PERIGENOMED-CLINICS 1—the first study on feasibility, acceptability and psychosocial impact of PERIGENOMED: a pilot project aimed at providing initial concrete evidence on the relevance of panel-based genome sequencing for newborn screening (NBS) in

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Publication Details

Journal
BMJ Open
Published
2025-10-01
DOI
https://doi.org/10.1136/bmjopen-2025-105752
Citations
2
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
3.63

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article

PERIGENOMED-CLINICS 1—the first study on feasibility, acceptability and psychosocial impact of PERIGENOMED: a pilot project aimed at providing initial concrete evidence on the relevance of panel-based genome sequencing for newborn screening (NBS) in

Caroline Racine, Amir Hassine, Juliette Piard, Emmanuel G. Simon et al.
2 citations
BMJ Open
Genomics and Rare Diseases
3.63
article

PERIGENOMED-CLINICS 1—the first study on feasibility, acceptability and psychosocial impact of PERIGENOMED: a pilot project aimed at providing initial concrete evidence on the relevance of panel-based genome sequencing for newborn screening (NBS) in

Caroline Racine, Amir Hassine, Juliette Piard, Emmanuel G. Simon, Christian Renaud, Paul Rollier, Marie de Tayrac, Frédéric Tran Mau‐Them, David Cheillan, Paul Kuentz, Laurence Olivier Faivre, Catherine Lejeune, Amandine Charreton, Laurent Pasquier, Julien Barc, Estelle Colin, Hana Safraou, Christine Binquet, Richard Redon, B. Chabrol, Anne‐Sophie Jannot, Virginie Loizeau, Catherine Cormier, Dominique Salvi, Emeline Davoine, Alban Ziegler, Maud Carpentier, Céline Bris, Frédéric Huet, Sylvie Odent, Nicolas Mottet, Sébastien Schmitt, Stéphane Bezieau, Martin Chevarin, Marlène Malbos, Camille Level, Léa Gaudillat, Mathilde Nizon, Ange-Line Bruel, Émilie Tisserant, M. Lemaître, Jean-Baptiste Arnoux, Marie-Laure Asensio, Véronique Tardy, Yannis Duffourd, Christel Thauvin-Robinet, Sandra Mercier, Emmanuelle Lecommandeur, Camille Lenelle
article en
2 citations

Abstract

No abstract available for this paper.
BMJ OpenVol. 15(10)
Hôpital Necker-Enfants Malades (FR), Centre National de la Recherche Scientifique (FR), Université Toulouse III - Paul Sabatier (FR), Inserm (FR), École des Hautes Études en Santé Publique (FR), Université de Bourgogne (FR), Université Fédérale de Toulouse Midi-Pyrénées (FR), Université Paris Cité (FR), Aix-Marseille Université (FR), Assistance Publique – Hôpitaux de Paris (FR), Hospices Civils de Lyon (FR), Centre Hospitalier Universitaire d'Angers (FR), CHU Dijon Bourgogne (FR), Institut de génétique et de développement de Rennes (FR), Centre de recherche Translationnelle en Médecine moléculaire (FR), Institut du Thorax (FR), Centre Hospitalier Universitaire de Rennes (FR), Génétique Médicale & Génomique Fonctionelle (FR), Hôpital de la Timone (FR), Université de Franche-Comté (FR), BNP Paribas (France) (FR)
Infrastructures en Biologie Santé et Agronomie
Openalex Percentile: Top 6%
Genomics and Rare Diseases
3.63
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