Heidi C. Howard, Ph.D.
Affiliations: | 2004 | McGill University, Montreal, QC, Canada |
Area:
NeurogeneticsGoogle:
"Heidi Howard"Mean distance: 19.61 (cluster 28)
Parents
Sign in to add mentor| Guy A. Rouleau | grad student | 2004 | McGill | |
| (Identification of the gene responsible for peripheral neuropathy associated with agenesis of the corpus callosum.) | ||||
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Publications
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| Middleton A, Milne R, Almarri MA, et al. (2020) Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data? American Journal of Human Genetics |
| Phillips A, Niemiec E, Howard HC, et al. (2020) Communicating genetic information to family members: analysis of consent forms for diagnostic genomic sequencing. European Journal of Human Genetics : Ejhg |
| Niemiec E, Howard HC. (2020) Ethical issues related to research on genome editing in human embryos. Computational and Structural Biotechnology Journal. 18: 887-896 |
| Voigt TH, Holtz V, Niemiec E, et al. (2020) Willingness to donate genomic and other medical data: results from Germany. European Journal of Human Genetics : Ejhg |
| Kalokairinou L, Borry P, Howard HC. (2020) 'It's much more grey than black and white': clinical geneticists' views on the oversight of consumer genomics in Europe. Personalized Medicine |
| Raz AE, Niemiec E, Howard HC, et al. (2020) 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 |
| Middleton A, Milne R, Howard H, et al. (2019) 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 |
| Milne R, Morley KI, Howard H, et al. (2019) Trust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia. Human Genetics |
| Ormond KE, Bombard Y, Bonham VL, et al. (2019) The clinical application of gene editing: ethical and social issues. Personalized Medicine |
| Fellmann F, van El CG, Charron P, et al. (2019) European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death. European Journal of Human Genetics : Ejhg |