Florence Coulet

13PUBLICATIONS
95CO-AUTHORS
Respiratory diseasesEpigenetics (incl. genome methylation and epigenomics)HaematologyNanomedicineComputational physiology
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Publications (13)

|Jun 18, 2026
Reply: <i>FLNA</i> loss-of-function variants in pulmonary hypertension: implications for genetic testing in congenital heart disease.

|Jun 09, 2026
Functional and Molecular Characterization of Novel <i>GDF2 (BMP9</i>) and <i>BMP10</i> Variants From the French PAH and HHT Cohorts.

|Feb 19, 2026
Pulmonary hypertension associated with hereditary haemorrhagic telangiectasia: from genetics to clinical management.

Etienne-Marie Jutant, Julien Grynblat, Matilde Pyrrait

|Dec 11, 2025
Pulmonary hypertension in patients with Noonan syndrome.

Julien Grynblat, Mathieu Farges, Pascal Magro

|Sep 17, 2025
SOX17 in pulmonary arterial hypertension: from development to clinical phenotype.

Thomas Lacoste-Palasset, Benoit Aguado, Julien Grynblat

|Jul 10, 2025
Cobalamin C deficiency: a rare but treatable genetic cause of pulmonary hypertension.

Julien Grynblat, Florence Coulet, David Montani

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Frequent Collaborators

9 joint publications

David Montani

7 joint publications

Julien Grynblat

6 joint publications

Marc Humbert

4 joint publications

Laurent Savale