Implementing electronic informed consent in rare disease genomics.

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Title: Implementing electronic informed consent in rare disease genomics.
Authors: Ekholm K; Department of Clinical Genetics and Genomics, Karolinska University Hospital, Stockholm, Sweden.; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden., Augustinsson A; Care in High Technological Environments, Department of Health Sciences, Lund University, Lund, Sweden.; Department of Clinical Genetics, Pathology and Molecular Diagnostics, Skåne University Hospital, Lund, Sweden., Sundström J; Department of Medical Sciences, Clinical Epidemiology, Uppsala University, Uppsala, Sweden., Johansen C; MinForskning AB, Uppsala, Sweden., Storgärds M; MinForskning AB, Uppsala, Sweden., Ljöstad L; Department of Clinical Genetics and Genomics, Karolinska University Hospital, Stockholm, Sweden., Taylan F; Department of Clinical Genetics and Genomics, Karolinska University Hospital, Stockholm, Sweden.; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden., Ekblom E; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden., Juran S; Rare Diseases Sweden, National alliance for people living with rare diseases, Sundbyberg, Sweden., Ek M; Department of Clinical Genetics and Genomics, Karolinska University Hospital, Stockholm, Sweden.; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden., Malmgren CI; Department of Clinical Genetics and Genomics, Karolinska University Hospital, Stockholm, Sweden.; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden., Soller MJ; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden., Friedman M; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden., Thunström S; Department of Clinical Genetics and Genomics, Sahlgrenska University Hospital, Region Vastra Gotaland, Gothenburg, Sweden., Lovmar L; Department of Clinical Genetics and Genomics, Sahlgrenska University Hospital, Region Vastra Gotaland, Gothenburg, Sweden., Nordgren A; Department of Clinical Genetics and Genomics, Karolinska University Hospital, Stockholm, Sweden.; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.; Department of Clinical Genetics and Genomics, Sahlgrenska University Hospital, Region Vastra Gotaland, Gothenburg, Sweden.; Department of Laboratory Medicine, Institute of Biomedicine, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden., Ehrencrona H; Department of Clinical Genetics, Pathology and Molecular Diagnostics, Skåne University Hospital, Lund, Sweden. hans.ehrencrona@med.lu.se.; Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden. hans.ehrencrona@med.lu.se., Lindstrand A; Department of Clinical Genetics and Genomics, Karolinska University Hospital, Stockholm, Sweden. anna.lindstrand@ki.se.; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden. anna.lindstrand@ki.se.
Source: Scientific reports [Sci Rep] 2025 Dec 23; Vol. 15 (1), pp. 44419. Date of Electronic Publication: 2025 Dec 23.
Publication Type: Journal Article; Multicenter Study
Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:2045-2322
DOI:10.1038/s41598-025-32740-1