Nicolas Lévy

发表

A new tool CovReport generates easy-to-understand sequencing coverage summary for diagnostic reports

Svetlana Gorokhova, Mark Gorokhov, Mathieu Cerino, 2020, Scientific Reports.

Average Worn Profile of Tires in Europe

Nicolas Lévy, Frédéric Biesse, Jérôme Mahé, 2014 .

Deciphering the complexity of the 4q and 10q subtelomeres by molecular combing in healthy individuals and patients with facioscapulohumeral dystrophy

Albert David, Jon Andoni Urtizberea, Bruno Eymard, 2019, Journal of Medical Genetics.

UMD‐Predictor: A High‐Throughput Sequencing Compliant System for Pathogenicity Prediction of any Human cDNA Substitution

Christophe Béroud, Arnaud Blanchard, Nicolas Lévy, 2016, Human mutation.

UMD‐DYSF, a novel locus specific database for the compilation and interactive analysis of mutations in the dysferlin gene

Nilah Monnier, Pierre Cau, Nicolas Lévy, 2012, Human mutation.

Combined treatment with statins and aminobisphosphonates extends longevity in a mouse model of human premature aging

Ignacio Varela, Sandrine Pereira, Pierre Cau, 2008, Nature Medicine.

Molecular bases of progeroid syndromes.

Pierre Cau, Nicolas Lévy, N. Lévy, 2006, Human molecular genetics.

SRPX2 mutations in disorders of language cortex and cognition.

Marie-Noëlle Metz-Lutz, Edouard Hirsch, Sandrine Pereira, 2006, Human molecular genetics.

Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspective.

Pierre Cau, Nicolas Lévy, N. Lévy, 2014, Seminars in cell & developmental biology.

Exome sequencing reveals a de novo POLD1 mutation causing phenotypic variability in mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome (MDPL).

Christophe Béroud, Nicolas Lévy, Richard Caswell, 2017, Metabolism: clinical and experimental.