Yann Hérault (Yann Herault)

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 68

Top Venues

Nature communications

Science translational medicine

Biomedicines

Communications biology

Centre National de la Recherche Scientifique

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

Affiliation History

Centre National de la Recherche Scientifique Nov 01 2004

France

Directeur de Recherche :: Institut des Sciences Biologiques

Centre National de la Recherche Scientifique Nov 01 1999 - Oct 31 2004

France

Chargé de Recherche :: Sciences de la Vie

Publications

Eva Lana-Elola, Rifdat Aoidi, Miriam Llorian Sopena, Dorota Gibbins, Callan Buechsenschuetz, Claudio Bussi, Helen R Flynn, Tegan Gilmore, Sheona Watson-Scales, Marie H Hansen, Darryl A Hayward, Ok-Ryul Song, Véronique Brault, Yann Hérault, Emmanuel Deau, Laurent Meijer, Ambrosius P Snijders, Maximiliano G Gutierrez, Elizabeth M C Fisher, Victor L J Tybulewicz
Increased dosage of DYRK1A leads to congenital heart defects in a mouse model of Down syndrome. Science translational medicine 16 (731) (2024)
Lydia Teboul, James M Amos-Landgraf, Fernando J Benavides, Marie-Christine Birling, Steve D M Brown, Elizabeth Bryda, Rosie K Bunton-Stasyshyn, Hsian-Jean Chin, Martina Crispo, Fabien Delerue, Michael Dobbie, Craig L Franklin, Ernst-Martin Fuchtbauer, Xiang Gao, Christelle Golzio, Rebecca Haffner, Yann Hérault, Martin Hrabě de Angelis, Kevin C Kent Lloyd, Terry R Magnuson, Lluís Montoliu, Stephen A Murray, Ki-Hoan Nam, Lauryl M J Nutter, Eric Pailhoux, Fernando Pardo-Manuel de Villena, Kevin A Peterson, Laura G Reinholdt, Radislav Sedlacek, Je-Kyung Seong, Toshihiko Shiroishi, Cynthia L Smith, Nobuyuki Mikoda, Louise Tinsley, Jean-Luc Vilotte, Søren Warming, Sara E Wells, C Bruce A Whitelaw, Atsushi Yoshiki, null null, null null, null null, null null, null null, null null, null null, null null, null null, Guillaume Pavlovic
Improving laboratory animal genetic reporting: LAG-R guidelines. Nature communications 15 (1) (2024)
Lydia Teboul, James M Amos-Landgraf, Fernando J Benavides, Marie-Christine Birling, Steve D M Brown, Elizabeth Bryda, Rosie K Bunton-Stasyshyn, Hsian-Jean Chin, Martina Crispo, Fabien Delerue, Michael Dobbie, Craig L Franklin, Ernst-Martin Fuchtbauer, Xiang Gao, Christelle Golzio, Rebecca Haffner, Yann Hérault, Martin Hrabě de Angelis, Kevin C Kent Lloyd, Terry R Magnuson, Lluís Montoliu, Stephen A Murray, Ki-Hoan Nam, Lauryl M J Nutter, Eric Pailhoux, Fernando Pardo-Manuel de Villena, Kevin A Peterson, Laura G Reinholdt, Radislav Sedlacek, Je-Kyung Seong, Toshihiko Shiroishi, Cynthia L Smith, Nobuyuki Mikoda, Louise Tinsley, Jean-Luc Vilotte, Søren Warming, Sara E Wells, C Bruce A Whitelaw, Atsushi Yoshiki, null null, null null, null null, null null, null null, null null, null null, null null, null null, Guillaume Pavlovic
Improving laboratory animal genetic reporting: LAG-R guidelines. Nature communications 15 (1) (2024)
Daniel Holl, Wing Fung Hau, Anais Julien, Shervin Banitalebi, Jannis Kalkitsas, Soniya Savant, Enric Llorens-Bobadilla, Yann Hérault, Guillaume Pavlovic, Mahmood Amiry-Moghaddam, David Oliveira Dias, Christian Göritz
Distinct origin and region-dependent contribution of stromal fibroblasts to fibrosis following traumatic injury in mice. Nature neuroscience 27 (7) (2024)
Eva Lana-Elola, Rifdat Aoidi, Miriam Llorian Sopena, Dorota Gibbins, Callan Buechsenschuetz, Claudio Bussi, Helen R Flynn, Tegan Gilmore, Sheona Watson-Scales, Marie H Hansen, Darryl A Hayward, Ok-Ryul Song, Véronique Brault, Yann Hérault, Emmanuel Deau, Laurent Meijer, Ambrosius P Snijders, Maximiliano G Gutierrez, Elizabeth M C Fisher, Victor L J Tybulewicz
Increased dosage of DYRK1A leads to congenital heart defects in a mouse model of Down syndrome. Science translational medicine 16 (731) (2024)
Lydia Teboul, James M Amos-Landgraf, Fernando J Benavides, Marie-Christine Birling, Steve D M Brown, Elizabeth Bryda, Rosie K Bunton-Stasyshyn, Hsian-Jean Chin, Martina Crispo, Fabien Delerue, Michael Dobbie, Craig L Franklin, Ernst-Martin Fuchtbauer, Xiang Gao, Christelle Golzio, Rebecca Haffner, Yann Hérault, Martin Hrabě de Angelis, Kevin C Kent Lloyd, Terry R Magnuson, Lluís Montoliu, Stephen A Murray, Ki-Hoan Nam, Lauryl M J Nutter, Eric Pailhoux, Fernando Pardo-Manuel de Villena, Kevin A Peterson, Laura G Reinholdt, Radislav Sedlacek, Je-Kyung Seong, Toshihiko Shiroishi, Cynthia L Smith, Nobuyuki Mikoda, Louise Tinsley, Jean-Luc Vilotte, Søren Warming, Sara E Wells, C Bruce A Whitelaw, Atsushi Yoshiki, null null, null null, null null, null null, null null, null null, null null, null null, null null, Guillaume Pavlovic
Improving laboratory animal genetic reporting: LAG-R guidelines. Nature communications 15 (1) (2024)
Lydia Teboul, James M Amos-Landgraf, Fernando J Benavides, Marie-Christine Birling, Steve D M Brown, Elizabeth Bryda, Rosie K Bunton-Stasyshyn, Hsian-Jean Chin, Martina Crispo, Fabien Delerue, Michael Dobbie, Craig L Franklin, Ernst-Martin Fuchtbauer, Xiang Gao, Christelle Golzio, Rebecca Haffner, Yann Hérault, Martin Hrabě de Angelis, Kevin C Kent Lloyd, Terry R Magnuson, Lluís Montoliu, Stephen A Murray, Ki-Hoan Nam, Lauryl M J Nutter, Eric Pailhoux, Fernando Pardo-Manuel de Villena, Kevin A Peterson, Laura G Reinholdt, Radislav Sedlacek, Je-Kyung Seong, Toshihiko Shiroishi, Cynthia L Smith, Nobuyuki Mikoda, Louise Tinsley, Jean-Luc Vilotte, Søren Warming, Sara E Wells, C Bruce A Whitelaw, Atsushi Yoshiki, null null, null null, null null, null null, null null, null null, null null, null null, null null, Guillaume Pavlovic
Improving laboratory animal genetic reporting: LAG-R guidelines. Nature communications 15 (1) (2024)
Daniel Holl, Wing Fung Hau, Anais Julien, Shervin Banitalebi, Jannis Kalkitsas, Soniya Savant, Enric Llorens-Bobadilla, Yann Hérault, Guillaume Pavlovic, Mahmood Amiry-Moghaddam, David Oliveira Dias, Christian Göritz
Distinct origin and region-dependent contribution of stromal fibroblasts to fibrosis following traumatic injury in mice. Nature neuroscience 27 (7) (2024)
Camille Sauter, Thomas Morin, Fabien Guidez, John Simonet, Cyril Fournier, Céline Row, Denis Masnikov, Baptiste Pernon, Anne Largeot, Aziza Aznague, Yann Hérault, Guy Sauvageau, Marc Maynadié, Mary Callanan, Jean-Noël Bastie, Romain Aucagne, Laurent Delva
Protein arginine methyltransferase 2 controls inflammatory signaling in acute myeloid leukemia. Communications biology 7 (1) (2024)
Daniel Holl, Wing Fung Hau, Anais Julien, Shervin Banitalebi, Jannis Kalkitsas, Soniya Savant, Enric Llorens-Bobadilla, Yann Hérault, Guillaume Pavlovic, Mahmood Amiry-Moghaddam, David Oliveira Dias, Christian Göritz
Distinct origin and region-dependent contribution of stromal fibroblasts to fibrosis following traumatic injury in mice. Nature neuroscience (2024)
Camille Sauter, Thomas Morin, Fabien Guidez, John Simonet, Cyril Fournier, Céline Row, Denis Masnikov, Baptiste Pernon, Anne Largeot, Aziza Aznague, Yann Hérault, Guy Sauvageau, Marc Maynadié, Mary Callanan, Jean-Noël Bastie, Romain Aucagne, Laurent Delva
Protein arginine methyltransferase 2 controls inflammatory signaling in acute myeloid leukemia. Communications biology 7 (1) (2024)
Eva Lana-Elola, Rifdat Aoidi, Miriam Llorian Sopena, Dorota Gibbins, Callan Buechsenschuetz, Claudio Bussi, Helen R Flynn, Tegan Gilmore, Sheona Watson-Scales, Marie H Hansen, Darryl A Hayward, Ok-Ryul Song, Véronique Brault, Yann Hérault, Emmanuel Deau, Laurent Meijer, Ambrosius P Snijders, Maximiliano G Gutierrez, Elizabeth M C Fisher, Victor L J Tybulewicz
Increased dosage of DYRK1A leads to congenital heart defects in a mouse model of Down syndrome. Science translational medicine 16 (731) (2024)
Camille Sauter, Thomas Morin, Fabien Guidez, John Simonet, Cyril Fournier, Céline Row, Denis Masnikov, Baptiste Pernon, Anne Largeot, Aziza Aznague, Yann Hérault, Guy Sauvageau, Marc Maynadié, Mary Callanan, Jean-Noël Bastie, Romain Aucagne, Laurent Delva
Protein arginine methyltransferase 2 controls inflammatory signaling in acute myeloid leukemia. Communications biology 7 (1) (2024)
Eva Lana-Elola, Rifdat Aoidi, Miriam Llorian Sopena, Dorota Gibbins, Callan Buechsenschuetz, Claudio Bussi, Helen R Flynn, Tegan Gilmore, Sheona Watson-Scales, Marie H Hansen, Darryl A Hayward, Ok-Ryul Song, Véronique Brault, Yann Hérault, Emmanuel Deau, Laurent Meijer, Ambrosius P Snijders, Maximiliano G Gutierrez, Elizabeth M C Fisher, Victor L J Tybulewicz
Increased dosage of DYRK1A leads to congenital heart defects in a mouse model of Down syndrome. Science translational medicine 16 (731) (2024)
Camille Sauter, Thomas Morin, Fabien Guidez, John Simonet, Cyril Fournier, Céline Row, Denis Masnikov, Baptiste Pernon, Anne Largeot, Aziza Aznague, Yann Hérault, Guy Sauvageau, Marc Maynadié, Mary Callanan, Jean-Noël Bastie, Romain Aucagne, Laurent Delva
Protein arginine methyltransferase 2 controls inflammatory signaling in acute myeloid leukemia. Communications biology 7 (1) (2024)
Eva Lana-Elola, Rifdat Aoidi, Miriam Llorian Sopena, Dorota Gibbins, Callan Buechsenschuetz, Claudio Bussi, Helen R Flynn, Tegan Gilmore, Sheona Watson-Scales, Marie H Hansen, Darryl A Hayward, Ok-Ryul Song, Véronique Brault, Yann Hérault, Emmanuel Deau, Laurent Meijer, Ambrosius P Snijders, Maximiliano G Gutierrez, Elizabeth M C Fisher, Victor L J Tybulewicz
Increased dosage of DYRK1A leads to congenital heart defects in a mouse model of Down syndrome. Science translational medicine 16 (731) (2024)
Eva Lana-Elola, Rifdat Aoidi, Miriam Llorian Sopena, Dorota Gibbins, Callan Buechsenschuetz, Claudio Bussi, Helen R Flynn, Tegan Gilmore, Sheona Watson-Scales, Marie H Hansen, Darryl A Hayward, Ok-Ryul Song, Véronique Brault, Yann Hérault, Emmanuel Deau, Laurent Meijer, Ambrosius P Snijders, Maximiliano G Gutierrez, Elizabeth M C Fisher, Victor L J Tybulewicz
Increased dosage of DYRK1A leads to congenital heart defects in a mouse model of Down syndrome. Science translational medicine 16 (731) (2024)
Lydia Teboul, James M Amos-Landgraf, Fernando J Benavides, Marie-Christine Birling, Steve D M Brown, Elizabeth Bryda, Rosie K Bunton-Stasyshyn, Hsian-Jean Chin, Martina Crispo, Fabien Delerue, Michael Dobbie, Craig L Franklin, Ernst-Martin Fuchtbauer, Xiang Gao, Christelle Golzio, Rebecca Haffner, Yann Hérault, Martin Hrabě de Angelis, Kevin C Kent Lloyd, Terry R Magnuson, Lluís Montoliu, Stephen A Murray, Ki-Hoan Nam, Lauryl M J Nutter, Eric Pailhoux, Fernando Pardo-Manuel de Villena, Kevin A Peterson, Laura G Reinholdt, Radislav Sedlacek, Je-Kyung Seong, Toshihiko Shiroishi, Cynthia L Smith, Nobuyuki Mikoda, Louise Tinsley, Jean-Luc Vilotte, Søren Warming, Sara E Wells, C Bruce A Whitelaw, Atsushi Yoshiki, null null, null null, null null, null null, null null, null null, null null, null null, null null, Guillaume Pavlovic
Improving laboratory animal genetic reporting: LAG-R guidelines. Nature communications 15 (1) (2024)
Eva Lana-Elola, Rifdat Aoidi, Miriam Llorian Sopena, Dorota Gibbins, Callan Buechsenschuetz, Claudio Bussi, Helen R Flynn, Tegan Gilmore, Sheona Watson-Scales, Marie H Hansen, Darryl A Hayward, Ok-Ryul Song, Véronique Brault, Yann Hérault, Emmanuel Deau, Laurent Meijer, Ambrosius P Snijders, Maximiliano G Gutierrez, Elizabeth M C Fisher, Victor L J Tybulewicz
Increased dosage of DYRK1A leads to congenital heart defects in a mouse model of Down syndrome. Science translational medicine 16 (731) (2024)
Maria Del Mar Muñiz Moreno, Claire Gavériaux-Ruff, Yann Hérault
Gdaphen, R pipeline to identify the most important qualitative and quantitative predictor variables from phenotypic data. BMC bioinformatics 24 (1) (2023)
Maria Del Mar Muñiz Moreno, Claire Gavériaux-Ruff, Yann Hérault
Gdaphen, R pipeline to identify the most important qualitative and quantitative predictor variables from phenotypic data. BMC bioinformatics 24 (1) (2023)
Brigitta B Gundersen, William T O'Brien, Melanie D Schaffler, Maria N Schultz, Tatsuya Tsukahara, Sandra Martin Lorenzo, Valerie Nalesso, Alice H Luo Clayton, Ted Abel, Jacqueline N Crawley, Sandeep Robert Datta, Yann Hérault
Towards Preclinical Validation of Arbaclofen (R-baclofen) Treatment for 16p11.2 Deletion Syndrome. bioRxiv : the preprint server for biology (2023)
Valérie Erbs, Romain Lorentz, Benjamin Eisenman, Laurence Schaeffer, Laurence Luppi, Loic Lindner, Yann Hérault, Guillaume Pavlovic, Marie Wattenhofer-Donzé, Marie-Christine Birling
Increased On-Target Rate and Risk of Concatemerization after CRISPR-Enhanced Targeting in ES Cells. Genes 14 (2) (2023)
Marius Teletin, Manuel Mark, Olivia Wendling, Nadège Vernet, Betty Féret, Muriel Klopfenstein, Yann Hérault, Norbert B Ghyselinck
Timeline of Developmental Defects Generated upon Genetic Inhibition of the Retinoic Acid Receptor Signaling Pathway. Biomedicines 11 (1) (2023)
Valérie Erbs, Romain Lorentz, Benjamin Eisenman, Laurence Schaeffer, Laurence Luppi, Loic Lindner, Yann Hérault, Guillaume Pavlovic, Marie Wattenhofer-Donzé, Marie-Christine Birling
Increased On-Target Rate and Risk of Concatemerization after CRISPR-Enhanced Targeting in ES Cells. Genes 14 (2) (2023)
Mojca Trstenjak-Prebanda, Monika Biasizzo, Klemen Dolinar, Sergej Pirkmajer, Boris Turk, Véronique Brault, Yann Hérault, Nataša Kopitar-Jerala
Stefin B Inhibits NLRP3 Inflammasome Activation via AMPK/mTOR Signalling. Cells 12 (23) (2023)
Valérie Erbs, Romain Lorentz, Benjamin Eisenman, Laurence Schaeffer, Laurence Luppi, Loic Lindner, Yann Hérault, Guillaume Pavlovic, Marie Wattenhofer-Donzé, Marie-Christine Birling
Increased On-Target Rate and Risk of Concatemerization after CRISPR-Enhanced Targeting in ES Cells. Genes 14 (2) (2023)
Valérie Erbs, Romain Lorentz, Benjamin Eisenman, Laurence Schaeffer, Laurence Luppi, Loic Lindner, Yann Hérault, Guillaume Pavlovic, Marie Wattenhofer-Donzé, Marie-Christine Birling
Increased On-Target Rate and Risk of Concatemerization after CRISPR-Enhanced Targeting in ES Cells. Genes 14 (2) (2023)
Maria Del Mar Muñiz Moreno, Claire Gavériaux-Ruff, Yann Hérault
Gdaphen, R pipeline to identify the most important qualitative and quantitative predictor variables from phenotypic data. BMC bioinformatics 24 (1) (2023)
Marius Teletin, Manuel Mark, Olivia Wendling, Nadège Vernet, Betty Féret, Muriel Klopfenstein, Yann Hérault, Norbert B Ghyselinck
Timeline of Developmental Defects Generated upon Genetic Inhibition of the Retinoic Acid Receptor Signaling Pathway. Biomedicines 11 (1) (2023)
Giuliana Giannuzzi, Nicolas Chatron, Katrin Mannik, Chiara Auwerx, Sylvain Pradervand, Gilles Willemin, Kendra Hoekzema, Xander Nuttle, Jacqueline Chrast, Marie C Sadler, Eleonora Porcu, null null, Yann Hérault, Bertrand Isidor, Brigitte Gilbert-Dussardier, Evan E Eichler, Zoltan Kutalik, Alexandre Reymond
Author Correction: Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts. NPJ genomic medicine 8 (1) (2023)
Hamid Meziane, Marie-Christine Birling, Olivia Wendling, Sophie Leblanc, Aline Dubos, Mohammed Selloum, Guillaume Pavlovic, Tania Sorg, Vera M Kalscheuer, Pierre Billuart, Frederic Laumonnier, Jamel Chelly, Hans van Bokhoven, Yann Hérault
Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models. Biomedicines 10 (12) (2022)
Giuliana Giannuzzi, Nicolas Chatron, Katrin Mannik, Chiara Auwerx, Sylvain Pradervand, Gilles Willemin, Kendra Hoekzema, Xander Nuttle, Jacqueline Chrast, Marie C Sadler, Eleonora Porcu, null null, Yann Hérault, Bertrand Isidor, Brigitte Gilbert-Dussardier, Evan E Eichler, Zoltan Kutalik, Alexandre Reymond
Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts. NPJ genomic medicine 7 (1) (2022)
Hamid Meziane, Marie-Christine Birling, Olivia Wendling, Sophie Leblanc, Aline Dubos, Mohammed Selloum, Guillaume Pavlovic, Tania Sorg, Vera M Kalscheuer, Pierre Billuart, Frederic Laumonnier, Jamel Chelly, Hans van Bokhoven, Yann Hérault
Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models. Biomedicines 10 (12) (2022)
Nadine Spielmann, Gregor Miller, Tudor I Oprea, Chih-Wei Hsu, Gisela Fobo, Goar Frishman, Corinna Montrone, Hamed Haseli Mashhadi, Jeremy C Mason, Violeta Munoz Fuentes, Stefanie Leuchtenberger, Andreas Ruepp, Matias Wagner, Dominik Sebastian Westphal, Cordula M Wolf, Agnes Görlach, Adrián Sanz-Moreno, Yi-Li Cho, Raffaele Teperino, Stefan Brandmaier, Sapna Sharma, Isabella Rikarda Galter, Manuela A Östereicher, Lilly Zapf, Philipp Mayer-Kuckuk, Jan Rozman, Lydia Teboul, Rosie K A Bunton-Stasyshyn, Heather L Cater, Michelle Stewart, Skevoulla Christou, Henrik Westerberg, Amelia M Willett, Janine M Wotton, Willson B Roper, Audrey E Christiansen, Christopher S Ward, Jason D Heaney, Corey L Reynolds, Jan Prochazka, Lynette Bower, Dave A Clary, Mohammed Selloum, Ghina Bou About, Olivia Wendling, Hugues Jacobs, Sophie Leblanc, Hamid Meziane, Tania Sorg, Enrique Audain, Arthur Gilly, Nigel William Rayner, null null, null null, Marc-Phillip Hitz, Eleftheria Zeggini, Eckhard Wolf, Radislav Sedlacek, Stephen A Murray, Karen L Svenson, Robert E Braun, Jaqueline K White, Lois Kelsey, Xiang Gao, Toshihiko Shiroishi, Ying Xu, Je-Kyung Seong, Fabio Mammano, Glauco P Tocchini-Valentini, Arthur L Beaudet, Terrence F Meehan, Helen Parkinson, Damian Smedley, Ann-Marie Mallon, Sara E Wells, Harald Grallert, Wolfgang Wurst, Susan Marschall, Helmut Fuchs, Steve D M Brown, Ann M Flenniken, Lauryl M J Nutter, Colin McKerlie, Yann Hérault, K C Kent Lloyd, Mary E Dickinson, Valérie Gailus-Durner, Martin Hrabě de Angelis
Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy. Nature cardiovascular research 1 (2) (2022)
Arnaud Duchon, Maria Del Mar Muñiz Moreno, Claire Chevalier, Valérie Nalesso, Philippe Andre, Marta Fructuoso-Castellar, Mary Mondino, Chrystelle Po, Vincent Noblet, Marie-Christine Birling, Marie-Claude Potier, Yann Hérault
Ts66Yah, a mouse model of Down syndrome with improved construct and face validity. Disease models & mechanisms 15 (12) (2022)
Julia Viard, Yann Loe-Mie, Rachel Daudin, Malik Khelfaoui, Christine Plancon, Anne Boland-Auge, Francisco J Tejedor, Richard L Huganir, Eunjoon Kim, Makoto Kinoshita, Guofa Liu, Volker Haucke, Thomas Moncion, Eugene Yu, Valérie Hindie, Henri Bléhaut, Clotilde Mircher, Yann Hérault, Jean-François Deleuze, Jean-Christophe Rain, Michel Simonneau, Aude-Marie Lepagnol-Bestel
Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer's disease. Life science alliance 5 (12) (2022)
Nadine Spielmann, Gregor Miller, Tudor I Oprea, Chih-Wei Hsu, Gisela Fobo, Goar Frishman, Corinna Montrone, Hamed Haseli Mashhadi, Jeremy C Mason, Violeta Munoz Fuentes, Stefanie Leuchtenberger, Andreas Ruepp, Matias Wagner, Dominik Sebastian Westphal, Cordula M Wolf, Agnes Görlach, Adrián Sanz-Moreno, Yi-Li Cho, Raffaele Teperino, Stefan Brandmaier, Sapna Sharma, Isabella Rikarda Galter, Manuela A Östereicher, Lilly Zapf, Philipp Mayer-Kuckuk, Jan Rozman, Lydia Teboul, Rosie K A Bunton-Stasyshyn, Heather L Cater, Michelle Stewart, Skevoulla Christou, Henrik Westerberg, Amelia M Willett, Janine M Wotton, Willson B Roper, Audrey E Christiansen, Christopher S Ward, Jason D Heaney, Corey L Reynolds, Jan Prochazka, Lynette Bower, Dave A Clary, Mohammed Selloum, Ghina Bou About, Olivia Wendling, Hugues Jacobs, Sophie Leblanc, Hamid Meziane, Tania Sorg, Enrique Audain, Arthur Gilly, Nigel William Rayner, null null, null null, Marc-Phillip Hitz, Eleftheria Zeggini, Eckhard Wolf, Radislav Sedlacek, Stephen A Murray, Karen L Svenson, Robert E Braun, Jaqueline K White, Lois Kelsey, Xiang Gao, Toshihiko Shiroishi, Ying Xu, Je-Kyung Seong, Fabio Mammano, Glauco P Tocchini-Valentini, Arthur L Beaudet, Terrence F Meehan, Helen Parkinson, Damian Smedley, Ann-Marie Mallon, Sara E Wells, Harald Grallert, Wolfgang Wurst, Susan Marschall, Helmut Fuchs, Steve D M Brown, Ann M Flenniken, Lauryl M J Nutter, Colin McKerlie, Yann Hérault, K C Kent Lloyd, Mary E Dickinson, Valérie Gailus-Durner, Martin Hrabě de Angelis
Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy. Nature cardiovascular research 1 (2) (2022)
Nadine Spielmann, Gregor Miller, Tudor I Oprea, Chih-Wei Hsu, Gisela Fobo, Goar Frishman, Corinna Montrone, Hamed Haseli Mashhadi, Jeremy C Mason, Violeta Munoz Fuentes, Stefanie Leuchtenberger, Andreas Ruepp, Matias Wagner, Dominik Sebastian Westphal, Cordula M Wolf, Agnes Görlach, Adrián Sanz-Moreno, Yi-Li Cho, Raffaele Teperino, Stefan Brandmaier, Sapna Sharma, Isabella Rikarda Galter, Manuela A Östereicher, Lilly Zapf, Philipp Mayer-Kuckuk, Jan Rozman, Lydia Teboul, Rosie K A Bunton-Stasyshyn, Heather L Cater, Michelle Stewart, Skevoulla Christou, Henrik Westerberg, Amelia M Willett, Janine M Wotton, Willson B Roper, Audrey E Christiansen, Christopher S Ward, Jason D Heaney, Corey L Reynolds, Jan Prochazka, Lynette Bower, Dave A Clary, Mohammed Selloum, Ghina Bou About, Olivia Wendling, Hugues Jacobs, Sophie Leblanc, Hamid Meziane, Tania Sorg, Enrique Audain, Arthur Gilly, Nigel William Rayner, null null, null null, Marc-Phillip Hitz, Eleftheria Zeggini, Eckhard Wolf, Radislav Sedlacek, Stephen A Murray, Karen L Svenson, Robert E Braun, Jaqueline K White, Lois Kelsey, Xiang Gao, Toshihiko Shiroishi, Ying Xu, Je-Kyung Seong, Fabio Mammano, Glauco P Tocchini-Valentini, Arthur L Beaudet, Terrence F Meehan, Helen Parkinson, Damian Smedley, Ann-Marie Mallon, Sara E Wells, Harald Grallert, Wolfgang Wurst, Susan Marschall, Helmut Fuchs, Steve D M Brown, Ann M Flenniken, Lauryl M J Nutter, Colin McKerlie, Yann Hérault, K C Kent Lloyd, Mary E Dickinson, Valérie Gailus-Durner, Martin Hrabě de Angelis
Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy. Nature cardiovascular research 1 (2) (2022)
Olivia Wendling, Didier Hentsch, Hugues Jacobs, Nicolas Lemercier, Serge Taubert, Fabien Pertuy, Jean-Luc Vonesch, Tania Sorg, Michela Di Michele, Laurent Le Cam, Thomas Rosahl, Ester Carballo-Jane, Mindy Liu, James Mu, Manuel Mark, Yann Hérault
High Resolution Episcopic Microscopy for Qualitative and Quantitative Data in Phenotyping Altered Embryos and Adult Mice Using the New "Histo3D" System. Biomedicines 9 (7) (2021)
Manuel Mark, Marius Teletin, Olivia Wendling, Jean-Luc Vonesch, Betty Féret, Yann Hérault, Norbert B Ghyselinck
Pathogenesis of Anorectal Malformations in Retinoic Acid Receptor Knockout Mice Studied by HREM. Biomedicines 9 (7) (2021)
Yixing Wu, Heather T Whittaker, Suzanna Noy, Karen Cleverley, Veronique Brault, Yann Hérault, Elizabeth M C Fisher, Frances K Wiseman
The effects of Cstb duplication on APP/amyloid-β pathology and cathepsin B activity in a mouse model. PloS one 16 (7) (2021)
Hilke Ehlich, Heather L Cater, Ann M Flenniken, Isabelle Goncalves Da Cruz, Anne-Marie Mura, Vasileios Ntafis, Michael Raess, Mohammed Selloum, Claudia Stoeger, Sarka Suchanova, Reetta Vuolteenaho, Steve D M Brown, Yann Hérault, Reetta M Hinttala, Martin Hrabě de Angelis, George Kollias, Dimitris L Kontoyiannis, Bernard Malissen, Colin McKerlie, Radislav Sedlacek, Sara E Wells, Ana Zarubica, Jan Rozman, Tania Sorg
INFRAFRONTIER quality principles in systemic phenotyping. Mammalian genome : official journal of the International Mammalian Genome Society (2021)
Alyssa Imbert, Magali Rompais, Mohammed Selloum, Florence Castelli, Emmanuelle Mouton-Barbosa, Marion Brandolini-Bunlon, Emeline Chu-Van, Charlotte Joly, Aurélie Hirschler, Pierrick Roger, Thomas Burger, Sophie Leblanc, Tania Sorg, Sadia Ouzia, Yves Vandenbrouck, Claudine Médigue, Christophe Junot, Myriam Ferro, Estelle Pujos-Guillot, Anne Gonzalez de Peredo, François Fenaille, Christine Carapito, Yann Hérault, Etienne A Thévenot
ProMetIS, deep phenotyping of mouse models by combined proteomics and metabolomics analysis. Scientific data 8 (1) (2021)
Sandra Martin Lorenzo, Valérie Nalesso, Claire Chevalier, Marie-Christine Birling, Yann Hérault
Targeting the RHOA pathway improves learning and memory in adult Kctd13 and 16p11.2 deletion mouse models. Molecular autism 12 (1) (2021)
Helin Atas-Ozcan, Véronique Brault, Arnaud Duchon, Yann Hérault
Dyrk1a from Gene Function in Development and Physiology to Dosage Correction across Life Span in Down Syndrome. Genes 12 (11) (2021)
Véronique Brault, Thu Lan Nguyen, Javier Flores-Gutiérrez, Giovanni Iacono, Marie-Christine Birling, Valérie Lalanne, Hamid Meziane, Antigoni Manousopoulou, Guillaume Pavlovic, Loic Lindner, Mohammed Selloum, Tania Sorg, Eugene Yu, Spiros D D Garbis, Yann Hérault
Dyrk1a gene dosage in glutamatergic neurons has key effects in cognitive deficits observed in mouse models of MRD7 and Down syndrome. PLoS genetics 17 (9) (2021)
Marie-Christine Birling, Atsushi Yoshiki, David J Adams, Shinya Ayabe, Arthur L Beaudet, Joanna Bottomley, Allan Bradley, Steve D M Brown, Antje Bürger, Wendy Bushell, Francesco Chiani, Hsian-Jean Genie Chin, Skevoulla Christou, Gemma F Codner, Francesco J DeMayo, Mary E Dickinson, Brendan Doe, Leah Rae Donahue, Martin D Fray, Alessia Gambadoro, Xiang Gao, Marina Gertsenstein, Alba Gomez-Segura, Leslie O Goodwin, Jason D Heaney, Yann Hérault, Martin Hrabě de Angelis, Si-Tse Jiang, Monica J Justice, Petr Kasparek, Ruairidh E King, Ralf Kühn, Ho Lee, Young-Jae Lee, Zhiwei Liu, Kevin C Kent Lloyd, Isabel Lorenzo, Ann-Marie Mallon, Colin McKerlie, Terrence F Meehan, Violeta Munoz Fuentes, Stuart Newman, Lauryl M J Nutter, Goo Taeg Oh, Guillaume Pavlovic, Ramiro Ramirez-Solis, Barry Rosen, Edward J Ryder, Luis A Santos, Joel A Schick, John R Seavitt, Radislav Sedlacek, Claudia Seisenberger, Je Kyung Seong, William C Skarnes, Tania Sorg, Karen P Steel, Masaru Tamura, Glauco P Tocchini-Valentini, Chi-Kuang Leo Wang, Hannah Wardle-Jones, Marie Wattenhofer-Donzé, Sara Wells, Michael V Wiles, Brandon J Willis, Joshua A Wood, Wolfgang Wurst, Ying Xu, null null, Lydia Teboul, Stephen A Murray
A resource of targeted mutant mouse lines for 5,061 genes. Nature genetics 53 (4) (2021)
Anna L Swan, Christine Schütt, Jan Rozman, Maria Del Mar Muñiz-Moreno, Stefan Brandmaier, Michelle Simon, Stefanie Leuchtenberger, Mark Griffiths, Robert Brommage, Piia Keskivali-Bond, Harald Grallert, Thomas Werner, Raffaele Teperino, Lore Becker, Gregor Miller, Ala Moshiri, John R Seavitt, Derek D Cissell, Terrence F Meehan, Elif F Acar, Christopher J Lelliott, Ann M Flenniken, Marie-France Champy, Tania Sorg, Abdel Ayadi, Robert E Braun, Heather L Cater, Mary E Dickinson, Paul Flicek, Juan Gallegos, Elena J Ghirardello, Jason D Heaney, Sylvie Jacquot, Connor Lally, John G Logan, Lydia Teboul, Jeremy C Mason, Nadine Spielmann, Colin McKerlie, Stephen A Murray, Lauryl M J Nutter, Kristian F Odfalk, Helen Parkinson, Jan Prochazka, Corey L Reynolds, Mohammed Selloum, Frantisek Spoutil, Karen L Svenson, Taylor S Vales, Sara E Wells, Jacqueline K White, Radislav Sedlacek, Wolfgang Wurst, Kevin C Kent Lloyd, Peter I Croucher, Helmut Fuchs, Graham R Williams, J H Duncan Bassett, Valerie Gailus-Durner, Yann Hérault, Ann-Marie Mallon, Steve D M Brown, Philipp Mayer-Kuckuk, Martin Hrabě de Angelis, null null
Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density. PLoS genetics 16 (12) (2020)
Valentina Maria Lionello, Anne-Sophie Nicot, Maxime Sartori, Christine Kretz, Pascal Kessler, Suzie Buono, Sarah Djerroud, Nadia Messaddeq, Pascale Koebel, Ivana Prokic, Yann Hérault, Norma B Romero, Jocelyn Laporte, Belinda S Cowling
Amphiphysin 2 modulation rescues myotubular myopathy and prevents focal adhesion defects in mice. Science translational medicine 11 (484) (2020)
Pilar Cacheiro, Violeta Munoz Fuentes, Stephen A Murray, Mary E Dickinson, Maja Bucan, Lauryl M J Nutter, Kevin A Peterson, Hamed Haseli Mashhadi, Ann M Flenniken, Hugh Morgan, Henrik Westerberg, Tomasz Konopka, Chih-Wei Hsu, Audrey Christiansen, Denise G Lanza, Arthur L Beaudet, Jason D Heaney, Helmut Fuchs, Valérie Gailus-Durner, Tania Sorg, Jan Prochazka, Vendula Novosadova, Christopher J Lelliott, Hannah Wardle-Jones, Sara Wells, Lydia Teboul, Heather Cater, Michelle Stewart, Tertius Hough, Wolfgang Wurst, Radislav Sedlacek, David J Adams, John R Seavitt, Glauco Tocchini-Valentini, Terrence F Meehan, Robert E Braun, Colin McKerlie, Yann Hérault, Martin Hrabě de Angelis, Ann-Marie Mallon, Kevin C Kent Lloyd, Steve D M Brown, Helen Parkinson, Terrence F Meehan, Damian Smedley, null null, null null
Human and mouse essentiality screens as a resource for disease gene discovery. Nature communications 11 (1) (2020)
Renaud Pourpre, Laurent Naudon, Hamid Meziane, Goran Lakisic, Luc Jouneau, Hugo Varet, Rachel Legendre, Olivia Wendling, Mohammed Selloum, Caroline Proux, Jean-Yves Coppée, Yann Hérault, Hélène Bierne
BAHD1 haploinsufficiency results in anxiety-like phenotypes in male mice. PloS one 15 (5) (2020)
Arnaud Duchon, Agnès Gruart, Christelle Albac, Benoît Delatour, Javier Zorrilla de San Martin, José María Delgado-García, Yann Hérault, Marie-Claude Potier
Long-lasting correction of in vivo LTP and cognitive deficits of mice modelling Down syndrome with an α5-selective GABAA inverse agonist. British journal of pharmacology 177 (5) (2020)
Jesus Ruberte, Paul N Schofield, Cord Brakebusch, Peter Vogel, Yann Hérault, Guillem Gracia, Colin McKerlie, Martin Hrabě de Angelis, Michael Hagn, John P Sundberg
PATHBIO: an international training program for precision mouse phenotyping. Mammalian genome : official journal of the International Mammalian Genome Society 31 (1-2) (2020)
Benoit Souchet, Arnaud Duchon, Yuchen Gu, Julien Dairou, Claire Chevalier, Fabrice Daubigney, Valérie Nalesso, Nicole Créau, Yuejin Yu, Nathalie Janel, Yann Hérault, Jean Maurice Delabar
Prenatal treatment with EGCG enriched green tea extract rescues GAD67 related developmental and cognitive defects in Down syndrome mouse models. Scientific reports 9 (1) (2019)
Ekaterina L Ivanova, Johan G Gilet, Vadym Sulimenko, Arnaud Duchon, Gabrielle Rudolf, Karen Runge, Stephan C Collins, Laure Asselin, Loic Broix, Nathalie Drouot, Peggy Tilly, Patrick Nusbaum, Alexandre Vincent, William Magnant, Valerie Skory, Marie-Christine Birling, Guillaume Pavlovic, Juliette D Godin, Binnaz Yalcin, Yann Hérault, Pavel Dráber, Jamel Chelly, Maria-Victoria Hinckelmann
TUBG1 missense variants underlying cortical malformations disrupt neuronal locomotion and microtubule dynamics but not neurogenesis. Nature communications 10 (1) (2019)
Bret A Moore, Brian C Leonard, Lionel Sebbag, Sydney G Edwards, Ann Cooper, Denise M Imai, Ewan Straiton, Luis Santos, Christopher Reilly, Stephen M Griffey, Lynette Bower, David Clary, Jeremy C Mason, Michel J Roux, Hamid Meziane, Yann Hérault, null null, Colin McKerlie, Ann M Flenniken, Lauryl M J Nutter, Zorana Berberovic, Celeste Owen, Susan Newbigging, Hibret Adissu, Mohammed Eskandarian, Chih-Wei Hsu, Sowmya Kalaga, Uchechukwu Udensi, Chinwe Asomugha, Ritu Bohat, Juan J Gallegos, John R Seavitt, Jason D Heaney, Arthur L Beaudet, Mary E Dickinson, Monica J Justice, Vivek Philip, Vivek Kumar, Karen L Svenson, Robert E Braun, Sara Wells, Heather Cater, Michelle Stewart, Sharon Clementson-Mobbs, Russell Joynson, Xiang Gao, Tomohiro Suzuki, Shigeharu Wakana, Damian Smedley, J K Seong, Glauco Tocchini-Valentini, Mark Moore, Colin Fletcher, Natasha Karp, Ramiro Ramirez-Solis, Jacqueline K White, Martin Hrabě de Angelis, Wolfgang Wurst, Sara M Thomasy, Paul Flicek, Helen Parkinson, Steve D M Brown, Terrence F Meehan, Patsy M Nishina, Stephen A Murray, Mark P Krebs, Ann-Marie Mallon, Kevin C Kent Lloyd, Christopher J Murphy, Ala Moshiri
Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts. Communications biology 2 (2019)
Elena Sügis, Jerome Dauvillier, Anna Leontjeva, Priit Adler, Valerie Hindie, Thomas Moncion, Vincent Collura, Rachel Daudin, Yann Loe-Mie, Yann Hérault, Jean-Charles Lambert, Henning Hermjakob, Tal Pupko, Jean-Christophe Rain, Ioannis Xenarios, Jaak Vilo, Michel Simonneau, Hedi Peterson
HENA, heterogeneous network-based data set for Alzheimer's disease. Scientific data 6 (1) (2019)
Yann Hérault, Jean Maurice Delabar, Elizabeth M C Fisher, Victor L J Tybulewicz, Eugene Yu, Véronique Brault
Rodent models in Down syndrome research: impact and future opportunities. Disease models & mechanisms 10 (10) (2018)
Jan Rozman, Birgit Rathkolb, Manuela A Oestereicher, Christine Schütt, Aakash Chavan Ravindranath, Stefanie Leuchtenberger, Sapna Sharma, Martin Kistler, Monja Willershäuser, Robert Brommage, Terrence F Meehan, Jeremy C Mason, Hamed Haselimashhadi, null null, Tertius Hough, Ann-Marie Mallon, Sara Wells, Luis Santos, Christopher J Lelliott, Jacqueline K White, Tania Sorg, Marie-France Champy, Lynette R Bower, Corey L Reynolds, Ann M Flenniken, Stephen A Murray, Lauryl M J Nutter, Karen L Svenson, David West, Glauco P Tocchini-Valentini, Arthur L Beaudet, Fatima Bosch, Robert B Braun, Michael S Dobbie, Xiang Gao, Yann Hérault, Ala Moshiri, Bret A Moore, Kevin C Kent Lloyd, Colin McKerlie, Hiroshi Masuya, Nobuhiko Tanaka, Paul Flicek, Helen E Parkinson, Radislav Sedlacek, Je Kyung Seong, Chi-Kuang Leo Wang, Mark Moore, Steve D Brown, Matthias H Tschöp, Wolfgang Wurst, Martin Klingenspor, Eckhard Wolf, Johannes Beckers, Fausto Machicao, Andreas Peter, Harald Staiger, Hans-Ulrich Häring, Harald Grallert, Monica Campillos, Holger Maier, Helmut Fuchs, Valerie Gailus-Durner, Thomas Werner, Martin Hrabě de Angelis
Identification of genetic elements in metabolism by high-throughput mouse phenotyping. Nature communications 9 (1) (2018)
Thu Lan Nguyen, Arnaud Duchon, Antigoni Manousopoulou, Nadège Loaëc, Benoît Villiers, Guillaume Pani, Meltem Karatas, Anna E Mechling, Laura-Adela Harsan, Emmanuelle Limanton, Jean-Pierre Bazureau, François Carreaux, Spiros D D Garbis, Laurent Meijer, Yann Hérault
Correction of cognitive deficits in mouse models of Down syndrome by a pharmacological inhibitor of DYRK1A. Disease models & mechanisms 11 (9) (2018)
Bret A Moore, Brian C Leonard, Lionel Sebbag, Sydney G Edwards, Ann Cooper, Denise M Imai, Ewan Straiton, Luis Santos, Christopher Reilly, Stephen M Griffey, Lynette Bower, David Clary, Jeremy C Mason, Michel J Roux, Hamid Meziane, Yann Hérault, null null, Colin McKerlie, Ann M Flenniken, Lauryl M J Nutter, Zorana Berberovic, Celeste Owen, Susan Newbigging, Hibret Adissu, Mohammed Eskandarian, Chih-Wei Hsu, Sowmya Kalaga, Uchechukwu Udensi, Chinwe Asomugha, Ritu Bohat, Juan J Gallegos, John R Seavitt, Jason D Heaney, Arthur L Beaudet, Mary E Dickinson, Monica J Justice, Vivek Philip, Vivek Kumar, Karen L Svenson, Robert E Braun, Sara Wells, Heather Cater, Michelle Stewart, Sharon Clementson-Mobbs, Russell Joynson, Xiang Gao, Tomohiro Suzuki, Shigeharu Wakana, Damian Smedley, J K Seong, Glauco Tocchini-Valentini, Mark Moore, Colin Fletcher, Natasha Karp, Ramiro Ramirez-Solis, Jacqueline K White, Martin Hrabě de Angelis, Wolfgang Wurst, Sara M Thomasy, Paul Flicek, Helen Parkinson, Steve D M Brown, Terrence F Meehan, Patsy M Nishina, Stephen A Murray, Mark P Krebs, Ann-Marie Mallon, Kevin C Kent Lloyd, Christopher J Murphy, Ala Moshiri
Identification of genes required for eye development by high-throughput screening of mouse knockouts. Communications biology 1 (2018)
Michael R Bowl, Michelle M Simon, Neil J Ingham, Simon Greenaway, Luis Santos, Heather Cater, Sarah Taylor, Jeremy C Mason, Natalja Kurbatova, Selina Pearson, Lynette R Bower, Dave A Clary, Hamid Meziane, Patrick Reilly, Osamu Minowa, Lois Kelsey, null null, Glauco P Tocchini-Valentini, Xiang Gao, Allan Bradley, William C Skarnes, Mark Moore, Arthur L Beaudet, Monica J Justice, John Seavitt, Mary E Dickinson, Wolfgang Wurst, Martin Hrabě de Angelis, Yann Hérault, Shigeharu Wakana, Lauryl M J Nutter, Ann M Flenniken, Colin McKerlie, Stephen A Murray, Karen L Svenson, Robert E Braun, David B West, Kevin C Kent Lloyd, David J Adams, Jacqui White, Natasha Karp, Paul Flicek, Damian Smedley, Terrence F Meehan, Helen E Parkinson, Lydia M Teboul, Sara Wells, Karen P Steel, Ann-Marie Mallon, Steve D M Brown
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction. Nature communications 8 (1) (2017)
Giovanni Iacono, Marco Benevento, Aline Dubos, Yann Hérault, Hans van Bokhoven, Nael Nadif Kasri, Hendrik G Stunnenberg
Integrated transcriptional analysis unveils the dynamics of cellular differentiation in the developing mouse hippocampus. Scientific reports 7 (1) (2017)
Thomas Arbogast, Giovanni Iacono, Claire Chevalier, Nurudeen O Afinowi, Xander Houbaert, Matthijs C van Eede, Christine Laliberte, Marie-Christine Birling, Katrin Linda, Hamid Meziane, Mohammed Selloum, Tania Sorg, Nael Nadif Kasri, David A Koolen, Henk G Stunnenberg, R Mark Henkelman, Maksym Kopanitsa, Yann Humeau, Bert B A De Vries, Yann Hérault
Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition. PLoS genetics 13 (7) (2017)
Olivia Wendling, Marie-France Champy, Solène Jaubert, Guillaume Pavlovic, Aline Dubos, Loic Lindner, Hugues Jacobs, Manuel Mark, Roy Combe, Isabelle Goncalves Da Cruz, Hervé Luche, John S Mudgett, Thomas Rosahl, Tania Sorg, Marie Malissen, Patrick T Reilly, Yann Hérault
Atp6ap2 ablation in adult mice impairs viability through multiple organ deficiencies. Scientific reports 7 (1) (2017)
Natasha A Karp, Jeremy C Mason, Arthur L Beaudet, Yoav Benjamini, Lynette Bower, Robert E Braun, Steve D M Brown, Elissa J Chesler, Mary E Dickinson, Ann M Flenniken, Helmut Fuchs, Martin Hrabě de Angelis, Xiang Gao, Shiying Guo, Simon Greenaway, Ruth Heller, Yann Hérault, Monica J Justice, Natalja Kurbatova, Christopher J Lelliott, K C Kent Lloyd, Ann-Marie Mallon, Judith E Mank, Hiroshi Masuya, Colin McKerlie, Terrence F Meehan, Richard F Mott, Stephen A Murray, Helen Parkinson, Ramiro Ramirez-Solis, Luis Santos, John R Seavitt, Damian Smedley, Tania Sorg, Anneliese O Speak, Karen P Steel, Karen L Svenson, null null, Shigeharu Wakana, David West, Sara Wells, Henrik Westerberg, Shay Yaacoby, Jacqueline K White
Prevalence of sexual dimorphism in mammalian phenotypic traits. Nature communications 8 (2017)
Terrence F Meehan, Nathalie Conte, David B West, Julius O Jacobsen, Jeremy C Mason, Jonathan Warren, Chao-Kung Chen, Ilinca Tudose, Mike Relac, Peter Matthews, Natasha Karp, Luis Santos, Tanja Fiegel, Natalie Ring, Henrik Westerberg, Simon Greenaway, Duncan Sneddon, Hugh Morgan, Gemma F Codner, Michelle E Stewart, James Brown, Neil Horner, null null, Melissa Haendel, Nicole Washington, Christopher J Mungall, Corey L Reynolds, Juan Gallegos, Valerie Gailus-Durner, Tania Sorg, Guillaume Pavlovic, Lynette R Bower, Mark Moore, Iva Morse, Xiang Gao, Glauco P Tocchini-Valentini, Yuichi Obata, Soo Young Cho, Je Kyung Seong, John Seavitt, Arthur L Beaudet, Mary E Dickinson, Yann Hérault, Wolfgang Wurst, Martin Hrabě de Angelis, Kevin C Kent Lloyd, Ann M Flenniken, Lauryl M J Nutter, Susan Newbigging, Colin McKerlie, Monica J Justice, Stephen A Murray, Karen L Svenson, Robert E Braun, Jacqueline K White, Allan Bradley, Paul Flicek, Sara Wells, William C Skarnes, David J Adams, Helen Parkinson, Ann-Marie Mallon, Steve D M Brown, Damian Smedley
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium. Nature genetics 49 (8) (2017)

Yann Hérault.css-eqlu8i{font-size:small;padding-left:4px;} (Yann Herault)

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Yann Hérault (Yann Herault)