Marie Legendre

基本信息

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职业迁徙

个人简介

Marie does research in Genetics, Cell Biology, Primary Ciliary Dyskinesia and Endocrinology.

研究兴趣

论文共 544 篇作者统计合作学者相似作者

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Bi-allelic LAMP3 Variants in Childhood Interstitial Lung Disease: a Surfactant-Related Disease

Camille Louvrier, Tifenn Desroziers, Yohan Soreze, Martha Delgado Rodriguez,Lucie Thomas, Valérie Nau, Florence Dastot-Le Moal,Jonathan A Bernstein,F Sessions Cole,Markus Damme, Anthony Fischer,Matthias Griese, Daniel Hinds, Laura Keehan,Carlos Milla, Hadhud Mohammad,Jonathan Rips,Jennifer A Wambach, Daniel J Wegner,Serge Amselem,Marie Legendre,Irina Giurgea,Sonia Athina Karabina,Oded Breuer, Aurore Coulomb l'Herminé,Nadia Nathan

EBioMedicine (2025): 105626-105626

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Efficacy and Safety of CFTR Modulators in Patients with Interstitial Lung Disease Caused by ABCA3 Transporter Deficiency

Mathilde Le Brun,Nadia Nathan,Camille Louvrier,Marie Legendre, Severine Feuillet,Justine Frija-Masson, Mwetty Onanga,Lise Morer,Marie-Pierre Debray,Isabelle Fajac,Pierre-Régis Burgel,Sylvain Marchand-Adam,Bruno Crestani,Raphaël Borie

ERJ open research（2025）

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Interleukin-34 Orchestrates Bone Formation Through Its Binding to Bone Morphogenic Proteins

Javier Muñoz-Garcia, Jorge W Vargas-Franco,Kristina Schiavone, Marcus T Keatinge, Robin Young,Jérôme Amiaud, Laurie Fradet,Jean-François Jégou,Hideo Yagita,Claudine Blin-Wakkach,Abdelilah Wakkach,Denis Cochonneau, Emilie Ollivier, Martine Pugière,Corinne Henriquet,Marie Legendre,Irina Giurgea,Serge Amselem, Marie-Françoise Heymann, Stéphane Télétchéa,Frédéric Lézot,Dominique Heymann

Theranosticsno. 7 (2025): 3185-3202

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Childhood Interstitial Lung Disease Survivors in Adulthood: a European Collaborative Study

Effrosyni D Manali,Matthias Griese,Nadia Nathan,Yurdagül Uzunhan,Raphael Borie,Katarzyna Michel,Nicolaus Schwerk,Justyna Fijolek,Elżbieta Radzikowska,Felix Chua,Rishi Pabary,Nesrin Mogulkoc,Cormac McCarthy,Maria Kallieri, Andriana I Papaioannou,Nural Kiper,Martina Koziar Vasakova,Ladislav Lacina,Maria Molina-Molina,Alba Torrent-Vernetta,Theofanis Tsiligiannis,Bulent Karadag,Maria Kokosi,Elisabetta A Renzoni,Coline H M van Moorsel,Ilaria Campo,Elisabeth Bendstrup,Thomas Skovhus Prior,Antje Prasse,Francesco Bonella,Vincent Cottin,Rémi Diesler,Antoine Froidure,Lykourgos Kolilekas,Lampros Fotis, Konstantinos Douros, Athanasios G Kaditis,Florence Jeny,Simon Chauveau,Hilario Nunes, Azrine Dahbia, Francesca Mariani,Joanne J van der Vis,Karlijn Groen,Ela Erdem Eralp,Yasemin Gokdemir,Derya Kocakaya,Sehnaz Olgun Yildizeli,Ebru Yalçın,Nagehan Emiralioğlu,Halime Nayir Buyuksahin, Helen O'Brien,Oguz Karcıoglu,Demet Can, Alper Ezircan,Gokcen Kartal Ozturk, Nesrin Ocal,Hasan Yuksel,Sedef Narin Tongal, Martina Safrankova,Katerina Kourtesi,Camille Louvrier,Caroline Kannengiesser,Aurelie Fabre,Marie Legendre,Bruno Crestani,Petr Pohunek,Andrew Bush,Spyros A Papiris

The European respiratory journalno. 2 (2025)

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High Risk of Lung Cancer in Surfactant-Related Gene Variant Carriers

European Respiratory Journalno. 5 (2024): 2301809-2301809

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TUBB4Bvariants Specifically Impact Ciliary Function, Causing a Ciliopathic Spectrum

Isabelle Perrault,Mechaussier Sabrina,Dodd Daniel,Yeyati Patricia,McPhie Fraser,Shoemark Amelia,Zariwala Maimoona,Marie Legendre,Lucas Fares Taie,Josseline Kaplan,Descartes Maria,Jabs Ethylin,Jean-Francois Papon,Laurent Pasquier,Marlene Murris,Heymut Omran,Amjad Horani,Jean-Michel Rozet,Pleasantine Mill

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 15-15

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Surfactant Protein B Deficiency: the RespiRare Cohort

Manon Fleury,Celine Delestrain,Lea Roditis,Caroline Perisson,Marie-Catherine Renoux,Caroline Thumerelle,Ralph Epaud,Camille Fletcher, Nouha Jedidi,Aurore Coulomb L'Hermine,Harriet Corvol,Hubert Ducou le Pointe,Pascale Fanen,Chiara Sileo,Camille Louvrier,Alix de Becdelievre,Marie Legendre,Nadia Nathan

THORAX (2024)

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Children’s ILDs Survivors in Adulthood: a European Study

Effrosyni D. Manali,Matthias Griese,Nadia Nathan,Yurdagul Uzunhan,Raphael Borie,Katarzyna Michel, Nikolaus Schwerk,Justyna Fijolek,Elzbieta Radzikowska,Felix Chua,Rishi Pabary,Nesrin Mogulkoc,Cormac Mccarthy,Maria Kallieri,Andriana Papaioannou,Nural Kiper,Martina Koziar Vasakova,Ladislav Lacina,Maria Molina-Molina,Alba Torrent-Vernetta,Theofanis Tsiligiannis,Bulent Karadag,Maria Kokosi, Elisabetta A. Renzoni,Coline Hm Van Moorsel,Ilaria Campo,Elisabeth Bendstrup,Thomas Skovhus Prior,Antje Prasse,Francesco Bonella,Vincent Cottin,Remi Diesler,Antoine Froidure,Lykourgos Kolilekas,Lampros Fotis,Konstantinos Douros, Athanasios G. Kaditis,Florence Jeny,Simon Chauveau,Hilario Nunes, Azrine Dahbia, Francesca Mariani,Joanne van der Vis,Karlijn Groen,Ela Erdem Eralp,Yasemin Gokdemir,Derya Kocakaya,Sehnaz Olgun Yildizeli,Olgun Yildizeli,Ebru Yalcin,Nagehan Emiralioglu,Halime Nayir Buyuksahin, Helen O'Brien,Oguz Karcioglu,Demet Can, Alper Ezircan,Gokcen Kartal Ozturk,Kartal Ozturk,Nesrin Ocal,Hasan Yuksel,Narin Tongal, Martina Safrankova,Katerina Kourtesi,Camille Louvrier,Caroline Kannengiesser,Aurelie Fabre,Marie Legendre,Bruno Crestani,Petr Pohunek,Andrew Bush,Spyros Papiris

EUROPEAN RESPIRATORY JOURNAL (2024)

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Mutation Hypomorphe De SFTPB Associée À Des Fibroses Pulmonaires Viables À L’âge Adulte

T. Desroziers,G. Prévot,A. Coulomb,V. Nau,F. Dastot-Le Moal,P. Duquesnoy, M. Héry,A. Le Borgne,S. Amselem,M. Legendre,N. Nathan

Revue des Maladies Respiratoires Actualités（2024）

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Molecular Geneticist

论文共 544 篇作者统计合作学者相似作者