Sylvie Odent

Affiliations

Service de Génétique Clinique, Centre de référence "Maladies Rares" CLAD-Ouest, université de Rennes 1, CNRS UMR6290, Hôpital SUD, Rennes, France.

Publications (74)

Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiency.

European journal of human genetics : EJHG

Avec: Nicolas Jullien , Pauline Romanet , Mélanie Philippon , Marie-Hélène Quentien , Paolo Beck-Peccoz , Ignacio Bergada , Sylvie Odent , Rachel Reynaud , Anne Barlier , Alexandru Saveanu , Thierry Brue , Frederic Castinetti

Care management in a French cohort with Down syndrome from the AnDDI-Rares/CNSA study.

European journal of medical genetics

Avec: Pierre-Henri Roux-Levy , Damien Sanlaville , Bénédicte De Freminville , Renaud Touraine , Alice Masurel , Isabelle Gueneau , Audrey Cotinaud-Ricou , Sophie Chancenotte , Frédérique Debomy , Delphine Minot , Marie Bournez , Isabelle Rousseau , Sandrine Daniel , Elodie Gautier , Didier Lacombe , Emmanuelle Taupiac , Sylvie Odent , Myriam Mikaty , Sylvie Manouvrier , Jamal Ghoumid , David Geneviève , Natacha Lehman , Tiffany Busa , Charles-Patrick Edery , Jenny Cornaton , Jennifer Gallard , Delphine Héron , Coralie Rastel , Christel Thauvin-Robinet , Alain Verloes , Christine Binquet , Laurence Faivre , Catherine Lejeune

Executive functioning in adolescents and adults with Silver-Russell syndrome.

PloS one

Avec: Mélissa Burgevin , Agnès Lacroix , Fanny Ollivier , Karine Bourdet , Régis Coutant , Bruno Donadille , Laurence Faivre , Sylvie Manouvrier-Hanu , Florence Petit , Christel Thauvin-Robinet , Annick Toutain , Irène Netchine , Sylvie Odent

Cat eye syndrome: Clinical, cytogenetics and familial findings in a large cohort of 43 patients highlighting the importance of congenital heart disease and inherited cases.

American journal of medical genetics. Part A

Avec: Guillaume Jedraszak , Florence Jobic , Aline Receveur , Frédéric Bilan , Brigitte Gilbert-Dussardier , Busa Tiffany , Chantal Missirian , Marjolaine Willems , Sylvie Odent , Josette Lucas , Christele Dubourg , Elise Schaefer , Sophie Scheidecker , James Lespinasse , Alice Goldenberg , Anne-Marie Guerrot , Géraldine Joly-Helas , Pascal Chambon , Cédric Le Caignec , Albert David , Charles Coutton , Véronique Satre , Gaëlle Vieville , Florence Amblard , Radu Harbuz , Damien Sanlaville , Marianne Till , Catherine Vincent-Delorme , Cindy Colson , Joris Andrieux , Sophie Naudion , Jérome Toutain , Caroline Rooryck , Bénédicte de Fréminville , Fabienne Prieur , Valérie Cormier Daire , Daniel Amram , Pascale Kleinfinger , Matthias B Schulze , Gisela Raabe-Meyer , Carolina Courage , Johannes Lemke , Eunice G Stefanou , Thomaidis Loretta , Manolakos Emmanouil , Sophia Kitsiou Tzeli , Henryka Sodowska , Jasen Anderson , Adayapalam Nandini , Henri Copin , Loïc Garçon , Thomas Liehr , Gilles Morin

Differential alternative splicing analysis links variation in ZRSR2 to a novel type of oral-facial-digital syndrome.

Genetics in medicine : official journal of the American College of Medical Genetics

Avec: Laurens Hannes , Marta Atzori , Alice Goldenberg , Jesús Argente , Tania Attie-Bitach , Jeanne Amiel , Catia Attanasio , Débora G Braslavsky , Ange-Line Bruel , Mireille Castanet , Christèle Dubourg , An Jacobs , Stanislas Lyonnet , Julian Martinez-Mayer , María Inés Pérez Millán , Nunziana Pezzella , Elise Pelgrims , Mio Aerden , Marijke Bauters , Anne Rochtus , Paula Scaglia , Ann Swillen , Alejandro Sifrim , Roberta Tammaro , Frederic Tran Mau-Them , Sylvie Odent , Christel Thauvin-Robinet , Brunella Franco , Jeroen Breckpot

Pathogenic variants affecting the TB5 domain of the fibrillin-1 protein: not only in geleophysic/acromicric dysplasias but also in Marfan syndrome.

Journal of medical genetics

Avec: Pauline Arnaud , Zakaria Mougin , Genevieve Baujat , Valérie Drouin-Garraud , Salima El Chehadeh , Laurent Gouya , Sylvie Odent , Guillaume Jondeau , Catherine Boileau , Nadine Hanna , Carine Le Goff

Incidence of cardiovascular events and risk markers in a prospective study of children diagnosed with Marfan syndrome.

Archives of cardiovascular diseases

Avec: Sebastien Hascoet , Thomas Edouard , Julie Plaisancie , Florence Arnoult , Olivier Milleron , Chantal Stheneur , Bertrand Chevallier , Cécile Zordan , Sylvie Odent , Laurence Bal , Laurence Faivre , Bruno Leheup , Sophie Dupuis-Girod , Jean-Bernard Ruidavets , Philippe Acar , Jean Ferrieres , Guillaume Jondeau , Yves Dulac

Diagnosis and management of individuals with Fetal Valproate Spectrum Disorder; a consensus statement from the European Reference Network for Congenital Malformations and Intellectual Disability.

Orphanet journal of rare diseases

Avec: Jill Clayton-Smith , Rebecca Bromley , John Dean , Hubert Journel , Sylvie Odent , Amanda Wood , Janet Williams , Verna Cuthbert , Latha Hackett , Neelo Aslam , Heli Malm , Gregory James , Lena Westbom , Ruth Day , Edmund Ladusans , Adam Jackson , Iain Bruce , Robert Walker , Sangeet Sidhu , Catrina Dyer , Jane Ashworth , Daniel Hindley , Gemma Arca Diaz , Myfanwy Rawson , Peter Turnpenny

Intellectual functioning in Silver-Russell syndrome: First study in adults.

Applied neuropsychology. Adult

Avec: Mélissa Burgevin , Agnès Lacroix , Genavee Brown , Myriam Mikaty , Virginie Coutinho , Irène Netchine , Sylvie Odent

Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature.

Human mutation

Avec: Claire Bar , Giulia Barcia , Mélanie Jennesson , Gwenaël Le Guyader , Amy Schneider , Cyril Mignot , Gaetan Lesca , Delphine Breuillard , Martino Montomoli , Boris Keren , Diane Doummar , Thierry Billette de Villemeur , Alexandra Afenjar , Isabelle Marey , Marion Gerard , Hervé Isnard , Alice Poisson , Sophie Dupont , Patrick Berquin , Pierre Meyer , David Genevieve , Anne De Saint Martin , Salima El Chehadeh , Jamel Chelly , Agnès Guët , Emmanuel Scalais , Nathalie Dorison , Candace T Myers , Heather C Mefford , Katherine B Howell , Carla Marini , Jeremy L Freeman , Anca Nica , Gaetano Terrone , Tayeb Sekhara , Anne-Sophie Lebre , Sylvie Odent , Lynette G Sadleir , Arnold Munnich , Renzo Guerrini , Ingrid E Scheffer , Edor Kabashi , Rima Nabbout

Heterozygous loss-of-function variants of MEIS2 cause a triad of palatal defects, congenital heart defects, and intellectual disability.

European journal of human genetics : EJHG

Avec: Rosalind Verheije , Gabriel S Kupchik , Bertrand Isidor , Hester Y Kroes , Sally Ann Lynch , Lara Hawkes , Maja Hempel , Bruce D Gelb , Jamal Ghoumid , Guylaine D'Amours , Kate Chandler , Christèle Dubourg , Sara Loddo , Zeynep Tümer , Charles Shaw-Smith , Mathilde Nizon , Michael Shevell , Evelien Van Hoof , Kwame Anyane-Yeboa , Gaetana Cerbone , Jill Clayton-Smith , Benjamin Cogné , Pierre Corre , Anniek Corveleyn , Marie De Borre , Tina Duelund Hjortshøj , Mélanie Fradin , Marc Gewillig , Elizabeth Goldmuntz , Greet Hens , Emmanuelle Lemyre , Hubert Journel , Usha Kini , Fanny Kortüm , Cedric Le Caignec , Antonio Novelli , Sylvie Odent , Florence Petit , Anya Revah-Politi , Nicholas Stong , Tim M Strom , Ellen van Binsbergen , Auteur inconnu , Koenraad Devriendt , Jeroen Breckpot

Next-generation sequencing in a series of 80 fetuses with complex cardiac malformations and/or heterotaxy.

Human mutation

Avec: Hui Liu , Anna-Gaëlle Giguet-Valard , Thomas Simonet , Emmanuelle Szenker-Ravi , Laetitia Lambert , Catherine Vincent-Delorme , Sophie Scheidecker , Mélanie Fradin , Fanny Morice-Picard , Sophie Naudion , Viorica Ciorna-Monferrato , Estelle Colin , Florence Fellmann , Sophie Blesson , Pierre-Simon Jouk , Christine Francannet , Florence Petit , Sébastien Moutton , Daphné Lehalle , Nicolas Chassaing , Loubna El Zein , Anne Bazin , Claire Bénéteau , Tania Attié-Bitach , Sylvie M Hanu , Marie-Pierre Brechard , Jean Chiesa , Laurent Pasquier , Caroline Rooryck-Thambo , Lionel Van Maldergem , Christelle Cabrol , Salima El Chehadeh , Alexandre Vasiljevic , Bertrand Isidor , Carine Abel , Julien Thevenon , Sylvie Di Filippo , Adeline Vigouroux-Castera , Jocelyne Attia , Chloé Quelin , Sylvie Odent , Juliette Piard , Fabienne Giuliano , Audrey Putoux , Philippe Khau Van Kien , Catherine Yardin , Renaud Touraine , Bruno Reversade , Patrice Bouvagnet

How do non-geneticist physicians deal with genetic tests? A qualitative analysis.

European journal of human genetics : EJHG

Avec: Laurent Pasquier , Guy Minguet , Sylvie Moisdon-Chataigner , Pascal Jarno , Philippe Denizeau , Ginette Volf , Sylvie Odent , Grégoire Moutel

Adult-onset diagnosis of urea cycle disorders: Results of a French cohort of 71 patients.

Journal of inherited metabolic disease

Avec: Ségolène Toquet , Marta Spodenkiewicz , Claire Douillard , François Maillot , Jean-Baptiste Arnoux , Lena Damaj , Sylvie Odent , Caroline Moreau , Isabelle Redonnet-Vernhet , Samir Mesli , Aude Servais , Esther Noel , Sybill Charriere , Vincent Rigalleau , Christian Lavigne , Elsa Kaphan , Agathe Roubertie , Gérard Besson , Adrien Bigot , Amélie Servettaz , Fanny Mochel , Roselyne Garnotel

High rate of hypomorphic variants as the cause of inherited ataxia and related diseases: study of a cohort of 366 families.

Genetics in medicine : official journal of the American College of Medical Genetics

Avec: Mehdi Benkirane , Cecilia Marelli , Claire Guissart , Agathe Roubertie , Elizabeth Ollagnon , Ariane Choumert , Frédérique Fluchère , Fabienne Ory Magne , Yosra Halleb , Mathilde Renaud , Lise Larrieu , David Baux , Olivier Patat , Idriss Bousquet , Jean-Marie Ravel , Danielle Cuntz-Shadfar , Catherine Sarret , Xavier Ayrignac , Anne Rolland , Raoul Morales , Morgane Pointaux , Cathy Lieutard-Haag , Brice Laurens , Caroline Tillikete , Emilien Bernard , Martial Mallaret , Clarisse Carra-Dallière , Christine Tranchant , Pierre Meyer , Lena Damaj , Laurent Pasquier , Cecile Acquaviva , Annabelle Chaussenot , Bertrand Isidor , Karine Nguyen , William Camu , Alexandre Eusebio , Nicolas Carrière , Audrey Riquet , Eric Thouvenot , Victoria Gonzales , Emilie Carme , Shahram Attarian , Sylvie Odent , Anna Castrioto , Claire Ewenczyk , Perrine Charles , Laurent Kremer , Samira Sissaoui , Nadia Bahi-Buisson , Elsa Kaphan , Adrian Degardin , Bérénice Doray , Sophie Julia , Ganaëlle Remerand , Valerie Fraix , Lydia Abou Haidar , Leila Lazaro , Vincent Laugel , Frederic Villega , Cyril Charlin , Solène Frismand , Marinha Costa Moreira , Tatiana Witjas , Christine Francannet , Ulrike Walther-Louvier , Mélanie Fradin , Brigitte Chabrol , Joel Fluss , Eric Bieth , Giovanni Castelnovo , Sylvain Vergnet , Isabelle Meunier , Alain Verloes , Elise Brischoux-Boucher , Christine Coubes , David Geneviève , Nicolas Lebouc , Jean Phillipe Azulay , Mathieu Anheim , Cyril Goizet , François Rivier , Pierre Labauge , Patrick Calvas , Michel Koenig

DNA methylation episignature in Gabriele-de Vries syndrome.

Genetics in medicine : official journal of the American College of Medical Genetics

Avec: Florian Cherik , Jack Reilly , Jennifer Kerkhof , Michael Levy , Haley McConkey , Mouna Barat-Houari , Kameryn M Butler , Christine Coubes , Jennifer A Lee , Gwenael Le Guyader , Raymond J Louie , Wesley G Patterson , Matthew L Tedder , Mads Bak , Trine Bjørg Hammer , William Craigen , Florence Démurger , Christèle Dubourg , Mélanie Fradin , Rachel Franciskovich , Eirik Frengen , Jennifer Friedman , Nathalie Ruiz Palares , Maria Iascone , Doriana Misceo , Pauline Monin , Sylvie Odent , Christophe Philippe , Flavien Rouxel , Veronica Saletti , Petter Strømme , Perla Cassayre Thulin , Bekim Sadikovic , David Genevieve

PHGDH-related microcephalic dwarfism in two fetuses: Expanding the phenotypical spectrum of L-serine biosynthesis defect.

European journal of medical genetics

Avec: Silvestre Cuinat , Chloé Quélin , Laurent Pasquier , Philippe Loget , Dominique Aussel , Sylvie Odent , Annie Laquerrière , Maia Proisy , Sylvie Mazoyer , Marion Delous , Patrick Edery , Nicolas Chatron , Gaetan Lesca , Audrey Putoux

Extending the clinical spectrum of X-linked Tonne-Kalscheuer syndrome (TOKAS): new insights from the fetal perspective.

Journal of medical genetics

Avec: Silvestre Cuinat , Chloé Quélin , Claire Effray , Christèle Dubourg , Gwenaelle Le Bouar , Anne-Sophie Cabaret-Dufour , Philippe Loget , Maia Proisy , Fanny Sauvestre , Mélie Sarreau , Sophie Martin-Berenguer , Claire Beneteau , Sophie Naudion , Vincent Michaud , Benoit Arveiler , Aurélien Trimouille , Pierre Macé , Sabine Sigaudy , Olga Glazunova , Julia Torrents , Laure Raymond , Marie-Hélène Saint-Frison , Tania Attié-Bitach , Mathilde Lefebvre , Yline Capri , Nicolas Bourgon , Christel Thauvin-Robinet , Frédéric Tran Mau-Them , Ange-Line Bruel , Antonio Vitobello , Anne-Sophie Denommé-Pichon , Laurence Faivre , Anne-Claire Brehin , Alice Goldenberg , Sophie Patrier-Sallebert , Alexandre Perani , Benjamin Dauriat , Sylvie Bourthoumieu , Catherine Yardin , Valentine Marquet , Marion Barnique , Maryse Fiorenza-Gasq , Isabelle Marey , Danielle Tournadre , Raïa Doumit , Frédérique Nugues , Tahsin Stefan Barakat , Francisco Bustos , Sylvie Jaillard , Erika Launay , Laurent Pasquier , Sylvie Odent

The NLRP3 p.A441V Mutation in

ACR open rheumatology

Avec: Fawaz Awad , Eman Assrawi , Claire Jumeau , Sylvie Odent , Veronique Despert , Gérard Cam , Aleth Perdriger , Camille Louvrier , Laetitia Cobret , Bruno Copin , Sandra Chantot-Bastaraud , Philippe Duquesnoy , William Piterboth , Claire Le Jeunne , Genevieve Quenum-Miraillet , Jean Pierre Siffroi , Sophie Georgin-Lavialle , Gilles Grateau , Marie Legendre , Irina Giurgea , Sonia-Athina Karabina , Serge Amselem

Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability.

American journal of human genetics

Avec: Benjamin Cogné , Sophie Ehresmann , Eliane Beauregard-Lacroix , Justine Rousseau , Thomas Besnard , Thomas Garcia , Slavé Petrovski , Shiri Avni , Kirsty McWalter , Patrick R Blackburn , Stephan J Sanders , Kévin Uguen , Jacqueline Harris , Julie S Cohen , Moira Blyth , Anna Lehman , Jonathan Berg , Mindy H Li , Usha Kini , Shelagh Joss , Charlotte von der Lippe , Christopher T Gordon , Jennifer B Humberson , Laurie Robak , Daryl A Scott , Vernon R Sutton , Cara M Skraban , Jennifer J Johnston , Annapurna Poduri , Magnus Nordenskjöld , Vandana Shashi , Erica H Gerkes , Ernie M H F Bongers , Christian Gilissen , Yuri A Zarate , Malin Kvarnung , Kevin P Lally , Peggy A Kulch , Brina Daniels , Andres Hernandez-Garcia , Nicholas Stong , Julie McGaughran , Kyle Retterer , Kristian Tveten , Jennifer Sullivan , Madeleine R Geisheker , Asbjorg Stray-Pedersen , Jennifer M Tarpinian , Eric W Klee , Julie C Sapp , Jacob Zyskind , Øystein L Holla , Emma Bedoukian , Francesca Filippini , Anne Guimier , Arnaud Picard , Øyvind L Busk , Jaya Punetha , Rolph Pfundt , Anna Lindstrand , Ann Nordgren , Fayth Kalb , Megha Desai , Ashley Harmon Ebanks , Shalini N Jhangiani , Tammie Dewan , Zeynep H Coban Akdemir , Aida Telegrafi , Elaine H Zackai , Amber Begtrup , Xiaofei Song , Annick Toutain , Ingrid M Wentzensen , Sylvie Odent , Dominique Bonneau , Xénia Latypova , Wallid Deb , Auteur inconnu , Sylvia Redon , Frédéric Bilan , Marine Legendre , Caitlin Troyer , Kerri Whitlock , Oana Caluseriu , Marine I Murphree , Pavel N Pichurin , Katherine Agre , Ralitza Gavrilova , Tuula Rinne , Meredith Park , Catherine Shain , Erin L Heinzen , Rui Xiao , Jeanne Amiel , Stanislas Lyonnet , Bertrand Isidor , Leslie G Biesecker , Dan Lowenstein , Jennifer E Posey , Anne-Sophie Denommé-Pichon , Auteur inconnu , Claude Férec , Xiang-Jiao Yang , Jill A Rosenfeld , Brigitte Gilbert-Dussardier , Séverine Audebert-Bellanger , Richard Redon , Holly A F Stessman , Christoffer Nellaker , Yaping Yang , James R Lupski , David B Goldstein , Evan E Eichler , Francois Bolduc , Stéphane Bézieau , Sébastien Küry , Philippe M Campeau

Genetic diversity and pathogenic variants as possible predictors of severity in a French sample of nonsyndromic heritable thoracic aortic aneurysms and dissections (nshTAAD).

Genetics in medicine : official journal of the American College of Medical Genetics

Avec: Pauline Arnaud , Nadine Hanna , Louise Benarroch , Mélodie Aubart , Laurence Bal , Patrice Bouvagnet , Tiffany Busa , Yves Dulac , Sophie Dupuis-Girod , Thomas Edouard , Laurence Faivre , Laurent Gouya , Didier Lacombe , Maud Langeois , Bruno Leheup , Olivier Milleron , Sophie Naudion , Sylvie Odent , Maria Tchitchinadze , Jacques Ropers , Guillaume Jondeau , Catherine Boileau

Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency.

Genetics in medicine : official journal of the American College of Medical Genetics

Avec: Ash Zawerton , Cyril Mignot , Ashley Sigafoos , Patrick R Blackburn , Abdul Haseeb , Kirsty McWalter , Shoji Ichikawa , Caroline Nava , Boris Keren , Perrine Charles , Isabelle Marey , Anne-Claude Tabet , Jonathan Levy , Laurence Perrin , Andreas Hartmann , Gaetan Lesca , Caroline Schluth-Bolard , Pauline Monin , Sophie Dupuis-Girod , Maria J Guillen Sacoto , Rhonda E Schnur , Zehua Zhu , Alice Poisson , Salima El Chehadeh , Yves Alembik , Ange-Line Bruel , Daphné Lehalle , Sophie Nambot , Sébastien Moutton , Sylvie Odent , Sylvie Jaillard , Christèle Dubourg , Yvonne Hilhorst-Hofstee , Tina Barbaro-Dieber , Lucia Ortega , Elizabeth J Bhoj , Diane Masser-Frye , Lynne M Bird , Kristin Lindstrom , Keri M Ramsey , Vinodh Narayanan , Emily Fassi , Marcia Willing , Trevor Cole , Claire G Salter , Rhoda Akilapa , Anthony Vandersteen , Natalie Canham , Patrick Rump , Erica H Gerkes , Jolien S Klein Wassink-Ruiter , Emilia Bijlsma , Mariëtte J V Hoffer , Marcelo Vargas , Antonina Wojcik , Florian Cherik , Christine Francannet , Jill A Rosenfeld , Keren Machol , Daryl A Scott , Carlos A Bacino , Xia Wang , Gary D Clark , Marta Bertoli , Simon Zwolinski , Rhys H Thomas , Ela Akay , Richard C Chang , Rebekah Bressi , Rossana Sanchez Russo , Myriam Srour , Laura Russell , Anne-Marie E Goyette , Lucie Dupuis , Roberto Mendoza-Londono , Catherine Karimov , Maries Joseph , Mathilde Nizon , Benjamin Cogné , Alma Kuechler , Amélie Piton , Auteur inconnu , Eric W Klee , Véronique Lefebvre , Karl J Clark , Christel Depienne

STAG3 homozygous missense variant causes primary ovarian insufficiency and male non-obstructive azoospermia.

Molecular human reproduction

Avec: Sylvie Jaillard , Kenneth McElreavy , Gorjana Robevska , Linda Akloul , Farah Ghieh , Rajini Sreenivasan , Marion Beaumont , Anu Bashamboo , Joelle Bignon-Topalovic , Anne-Sophie Neyroud , Katrina Bell , Elisabeth Veron-Gastard , Erika Launay , Jocelyn van den Bergen , Bénédicte Nouyou , François Vialard , Marc-Antoine Belaud-Rotureau , Katie L Ayers , Sylvie Odent , Célia Ravel , Elena J Tucker , Andrew H Sinclair

Incidental diagnosis of mucopolysaccharidosis type I in an infant with chronic intestinal pseudoobstruction by exome sequencing.

Molecular genetics and metabolism reports

Avec: Auriane Cospain , Christèle Dubourg , Swellen Gastineau , Samia Pichard , Virginie Gandemer , Jacinthe Bonneau , Marie de Tayrac , Caroline Moreau , Sylvie Odent , Laurent Pasquier , Lena Damaj , Alinoë Lavillaureix

Renal cell carcinoma with leiomyomatous stroma in tuberous sclerosis complex: a distinct entity.

Virchows Archiv : an international journal of pathology

Avec: Marjorie Gournay , Frédéric Dugay , Marc-Antoine Belaud-Rotureau , Benoit Peyronnet , Romain Mathieu , Gregory Verhoest , Karim Bensalah , Sylvie Odent , Philippe Denizeau , Cécile Vigneau , Aurélien Morini , Nathalie Rioux-Leclercq , Solène-Florence Kammerer-Jacquet

Phenotypic spectrum of TGFB3 disease-causing variants in a Dutch-French cohort and first report of a homozygous patient.

Clinical genetics

Avec: Luisa Marsili , Eline Overwater , Nadine Hanna , Geneviève Baujat , Marieke J H Baars , Catherine Boileau , Dominique Bonneau , Anne Claire Brehin , Yline Capri , Ho Y Cheung , Eelco Dulfer , Marion Gerard , Laurent Gouya , Yvonne Hilhorst-Hofstee , Arjan C Houweling , Bertrand Isidor , Lauriane Le Gloan , Leonie A Menke , Sylvie Odent , Fanny Morice-Picard , Clemence Vanlerberghe , Els Voorhoeve , J Peter van Tintelen , Alessandra Maugeri , Pauline Arnaud

ATP7A mutation with occipital horns and distal motor neuropathy: A continuum.

European journal of medical genetics

Avec: Melanie Fradin , Alinoe Lavillaureix , Sylvie Jaillard , Chloe Quelin , Paul Sauleau , Marie-Christine Minot , Dominique Menard , Gilles Edan , Irene Ceballos , Catherine Treguier , Maia Proisy , Corinne Magdelaine , Anne-Sophie Lia , Sylvie Odent , Laurent Pasquier

Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction.

American journal of human genetics

Avec: Joery den Hoed , Elke de Boer , Norine Voisin , Alexander J M Dingemans , Nicolas Guex , Laurens Wiel , Christoffer Nellaker , Shivarajan M Amudhavalli , Siddharth Banka , Frederique S Bena , Bruria Ben-Zeev , Vincent R Bonagura , Ange-Line Bruel , Theresa Brunet , Han G Brunner , Hui B Chew , Jacqueline Chrast , Loreta Cimbalistienė , Hilary Coon , Auteur inconnu , Emmanuèlle C Délot , Florence Démurger , Anne-Sophie Denommé-Pichon , Christel Depienne , Dian Donnai , David A Dyment , Orly Elpeleg , Laurence Faivre , Christian Gilissen , Leslie Granger , Benjamin Haber , Yasuo Hachiya , Yasmin Hamzavi Abedi , Jennifer Hanebeck , Jayne Y Hehir-Kwa , Brooke Horist , Toshiyuki Itai , Adam Jackson , Rosalyn Jewell , Kelly L Jones , Shelagh Joss , Hirofumi Kashii , Mitsuhiro Kato , Anja A Kattentidt-Mouravieva , Fernando Kok , Urania Kotzaeridou , Vidya Krishnamurthy , Vaidutis Kučinskas , Alma Kuechler , Alinoë Lavillaureix , Pengfei Liu , Linda Manwaring , Naomichi Matsumoto , Benoît Mazel , Kirsty McWalter , Vardiella Meiner , Mohamad A Mikati , Satoko Miyatake , Takeshi Mizuguchi , Lip H Moey , Shehla Mohammed , Hagar Mor-Shaked , Hayley Mountford , Ruth Newbury-Ecob , Sylvie Odent , Laura Orec , Matthew Osmond , Timothy B Palculict , Michael Parker , Andrea K Petersen , Rolph Pfundt , Eglė Preikšaitienė , Kelly Radtke , Emmanuelle Ranza , Jill A Rosenfeld , Teresa Santiago-Sim , Caitlin Schwager , Margje Sinnema , Lot Snijders Blok , Rebecca C Spillmann , Alexander P A Stegmann , Isabelle Thiffault , Linh Tran , Adi Vaknin-Dembinsky , Juliana H Vedovato-Dos-Santos , Samantha A Schrier Vergano , Eric Vilain , Antonio Vitobello , Matias Wagner , Androu Waheeb , Marcia Willing , Britton Zuccarelli , Usha Kini , Dianne F Newbury , Tjitske Kleefstra , Alexandre Reymond , Simon E Fisher , Lisenka E L M Vissers

Associations between cognitive performance and the rehabilitation, medical care and social support provided to French children with Prader-Willi syndrome.

European journal of medical genetics

Avec: Pierre-Henri Roux-Levy , Marie Bournez , Alice Masurel , Nolwenn Jean , Sophie Chancenotte , Mathieu Bordes , Frédérique Debomy , Delphine Minot , Emilie Schmitt , Sandrine Vinault , Elodie Gautier , Didier Lacombe , Sylvie Odent , Myriam Mikaty , Sylvie Manouvrier , Jamal Ghoumid , David Geneviève , Natacha Lehman , Nicole Philip , Patrick Edery , Jenny Cornaton , Jennifer Gallard , Delphine Héron , Coralie Rastel , Frédéric Huet , Christel Thauvin-Robinet , Alain Verloes , Christine Binquet , Maïté Tauber , Catherine Lejeune , Laurence Faivre

Developmental and epilepsy spectrum of KCNB1 encephalopathy with long-term outcome.

Epilepsia

Avec: Claire Bar , Mathieu Kuchenbuch , Giulia Barcia , Amy Schneider , Mélanie Jennesson , Gwenaël Le Guyader , Gaetan Lesca , Cyril Mignot , Martino Montomoli , Elena Parrini , Hervé Isnard , Anne Rolland , Boris Keren , Alexandra Afenjar , Nathalie Dorison , Lynette G Sadleir , Delphine Breuillard , Raphael Levy , Marlène Rio , Sophie Dupont , Susanna Negrin , Alberto Danieli , Emmanuel Scalais , Anne De Saint Martin , Salima El Chehadeh , Jamel Chelly , Alice Poisson , Anne-Sophie Lebre , Anca Nica , Sylvie Odent , Tayeb Sekhara , Vesna Brankovic , Alice Goldenberg , Pascal Vrielynck , Damien Lederer , Hélène Maurey , Gaetano Terrone , Claude Besmond , Laurence Hubert , Patrick Berquin , Thierry Billette de Villemeur , Bertrand Isidor , Jeremy L Freeman , Heather C Mefford , Candace T Myers , Katherine B Howell , Andrés Rodríguez-Sacristán Cascajo , Pierre Meyer , David Genevieve , Agnès Guët , Diane Doummar , Julien Durigneux , Marieke F van Dooren , Marie Claire Y de Wit , Marion Gerard , Isabelle Marey , Arnold Munnich , Renzo Guerrini , Ingrid E Scheffer , Edor Kabashi , Rima Nabbout

Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder.

American journal of human genetics

Avec: Sébastien Küry , Frédéric Ebstein , Alice Mollé , Thomas Besnard , Ming-Kang Lee , Virginie Vignard , Tiphaine Hery , Mathilde Nizon , Grazia M S Mancini , Jacques C Giltay , Benjamin Cogné , Kirsty McWalter , Wallid Deb , Hagar Mor-Shaked , Hong Li , Rhonda E Schnur , Ingrid M Wentzensen , Anne-Sophie Denommé-Pichon , Cynthia Fourgeux , Frans W Verheijen , Eva Faurie , Rachel Schot , Cathy A Stevens , Daphne J Smits , Eileen Barr , Ruth Sheffer , Jonathan A Bernstein , Chandler L Stimach , Eliana Kovitch , Vandana Shashi , Kelly Schoch , Whitney Smith , Richard H van Jaarsveld , Anna C E Hurst , Kirstin Smith , Evan H Baugh , Suzanne G Bohm , Emílie Vyhnálková , Lukáš Ryba , Capucine Delnatte , Juanita Neira , Dominique Bonneau , Annick Toutain , Jill A Rosenfeld , Auteur inconnu , Séverine Audebert-Bellanger , Brigitte Gilbert-Dussardier , Sylvie Odent , Frédéric Laumonnier , Seth I Berger , Ann C M Smith , Franck Bourdeaut , Marc-Henri Stern , Richard Redon , Elke Krüger , Raphaël Margueron , Stéphane Bézieau , Jeremie Poschmann , Bertrand Isidor

Adaptive behavior and psychiatric comorbidities in KCNB1 encephalopathy.

Epilepsy & behavior : E&B

Avec: Claire Bar , Delphine Breuillard , Mathieu Kuchenbuch , Mélanie Jennesson , Gwenaël Le Guyader , Hervé Isnard , Anne Rolland , Diane Doummar , Joel Fluss , Alexandra Afenjar , Patrick Berquin , Anne De Saint Martin , Sophie Dupont , Alice Goldenberg , Damien Lederer , Gaétan Lesca , Hélène Maurey , Pierre Meyer , Cyril Mignot , Anca Nica , Sylvie Odent , Alice Poisson , Emmanuel Scalais , Tayeb Sekhara , Pascal Vrielynck , Giulia Barcia , Rima Nabbout

SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidance.

Human molecular genetics

Avec: Amélie Cordovado , Martina Schaettin , Médéric Jeanne , Veranika Panasenkava , Anne-Sophie Denommé-Pichon , Boris Keren , Cyril Mignot , Martine Doco-Fenzy , Lance Rodan , Keri Ramsey , Vinodh Narayanan , Julie R Jones , Eloise J Prijoles , Wendy G Mitchell , Jillian R Ozmore , Kali Juliette , Erin Torti , Elizabeth A Normand , Leslie Granger , Andrea K Petersen , Margaret G Au , Juliann P Matheny , Chanika Phornphutkul , Mary-Kathryn Chambers , Joaquín-Alejandro Fernández-Ramos , Eduardo López-Laso , Michael C Kruer , Somayeh Bakhtiari , Marcella Zollino , Manuela Morleo , Giuseppe Marangi , Davide Mei , Tiziana Pisano , Renzo Guerrini , Raymond J Louie , Anna Childers , David B Everman , Betrand Isidor , Séverine Audebert-Bellanger , Sylvie Odent , Dominique Bonneau , Brigitte Gilbert-Dussardier , Richard Redon , Stéphane Bézieau , Frédéric Laumonnier , Esther T Stoeckli , Annick Toutain , Marie-Laure Vuillaume

Deficiency of the minor spliceosome component U4atac snRNA secondarily results in ciliary defects in human and zebrafish.

Proceedings of the National Academy of Sciences of the United States of America

Avec: Deepak Khatri , Audrey Putoux , Audric Cologne , Sophie Kaltenbach , Alicia Besson , Eloïse Bertiaux , Justine Guguin , Adèle Fendler , Marie A Dupont , Clara Benoit-Pilven , Leila Qebibo , Samira Ahmed-Elie , Séverine Audebert-Bellanger , Pierre Blanc , Thomas Rambaud , Martin Castelle , Gaëlle Cornen , Sarah Grotto , Agnès Guët , Laurent Guibaud , Caroline Michot , Sylvie Odent , Lyse Ruaud , Elise Sacaze , Virginie Hamel , Rémy Bordonné , Anne-Louise Leutenegger , Patrick Edery , Lydie Burglen , Tania Attié-Bitach , Sylvie Mazoyer , Marion Delous

Changes in French family medicine residents' perspectives about patient partners' participation in teaching: A qualitative study in co-facilitated practice exchange groups.

Medical teacher

Avec: Juliette Guary , Priscille Hébert , Arnaud Maury , Maud Le Ridant , Pierric Renaut , Sylvie Odent , Laure Fiquet , Emmanuel Allory

DISP1 deficiency: monoallelic and biallelic variants cause a spectrum of midline craniofacial malformations.

Genetics in medicine : official journal of the American College of Medical Genetics

Avec: Alinoë Lavillaureix , Paul Rollier , Artem Kim , Veranika Panasenkava , Marie De Tayrac , Wilfrid Carré , Hélène Guyodo , Marie Faoucher , Elisabeth Poirel , Linda Akloul , Chloe Quelin , Sandra Whalen , Jessica Bos , Marjoleine Broekema , Johanna M van Hagen , Katheryn Grand , Michelle Allen-Sharpley , Emily Magness , Scott McLean , Hülya Kayserili , Umut Altunoglu , Angie En Qi Chong , Shifeng Xue , Mederic Jeanne , Naif Almontashiri , Wisam Habhab , Clemence Vanlerberghe , Laurence Faivre , Eleonore Viora Dupont , Christophe Philippe , Hana Safraou , Fanny Laffargue , Luisa Mittendorf , Rami Abou Jamra , Siddaramappa Jagdish Patil , Ashwin Dalal , Asodu Sandeep Sarma , Boris Keren , Bruno Reversade , Christèle Dubourg , Sylvie Odent , Valérie Dupé

Gene Editing Corrects

The CRISPR journal

Avec: Delphine Leclerc , Louise Goujon , Sylvie Jaillard , Bénédicte Nouyou , Laurence Cluzeau , Léna Damaj , Christèle Dubourg , Amandine Etcheverry , Thierry Levade , Roseline Froissart , Stéphane Dréano , Xavier Guillory , Leif A Eriksson , Erika Launay , Frédéric Mouriaux , Marc-Antoine Belaud-Rotureau , Sylvie Odent , David Gilot

BRAT1-related disorders: phenotypic spectrum and phenotype-genotype correlations from 97 patients.

European journal of human genetics : EJHG

Avec: Camille Engel , Stéphanie Valence , Geoffroy Delplancq , Reza Maroofian , Andrea Accogli , Emanuele Agolini , Fowzan S Alkuraya , Valentina Baglioni , Irene Bagnasco , Mathilde Becmeur-Lefebvre , Enrico Bertini , Ingo Borggraefe , Elise Brischoux-Boucher , Ange-Line Bruel , Alfredo Brusco , Dalal K Bubshait , Christelle Cabrol , Maria Roberta Cilio , Marie-Coralie Cornet , Christine Coubes , Olivier Danhaive , Valérie Delague , Anne-Sophie Denommé-Pichon , Marilena Carmela Di Giacomo , Martine Doco-Fenzy , Hartmut Engels , Kirsten Cremer , Marion Gérard , Joseph G Gleeson , Delphine Heron , Joanna Goffeney , Anne Guimier , Frederike L Harms , Henry Houlden , Michele Iacomino , Rauan Kaiyrzhanov , Benjamin Kamien , Ehsan Ghayoor Karimiani , Dror Kraus , Paul Kuentz , Kerstin Kutsche , Damien Lederer , Lauren Massingham , Cyril Mignot , Déborah Morris-Rosendahl , Lakshmi Nagarajan , Sylvie Odent , Clothilde Ormières , Jennifer Neil Partlow , Laurent Pasquier , Lynette Penney , Christophe Philippe , Gianluca Piccolo , Cathryn Poulton , Audrey Putoux , Marlène Rio , Christelle Rougeot , Vincenzo Salpietro , Ingrid Scheffer , Amy Schneider , Siddharth Srivastava , Rachel Straussberg , Pasquale Striano , Enza Maria Valente , Perrine Venot , Laurent Villard , Antonio Vitobello , Johanna Wagner , Matias Wagner , Maha S Zaki , Federizo Zara , Gaetan Lesca , Vahid Reza Yassaee , Mohammad Miryounesi , Farzad Hashemi-Gorji , Mehran Beiraghi , Farah Ashrafzadeh , Hamid Galehdari , Christopher Walsh , Antonio Novelli , Moritz Tacke , Dinara Sadykova , Yerdan Maidyrov , Kairgali Koneev , Chingiz Shashkin , Valeria Capra , Mina Zamani , Lionel Van Maldergem , Lydie Burglen , Juliette Piard

Episignatures in practice: independent evaluation of published episignatures for the molecular diagnostics of ten neurodevelopmental disorders.

European journal of human genetics : EJHG

Avec: 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 , Perrine Brunelle , Roseline Caumes , Perrine Charles , Nicolas Chassaing , Nicolas Chatron , Benjamin Cogné , Estelle Colin , Valérie Cormier-Daire , Rodolphe Dard , Benjamin Dauriat , Julian Delanne , Jean-François Deleuze , Florence Demurger , Anne-Sophie Denommé-Pichon , Christel Depienne , Anne Dieux , Christèle Dubourg , Patrick Edery , Salima El Chehadeh , Laurence Faivre , Patricia Fergelot , Mélanie Fradin , Aurore Garde , David Geneviève , Brigitte Gilbert-Dussardier , Cyril Goizet , Alice Goldenberg , Evan Gouy , Anne-Marie Guerrot , Anne Guimier , Inès Harzalla , Delphine Héron , Bertrand Isidor , Didier Lacombe , Xavier Le Guillou Horn , Boris Keren , Alma Kuechler , Elodie Lacaze , Alinoë Lavillaureix , Daphné Lehalle , Gaëtan Lesca , James Lespinasse , Jonathan Levy , Stanislas Lyonnet , Godeliève Morel , Nolwenn Jean-Marçais , Sandrine Marlin , Luisa Marsili , Cyril Mignot , Sophie Nambot , Mathilde Nizon , Robert Olaso , Laurent Pasquier , Laurine Perrin , Florence Petit , Veronique Pingault , Amélie Piton , Fabienne Prieur , Audrey Putoux , Marc Planes , Sylvie Odent , Chloé Quélin , Sylvia Quemener-Redon , Mélanie Rama , Marlène Rio , Massimiliano Rossi , Elise Schaefer , Sophie Rondeau , Pascale Saugier-Veber , Thomas Smol , Sabine Sigaudy , Renaud Touraine , Frederic Tran Mau-Them , Aurélien Trimouille , Julien Van Gils , Clémence Vanlerberghe , Valérie Vantalon , Gabriella Vera , Marie Vincent , Alban Ziegler , Olivier Guillin , Dominique Campion , Camille Charbonnier

Intellectual Disability and Behavioral Deficits Linked to CYFIP1 Missense Variants Disrupting Actin Polymerization.

Biological psychiatry

Avec: Vittoria Mariano , Alexandros K Kanellopoulos , Carlotta Ricci , Daniele Di Marino , Sarah C Borrie , Sebastian Dupraz , Frank Bradke , Tilmann Achsel , Eric Legius , Sylvie Odent , Pierre Billuart , Thierry Bienvenu , Claudia Bagni

Integrating RNA-Seq into genome sequencing workflow enhances the analysis of structural variants causing neurodevelopmental disorders.

Journal of medical genetics

Avec: Kevin Riquin , Bertrand Isidor , Sandra Mercier , Mathilde Nizon , Estelle Colin , Dominique Bonneau , Laurent Pasquier , Sylvie Odent , Xavier Maximin Le Guillou Horn , Gwenaël Le Guyader , Annick Toutain , Vincent Meyer , Jean-François Deleuze , Olivier Pichon , Martine Doco-Fenzy , Stéphane Bézieau , Benjamin Cogné

Synonymous variants in holoprosencephaly alter codon usage and impact the Sonic Hedgehog protein.

Brain : a journal of neurology

Avec: Artem Kim , Jérôme Le Douce , Farah Diab , Monika Ferovova , Christèle Dubourg , Sylvie Odent , Valérie Dupé , Véronique David , Luis Diambra , Erwan Watrin , Marie de Tayrac

Disrupted Hypothalamo-Pituitary Axis in Association With Reduced SHH Underlies the Pathogenesis of NOTCH-Deficiency.

The Journal of clinical endocrinology and metabolism

Avec: Houda Hamdi-Rozé , Michelle Ware , Hélène Guyodo , Aurélie Rizzo , Leslie Ratié , Maïlys Rupin , Wilfrid Carré , Artem Kim , Sylvie Odent , Christèle Dubourg , Véronique David , Marie de Tayrac , Valérie Dupé

De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides-Baraitser syndrome.

Genetics in medicine : official journal of the American College of Medical Genetics

Avec: Gerarda Cappuccio , Camille Sayou , Pauline Le Tanno , Emilie Tisserant , Ange-Line Bruel , Sara El Kennani , Joaquim Sá , Karen J Low , Cristina Dias , Markéta Havlovicová , Miroslava Hančárová , Evan E Eichler , Françoise Devillard , Sébastien Moutton , Julien Van-Gils , Christèle Dubourg , Sylvie Odent , Bénédicte Gerard , Amélie Piton , Toshiyuki Yamamoto , Nobuhiko Okamoto , Helen Firth , Kay Metcalfe , Anna Moh , Kimberly A Chapman , Erfan Aref-Eshghi , Jennifer Kerkhof , Annalaura Torella , Vincenzo Nigro , Laurence Perrin , Juliette Piard , Gwenaël Le Guyader , Thibaud Jouan , Christel Thauvin-Robinet , Yannis Duffourd , Jaya K George-Abraham , Catherine A Buchanan , Denise Williams , Usha Kini , Kate Wilson , Auteur inconnu , Sérgio B Sousa , Raoul C M Hennekam , Bekim Sadikovic , Julien Thevenon , Jérôme Govin , Antonio Vitobello , Nicola Brunetti-Pierri

A new mutational hotspot in the SKI gene in the context of MFS/TAA molecular diagnosis.

Human genetics

Avec: Pauline Arnaud , Caroline Racine , Nadine Hanna , Julien Thevenon , Jean-Luc Alessandri , Dominique Bonneau , Jill Clayton-Smith , Christine Coubes , Bruno Delobel , Sophie Dupuis-Girod , Laurent Gouya , Sylvie Odent , Virginie Carmignac , Christel Thauvin-Robinet , Carine Le Goff , Guillaume Jondeau , Catherine Boileau , Laurence Faivre

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

Journal of medical genetics

Avec: Martin Chevarin , 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

Expanding the phenotype of the X-linked BCOR microphthalmia syndromes.

Human genetics

Avec: Nicola Ragge , Bertrand Isidor , Pierre Bitoun , Sylvie Odent , Irina Giurgea , Benjamin Cogné , Wallid Deb , Marie Vincent , Jessica Le Gall , Jenny Morton , Derek Lim , Auteur inconnu , Guylène Le Meur , Celia Zazo Seco , Dimitra Zafeiropoulou , Dorine Bax , Petra Zwijnenburg , Anara Arteche , Saoud Tahsin Swafiri , Ruth Cleaver , Meriel McEntagart , Usha Kini , William Newman , Carmen Ayuso , Marta Corton , Yvan Herenger , Médéric Jeanne , Patrick Calvas , Nicolas Chassaing

Immunopathological manifestations in Kabuki syndrome: a registry study of 177 individuals.

Genetics in medicine : official journal of the American College of Medical Genetics

Avec: Henri Margot , Guilaine Boursier , Claire Duflos , Elodie Sanchez , Jeanne Amiel , Jean-Christophe Andrau , Stéphanie Arpin , Elise Brischoux-Boucher , Odile Boute , Lydie Burglen , Charlotte Caille , Yline Capri , Patrick Collignon , Solène Conrad , Valérie Cormier-Daire , Geoffroy Delplancq , Klaus Dieterich , Hélène Dollfus , Mélanie Fradin , Laurence Faivre , Helder Fernandes , Christine Francannet , Vincent Gatinois , Marion Gerard , Alice Goldenberg , Jamal Ghoumid , Sarah Grotto , Anne-Marie Guerrot , Agnès Guichet , Bertrand Isidor , Marie-Line Jacquemont , Sophie Julia , Philippe Khau Van Kien , Marine Legendre , K H Le Quan Sang , Bruno Leheup , Stanislas Lyonnet , Virginie Magry , Sylvie Manouvrier , Dominique Martin , Godelieve Morel , Arnold Munnich , Sophie Naudion , Sylvie Odent , Laurence Perrin , Florence Petit , Nicole Philip , Marlène Rio , Julie Robbe , Massimiliano Rossi , Elisabeth Sarrazin , Annick Toutain , Julien Van Gils , Gabriella Vera , Alain Verloes , Sacha Weber , Sandra Whalen , Damien Sanlaville , Didier Lacombe , Nathalie Aladjidi , David Geneviève

Targeted panel sequencing establishes the implication of planar cell polarity pathway and involves new candidate genes in neural tube defect disorders.

Human genetics

Avec: Marie Beaumont , Linda Akloul , Wilfrid Carré , Chloé Quélin , Hubert Journel , Laurent Pasquier , Mélanie Fradin , Sylvie Odent , Houda Hamdi-Rozé , Erwan Watrin , Valérie Dupé , Christèle Dubourg , Véronique David

Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly.

Brain : a journal of neurology

Avec: Artem Kim , Clara Savary , Christèle Dubourg , Wilfrid Carré , Charlotte Mouden , Houda Hamdi-Rozé , Hélène Guyodo , Jerome Le Douce , Auteur inconnu , Auteur inconnu , Laurent Pasquier , Elisabeth Flori , Marie Gonzales , Claire Bénéteau , Odile Boute , Tania Attié-Bitach , Joelle Roume , Louise Goujon , Linda Akloul , Sylvie Odent , Erwan Watrin , Valérie Dupé , Marie de Tayrac , Véronique David

The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorder.

Human mutation

Avec: Smitha Kumble , Amanda M Levy , Jaya Punetha , Hua Gao , Nicholas Ah Mew , Kwame Anyane-Yeboa , Paul J Benke , Sara M Berger , Lise Bjerglund , Belinda Campos-Xavier , Michael Ciliberto , Julie S Cohen , Anne M Comi , Cynthia Curry , Lena Damaj , Anne-Sophie Denommé-Pichon , Lisa Emrick , Laurence Faivre , Mary Beth Fasano , Alice Fiévet , Richard S Finkel , Sixto García-Miñaúr , Amanda Gerard , Paulino Gomez-Puertas , Maria J Guillen Sacoto , Trevor L Hoffman , Lillian Howard , Alejandro D Iglesias , Kosuke Izumi , Austin Larson , Anja Leiber , Reymundo Lozano , Iñigo Marcos-Alcalde , Cassie S Mintz , Sureni V Mullegama , Rikke S Møller , Sylvie Odent , Henry Oppermann , Elsebet Ostergaard , Marta Pacio-Míguez , Maria Palomares-Bralo , Sumit Parikh , Anna M Paulson , Konrad Platzer , Jennifer E Posey , Lorraine Potocki , Anya Revah-Politi , Marlene Rio , Alyssa L Ritter , Scott Robinson , Jill A Rosenfeld , Fernando Santos-Simarro , Sérgio B Sousa , Auteur inconnu , Mathys Wéber , Yili Xie , Wendy K Chung , Natasha J Brown , Zeynep Tümer

The Study of a 231 French Patient Cohort Significantly Extends the Mutational Spectrum of the Two Major Usher Genes

International journal of molecular sciences

Avec: Luke Mansard , David Baux , Christel Vaché , Catherine Blanchet , Isabelle Meunier , Marjolaine Willems , Valérie Faugère , Corinne Baudoin , Melody Moclyn , Julie Bianchi , Helene Dollfus , Brigitte Gilbert-Dussardier , Delphine Dupin-Deguine , Dominique Bonneau , Isabelle Drumare , Sylvie Odent , Xavier Zanlonghi , Mireille Claustres , Michel Koenig , Vasiliki Kalatzis , Anne-Françoise Roux

Multicolor-FISH Characterization of a Prenatal Mosaicism for a Chromosomal Rearrangement Undetected by Molecular Cytogenetics.

Cytogenetic and genome research

Avec: Laura Mary , Philippe Loget , Sylvie Odent , Dominique Aussel , Gwenaelle Le Bouar , Erika Launay , Catherine Henry , Marc-Antoine Belaud-Rotureau , Sylvie Jaillard

Histone H3.3 beyond cancer: Germline mutations in

Science advances

Avec: Laura Bryant , Dong Li , Samuel G Cox , Dylan Marchione , Evan F Joiner , Khadija Wilson , Kevin Janssen , Pearl Lee , Michael E March , Divya Nair , Elliott Sherr , Brieana Fregeau , Klaas J Wierenga , Alexandrea Wadley , Grazia M S Mancini , Nina Powell-Hamilton , Jiddeke van de Kamp , Theresa Grebe , John Dean , Alison Ross , Heather P Crawford , Zoe Powis , Megan T Cho , Marcia C Willing , Linda Manwaring , Rachel Schot , Caroline Nava , Alexandra Afenjar , Davor Lessel , Matias Wagner , Thomas Klopstock , Juliane Winkelmann , Claudia B Catarino , Kyle Retterer , Jane L Schuette , Jeffrey W Innis , Amy Pizzino , Sabine Lüttgen , Jonas Denecke , Tim M Strom , Kristin G Monaghan , Auteur inconnu , Zuo-Fei Yuan , Holly Dubbs , Renee Bend , Jennifer A Lee , Michael J Lyons , Julia Hoefele , Roman Günthner , Heiko Reutter , Boris Keren , Kelly Radtke , Omar Sherbini , Cameron Mrokse , Katherine L Helbig , Sylvie Odent , Benjamin Cogne , Sandra Mercier , Stephane Bezieau , Thomas Besnard , Sebastien Kury , Richard Redon , Karit Reinson , Monica H Wojcik , Katrin Õunap , Pilvi Ilves , A Micheil Innes , Kristin D Kernohan , Auteur inconnu , Gregory Costain , M Stephen Meyn , David Chitayat , Elaine Zackai , Anna Lehman , Hilary Kitson , Auteur inconnu , Martin G Martin , Julian A Martinez-Agosto , Auteur inconnu , Stan F Nelson , Christina G S Palmer , Jeanette C Papp , Neil H Parker , Janet S Sinsheimer , Eric Vilain , Jijun Wan , Amanda J Yoon , Allison Zheng , Elise Brimble , Giovanni Battista Ferrero , Francesca Clementina Radio , Diana Carli , Sabina Barresi , Alfredo Brusco , Marco Tartaglia , Jennifer Muncy Thomas , Luis Umana , Marjan M Weiss , Garrett Gotway , K E Stuurman , Michelle L Thompson , Kirsty McWalter , Constance T R M Stumpel , Servi J C Stevens , Alexander P A Stegmann , Kristian Tveten , Arve Vøllo , Trine Prescott , Christina Fagerberg , Lone Walentin Laulund , Martin J Larsen , Melissa Byler , Robert Roger Lebel , Anna C Hurst , Joy Dean , Samantha A Schrier Vergano , Jennifer Norman , Saadet Mercimek-Andrews , Juanita Neira , Margot I Van Allen , Nicola Longo , Elizabeth Sellars , Raymond J Louie , Sara S Cathey , Elly Brokamp , Delphine Heron , Molly Snyder , Adeline Vanderver , Celeste Simon , Xavier de la Cruz , Natália Padilla , J Gage Crump , Wendy Chung , Benjamin Garcia , Hakon H Hakonarson , Elizabeth J Bhoj

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

Smith-Magenis syndrome: Clinical and behavioral characteristics in a large retrospective cohort.

Clinical genetics

Avec: Nicolas Rive Le Gouard , Adeline Jacquinet , Lyse Ruaud , Hélène Deleersnyder , Faustine Ageorges , Jennifer Gallard , Didier Lacombe , Sylvie Odent , Myriam Mikaty , Sylvie Manouvrier-Hanu , Jamal Ghoumid , David Geneviève , Natacha Lehman , Nicole Philip , Patrick Edery , Delphine Héron , Coralie Rastel , Sophie Chancenotte , Christel Thauvin-Robinet , Laurence Faivre , Laurence Perrin , Alain Verloes

Pseudodicentric Chromosome Originating from an X-Autosome Translocation in a Male Patient with Cryptozoospermia.

Cytogenetic and genome research

Avec: Saloua Toujani , Elena J Tucker , Linda Akloul , Laura Mary , Céline Pimentel , Erika Launay , Lucas Freton , Guilhem Jouve , Catherine Henry , Sylvie Odent , Marc-Antoine Belaud-Rotureau , Sylvie Jaillard

Heterozygous HMGB1 loss-of-function variants are associated with developmental delay and microcephaly.

Clinical genetics

Avec: Kévin Uguen , Kilannin Krysiak , Séverine Audebert-Bellanger , Sylvia Redon , Caroline Benech , Eléonore Viora-Dupont , Frederic Tran Mau-Them , Sophie Rondeau , Ibrahim Elsharkawi , Jorge L Granadillo , Julie Neidich , Celia Azevedo Soares , Natáliya Tkachenko , Shivarajan M Amudhavalli , Kendra Engleman , Anne Boland , Jean-François Deleuze , Stéphane Bezieau , Sylvie Odent , Annick Toutain , Dominique Bonneau , Brigitte Gilbert-Dussardier , Laurence Faivre , Marlène Rio , Cedric Le Marechal , Claude Ferec , Elena Repnikova , Yang Cao

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

Primary Non-Aortic Lesions Are Not Rare in Marfan Syndrome and Are Associated with Aortic Dissection Independently of Age.

Journal of clinical medicine

Avec: Jean Sénémaud , Marine Gaudry , Elisabeth Jouve , Arnaud Blanchard , Olivier Milleron , Yves Dulac , Laurence Olivier-Faivre , Dominique Stephan , Sylvie Odent , Damien Lanéelle , Sophie Dupuis-Girod , Guillaume Jondeau , Laurence Bal-Theoleyre

Cost of exome analysis in patients with intellectual disability: a micro-costing study in a French setting.

BMC health services research

Avec: A L Soilly , C Robert-Viard , C Besse , A L Bruel , B Gerard , A Boland , A Piton , Y Duffourd , J Muller , C Poë , T Jouan , S El Doueiri , L Faivre , D Bacq-Daian , B Isidor , D Genevieve , S Odent , N Philip , M Doco-Fenzy , D Lacombe , M L Asensio , J F Deleuze , C Binquet , Auteur inconnu , C Thauvin-Robinet , C Lejeune

Antenatal ultrasound features of isolated recurrent copy number variation in 7q11.23 (Williams syndrome and 7q11.23 duplication syndrome).

Prenatal diagnosis

Avec: Cécile Courdier , John Boudjarane , Valérie Malan , Christine Muti , Brian Sperelakis-Beedham , Sylvie Odent , Sylvie Jaillard , Chloé Quelin , Cédric Le Caignec , Olivier Patat , Charlotte Dubucs , Sophie Julia , Caroline Schluth-Bolard , Carole Goumy , Sylvia Redon , Jean-Baptiste Gaillard , Minh Tuan Huynh , Céline Dupont , Anne-Claude Tabet , Guillaume Cogan , François Vialard , Rodolphe Dard , Guillaume Jedraszak , Florence Jobic , Mathilde Lefebvre , Geneviève Quenum , Saori Inai , Mélanie Rama , Fanny Sauvestre , Frédéric Coatleven , Julie Thomas , Caroline Rooryck

Role of chromosomal imbalances in the pathogenesis of DSD: A retrospective analysis of 115 prenatal samples.

European journal of medical genetics

Avec: L Mary , M Fradin , L Pasquier , C Quelin , P Loget , M Le Lous , G Le Bouar , S Nivot-Adamiak , A Lokchine , C Dubourg , V Jauffret , B Nouyou , C Henry , E Launay , S Odent , S Jaillard , M A Belaud-Rotureau

Impact of Sonic Hedgehog-dependent sphenoid bone defect on craniofacial growth.

Clinical and experimental dental research

Avec: Hélène Guyodo , Aurélie Rizzo , Farah Diab , Fanny Noury , Svetlana Mironov , Marie de Tayrac , Véronique David , Sylvie Odent , Christèle Dubourg , Valérie Dupé

Expanding the genetic and clinical spectrum of Tatton-Brown-Rahman syndrome in a series of 24 French patients.

Journal of medical genetics

Avec: Hortense Thomas , Tom Alix , Émeline Renard , Mathilde Renaud , Justine Wourms , Stéphane Zuily , Bruno Leheup , David Geneviève , Natacha Dreumont , Emmanuelle Schmitt , Myriam Bronner , Marc Muller , Marion Divoux , Marion Wandzel , Jean-Marie Ravel , Mylène Dexheimer , Aurélie Becker , Virginie Roth , Marjolaine Willems , Christine Coubes , Gaëlle Vieville , Françoise Devillard , Élise Schaefer , Sarah Baer , Amélie Piton , Bénédicte Gérard , Marie Vincent , Mathilde Nizon , Benjamin Cogné , Lyse Ruaud , Nathalie Couque , Audrey Putoux , Patrick Edery , Gaëtan Lesca , Nicolas Chatron , Marianne Till , Laurence Faivre , Frédéric Tran-Mau-Them , Jean-Luc Alessandri , Marine Lebrun , Chloé Quélin , Sylvie Odent , Christèle Dubourg , Véronique David , Marie Faoucher , Cyril Mignot , Boris Keren , Élise Pisan , Alexandra Afenjar , Sophie Julia , Éric Bieth , Guillaume Banneau , Alice Goldenberg , Thomas Husson , Dominique Campion , François Lecoquierre , Gaël Nicolas , Camille Charbonnier , Anne De Saint Martin , Sophie Naudion , Manon Degoutin , Sophie Rondeau , Caroline Michot , Valérie Cormier-Daire , Abderrahim Oussalah , Carine Pourié , Laëtitia Lambert , Céline Bonnet

Optimizing care for MRKH patients: From malformation screening to uterus transplantation eligibility.

Acta obstetricia et gynecologica Scandinavica

Avec: Auriane Cospain , Ludivine Dion , Maud Bidet , Krystel Nyangoh Timoh , Chloé Quelin , Isis Carton , Alinoe Lavillaureix , Karine Morcel , Paul Rollier , Laurent Pasquier , Bénédicte Nouyou , Sylvie Odent , Daniel Guerrier , Erika Launay , Marc-Antoine Belaud Rotureau , Mélanie Fradin , Sylvie Jaillard , Vincent Lavoué

Analysis of NR5A1 in 142 patients with premature ovarian insufficiency, diminished ovarian reserve, or unexplained infertility.

Maturitas

Avec: Sylvie Jaillard , Rajini Sreenivasan , Marion Beaumont , Gorjana Robevska , Christèle Dubourg , Ingrid M Knarston , Linda Akloul , Jocelyn van den Bergen , Sylvie Odent , Brittany Croft , Guilhem Jouve , Sonia R Grover , Solène Duros , Céline Pimentel , Marc-Antoine Belaud-Rotureau , Katie L Ayers , Célia Ravel , Elena J Tucker , Andrew H Sinclair

Genotype-first in a cohort of 95 fetuses with multiple congenital abnormalities: when exome sequencing reveals unexpected fetal phenotype-genotype correlations.

Journal of medical genetics

Avec: Mathilde Lefebvre , Ange-Line Bruel , Emilie Tisserant , Nicolas Bourgon , Yannis Duffourd , Sophie Collardeau-Frachon , Tania Attie-Bitach , Paul Kuentz , Mirna Assoum , Elise Schaefer , Salima El Chehadeh , Maria Cristina Antal , Valérie Kremer , Françoise Girard-Lemaitre , Jean-Louis Mandel , Daphne Lehalle , Sophie Nambot , Nolwenn Jean-Marçais , Nada Houcinat , Sébastien Moutton , Nathalie Marle , Laetita Lambert , Philippe Jonveaux , Bernard Foliguet , Jean-Pierre Mazutti , Dominique Gaillard , Elisabeth Alanio , Celine Poirisier , Anne-Sophie Lebre , Marion Aubert-Lenoir , Francine Arbez-Gindre , Sylvie Odent , Chloé Quélin , Philippe Loget , Melanie Fradin , Marjolaine Willems , Nicole Bigi , Marie-José Perez , Sophie Blesson , Christine Francannet , Anne-Marie Beaufrere , Sophie Patrier-Sallebert , Anne-Marie Guerrot , Alice Goldenberg , Anne-Claire Brehin , James Lespinasse , Renaud Touraine , Yline Capri , Marie-Hélène Saint-Frison , Nicole Laurent , Christophe Philippe , Frederic Tran Mau-Them , Julien Thevenon , Laurence Faivre , Christel Thauvin-Robinet , Antonio Vitobello

Population and evolutionary genetics of the PAH locus to uncover overdominance and adaptive mechanisms in phenylketonuria: Results from a multiethnic study.

EBioMedicine

Avec: Abderrahim Oussalah , Elise Jeannesson-Thivisol , Céline Chéry , Pascal Perrin , Pierre Rouyer , Thomas Josse , Aline Cano , Magalie Barth , Alain Fouilhoux , Karine Mention , François Labarthe , Jean-Baptiste Arnoux , François Maillot , Catherine Lenaerts , Cécile Dumesnil , Kathy Wagner , Daniel Terral , Pierre Broué , Loic De Parscau , Claire Gay , Alice Kuster , Antoine Bédu , Gérard Besson , Delphine Lamireau , Sylvie Odent , Alice Masurel , Rosa-Maria Rodriguez-Guéant , François Feillet , Jean-Louis Guéant , Fares Namour

Growth charts in Kabuki syndrome 1.

American journal of medical genetics. Part A

Avec: Valentin Ruault , Carole Corsini , Claire Duflos , Sandrine Akouete , Véra Georgescu , Mario Abaji , Yves Alembick , Eudeline Alix , Jeanne Amiel , Cyril Amouroux , Mouna Barat-Houari , Clarisse Baumann , Adeline Bonnard , Guilaine Boursier , Odile Boute , Lydie Burglen , Tiffany Busa , Marie-Pierre Cordier , Valérie Cormier-Daire , Marie-Ange Delrue , Bérénice Doray , Laurence Faivre , Mélanie Fradin , Brigitte Gilbert-Dussardier , Fabienne Giuliano , Alice Goldenberg , Svetlana Gorokhova , Delphine Héron , Bertrand Isidor , Marie-Line Jacquemont , Aurélia Jacquette , Claire Jeandel , Didier Lacombe , Martine Le Merrer , Kim Hanh Le Quan Sang , Stanislas Lyonnet , Sylvie Manouvrier , Caroline Michot , Anne Moncla , Sébastien Moutton , Sylvie Odent , Anna Pelet , Nicole Philip , Lucile Pinson , Julie Reversat , Joëlle Roume , Elodie Sanchez , Damien Sanlaville , Pierre Sarda , Elise Schaefer , Marianne Till , Isabelle Touitou , Annick Toutain , Marjolaine Willems , Vincent Gatinois , David Geneviève

Maternal Transmission Ratio Distortion of GNAS Loss-of-Function Mutations.

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research

Avec: Sarah Snanoudj , Arnaud Molin , Cindy Colson , Nadia Coudray , Sylvie Paulien , Hervé Mittre , Marion Gérard , Elise Schaefer , Alice Goldenberg , Justine Bacchetta , Sylvie Odent , Sophie Naudion , Bénédicte Demeer , Laurence Faivre , Nicolas Gruchy , Marie-Laure Kottler , Nicolas Richard

Pseudodicentric Chromosome Originating from Autosomes 9 and 21 in a Male Patient with Oligozoospermia.

Cytogenetic and genome research

Avec: Marion Beaumont , Elena J Tucker , Laura Mary , Erika Launay , Yann Lurton , Céline Pimentel , Paul Rollier , Linda Akloul , Claire Beneteau , Solène Chevallier-Bordeau , Anne-Sophie Neyroud , Olivier Pichon , Célia Ravel , Sylvie Odent , Marc-Antoine Belaud-Rotureau , Sylvie Jaillard

Clinical and Molecular Spectrum of Nonsyndromic Early-Onset Osteoarthritis.

Arthritis & rheumatology (Hoboken, N.J.)

Avec: Valentin Ruault , Kevin Yauy , Aurélie Fabre , Mélanie Fradin , Julien Van-Gils , Chloé Angelini , Geneviève Baujat , Patricia Blanchet , Silvestre Cuinat , Bertrand Isidor , Christian Jorgensen , Didier Lacombe , Sébastien Moutton , Sylvie Odent , Elodie Sanchez , Sabine Sigaudy , Isabelle Touitou , Marjolaine Willems , Florence Apparailly , David Geneviève , Mouna Barat-Houari

Primal health research in the age of epigenetic clocks.

Medical hypotheses

Avec: Sylvie Odent , Michel Odent

Réseau de co-auteurs

Laurence Faivre 21 collaborations

Christèle Dubourg 18 collaborations

None None 16 collaborations

Bertrand Isidor 14 collaborations

Laurent Pasquier 13 collaborations

David Geneviève 12 collaborations

Alice Goldenberg 12 collaborations

Christel Thauvin-Robinet 11 collaborations

Sylvie Jaillard 11 collaborations

Mélanie Fradin 10 collaborations

Didier Lacombe 9 collaborations

Annick Toutain 9 collaborations

Ange-Line Bruel 9 collaborations

Cyril Mignot 9 collaborations

Boris Keren 9 collaborations

Benjamin Cogné 9 collaborations

Anne-Sophie Denommé-Pichon 9 collaborations

Brigitte Gilbert-Dussardier 8 collaborations

Salima El Chehadeh 8 collaborations

Sébastien Moutton 8 collaborations

Audrey Putoux 8 collaborations

Antonio Vitobello 8 collaborations

Dominique Bonneau 8 collaborations

Sophie Naudion 7 collaborations

Alexandra Afenjar 7 collaborations

Christine Coubes 7 collaborations

Erika Launay 7 collaborations

Linda Akloul 7 collaborations

Marc-Antoine Belaud-Rotureau 7 collaborations

Delphine Héron 6 collaborations

Florence Petit 6 collaborations

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Elise Schaefer 6 collaborations

Stanislas Lyonnet 6 collaborations

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Usha Kini 6 collaborations

Christophe Philippe 6 collaborations

Chloé Quélin 6 collaborations

Patrick Edery 6 collaborations

Séverine Audebert-Bellanger 6 collaborations

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