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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. Among authors: howard hc. 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 newborn screening? A statement on the continued importance of targeted approaches in newborn screening programmes.
Howard HC, Knoppers BM, Cornel MC, Wright Clayton E, Sénécal K, Borry P; European Society of Human Genetics; P3G International Paediatric Platform; Human Genome Organisation; and the PHG Foundation. Howard HC, et al. Eur J Hum Genet. 2015 Dec;23(12):1593-600. doi: 10.1038/ejhg.2014.289. Epub 2015 Jan 28. Eur J Hum Genet. 2015. PMID: 25626707 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. Among authors: howard hc. 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. 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: howard hc. 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.
Responsible implementation of expanded carrier screening.
Henneman L, Borry P, Chokoshvili D, Cornel MC, van El CG, Forzano F, Hall A, Howard HC, Janssens S, Kayserili H, Lakeman P, Lucassen A, Metcalfe SA, Vidmar L, de Wert G, Dondorp WJ, Peterlin B. Henneman L, et al. Among authors: howard hc. Eur J Hum Genet. 2016 Jun;24(6):e1-e12. doi: 10.1038/ejhg.2015.271. Epub 2016 Mar 16. Eur J Hum Genet. 2016. PMID: 26980105 Free PMC article.
Human germline gene editing: Recommendations of ESHG and ESHRE.
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. de Wert G, et al. Among authors: howard hc. Eur J Hum Genet. 2018 Apr;26(4):445-449. doi: 10.1038/s41431-017-0076-0. Epub 2018 Jan 12. Eur J Hum Genet. 2018. PMID: 29326428 Free PMC article.
Responsible innovation in human germline gene editing: Background document to the recommendations of ESHG and ESHRE.
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; European Society of Human Genetics and the European Society of Human Reproduction and Embryology. De Wert G, et al. Among authors: howard hc. Eur J Hum Genet. 2018 Apr;26(4):450-470. doi: 10.1038/s41431-017-0077-z. Epub 2018 Jan 12. Eur J Hum Genet. 2018. PMID: 29326429 Free PMC article.
Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics.
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. Carrieri D, et al. Among authors: howard hc. Eur J Hum Genet. 2019 Feb;27(2):169-182. doi: 10.1038/s41431-018-0285-1. Epub 2018 Oct 11. Eur J Hum Genet. 2019. PMID: 30310124 Free PMC article.
Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness.
Severin F, Borry P, Cornel MC, Daniels N, Fellmann F, Victoria Hodgson S, Howard HC, John J, Kääriäinen H, Kayserili H, Kent A, Koerber F, Kristoffersson U, Kroese M, Lewis C, Marckmann G, Meyer P, Pfeufer A, Schmidtke J, Skirton H, Tranebjærg L, Rogowski WH; EuroGentest and ESHG/PPPC Priority Consortium. Severin F, et al. Among authors: howard hc. Eur J Hum Genet. 2015 Jun;23(6):729-35. doi: 10.1038/ejhg.2014.190. Epub 2014 Sep 24. Eur J Hum Genet. 2015. PMID: 25248395 Free PMC article.
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: howard hc. 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.
86 results