Julien Thevenon (J Thevenon)

ORCID

Publication Activity (10 Years)

Years Active: 2013-2022
Publications (10 Years): 23

Top Venues

European journal of human genetics : EJHG

Clinical genetics

Journal of medical genetics

Nature genetics

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

Publications

Emilie Tisserant, Antonio Vitobello, Davide Callegarin, Simon Verdez, Ange-Line Bruel, Ludwig Serge Aho Glélé, Arthur Sorlin, Eleonore Viora-Dupont, Marina Konyukh, Nathalie Marle, Sophie Nambot, Sebastien 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 Olivier-Faivre, Anne-Laure Mosca-Boidron, Julien Thevenon, Yannis Duffourd, Patrick Callier
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 86 (4) (2022)
Nicolas Bourgon, Aurore Garde, Ange-Line Bruel, Mathilde Lefebvre, Frédéric 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
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 30 (8) (2022)
Quentin Testard, Xavier Vanhoye, Kevin Yauy, Marie-Emmanuelle Naud, Gaelle Vieville, Francis Rousseau, Benjamin Dauriat, Valentine Marquet, Sylvie Bourthoumieu, David Geneviève, Vincent Gatinois, Constance Wells, Marjolaine Willems, Christine Coubes, Lucile Pinson, Rodolphe Dard, Aude Tessier, Bérénice Hervé, François Vialard, Ines Harzallah, Renaud Touraine, Benjamin Cogné, Wallid Deb, Thomas Besnard, Olivier Pichon, Béatrice Laudier, Laurent Mesnard, Alice Doreille, Tiffany Busa, Chantal Missirian, Véronique Satre, Charles Coutton, Tristan Celse, Radu Harbuz, Laure Raymond, Jean-François Taly, Julien Thevenon
Exome sequencing as a first-tier test for copy number variant detection: retrospective evaluation and prospective screening in 2418 cases. Journal of medical genetics 59 (12) (2022)
Sophie Nambot, Laurence Faivre, Ghayda Mirzaa, Julien Thevenon, Ange-Line Bruel, Anne-Laure Mosca-Boidron, Alice Masurel-Paulet, Alice Goldenberg, Nathalie Le Meur, Aude Charollais, Cyril Mignot, Florence Petit, Massimiliano Rossi, Julia Metreau, Valérie Layet, Daniel Amram, Odile Boute-Bénéjean, Elizabeth Bhoj, Margot A Cousin, Teresa M Kruisselbrink, Brendan C Lanpher, Eric W Klee, Elise Fiala, Dorothy K Grange, Wendy S Meschino, Susan M Hiatt, Gregory M Cooper, Hilde Olivié, Wendy E Smith, Meghan Dumas, Anna Lehman, null null, Cara Inglese, Mathilde Nizon, Renzo Guerrini, Annalisa Vetro, Eitan S Kaplan, Dolores Miramar, Julien Van Gils, Patricia Fergelot, Olaf Bodamer, Johanna C Herkert, Sander Pajusalu, Katrin Õunap, James J Filiano, Thomas Smol, Amelie Piton, Bénédicte Gérard, Sandra Chantot-Bastaraud, Thierry Bienvenu, Dong Li, Jane Juusola, Koen Devriendt, Frederic Bilan, Charlotte Poé, Martin Chevarin, Thibaud Jouan, Emilie Tisserant, Jean-Baptiste Rivière, Frédéric Tran Mau-Them, Christophe Philippe, Yannis Duffourd, William B Dobyns, Robert F Hevner, Christel Thauvin-Robinet
De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature. European journal of human genetics : EJHG 28 (6) (2020)
Ange-Line Bruel, Sophie Nambot, Virginie Quéré, Antonio Vitobello, Julien Thevenon, Mirna Assoum, Sébastien Moutton, Nada Houcinat, Daphné Lehalle, Nolwenn Jean-Marçais, null null, Martin Chevarin, Thibaud Jouan, Charlotte Poë, Patrick Callier, Emilie Tisserand, Christophe Philippe, Frédéric Tran Mau Them, Yannis Duffourd, Laurence Faivre, Christel Thauvin-Robinet
Increased diagnostic and new genes identification outcome using research reanalysis of singleton exome sequencing. European journal of human genetics : EJHG 27 (10) (2019)
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
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 27 (8) (2019)
Aline Chassagne, Aurore Pélissier, Françoise Houdayer, Elodie Cretin, Elodie Gautier, Dominique Salvi, Sarah Kidri, Aurélie Godard, Christel Thauvin-Robinet, Alice Masurel, Daphne Lehalle, Nolwenn Jean-Marçais, Julien Thevenon, Gaetan Lesca, Audrey Putoux, Marie-Pierre Cordier, Sophie Dupuis-Girod, Marianne Till, Yannis Duffourd, Jean-Baptiste Rivière, Lorraine Joly, Christine Juif, Olivier Putois, Pierre Ancet, Anne-Sophie Lapointe, Paulette Morin, Patrick Edery, Massimiliano Rossi, Damien Sanlaville, Sophie Béjean, Christine Peyron, Laurence Faivre
Exome sequencing in clinical settings: preferences and experiences of parents of children with rare diseases (SEQUAPRE study). European journal of human genetics : EJHG 27 (5) (2019)
Camille Lemattre, Marion Imbert-Bouteille, Vincent Gatinois, Paule Benit, Elodie Sanchez, Thomas Guignard, Frédéric Tran Mau-Them, Emmanuelle Haquet, François Rivier, Emilie Carme, Agathe Roubertie, Anne Boland, Doris Lechner, Vincent Meyer, Julien Thevenon, Yannis Duffourd, Jean-Baptiste Rivière, Jean-François Deleuze, Constance Wells, Florence Molinari, Pierre Rustin, Patricia Blanchet, David Geneviève
Report on three additional patients and genotype-phenotype correlation in SLC25A22-related disorders group. European journal of human genetics : EJHG 27 (11) (2019)
Ange-Line Bruel, Julien Thevenon, F Huet, N Jean-Marcais, S Odent, C Dubourg, D Lehalle, F Tran Mau-Them, C Philippe, S Moutton, N Houcinat, S Gay, L Guibaud, Y Duffourd, J-B Rivière, L Faivre, C Thauvin-Robinet
Unexpected diagnosis of a SHH nonsense variant causing a variable phenotype ranging from familial coloboma and Intellectual disability to isolated microcephaly. Clinical genetics 94 (1) (2018)
Daphne Lehalle, Anne-Laure Mosca-Boidron, Amber Begtrup, Odile Boute-Benejean, Perrine Charles, Megan T Cho, Amanda Clarkson, Orrin Devinsky, Yannis Duffourd, Laurence Duplomb-Jego, Bénédicte Gérard, Aurélia Jacquette, Paul Kuentz, Alice Masurel-Paulet, Carey McDougall, Sébastien Moutton, Hilde Olivié, Soo-Mi Park, Anita Rauch, Nicole Revencu, Jean-Baptiste Rivière, Karol Rubin, Ingrid Simonic, Deborah J Shears, Thomas Smol, Ana Lisa Taylor Tavares, Paulien Terhal, Julien Thevenon, Koen Van Gassen, Catherine Vincent-Delorme, Marjolein H Willemsen, Golder N Wilson, Elaine Zackai, Christiane Zweier, Patrick Callier, Christel Thauvin-Robinet, Laurence Faivre
STAG1 mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability. Journal of medical genetics 54 (7) (2017)
Hsiang-Chih Lu, Qiumin Tan, Maxime W C Rousseaux, Wei Wang, Ji-Yoen Kim, Ronald Richman, Ying-Wooi Wan, Szu-Ying Yeh, Jay M Patel, Xiuyun Liu, Tao Lin, Yoontae Lee, John D Fryer, Jing Han, Maria H Chahrour, Richard H Finnell, Yunping Lei, Maria E Zurita-Jimenez, Priyanka Ahimaz, Kwame Anyane-Yeboa, Lionel Van Maldergem, Daphne Lehalle, Nolwenn Jean-Marcais, Anne-Laure Mosca-Boidron, Julien Thevenon, Margot A Cousin, Della E Bro, Brendan C Lanpher, Eric W Klee, Nora Alexander, Matthew N Bainbridge, Harry T Orr, Roy V Sillitoe, M Cecilia Ljungberg, Zhandong Liu, Christian Patrick Schaaf, Huda Y Zoghbi
Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans. Nature genetics 49 (4) (2017)
S El Chehadeh, R Touraine, F Prieur, W Reardon, T Bienvenu, S Chantot-Bastaraud, M Doco-Fenzy, E Landais, C Philippe, N Marle, P Callier, A-L Mosca-Boidron, F Mugneret, N Le Meur, A Goldenberg, A-M Guerrot, P Chambon, V Satre, C Coutton, P-S Jouk, F Devillard, K Dieterich, A Afenjar, L Burglen, M-L Moutard, M-C Addor, S Lebon, D Martinet, J-L Alessandri, B Doray, M Miguet, D Devys, P Saugier-Veber, S Drunat, B Aral, V Kremer, S Rondeau, A-C Tabet, Julien Thevenon, C Thauvin-Robinet, N Perreton, V Des Portes, L Faivre
Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling? Clinical genetics 91 (4) (2017)
Angélique Quartier, Hélène Poquet, Brigitte Gilbert-Dussardier, Massimiliano Rossi, Anne-Sophie Casteleyn, Vincent des Portes, Claire Feger, Elsa Nourisson, Paul Kuentz, Claire Redin, Julien Thevenon, Anne-Laure Mosca-Boidron, Patrick Callier, Jean Muller, Gaetan Lesca, Frédéric Huet, Véronique Geoffroy, Salima El Chehadeh, Matthieu Jung, Benoit Trojak, Stéphanie Le Gras, Daphné Lehalle, Bernard Jost, Stéphanie Maury, Alice Masurel, Patrick Edery, Christel Thauvin-Robinet, Bénédicte Gérard, Jean-Louis Mandel, Laurence Faivre, Amélie Piton
Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndrome. European journal of human genetics : EJHG 25 (4) (2017)
M Lefebvre, Y Duffourd, T Jouan, C Poe, N Jean-Marçais, Alain Verloes, J St-Onge, J-B Riviere, F Petit, G Pierquin, B Demeer, P Callier, C Thauvin-Robinet, L Faivre, Julien Thevenon
Autosomal recessive variations of TBX6, from congenital scoliosis to spondylocostal dysostosis. Clinical genetics 91 (6) (2017)
Sophie Nambot, D Gavrilov, Julien Thevenon, A L Bruel, M Bainbridge, M Rio, C Goizet, A Rötig, J Jaeken, N Niu, F Xia, A Vital, N Houcinat, F Mochel, P Kuentz, D Lehalle, Y Duffourd, J B Rivière, C Thauvin-Robinet, A L Beaudet, L Faivre
Further delineation of a rare recessive encephalomyopathy linked to mutations in GFER thanks to data sharing of whole exome sequencing data. Clinical genetics 92 (2) (2017)
L Allou, S Julia, D Amsallem, S El Chehadeh, L Lambert, Julien Thevenon, Y Duffourd, A Saunier, P Bouquet, S Pere, A Moustaïne, L Ruaud, V Roth, P Jonveaux, C Philippe
Rett-like phenotypes: expanding the genetic heterogeneity to the KCNA2 gene and first familial case of CDKL5-related disease. Clinical genetics 91 (3) (2016)
J S Amos, L Huang, Julien Thevenon, A Kariminedjad, C L Beaulieu, A Masurel-Paulet, H Najmabadi, Z Fattahi, M Beheshtian, S H Tonekaboni, S Tang, K L Helbig, W Alcaraz, J-B Rivière, L Faivre, A M Innes, R R Lebel, K M Boycott, null null
Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotyping. Clinical genetics 91 (1) (2016)
Julien Thevenon, L Duplomb, S Phadke, T Eguether, A Saunier, M Avila, V Carmignac, A-L Bruel, J St-Onge, Y Duffourd, G J Pazour, B Franco, T Attie-Bitach, A Masurel-Paulet, J-B Rivière, V Cormier-Daire, C Philippe, L Faivre, C Thauvin-Robinet
Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangia. Clinical genetics 90 (6) (2016)
Julien Thevenon, Y Duffourd, A Masurel-Paulet, M Lefebvre, F Feillet, S El Chehadeh-Djebbar, J St-Onge, A Steinmetz, F Huet, M Chouchane, V Darmency-Stamboul, P Callier, C Thauvin-Robinet, L Faivre, J B Rivière
Diagnostic odyssey in severe neurodevelopmental disorders: toward clinical whole-exome sequencing as a first-line diagnostic test. Clinical genetics 89 (6) (2016)
M Lefebvre, D Sanlaville, N Marle, C Thauvin-Robinet, E Gautier, S E Chehadeh, A-L Mosca-Boidron, Julien Thevenon, P Edery, M-P Alex-Cordier, M Till, S Lyonnet, V Cormier-Daire, J Amiel, A Philippe, S Romana, V Malan, A Afenjar, S Marlin, S Chantot-Bastaraud, P Bitoun, B Heron, E Piparas, F Morice-Picard, S Moutton, N Chassaing, A Vigouroux-Castera, J Lespinasse, S Manouvrier-Hanu, O Boute-Benejean, C Vincent-Delorme, F Petit, N L Meur, M Marti-Dramard, A-M Guerrot, A Goldenberg, S Redon, C Ferrec, S Odent, C L Caignec, S Mercier, B Gilbert-Dussardier, A Toutain, S Arpin, S Blesson, I Mortemousque, E Schaefer, D Martin, N Philip, S Sigaudy, T Busa, C Missirian, F Giuliano, H K Benailly, P K V Kien, B Leheup, C Benneteau, L Lambert, R Caumes, P Kuentz, I François, D Heron, B Keren, E Cretin, P Callier, S Julia, L Faivre
Genetic counselling difficulties and ethical implications of incidental findings from array-CGH: a 7-year national survey. Clinical genetics 89 (5) (2016)
C Thauvin-Robinet, L Duplomb-Jego, F Limoge, D Picot, A Masurel, B Terriat, C Champilou, D Minot, J St-Onge, P Kuentz, Y Duffourd, Julien Thevenon, J-B Rivière, L Faivre
Homozygous FIBP nonsense variant responsible of syndromic overgrowth, with overgrowth, macrocephaly, retinal coloboma and learning disabilities. Clinical genetics 89 (5) (2016)
Salima El Chehadeh, Wilhelmina S Kerstjens-Frederikse, Julien Thevenon, Paul Kuentz, Ange-Line Bruel, Christel Thauvin-Robinet, Candace Bensignor, Hélène Dollfus, Vincent Laugel, Jean-Baptiste Rivière, Yannis Duffourd, Caroline Bonnet, Matthieu P Robert, Rodica Isaiko, Morgane Straub, Catherine Creuzot-Garcher, Patrick Calvas, Nicolas Chassaing, Bart Loeys, Edwin Reyniers, Geert Vandeweyer, R Frank Kooy, Miroslava Hančárová, Marketa Havlovicová, Darina Prchalová, Zdenek Sedláček, Christian Gilissen, Rolph Pfundt, Jolien S Klein Wassink-Ruiter, Laurence Faivre
Dominant variants in the splicing factor PUF60 cause a recognizable syndrome with intellectual disability, heart defects and short stature. European journal of human genetics : EJHG 25 (1) (2016)
A-L Bruel, A Masurel-Paulet, J-B Rivière, Y Duffourd, D Lehalle, C Bensignor, F Huet, J Borgnon, F Roucher, P Kuentz, J-F Deleuze, C Thauvin-Robinet, L Faivre, Julien Thevenon
Autosomal recessive truncating MAB21L1 mutation associated with a syndromic scrotal agenesis. Clinical genetics 91 (2) (2016)
Sophie Nambot, Alice Masurel, Salima El Chehadeh, Anne-Laure Mosca-Boidron, Christel Thauvin-Robinet, Mathilde Lefebvre, Nathalie Marle, Julien Thevenon, Stéphanie Perez-Martin, Véronique Dulieu, Frédéric Huet, Ghislaine Plessis, Joris Andrieux, Pierre-Simon Jouk, Gipsy Billy-Lopez, Charles Coutton, Fanny Morice-Picard, Marie-Ange Delrue, Delphine Heron, Caroline Rooryck, Alice Goldenberg, Pascale Saugier-Veber, Géraldine Joly-Hélas, Patricia Calenda, Paul Kuentz, Sylvie Manouvrier-Hanu, Sophie Dupuis-Girod, Patrick Callier, Laurence Faivre
9q33.3q34.11 microdeletion: new contiguous gene syndrome encompassing STXBP1, LMX1B and ENG genes assessed using reverse phenotyping. European journal of human genetics : EJHG 24 (6) (2015)
Julien Thevenon, Céline Souchay, Gail K Seabold, Inna Dygai-Cochet, Patrick Callier, Sébastien Gay, Lucie Corbin, Laurence Duplomb, Christel Thauvin-Robinet, Alice Masurel-Paulet, Salima El Chehadeh, Magali Avila, Delphine Minot, Eric Guedj, Sophie Chancenotte, Marlène Bonnet, Daphne Lehalle, Ya-Xian Wang, Paul Kuentz, Frédéric Huet, Anne-Laure Mosca-Boidron, Nathalie Marle, Ronald S Petralia, Laurence Faivre
Heterozygous deletion of the LRFN2 gene is associated with working memory deficits. European journal of human genetics : EJHG 24 (6) (2015)
Lucas M Bronicki, Claire Redin, Severine Drunat, Amélie Piton, Michael Lyons, Sandrine Passemard, Clarisse Baumann, Laurence Faivre, Julien Thevenon, Jean-Baptiste Rivière, Bertrand Isidor, Grace Gan, Christine Francannet, Marjolaine Willems, Murat Gunel, Julie R Jones, Joseph G Gleeson, Jean-Louis Mandel, Roger E Stevenson, Michael J Friez, Arthur S Aylsworth
Ten new cases further delineate the syndromic intellectual disability phenotype caused by mutations in DYRK1A. European journal of human genetics : EJHG 23 (11) (2015)
Anne-Laure Mosca-Boidron, Lucie Gueneau, Guillaume Huguet, Alice Goldenberg, Céline Henry, Nadège Gigot, Emilie Pallesi-Pocachard, Antonio Falace, Laurence Duplomb, Julien Thevenon, Yannis Duffourd, Judith St-Onge, Pascal Chambon, Jean-Baptiste Rivière, Christel Thauvin-Robinet, Patrick Callier, Nathalie Marle, Muriel Payet, Clemence Ragon, Hany Goubran Botros, Julien Buratti, Sophie Calderari, Guillaume Dumas, Richard Delorme, Nathalie Lagarde, Jean-Michel Pinoit, Antoine Rosier, Alice Masurel-Paulet, Carlos Cardoso, Francine Mugneret, Pascale Saugier-Veber, Dominique Campion, Laurence Faivre, Thomas Bourgeron
A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability. European journal of human genetics : EJHG 24 (6) (2015)
Christel Thauvin-Robinet, Jaclyn S Lee, Estelle Lopez, Vicente Herranz-Pérez, Toshinobu Shida, Brunella Franco, Laurence Jego, Fan Ye, Laurent Pasquier, Philippe Loget, Nadège Gigot, Bernard Aral, Carla A M Lopes, Judith St-Onge, Ange-Line Bruel, Julien Thevenon, Susana González-Granero, Caroline Alby, Arnold Munnich, Michel Vekemans, Frédéric Huet, Andrew M Fry, Sophie Saunier, Jean-Baptiste Rivière, Tania Attié-Bitach, Jose Manuel Garcia-Verdugo, Laurence Faivre, André Mégarbané, Maxence V Nachury
The oral-facial-digital syndrome gene C2CD3 encodes a positive regulator of centriole elongation. Nature genetics 46 (8) (2014)
Claire Redin, Bénédicte Gérard, Julia Lauer, Yvan Herenger, Jean Muller, Angélique Quartier, Alice Masurel-Paulet, Marjolaine Willems, Gaétan Lesca, Salima El-Chehadeh, Stéphanie Le Gras, Serge Vicaire, Muriel Philipps, Michaël Dumas, Véronique Geoffroy, Claire Feger, Nicolas Haumesser, Yves Alembik, Magalie Barth, Dominique Bonneau, Estelle Colin, Hélène Dollfus, Bérénice Doray, Marie-Ange Delrue, Valérie Drouin-Garraud, Elisabeth Flori, Mélanie Fradin, Christine Francannet, Alice Goldenberg, Serge Lumbroso, Michèle Mathieu-Dramard, Dominique Martin-Coignard, Didier Lacombe, Gilles Morin, Anne Polge, Sylvie Sukno, Christel Thauvin-Robinet, Julien Thevenon, Martine Doco-Fenzy, David Genevieve, Pierre Sarda, Patrick Edery, Bertrand Isidor, Bernard Jost, Laurence Olivier-Faivre, Jean-Louis Mandel, Amélie Piton
Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing. Journal of medical genetics 51 (11) (2014)
Amélie Piton, Hélène Poquet, Claire Redin, Alice Masurel, Julia Lauer, Jean Muller, Julien Thevenon, Yvan Herenger, Sophie Chancenotte, Marlène Bonnet, Jean-Michel Pinoit, Frédéric Huet, Christel Thauvin-Robinet, Anne-Sophie Jaeger, Stéphanie Le Gras, Bernard Jost, Bénédicte Gérard, Katell Peoc'h, Jean-Marie Launay, Laurence Faivre, Jean-Louis Mandel
20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition. European journal of human genetics : EJHG 22 (6) (2013)

Julien Thevenon.css-eqlu8i{font-size:small;padding-left:4px;} (J Thevenon)

Publication Activity (10 Years)

Top Topics

Top Venues

Julien Thevenon (J Thevenon)