All papers authored by Jonathan Levy
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2023
Thomas Husson 
,
François Lecoquierre,
Gaël Nicolas ,
Anne-Claire Richard,
Alexandra Afenjar,
Séverine Audebert-Bellanger,
Catherine Badens,
Frédéric Bilan,
Varoona Bizaoui,
Anne Boland,
Marie-Noëlle Bonnet-Dupeyron,
Elise Brischoux-Boucher ,
Céline Bonnet ,
Marie Bournez ,
Odile Boute
and 89 other authors
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,
François Lecoquierre,
Gaël Nicolas ,
Anne-Claire Richard,
Alexandra Afenjar,
Séverine Audebert-Bellanger,
Catherine Badens,
Frédéric Bilan,
Varoona Bizaoui,
Anne Boland,
Marie-Noëlle Bonnet-Dupeyron,
Elise Brischoux-Boucher ,
Céline Bonnet ,
Marie Bournez ,
Odile Boute
and 89 other authors
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2022
Ethiraj Ravindran ,
Nobuto Arashiki,
Lena-Luise Becker,
Kohtaro Takizawa,
Jonathan Lévy ,
Thomas Rambaud,
Konstantin L. Makridis ,
Makridis Kl,
Yoshio Goshima,
Na Li,
Maaike Vreeburg,
Bénédicte Demeer,
Achim Dickmanns,
Alexander Pa Stegmann ,
Stegmann Ap
and 4 other authors
,
Nobuto Arashiki,
Lena-Luise Becker,
Kohtaro Takizawa,
Jonathan Lévy ,
Thomas Rambaud,
Konstantin L. Makridis ,
Makridis Kl,
Yoshio Goshima,
Na Li,
Maaike Vreeburg,
Bénédicte Demeer,
Achim Dickmanns,
Alexander Pa Stegmann ,
Stegmann Ap
and 4 other authors
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder
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Ilaria Parenti ,
Elsa Leitão,
Alma Kuechler,
Laurent Villard,
Cyril Goizet,
Cécile Courdier,
Allan Bayat,
Alessandra Rossi,
Sophie Julia,
Ange-Line Bruel,
Frédéric Tran Mau-Them,
Sophie Nambot,
Daphné Lehalle,
Marjolaine Willems,
James Lespinasse
and 37 other authors
,
Elsa Leitão,
Alma Kuechler,
Laurent Villard,
Cyril Goizet,
Cécile Courdier,
Allan Bayat,
Alessandra Rossi,
Sophie Julia,
Ange-Line Bruel,
Frédéric Tran Mau-Them,
Sophie Nambot,
Daphné Lehalle,
Marjolaine Willems,
James Lespinasse
and 37 other authors
The different clinical facets of SYN1-related neurodevelopmental disorders
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Marcello Niceta ,
Simone Pizzi,
Francesca Inzana,
Angela Peron ,
Somayeh Bakhtiari,
Mathilde Nizon,
Jonathan Levy ,
Cecilia Mancini,
Benjamin Cogné,
Francesca Clementina Radio ,
Emanuele Agolini ,
Dario Cocciadiferro,
Antonio Novelli,
Mustafa A. Salih,
Maria Paola Recalcati
and 7 other authors
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,
Simone Pizzi,
Francesca Inzana,
Angela Peron ,
Somayeh Bakhtiari,
Mathilde Nizon,
Jonathan Levy ,
Cecilia Mancini,
Benjamin Cogné,
Francesca Clementina Radio ,
Emanuele Agolini ,
Dario Cocciadiferro,
Antonio Novelli,
Mustafa A. Salih,
Maria Paola Recalcati
and 7 other authors
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Guillaume Jouret ,
Matthieu Egloff ,
Emilie Landais,
Olivier Tassy,
Fabienne Giuliano,
Houda Karmous‐Benailly,
Charles Coutton,
Véronique Satre,
Françoise Devillard,
Klaus Dieterich,
Gaëlle Vieville,
Paul Kuentz ,
Cédric le Caignec,
Claire Beneteau,
Bertrand Isidor
and 20 other authors
,
Matthieu Egloff ,
Emilie Landais,
Olivier Tassy,
Fabienne Giuliano,
Houda Karmous‐Benailly,
Charles Coutton,
Véronique Satre,
Françoise Devillard,
Klaus Dieterich,
Gaëlle Vieville,
Paul Kuentz ,
Cédric le Caignec,
Claire Beneteau,
Bertrand Isidor
and 20 other authors
Clinical and genomic delineation of the new proximal 19p13.3 microduplication syndrome
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Julien Rossignol ,
Zakia Belaid,
Guillemette Fouquet,
Flavia Guillem,
Rachel Rignault,
Pierre Milpied,
Amédée Renand,
Tereza Coman ,
Maud D’Aveni,
Michael Dussiot,
Elia Colin,
Jonathan Levy ,
Caroline Carvalho,
Nicolas Goudin ,
Nicolas Cagnard
and 23 other authors
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,
Zakia Belaid,
Guillemette Fouquet,
Flavia Guillem,
Rachel Rignault,
Pierre Milpied,
Amédée Renand,
Tereza Coman ,
Maud D’Aveni,
Michael Dussiot,
Elia Colin,
Jonathan Levy ,
Caroline Carvalho,
Nicolas Goudin ,
Nicolas Cagnard
and 23 other authors
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2021
Jonathan Lévy ,
Guillaume Cogan,
Anna Maruani,
Arnaud Maillard,
Céline Dupont,
Séverine Drunat,
Myriam Rachid,
Paola Atzori,
Richard Delorme,
Sabatini Jeyarajah,
Bertrand Isidor,
Olivier Pichon,
Kamran Moradkhani,
Alain Verloes ,
Anne‐Claude Tabet
,
Guillaume Cogan,
Anna Maruani,
Arnaud Maillard,
Céline Dupont,
Séverine Drunat,
Myriam Rachid,
Paola Atzori,
Richard Delorme,
Sabatini Jeyarajah,
Bertrand Isidor,
Olivier Pichon,
Kamran Moradkhani,
Alain Verloes ,
Anne‐Claude Tabet
Rare and de novo duplications containing TCF20 are associated with a neurodevelopmental disorder
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Charlotte Lippe,
Charlotte von der Lippe ,
Kristian Tveten,
Trine E. Prescott,
Øystein L. Holla,
Øyvind L. Busk,
Katherine B. Burke,
Francis H. Sansbury,
Júlia Baptista ,
Andrew E. Fry ,
Derek Lim,
Stephen Jolles ,
Jennifer Evans,
Deborah Osio,
Carol Macmillan
and 17 other authors
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,
Kristian Tveten,
Trine E. Prescott,
Øystein L. Holla,
Øyvind L. Busk,
Katherine B. Burke,
Francis H. Sansbury,
Júlia Baptista ,
Andrew E. Fry ,
Derek Lim,
Stephen Jolles ,
Jennifer Evans,
Deborah Osio,
Carol Macmillan
and 17 other authors
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Conny M. A. van Ravenswaaij‐Arts,
Jonathan Lévy ,
Alain Verloes ,
Anne‐Claude Tabet ,
Bérénice Schell,
Hala Nasser,
Myriam Rachid,
Lyse Ruaud ,
Nathalie Couque ,
Patrick Callier,
Morgane Plutino,
Houda Karmous‐Benailly,
Laurence Faivre ,
Caroline Benech,
Sylvia Redon
and 9 other authors
,
Alain Verloes ,
Anne‐Claude Tabet ,
Bérénice Schell,
Hala Nasser,
Myriam Rachid,
Lyse Ruaud ,
Nathalie Couque ,
Patrick Callier,
Morgane Plutino,
Houda Karmous‐Benailly,
Laurence Faivre ,
Caroline Benech,
Sylvia Redon
and 9 other authors
EPHA7 haploinsufficiency is associated with a neurodevelopmental disorder
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2017
Anne-Claude Tabet ,
Thomas Rolland ,
Marie Ducloy,
Jonathan Lévy ,
Julien Buratti,
Alexandre Mathieu,
Damien Haye,
Laurence Perrin,
Alain Verloes,
Yline Capri,
Céline Dupont ,
Séverine Drunat,
Sandrine Passemard,
Boris Keren,
Cyril Mignot
and 47 other authors
,
Thomas Rolland ,
Marie Ducloy,
Jonathan Lévy ,
Julien Buratti,
Alexandre Mathieu,
Damien Haye,
Laurence Perrin,
Alain Verloes,
Yline Capri,
Céline Dupont ,
Séverine Drunat,
Sandrine Passemard,
Boris Keren,
Cyril Mignot
and 47 other authors
A framework to identify contributing genes in patients with Phelan-McDermid syndrome
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Jonathan Lévy ,
Aurélie Coussement,
Céline Dupont,
Fabien Guimiot,
Clarisse Baumann,
Géraldine Viot,
Sandrine Passemard,
Yline Capri,
Séverine Drunat,
Alain Verloes,
Eva Pipiras,
Brigitte Benzacken,
Jean-Michel Dupont,
Anne-Claude Tabet
,
Aurélie Coussement,
Céline Dupont,
Fabien Guimiot,
Clarisse Baumann,
Géraldine Viot,
Sandrine Passemard,
Yline Capri,
Séverine Drunat,
Alain Verloes,
Eva Pipiras,
Brigitte Benzacken,
Jean-Michel Dupont,
Anne-Claude Tabet
Molecular and clinical delineation of 2p15p16.1 microdeletion syndrome
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2014
Jonathan Lévy ,
Aline Receveur,
Guillaume Jedraszak,
Sandra Chantot‐Bastaraud,
Florence Renaldo,
Jean Gondry,
Joris Andrieux,
Henri Copin,
Jean‐Pierre Siffroi,
Marie‐France Portnoï
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,
Aline Receveur,
Guillaume Jedraszak,
Sandra Chantot‐Bastaraud,
Florence Renaldo,
Jean Gondry,
Joris Andrieux,
Henri Copin,
Jean‐Pierre Siffroi,
Marie‐France Portnoï
Download from api.wiley.com
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