Richard Redon

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2013-2024
Publications (10 Years): 14

Top Venues

Nature communications

Nature genetics

Stroke

Circulation. Genomic and precision medicine

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

Publications

Manon Baudic, Hiroshige Murata, Fernanda M Bosada, Uirá Souto Melo, Takanori Aizawa, Pierre Lindenbaum, Lieve E van der Maarel, Amaury Guedon, Estelle Baron, Enora Fremy, Adrien Foucal, Taisuke Ishikawa, Hiroya Ushinohama, Sean Joseph Jurgens, Seung Hoan Choi, Florence Kyndt, Solena Le Scouarnec, Vincent Wakker, Aurélie Thollet, Annabelle Rajalu, Tadashi Takaki, Seiko Ohno, Wataru Shimizu, Minoru Horie, Takeshi Kimura, Patrick T Ellinor, Florence Petit, Yves Dulac, Paul Bru, Anne Boland, Jean-François Deleuze, Richard Redon, Hervé Le Marec, Thierry Le Tourneau, Jean-Baptiste Gourraud, Yoshinori Yoshida, Naomasa Makita, Claude Vieyres, Takeru Makiyama, Stephan Mundlos, Vincent M Christoffels, Vincent Probst, Jean-Jacques Schott, Julien Barc
TAD boundary deletion causes PITX2-related cardiac electrical and structural defects. Nature communications 15 (1) (2024)
Isabel Alves, Joanna Giemza, Michael G B Blum, Carolina Bernhardsson, Stéphanie Chatel, Matilde Karakachoff, Aude Saint Pierre, Anthony Francis Herzig, Robert Olaso, Martial Monteil, Véronique Gallien, Elodie Cabot, Emma Svensson, Delphine Bacq, Estelle Baron, Charlotte Berthelier, Céline Besse, Hélène Blanché, Ozvan Bocher, Anne Boland-Auge, Stéphanie Bonnaud, Eric Charpentier, Claire Dandine-Roulland, Claude Férec, Christine Fruchet, Simon Lecointe, Edith Le Floch, Thomas E Ludwig, Gaelle Marenne, Vincent Meyer, Elisabeth Quellery, Fernando Racimo, Karen Rouault, Florian Sandron, Jean-Jacques Schott, Lourdes Velo-Suarez, Jade Violleau, Eske Willerslev, Yves Coativy, Mael Jézéquel, Daniel Le Bris, Clément Nicolas, Yvan Pailler, Marcel Goldberg, Marie Zins, Hervé Le Marec, Mattias Jakobsson, Pierre Darlu, French Exome Consortium, Jean François Deleuze, Richard Redon, Christian Dina
Human genetic structure in Northwest France provides new insights into West European historical demography. Nature communications 15 (1) (2024)
Manon Baudic, Hiroshige Murata, Fernanda M Bosada, Uirá Souto Melo, Takanori Aizawa, Pierre Lindenbaum, Lieve E van der Maarel, Amaury Guedon, Estelle Baron, Enora Fremy, Adrien Foucal, Taisuke Ishikawa, Hiroya Ushinohama, Sean Joseph Jurgens, Seung Hoan Choi, Florence Kyndt, Solena Le Scouarnec, Vincent Wakker, Aurélie Thollet, Annabelle Rajalu, Tadashi Takaki, Seiko Ohno, Wataru Shimizu, Minoru Horie, Takeshi Kimura, Patrick T Ellinor, Florence Petit, Yves Dulac, Paul Bru, Anne Boland, Jean-François Deleuze, Richard Redon, Hervé Le Marec, Thierry Le Tourneau, Jean-Baptiste Gourraud, Yoshinori Yoshida, Naomasa Makita, Claude Vieyres, Takeru Makiyama, Stephan Mundlos, Vincent M Christoffels, Vincent Probst, Jean-Jacques Schott, Julien Barc
TAD boundary deletion causes PITX2-related cardiac electrical and structural defects. Nature communications 15 (1) (2024)
Isabel Alves, Joanna Giemza, Michael G B Blum, Carolina Bernhardsson, Stéphanie Chatel, Matilde Karakachoff, Aude Saint Pierre, Anthony Francis Herzig, Robert Olaso, Martial Monteil, Véronique Gallien, Elodie Cabot, Emma Svensson, Delphine Bacq, Estelle Baron, Charlotte Berthelier, Céline Besse, Hélène Blanché, Ozvan Bocher, Anne Boland-Auge, Stéphanie Bonnaud, Eric Charpentier, Claire Dandine-Roulland, Claude Férec, Christine Fruchet, Simon Lecointe, Edith Le Floch, Thomas E Ludwig, Gaelle Marenne, Vincent Meyer, Elisabeth Quellery, Fernando Racimo, Karen Rouault, Florian Sandron, Jean-Jacques Schott, Lourdes Velo-Suarez, Jade Violleau, Eske Willerslev, Yves Coativy, Mael Jézéquel, Daniel Le Bris, Clément Nicolas, Yvan Pailler, Marcel Goldberg, Marie Zins, Hervé Le Marec, Mattias Jakobsson, Pierre Darlu, French Exome Consortium, Jean François Deleuze, Richard Redon, Christian Dina
Human genetic structure in Northwest France provides new insights into West European historical demography. Nature communications 15 (1) (2024)
Isabel Alves, Joanna Giemza, Michael G B Blum, Carolina Bernhardsson, Stéphanie Chatel, Matilde Karakachoff, Aude Saint Pierre, Anthony Francis Herzig, Robert Olaso, Martial Monteil, Véronique Gallien, Elodie Cabot, Emma Svensson, Delphine Bacq, Estelle Baron, Charlotte Berthelier, Céline Besse, Hélène Blanché, Ozvan Bocher, Anne Boland-Auge, Stéphanie Bonnaud, Eric Charpentier, Claire Dandine-Roulland, Claude Férec, Christine Fruchet, Simon Lecointe, Edith Le Floch, Thomas E Ludwig, Gaelle Marenne, Vincent Meyer, Elisabeth Quellery, Fernando Racimo, Karen Rouault, Florian Sandron, Jean-Jacques Schott, Lourdes Velo-Suarez, Jade Violleau, Eske Willerslev, Yves Coativy, Mael Jézéquel, Daniel Le Bris, Clément Nicolas, Yvan Pailler, Marcel Goldberg, Marie Zins, Hervé Le Marec, Mattias Jakobsson, Pierre Darlu, French Exome Consortium, Jean François Deleuze, Richard Redon, Christian Dina
Human genetic structure in Northwest France provides new insights into West European historical demography. Nature communications 15 (1) (2024)
Manon Baudic, Hiroshige Murata, Fernanda M Bosada, Uirá Souto Melo, Takanori Aizawa, Pierre Lindenbaum, Lieve E van der Maarel, Amaury Guedon, Estelle Baron, Enora Fremy, Adrien Foucal, Taisuke Ishikawa, Hiroya Ushinohama, Sean Joseph Jurgens, Seung Hoan Choi, Florence Kyndt, Solena Le Scouarnec, Vincent Wakker, Aurélie Thollet, Annabelle Rajalu, Tadashi Takaki, Seiko Ohno, Wataru Shimizu, Minoru Horie, Takeshi Kimura, Patrick T Ellinor, Florence Petit, Yves Dulac, Paul Bru, Anne Boland, Jean-François Deleuze, Richard Redon, Hervé Le Marec, Thierry Le Tourneau, Jean-Baptiste Gourraud, Yoshinori Yoshida, Naomasa Makita, Claude Vieyres, Takeru Makiyama, Stephan Mundlos, Vincent M Christoffels, Vincent Probst, Jean-Jacques Schott, Julien Barc
TAD boundary deletion causes PITX2-related cardiac electrical and structural defects. Nature communications 15 (1) (2024)
Manon Baudic, Hiroshige Murata, Fernanda M Bosada, Uirá Souto Melo, Takanori Aizawa, Pierre Lindenbaum, Lieve E van der Maarel, Amaury Guedon, Estelle Baron, Enora Fremy, Adrien Foucal, Taisuke Ishikawa, Hiroya Ushinohama, Sean Joseph Jurgens, Seung Hoan Choi, Florence Kyndt, Solena Le Scouarnec, Vincent Wakker, Aurélie Thollet, Annabelle Rajalu, Tadashi Takaki, Seiko Ohno, Wataru Shimizu, Minoru Horie, Takeshi Kimura, Patrick T Ellinor, Florence Petit, Yves Dulac, Paul Bru, Anne Boland, Jean-François Deleuze, Richard Redon, Hervé Le Marec, Thierry Le Tourneau, Jean-Baptiste Gourraud, Yoshinori Yoshida, Naomasa Makita, Claude Vieyres, Takeru Makiyama, Stephan Mundlos, Vincent M Christoffels, Vincent Probst, Jean-Jacques Schott, Julien Barc
TAD boundary deletion causes PITX2-related cardiac electrical and structural defects. Nature communications 15 (1) (2024)
Charlotte C M Zuurbier, Romain Bourcier, Pacôme Constant Dit Beaufils, Richard Redon, Hubert Desal, null null, Anne S E Bor, Gabriel J E Rinkel, Jacoba P Greving, Ynte M Ruigrok
Risk Prediction of New Intracranial Aneurysms at Follow-Up Screening in People With a Positive Family History. Stroke (2023)
Marine Tortigue, Lynne E Nield, Matilde Karakachoff, Christopher J McLeod, Emre Belli, Sonya V Babu-Narayan, Solène Prigent, Angèle Boet, Miriam Conway, Robert W Elder, Magalie Ladouceur, Paul Khairy, Ewa Kowalik, David M Kalfa, David J Barron, Shafi Mussa, Anita Hiippala, Joel Temple, Sylvia Abadir, Laurianne Le Gloan, Matthias Lachaud, Shubhayan Sanatani, Jean-Benoit Thambo, Céline Grunenwald Gronier, Pascal Amedro, Guy Vaksmann, Anne Charbonneau, Linda Koutbi, Caroline Ovaert, Ali Houeijeh, Nicolas Combes, Philippe Maury, Guillaume Duthoit, Bérengère Hiel, Christopher C Erickson, Caroline Bonnet, George F Van Hare, Christian Dina, Clément Karsenty, Emmanuelle Fournier, Mathieu Le Bloa, Robert H Pass, Leonardo Liberman, Juha-Matti Happonen, James C Perry, Bénédicte Romefort, Nadir Benbrik, Quentin Hauet, Alain Fraisse, Michael A Gatzoulis, Dominic J R Abrams, Anne M Dubin, Siew Yen Ho, Richard Redon, Emile A Bacha, Jean-Jacques Schott, Alban-Elouen Baruteau
Familial Recurrence Patterns in Congenitally Corrected Transposition of the Great Arteries: An International Study. Circulation. Genomic and precision medicine 15 (3) (2022)
Zeina R Al Sayed, Mariam Jouni, Jean-Baptiste Gourraud, Nadjet Belbachir, Julien Barc, Aurore Girardeau, Virginie Forest, Aude Derevier, Anne Gaignerie, Caroline Chariau, Bastien Cimarosti, Robin Canac, Pierre Olchesqui, Eric Charpentier, Jean-Jacques Schott, Richard Redon, Isabelle Baró, Vincent Probst, Flavien Charpentier, Gildas Loussouarn, Kazem Zibara, Guillaume Lamirault, Patricia Lemarchand, Nathalie Gaborit
A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype. Clinical and translational medicine 11 (6) (2022)
Henne Holstege, Marc Hulsman, Camille Charbonnier, Benjamin Grenier-Boley, Olivier Quenez, Detelina Grozeva, Jeroen G J van Rooij, Rebecca Sims, Shahzad Ahmad, Ivana Nedeljković, Penny J Norsworthy, Oriol Dols-Icardo, Holger Hummerich, Amit Kawalia, Phillippe Amouyel, Gary W Beecham, Claudine Berr, Joshua C Bis, Anne Boland, Paola Bossù, Femke Bouwman, Jose Bras, Dominique Campion, Jesse Nicholas Cochran, Antonio Daniele, Jean-François Dartigues, Stephanie Debette, Jean-François Deleuze, Nicola Denning, Anita L DeStefano, Lindsay A Farrer, Maria Victoria Fernandez, Nick C Fox, Daniela Galimberti, French Exome Consortium, Johan J P Gille, Yann Le Guen, Rita Guerreiro, Jonathan L Haines, Clive Holmes, Mohammad Arfan Ikram, M Kamran Ikram, Iris E Jansen, Robert Kraaij, Marc Lathrop, Afina W Lemstra, Alberto Lleó, Lauren Luckcuck, Marcel M A M Mannens, Rachel Marshall, Eden R Martin, Carlo Masullo, Richard Mayeux, Patrizia Mecocci, Alun Meggy, Merel O Mol, Kevin Morgan, Richard M Myers, Benedetta Nacmias, Adam C Naj, Valerio Napolioni, Florence Pasquier, Pau Pastor, Margaret A Pericak-Vance, Rachel Raybould, Richard Redon, Marcel J T Reinders, Anne-Claire Richard, Steffi G Riedel-Heller, Fernando Rivadeneira, Stéphane Rousseau, Natalie S Ryan, Salha Saad, Pascual Sánchez Juan, Gerard D Schellenberg, Philip Scheltens, Jonathan M Schott, Davide Seripa, Sudha Seshadri, Daoud Sie, Erik A Sistermans, Sandro Sorbi, Rosalina M L van Spaendonk, Gianfranco Spalletta, Niccolo' Tesi, Betty Tijms, Andre G Uitterlinden, Sven J Van der Lee, Pieter Jelle Visser, Michael Wagner, David Wallon, Li-San Wang, Aline Zarea, Jordi Clarimon, John C van Swieten, Michael D Greicius, Jennifer S Yokoyama, Carlos Cruchaga, John Hardy, Alfredo Ramirez, Simon Mead, Wiesje Maria van der Flier, Cornelia M Van Duijn, Julie Williams, Gaël Nicolas, Celine Bellenguez, Jean-Charles Lambert
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease. Nature genetics 54 (12) (2022)
Julien Barc, Rafik Tadros, Charlotte Glinge, David Y Chiang, Mariam Jouni, Floriane Simonet, Sean Joseph Jurgens, Manon Baudic, Michele Nicastro, Franck Potet, Joost A Offerhaus, Roddy Walsh, Seung Hoan Choi, Arjan C Houweling, Yuka Mizusawa, Soraya Anys, Damien Minois, Marine Arnaud, Josselin Duchateau, Yanushi D Wijeyeratne, Alison Muir, Michael Papadakis, Silvia Castelletti, Margherita Torchio, Cristina Gil Ortuño, Javier Lacunza, Daniela Francesca Giachino, Natascia Cerrato, Raphaël P Martins, Òscar Campuzano, Sonia Van Dooren, Aurélie Thollet, Florence Kyndt, Andrea Mazzanti, Nicolas Clémenty, Arnaud Bisson, Anniek Corveleyn, Birgit Stallmeyer, Sven Dittmann, Johan Saenen, Antoine Noël, Shohreh Honarbakhsh, Boris Rudic, Halim Marzak, Matthew K Rowe, Claire Federspiel, Sophie Le Page, Leslie Placide, Antoine Milhem, Hector Barajas-Martinez, Britt-Maria Beckmann, Ingrid P Krapels, Johannes Steinfurt, Bo Gregers Winkel, Reza Jabbari, Moore B Shoemaker, Bas J Boukens, Doris Škorić-Milosavljević, Hennie Bikker, Federico Manevy, Peter Lichtner, Marta Ribasés, Thomas Meitinger, Martina Müller-Nuraysid, null null, Jan Herman Veldink, Leonard H van den Berg, Philip Van Damme, Daniele Cusi, Chiara Lanzani, Sidwell Rigade, Eric Charpentier, Estelle Baron, Stéphanie Bonnaud, Simon Lecointe, Audrey Donnart, Hervé Le Marec, Stéphanie Chatel, Matilde Karakachoff, Stephane Bezieau, Barry London, Jacob Tfelt-Hansen, Dan Roden, Katja E Odening, Marina Cerrone, Larry A Chinitz, Paul G Volders, Maarten P van den Berg, Gabriel Laurent, Laurence Faivre, Charles Antzelevitch, Stefan Kääb, Alain Al Arnaout, Jean-Marc Dupuis, Jean-Luc Pasquie, Olivier Billon, Jason D Roberts, Laurence Jesel, Martin Borggrefe, Pier D Lambiase, Jacques Mansourati, Bart Loeys, Antoine Leenhardt, Pascale Guicheney, Philippe Maury, Eric Schulze-Bahr, Tomas Robyns, Jeroen Breckpot, Dominique Babuty, Silvia G Priori, Carlo Napolitano, null null, Carlos De Asmundis, Pedro Brugada, Ramon Brugada, Elena Arbelo, Josep Brugada, Philippe Mabo, Nathalie Behar, Carla Giustetto, Maria Sabater Molina, Juan R Gimeno, Can Hasdemir, Peter J Schwartz, Lia Crotti, Pascal P McKeown, Sanjay Sharma, Elijah R Behr, Michel Haissaguerre, Frédéric Sacher, Caroline Rooryck, Hanno L Tan, Carol A Remme, Pieter G Postema, Mario Delmar, Patrick T Ellinor, Steven A Lubitz, Jean-Baptiste Gourraud, Michael W T Tanck, Alfred L George, Calum A MacRae, Maged M Costantine, Christian Dina, Vincent Probst, Arthur A Wilde, Jean-Jacques Schott, Richard Redon, Connie R Bezzina
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nature genetics 54 (3) (2022)
Charlotte C M Zuurbier, Romain Bourcier, Pacôme Constant Dit Beaufils, Richard Redon, Hubert Desal, null null, Anne S E Bor, Antti E Lindgren, Gabriel J E Rinkel, Jacoba P Greving, Ynte M Ruigrok
Number of Affected Relatives, Age, Smoking, and Hypertension Prediction Score for Intracranial Aneurysms in Persons With a Family History for Subarachnoid Hemorrhage. Stroke 53 (5) (2022)
Mark K Bakker, Rick A A van der Spek, Wouter Van Rheenen, Sandrine Morel, Romain Bourcier, Isabel Charlotte Hostettler, Varinder S Alg, Kristel R van Eijk, Masaru Koido, Masato Akiyama, Chikashi C Terao, Koichi Matsuda, Robin G Walters, Kuang Lin, Liming Li, Iona Y Millwood, Zhengming Chen, Guy A Rouleau, Sirui Zhou, Kristiina Rannikmäe, Cathie L M Sudlow, Henry Houlden, Leonard H van den Berg, Christian Dina, Olivier Naggara, Jean-Christophe Gentric, Eimad Shotar, Francisco Macian, Hubert Desal, Bendik Slagsvold Winsvold, Sigrid Børte, Marianne Bakke Johnsen, Ben Michael Brumpton, Marie Søfteland Sandvei, Cristen J Willer, Kristian Hveem, John-Anker Zwart, W M Monique Verschuren, Christoph M Friedrich, Sven Hirsch, Sabine Schilling, Jérôme Dauvillier, Olivier Martin, null null, null null, null null, null null, null null, null null, null null, Gregory T Jones, Matthew J Bown, Nerissa U Ko, Helen Kim, Jonathan R I Coleman, Gerome Breen, Jonathan G Zaroff, Catharina J M Klijn, Rainer Malik, Martin Dichgans, Muralidharan Sargurupremraj, Turgut Tatlisumak, Phillippe Amouyel, Stephanie Debette, Gabriel J E Rinkel, Bradford B Worrall, Joanna Pera, Agnieszka Slowik, Emília I Gaál-Paavola, Mika Niemelä, Juha E Jääskeläinen, Mikael von Und Zu Fraunberg, Antti E Lindgren, Joseph P Broderick, David John Werring, Daniel Woo, Richard Redon, Philippe Bijlenga, Yoichiro Kamatani, Jan Herman Veldink, Ynte M Ruigrok
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors. Nature genetics 52 (12) (2020)
Connie R Bezzina, Julien Barc, Yuka Mizusawa, Carol Ann Remme, Jean-Baptiste Gourraud, Floriane Simonet, Arie O Verkerk, Peter J Schwartz, Lia Crotti, Federica Dagradi, Pascale Guicheney, Véronique Fressart, Antoine Leenhardt, Charles Antzelevitch, Susan Bartkowiak, Martin Borggrefe, Rainer Schimpf, Eric Schulze-Bahr, Sven Zumhagen, Elijah R Behr, Rachel Bastiaenen, Jacob Tfelt-Hansen, Morten Salling Olesen, Stefan Kääb, Britt M Beckmann, Peter Weeke, Hiroshi Watanabe, Naoto Endo, Tohru Minamino, Minoru Horie, Seiko Ohno, Kanae Hasegawa, Naomasa Makita, Akihiko Nogami, Wataru Shimizu, Takeshi Aiba, Philippe Froguel, Beverley Balkau, Olivier Lantieri, Margherita Torchio, Cornelia Wiese, David Weber, Rianne Wolswinkel, Ruben Coronel, Bas J Boukens, Stéphane Bézieau, Eric Charpentier, Stéphanie Chatel, Aurore Despres, Françoise Gros, Florence Kyndt, Simon Lecointe, Pierre Lindenbaum, Vincent Portero, Jade Violleau, Manfred Gessler, Hanno L Tan, Dan M Roden, Vincent M Christoffels, Hervé Le Marec, Arthur A Wilde, Vincent Probst, Jean-Jacques Schott, Christian Dina, Richard Redon
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. Nature genetics 45 (9) (2013)

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Publication Activity (10 Years)

Top Topics

Top Venues

Richard Redon