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Page 1
Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice.
Forzano F, Antonova O, Clarke A, de Wert G, Hentze S, Jamshidi Y, Moreau Y, Perola M, Prokopenko I, Read A, Reymond A, Stefansdottir V, van El C, Genuardi M; Executive Committee of the European Society of Human Genetics; Public and Professional Policy Committee of the European Society of Human Genetics. Forzano F, et al. Among authors: van el c. Eur J Hum Genet. 2022 May;30(5):628. doi: 10.1038/s41431-022-01067-0. Eur J Hum Genet. 2022. PMID: 35283483 Free PMC article. No abstract available.
Italian appeal court: a genetic predisposition to commit murder?
Forzano F, Borry P, Cambon-Thomsen A, Hodgson SV, Tibben A, de Vries P, van El C, Cornel M. Forzano F, et al. Among authors: van el c. Eur J Hum Genet. 2010 May;18(5):519-21. doi: 10.1038/ejhg.2010.31. Epub 2010 Mar 10. Eur J Hum Genet. 2010. PMID: 20216573 Free PMC article.
Genetic testing and common disorders in a public health framework.
van El CG, Cornel MC; ESHG Public and Professional Policy Committee. van El CG, et al. Eur J Hum Genet. 2011 Apr;19(4):377-81. doi: 10.1038/ejhg.2010.176. Epub 2011 Jan 26. Eur J Hum Genet. 2011. PMID: 21267009 Free PMC article. No abstract available.
Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disorders.
Becker F, van El CG, Ibarreta D, Zika E, Hogarth S, Borry P, Cambon-Thomsen A, Cassiman JJ, Evers-Kiebooms G, Hodgson S, Janssens AC, 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. Becker F, et al. Among authors: van el cg, van langen im. Eur J Hum Genet. 2011 Apr;19 Suppl 1(Suppl 1):S6-44. doi: 10.1038/ejhg.2010.249. Eur J Hum Genet. 2011. PMID: 21412252 Free PMC article. Review. No abstract available.
The changing landscape of genetic testing and its impact on clinical and laboratory services and research in Europe.
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. Hastings R, et al. Among authors: van el cg. Eur J Hum Genet. 2012 Sep;20(9):911-6. doi: 10.1038/ejhg.2012.56. Epub 2012 Mar 28. Eur J Hum Genet. 2012. PMID: 22453292 Free PMC article.
Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.
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 GM; ESHG Public and Professional Policy Committee. van El CG, et al. Eur J Hum Genet. 2013 Jun;21(6):580-4. doi: 10.1038/ejhg.2013.46. Eur J Hum Genet. 2013. PMID: 23676617 Free PMC article. No abstract available.
Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.
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 GM; ESHG Public and Professional Policy Committee. van El CG, et al. Eur J Hum Genet. 2013 Jun;21 Suppl 1(Suppl 1):S1-5. Eur J Hum Genet. 2013. PMID: 23819146 Free PMC article. No abstract available.
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.
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; European Society of Human Genetics; American Society of Human Genetics. Dondorp W, et al. Among authors: van el cg. Eur J Hum Genet. 2015 Nov;23(11):1438-50. doi: 10.1038/ejhg.2015.57. Epub 2015 Mar 18. Eur J Hum Genet. 2015. PMID: 25782669 Free PMC article.
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations.
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. Dondorp W, et al. Among authors: van el cg. Eur J Hum Genet. 2015 Apr 1. doi: 10.1038/ejhg.2015.56. Online ahead of print. Eur J Hum Genet. 2015. PMID: 25828867 Free article. No abstract available.
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