Arthur Sorlin

Affiliations
  • Centre de Génétique, CHU Dijon Bourgogne, Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, INSERM 1231, Génétique des Anomalies du Développement, Université Bourgogne Franche-Comté, Dijon, France.

Publications (47)

Clinical and molecular description of 19 patients with GATAD2B-Associated Neurodevelopmental Disorder (GAND).

European journal of medical genetics
Avec: Gabriella Vera , Arthur Sorlin , Geoffroy Delplancq , François Lecoquierre , Marie Brasseur-Daudruy , Florence Petit , Thomas Smol , Alban Ziegler , Dominique Bonneau , Estelle Colin , Sandra Mercier , Benjamin Cogné , Stéphane Bézieau , Patrick Edery , Gaetan Lesca , Nicolas Chatron , Isabelle Sabatier , Bénédicte Duban-Bedu , Cindy Colson , Amélie Piton , Benjamin Durand , Yline Capri , Laurence Perrin , Antje Wiesener , Christiane Zweier , Reza Maroofian , Christopher J Carroll , Hamid Galehdari , Neda Mazaheri , Bert Callewaert , Fabienne Giulianno , Khaoula Zaafrane-Khachnaoui , Rebecca Buchert-Lo , Tobias Haack , Janine Magg , Angelika Rieß , Maria Blandfort , Stephan Waldmüller , Veronka Horber , Emanuela Leonardi , Roberta Polli , Licia Turolla , Alessandra Murgia , Thierry Frebourg , Anne Sophie Lebre , Gaël Nicolas , Pascale Saugier-Veber , Anne-Marie Guerrot

Understanding the new BRD4-related syndrome: Clinical and genomic delineation with an international cohort study.

Clinical genetics
Avec: Guillaume Jouret , Solveig Heide , Arthur Sorlin , Laurence Faivre , Sandra Chantot-Bastaraud , Claire Beneteau , Marie Denis-Musquer , Peter D Turnpenny , Charles Coutton , Gaëlle Vieville , Julien Thevenon , Austin Larson , Florence Petit , Elise Boudry , Thomas Smol , Bruno Delobel , Bénédicte Duban-Bedu , Chiara Fallerini , Francesca Mari , Caterina Lo Rizzo , Alessandra Renieri , Jean-Hubert Caberg , Anne-Sophie Denommé-Pichon , Frédéric Tran Mau-Them , Isabelle Maystadt , Thomas Courtin , Boris Keren , Linda Mouthon , Perrine Charles , Silvestre Cuinat , Bertrand Isidor , Philippe Theis , Christian Müller , Marizela Kulisic , Seval Türkmen , Daniel Stieber , Dominique Bourgeois , Emmanuel Scalais , Barbara Klink

Molecular consequences of PQBP1 deficiency, involved in the X-linked Renpenning syndrome.

Molecular psychiatry
Avec: Jérémie Courraud , Camille Engel , Angélique Quartier , Nathalie Drouot , Ursula Houessou , Damien Plassard , Arthur Sorlin , Elise Brischoux-Boucher , Evan Gouy , Lionel Van Maldergem , Massimiliano Rossi , Gaetan Lesca , Patrick Edery , Audrey Putoux , Frederic Bilan , Brigitte Gilbert-Dussardier , Isis Atallah , Vera M Kalscheuer , Jean-Louis Mandel , Amélie Piton

Further delineation of the female phenotype with KDM5C disease causing variants: 19 new individuals and review of the literature.

Clinical genetics
Avec: Virginie Carmignac , Sophie Nambot , Daphné Lehalle , Patrick Callier , Stephanie Moortgat , Valérie Benoit , Jamal Ghoumid , Bruno Delobel , Thomas Smol , Caroline Thuillier , Cécile Zordan , Sophie Naudion , Thierry Bienvenu , Renaud Touraine , Francis Ramond , Christiane Zweier , André Reis , Cornelia Kraus , Mathilde Nizon , Benjamin Cogné , Alain Verloes , Frédéric Tran Mau-Them , Arthur Sorlin , Thibaud Jouan , Yannis Duffourd , Emilie Tisserant , Christophe Philippe , Antonio Vitobello , Julien Thevenon , Laurence Faivre , Christel Thauvin-Robinet

NR2F1 regulates regional progenitor dynamics in the mouse neocortex and cortical gyrification in BBSOAS patients.

The EMBO journal
Avec: Michele Bertacchi , Anna Lisa Romano , Agnès Loubat , Frederic Tran Mau-Them , Marjolaine Willems , Laurence Faivre , Philippe Khau van Kien , Laurence Perrin , Françoise Devillard , Arthur Sorlin , Paul Kuentz , Christophe Philippe , Aurore Garde , Francesco Neri , Rossella Di Giaimo , Salvatore Oliviero , Silvia Cappello , Ludovico D'Incerti , Carolina Frassoni , Michèle Studer

Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome.

Nature genetics
Avec: Pierre Vabres , Arthur Sorlin , Stanislav S Kholmanskikh , Bénédicte Demeer , Judith St-Onge , Yannis Duffourd , Paul Kuentz , Jean-Benoît Courcet , Virginie Carmignac , Philippine Garret , Didier Bessis , Odile Boute , Alain Bron , Guillaume Captier , Esther Carmi , Bernard Devauchelle , David Geneviève , Catherine Gondry-Jouet , Laurent Guibaud , Arnaud Lafon , Michèle Mathieu-Dramard , Julien Thevenon , William B Dobyns , Geneviève Bernard , Satyamaanasa Polubothu , Francesca Faravelli , Veronica A Kinsler , Christel Thauvin , Laurence Faivre , M Elizabeth Ross , Jean-Baptiste Rivière

Performance of semiconductor sequencing platform for non-invasive prenatal genetic screening for fetal aneuploidy: results from a multicenter prospective cohort study in a clinical setting.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Avec: L Allach El Khattabi , S Brun , P Gueguen , N Chatron , E Guichoux , S Schutz , J Nectoux , A Sorlin , M Quere , J Boudjarane , V Tsatsaris , L Mandelbrot , C Schluth-Bolard , J M Dupont , C Rooryck , Auteur inconnu

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 , Martin Chevarin , Antonio Vitobello , Christophe Philippe , Christel Thauvin-Robinet , Laurence Faivre

Heterozygous Variants in KDM4B Lead to Global Developmental Delay and Neuroanatomical Defects.

American journal of human genetics
Avec: Anna R Duncan , Antonio Vitobello , Stephan C Collins , Valerie E Vancollie , Christopher J Lelliott , Lance Rodan , Jiahai Shi , Ann R Seman , Emanuele Agolini , Antonio Novelli , Paolo Prontera , Maria J Guillen Sacoto , Teresa Santiago-Sim , Aurélien Trimouille , Cyril Goizet , Mathilde Nizon , Ange-Line Bruel , Christophe Philippe , Patricia E Grant , Monica H Wojcik , Joan Stoler , Casie A Genetti , Marieke F van Dooren , Saskia M Maas , Marielle Alders , Laurence Faivre , Arthur Sorlin , Grace Yoon , Binnaz Yalcin , Pankaj B Agrawal

Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy.

Human genetics
Avec: Ilaria Parenti , Daphné Lehalle , Caroline Nava , Erin Torti , Elsa Leitão , Richard Person , Takeshi Mizuguchi , Naomichi Matsumoto , Mitsuhiro Kato , Kazuyuki Nakamura , Stella A de Man , Heidi Cope , Vandana Shashi , Auteur inconnu , Jennifer Friedman , Pascal Joset , Katharina Steindl , Anita Rauch , Irena Muffels , Peter M van Hasselt , Florence Petit , Thomas Smol , Gwenaël Le Guyader , Frédéric Bilan , Arthur Sorlin , Antonio Vitobello , Christophe Philippe , Ingrid M B H van de Laar , Marjon A van Slegtenhorst , Philippe M Campeau , Ping Yee Billie Au , Mitsuko Nakashima , Hirotomo Saitsu , Tatsuya Yamamoto , Yumiko Nomura , Raymond J Louie , Michael J Lyons , Amy Dobson , Astrid S Plomp , M Mahdi Motazacker , Frank J Kaiser , Andrew T Timberlake , Sabine A Fuchs , Christel Depienne , Cyril Mignot

High efficiency and clinical relevance of exome sequencing in the daily practice of neurogenetics.

Journal of medical genetics
Avec: Quentin Thomas , Antonio Vitobello , Frederic Tran Mau-Them , Yannis Duffourd , Agnès Fromont , Maurice Giroud , Benoit Daubail , Agnès Jacquin-Piques , Marie Hervieu-Begue , Thibault Moreau , Guy-Victor Osseby , Philippine Garret , Sophie Nambot , Julian Delanne , Ange-Line Bruel , Arthur Sorlin , Patrick Callier , Anne-Sophie Denomme-Pichon , Laurence Faivre , Yannick Béjot , Christophe Philippe , Christel Thauvin-Robinet , Sébastien Moutton

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 , Martin Chevarin , 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

Copy number variants calling from WES data through eXome hidden Markov model (XHMM) identifies additional 2.5% pathogenic genomic imbalances smaller than 30 kb undetected by array-CGH.

Annals of human genetics
Avec: Emilie Tisserant , Antonio Vitobello , Davide Callegarin , Simon Verdez , Ange-Line Bruel , Ludwig Serge Aho Glele , Arthur Sorlin , Eleonore Viora-Dupont , Marina Konyukh , Nathalie Marle , Sophie Nambot , Sébastien Moutton , Caroline Racine , Aurore Garde , Julian Delanne , Frédéric Tran-Mau-Them , Christophe Philippe , Paul Kuentz , Marlène Poulleau , Muriel Payet , Charlotte Poe , Christel Thauvin-Robinet , Laurence Faivre , Anne-Laure Mosca-Boidron , Julien Thevenon , Yannis Duffourd , Patrick Callier

Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Elke de Boer , Charlotte W Ockeloen , Rosalie A Kampen , Juliet E Hampstead , Alexander J M Dingemans , Dmitrijs Rots , Lukas Lütje , Tazeen Ashraf , Rachel Baker , Mouna Barat-Houari , Brad Angle , Nicolas Chatron , Anne-Sophie Denommé-Pichon , Orrin Devinsky , Christèle Dubourg , Frances Elmslie , Houda Zghal Elloumi , Laurence Faivre , Sarah Fitzgerald-Butt , David Geneviève , Jacqueline A C Goos , Benjamin M Helm , Usha Kini , Amaia Lasa-Aranzasti , Gaetan Lesca , Sally A Lynch , Irene M J Mathijssen , Ruth McGowan , Kristin G Monaghan , Sylvie Odent , Rolph Pfundt , Audrey Putoux , Jeroen van Reeuwijk , Gijs W E Santen , Erina Sasaki , Arthur Sorlin , Peter J van der Spek , Alexander P A Stegmann , Sigrid M A Swagemakers , Irene Valenzuela , Eléonore Viora-Dupont , Antonio Vitobello , Stephanie M Ware , Mathys Wéber , Christian Gilissen , Karen J Low , Simon E Fisher , Lisenka E L M Vissers , Maggie M K Wong , Tjitske Kleefstra

Compassionate use of everolimus for refractory epilepsy in a patient with MTOR mosaic mutation.

European journal of medical genetics
Avec: Nawale Hadouiri , Veronique Darmency , Laurent Guibaud , Alexis Arzimanoglou , Arthur Sorlin , Virginie Carmignac , Jean-Baptiste Rivière , Frédéric Huet , Maxime Luu , Marc Bardou , Christel Thauvin-Robinet , Pierre Vabres , Laurence Faivre

Deciphering exome sequencing data: Bringing mitochondrial DNA variants to light.

Human mutation
Avec: Philippine Garret , Céline Bris , Vincent Procaccio , Patrizia Amati-Bonneau , Pierre Vabres , Nada Houcinat , Emilie Tisserant , François Feillet , Ange-Line Bruel , Virginie Quéré , Christophe Philippe , Arthur Sorlin , Frédéric Tran Mau-Them , Antonio Vitobello , Jean-Marc Costa , Aïcha Boughalem , Detlef Trost , Laurence Faivre , Christel Thauvin-Robinet , Yannis Duffourd

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 , Martin Chevarin , Thibaud Jouan , Sébastien Moutton , Auteur inconnu , Frédéric Tran-Mau-Them , Christophe Philippe , Arthur Sorlin , 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 , Martin Chevarin , Charlotte Poe , Anne-Laure Mosca-Boidron , Patrick Callier , Hana Safraou , Laurence Faivre , Christophe Philippe , Christel Thauvin-Robinet

Clinical and neuroimaging findings in 33 patients with MCAP syndrome: A survey to evaluate relevant endpoints for future clinical trials.

Clinical genetics
Avec: Aurore Garde , Laurent Guibaud , Alice Goldenberg , Florence Petit , Rodolphe Dard , Joelle Roume , Juliette Mazereeuw-Hautier , Nicolas Chassaing , Didier Lacombe , Fanny Morice-Picard , Annick Toutain , Stéphanie Arpin , Olivia Boccara , Renaud Touraine , Patricia Blanchet , Christine Coubes , Marjolaine Willems , Lucile Pinson , Philippe Khau Van Kien , Christine Chiaverini , Fabienne Giuliano , Jean-Luc Alessandri , Michèle Mathieu-Dramard , Gilles Morin , Anne-Claire Bursztejn , Cyril Mignot , Diane Doummar , Frederico Di Rocco , Jenny Cornaton , Claire Nicolas , Elodie Gautier , Maxime Luu , Marc Bardou , Arthur Sorlin , Christophe Philippe , Patrick Edery , Massimiliano Rossi , Virginie Carmignac , Christel Thauvin-Robinet , Pierre Vabres , Laurence Faivre

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

TAOK1 is associated with neurodevelopmental disorder and essential for neuronal maturation and cortical development.

Human mutation
Avec: Geeske M van Woerden , Melanie Bos , Charlotte de Konink , Ben Distel , Rossella Avagliano Trezza , Natasha E Shur , Kristin Barañano , Sonal Mahida , Anna Chassevent , Allison Schreiber , Angelika L Erwin , Karen W Gripp , Fatima Rehman , Saskia Brulleman , Róisín McCormack , Gwynna de Geus , Louisa Kalsner , Arthur Sorlin , Ange-Line Bruel , David A Koolen , Melissa K Gabriel , Mari Rossi , David R Fitzpatrick , Andrew O M Wilkie , Eduardo Calpena , David Johnson , Alice Brooks , Marjon van Slegtenhorst , Julie Fleischer , Daniel Groepper , Kristin Lindstrom , A Micheil Innes , Allison Goodwin , Jennifer Humberson , Amanda Noyes , Katherine G Langley , Aida Telegrafi , Amy Blevins , Jessica Hoffman , Maria J Guillen Sacoto , Jane Juusola , Kristin G Monaghan , Sumit Punj , Marleen Simon , Rolph Pfundt , Ype Elgersma , Tjitske Kleefstra

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 , Martin Chevarin , 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

ATP6V0C variants impair V-ATPase function causing a neurodevelopmental disorder often associated with epilepsy.

Brain : a journal of neurology
Avec: Kari A Mattison , Gilles Tossing , Fred Mulroe , Callum Simmons , Kameryn M Butler , Alison Schreiber , Adnan Alsadah , Derek E Neilson , Karin Naess , Anna Wedell , Anna Wredenberg , Arthur Sorlin , Emma McCann , George J Burghel , Beatriz Menendez , George E Hoganson , Lorenzo D Botto , Francis M Filloux , Ángel Aledo-Serrano , Antonio Gil-Nagel , Katrina Tatton-Brown , Nienke E Verbeek , Bert van der Zwaag , Kyrieckos A Aleck , Andrew C Fazenbaker , Jorune Balciuniene , Holly A Dubbs , Eric D Marsh , Kathryn Garber , Jakob Ek , Morten Duno , Christina E Hoei-Hansen , Matthew A Deardorff , Gordana Raca , Catherine Quindipan , Michele van Hirtum-Das , Jeroen Breckpot , Trine Bjørg Hammer , Rikke S Møller , Andrea Whitney , Andrew G L Douglas , Mira Kharbanda , Nicola Brunetti-Pierri , Manuela Morleo , Vincenzo Nigro , Halie J May , James X Tao , Emanuela Argilli , Elliot H Sherr , William B Dobyns , Auteur inconnu , Richard A Baines , Jim Warwicker , J Alex Parker , Siddharth Banka , Philippe M Campeau , Andrew Escayg

Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish.

Science advances
Avec: Victoria Patterson , Farid Ullah , Laura Bryant , John N Griffin , Alpa Sidhu , Sheila Saliganan , Mackenzie Blaile , Margarita S Saenz , Rosemarie Smith , Sara Ellingwood , Dorothy K Grange , Xuyun Hu , Maimaiti Mireguli , Yanfei Luo , Yiping Shen , Maureen Mulhern , Elaine Zackai , Alyssa Ritter , Kosaki Izumi , Julia Hoefele , Matias Wagner , Korbinian M Riedhammer , Barbara Seitz , Nathaniel H Robin , Dana Goodloe , Cyril Mignot , Boris Keren , Helen Cox , Joanna Jarvis , Maja Hempel , Cynthia Forster Gibson , Frederic Tran Mau-Them , Antonio Vitobello , Ange-Line Bruel , Arthur Sorlin , Sarju Mehta , F Lucy Raymond , Kelly Gilmore , Bradford C Powell , Karen Weck , Chumei Li , Anneke T Vulto-van Silfhout , Thea Giacomini , Maria Margherita Mancardi , Andrea Accogli , Vincenzo Salpietro , Federico Zara , Neeta L Vora , Erica E Davis , Rebecca Burdine , Elizabeth Bhoj

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 , Martin Chevarin , Victor Couturier , Philippine Garret , Christophe Philippe , Yannis Duffourd , Laurence Faivre , Christel Thauvin-Robinet

Variants of NAV3, a neuronal morphogenesis protein, cause intellectual disability, developmental delay, and microcephaly.

Communications biology
Avec: Amama Ghaffar , Tehmeena Akhter , Petter Strømme , Doriana Misceo , Amjad Khan , Eirik Frengen , Muhammad Umair , Bertrand Isidor , Benjamin Cogné , Asma A Khan , Ange-Line Bruel , Arthur Sorlin , Paul Kuentz , Christine Chiaverini , A Micheil Innes , Michael Zech , Marek Baláž , Petra Havrankova , Robert Jech , Zubair M Ahmed , Sheikh Riazuddin , Saima Riazuddin

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 , Martin Chevarin , 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

Next-generation sequencing approaches and challenges in the diagnosis of developmental anomalies and intellectual disability.

Clinical genetics
Avec: Ange-Line Bruel , Antonio Vitobello , Frédéric Tran Mau-Them , Sophie Nambot , Arthur Sorlin , Anne-Sophie Denommé-Pichon , Julian Delanne , Sébastien Moutton , Patrick Callier , Yannis Duffourd , Christophe Philippe , Laurence Faivre , Christel Thauvin-Robinet

Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome.

Nature genetics
Avec: Pierre Vabres , Arthur Sorlin , Stanislav S Kholmanskikh , Bénédicte Demeer , Judith St-Onge , Yannis Duffourd , Paul Kuentz , Jean-Benoît Courcet , Virginie Carmignac , Philippine Garret , Didier Bessis , Odile Boute , Alain Bron , Guillaume Captier , Esther Carmi , Bernard Devauchelle , David Geneviève , Catherine Gondry-Jouet , Laurent Guibaud , Arnaud Lafon , Michèle Mathieu-Dramard , Julien Thevenon , William B Dobyns , Geneviève Bernard , Satyamaanasa Polubothu , Francesca Faravelli , Veronica A Kinsler , Christel Thauvin , Laurence Faivre , M Elizabeth Ross , Jean-Baptiste Rivière

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 , Martin Chevarin , Gilles Millat , Bouchra Khallouk , Thierry Rousseau , Sylvie Falcon-Eicher , Alexandre Vasiljevic , Fara T Harizay , Christel Thauvin-Robinet , Laurence Faivre , Paul Kuentz

Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism.

Molecular autism
Avec: Hyung-Goo Kim , Jill A Rosenfeld , Daryl A Scott , Gerard Bénédicte , Jonathan D Labonne , Jason Brown , Marianne McGuire , Sonal Mahida , Sakkubai Naidu , Jacqueline Gutierrez , Gaetan Lesca , Vincent des Portes , Ange-Line Bruel , Arthur Sorlin , Fan Xia , Yline Capri , Eric Muller , Dianalee McKnight , Erin Torti , Franz Rüschendorf , Oliver Hummel , Zeyaul Islam , Prasanna R Kolatkar , Lawrence C Layman , Duchwan Ryu , Il-Keun Kong , Suneeta Madan-Khetarpal , Cheol-Hee Kim

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 , Martin Chevarin , Mathilde Lefebvre , Marc Bardou , Emilie Tisserant , Maxime Luu , Christine Binquet , Jean-François Deleuze , Céline Verstuyft , Yannis Duffourd , Laurence Faivre

Hearing impairment as an early sign of alpha-mannosidosis in children with a mild phenotype: Report of seven new cases.

American journal of medical genetics. Part A
Avec: Daphné Lehalle , Roberto Colombo , Michael O'Grady , Bénédicte Héron , Nada Houcinat , Paul Kuentz , Sebastien Moutton , Arthur Sorlin , Julien Thevenon , Julian Delanne , Sebastien Gay , Caroline Racine , Aurore Garde , Frédéric Tran Mau-Them , Christophe Philippe , Antonio Vitobello , Sophie Nambot , Frédéric Huet , Yannis Duffourd , François Feillet , Christel Thauvin-Robinet , Sandrine Marlin , Laurence Faivre

The diagnostic rate of inherited metabolic disorders by exome sequencing in a cohort of 547 individuals with developmental disorders.

Molecular genetics and metabolism reports
Avec: Julian Delanne , Ange-Line Bruel , Frédéric Huet , Sébastien Moutton , Sophie Nambot , Margot Grisval , Nada Houcinat , Paul Kuentz , Arthur Sorlin , Patrick Callier , Nolwenn Jean-Marcais , Anne-Laure Mosca-Boidron , Frédéric Tran Mau-Them , Anne-Sophie Denommé-Pichon , Antonio Vitobello , Daphné Lehalle , Salima El Chehadeh , Christine Francannet , Marine Lebrun , Laetitia Lambert , Marie-Line Jacquemont , Marion Gerard-Blanluet , Jean-Luc Alessandri , Marjolaine Willems , Julien Thevenon , Mondher Chouchane , Véronique Darmency , Clémence Fatus-Fauconnier , Sébastien Gay , Marie Bournez , Alice Masurel , Vanessa Leguy , Yannis Duffourd , Christophe Philippe , François Feillet , Laurence Faivre , Christel Thauvin-Robinet

Clinical and molecular data in cases of prenatal localized overgrowth disorder: major implication of genetic variants in PI3K-AKT-mTOR signaling pathway.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Avec: N Bourgon , V Carmignac , A Sorlin , Y Duffourd , C Philippe , C Thauvin-Robinet , L Guibaud , L Faivre , P Vabres , P Kuentz , Auteur inconnu

Fertility in McCune Albright syndrome female: A case study focusing on AMH as a marker of ovarian dysfunction and a literature review.

Journal of gynecology obstetrics and human reproduction
Avec: Mikaël Agopiantz , Arthur Sorlin , Pierre Vabres , Bruno Leheup , Virginie Carmignac , Catherine Malaplate-Armand , Catherine Diligent , Céline Bonnet , Guillaume Gauchotte

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 , Martin Chevarin , 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

Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome.

American journal of human genetics
Avec: Federico Tessadori , Karen Duran , Karen Knapp , Matthias Fellner , Auteur inconnu , Sarah Smithson , Ana Beleza Meireles , Mariet W Elting , Quinten Waisfisz , Anne O'Donnell-Luria , Catherine Nowak , Jessica Douglas , Anne Ronan , Theresa Brunet , Urania Kotzaeridou , Shayna Svihovec , Margarita S Saenz , Isabelle Thiffault , Florencia Del Viso , Patrick Devine , Shannon Rego , Jessica Tenney , Arie van Haeringen , Claudia A L Ruivenkamp , Saskia Koene , Stephen P Robertson , Charulata Deshpande , Rolph Pfundt , Nienke Verbeek , Jiddeke M van de Kamp , Janneke M M Weiss , Anna Ruiz , Elisabeth Gabau , Ehud Banne , Alexander Pepler , Armand Bottani , Sacha Laurent , Michel Guipponi , Emilia Bijlsma , Ange-Line Bruel , Arthur Sorlin , Mary Willis , Zoe Powis , Thomas Smol , Catherine Vincent-Delorme , Diana Baralle , Estelle Colin , Nicole Revencu , Eduardo Calpena , Andrew O M Wilkie , Maya Chopra , Valerie Cormier-Daire , Boris Keren , Alexandra Afenjar , Marcello Niceta , Alessandra Terracciano , Nicola Specchio , Marco Tartaglia , Marlene Rio , Giulia Barcia , Sophie Rondeau , Cindy Colson , Jeroen Bakkers , Peter D Mace , Louise S Bicknell , Gijs van Haaften

Clinico-biological refinement of BCL11B-related disorder and identification of an episignature: A series of 20 unreported individuals.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Quentin Sabbagh , Sadegheh Haghshenas , Juliette Piard , Chloé Trouvé , Jeanne Amiel , Tania Attié-Bitach , Tugce Balci , Mouna Barat-Houari , Alyce Belonis , Odile Boute , Diana S Brightman , Ange-Line Bruel , Stefano Giuseppe Caraffi , Nicolas Chatron , Corinne Collet , William Dufour , Patrick Edery , Chin-To Fong , Carlo Fusco , Vincent Gatinois , Evan Gouy , Anne-Marie Guerrot , Solveig Heide , Aakash Joshi , Natalya Karp , Boris Keren , Marion Lesieur-Sebellin , Jonathan Levy , Michael A Levy , Claire Lozano , Stanislas Lyonnet , Henri Margot , Pauline Marzin , Haley McConkey , Vincent Michaud , Gaël Nicolas , Mevyn Nizard , Alix Paulet , Francesca Peluso , Vincent Pernin , Laurence Perrin , Christophe Philippe , Chitra Prasad , Madhavi Prasad , Raissa Relator , Marlène Rio , Sophie Rondeau , Valentin Ruault , Nathalie Ruiz-Pallares , Elodie Sanchez , Debbie Shears , Victoria Mok Siu , Arthur Sorlin , Matthew Tedder , Mylène Tharreau , Frédéric Tran Mau-Them , Liselot van der Laan , Julien Van Gils , Alain Verloes , Sandra Whalen , Marjolaine Willems , Kévin Yauy , Roberta Zuntini , Jennifer Kerkhof , Bekim Sadikovic , David Geneviève

Expectations, needs and mid-term outcomes in people accessing to secondary findings from ES: 1st French mixed study (FIND Study).

European journal of human genetics : EJHG
Avec: Eléonore Viora-Dupont , Françoise Robert , Aline Chassagne , Aurore Pélissier , Stéphanie Staraci , Damien Sanlaville , Patrick Edery , Gaetan Lesca , Audrey Putoux , Linda Pons , Amandine Cadenes , Amandine Baurand , Caroline Sawka , Geoffrey Bertolone , Myrtille Spetchian , Meriem Yousfi , Dominique Salvi , Elodie Gautier , Antonio Vitobello , Anne-Sophie Denommé-Pichon , Ange-Line Bruel , Frédéric Tran Mau-Them , Anne Faudet , Boris Keren , Audrey Labalme , Nicolas Chatron , Carine Abel , Sophie Dupuis-Girod , Alice Poisson , Julien Buratti , Cyril Mignot , Alexandra Afenjar , Sandra Whalen , Perrine Charles , Solveig Heide , Linda Mouthon , Sébastien Moutton , Arthur Sorlin , Sophie Nambot , Anne-Sophie Briffaut , Marie-Laure Asensio , Christophe Philippe , Christel Thauvin-Robinet , Delphine Héron , Massimiliano Rossi , Nicolas Meunier-Bellard , Marcela Gargiulo , Christine Peyron , Christine Binquet , Laurence Faivre

Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviors.

Nature communications
Avec: Jana Willim , Daniel Woike , Daniel Greene , Sarada Das , Kevin Pfeifer , Weimin Yuan , Anika Lindsey , Omar Itani , Amber L Böhme , Debora Tibbe , Hans-Hinrich Hönck , Fatemeh Hassani Nia , Auteur inconnu , Michael Zech , Theresa Brunet , Laurence Faivre , Arthur Sorlin , Antonio Vitobello , Thomas Smol , Cindy Colson , Kristin Baranano , Krista Schatz , Allan Bayat , Kelly Schoch , Rebecca Spillmann , Erica E Davis , Erin Conboy , Francesco Vetrini , Konrad Platzer , Sonja Neuser , Janina Gburek-Augustat , Alexandra Noel Grace , Bailey Mitchell , Alexander Stegmann , Margje Sinnema , Naomi Meeks , Carol Saunders , Maxime Cadieux-Dion , Juliane Hoyer , Julien Van-Gils , Jean-Madeleine de Sainte-Agathe , Michelle L Thompson , E Martina Bebin , Monika Weisz-Hubshman , Anne-Claude Tabet , Alain Verloes , Jonathan Levy , Xenia Latypova , Sönke Harder , Gary A Silverman , Stephen C Pak , Tim Schedl , Kathleen Freson , Andrew Mumford , Ernest Turro , Christian Schlein , Vandana Shashi , Hans-Jürgen Kreienkamp

Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome.

Nature genetics
Avec: Pierre Vabres , Arthur Sorlin , Stanislav S Kholmanskikh , Bénédicte Demeer , Judith St-Onge , Yannis Duffourd , Paul Kuentz , Jean-Benoît Courcet , Virginie Carmignac , Philippine Garret , Didier Bessis , Odile Boute , Alain Bron , Guillaume Captier , Esther Carmi , Bernard Devauchelle , David Geneviève , Catherine Gondry-Jouet , Laurent Guibaud , Arnaud Lafon , Michèle Mathieu-Dramard , Julien Thevenon , William B Dobyns , Geneviève Bernard , Satyamaanasa Polubothu , Francesca Faravelli , Veronica A Kinsler , Christel Thauvin , Laurence Faivre , M Elizabeth Ross , Jean-Baptiste Rivière

Kosaki overgrowth syndrome: A novel pathogenic variant in PDGFRB and expansion of the phenotype including cerebrovascular complications.

Clinical genetics
Avec: Alison Foster , Basile Chalot , Thalia Antoniadi , Elise Schaefer , Rebecca Keelagher , Gavin Ryan , Quentin Thomas , Christophe Philippe , Ange-Line Bruel , Arthur Sorlin , Christel Thauvin-Robinet , Marc Bardou , Maxime Luu , Veronique Quenardelle , Valerie Wolff , Jessica Woodley , Pierre Vabres , Derek Lim , Rebecca Igbokwe , Annie Joseph , Harriet Walker , Andrea Jester , Jonathan Ellenbogen , Diana Johnson , Bethanie Rooke , Celia Moss , Trevor Cole , Laurence Faivre

Journal of medical genetics
Avec: Daphné Lehalle , Pierre Vabres , Arthur Sorlin , Tatjana Bierhals , Magali Avila , Virginie Carmignac , Martin Chevarin , 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

De Novo Variants in CNOT1, a Central Component of the CCR4-NOT Complex Involved in Gene Expression and RNA and Protein Stability, Cause Neurodevelopmental Delay.

American journal of human genetics
Avec: Lisenka E L M Vissers , Sreehari Kalvakuri , Elke de Boer , Sinje Geuer , Machteld Oud , Inge van Outersterp , Michael Kwint , Melde Witmond , Simone Kersten , Daniel L Polla , Dilys Weijers , Amber Begtrup , Kirsty McWalter , Anna Ruiz , Elisabeth Gabau , Jenny E V Morton , Christopher Griffith , Karin Weiss , Candace Gamble , James Bartley , Hilary J Vernon , Kendra Brunet , Claudia Ruivenkamp , Sarina G Kant , Paul Kruszka , Austin Larson , Alexandra Afenjar , Thierry Billette de Villemeur , Kimberly Nugent , Auteur inconnu , F Lucy Raymond , Hanka Venselaar , Florence Demurger , Claudia Soler-Alfonso , Dong Li , Elizabeth Bhoj , Ian Hayes , Nina Powell Hamilton , Ayesha Ahmad , Rachel Fisher , Myrthe van den Born , Marjolaine Willems , Arthur Sorlin , Julian Delanne , Sebastien Moutton , Philippe Christophe , Frederic Tran Mau-Them , Antonio Vitobello , Himanshu Goel , Lauren Massingham , Chanika Phornphutkul , Jennifer Schwab , Boris Keren , Perrine Charles , Maaike Vreeburg , Lenika De Simone , George Hoganson , Maria Iascone , Donatella Milani , Lucie Evenepoel , Nicole Revencu , D Isum Ward , Kaitlyn Burns , Ian Krantz , Sarah E Raible , Jill R Murrell , Kathleen Wood , Megan T Cho , Hans van Bokhoven , Maximilian Muenke , Tjitske Kleefstra , Rolf Bodmer , Arjan P M de Brouwer

Accelerated genome sequencing with controlled costs for infants in intensive care units: a feasibility study in a French hospital network.

European journal of human genetics : EJHG
Avec: Anne-Sophie Denommé-Pichon , Antonio Vitobello , Robert Olaso , Alban Ziegler , Médéric Jeanne , Frédéric Tran Mau-Them , Victor Couturier , Caroline Racine , Bertrand Isidor , Charlotte Poë , Thibaud Jouan , Anne Boland , Bertrand Fin , Delphine Bacq-Daian , Céline Besse , Aurore Garde , Adeline Prost , Philippine Garret , Émilie Tisserant , Julian Delanne , Sophie Nambot , Aurélien Juven , Magali Gorce , Mathilde Nizon , Marie Vincent , Sébastien Moutton , Mélanie Fradin , Alinoë Lavillaureix , Paul Rollier , Yline Capri , Julien Van-Gils , Tiffany Busa , Sabine Sigaudy , Laurent Pasquier , Magalie Barth , Ange-Line Bruel , Cyril Flamant , Clément Prouteau , Dominique Bonneau , Annick Toutain , Corinne Chantegret , Patrick Callier , Christophe Philippe , Yannis Duffourd , Jean-François Deleuze , Arthur Sorlin , Laurence Faivre , Christel Thauvin-Robinet

Unveiling the crucial neuronal role of the proteasomal ATPase subunit gene

medRxiv : the preprint server for health sciences
Avec: Sébastien Küry , Janelle E Stanton , Geeske van Woerden , Tzung-Chien Hsieh , Cory Rosenfelt , Marie Pier Scott-Boyer , Victoria Most , Tianyun Wang , Jonas Johannes Papendorf , Charlotte de Konink , Wallid Deb , Virginie Vignard , Maja Studencka-Turski , Thomas Besnard , Anna Marta Hajdukowicz , Franziska Thiel , Sophie Möller , Laëtitia Florenceau , Silvestre Cuinat , Sylvain Marsac , Ingrid Wentzensen , Annabelle Tuttle , Cara Forster , Johanna Striesow , Richard Golnik , Damara Ortiz , Laura Jenkins , Jill A Rosenfeld , Alban Ziegler , Clara Houdayer , Dominique Bonneau , Erin Torti , Amber Begtrup , Kristin G Monaghan , Sureni V Mullegama , C M L Nienke Volker-Touw , Koen L I van Gassen , Renske Oegema , Mirjam de Pagter , Katharina Steindl , Anita Rauch , Ivan Ivanovski , Kimberly McDonald , Emily Boothe , Andrew Dauber , Janice Baker , Noelle Andrea V Fabie , Raphael A Bernier , Tychele N Turner , Siddharth Srivastava , Kira A Dies , Lindsay Swanson , Carrie Costin , Rebekah K Jobling , John Pappas , Rachel Rabin , Dmitriy Niyazov , Anne Chun-Hui Tsai , Karen Kovak , David B Beck , McV Malicdan , David R Adams , Lynne Wolfe , Rebecca D Ganetzky , Colleen Muraresku , Davit Babikyan , Zdeněk Sedláček , Miroslava Hančárová , Andrew T Timberlake , Hind Al Saif , Berkley Nestler , Kayla King , M J Hajianpour , Gregory Costain , D'Arcy Prendergast , Chumei Li , David Geneviève , Antonio Vitobello , Arthur Sorlin , Christophe Philippe , Tamar Harel , Ori Toker , Ataf Sabir , Derek Lim , Mark Hamilton , Lisa Bryson , Elaine Cleary , Sacha Weber , Trevor L Hoffman , Anna Maria Cueto-González , Eduardo Fidel Tizzano , David Gómez-Andrés , Marta Codina-Solà , Athina Ververi , Efterpi Pavlidou , Alexandros Lambropoulos , Kyriakos Garganis , Marlène Rio , Jonathan Levy , Sarah Jurgensmeyer , Anne M McRae , Mathieu Kent Lessard , Maria Daniela D'Agostino , Isabelle De Bie , Meret Wegler , Rami Abou Jamra , Susanne B Kamphausen , Viktoria Bothe , Larissa M Busch , Uwe Völker , Elke Hammer , Kristian Wende , Benjamin Cogné , Bertrand Isidor , Jens Meiler , Amélie Bosc-Rosati , Julien Marcoux , Marie-Pierre Bousquet , Jeremie Poschmann , Frédéric Laumonnier , Peter W Hildebrand , Evan E Eichler , Kirsty McWalter , Peter M Krawitz , Arnaud Droit , Ype Elgersma , Andreas M Grabrucker , Francois V Bolduc , Stéphane Bézieau , Frédéric Ebstein , Elke Krüger

Réseau de co-auteurs

Laurence Faivre 31 collaborations
Christophe Philippe 26 collaborations
Antonio Vitobello 25 collaborations
Ange-Line Bruel 23 collaborations
Christel Thauvin-Robinet 22 collaborations
Yannis Duffourd 21 collaborations
Sophie Nambot 15 collaborations
Julien Thevenon 13 collaborations
Paul Kuentz 13 collaborations
Julian Delanne 13 collaborations
Frédéric Tran Mau-Them 11 collaborations
Patrick Callier 11 collaborations
Pierre Vabres 11 collaborations
David Geneviève 11 collaborations
Martin Chevarin 11 collaborations
Virginie Carmignac 10 collaborations
None None 10 collaborations
Sébastien Moutton 10 collaborations
Frederic Tran Mau-Them 9 collaborations
Marjolaine Willems 9 collaborations
Philippine Garret 9 collaborations
Anne-Sophie Denommé-Pichon 8 collaborations
Daphné Lehalle 8 collaborations
Aurore Garde 8 collaborations
Thomas Smol 7 collaborations
Benjamin Cogné 7 collaborations
Boris Keren 7 collaborations
Bertrand Isidor 6 collaborations
Laurent Guibaud 6 collaborations
Jean-Baptiste Rivière 6 collaborations
Patrick Edery 5 collaborations
Gaetan Lesca 5 collaborations
Yline Capri 5 collaborations
Laurence Perrin 5 collaborations
Thibaud Jouan 5 collaborations
Emilie Tisserant 5 collaborations
Cyril Mignot 5 collaborations
Caroline Racine 5 collaborations
Anne-Laure Mosca-Boidron 5 collaborations
Sebastien Moutton 5 collaborations
Florence Petit 4 collaborations
Nicolas Chatron 4 collaborations
Solveig Heide 4 collaborations
Judith St-Onge 4 collaborations
Jean-Benoît Courcet 4 collaborations
Didier Bessis 4 collaborations
Odile Boute 4 collaborations
Michèle Mathieu-Dramard 4 collaborations
William B Dobyns 4 collaborations
Satyamaanasa Polubothu 4 collaborations
Veronica A Kinsler 4 collaborations
Christel Thauvin 4 collaborations
Alexandra Afenjar 4 collaborations
Christine Coubes 4 collaborations
Erin Torti 4 collaborations
Charlotte Poe 4 collaborations
Maxime Luu 4 collaborations
Marc Bardou 4 collaborations
Nada Houcinat 4 collaborations
François Lecoquierre 3 collaborations
Alban Ziegler 3 collaborations
Dominique Bonneau 3 collaborations
Estelle Colin 3 collaborations
Cindy Colson 3 collaborations
Amélie Piton 3 collaborations
Perrine Charles 3 collaborations
Massimiliano Rossi 3 collaborations
Audrey Putoux 3 collaborations
Mathilde Nizon 3 collaborations
Alain Verloes 3 collaborations
Stanislav S Kholmanskikh 3 collaborations
Bénédicte Demeer 3 collaborations
Alain Bron 3 collaborations
Guillaume Captier 3 collaborations
Esther Carmi 3 collaborations
Bernard Devauchelle 3 collaborations
Catherine Gondry-Jouet 3 collaborations
Arnaud Lafon 3 collaborations
Geneviève Bernard 3 collaborations
Francesca Faravelli 3 collaborations
M Elizabeth Ross 3 collaborations
A Sorlin 3 collaborations
Catherine Vincent-Delorme 3 collaborations
Annick Toutain 3 collaborations
Sylvie Odent 3 collaborations
Elise Schaefer 3 collaborations
Maria J Guillen Sacoto 3 collaborations
Quentin Thomas 3 collaborations
Kristin G Monaghan 3 collaborations
Rolph Pfundt 3 collaborations
Tjitske Kleefstra 3 collaborations
Frédéric Huet 3 collaborations
François Feillet 3 collaborations
Victor Couturier 3 collaborations
Elodie Gautier 3 collaborations
Jean-François Deleuze 3 collaborations
Nolwenn Jean-Marçais 3 collaborations
Laetitia Lambert 3 collaborations
Christine Binquet 3 collaborations
Jonathan Levy 3 collaborations
Geoffroy Delplancq 2 collaborations
Stéphane Bézieau 2 collaborations
Bénédicte Duban-Bedu 2 collaborations
Christiane Zweier 2 collaborations
Gaël Nicolas 2 collaborations
Anne-Marie Guerrot 2 collaborations
Austin Larson 2 collaborations
Bruno Delobel 2 collaborations
Linda Mouthon 2 collaborations
Silvestre Cuinat 2 collaborations
Camille Engel 2 collaborations
Evan Gouy 2 collaborations
Renaud Touraine 2 collaborations
Jenny Cornaton 2 collaborations
Claire Nicolas 2 collaborations
Catherine Sarret 2 collaborations
Juliette Piard 2 collaborations
Pankaj B Agrawal 2 collaborations
Vandana Shashi 2 collaborations
Katharina Steindl 2 collaborations
Anita Rauch 2 collaborations
Philippe M Campeau 2 collaborations
Andrew T Timberlake 2 collaborations
Anne-Sophie Denomme-Pichon 2 collaborations
Thomas Besnard 2 collaborations
Maria Iascone 2 collaborations
Alice Masurel 2 collaborations
Siddharth Banka 2 collaborations
Diana Rodriguez 2 collaborations
Nathalie Marle 2 collaborations
Laurence Duplomb 2 collaborations
Frédéric Tran-Mau-Them 2 collaborations
Elke de Boer 2 collaborations
Mouna Barat-Houari 2 collaborations
Irene Valenzuela 2 collaborations
Eléonore Viora-Dupont 2 collaborations
Lisenka E L M Vissers 2 collaborations
Alexis Arzimanoglou 2 collaborations
Valentin Bourgeois 2 collaborations
Hana Safraou 2 collaborations
Alice Goldenberg 2 collaborations
Lucile Pinson 2 collaborations
Christine Chiaverini 2 collaborations
Jean-Luc Alessandri 2 collaborations
V Carmignac 2 collaborations
C Thauvin-Robinet 2 collaborations
C Philippe 2 collaborations
L Faivre 2 collaborations
P Vabres 2 collaborations
P Kuentz 2 collaborations
Charlotte de Konink 2 collaborations
Sonal Mahida 2 collaborations
Andrew O M Wilkie 2 collaborations
Eduardo Calpena 2 collaborations
A Micheil Innes 2 collaborations
Ype Elgersma 2 collaborations
Anne Boland 2 collaborations
Robert Olaso 2 collaborations
Véronique Darmency 2 collaborations
Paul Rollier 2 collaborations
Marie-Line Jacquemont 2 collaborations
Margarita S Saenz 2 collaborations
Maja Hempel 2 collaborations
F Lucy Raymond 2 collaborations
Chumei Li 2 collaborations
Erica E Davis 2 collaborations
Elizabeth Bhoj 2 collaborations
Fanny Laffargue 2 collaborations
Michael Zech 2 collaborations
Thierry Rousseau 2 collaborations
Jill A Rosenfeld 2 collaborations
Aline Chassagne 2 collaborations
Mathilde Lefebvre 2 collaborations
Salima El Chehadeh 2 collaborations
Christine Francannet 2 collaborations
Mélanie Fradin 2 collaborations
Theresa Brunet 2 collaborations
Anna Ruiz 2 collaborations
Elisabeth Gabau 2 collaborations
Nicole Revencu 2 collaborations
Sophie Rondeau 2 collaborations
Marlène Rio 2 collaborations
Sandra Whalen 2 collaborations
Julien Van-Gils 2 collaborations
Derek Lim 2 collaborations
Laurent Pasquier 2 collaborations
Rami Abou Jamra 2 collaborations
Amber Begtrup 2 collaborations
Kirsty McWalter 2 collaborations
Gabriella Vera 1 collaboration
Marie Brasseur-Daudruy 1 collaboration
Sandra Mercier 1 collaboration
Isabelle Sabatier 1 collaboration
Benjamin Durand 1 collaboration
Antje Wiesener 1 collaboration
Reza Maroofian 1 collaboration
Christopher J Carroll 1 collaboration
Hamid Galehdari 1 collaboration
Neda Mazaheri 1 collaboration
Bert Callewaert 1 collaboration
Fabienne Giulianno 1 collaboration
Khaoula Zaafrane-Khachnaoui 1 collaboration
Rebecca Buchert-Lo 1 collaboration
Tobias Haack 1 collaboration
Janine Magg 1 collaboration
Angelika Rieß 1 collaboration
Maria Blandfort 1 collaboration
Stephan Waldmüller 1 collaboration
Veronka Horber 1 collaboration
Emanuela Leonardi 1 collaboration
Roberta Polli 1 collaboration
Licia Turolla 1 collaboration
Alessandra Murgia 1 collaboration
Thierry Frebourg 1 collaboration
Anne Sophie Lebre 1 collaboration
Pascale Saugier-Veber 1 collaboration
Guillaume Jouret 1 collaboration
Sandra Chantot-Bastaraud 1 collaboration
Claire Beneteau 1 collaboration
Marie Denis-Musquer 1 collaboration
Peter D Turnpenny 1 collaboration
Charles Coutton 1 collaboration
Gaëlle Vieville 1 collaboration
Elise Boudry 1 collaboration
Chiara Fallerini 1 collaboration
Francesca Mari 1 collaboration
Caterina Lo Rizzo 1 collaboration
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Jean-Hubert Caberg 1 collaboration
Isabelle Maystadt 1 collaboration
Thomas Courtin 1 collaboration
Philippe Theis 1 collaboration
Christian Müller 1 collaboration
Marizela Kulisic 1 collaboration
Seval Türkmen 1 collaboration
Daniel Stieber 1 collaboration
Dominique Bourgeois 1 collaboration
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Angélique Quartier 1 collaboration
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Elise Brischoux-Boucher 1 collaboration
Lionel Van Maldergem 1 collaboration
Frederic Bilan 1 collaboration
Brigitte Gilbert-Dussardier 1 collaboration
Isis Atallah 1 collaboration
Vera M Kalscheuer 1 collaboration
Jean-Louis Mandel 1 collaboration
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Valérie Benoit 1 collaboration
Jamal Ghoumid 1 collaboration
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N Chatron 1 collaboration
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J M Dupont 1 collaboration
C Rooryck 1 collaboration
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Kim Giraudat 1 collaboration
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Pascal Joset 1 collaboration
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