Pascale Fanen

Prof. Dr. Pascale Fanen is a senior academic and researcher specializing in genetics and respiratory diseases, with a focus on rare monogenic disorders and surfactant-related lung conditions. Her collaborative research spans molecular pharmacology, pediatric pulmonology, and genetic mechanisms of lung disease.

Her research interests include ABC transporters, surfactant protein disorders, idiopathic pulmonary fibrosis, and genetic variants in lung carcinogenesis. She investigates how monogenic mutations contribute to isolated and systemic respiratory phenotypes, particularly in pediatric and rare disease contexts.

The recent publications highlight a strong trend in identifying genetic underpinnings of rare lung diseases, integrating molecular biology with clinical phenotyping. Her work frequently involves international collaboration and contributes to the understanding of disease mechanisms in Cystic Fibrosis, interstitial lung disease, and hereditary cancer risk.

While no specific awards are listed in the provided text, her publication record in high-impact journals such as Biochemical Pharmacology and European Respiratory Journal reflects significant scientific contributions. She actively collaborates with laboratory heads and clinical researchers, suggesting a leadership role in research teams focused on genetic lung disorders.

Pascale Fanen advises or mentors students in genetics and respiratory medicine, though specific names are not provided. She is involved in multi-center research networks such as the OrphaLung network, indicating active participation in collaborative grants and rare disease research initiatives. Her work likely involves funding from national or European rare disease research programs.

She is affiliated with research teams investigating monogenic respiratory diseases, possibly within a university medical or life sciences faculty. Her collaborations suggest integration in labs focused on molecular genetics, pediatric pulmonology, and translational respiratory research.