Yoann Vial

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 20

Top Topics

Iron Deficiency

Intellectual Disability

Top Venues

Journal of the European Academy of Dermatology and Venereology : JEADV

Pediatric blood & cancer

European journal of human genetics : EJHG

Hôpital Universitaire Robert-Debré

Université Paris Descartes (MSC)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Hôpital Universitaire Robert-Debré

France

Clinical Biologist :: Molecular Genetic

Université Paris Diderot

France

Teacher :: Faculty of Medicine

Centre Hospitalier Universitaire de Rouen

France

Resident :: Molecular Genetic

Hôpital Universitaire Robert-Debré

France

Research Grant :: Molecular Genetic

Centre Hospitalier Universitaire de Rouen

France

Resident :: Cytogenetic

Centre Hospitalier Universitaire de Rouen

France

Resident :: Molecular Genetic

Centre Hospitalier Universitaire de Rouen

France

Resident :: Immunology

Centre Hospitalier Universitaire de Rouen

France

Resident :: Hematology

Centre Hospitalier Universitaire de Rouen

France

Resident :: Microbiology

Centre Hospitalier Universitaire de Rouen

France

Resident :: Biochemistry

Education History

Université Paris Descartes

France

MSC :: Genetic

Université Paris Descartes

France

MSC :: Genetic

Publications

Yoann Vial, Jeannette Nardelli, Adeline A Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressens, Hélène Cave, Séverine Drunat
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis. EMBO reports 25 (5) (2024)
Didier Bessis, Anne-Claire Bursztejn, Fanny Morice-Picard, Yline Capri, Sébastien Barbarot, Hélène Aubert, Damien Bodet, Emmanuelle Bourrat, Christine Chiaverini, Laura Poujade, Marjolaine Willems, Jacques Rouanet, Anne Dompmartin-Blanchère, David Geneviève, Marion Gerard, Emmanuelle Ginglinger, Smail Hadj Rabia, Ludovic Martin, Juliette Mazereeuw-Hautier, Nathalie Bibas, Nicolas Molinari, Fanchon Herman, Alice Phan, Julien Rod, Hugues Roger, Sabine Sigaudy, Alban Ziegler, Yoann Vial, Alain Verloes, Hélène Cave, Didier Lacombe
Dermatological manifestations in Costello syndrome: A prospective multicentric study of 31 HRAS-positive variant patients. Journal of the European Academy of Dermatology and Venereology : JEADV (2024)
Yoann Vial, Jeannette Nardelli, Adeline A Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressens, Hélène Cave, Séverine Drunat
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis. EMBO reports 25 (5) (2024)
Yoann Vial, Jeannette Nardelli, Adeline A Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressens, Hélène Cave, Séverine Drunat
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis. EMBO reports 25 (5) (2024)
Yoann Vial, Jeannette Nardelli, Adeline A Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressens, Hélène Cave, Séverine Drunat
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis. EMBO reports 25 (5) (2024)
Yoann Vial, Jeannette Nardelli, Adeline A Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressens, Hélène Cave, Séverine Drunat
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis. EMBO reports (2024)
Yoann Vial, Jeannette Nardelli, Adeline A Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressens, Hélène Cave, Séverine Drunat
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis. EMBO reports 25 (5) (2024)
Didier Bessis, Anne-Claire Bursztejn, Fanny Morice-Picard, Yline Capri, Sébastien Barbarot, Hélène Aubert, Damien Bodet, Emmanuelle Bourrat, Christine Chiaverini, Laura Poujade, Marjolaine Willems, Jacques Rouanet, Anne Dompmartin-Blanchère, David Geneviève, Marion Gerard, Emmanuelle Ginglinger, Smail Hadj Rabia, Ludovic Martin, Juliette Mazereeuw-Hautier, Nathalie Bibas, Nicolas Molinari, Fanchon Herman, Alice Phan, Julien Rod, Hugues Roger, Sabine Sigaudy, Alban Ziegler, Yoann Vial, Alain Verloes, Hélène Cave, Didier Lacombe
Dermatological manifestations in Costello syndrome: A prospective multicentric study of 31 HRAS-positive variant patients. Journal of the European Academy of Dermatology and Venereology : JEADV 38 (9) (2024)
Didier Bessis, Anne-Claire Bursztejn, Fanny Morice-Picard, Yline Capri, Sébastien Barbarot, Hélène Aubert, Damien Bodet, Emmanuelle Bourrat, Christine Chiaverini, Laura Poujade, Marjolaine Willems, Jacques Rouanet, Anne Dompmartin-Blanchère, David Geneviève, Marion Gerard, Emmanuelle Ginglinger, Smail Hadj Rabia, Ludovic Martin, Juliette Mazereeuw-Hautier, Nathalie Bibas, Nicolas Molinari, Fanchon Herman, Alice Phan, Julien Rod, Hugues Roger, Sabine Sigaudy, Alban Ziegler, Yoann Vial, Alain Verloes, Hélène Cave, Didier Lacombe
Dermatological manifestations in Costello syndrome: A prospective multicentric study of 31 HRAS-positive variant patients. Journal of the European Academy of Dermatology and Venereology : JEADV 38 (9) (2024)
Brian Sperelakis-Beedham, Lyse Ruaud, Yoann Vial, Myriam Rachid, Faustine Ageorges, Louise Goujon, Alain Verloes, Anne-Claude Tabet, Emmanuelle Bourrat, Jonathan Lévy
Expanding the phenotype of GTF2E2-associated trichothiodystrophy. Journal of the European Academy of Dermatology and Venereology : JEADV (2023)
Yoann Vial, Elodie Lainey, Thierry Leblanc, Véronique Baudouin, Marie Emilie Dourthe, Pierre Gressens, Alain Verloes, Hélène Cavé, Séverine Drunat
De novo NUF2 variant in a novel inherited bone marrow failure syndrome including microcephaly and renal hypoplasia. British journal of haematology 199 (5) (2022)
Marialetizia Motta, Maja Solman, Adeline A Bonnard, Alma Kuechler, Francesca Pantaleoni, Manuela Priolo, Balasubramanian Chandramouli, Simona Coppola, Simone Pizzi, Erika Zara, Marco Ferilli, Hülya Kayserili, Roberta Onesimo, Chiara Leoni, Julia Brinkmann, Yoann Vial, Susanne B Kamphausen, Cécile Thomas-Teinturier, Anne Guimier, Viviana Cordeddu, Laura Mazzanti, Giuseppe Zampino, Giovanni Chillemi, Martin Zenker, Hélène Cavé, Jeroen den Hertog, Tartaglia Marco
Expanding the molecular spectrum of pathogenic SHOC2 variants underlying Mazzanti syndrome. Human molecular genetics 31 (16) (2022)
Sarah Faggetter, Alina Ferster, Laurence Dedeken, Anne Demulder, Ludvine David-Nguyen, Odile Fenneteau, Melanie Parisot, Patrick Nitschke, Yoann Vial, Lydie Da Costa
Hereditary spherocytosis associated with Noonan syndrome mimicking a dyserythropoietic anaemia. Pediatric blood & cancer 70 (4) (2022)
Sarah Faggetter, Alina Ferster, Laurence Dedeken, Anne Demulder, Ludvine David-Nguyen, Odile Fenneteau, Melanie Parisot, Patrick Nitschke, Yoann Vial, Lydie Da Costa
Hereditary spherocytosis associated with Noonan syndrome mimicking a dyserythropoietic anaemia. Pediatric blood & cancer 70 (4) (2022)
Sarah Faggetter, Alina Ferster, Laurence Dedeken, Anne Demulder, Ludvine David-Nguyen, Odile Fenneteau, Melanie Parisot, Patrick Nitschke, Yoann Vial, Lydie Da Costa
Hereditary spherocytosis associated with Noonan syndrome mimicking a dyserythropoietic anaemia. Pediatric blood & cancer (2022)
Sarah Faggetter, Alina Ferster, Laurence Dedeken, Anne Demulder, Ludvine David-Nguyen, Odile Fenneteau, Melanie Parisot, Patrick Nitschke, Yoann Vial, Lydie Da Costa
Hereditary spherocytosis associated with Noonan syndrome mimicking a dyserythropoietic anaemia. Pediatric blood & cancer 70 (4) (2022)
Christina Lissewski, Valérie Chune, Francesca Pantaleoni, Alessandro De Luca, Yline Capri, Julia Brinkmann, Francesca Lepri, Paola Daniele, Erika Leenders, Laura Mazzanti, Emanuela Scarano, Francesca Clementina Radio, Kerstin Kutsche, Alma Kuechler, Marion Gérard, Kara Ranguin, Marine Legendre, Yoann Vial, Ineke van der Burgt, Tuula Rinne, Elena Andreucci, Gioia Mastromoro, Maria Cristina Digilio, Hélène Cave, Tartaglia Marco, Martin Zenker
Variants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications. European journal of human genetics : EJHG 29 (1) (2020)
Anne Welfringer-Morin, Graziella Pinto, Geneviève Baujat, Yoann Vial, Smail Hadj-Rabia, Christine Bodemer, Olivia Boccara
Hypophosphatemic rickets: A rare complication of congenital melanocytic nevus syndrome. Pediatric dermatology 37 (3) (2020)
Julia Brinkmann, Christina Lissewski, Valentina Pinna, Yoann Vial, Francesca Pantaleoni, Francesca Lepri, Paola Daniele, Birute Burnyte, Goran Cuturilo, Christine Fauth, Alper Gezdirici, Dieter Kotzot, Elif Yılmaz Güleç, Violeta Iotova, Denny Schanze, Francis Ramond, Markéta Havlovicová, Gulen Eda Utine, Pelin Ozlem Simsek-Kiper, Milena Stoyanova, Alain Verloes, Alessandro De Luca, Tartaglia Marco, Hélène Cave, Martin Zenker
The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered. European journal of human genetics : EJHG 29 (3) (2020)
Sarah Duerinckx, Valérie Jacquemin, Séverine Drunat, Yoann Vial, Sandrine Passemard, Camille Perazzolo, Annick Massart, Julie Soblet, Judith Racapé, Laurence Desmyter, Cindy Badoer, Sofia Papadimitriou, Yann-Aël Le Borgne, Anne Lefort, Frédérick Libert, Viviane De Maertelaer, Marianne Rooman, Sabine Costagliola, Alain Verloes, Tom Lenaerts, Isabelle Pirson, Marc Abramowicz
Digenic inheritance of human primary microcephaly delineates centrosomal and non-centrosomal pathways. Human mutation 41 (2) (2019)