Gérard Tachdjian - Lab Cytogenet, Univ Paris Saclay

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Generation of Human Induced Pluripotent Stem Cell Lines from Five Patients with Myofibrillar Myopathy Carrying Different Heterozygous Mutations in the DES Gene

Pierre Joanne,Yeranuhi Hovhannisyan,Alexandre Simon,Gaelle Revet,Romain Diot, Gabriel Friob, Denisa Calin,Zhenlin Li,Anthony Behin,Karim Wahbi,Gerard Tachdjian,Onnik Agbulut

STEM CELL RESEARCH (2024)

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KDM1A Genotyping and Expression in 146 Sporadic Somatotroph Pituitary Adenomas

Fanny Chasseloup,Daniela Regazzo,Lucie Tosca,Alexis Proust,Emmanuelle Kuhn,Mirella Hage,Christel Jublanc,Karima Mokhtari, Mattia Dalle Nogare, Serena Avallone,Filippo Ceccato,Gerard Tachdjian,Sylvie Salenave,Jacques Young,Stephan Gaillard,Fabrice Parker,Anne-Laure Boch,Philippe Chanson,Jerome Bouligand,Gianluca Occhi,Peter Kamenicky

EUROPEAN JOURNAL OF ENDOCRINOLOGYno. 2 (2024): 173-181

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Improved Functionality of Hepatic Spheroids Cultured in Acoustic Levitation Compared to Existing 2D and 3D Models

Lucile Rabiet,Nathan Jeger-Madiot, Duvan Rojas Garcia,Lucie Tosca,Gerard Tachdjian,Sabrina Kellouche,Remy Agniel,Jerome Larghero,Jean-Luc Aider,Lousineh Arakelian

SCIENTIFIC REPORTSno. 1 (2024)

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Critical Contribution of Mitochondria in the Development of Cardiomyopathy Linked to Desmin Mutation

STEM CELL RESEARCH & THERAPYno. 1 (2024)

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An Early Onset Benign Myopathy with Glycogen Storage Caused by a De Novo 1.4 Mb-deletion of Chromosome 14

Gianmarco Severa,Alessandra Pennisi,Christine Barnerias,Chiara Fiorillo,Marcello Scala,Valentina Taglietti, Andreea Iuliana Cojocaru,Dima Jouni,Lucie Tosca,Gerard Tachdjian,Isabelle Desguerre,Francois-Jerome Authier,Robert-Yves Carlier,Corinne Metay,Camille Verebi,Edoardo Malfatti

Neuromuscular Disordersno. 10 (2023): 817-821

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Lysine Demethylase KDM1A and Ectopic Expression of GIP-receptor in Somatotropinomas of Patients with Paradoxical Response to Oral Glucose

Fanny Chasseloup,Lucie Tosca,Daniela Regazzo,Alexis Proust,Mirella Hage,Emmanuelle Kuhn,Christel Jublanc, Karima Mokhtari,Sylvie Salenave,Stephan Gaillard,Fabrice Parker,Anne-Laure Boch,Gerard Tachdjian,Philippe Chanson,Jerome Bouligand,Gianluca Occhi,Peter Kamenicky

Endocrine Abstracts (2023)

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P342 an Early Onset Benign Myopathy with Glycogen Storage Caused by a De Novo 1.3 Microdeletion of Chromosome 14

G. Severa,C. Fiorillo,M. Scala,V. Taglietti,A. Cojocaru,G. Tachdjian,D. Jouni,L. Tosca,F. Authier,R. Carlier,C. Verebi,C. Metay,E. Malfatti

Neuromuscular Disorders (2023): S180-S181

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OR17-05 Lysine Demethylase KDM1A and Ectopic Expression of GIP-Receptor in Somatotropinomas of Patients with Paradoxical Response to Oral Glucose

Fanny Chasseloup,Lucie Tosca,Daniela Regazzo,Alexis Proust,Mirella Hage,Emmanuelle Kuhn,Christel Jublanc, Karima Mokhtari,Sylvie Salenave,Stéphan Gaillard,Fabrice Parker,Anne‐Laure Boch,Gérard Tachdjian,Philippe Chanson,Jérôme Bouligand,Gianluca Occhi,Peter Kamenický

Journal of the Endocrine Societyno. Supplement_1 (2023)

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OR04-4 Loss of KDM1A in Bilateral Macronodular Adrenal Hyperplasia with GIP-Dependent Cushing's Syndrome and in Acromegaly with Paradoxical GH Response to Oral Glucose

Journal of the Endocrine Societyno. Supplement_1 (2022)

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