Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by Crossref.
Bybjerg-Grauholm, Jonas Hagen, Christian Munch Khoo, Sok Kean Johannesen, Maria Louise Hansen, Christine Søholm Bækvad-Hansen, Marie Christiansen, Michael Hougaard, David Michael and Hollegaard, Mads V. 2017. RNA sequencing of archived neonatal dried blood spots. Molecular Genetics and Metabolism Reports, Vol. 10, Issue. , p. 33.
Pedersen, C B Bybjerg-Grauholm, J Pedersen, M G Grove, J Agerbo, E Bækvad-Hansen, M Poulsen, J B Hansen, C S McGrath, J J Als, T D Goldstein, J I Neale, B M Daly, M J Hougaard, D M Mors, O Nordentoft, M Børglum, A D Werge, T and Mortensen, P B 2018. The iPSYCH2012 case–cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders. Molecular Psychiatry, Vol. 23, Issue. 1, p. 6.
Przhilenskiy, V. I. and Vergun, A. A. 2019. The legal regulation of genomic DNA banks in the context of social, cultural and regulatory diversity. Actual Problems of Russian Law, p. 30.
Nordfalk, Francisca and Ekstrøm, Claus Thorn 2019. Newborn dried blood spot samples in Denmark: the hidden figures of secondary use and research participation. European Journal of Human Genetics, Vol. 27, Issue. 2, p. 203.
Tupasela, Aaro Snell, Karoliina and Tarkkala, Heta 2020. The Nordic data imaginary. Big Data & Society, Vol. 7, Issue. 1, p. 205395172090710.
Hartlev, Mette 2021. GDPR and Biobanking. Vol. 43, Issue. , p. 215.
Nordfalk, Francisca and Jensen, Anja 2022. Mothering a population: How Danish mothers experience newborn dried blood spot samples and their considerations about re-use of samples for research purposes. European Journal of Midwifery, Vol. 6, Issue. September, p. 1.
Martani, Andrea Egli, Sophia Mira Geneviève, Lester Darryl Elger, Bernice Simone and Wangmo, Tenzin 2022. A role-model for data policies? Qualitative study on the governance of health data in Denmark. Health Policy and Technology, Vol. 11, Issue. 4, p. 100683.
Przhilenskiy, V. I. 2023. Discussions on the Status of the Ethics Committee and Biobanking Practices in the Nordic Countries. Kutafin Law Review, Vol. 10, Issue. 3, p. 544.
Lutomski, Jennifer E. Manders, Peggy and Chandna, Arjun 2024. From opt-out to opt-in consent for secondary use of medical data and residual biomaterial: An evaluation using the RE-AIM framework. PLOS ONE, Vol. 19, Issue. 3, p. e0299430.
Przhilenskiy, Vladimir I. 2024. Philosophy, Governance and Law in the System of Social Action: Moral and Instrumental Problems of Genetic Research. RUDN Journal of Philosophy, Vol. 28, Issue. 1, p. 244.