Implementing electronic informed consent in rare disease genomics.
Saved in:
| 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 |
| FullText | Text: Availability: 0 |
|---|---|
| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 41436845 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Implementing electronic informed consent in rare disease genomics. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Ekholm+K%22">Ekholm K</searchLink>; Department of Clinical Genetics and Genomics, Karolinska University Hospital, Stockholm, Sweden.; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.<br /><searchLink fieldCode="AU" term="%22Augustinsson+A%22">Augustinsson A</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Sundström+J%22">Sundström J</searchLink>; Department of Medical Sciences, Clinical Epidemiology, Uppsala University, Uppsala, Sweden.<br /><searchLink fieldCode="AU" term="%22Johansen+C%22">Johansen C</searchLink>; MinForskning AB, Uppsala, Sweden.<br /><searchLink fieldCode="AU" term="%22Storgärds+M%22">Storgärds M</searchLink>; MinForskning AB, Uppsala, Sweden.<br /><searchLink fieldCode="AU" term="%22Ljöstad+L%22">Ljöstad L</searchLink>; Department of Clinical Genetics and Genomics, Karolinska University Hospital, Stockholm, Sweden.<br /><searchLink fieldCode="AU" term="%22Taylan+F%22">Taylan F</searchLink>; Department of Clinical Genetics and Genomics, Karolinska University Hospital, Stockholm, Sweden.; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.<br /><searchLink fieldCode="AU" term="%22Ekblom+E%22">Ekblom E</searchLink>; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.<br /><searchLink fieldCode="AU" term="%22Juran+S%22">Juran S</searchLink>; Rare Diseases Sweden, National alliance for people living with rare diseases, Sundbyberg, Sweden.<br /><searchLink fieldCode="AU" term="%22Ek+M%22">Ek M</searchLink>; Department of Clinical Genetics and Genomics, Karolinska University Hospital, Stockholm, Sweden.; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.<br /><searchLink fieldCode="AU" term="%22Malmgren+CI%22">Malmgren CI</searchLink>; Department of Clinical Genetics and Genomics, Karolinska University Hospital, Stockholm, Sweden.; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.<br /><searchLink fieldCode="AU" term="%22Soller+MJ%22">Soller MJ</searchLink>; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.<br /><searchLink fieldCode="AU" term="%22Friedman+M%22">Friedman M</searchLink>; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.<br /><searchLink fieldCode="AU" term="%22Thunström+S%22">Thunström S</searchLink>; Department of Clinical Genetics and Genomics, Sahlgrenska University Hospital, Region Vastra Gotaland, Gothenburg, Sweden.<br /><searchLink fieldCode="AU" term="%22Lovmar+L%22">Lovmar L</searchLink>; Department of Clinical Genetics and Genomics, Sahlgrenska University Hospital, Region Vastra Gotaland, Gothenburg, Sweden.<br /><searchLink fieldCode="AU" term="%22Nordgren+A%22">Nordgren A</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Ehrencrona+H%22">Ehrencrona H</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Lindstrand+A%22">Lindstrand A</searchLink>; 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. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101563288%22">Scientific reports</searchLink> [Sci Rep] 2025 Dec 23; Vol. 15 (1), pp. 44419. <i>Date of Electronic Publication: </i>2025 Dec 23. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Multicenter Study – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Nature+Publishing+Group%22">Nature Publishing Group </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101563288 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2045-2322 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2220452322%22">20452322 </searchLink><i>NLM ISO Abbreviation: </i>Sci Rep <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=41436845 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1038/s41598-025-32740-1 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 44419 Titles: – TitleFull: Implementing electronic informed consent in rare disease genomics. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Ekholm K – PersonEntity: Name: NameFull: Augustinsson A – PersonEntity: Name: NameFull: Sundström J – PersonEntity: Name: NameFull: Johansen C – PersonEntity: Name: NameFull: Storgärds M – PersonEntity: Name: NameFull: Ljöstad L – PersonEntity: Name: NameFull: Taylan F – PersonEntity: Name: NameFull: Ekblom E – PersonEntity: Name: NameFull: Juran S – PersonEntity: Name: NameFull: Ek M – PersonEntity: Name: NameFull: Malmgren CI – PersonEntity: Name: NameFull: Soller MJ – PersonEntity: Name: NameFull: Friedman M – PersonEntity: Name: NameFull: Thunström S – PersonEntity: Name: NameFull: Lovmar L – PersonEntity: Name: NameFull: Nordgren A – PersonEntity: Name: NameFull: Ehrencrona H – PersonEntity: Name: NameFull: Lindstrand A IsPartOfRelationships: – BibEntity: Dates: – D: 23 M: 12 Text: 2025 Dec 23 Type: published Y: 2025 Identifiers: – Type: issn-electronic Value: 2045-2322 Numbering: – Type: volume Value: 15 – Type: issue Value: 1 Titles: – TitleFull: Scientific reports Type: main |
| ResultId | 1 |