Martin Chevarin

Affiliations
  • Inserm UMR 1231 GAD (Génétique des Anomalies du Développement), Université de Bourgogne, Dijon, France.
ORCID: http://orcid.org/0000-0002-5010-4161

Publications (27)

De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature.

European journal of human genetics : EJHG
Avec: Sophie Nambot , Laurence Faivre , Ghayda Mirzaa , Julien Thevenon , Ange-Line Bruel , Anne-Laure Mosca-Boidron , Alice Masurel-Paulet , Alice Goldenberg , Nathalie Le Meur , Aude Charollais , Cyril Mignot , Florence Petit , Massimiliano Rossi , Julia Metreau , Valérie Layet , Daniel Amram , Odile Boute-Bénéjean , Elizabeth Bhoj , Margot A Cousin , Teresa M Kruisselbrink , Brendan C Lanpher , Eric W Klee , Elise Fiala , Dorothy K Grange , Wendy S Meschino , Susan M Hiatt , Gregory M Cooper , Hilde Olivié , Wendy E Smith , Meghan Dumas , Anna Lehman , Auteur inconnu , Cara Inglese , Mathilde Nizon , Renzo Guerrini , Annalisa Vetro , Eitan S Kaplan , Dolores Miramar , Julien Van Gils , Patricia Fergelot , Olaf Bodamer , Johanna C Herkert , Sander Pajusalu , Katrin Õunap , James J Filiano , Thomas Smol , Amélie Piton , Bénédicte Gérard , Sandra Chantot-Bastaraud , Thierry Bienvenu , Dong Li , Jane Juusola , Koen Devriendt , Frederic Bilan , Charlotte Poé , Thibaud Jouan , Emilie Tisserant , Jean-Baptiste Rivière , Frédéric Tran Mau-Them , Christophe Philippe , Yannis Duffourd , William B Dobyns , Robert Hevner , Christel Thauvin-Robinet

Further clinical and molecular characterization of an XLID syndrome associated with BRWD3 variants, a gene implicated in the leukemia-related JAK-STAT pathway.

European journal of medical genetics
Avec: Julian Delanne , Magaly Lecat , Patrick R Blackburn , Eric W Klee , Constance T R M Stumpel , Sander Stegmann , Servi J C Stevens , Caroline Nava , Delphine Heron , Boris Keren , Sonal Mahida , Sakkubai Naidu , Dusica Babovic-Vuksanovic , Johanna C Herkert , Pernille M Torring , Maria Kibæk , Isabelle De Bie , Rolph Pfundt , Yvonne M C Hendriks , Lilian Bomme Ousager , Renee Bend , Hannah Warren , Steven A Skinner , Michael J Lyons , Charlotte Pöe , Thibaud Jouan , Aurore Garde , Quentin Thomas , Paul Kuentz , Emilie Tisserant , Yannis Duffourd , Christophe Philippe , Laurence Faivre , Christel Thauvin-Robinet

Journal of medical genetics
Avec: Daphné Lehalle , Pierre Vabres , Arthur Sorlin , Tatjana Bierhals , Magali Avila , Virginie Carmignac , Erin Torti , Yuichi Abe , Tobias Bartolomaeus , Jill Clayton-Smith , Benjamin Cogné , Ivon Cusco , Laurence Duplomb , Eveline De Bont , Yannis Duffourd , Floor Duijkers , Orly Elpeleg , Aviva Fattal , David Geneviève , Maria J Guillen Sacoto , Anne Guimier , David J Harris , Maja Hempel , Bertrand Isidor , Thibaud Jouan , Paul Kuentz , Eriko Koshimizu , Klaske Lichtenbelt , Valerie Loik Ramey , Miriam Maik , Sakoto Miyakate , Yoshiko Murakami , Laurent Pasquier , Helio Pedro , Laurie Simone , Krista Sondergaard-Schatz , Judith St-Onge , Julien Thevenon , Irene Valenzuela , Rami Abou Jamra , Koen van Gassen , Mieke M van Haelst , Silvana van Koningsbruggen , Edgard Verdura , Christa Whelan Habela , Pia Zacher , Jean-Baptiste Rivière , Christel Thauvin-Robinet , Joerg Betschinger , Laurence Faivre

The "extreme phenotype approach" applied to male breast cancer allows the identification of rare variants of ATR as potential breast cancer susceptibility alleles.

Oncotarget
Avec: Diana Alcantara , Juliette Albuisson , Marie-Agnès Collonge-Rame , Céline Populaire , Zohair Selmani , Amandine Baurand , Caroline Sawka , Geoffrey Bertolone , Patrick Callier , Yannis Duffourd , Philippe Jonveaux , Yves-Jean Bignon , Isabelle Coupier , François Cornelis , Christophe Cordier , Monique Mozelle-Nivoix , Jean-Baptiste Rivière , Paul Kuentz , Christel Thauvin , Romain Boidot , François Ghiringhelli , Marc O'Driscoll , Laurence Faivre , Sophie Nambot

Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples.

European journal of human genetics : EJHG
Avec: Robin Wijngaard , German Demidov , Luke O'Gorman , Jordi Corominas-Galbany , Burcu Yaldiz , Wouter Steyaert , Elke de Boer , Lisenka E L M Vissers , Erik-Jan Kamsteeg , Rolph Pfundt , Hilde Swinkels , Amber den Ouden , Iris B A W Te Paske , Richarda M de Voer , Laurence Faivre , Anne-Sophie Denommé-Pichon , Yannis Duffourd , Antonio Vitobello , Volker Straub , Ana Töpf , Anneke J van der Kooi , Francesca Magrinelli , Clarissa Rocca , Michael G Hanna , Jana Vandrovcova , Auteur inconnu , Stephan Ossowski , Steven Laurie , Christian Gilissen

Identification of the first homozygous intragenic deletion in the YY1AP1 gene in a consanguineous family: New insights into the phenotypic variability associated with Grange syndrome.

American journal of medical genetics. Part A
Avec: E Viora-Dupont , A Denommé-Pichon , M Chevarin , O Patat , M Willems , N Bourgon , A Bruel , M Aubert-Mucca , M Galinier , R Itier , S Decramer , A Piton , B Gerard , C Billon , X Jeunemaitre , Y Duffourd , P Callier , C Thauvin , C Philippe , L Faivre , J Albuisson , A Vitobello

Second-tier trio exome sequencing after negative solo clinical exome sequencing: an efficient strategy to increase diagnostic yield and decipher molecular bases in undiagnosed developmental disorders.

Human genetics
Avec: Frederic Tran Mau-Them , Sebastien Moutton , Caroline Racine , Antonio Vitobello , Ange-Line Bruel , Sophie Nambot , Steven A Kushner , Femke M S de Vrij , Daphné Lehalle , Nolwenn Jean-Marçais , François Lecoquierre , Julian Delanne , Julien Thevenon , Charlotte Poe , Thibaut Jouan , David Geneviève , Marjolaine Willems , Christine Coubes , Nada Houcinat , Alice Masurel-Paulet , Anne-Laure Mosca-Boidron , Emilie Tisserant , Patrick Callier , Arthur Sorlin , Yannis Duffourd , Laurence Faivre , Christophe Philippe , Christel Thauvin-Robinet

Cardiomyopathy due to PRDM16 mutation: First description of a fetal presentation, with possible modifier genes.

American journal of medical genetics. Part C, Seminars in medical genetics
Avec: Geoffroy Delplancq , Georges Tarris , Antonio Vitobello , Sophie Nambot , Arthur Sorlin , Christophe Philippe , Virginie Carmignac , Yannis Duffourd , Charlotte Denis , Jean Christophe Eicher , Gilles Millat , Bouchra Khallouk , Thierry Rousseau , Sylvie Falcon-Eicher , Alexandre Vasiljevic , Fara T Harizay , Christel Thauvin-Robinet , Laurence Faivre , Paul Kuentz

Secondary actionable findings identified by exome sequencing: expected impact on the organisation of care from the study of 700 consecutive tests.

European journal of human genetics : EJHG
Avec: Christel Thauvin-Robinet , Julien Thevenon , Sophie Nambot , Julian Delanne , Paul Kuentz , Ange-Line Bruel , Aline Chassagne , Elodie Cretin , Aurore Pelissier , Chritine Peyron , Elodie Gautier , Daphné Lehalle , Nolwenn Jean-Marçais , Patrick Callier , Anne-Laure Mosca-Boidron , Antonio Vitobello , Arthur Sorlin , Frédéric Tran Mau-Them , Christophe Philippe , Pierre Vabres , Laurent Demougeot , Charlotte Poé , Thibaud Jouan , Mathilde Lefebvre , Marc Bardou , Emilie Tisserant , Maxime Luu , Christine Binquet , Jean-François Deleuze , Céline Verstuyft , Yannis Duffourd , Laurence Faivre

Same performance of exome sequencing before and after fetal autopsy for congenital abnormalities: toward a paradigm shift in prenatal diagnosis?

European journal of human genetics : EJHG
Avec: Nicolas Bourgon , Aurore Garde , Ange-Line Bruel , Mathilde Lefebvre , Frederic Tran Mau-Them , Sebastien Moutton , Arthur Sorlin , Sophie Nambot , Julian Delanne , Charlotte Pöe , Julien Thevenon , Daphné Lehalle , Nolween Jean-Marçais , Paul Kuentz , Laetitia Lambert , Salima El Chehadeh , Elise Schaefer , Marjolaine Willems , Fanny Laffargue , Christine Francannet , Mélanie Fradin , Dominique Gaillard , Sophie Blesson , Alice Goldenberg , Yline Capri , Paul Sagot , Thierry Rousseau , Emmanuel Simon , Christine Binquet , Marie-Laure Ascencio , Yannis Duffourd , Christophe Philippe , Laurence Faivre , Antonio Vitobello , Christel Thauvin-Robinet

Surgical management of Chiari malformation type 1 associated to MCAP syndrome and study of cerebellar and adjacent tissues for PIK3CA mosaicism.

European journal of medical genetics
Avec: Federico Di Rocco , Maria Lucia Licci , Aurore Garde , Carmine Mottolese , Christel Thauvin-Robinet , Laurent Guibaud , Pierre Vabres , Paul Kuentz , Laurence Faivre

A second look at exome sequencing data: detecting mobile elements insertion in a rare disease cohort.

European journal of human genetics : EJHG
Avec: Philippine Garret , Antonio Vitobello , Simon Verdez , Cyril Fournier , Alain Verloes , Emilie Tisserant , Pierre Vabres , Orlane Prevel , Christophe Philippe , Anne-Sophie Denommé-Pichon , Ange-Line Bruel , Frédéric Tran Mau-Them , Hana Safraou , Aïcha Boughalem , Jean-Marc Costa , Detlef Trost , Christel Thauvin-Robinet , Laurence Faivre , Yannis Duffourd

Neutralization of HSF1 in cells from PIK3CA-related overgrowth spectrum patients blocks abnormal proliferation.

Biochemical and biophysical research communications
Avec: Romain Da Costa , Steven De Almeida , Smail Hadj-Rabia , Stéphanie Leclerc-Mercier , Christel Thauvin-Robinet , Carmen Garrido , Laurence Faivre , Pierre Vabres , Laurence Duplomb , Gaëtan Jego

Excess of de novo variants in genes involved in chromatin remodelling in patients with marfanoid habitus and intellectual disability.

Journal of medical genetics
Avec: Yannis Duffourd , Rebecca A Barnard , Sébastien Moutton , François Lecoquierre , Fatma Daoud , Paul Kuentz , Caroline Cabret , Julien Thevenon , Elodie Gautier , Patrick Callier , Judith St-Onge , Thibaud Jouan , Didier Lacombe , Marie Ange Delrue , Cyril Goizet , Fanny Morice-Picard , Julien Van-Gils , Arnold Munnich , Stanislas Lyonnet , Valérie Cormier-Daire , Geneviève Baujat , Muriel Holder , Florence Petit , Bruno Leheup , Sylvie Odent , Pierre-Simon Jouk , Gipsy Lopez , David Geneviève , Patrick Collignon , Dominique Martin-Coignard , Aurélia Jacquette , Laurence Perrin , Audrey Putoux , Elisabeth Sarrazin , Khadija Amarof , Isabelle Missotte , Christine Coubes , Sujatha Jagadeesh , Elisabetta Lapi , Florence Demurger , Alice Goldenberg , Martine Doco-Fenzy , Cyril Mignot , Delphine Héron , Nolwenn Jean-Marçais , Alice Masurel , Salima El Chehadeh , Nathalie Marle , Frédéric Huet , Christine Binquet , Gwenaëlle Collod-Beroud , Pauline Arnaud , Nadine Hanna , Catherine Boileau , Guillaume Jondeau , Robert Olaso , Doris Lechner , Charlotte Poe , Mirna Assoum , Virginie Carmignac , Laurence Duplomb , Frédéric Tran Mau-Them , Christophe Philippe , Antonio Vitobello , Ange-Line Bruel , Anne Boland , Jean-François Deleuze , Christel Thauvin-Robinet , Jean-Baptiste Rivière , Brian J O'Roak , Laurence Faivre

Neuropsychological study in 19 French patients with White-Sutton syndrome and POGZ mutations.

Clinical genetics
Avec: Aurore Garde , Jenny Cornaton , Arthur Sorlin , Sébastien Moutton , Claire Nicolas , Christine Juif , David Geneviève , Laurence Perrin , Philippe Khau-Van-Kien , Thomas Smol , Catherine Vincent-Delorme , Bertrand Isidor , Benjamin Cogné , Alexandra Afenjar , Boris Keren , Christine Coubes , Fabienne Prieur , Annick Toutain , Yann Trousselet , Solène Bourgouin , Coralie Gonin-Olympiade , Kim Giraudat , Amélie Piton , Bénédicte Gérard , Sylvie Odent , Fanny Tessier , Lola Lemasson , Solveig Heide , Anne-Claire Gelineau , Catherine Sarret , Anne Miret , Elise Schaefer , Juliette Piard , Rémi Mathevet , Marion Boucon , Ange-Line Bruel , Frederic Tran Mau-Them , Antonio Vitobello , Christophe Philippe , Christel Thauvin-Robinet , Laurence Faivre

Haploinsufficiency of ARFGEF1 is associated with developmental delay, intellectual disability, and epilepsy with variable expressivity.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Quentin Thomas , Thierry Gautier , Dana Marafi , Thomas Besnard , Marjolaine Willems , Sébastien Moutton , Bertand Isidor , Benjamin Cogné , Solène Conrad , Romano Tenconi , Maria Iascone , Arthur Sorlin , Alice Masurel , Tabib Dabir , Adam Jackson , Siddharth Banka , Julian Delanne , James R Lupski , Nebal Waill Saadi , Fowzan S Alkuraya , Fatema Al Zahrani , Pankaj B Agrawal , Eleina England , Jill A Madden , Jennifer E Posey , Lydie Burglen , Diana Rodriguez , Sylvie Nguyen , Frédéric Tran Mau-Them , Yannis Duffourd , Philippine Garret , Ange-Line Bruel , Patrick Callier , Nathalie Marle , Anne-Sophie Denomme-Pichon , Laurence Duplomb , Christophe Philippe , Christel Thauvin-Robinet , Jérôme Govin , Laurence Faivre , Antonio Vitobello

Detection of the novel allele, HLA-A*32:165, in a French individual by next-generation sequencing.

HLA
Avec: Simon Verdez , Victor Couturier , Damien Leleu , Christel Thauvin-Robinet

Low risk of embryonic and other cancers in PIK3CA-related overgrowth spectrum: Impact on screening recommendations.

Clinical genetics
Avec: Laurence Faivre , Jean-Charles Crépin , Manon Réda , Sophie Nambot , Virginie Carmignac , Caroline Abadie , Tristan Mirault , Cécile Faure-Conter , Juliette Mazereeuw-Hautier , Aude Maza , Eve Puzenat , Marie-Agnès Collonge-Rame , Anne-Claire Bursztejn , Christophe Philippe , Christel Thauvin-Robinet , Claire Abasq-Thomas , Jeanne Amiel , Stéphanie Arpin , Sébastien Barbarot , Geneviève Baujat , Didier Bessis , Emmanuelle Bourrat , Odile Boute , Nicolas Chassaing , Christine Coubes , Bénédicte Demeer , Patrick Edery , Salima El Chehadeh , Alice Goldenberg , Smail Hadj-Rabia , Damien Haye , Bertrand Isidor , Marie-Line Jacquemont , Philippe Khau Van Kien , Didier Lacombe , Daphné Lehalle , Laetitia Lambert , Ludovic Martin , Annabel Maruani , Fanny Morice-Picard , Florence Petit , Alice Phan , Lucile Pinson , Massimiliano Rossi , Renaud Touraine , Clémence Vanlerberghe , Marie Vincent , Catherine Vincent-Delorme , Sandra Whalen , Marjolaine Willems , Nathalie Marle , Virginie Verkarre , Christine Devalland , Mojgan Devouassoux-Shisheboran , Marine Abad , Nathalie Rioux-Leclercq , Bertille Bonniaud , Yannis Duffourd , Jehanne Martel , Christine Binquet , Paul Kuentz , Pierre Vabres

YWHAE loss of function causes a rare neurodevelopmental disease with brain abnormalities in human and mouse.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Anne-Sophie Denommé-Pichon , Stephan C Collins , Ange-Line Bruel , Anna Mikhaleva , Christel Wagner , Valerie E Vancollie , Quentin Thomas , Mathys Weber , Carlos E Prada , Alexis Overs , María Palomares-Bralo , Fernando Santos-Simarro , Marta Pacio-Míguez , Tiffany Busa , Eric Legius , Carlos A Bacino , Jill A Rosenfeld , Gwenaël Le Guyader , Matthieu Egloff , Xavier Le Guillou , Maria Antonietta Mencarelli , Alessandra Renieri , Salvatore Grosso , Jonathan Levy , Blandine Dozières , Isabelle Desguerre , Antonio Vitobello , Yannis Duffourd , Christopher J Lelliott , Christel Thauvin-Robinet , Christophe Philippe , Laurence Faivre , Binnaz Yalcin

Allelic heterogeneity in a patient with postzygotic MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities.

Clinical genetics
Avec: Camille Engel , Juliette Piard , Marine Abad , Quentin Thomas , Virginie Carmignac , Yannis Duffourd , Martine Lemesle-Martin , Georges Tarris , Christel Thauvin-Robinet , Pierre Vabres , Laurence Faivre , Paul Kuentz

Primrose syndrome: a phenotypic comparison of patients with a ZBTB20 missense variant versus a 3q13.31 microdeletion including ZBTB20.

European journal of human genetics : EJHG
Avec: Aurélien Juven , Sophie Nambot , Amélie Piton , Nolwenn Jean-Marçais , Alice Masurel , Patrick Callier , Nathalie Marle , Anne-Laure Mosca-Boidron , Paul Kuentz , Christophe Philippe , Yannis Duffourd , Elodie Gautier , Arnold Munnich , Marlène Rio , Sophie Rondeau , Salima El Chehadeh , Élise Schaefer , Bénédicte Gérard , Sonia Bouquillon , Catherine Vincent Delorme , Christine Francannet , Fanny Laffargue , Laetitia Gouas , Bertrand Isidor , Marie Vincent , Sophie Blesson , Fabienne Giuliano , Olivier Pichon , Cédric Le Caignec , Hubert Journel , Laurence Perrin-Sabourin , Jennifer Fabre-Teste , Dominique Martin , Gaelle Vieville , Klaus Dieterich , Didier Lacombe , Anne-Sophie Denommé-Pichon , Christel Thauvin-Robinet , Laurence Faivre

Variant recurrence in neurodevelopmental disorders: the use of publicly available genomic data identifies clinically relevant pathogenic missense variants.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: François Lecoquierre , Yannis Duffourd , Antonio Vitobello , Ange-Line Bruel , Benoit Urteaga , Christine Coubes , Philippine Garret , Sophie Nambot , Thibaud Jouan , Sébastien Moutton , Auteur inconnu , Frédéric Tran-Mau-Them , Christophe Philippe , Arthur Sorlin , Laurence Faivre , Christel Thauvin-Robinet

Increased diagnostic and new genes identification outcome using research reanalysis of singleton exome sequencing.

European journal of human genetics : EJHG
Avec: Ange-Line Bruel , Sophie Nambot , Virginie Quéré , Antonio Vitobello , Julien Thevenon , Mirna Assoum , Sébastien Moutton , Nada Houcinat , Daphné Lehalle , Nolwenn Jean-Marçais , Auteur inconnu , Thibaud Jouan , Charlotte Poë , Patrick Callier , Emilie Tisserand , Christophe Philippe , Frédéric Tran Mau Them , Yannis Duffourd , Laurence Faivre , Christel Thauvin-Robinet

Interest of exome sequencing trio-like strategy based on pooled parental DNA for diagnosis and translational research in rare diseases.

Molecular genetics & genomic medicine
Avec: Frederic Tran Mau-Them , Yannis Duffourd , Antonio Vitobello , Ange-Line Bruel , Anne-Sophie Denommé-Pichon , Sophie Nambot , Julian Delanne , Sebastien Moutton , Arthur Sorlin , Auteur inconnu , Victor Couturier , Valentin Bourgeois , Charlotte Poe , Anne-Laure Mosca-Boidron , Patrick Callier , Hana Safraou , Laurence Faivre , Christophe Philippe , Christel Thauvin-Robinet

Cerebriform sebaceous nevus: a subtype of organoid nevus due to specific postzygotic FGFR2 mutations.

Journal of the European Academy of Dermatology and Venereology : JEADV
Avec: M Theiler , L Weibel , S Christen-Zaech , V Carmignac , A Sorlin , K Neuhaus , M Chevarin , C Thauvin-Robinet , C Philippe , L Faivre , P Vabres , P Kuentz

Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Virginie Carmignac , Cyril Mignot , Emmanuelle Blanchard , Paul Kuentz , Marie-Hélène Aubriot-Lorton , Victoria E R Parker , Arthur Sorlin , Sylvie Fraitag , Jean-Benoît Courcet , Yannis Duffourd , Diana Rodriguez , Rachel G Knox , Satyamaanasa Polubothu , Anne Boland , Robert Olaso , Marc Delepine , Véronique Darmency , Melissa Riachi , Chloé Quelin , Paul Rollier , Louise Goujon , Sarah Grotto , Yline Capri , Marie-Line Jacquemont , Sylvie Odent , Daniel Amram , Catherine Vincent-Delorme , Benoît Catteau , Laurent Guibaud , Alexis Arzimanoglou , Malika Keddar , Catherine Sarret , Patrick Callier , Didier Bessis , David Geneviève , Jean-François Deleuze , Christel Thauvin , Robert K Semple , Christophe Philippe , Jean-Baptiste Rivière , Veronica A Kinsler , Laurence Faivre , Pierre Vabres

Multiple molecular diagnoses in the field of intellectual disability and congenital anomalies: 3.5% of all positive cases.

Journal of medical genetics
Avec: Caroline Racine , Anne-Sophie Denommé-Pichon , Camille Engel , Frederic Tran Mau-Them , Ange-Line Bruel , Antonio Vitobello , Hana Safraou , Arthur Sorlin , Sophie Nambot , Julian Delanne , Aurore Garde , Estelle Colin , Sébastien Moutton , Julien Thevenon , Nolwenn Jean-Marçais , Marjolaine Willems , David Geneviève , Lucile Pinson , Laurence Perrin , Fanny Laffargue , James Lespinasse , Elodie Lacaze , Arnaud Molin , Marion Gerard , Laetitia Lambert , Charlotte Benigni , Olivier Patat , Auteur inconnu , Valentin Bourgeois , Charlotte Poe , Victor Couturier , Philippine Garret , Christophe Philippe , Yannis Duffourd , Laurence Faivre , Christel Thauvin-Robinet

Réseau de co-auteurs

Laurence Faivre 24 collaborations
Christel Thauvin-Robinet 22 collaborations
Yannis Duffourd 21 collaborations
Christophe Philippe 18 collaborations
Antonio Vitobello 14 collaborations
Ange-Line Bruel 13 collaborations
Sophie Nambot 12 collaborations
Paul Kuentz 12 collaborations
Arthur Sorlin 11 collaborations
Patrick Callier 9 collaborations
Julien Thevenon 8 collaborations
Pierre Vabres 8 collaborations
Thibaud Jouan 7 collaborations
Julian Delanne 7 collaborations
None None 6 collaborations
Daphné Lehalle 6 collaborations
Virginie Carmignac 6 collaborations
David Geneviève 6 collaborations
Anne-Sophie Denommé-Pichon 6 collaborations
Nolwenn Jean-Marçais 6 collaborations
Sébastien Moutton 6 collaborations
Anne-Laure Mosca-Boidron 5 collaborations
Emilie Tisserant 5 collaborations
Jean-Baptiste Rivière 5 collaborations
Frédéric Tran Mau-Them 5 collaborations
Aurore Garde 5 collaborations
Frederic Tran Mau-Them 5 collaborations
Marjolaine Willems 5 collaborations
Christine Coubes 5 collaborations
Alice Goldenberg 4 collaborations
Quentin Thomas 4 collaborations
Laurence Duplomb 4 collaborations
Bertrand Isidor 4 collaborations
Charlotte Poe 4 collaborations
Christine Binquet 4 collaborations
Salima El Chehadeh 4 collaborations
Philippine Garret 4 collaborations
Nathalie Marle 4 collaborations
Cyril Mignot 3 collaborations
Florence Petit 3 collaborations
Amélie Piton 3 collaborations
Bénédicte Gérard 3 collaborations
Benjamin Cogné 3 collaborations
Sebastien Moutton 3 collaborations
François Lecoquierre 3 collaborations
Elodie Gautier 3 collaborations
Jean-François Deleuze 3 collaborations
Laetitia Lambert 3 collaborations
Fanny Laffargue 3 collaborations
Hana Safraou 3 collaborations
Didier Lacombe 3 collaborations
Sylvie Odent 3 collaborations
Laurence Perrin 3 collaborations
Alice Masurel 3 collaborations
Catherine Vincent-Delorme 3 collaborations
Victor Couturier 3 collaborations
Alice Masurel-Paulet 2 collaborations
Massimiliano Rossi 2 collaborations
Daniel Amram 2 collaborations
Eric W Klee 2 collaborations
Johanna C Herkert 2 collaborations
Thomas Smol 2 collaborations
Charlotte Poé 2 collaborations
Boris Keren 2 collaborations
Rolph Pfundt 2 collaborations
Charlotte Pöe 2 collaborations
Judith St-Onge 2 collaborations
Marie-Agnès Collonge-Rame 2 collaborations
Christel Thauvin 2 collaborations
M Chevarin 2 collaborations
C Philippe 2 collaborations
L Faivre 2 collaborations
Caroline Racine 2 collaborations
Nada Houcinat 2 collaborations
Georges Tarris 2 collaborations
Thierry Rousseau 2 collaborations
Mathilde Lefebvre 2 collaborations
Elise Schaefer 2 collaborations
Christine Francannet 2 collaborations
Sophie Blesson 2 collaborations
Yline Capri 2 collaborations
Laurent Guibaud 2 collaborations
Simon Verdez 2 collaborations
Smail Hadj-Rabia 2 collaborations
Fanny Morice-Picard 2 collaborations
Arnold Munnich 2 collaborations
Geneviève Baujat 2 collaborations
Robert Olaso 2 collaborations
Mirna Assoum 2 collaborations
Anne Boland 2 collaborations
Catherine Sarret 2 collaborations
Juliette Piard 2 collaborations
Diana Rodriguez 2 collaborations
Didier Bessis 2 collaborations
Marie-Line Jacquemont 2 collaborations
Lucile Pinson 2 collaborations
Marie Vincent 2 collaborations
Marine Abad 2 collaborations
Camille Engel 2 collaborations
Valentin Bourgeois 2 collaborations
Ghayda Mirzaa 1 collaboration
Nathalie Le Meur 1 collaboration
Aude Charollais 1 collaboration
Julia Metreau 1 collaboration
Valérie Layet 1 collaboration
Odile Boute-Bénéjean 1 collaboration
Elizabeth Bhoj 1 collaboration
Margot A Cousin 1 collaboration
Teresa M Kruisselbrink 1 collaboration
Brendan C Lanpher 1 collaboration
Elise Fiala 1 collaboration
Dorothy K Grange 1 collaboration
Wendy S Meschino 1 collaboration
Susan M Hiatt 1 collaboration
Gregory M Cooper 1 collaboration
Hilde Olivié 1 collaboration
Wendy E Smith 1 collaboration
Meghan Dumas 1 collaboration
Anna Lehman 1 collaboration
Cara Inglese 1 collaboration
Mathilde Nizon 1 collaboration
Renzo Guerrini 1 collaboration
Annalisa Vetro 1 collaboration
Eitan S Kaplan 1 collaboration
Dolores Miramar 1 collaboration
Julien Van Gils 1 collaboration
Patricia Fergelot 1 collaboration
Olaf Bodamer 1 collaboration
Sander Pajusalu 1 collaboration
Katrin Õunap 1 collaboration
James J Filiano 1 collaboration
Sandra Chantot-Bastaraud 1 collaboration
Thierry Bienvenu 1 collaboration
Dong Li 1 collaboration
Jane Juusola 1 collaboration
Koen Devriendt 1 collaboration
Frederic Bilan 1 collaboration
William B Dobyns 1 collaboration
Robert Hevner 1 collaboration
Magaly Lecat 1 collaboration
Patrick R Blackburn 1 collaboration
Constance T R M Stumpel 1 collaboration
Sander Stegmann 1 collaboration
Servi J C Stevens 1 collaboration
Caroline Nava 1 collaboration
Delphine Heron 1 collaboration
Sonal Mahida 1 collaboration
Sakkubai Naidu 1 collaboration
Dusica Babovic-Vuksanovic 1 collaboration
Pernille M Torring 1 collaboration
Maria Kibæk 1 collaboration
Isabelle De Bie 1 collaboration
Yvonne M C Hendriks 1 collaboration
Lilian Bomme Ousager 1 collaboration
Renee Bend 1 collaboration
Hannah Warren 1 collaboration
Steven A Skinner 1 collaboration
Michael J Lyons 1 collaboration
Tatjana Bierhals 1 collaboration
Magali Avila 1 collaboration
Erin Torti 1 collaboration
Yuichi Abe 1 collaboration
Tobias Bartolomaeus 1 collaboration
Jill Clayton-Smith 1 collaboration
Ivon Cusco 1 collaboration
Eveline De Bont 1 collaboration
Floor Duijkers 1 collaboration
Orly Elpeleg 1 collaboration
Aviva Fattal 1 collaboration
Maria J Guillen Sacoto 1 collaboration
Anne Guimier 1 collaboration
David J Harris 1 collaboration
Maja Hempel 1 collaboration
Eriko Koshimizu 1 collaboration
Klaske Lichtenbelt 1 collaboration
Valerie Loik Ramey 1 collaboration
Miriam Maik 1 collaboration
Sakoto Miyakate 1 collaboration
Yoshiko Murakami 1 collaboration
Laurent Pasquier 1 collaboration
Helio Pedro 1 collaboration
Laurie Simone 1 collaboration
Krista Sondergaard-Schatz 1 collaboration
Irene Valenzuela 1 collaboration
Rami Abou Jamra 1 collaboration
Koen van Gassen 1 collaboration
Mieke M van Haelst 1 collaboration
Silvana van Koningsbruggen 1 collaboration
Edgard Verdura 1 collaboration
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