April 11, 2018 article Open access Identification of rare sequence variation underlying heritable pulmonary arterial hypertension Nature Communications DOI: 10.1038/s41467-018-03672-4 Full text (OA) OpenAlex Authors 0 Author list not loaded yet. Cited by 7 stored of 397 Search Sort Most cited Newest Oldest Patent citations Title Any typearticle review book-chapter conference-paper preprint dissertation book dataset other Any fieldAgricultural and Biological Sciences Arts and Humanities Biochemistry, Genetics and Molecular Biology Business, Management and Accounting Chemical Engineering Chemistry Computer Science Decision Sciences Dentistry Earth and Planetary Sciences Economics, Econometrics and Finance Energy Engineering Environmental Science Health Professions Immunology and Microbiology Materials Science Mathematics Medicine Neuroscience Nursing Pharmacology, Toxicology and Pharmaceutics Physics and Astronomy Psychology Social Sciences Veterinary Open access Expanding the phenotypic spectrum of MECOM -associated syndrome: rare variants are associated with syndromic pulmonary arterial hypertension 2026 Journal of Medical Genetics article Medicine Pulmonary Hypertension Research and Treatments 1 citations Pulmonary hypertension in adults with congenital heart defects (ACHDs)—in light of the 2022 ESC PAH guidelines—part I: definition, epidemiology, classification, diagnostics, genetics, risk stratification and follow-up, gender aspects 2024 Cardiovascular Diagnosis and Therapy article Medicine Pulmonary Hypertension Research and Treatments Open access 3 citations Sex-biased TGFβ signalling in pulmonary arterial hypertension 2023 Cardiovascular Research article Medicine Pulmonary Hypertension Research and Treatments Open access 27 citations Crystal structures of BMPRII extracellular domain in binary and ternary receptor complexes with BMP10 2022 Nature Communications article Biochemistry, Genetics and Molecular Biology TGF-β signaling in diseases Open access 23 citations Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot 2021 Genetics in Medicine article Biochemistry, Genetics and Molecular Biology Congenital heart defects research Open access 18 citations Endothelial Dysfunction in Pulmonary Hypertension: Cause or Consequence? 2021 Biomedicines article Medicine Pulmonary Hypertension Research and Treatments Open access 148 citations Bone morphogenetic protein receptors: Structure, function and targeting by selective small molecule kinase inhibitors 2020 Bone article Biochemistry, Genetics and Molecular Biology TGF-β signaling in diseases Open access cited by 13 patents 118 citations 7 results References 0