PFMG2025–integrating genomic medicine into the national healthcare system in France
Caroline Abadie, Giulia Barcia(Hôpital Necker-Enfants Malades), Salma Adham(Délégation Paris 5), Violaine Alunni, Xavier Ayrignac, Inês F. Amado, Chloé Angelini(Centre Hospitalier Universitaire de Bordeaux), Claire Bar(Centre National de la Recherche Scientifique), Flavie Ader(Inserm), Ralyath Balogoun, Isabelle Audo(Inserm), Lise Allard(Unknown), Nathalie Aladjidi, Chloé Arfeuille, Anne‐Sophie Alary(Centre National de la Recherche Scientifique), Thomas Aparicio(Université Paris Cité), O. Ackermann, Cécile Acquaviva(Hospices Civils de Lyon), Ibrahima Ba(Centre National de la Recherche Scientifique), Stéphanie Baert‐Desurmont, Brigitte Bader‐Meunier(Hôpital Necker-Enfants Malades), Maxime Auroux, Pauline Arnaud, Céline Auzanneau, Sarah Baer(Centre National de la Recherche Scientifique), Marie‐Pierre Audrézet(Inserm), Cyril Amouroux, Carine Abel(Hôpital de la Croix-Rousse), Dalila Adjaoud, Ingrid Allix, Marion Aubert‐Mucca(Hôpital Purpan), F. Albarel, Philippe Baltzinger, Sabrina Albert, Anne Bachelot, Mathieu Anheim(Centre National de la Recherche Scientifique), Guilhem Arnold, Laurence Bal-Theoleyre, Nicolas André(Ben-Gurion University of the Negev), Lionel Arnaud, Guillaume Banneau(Hôpital Purpan), Alexandra Afenjar(Sorbonne Université), Delphine Bacq(Inserm), J Arlet, Aldja Abderrahmane, Ignacio Antolin Sanfelliz, Ouarda Abdous, Tania Attié‐Bitach(Hôpital Necker-Enfants Malades), Audrey Barbet, Séverine Bacrot(Centre Hospitalier de Versailles)
Cited by 46
Related Papers
Seven new loci associated with age-related macular degeneration
|Nature Genetics|2013|802
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome
|Nature Genetics|2007|495
Brain MRI Findings in Severe COVID-19: A Retrospective Observational Study
|Radiology|2020|471
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
|The American Journal of Human Genetics|2016|454
Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome
|The American Journal of Human Genetics|2008|399