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National clinical Genetic Networks - GENets - Establishment of expert collaborations in Denmark.
Lildballe, Dorte L; Frederiksen, Anja Lisbeth; Schönewolf-Greulich, Bitten; Brasch-Andersen, Charlotte; Lautrup, Charlotte Kvist; Karstensen, Helena Gásdal; Pedersen, Inge Søkilde; Sunde, Lone; Risom, Lotte; Rasmussen, Maria; Bertelsen, Mette; Andersen, Mette Klarskov; Rendtorff, Nanna Dahl; Gregersen, Pernille Axél; Tørring, Pernille M; Hammer-Hansen, Sophia; Boonen, Susanne E; Lindquist, Suzanne Granhøj; Hammer, Trine Bjørg; Diness, Birgitte R.
Afiliação
  • Lildballe DL; Department Molecular Medicine, Aarhus University Hospital, Aarhus, Denmark; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
  • Frederiksen AL; Department of Clinical Genetics, Aalborg University Hospital, Aalborg, Denmark; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.
  • Schönewolf-Greulich B; Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
  • Brasch-Andersen C; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark; Human Genetics, Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
  • Lautrup CK; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.
  • Karstensen HG; Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark; Department of Clinical Medicine, Copenhagen University, Copenhagen, Denmark.
  • Pedersen IS; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark; Molecular Diagnostics, Aalborg University Hospital, Aalborg, Denmark.
  • Sunde L; Department of Clinical Genetics, Aalborg University Hospital, Aalborg, Denmark; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.
  • Risom L; Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
  • Rasmussen M; Department of Clinical Genetics, Lillebaelt Hospital, University Hospital of Southern Denmark, Vejle, Denmark; Department of Regional Health Research, University of Southern Denmark, Odense M, Denmark.
  • Bertelsen M; Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
  • Andersen MK; Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
  • Rendtorff ND; Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
  • Gregersen PA; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark; Centre for Rare Diseases, Aarhus University Hospital, Aarhus, Denmark.
  • Tørring PM; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.
  • Hammer-Hansen S; Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
  • Boonen SE; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark; Department of Clinical Research, Faculty of Health Sciences, University of Southern Denmark, Odense, Denmark.
  • Lindquist SG; Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark; Department of Clinical Medicine, Copenhagen University, Copenhagen, Denmark; Neurogenetics Clinic and Research Lab, Danish Dementia Research Centre, Department of Neurology, Copenhagen University Hos
  • Hammer TB; Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark; Department of Epilepsy Genetics and Personalized Medicine. Danish Epilepsy Centre, Filadelfia, Dianalund, Denmark.
  • Diness BR; Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark; Department of Clinical Medicine, Copenhagen University, Copenhagen, Denmark. Electronic address: Birgitte.rode.diness@regionh.dk.
Eur J Med Genet ; 66(12): 104872, 2023 Dec.
Article em En | MEDLINE | ID: mdl-37967791
ABSTRACT
Genetic conditions are often familial, but not all relatives receive counseling from the same institution. It is therefore necessary to ensure consistency in variant interpretation, counseling practices, and clinical follow up across health care providers. Furthermore, as new possibilities for gene-specific treatments emerge and whole genome sequencing becomes more widely available, efficient data handling and knowledge sharing between clinical laboratory geneticists and medical specialists in clinical genetics are increasingly important. In Denmark, these needs have been addressed through the establishment of collaborative national networks called Genetic Expert Networks or "GENets". These networks have enhanced patient and family care significantly by bringing together groups of experts in national collaborations. This promotes coordinated clinical care, the dissemination of best clinical practices, and facilitates the exchange of new knowledge.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Viverridae / Redes Reguladoras de Genes Limite: Animals / Humans País/Região como assunto: Europa Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Dinamarca

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Viverridae / Redes Reguladoras de Genes Limite: Animals / Humans País/Região como assunto: Europa Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Dinamarca