Anne-Sophie Lèbre
5PUBLICATIONS
101CO-AUTHORS
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Publications (5)
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|Mar 30, 2026
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.Elsa Leitão, Amandine Santini, Benjamin Cogne
|Jun 16, 2025
Nephrogenomics, precision medicine and the role of genetic testing in adult kidney disease management.Ilias Bensouna, Alice Doreille, Marine Dancer
|Feb 15, 2022
Clinical Utility of a Unique Genome-Wide DNA Methylation Signature for KMT2A-Related Syndrome.Aidin Foroutan, Sadegheh Haghshenas, Pratibha Bhai
|May 28, 2020
Clinical Genetics of Prolidase Deficiency: An Updated Review.Marta Spodenkiewicz, Michel Spodenkiewicz, Maureen Cleary
|Jan 26, 2020
Prolidase deficiency: a new genetic cause of combined pulmonary fibrosis and emphysema syndrome in the adult.Vincent Cottin, Mouhamad Nasser, Julie Traclet
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Frequent Collaborators
1 joint publications
Vincent Cottin
1 joint publications
Mouhamad Nasser
1 joint publications
Aidin Foroutan
1 joint publications
Sadegheh Haghshenas
1 joint publications
Jennifer Kerkhof
1 joint publications
Marcello Niceta
1 joint publications
Evelina Miele
1 joint publications
Giuseppe Merla
1 joint publications
Klaus Dieterich
1 joint publications
Elise Schaefer
