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Expectations, needs and mid-term outcomes in people accessing to secondary findings from ES: 1st French mixed study (FIND Study).

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Title: Expectations, needs and mid-term outcomes in people accessing to secondary findings from ES: 1st French mixed study (FIND Study).
Authors: Viora-Dupont E; FHU TRANSLAD, GAD INSERM UMR 1231, University of Burgundy, Dijon, France. eleonore.viora-dupont@chu-dijon.fr.; Genetics Department, Reference Center for Developmental Disorders, University Hospital, Dijon, France. eleonore.viora-dupont@chu-dijon.fr., Robert F; Genetics Department, Reference Center for Developmental Disorders, HCL, Bron, France.; Clinical Psychology Lab., Psychopathology, Psychoanalysis (EA4056, ED 261), University of Paris, Sorbonne Paris City, Paris, France., Chassagne A; FHU TRANSLAD, GAD INSERM UMR 1231, University of Burgundy, Dijon, France.; Laboratory of Sociology and Anthropology (LaSA, EA3189), University of Burgundy-Franche-Comté, Besançon, France., Pélissier A; FHU TRANSLAD, GAD INSERM UMR 1231, University of Burgundy, Dijon, France.; Laboratory of economy (LEDi), University of Burgundy, Dijon, France., Staraci S; Genetics Department, Reference Center for Hereditary Cardiac Disorders, GH APHP, Paris, France., Sanlaville D; Genetics Department, Reference Center for Developmental Disorders, HCL, Bron, France.; Univ Lyon, Univ Lyon 1, CNRS, INSERM, Physiopathologie et Génétique du Neurone et du Muscle, UMR5261, U1315, Institut NeuroMyoGène, 69008, Lyon, France., Edery P; Genetics Department, Reference Center for Developmental Disorders, HCL, Bron, France.; INSERM U1028, CNRS UMR5292, CRNL, GENDEV Team, University of Claude Bernard Lyon 1, Bron, France., Lesca G; Genetics Department, Reference Center for Developmental Disorders, HCL, Bron, France.; Univ Lyon, Univ Lyon 1, CNRS, INSERM, Physiopathologie et Génétique du Neurone et du Muscle, UMR5261, U1315, Institut NeuroMyoGène, 69008, Lyon, France., Putoux A; Genetics Department, Reference Center for Developmental Disorders, HCL, Bron, France.; INSERM U1028, CNRS UMR5292, CRNL, GENDEV Team, University of Claude Bernard Lyon 1, Bron, France., Pons L; Genetics Department, Reference Center for Developmental Disorders, HCL, Bron, France., Cadenes A; Genetics Department, Reference Center for Developmental Disorders, HCL, Bron, France., Baurand A; Genetics Department, Reference Center for Developmental Disorders, University Hospital, Dijon, France., Sawka C; Genetics Department, Reference Center for Developmental Disorders, University Hospital, Dijon, France., Bertolone G; Genetics Department, Reference Center for Developmental Disorders, University Hospital, Dijon, France., Spetchian M; Genetics Department, Reference Center for Developmental Disorders, GH APHP, Paris, France., Yousfi M; Genetics Department, Reference Center for Developmental Disorders, University Hospital, Dijon, France., Salvi D; Laboratory of economy (LEDi), University of Burgundy, Dijon, France., Gautier E; Genetics Department, Reference Center for Developmental Disorders, University Hospital, Dijon, France., Vitobello A; FHU TRANSLAD, GAD INSERM UMR 1231, University of Burgundy, Dijon, France., Denommé-Pichon AS; FHU TRANSLAD, GAD INSERM UMR 1231, University of Burgundy, Dijon, France., Bruel AL; FHU TRANSLAD, GAD INSERM UMR 1231, University of Burgundy, Dijon, France., Tran Mau-Them F; FHU TRANSLAD, GAD INSERM UMR 1231, University of Burgundy, Dijon, France., Faudet A; Genetics Department, Reference Center for Developmental Disorders, GH APHP, Paris, France., Keren B; Genetics Department, Reference Center for Developmental Disorders, GH APHP, Paris, France., Labalme A; Genetics Department, Reference Center for Developmental Disorders, HCL, Bron, France., Chatron N; Genetics Department, Reference Center for Developmental Disorders, HCL, Bron, France.; Univ Lyon, Univ Lyon 1, CNRS, INSERM, Physiopathologie et Génétique du Neurone et du Muscle, UMR5261, U1315, Institut NeuroMyoGène, 69008, Lyon, France., Abel C; Genetics Department, Reference Center for Developmental Disorders, HCL, Bron, France., Dupuis-Girod S; Genetics Department, Reference Center for Developmental Disorders, HCL, Bron, France., Poisson A; Reference Center for Rare Disorders with psychiatric expression C.H. Le Vinatier, Bron, France.; Equipe de recherche AESIO santé, unité de Sant Etienne, Clinique médico chirurgicale mutualiste, Saint Etienne, France., Buratti J; Genetics Department, Reference Center for Developmental Disorders, GH APHP, Paris, France., Mignot C; Genetics Department, Reference Center for Developmental Disorders, GH APHP, Paris, France., Afenjar A; Genetics Department, Reference Center for Developmental Disorders, GH APHP, Paris, France., Whalen S; Genetics Department, Reference Center for Developmental Disorders, GH APHP, Paris, France., Charles P; Genetics Department, Reference Center for Developmental Disorders, GH APHP, Paris, France., Heide S; Genetics Department, Reference Center for Developmental Disorders, GH APHP, Paris, France., Mouthon L; Genetics Department, Reference Center for Developmental Disorders, GH APHP, Paris, France., Moutton S; Genetics Department, Reference Center for Developmental Disorders, University Hospital, Dijon, France., Sorlin A; Genetics Department, Reference Center for Developmental Disorders, University Hospital, Dijon, France., Nambot S; Genetics Department, Reference Center for Developmental Disorders, University Hospital, Dijon, France., Briffaut AS; FHU TRANSLAD, GAD INSERM UMR 1231, University of Burgundy, Dijon, France.; CHU Dijon Bourgogne, INSERM, Université de Bourgogne, CIC 1432, Module Épidémiologie Clinique, Dijon, France., Asensio ML; CHU Dijon Bourgogne, INSERM, Université de Bourgogne, CIC 1432, Module Épidémiologie Clinique, Dijon, France., Philippe C; FHU TRANSLAD, GAD INSERM UMR 1231, University of Burgundy, Dijon, France., Thauvin-Robinet C; FHU TRANSLAD, GAD INSERM UMR 1231, University of Burgundy, Dijon, France.; Genetics Department, Reference Center for Intellectual Disabilities, University Hospital, Dijon, France., Héron D; Genetics Department, Reference Center for Developmental Disorders, GH APHP, Paris, France., Rossi M; Genetics Department, Reference Center for Developmental Disorders, HCL, Bron, France.; INSERM U1028, CNRS UMR5292, CRNL, GENDEV Team, University of Claude Bernard Lyon 1, Bron, France., Meunier-Bellard N; FHU TRANSLAD, GAD INSERM UMR 1231, University of Burgundy, Dijon, France.; CHU Dijon Bourgogne, INSERM, Université de Bourgogne, CIC 1432, Module Épidémiologie Clinique, Dijon, France., Gargiulo M; Clinical Psychology Lab., Psychopathology, Psychoanalysis (EA4056, ED 261), University of Paris, Sorbonne Paris City, Paris, France.; Institute of myology, GH APHP, Paris, France., Peyron C; FHU TRANSLAD, GAD INSERM UMR 1231, University of Burgundy, Dijon, France.; Laboratory of economy (LEDi), University of Burgundy, Dijon, France., Binquet C; FHU TRANSLAD, GAD INSERM UMR 1231, University of Burgundy, Dijon, France.; CHU Dijon Bourgogne, INSERM, Université de Bourgogne, CIC 1432, Module Épidémiologie Clinique, Dijon, France., Faivre L; FHU TRANSLAD, GAD INSERM UMR 1231, University of Burgundy, Dijon, France. laurence.faivre@chu-dijon.fr.; Genetics Department, Reference Center for Developmental Disorders, University Hospital, Dijon, France. laurence.faivre@chu-dijon.fr.
Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2024 Sep; Vol. 32 (9), pp. 1166-1183. Date of Electronic Publication: 2024 May 27.
Publication Type: Journal Article; Multicenter Study
Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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PubType: Academic Journal
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  Data: Expectations, needs and mid-term outcomes in people accessing to secondary findings from ES: 1st French mixed study (FIND Study).
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  Data: <searchLink fieldCode="AU" term="%22Viora-Dupont+E%22">Viora-Dupont E</searchLink>; FHU TRANSLAD, GAD INSERM UMR 1231, University of Burgundy, Dijon, France. eleonore.viora-dupont@chu-dijon.fr.; Genetics Department, Reference Center for Developmental Disorders, University Hospital, Dijon, France. eleonore.viora-dupont@chu-dijon.fr.<br /><searchLink fieldCode="AU" term="%22Robert+F%22">Robert F</searchLink>; Genetics Department, Reference Center for Developmental Disorders, HCL, Bron, France.; Clinical Psychology Lab., Psychopathology, Psychoanalysis (EA4056, ED 261), University of Paris, Sorbonne Paris City, Paris, France.<br /><searchLink fieldCode="AU" term="%22Chassagne+A%22">Chassagne A</searchLink>; FHU TRANSLAD, GAD INSERM UMR 1231, University of Burgundy, Dijon, France.; Laboratory of Sociology and Anthropology (LaSA, EA3189), University of Burgundy-Franche-Comté, Besançon, France.<br /><searchLink fieldCode="AU" term="%22Pélissier+A%22">Pélissier A</searchLink>; FHU TRANSLAD, GAD INSERM UMR 1231, University of Burgundy, Dijon, France.; 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Genetics Department, Reference Center for Developmental Disorders, HCL, Bron, France.; INSERM U1028, CNRS UMR5292, CRNL, GENDEV Team, University of Claude Bernard Lyon 1, Bron, France.<br /><searchLink fieldCode="AU" term="%22Pons+L%22">Pons L</searchLink>; Genetics Department, Reference Center for Developmental Disorders, HCL, Bron, France.<br /><searchLink fieldCode="AU" term="%22Cadenes+A%22">Cadenes A</searchLink>; Genetics Department, Reference Center for Developmental Disorders, HCL, Bron, France.<br /><searchLink fieldCode="AU" term="%22Baurand+A%22">Baurand A</searchLink>; Genetics Department, Reference Center for Developmental Disorders, University Hospital, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Sawka+C%22">Sawka C</searchLink>; Genetics Department, Reference Center for Developmental Disorders, University Hospital, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Bertolone+G%22">Bertolone G</searchLink>; Genetics Department, Reference Center for Developmental Disorders, University Hospital, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Spetchian+M%22">Spetchian M</searchLink>; 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            NameFull: Asensio ML
      – PersonEntity:
          Name:
            NameFull: Philippe C
      – PersonEntity:
          Name:
            NameFull: Thauvin-Robinet C
      – PersonEntity:
          Name:
            NameFull: Héron D
      – PersonEntity:
          Name:
            NameFull: Rossi M
      – PersonEntity:
          Name:
            NameFull: Meunier-Bellard N
      – PersonEntity:
          Name:
            NameFull: Gargiulo M
      – PersonEntity:
          Name:
            NameFull: Peyron C
      – PersonEntity:
          Name:
            NameFull: Binquet C
      – PersonEntity:
          Name:
            NameFull: Faivre L
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 09
              Text: 2024 Sep
              Type: published
              Y: 2024
          Identifiers:
            – Type: issn-electronic
              Value: 1476-5438
          Numbering:
            – Type: volume
              Value: 32
            – Type: issue
              Value: 9
          Titles:
            – TitleFull: European journal of human genetics : EJHG
              Type: main
ResultId 1