| Year |
Citation |
Score |
| 2020 |
Middleton A, Milne R, Almarri MA, Anwer S, Atutornu J, Baranova EE, Bevan P, Cerezo M, Cong Y, Critchley C, Fernow J, Goodhand P, Hasan Q, Hibino A, Houeland G, ... Howard HC, et al. Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data? American Journal of Human Genetics. PMID 32946764 DOI: 10.1016/J.Ajhg.2020.08.023 |
0.389 |
|
| 2020 |
Phillips A, Niemiec E, Howard HC, Kagkelari K, Borry P, Vears DF. Communicating genetic information to family members: analysis of consent forms for diagnostic genomic sequencing. European Journal of Human Genetics : Ejhg. PMID 32341470 DOI: 10.1038/S41431-020-0627-7 |
0.33 |
|
| 2020 |
Niemiec E, Howard HC. Ethical issues related to research on genome editing in human embryos. Computational and Structural Biotechnology Journal. 18: 887-896. PMID 32322370 DOI: 10.1016/J.Csbj.2020.03.014 |
0.34 |
|
| 2020 |
Voigt TH, Holtz V, Niemiec E, Howard HC, Middleton A, Prainsack B. Willingness to donate genomic and other medical data: results from Germany. European Journal of Human Genetics : Ejhg. PMID 32238912 DOI: 10.1038/S41431-020-0611-2 |
0.359 |
|
| 2020 |
Kalokairinou L, Borry P, Howard HC. 'It's much more grey than black and white': clinical geneticists' views on the oversight of consumer genomics in Europe. Personalized Medicine. PMID 32154757 DOI: 10.2217/Pme-2019-0064 |
0.373 |
|
| 2020 |
Raz AE, Niemiec E, Howard HC, Sterckx S, Cockbain J, Prainsack B. Transparency, consent and trust in the use of customers' data by an online genetic testing company: an Exploratory survey among 23andMe users New Genetics and Society. 1-24. DOI: 10.1080/14636778.2020.1755636 |
0.376 |
|
| 2019 |
Middleton A, Milne R, Howard H, Niemiec E, Robarts L, Critchley C, Nicol D, Prainsack B, Atutornu J, Vears DF, Smith J, Steed C, Bevan P, Scott ER, Bobe J, et al. Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data. European Journal of Human Genetics : Ejhg. PMID 31784701 DOI: 10.1038/S41431-019-0550-Y |
0.397 |
|
| 2019 |
Milne R, Morley KI, Howard H, Niemiec E, Nicol D, Critchley C, Prainsack B, Vears D, Smith J, Steed C, Bevan P, Atutornu J, Farley L, Goodhand P, Thorogood A, et al. Trust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia. Human Genetics. PMID 31531740 DOI: 10.1007/S00439-019-02062-0 |
0.392 |
|
| 2019 |
Ormond KE, Bombard Y, Bonham VL, Hoffman-Andrews L, Howard H, Isasi R, Musunuru K, Riggan KA, Michie M, Allyse M. The clinical application of gene editing: ethical and social issues. Personalized Medicine. PMID 31331245 DOI: 10.2217/Pme-2018-0155 |
0.338 |
|
| 2019 |
Fellmann F, van El CG, Charron P, Michaud K, Howard HC, Boers SN, Clarke AJ, Duguet AM, Forzano F, Kauferstein S, Kayserili H, Lucassen A, Mendes Á, Patch C, Radojkovic D, et al. European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death. European Journal of Human Genetics : Ejhg. PMID 31235869 DOI: 10.1038/S41431-019-0445-Y |
0.412 |
|
| 2019 |
Kalokairinou L, Borry P, Howard HC. Attitudes and experiences of European clinical geneticists towards direct-to-consumer genetic testing: a qualitative interview study New Genetics and Society. 38: 410-429. DOI: 10.1080/14636778.2019.1677149 |
0.422 |
|
| 2018 |
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. Human germline gene editing. Recommendations of ESHG and ESHRE. Human Reproduction Open. 2018: hox025. PMID 31490463 DOI: 10.1093/Hropen/Hox025 |
0.385 |
|
| 2018 |
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. Human Reproduction Open. 2018: hox024. PMID 31490459 DOI: 10.1093/Hropen/Hox024 |
0.389 |
|
| 2018 |
Cornel MC, Howard HC, Lim D, Bonham VL, Wartiovaara K. Moving towards a cure in genetics: what is needed to bring somatic gene therapy to the clinic? European Journal of Human Genetics : Ejhg. PMID 30568241 DOI: 10.1038/S41431-018-0309-X |
0.354 |
|
| 2018 |
Middleton A, Milne R, Thorogood A, Kleiderman E, Niemiec E, Prainsack B, Farley L, Bevan P, Steed C, Smith J, Vears D, Atutornu J, Howard HC, Morley KI. Attitudes of publics who are unwilling to donate DNA data for research. European Journal of Medical Genetics. PMID 30476628 DOI: 10.1016/J.Ejmg.2018.11.014 |
0.375 |
|
| 2018 |
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, et al. Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics. European Journal of Human Genetics : Ejhg. PMID 30310124 DOI: 10.1038/S41431-018-0285-1 |
0.423 |
|
| 2018 |
Vears DF, Niemiec E, Howard HC, Borry P. Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms. European Journal of Human Genetics : Ejhg. PMID 30143804 DOI: 10.1038/S41431-018-0239-7 |
0.331 |
|
| 2018 |
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 Science International. Genetics. PMID 30030012 DOI: 10.1016/J.Fsigen.2018.07.002 |
0.331 |
|
| 2018 |
Vears DF, Niemiec E, Howard HC, Borry P. How do consent forms for diagnostic high-throughput sequencing address unsolicited and secondary findings? A content analysis. Clinical Genetics. PMID 29888485 DOI: 10.1111/Cge.13391 |
0.34 |
|
| 2018 |
Middleton A, Niemiec E, Prainsack B, Bobe J, Farley L, Steed C, Smith J, Bevan P, Bonhomme N, Kleiderman E, Thorogood A, Schickhardt C, Garattini C, Vears D, Littler K, ... ... Howard HC, et al. 'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methods. Personalized Medicine. PMID 29856292 DOI: 10.2217/Pme-2018-0032 |
0.323 |
|
| 2018 |
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 Journal of Human Genetics : Ejhg. PMID 29326429 DOI: 10.1038/S41431-017-0077-Z |
0.389 |
|
| 2018 |
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. Human germline gene editing: Recommendations of ESHG and ESHRE. European Journal of Human Genetics : Ejhg. PMID 29326428 DOI: 10.1038/S41431-017-0076-0 |
0.39 |
|
| 2017 |
Middleton A, Mendes Á, Benjamin CM, Howard HC. Direct-to-consumer genetic testing: where and how does genetic counseling fit? Personalized Medicine. 14: 249-257. PMID 29767582 DOI: 10.2217/Pme-2017-0001 |
0.432 |
|
| 2017 |
Niemiec E, Kalokairinou L, Howard HC. Current ethical and legal issues in health-related direct-to-consumer genetic testing. Personalized Medicine. 14: 433-445. PMID 29754566 DOI: 10.2217/Pme-2017-0029 |
0.429 |
|
| 2017 |
Howard HC, van El CG, Forzano F, Radojkovic D, Rial-Sebbag E, de Wert G, Borry P, Cornel MC. 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. European Journal of Human Genetics : Ejhg. PMID 29192152 DOI: 10.1038/S41431-017-0024-Z |
0.349 |
|
| 2017 |
Kalokairinou L, Howard HC, Slokenberga S, Fisher E, Flatscher-Thöni M, Hartlev M, van Hellemondt R, Juškevičius J, Kapelenska-Pregowska J, Kováč P, Lovrečić L, Nys H, de Paor A, Phillips A, Prudil L, et al. Legislation of direct-to-consumer genetic testing in Europe: a fragmented regulatory landscape. Journal of Community Genetics. PMID 29150824 DOI: 10.1007/S12687-017-0344-2 |
0.432 |
|
| 2017 |
Borry P, Bentzen HB, Budin-Ljøsne I, Cornel MC, Howard HC, Feeney O, Jackson L, Mascalzoni D, Mendes Á, Peterlin B, Riso B, Shabani M, Skirton H, Sterckx S, Vears D, et al. The challenges of the expanded availability of genomic information: an agenda-setting paper. Journal of Community Genetics. PMID 28952070 DOI: 10.1007/S12687-017-0331-7 |
0.394 |
|
| 2017 |
Howard HC, Mascalzoni D, Mabile L, Houeland G, Rial-Sebbag E, Cambon-Thomsen A. How to responsibly acknowledge research work in the era of big data and biobanks: ethical aspects of the Bioresource Research Impact Factor (BRIF). Journal of Community Genetics. PMID 28948532 DOI: 10.1007/S12687-017-0332-6 |
0.36 |
|
| 2017 |
Niemiec E, Vears DF, Borry P, Howard HC. Readability of informed consent forms for whole-exome and whole-genome sequencing. Journal of Community Genetics. PMID 28856579 DOI: 10.1007/S12687-017-0324-6 |
0.304 |
|
| 2017 |
Kalokairinou L, Borry P, Howard HC. Regulating the advertising of genetic tests in Europe: a balancing act. Journal of Medical Genetics. PMID 28735297 DOI: 10.1136/Jmedgenet-2017-104531 |
0.389 |
|
| 2017 |
Hansson MG, Bouder F, Howard HC. Genetics and risk – an exploration of conceptual approaches to genetic risk Journal of Risk Research. 21: 101-108. DOI: 10.1080/13669877.2017.1382562 |
0.312 |
|
| 2017 |
Howard HC, Iwarsson E. Mapping uncertainty in genomics Journal of Risk Research. 21: 117-128. DOI: 10.1080/13669877.2016.1215344 |
0.302 |
|
| 2016 |
Oliveri S, Howard HC, Renzi C, Hansson MG, Pravettoni G. Anxiety delivered direct-to-consumer: are we asking the right questions about the impacts of DTC genetic testing? Journal of Medical Genetics. PMID 27647845 DOI: 10.1136/Jmedgenet-2016-104184 |
0.442 |
|
| 2016 |
Niemiec E, Borry P, Pinxten W, Howard HC. Content Analysis of Informed Consent for whole Genome Sequencing Offered by Direct-to-Consumer Genetic testing Companies. Human Mutation. PMID 27647801 DOI: 10.1002/Humu.23122 |
0.402 |
|
| 2016 |
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, et al. Responsible implementation of expanded carrier screening. European Journal of Human Genetics : Ejhg. PMID 26980105 DOI: 10.1038/Ejhg.2015.271 |
0.369 |
|
| 2016 |
Borry P, Shabani M, Howard HC. Is There a Right Time to Know? The Right Not to Know and Genetic Testing in Children. The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics. 42: 19-27. PMID 26767473 DOI: 10.1111/jlme.12115 |
0.314 |
|
| 2016 |
Borry P, Shabani M, Howard HC. Is There a Right Time to Know? The Right Not to Know and Genetic Testing in Children. The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics. 42: 19-27. PMID 26767473 DOI: 10.1111/jlme.12115 |
0.314 |
|
| 2016 |
Niemiec E, Howard HC. Ethical issues in consumer genome sequencing: Use of consumers' samples and data Applied and Translational Genomics. 8: 23-30. DOI: 10.1016/J.Atg.2016.01.005 |
0.305 |
|
| 2015 |
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, et al. Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. European Journal of Human Genetics : Ejhg. PMID 25782669 DOI: 10.1038/Ejhg.2015.57 |
0.308 |
|
| 2015 |
Howard HC, Knoppers BM, Cornel MC, Wright Clayton E, Sénécal K, Borry P. Whole-genome sequencing in newborn screening? A statement on the continued importance of targeted approaches in newborn screening programmes. European Journal of Human Genetics : Ejhg. PMID 25626707 DOI: 10.1038/Ejhg.2014.289 |
0.352 |
|
| 2015 |
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, et al. Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness. European Journal of Human Genetics : Ejhg. 23: 729-35. PMID 25248395 DOI: 10.1038/Ejhg.2014.190 |
0.386 |
|
| 2015 |
Kalokairinou L, Howard HC, Borry P. Current developments in the regulation of direct-to-consumer genetic testing in Europe Medical Law International. 15: 97-123. DOI: 10.1177/0968533215618441 |
0.4 |
|
| 2014 |
Kalokairinou L, Howard HC, Borry P. Science and Regulation. Changes on the horizon for consumer genomics in the EU. Science (New York, N.Y.). 346: 296-8. PMID 25324369 DOI: 10.1126/Science.1256396 |
0.403 |
|
| 2014 |
Pinxten W, Howard HC. Ethical issues raised by whole genome sequencing. Best Practice & Research. Clinical Gastroenterology. 28: 269-79. PMID 24810188 DOI: 10.1016/J.Bpg.2014.02.004 |
0.336 |
|
| 2013 |
Su Y, Borry P, Otte IC, Howard HC. "It's our DNA, we deserve the right to test!" A content analysis of a petition for the right to access direct-to-consumer genetic testing. Personalized Medicine. 10: 729-739. PMID 29768761 DOI: 10.2217/Pme.13.69 |
0.428 |
|
| 2013 |
Colledge F, Elger B, Howard HC. A review of the barriers to sharing in biobanking. Biopreservation and Biobanking. 11: 339-46. PMID 24835363 DOI: 10.1089/Bio.2013.0039 |
0.302 |
|
| 2013 |
Howard HC, Borry P. Survey of European clinical geneticists on awareness, experiences and attitudes towards direct-to-consumer genetic testing. Genome Medicine. 5: 45. PMID 23697740 DOI: 10.1186/Gm449 |
0.414 |
|
| 2013 |
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. Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics. European Journal of Human Genetics : Ejhg. 21: 580-4. PMID 23676617 DOI: 10.1038/Ejhg.2013.46 |
0.311 |
|
| 2012 |
Howard HC, Borry P. To ban or not to ban? Clinical geneticists' views on the regulation of direct-to-consumer genetic testing. Embo Reports. 13: 791-4. PMID 22890467 DOI: 10.1038/Embor.2012.114 |
0.408 |
|
| 2012 |
Borry P, Van Hellemondt RE, Sprumont D, Jales CFD, Rial-Sebbag E, Spranger TM, Curren L, Kaye J, Nys H, Howard H. Legislation on direct-to-consumer genetic testing in seven European countries European Journal of Human Genetics. 20: 715-721. PMID 22274578 DOI: 10.1038/Ejhg.2011.278 |
0.438 |
|
| 2012 |
Howard HC, Borry P. Is there a doctor in the house? : The presence of physicians in the direct-to-consumer genetic testing context. Journal of Community Genetics. 3: 105-12. PMID 22109907 DOI: 10.1007/S12687-011-0062-0 |
0.402 |
|
| 2011 |
Howard HC, Borry P. Europe and direct-to-consumer genetic tests. Nature Reviews. Genetics. 13: 146; author reply 14. PMID 22158309 DOI: 10.1038/Nrg3073-C1 |
0.426 |
|
| 2011 |
Su Y, Howard HC, Borry P. Users' motivations to purchase direct-to-consumer genome-wide testing: an exploratory study of personal stories. Journal of Community Genetics. 2: 135-46. PMID 22109820 DOI: 10.1007/S12687-011-0048-Y |
0.407 |
|
| 2011 |
Zawati MH, Borry P, Howard HC. Closure of population biobanks and direct-to-consumer genetic testing companies. Human Genetics. 130: 425-32. PMID 21706343 DOI: 10.1007/S00439-011-1019-4 |
0.455 |
|
| 2011 |
Howard HC, Avard D, Borry P. Are the kids really all right? Direct-to-consumer genetic testing in children: are company policies clashing with professional norms? European Journal of Human Genetics : Ejhg. 19: 1122-6. PMID 21629297 DOI: 10.1038/Ejhg.2011.94 |
0.403 |
|
| 2011 |
Borry P, Henneman L, Lakeman P, ten Kate LP, Cornel MC, Howard HC. Preconceptional genetic carrier testing and the commercial offer directly-to-consumers. Human Reproduction (Oxford, England). 26: 972-7. PMID 21362685 DOI: 10.1093/Humrep/Der042 |
0.405 |
|
| 2010 |
Borry P, Cornel MC, Howard HC. Where are you going, where have you been: a recent history of the direct-to-consumer genetic testing market. Journal of Community Genetics. 1: 101-106. PMID 21475669 DOI: 10.1007/S12687-010-0023-Z |
0.368 |
|
| 2010 |
Knoppers BM, Avard D, Howard HC. Direct-to-consumer genetic testing: driving choice? Expert Review of Molecular Diagnostics. 10: 965-8. PMID 21080811 DOI: 10.1586/Erm.10.84 |
0.393 |
|
| 2010 |
Howard HC, Knoppers BM, Borry P. Blurring lines. The research activities of direct-to-consumer genetic testing companies raise questions about consumers as research subjects. Embo Reports. 11: 579-82. PMID 20634807 DOI: 10.1038/Embor.2010.105 |
0.341 |
|
| 2010 |
Borry P, Howard HC, Sénécal K, Avard D. Health-related direct-to-consumer genetic testing: a review of companies' policies with regard to genetic testing in minors. Familial Cancer. 9: 51-9. PMID 19488835 DOI: 10.1007/S10689-009-9253-9 |
0.433 |
|
| 2009 |
Howard HC, Borry P. Personal genome testing: do you know what you are buying? The American Journal of Bioethics : Ajob. 9: 11-3. PMID 19998102 DOI: 10.1080/15265160902894005 |
0.326 |
|
| 2008 |
Howard HC, Borry P. Direct-to-consumer genetic testing: more questions than benefits? Personalized Medicine. 5: 317-320. PMID 29783456 DOI: 10.2217/17410541.5.4.317 |
0.448 |
|
| 2008 |
Borry P, Howard H. DTC genetic services: A look across the pond American Journal of Bioethics. 8: 14-16. PMID 18726773 DOI: 10.1080/15265160802248252 |
0.407 |
|
| 2008 |
Howard HC, Borry P. Direct-to-consumer genetic testing: More questions than benefits? Personalized Medicine. 5: 317-320. DOI: 10.2217/17410541.5.4.317 |
0.306 |
|
| 2003 |
Dupré N, Howard HC, Mathieu J, Karpati G, Vanasse M, Bouchard JP, Carpenter S, Rouleau GA. Hereditary motor and sensory neuropathy with agenesis of the corpus callosum. Annals of Neurology. 54: 9-18. PMID 12838516 DOI: 10.1002/Ana.77777 |
0.424 |
|
| 2003 |
Howard HC, Dupré N, Mathieu J, Bouchard JP, Rouleau GA. [Severe neuropathy with agenesis of the corpus callosum]. MéDecine Sciences : M/S. 19: 414-6. PMID 12836214 DOI: 10.1051/Medsci/2003194414 |
0.353 |
|
| 2003 |
Howard HC, Dupré N, Mathieu J, Bouchard J, Rouleau GA. La neuropathie sensitivo-motrice héréditaire avec agénésie du corps calleux M S-Medecine Sciences. 19: 414-416. DOI: 10.7202/006492Ar |
0.348 |
|
| 2002 |
Howard HC, Mount DB, Rochefort D, Byun N, Dupré N, Lu J, Fan X, Song L, Rivière JB, Prévost C, Horst J, Simonati A, Lemcke B, Welch R, England R, et al. The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum. Nature Genetics. 32: 384-92. PMID 12368912 DOI: 10.1038/Ng1002 |
0.543 |
|
| 2002 |
Howard HC, Dubé MP, Prévost C, Bouchard JP, Mathieu J, Rouleau GA. Fine mapping the candidate region for peripheral neuropathy with or without agenesis of the corpus callosum in the French Canadian population. European Journal of Human Genetics : Ejhg. 10: 406-12. PMID 12107814 DOI: 10.1038/Sj.Ejhg.5200815 |
0.547 |
|
| 1998 |
Xie YG, Rochefort D, Brais B, Howard H, Han FY, Gou LP, Maciel P, The BT, Larsson C, Rouleau GA. Restriction map of a YAC and cosmid contig encompassing the oculopharyngeal muscular dystrophy candidate region on chromosome 14q11.2-q13. Genomics. 52: 201-4. PMID 9782086 DOI: 10.1006/Geno.1998.5421 |
0.559 |
|
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