman L, Radstake M, Cornel MC. Mothers' views on longer storage of neonatal dried blood spots for specific secondary uses. Public Health Genomics 2016;19:25-33. PDF

Dondorp W, De Wert G, Bombard Y, Bianchi DW, Bergmann C, Borry P, Chitty LS, Fellmann F, Forzano F, Hall A, Henneman L, Howard HC, Lucassen A, Ormond K, Peterlin B, Radojkovic D, Rogowski W, Soller M, Tibben A, Tranebjærg L, Van El CG, Cornel MC, on behalf of the European Society of Human Genetics (ESHG) and the American Society of Human Genetics (ASHG). Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Eur J Hum Genet advance online publication, March 18, 2015; doi:10.1038/ejhg.2015.57 

Dondorp W, de Wert G, Bombard Y, Bianchi DW, Bergmann C, Borry P, Chitty LS, Fellmann F, Forzano F, Hall A, Henneman L, Howard HC, Lucassen A, Ormond K, Peterlin B, Radojkovic D, Rogowski W, Soller M, Tibben A, Tranebjærg L, van El CG, Cornel MC. Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations. Eur J Hum Genet. advanced online publication, 1 April 2015; doi:10.1038/ejhg.2015.56

Horstkoetter D, Van El CG, Rinne T, De Wert GMWR, Pieters T. Forensische psychologie, neurobiologie en preventie: kritische reflectie op nieuwe ontwikkelingen. 
http://www.boomlemmatijdschriften.nl/tijdschrift/tijdschriftcriminologie/2015/1/TvC_0165-182X_2015_057_001_005, Aflevering 1 2015 (Article in Dutch).

Vermeulen E, Henneman L, van El CG, Cornel MC. Public attitudes towards preventive genomics and personal interest in genetic testing to prevent disease: a survey study. Eur J Public Health 2014; 24:768-75.

Van der Gronde T, Kempes M, Van El CG, Rinne T, Pieters T. Neurobiological correlates in forensic assessment: a systematic review. PLOS One, 2014.

Van El CG, Rigter T, Reuser AJJ, Van der Ploeg AT, Weinreich SS, Cornel MC. Newborn screening for Pompe disease? A qualitative study exploring professional views. BMC Pediatrics 2014;14:203.

Horstkoetter D, Van EL CG, Kempes M, Egger J, Rinne T, Pieters T, De Wert G de. Neuroimaging in the courtroom: Normative Frameworks and Consensual Practices. AJOB Neuroscience 2014;5(2):37-39.

Dondorp WJ, Van El CG, De Wert GMWR, Cornel MC. Raw Data: Research and Health Care Goals Differ. Science  2014;343:968-969. Letter to the editor.

Van El CG, Dondorp WJ, De Wert GMWR, Cornel MC. Call for prudence in whole genome testing. Science 2013;341:958-959. Letter to the Editor. PDF

Van El CG, Cornel MC, Borry P, Hastings RJ, Fellmann F, Hodgson SV, Howard HC, Cambon-Thomsen A, Knoppers BM, Meijers-Heijboer H, Scheffer H, Tranebjaerg L, Dondorp W, de Wert GMWR. Whole-genome sequencing in health careEur J Hum Genet. 2013 Jun;21(6):580-4. doi: 10.1038/ejhg.2013.46. 

Henneman L, El CG van, Cornel MC. Editorial. Genetic testing and implications for personalized medicine: changes in public and healthcare professional perspectives. Personalized medicine 2013;10( 3): 217-219 , DOI 10.2217/pme.13.21.

SMPJ Jans, Henneman L, De Jonge A, Van El, CG, Van Tuyl, H. A morass of considerations: exploring attitudes towards ethnicity-based haemoglobinopathy-carrier screening in primary care. Family Practice. Advance Access 29 April 2013. doi:10.1093/fampra/cmt019 http://www.ncbi.nlm.nih.gov/pubmed/23629736

Henneman L, Vermeulen E, El CG van, Claassen L, Timmermans DRM, Cornel MC. Public attitudes towards genetic testing revisited: comparing opinions between 2002 and 2010. Eur J Hum Genet.  2013;21:793-9. PDF

Cornel MC, van El CG, Borry P. The challenge of implementing genetic tests with clinical utility while avoiding unsound applications.J Community Genet. DOI 10.1007/s12687-012-0121-1 http://www.springerlink.com/content/t2448750x60281q7/fulltext.pdf

Van El CG, Pieters T, Cornel M. Genetic screening and democracy: lessons from debating genetic screening criteria in the Netherlands. J Community Genet. 2012 Apr;3(2):79-89. Free PMC Article

Cornel MC, van El CG, Dondorp WJ. The promises of genomic screening: building a governance infrastructure. Special issue: genetics and democracy. J Community Genetics 2012;3(2):73-7.  PDF

Douglas CM, van El CG, Faulkner A, Cornel MC. Governing biological material at the intersection of care and research: the use of dried blood spots for biobanking. Croat Med J. 2012;53:390-7. PDF

Douglas C, van El C, Radstake M, van Teeffelen S, Cornel MC. The politics of representation in the governance of emergent ‘secondary use’ biobanks: The case of dried blood spot cards in The Netherlands. Studies in Ethics, Law, and Technology 2012. Vol. 6: Iss. 1, Article 4. DOI: 10.1515/1941-6008.1178 PDF

Hens K, Van El CG, Borry P, Cambon-Thomsen A, Cornel MC, Forzano F, Lucassen A, Patch C, Tranebjaerg L, Vermeulen E, Salvaterra E, Tibben A, Dierickx K. Developing a policy for paediatric biobanks: principles for good practice. Eur J Hum Genet. 2012 Jun 20. doi: 10.1038/ejhg.2012.99. PDF

Jans SM, van El CG, Houwaart ES, Westerman MJ, Janssens RJ, Lagro-Janssen AL, Plass AM, Cornel MC. A case study of haemoglobinopathy screening in the Netherlands: witnessing the past, lessons for the future. Ethn Health. 2012 Jun;17(3):217-39. Free PMC Article

Rigter T, Weinreich SS, van El CG, de Vries JM, van Gelder CM, Güngör D, Reuser AJJ, Hagemans MLC, Cornel MC, van der Ploeg AT. Severely impaired health status at diagnosis of Pompe disease: A crosssectional analysis to explore the potential utility of neonatal screening, Molecular Genetics and Metabolism (2012), doi: 10.1016/j.ymgme.2012.09.017 PDF

Weinreich SS, Rigter T, van El CG, Dondorp WJ, Kostense PJ, van der Ploeg AT, Reuser AJ, Cornel MC, Hagemans ML.Orphanet J Rare Dis. 2012 Mar 14;7:15. Free PMC Article

Hastings R, de Wert G, Fowler B, Krawczak M, Vermeulen E, Bakker E, Borry P, Dondorp W, Nijsingh N, Barton D, Schmidtke J, van El CG, Vermeesch J, Stol Y, Carmen Howard H, Cornel MC. The changing landscape of genetic testing and its impact on clinical and laboratory services and research in Europe. Eur J Hum Genet. 2012;20:911-6. PDF

Van El CG, Cornel MC on behalf of the ESHG Public and Professional Policy Committee. Genetic testing and common disorders in a public health framework. Recommendations of the European Society of Human Genetics. Eur J Hum Genet 2011;19:377-81. PDF

Becker F, van El CG, Ibarreta D, Zika E, Hogarth S, Borry P, Cambon-Thomsen A, Cassiman JJ, Evers-Kiebooms G, Hodgson S, Janssens ACJW, Kaariainen H, Krawczak M, Kristoffersson U, Lubinski J, Patch C, Penchaszadeh VB, Read A, Rogowski W, Sequeiros J, Tranebjaerg L, van Langen IM, Wallace H, Zimmern R, Schmidtke J, Cornel MC. Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Eur J Hum Genet 2011;19:S6-S44. PDF

Plass AMC, Van EL CG, Pieters T, Cornel MC. Neonatal screening for treatable and untreatable disorders: Prospective parents’ opinion in the Netherlands. Pediatrics 2010.

Forzano F, Borry P, Cambon-Thomsen A, Hodgson SV, Tibben A, de Vries P, van El C, Cornel M. Italian appeal court: A genetic predisposition to commit murder? Eur J Hum Genet 2010; 18:519-21. PDF

Krijgsman L, Van El CG, Ten Horn MH, Pieters T, Cornel MC. Genetische screening: het perspectief van de potentiële gebruiker – een verkennend kwalitatief onderzoek. TSG 2008;86(4):189-197.

Van El CG, Krijgsman L, Pieters T, Cornel MC. Genetische screening en preventie van erfelijke en aangeboren aandoeningen: een problematische combinatie. Tijdschrift voor Gezondheidszorg en Ethiek 2007;17(4):105-111.

Cornel MC, Van El CG, Krijgsman L, Pieters. Bied ouders de keus. Medisch Contact 2007;62(23):1003.

 

Books:

Loeber JG, Van El CG. Veertig jaar hielprikscreening in Nederland. [Forty years heel prick screening in the Netherlands]. Uitgeverij Prelum, Houten, 2014. 
English translation: MDPI 2016  https://www.bol.com/nl/p/forty-years-of-heel-prick-screening-in-the-netherlands/9200000058525321/?suggestionType=typedsearchEnglish

Van El CG, Cornel MC, Pieters T, Houwaart ES (redactie). Witness seminar. Debatteren over genetische screeningscriteria. [Debating genetic screening criteria]. Uitgeverij Prelum, Houten, 2010. 

Book chapter:

De Vries M en Van El C, Zorg rond de geboorte, in: Pieters T. en Widdershoven G., Basisboek Filosofie en Geschiedenis van de Gezondheidszorg, Amsterdam: Boom, pp.45-67. 

Van El CG, Henneman L, Cell-free DNA-based Noninvasive Prenatal Testing and Society, in: Page-Christiaens L, and Klein HG, Noninvasive Prenatal Testing (NIPT). London: Elsevier Academic Press, 2018, pp. 235-250.

Van El CG, Pieters T, Cornel MC. The changing focus of screening criteria in the age of Genomics: A brief history from the Netherlands. In: Assessing Life: on the organisation of genetic testing. Wieser, Bernhard; Berger, Wilhelm (eds.). Science and Technology Studies Vol. 59, München/Wien: Profil, 2010. pp 203-224. ISBN 978-3-89019-643-5.

Van El CG and Henneman L. Cell-free DNA based NIPT and Society. In: Noninvasive Prenatal Testing (NIPT) Applied Genomics in Prenatal Screening and Diagnosis. Page-Christiaens L, and  Klein H-G (eds). eBook ISBN: 9780128141908. Academic Press, London: Elsevier, 2018.