Julien Grynblat

Paris, France

Last Updated: 09/26/2026

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Found 29 publications

Functional and Molecular Characterization of Novel GDF2 (BMP9) and BMP10 Variants From the French PAH and HHT Cohorts.

Functional and Molecular Characterization of Novel GDF2 (BMP9) and BMP10 Variants From the French PAH and HHT Cohorts.

Journal: Circulation. Genomic and precision medicine

Published: June 09, 2026

Reply: FLNA loss-of-function variants in pulmonary hypertension: implications for genetic testing in congenital heart disease.

Reply: FLNA loss-of-function variants in pulmonary hypertension: implications for genetic testing in congenital heart disease.

Journal: The European respiratory journal

Published: April 06, 2026

ERS Congress 2025: highlights from the Pulmonary Vascular Diseases Assembly.

ERS Congress 2025: highlights from the Pulmonary Vascular Diseases Assembly.

Journal: ERJ open research

Published: March 26, 2026

SOX17 variants in pulmonary arterial hypertension and beyond: When genetics redefines the phenotype.

SOX17 variants in pulmonary arterial hypertension and beyond: When genetics redefines the phenotype.

Journal: International journal of cardiology

Published: March 17, 2026

Improved Outcomes with Early Aggressive Therapy in Pediatric Pulmonary Hypertension.

Improved Outcomes with Early Aggressive Therapy in Pediatric Pulmonary Hypertension.

Journal: The European respiratory journal

Published: February 11, 2026

Pulmonary hypertension in patients with Noonan syndrome.

Pulmonary hypertension in patients with Noonan syndrome.

Journal: The European respiratory journal

Published: August 27, 2025

Pulmonary arterial hypertension associated with toxic rapeseed oil: a continuous disease?

Pulmonary arterial hypertension associated with toxic rapeseed oil: a continuous disease?

Journal: ERJ open research

Published: August 13, 2025

Pulmonary hypertension associated with hereditary haemorrhagic telangiectasia: from genetics to clinical management.

Pulmonary hypertension associated with hereditary haemorrhagic telangiectasia: from genetics to clinical management.

Journal: The European respiratory journal

Published: July 22, 2025

Cobalamin C deficiency: a rare but treatable genetic cause of pulmonary hypertension.

Cobalamin C deficiency: a rare but treatable genetic cause of pulmonary hypertension.

Journal: Orphanet journal of rare diseases

Published: July 10, 2025

Detection and Evaluation of Drug-associated Pulmonary Arterial Hypertension.

Detection and Evaluation of Drug-associated Pulmonary Arterial Hypertension.

Journal: American journal of respiratory and critical care medicine

Published: June 12, 2025

Pulmonary veno-occlusive disease: a paradigm of diagnosis and therapeutic challenges in pulmonary hypertension.

Pulmonary veno-occlusive disease: a paradigm of diagnosis and therapeutic challenges in pulmonary hypertension.

Journal: Current opinion in pulmonary medicine

Published: June 05, 2025

Ca2+ Cycling Alteration in a Porcine Model of Right Ventricular Dysfunction.

Ca2+ Cycling Alteration in a Porcine Model of Right Ventricular Dysfunction.

Journal: Circulation. Heart failure

Published: April 18, 2025

Showing 1-12 of 29

Last Updated: 09/26/2026