Karine Aouchiche

5PUBLICATIONS
14CO-AUTHORS
NeonatologyFamily careCardiology (incl. cardiovascular diseases)Gene expression (incl. microarray and other genome-wide approaches)Nanotoxicology, health and safety
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Publications (5)

|Sep 24, 2026
Genetic landscape of a neonatal hypogonadotropic hypogonadism series: Novel variants and phenotypic spectrum.

|Aug 19, 2025
Sucessful Transition in Rare Endocrine Diseases: Patient Experiences in a French Reference Centre.

Karine Aouchiche, Thierry Brue, Emeline Marquant

|May 06, 2025
Cascade screening in familial hypercholesterolaemia is associated with earlier statin initiation and fewer cardiovascular events than opportunistic screening.

Florian Mourre, Roch Giorgi, Lauranne Cattieuw

|Feb 12, 2025
Phenotype and genotype of 23 patients with hypopituitarism and pathogenic GLI2 variants.

Karine Aouchiche, Camille Charmensat, Pertuit Morgane

|Dec 16, 2024
CSNK2B Mutation: A Rare Cause of IGHD.

Karine Aouchiche, Pauline Romanet, Anne Barlier

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Frequent Collaborators

2 joint publications

Anne Barlier

2 joint publications

Thierry Brue

1 joint publications

Aude Brac de la Perriere

1 joint publications

Frederic Castinetti