Memoona M. Shaukat

Heidelberg, BW, Germany

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 13 publications

Author Correction: Development and life cycle assessment (LCA) of super-oleophobic (under water) and super-hydrophilic (in-air) mesh membrane for oily water treatment.

Author Correction: Development and life cycle assessment (LCA) of super-oleophobic (under water) and super-hydrophilic (in-air) mesh membrane for oily water treatment.

Journal: Scientific reports

Published: November 01, 2025

Reduced gastrointestinal iron uptake in pulmonary arterial hypertension: a prospective cross-sectional study.

Reduced gastrointestinal iron uptake in pulmonary arterial hypertension: a prospective cross-sectional study.

Journal: Respiratory research

Published: September 04, 2025

Heritable pulmonary arterial hypertension: new genetic findings and environmental triggers.

Heritable pulmonary arterial hypertension: new genetic findings and environmental triggers.

Journal: Scientific reports

Published: September 03, 2025

Adaptation of ACMG/AMP Guidelines for Clinical Classification of BMPR2 Variants in Pulmonary Arterial Hypertension Resolves Variants of Unclear Pathogenicity in ClinVar.

Adaptation of ACMG/AMP Guidelines for Clinical Classification of BMPR2 Variants in Pulmonary Arterial Hypertension Resolves Variants of Unclear Pathogenicity in ClinVar.

Journal: Human mutation

Published: January 06, 2025

Adaptation of ACMG/AMP guidelines for clinical classification of BMPR2 variants in Pulmonary Arterial Hypertension resolves variants of unclear pathogenicity in ClinVar.

Adaptation of ACMG/AMP guidelines for clinical classification of BMPR2 variants in Pulmonary Arterial Hypertension resolves variants of unclear pathogenicity in ClinVar.

Journal: medRxiv : the preprint server for health sciences

Published: December 09, 2024

Pathogenic SMAD6 variants in patients with idiopathic and complex congenital heart disease associated pulmonary arterial hypertension.

Pathogenic SMAD6 variants in patients with idiopathic and complex congenital heart disease associated pulmonary arterial hypertension.

Journal: NPJ genomic medicine

Published: August 02, 2024

Genetic background of pulmonary (vascular) diseases - how much is written in the codes?

Genetic background of pulmonary (vascular) diseases - how much is written in the codes?

Journal: Current opinion in pulmonary medicine

Published: June 24, 2024

Heritable pulmonary arterial hypertension

Heritable pulmonary arterial hypertension

Journal: Innere Medizin (Heidelberg, Germany)

Published: April 24, 2024

Development and life cycle assessment (LCA) of super-oleophobic (under water) and super-hydrophilic (in-air) mesh membrane for oily water treatment.

Development and life cycle assessment (LCA) of super-oleophobic (under water) and super-hydrophilic (in-air) mesh membrane for oily water treatment.

Journal: Scientific reports

Published: April 11, 2024

Defining the clinical validity of genes reported to cause pulmonary arterial hypertension.

Defining the clinical validity of genes reported to cause pulmonary arterial hypertension.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: January 28, 2023

Gene panel diagnostics reveals new pathogenic variants in pulmonary arterial hypertension.

Gene panel diagnostics reveals new pathogenic variants in pulmonary arterial hypertension.

Journal: Respiratory research

Published: October 23, 2021

Prognostic impact of hypochromic erythrocytes in patients with pulmonary arterial hypertension.

Prognostic impact of hypochromic erythrocytes in patients with pulmonary arterial hypertension.

Journal: Respiratory research

Published: August 30, 2021

Showing 1-12 of 13

Last Updated: 09/26/2026