Xavier Jeunemaitre

ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 9

Top Venues

Nature communications

PLoS genetics

Nature genetics

European journal of human genetics : EJHG

UNIVERSITE DE PARIS

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

Affiliation History

UNIVERSITE DE PARIS Jul 01 2019

France

DEAN :: FACULTY OF HEALTH

Publications

Helene Quelquejay, Rida Al-Rifai, Michele Silvestro, Marie Vandestienne, Irmine Loisel-Ferreira, Tristan Mirault, Henrion Daniel, Xiaodan Zhong, Icia Santos-Zas, Guillaume Goudot, Paul Alayrac, Estelle Robidel, Gwennhael Autret, Daniel Balvay, Soraya Taleb, Alain Tedgui, Chantal M Boulanger, Alma Zernecke, Antoine-Emmanuel Saliba, Juliette Hadchouel, Bhama Ramkhelawon, Clément Cochain, Sonia Bergaya, Xavier Jeunemaitre, Hafid Ait Oufella
L-Wnk1 Deletion in Smooth Muscle Cells Causes Aortitis and Inflammatory Shift. Circulation research (2024)
Edith Le Floch, Teresa Cosentino, Casper K Larsen, Felix Beuschlein, Martin Reincke, Laurence Amar, Gian-Paolo Rossi, Kelly De Sousa, Stéphanie Baron, Sophie Chantalat, Benjamin Saintpierre, Livia Lenzini, Arthur Frouin, Isabelle Giscos-Douriez, Matthis Ferey, Alaa B Abdellatif, Tchao Meatchi, Jean-Philippe Empana, Xavier Jouven, Christian Gieger, Melanie Waldenberger, Annette Peters, Daniele Cusi, Mirna Andelic, Pierre Meneton, Mathilde Touvier, Mélanie Deschasaux, Nathalie Druesne-Pecollo, Sheerazed Boulkroun, Fabio L Fernandes-Rosa, Jean François Deleuze, Xavier Jeunemaitre, Maria-Christina Zennaro
Identification of risk loci for primary aldosteronism in genome-wide association studies. Nature communications 13 (1) (2022)
Anne Legrand, Charline Guery, Julie Faugeroux, Erika Fontaine, Carole Beugnon, Amélie Gianfermi, Irmine Loisel-Ferreira, Marie-Christine Verpont, Salma Adham, Tristan Mirault, Juliette Hadchouel, Xavier Jeunemaitre
Comparative therapeutic strategies for preventing aortic rupture in a mouse model of vascular Ehlers-Danlos syndrome. PLoS genetics 18 (3) (2022)
Adrien Georges, Min-Lee Yang, Takiy-Eddine Berrandou, Mark K Bakker, Ozan Dikilitas, Soto Romuald Kiando, Lijiang Ma, Benjamin A Satterfield, Sebanti Sengupta, Mengyao Yu, Jean François Deleuze, Delia Dupré, Kristina L Hunker, Sergiy Kyryachenko, Lu Liu, Ines Sayoud-Sadeg, Laurence Amar, Chad M Brummett, Dawn M Coleman, Valentina d'Escamard, Peter W de Leeuw, Natalia Fendrikova-Mahlay, Daniella Kadian-Dodov, Jun Z Li, Aurélien Lorthioir, Marco Pappaccogli, Aleksander Prejbisz, Witold Smigielski, James C Stanley, Matthew Zawistowski, Xiang Zhou, Sebastian Zöllner, null null, null null, null null, Phillippe Amouyel, Marc L De Buyzere, Stephanie Debette, Piotr Dobrowolski, Wojciech Drygas, Heather L Gornik, Jeffrey W Olin, Jerzy Piwonski, Ernst R Rietzschel, Ynte M Ruigrok, Miikka Vikkula, Ewa Warchol Celinska, Andrzej Januszewicz, Iftikhar J Kullo, Michel Azizi, null null, Xavier Jeunemaitre, Alexandre Persu, Jason C Kovacic, Santhi K Ganesh, Nabila Bouatia-Naji
Author Correction: Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases. Nature communications 13 (1) (2022)
Adrien Georges, Min-Lee Yang, Takiy-Eddine Berrandou, Mark K Bakker, Ozan Dikilitas, Soto Romuald Kiando, Lijiang Ma, Benjamin A Satterfield, Sebanti Sengupta, Mengyao Yu, Jean François Deleuze, Delia Dupré, Kristina L Hunker, Sergiy Kyryachenko, Lu Liu, Ines Sayoud-Sadeg, Laurence Amar, Chad M Brummett, Dawn M Coleman, Valentina d'Escamard, Peter W de Leeuw, Natalia Fendrikova-Mahlay, Daniella Kadian-Dodov, Jun Z Li, Aurélien Lorthioir, Marco Pappaccogli, Aleksander Prejbisz, Witold Smigielski, James C Stanley, Matthew Zawistowski, Xiang Zhou, Sebastian Zöllner, null null, null null, null null, Phillippe Amouyel, Marc L De Buyzere, Stephanie Debette, Piotr Dobrowolski, Wojciech Drygas, Heather L Gornik, Jeffrey W Olin, Jerzy Piwonski, Ernst R Rietzschel, Ynte M Ruigrok, Miikka Vikkula, Ewa Warchol Celinska, Andrzej Januszewicz, Iftikhar J Kullo, Michel Azizi, Xavier Jeunemaitre, Alexandre Persu, Jason C Kovacic, Santhi K Ganesh, Nabila Bouatia-Naji
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases. Nature communications 12 (1) (2021)
Ilse Luyckx, Ajay A Kumar, Edwin Reyniers, Emily Dekeyser, Kathleen Vanderstraeten, Geert Vandeweyer, Florian Wünnemann, Christoph Preuss, Jean-Michaël Mazzella, Guillaume Goudot, Emmanuel Messas, Juliette Albuisson, Xavier Jeunemaitre, Per Eriksson, Salah A Mohamed, Marlies Kempers, Simone Salemink, Anthonie L Duijnhouwer, Gregor U Andelfinger, Harry C Dietz, Aline Verstraeten, Lut Van Laer, Bart L Loeys, null null
Copy number variation analysis in bicuspid aortic valve-related aortopathy identifies TBX20 as a contributing gene. European journal of human genetics : EJHG 27 (7) (2019)
Martina Tetti, Silvia Monticone, Jacopo Burrello, Patrizia Matarazzo, Franco Veglio, Barbara Pasini, Xavier Jeunemaitre, Paolo Mulatero
Liddle Syndrome: Review of the Literature and Description of a New Case. International journal of molecular sciences 19 (3) (2018)
Fabio L Fernandes-Rosa, Georgios Daniil, Ian J Orozco, Corinna Göppner, Rami El Zein, Vandana Jain, Sheerazed Boulkroun, Xavier Jeunemaitre, Laurence Amar, Hervé Lefebvre, Thomas Schwarzmayr, Tim M Strom, Thomas J Jentsch, Maria-Christina Zennaro
A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism. Nature genetics 50 (3) (2018)
Soto Romuald Kiando, Nathan R Tucker, Luis-Jaime Castro-Vega, Alexander Katz, Valentina D'Escamard, Cyrielle Tréard, Daniel Fraher, Juliette Albuisson, Daniella Kadian-Dodov, Zi Ye, Erin Austin, Min-Lee Yang, Kristina Hunker, Cristina Barlassina, Daniele Cusi, Pilar Galan, Jean-Philippe Empana, Xavier Jouven, Anne-Paule Gimenez-Roqueplo, Patrick Bruneval, Esther Soo Hyun Kim, Jeffrey W Olin, Heather L Gornik, Michel Azizi, Pierre-François Plouin, Patrick T Ellinor, Iftikhar J Kullo, David J Milan, Santhi K Ganesh, Pierre Boutouyrie, Jason C Kovacic, Xavier Jeunemaitre, Nabila Bouatia-Naji
PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance. PLoS genetics 12 (10) (2016)
Christian Dina, Nabila Bouatia-Naji, Nathan Tucker, Francesca N Delling, Katelynn Toomer, Ronen Durst, Maelle Perrocheau, Leticia Fernandez-Friera, Jorge Solis, null null, Thierry Le Tourneau, Ming-Huei Chen, Vincent Probst, Yohan Bosse, Philippe Pibarot, Diana Zelenika, Mark Lathrop, Serge Hercberg, Ronan Roussel, Emelia J Benjamin, Fabrice Bonnet, Su Hao Lo, Elena Dolmatova, Floriane Simonet, Simon Lecointe, Florence Kyndt, Richard Redon, Hervé Le Marec, Philippe Froguel, Patrick T Ellinor, Ramachandran S Vasan, Patrick Bruneval, Roger R Markwald, Russell A Norris, David J Milan, Susan A Slaugenhaupt, Robert A Levine, Jean-Jacques Schott, Albert A Hagege, null null, Xavier Jeunemaitre, null null
Genetic association analyses highlight biological pathways underlying mitral valve prolapse. Nature genetics 47 (10) (2015)

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Publication Activity (10 Years)

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Xavier Jeunemaitre