Arnaud N Molin

4PUBLICATIONS
17CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Solid mechanics
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Publications (4)

|Jul 07, 2026
Abnormal position of a GNAS methylation regulatory element causes autosomal dominant pseudohypoparathyroidism type 1B (PHP1B).

|Mar 03, 2026
Non-coding genome in nail-patella syndrome: Genetic diagnosis as a guide for personalized follow-up.

Perrine Brunelle, Anne-Sophie Jourdain, Fabienne Escande

|Feb 12, 2024
Skeletal growth is enhanced by a shared role for SOX8 and SOX9 in promoting reserve chondrocyte commitment to columnar proliferation.

Arnaud N Molin, Romain Contentin, Marco Angelozzi

|Nov 02, 2022
Genotype-phenotype Description of Vitamin D-dependent Rickets 1A: CYP27B1 p.(Ala129Thr) Variant Induces a Milder Disease.

Marie-Noëlle Méaux, Jérôme Harambat, Anya Rothenbuhler

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Frequent Collaborators

1 joint publications

Marie-Noëlle Méaux

1 joint publications

Bruno Francou

1 joint publications

Agnès Linglart

1 joint publications

Justine Bacchetta