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by Rhodes, Christopher J and Batai, Ken and Bleda, Marta and Haimel, Matthias and Southgate, Laura and Germain, Marine and Pauciulo, Michael W and Hadinnapola, Charaka and Aman, Jurjan and Girerd, Barbara and Arora, Amit and Knight, Jo and Hanscombe, Ken B and Karnes, Jason H and Kaakinen, Marika and Gall, Henning and Ulrich, Anna and Harbaum, Lars and Cebola, Inês and Ferrer, Jorge and Lutz, Katie and Swietlik, Emilia M and Ahmad, Ferhaan and Amouyel, Philippe and Archer, Stephen L and Argula, Rahul and Austin, Eric D and Badesch, David and Bakshi, Sahil and Barnett, Christopher and Benza, Raymond and Bhatt, Nitin and Bogaard, Harm J and Burger, Charles D and Chakinala, Murali and Church, Colin and Coghlan, John G and Condliffe, Robin and Corris, Paul A and Danesino, Cesare and Debette, Stéphanie and Elliott, C Gregory and Elwing, Jean and Eyries, Melanie and Fortin, Terry and Franke, Andre and Frantz, Robert P and Frost, Adaani and Garcia, Joe G N and Ghio, Stefano and Ghofrani, Hossein-Ardeschir and Gibbs, J Simon R and Harley, John and He, Hua and Hill, Nicholas S and Hirsch, Russel and Houweling, Arjan C and Howard, Luke S and Ivy, Dunbar and Kiely, David G and Klinger, James and Kovacs, Gabor and Lahm, Tim and Laudes, Matthias and Machado, Rajiv D and MacKenzie Ross, Robert V and Marsolo, Keith and Martin, Lisa J and Moledina, Shahin and Montani, David and Nathan, Steven D and Newnham, Michael and Olschewski, Andrea and Olschewski, Horst and Oudiz, Ronald J and Ouwehand, Willem H and Peacock, Andrew J and Pepke-Zaba, Joanna and Rehman, Zia and Robbins, Ivan and Roden, Dan M and Rosenzweig, Erika B and Saydain, Ghulam and Scelsi, Laura and Schilz, Robert and Seeger, Werner and Shaffer, Christian M and Simms, Robert W and Simon, Marc and Sitbon, Olivier and Suntharalingam, Jay and Tang, Haiyang and Tchourbanov, Alexander Y and Thenappan, Thenappan and Torres, Fernando and Toshner, Mark R and Treacy, Carmen M and Vonk Noordegraaf, Anton and Waisfisz, Quinten and Walsworth, Anna K and ... and US PAH Biobank Consortium and UK PAH Cohort Study Consortium and UK NIHR BioResource Rare Diseases Consortium and UK NIHR Bioresource Rare Dis Conso
The Lancet Respiratory Medicine, ISSN 2213-2600, 03/2019, Volume 7, Issue 3, pp. 227 - 238
Rare genetic variants cause pulmonary arterial hypertension, but the contribution of common genetic variation to disease risk and natural history is poorly... 
SOX17 | ENDODERM FORMATION | RESPIRATORY SYSTEM | SUSCEPTIBILITY | DISEASE | ALPHA | CRITICAL CARE MEDICINE | Life Sciences
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 08/2001, Volume 345, Issue 5, pp. 325 - 334
Journal Article
Genome Medicine, ISSN 1756-994X, 07/2018, Volume 10, Issue 1, pp. 56 - 11
Journal Article
EUROPEAN RESPIRATORY JOURNAL, ISSN 0903-1936, 08/2019, Volume 54, Issue 2
Rare variants in the T-box transcription factor 4 gene (TBX4) have recently been recognised as an emerging cause of paediatric pulmonary hypertension (PH).... 
LIMB | RESPIRATORY SYSTEM | ARTERIAL-HYPERTENSION | GUIDELINES | ALVEOLAR-CAPILLARY DYSPLASIA | AMERICAN-COLLEGE | LUNG-DISEASE | CLASSIFICATION | MEDICAL GENETICS | COHORT | CHILDREN
Journal Article
American journal of respiratory cell and molecular biology, ISSN 1044-1549, 01/2019, Volume 60, Issue 1, pp. 106 - 116
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2012, Volume 7, Issue 3, p. e32468
Loss-of-function mutations in the bone morphogenetic protein receptor type 2 (BMPR2) gene have been identified in patients with heritable pulmonary arterial... 
SIGNAL-TRANSDUCTION | MULTIDISCIPLINARY SCIENCES | ARTERIAL-HYPERTENSION | II RECEPTOR | DISEASE | AIRWAY INFLAMMATION | ASTHMA | HETEROZYGOUS BMPR2-MUTANT MICE | MUTATIONS | MORPHOGENETIC PROTEIN-RECEPTOR | EXPOSURE | Blood Pressure | Immunohistochemistry | Bone Morphogenetic Protein Receptors, Type II - genetics | Enzyme-Linked Immunosorbent Assay | Bronchoalveolar Lavage | Genotype | DNA Primers - genetics | Hypersensitivity - complications | Mutation - genetics | Blotting, Western | Bone Morphogenetic Protein Receptors, Type II - metabolism | Arterioles - pathology | Inflammation - complications | Animals | Analysis of Variance | Polymerase Chain Reaction | Pyroglyphidae | Signal Transduction - physiology | Mice | Mice, Inbred BALB C | Hypertension, Pulmonary - etiology | Methacholine Chloride | Allergens | Bone morphogenetic proteins | Inflammation | B cells | Pulmonary hypertension | Heart | Pediatrics | Systolic pressure | Pathogenesis | Arterioles | Cardiovascular disease | Remodeling | Respiratory tract | Morphogenesis | Genotype & phenotype | Epidermal growth factor | Rodents | Methacholine | Blood pressure | Heart diseases | Deoxyribonucleic acid--DNA | Hypertension | Congenital diseases | Bone morphogenetic protein receptor type II | Cytokines | Catheterization | Dendritic cells | Pulmonary arteries | Hypersensitivity | House dust | Exposure | Wall thickness | Allergies | Children & youth | Asthma | Studies | Signaling | Hospitals | Ligands | Ventricle | Mutation | Deoxyribonucleic acid | DNA
Journal Article
Nature Genetics, ISSN 1061-4036, 09/2000, Volume 26, Issue 1, pp. 81 - 84
Journal Article
GENOME MEDICINE, ISSN 1756-994X, 11/2019, Volume 11, Issue 1, pp. 69 - 16
Background Group 1 pulmonary arterial hypertension (PAH) is a rare disease with high mortality despite recent therapeutic advances. Pathogenic remodeling of... 
SURVIVAL | TISSUE KALLIKREIN | BMPR2 | RARE | RECEPTOR | PATHOGENICITY | Exome sequencing | GENETICS & HEREDITY | FRAMEWORK | Genetics | Pulmonary arterial hypertension | MUTATIONS | Case-control association testing | ASSOCIATION
Journal Article
Movement Disorders, ISSN 0885-3185, 02/2015, Volume 30, Issue 2, pp. 278 - 283
Journal Article
Circulation. Genomic and precision medicine, ISSN 2574-8300, 04/2018, Volume 11, Issue 4, pp. e001887 - e001887
Journal Article
Journal Article