| human | Q5 |
| P227 | GND ID | 1228352437 |
| P269 | IdRef ID | 203008731 |
| P496 | ORCID iD | 0000-0003-2571-7932 |
| P214 | VIAF ID | 95150565571806250635 |
| P69 | educated at | Sorbonne University | Q41497113 |
| P108 | employer | Assistance Publique – Hôpitaux de Paris | Q2867205 |
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q37219463 | A novel channelopathy in pulmonary arterial hypertension |
| Q33968765 | Absence of influence of gender and BMPR2 mutation type on clinical phenotypes of pulmonary arterial hypertension. |
| Q46262263 | Angiotensin-1-converting enzyme (ACE) plasma concentration is influenced by multiple ACE-linked quantitative trait nucleotides |
| Q57149089 | BMPR2 gene rearrangements account for a significant proportion of mutations in familial and idiopathic pulmonary arterial hypertension |
| Q39218460 | BMPR2 mutation status influences bronchial vascular changes in pulmonary arterial hypertension. |
| Q31038854 | BMPR2 mutations and survival in pulmonary arterial hypertension: an individual participant data meta-analysis |
| Q55070015 | Characteristics of pulmonary arterial hypertension in affected carriers of a mutation located in the cytoplasmic tail of bone morphogenetic protein receptor type 2. |
| Q44096475 | Clinical outcomes of pulmonary arterial hypertension in carriers of BMPR2 mutation. |
| Q43199840 | Clinical outcomes of pulmonary arterial hypertension in patients carrying an ACVRL1 (ALK1) mutation |
| Q39021300 | Clinical phenotypes and outcomes of heritable and sporadic pulmonary veno-occlusive disease: a population-based study. |
| Q56893651 | Detection of putative functional angiotensinogen (AGT) gene variants controlling plasma AGT levels by combined segregation-linkage analysis |
| Q44360290 | EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension. |
| Q92931394 | Familial pulmonary arterial hypertension by KDR heterozygous loss of function |
| Q48275337 | Genetic counselling in a national referral centre for pulmonary hypertension. |
| Q57398334 | Genetic determinants of diastolic and pulse pressure map to different loci in Lyon hypertensive rats |
| Q57605580 | Genetic determinants of risk and survival in pulmonary arterial hypertension |
| Q61810186 | Genetics and genomics of pulmonary arterial hypertension |
| Q37698113 | Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension |
| Q60363751 | Identification of novel rare sequence variation underlying heritable pulmonary arterial hypertension |
| Q52590989 | Identification of rare sequence variation underlying heritable pulmonary arterial hypertension. |
| Q57818787 | Loss-of-Function ABCC8 Mutations in Pulmonary Arterial Hypertension |
| Q51702702 | Mechanisms of exertional dyspnoea in pulmonary veno-occlusive disease with EIF2AK4 mutations. |
| Q91343649 | Mendelian randomisation analysis of red cell distribution width in pulmonary arterial hypertension |
| Q52997994 | Mutations of the TGF-beta type II receptor BMPR2 in pulmonary arterial hypertension. |
| Q40351526 | Occupational exposure to organic solvents: a risk factor for pulmonary veno-occlusive disease |
| Q89807935 | Phenotype and outcome of PAH patients carrying a TBX4 mutation |
| Q47253821 | Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension |
| Q61818948 | Pulmonary Arterial Hypertension in a Patient With Cowden Syndrome and Anorexigen Exposure |
| Q44805780 | Pulmonary arterial hypertension in familial hemiplegic migraine with ATP1A2 channelopathy |
| Q51472493 | Pulmonary hypertension in patients with neurofibromatosis type I. |
| Q47434868 | Pulmonary vascular remodeling patterns and expression of general control nonderepressible 2 (GCN2) in pulmonary veno-occlusive disease. |
| Q55982322 | Pulmonary veno-occlusive disease |
| Q60017484 | Resident PW1 + Progenitor Cells Participate in Vascular Remodeling During Pulmonary Arterial Hypertension |
| Q104679618 | Screening for pulmonary arterial hypertension in adults carrying a BMPR2 mutation |
| Q54469933 | Small platelet microparticle levels are increased in pulmonary arterial hypertension. |
| Q90711882 | Widening the landscape of heritable pulmonary hypertension mutations in paediatric and adult cases |
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