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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2012 1
2013 17
2014 10
2015 9
2016 9
2017 12
2018 13
2019 5
2020 6
2021 6
2022 3
2024 0

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83 results

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Page 1
A pilot study to examine association of BMI with functional class and 6 min walk distance in idiopathic and heritable PAH: Possible association with estrogen metabolism.
MacLean MR, Pandya D, Swietlik EM, Denver N, Mair K, Morrell NW, Gräf S; National Cohort Study for Idiopathic and Heritable Pulmonary Arterial Hypertension Consortium. MacLean MR, et al. Pulm Circ. 2022 Jul 1;12(3):e12139. doi: 10.1002/pul2.12139. eCollection 2022 Jul. Pulm Circ. 2022. PMID: 36186719 Free PMC article.
Different Cytokine Patterns in BMPR2-Mutation-Positive Patients and Patients With Pulmonary Arterial Hypertension Without Mutations and Their Influence on Survival.
Schwiening M, Swietlik EM, Pandya D, Burling K, Barker P, Feng OY, Treacy CM, Abreu S, Wort SJ, Pepke-Zaba J, Graf S, Marciniak SJ, Morrell NW, Soon E. Schwiening M, et al. Chest. 2022 Jun;161(6):1651-1656. doi: 10.1016/j.chest.2022.01.019. Epub 2022 Jan 19. Chest. 2022. PMID: 35063447 Free PMC article. No abstract available.
Single-cell RNA sequencing profiling of mouse endothelial cells in response to pulmonary arterial hypertension.
Rodor J, Chen SH, Scanlon JP, Monteiro JP, Caudrillier A, Sweta S, Stewart KR, Shmakova A, Dobie R, Henderson BEP, Stewart K, Hadoke PWF, Southwood M, Moore SD, Upton PD, Morrell NW, Li Z, Chan SY, Handen A, Lafyatis R, de Rooij LPMH, Henderson NC, Carmeliet P, Spiroski AM, Brittan M, Baker AH. Rodor J, et al. Cardiovasc Res. 2022 Aug 24;118(11):2519-2534. doi: 10.1093/cvr/cvab296. Cardiovasc Res. 2022. PMID: 34528097 Free PMC article.
Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH.
Zhu N, Swietlik EM, Welch CL, Pauciulo MW, Hagen JJ, Zhou X, Guo Y, Karten J, Pandya D, Tilly T, Lutz KA, Martin JM, Treacy CM, Rosenzweig EB, Krishnan U, Coleman AW, Gonzaga-Jauregui C, Lawrie A, Trembath RC, Wilkins MR; Regeneron Genetics Center; PAH Biobank Enrolling Centers’ Investigators; NIHR BioResource for Translational Research - Rare Diseases; National Cohort Study of Idiopathic and Heritable PAH; Morrell NW, Shen Y, Gräf S, Nichols WC, Chung WK. Zhu N, et al. Genome Med. 2021 May 10;13(1):80. doi: 10.1186/s13073-021-00891-1. Genome Med. 2021. PMID: 33971972 Free PMC article.
Homozygous GDF2 nonsense mutations result in a loss of circulating BMP9 and BMP10 and are associated with either PAH or an "HHT-like" syndrome in children.
Hodgson J, Ruiz-Llorente L, McDonald J, Quarrell O, Ugonna K, Bentham J, Mason R, Martin J, Moore D, Bergstrom K, Bayrak-Toydemir P, Wooderchak-Donahue W, Morrell NW, Condliffe R, Bernabeu C, Upton PD. Hodgson J, et al. Mol Genet Genomic Med. 2021 Dec;9(12):e1685. doi: 10.1002/mgg3.1685. Epub 2021 Apr 9. Mol Genet Genomic Med. 2021. PMID: 33834622 Free PMC article.
Circulating BMP9 Protects the Pulmonary Endothelium during Inflammation-induced Lung Injury in Mice.
Li W, Long L, Yang X, Tong Z, Southwood M, King R, Caruso P, Upton PD, Yang P, Bocobo GA, Nikolic I, Higuera A, Salmon RM, Jiang H, Lodge KM, Hoenderdos K, Baron RM, Yu PB, Condliffe AM, Summers C, Nourshargh S, Chilvers ER, Morrell NW. Li W, et al. Am J Respir Crit Care Med. 2021 Jun 1;203(11):1419-1430. doi: 10.1164/rccm.202005-1761OC. Am J Respir Crit Care Med. 2021. PMID: 33320799 Free PMC article.
Expression Quantitative Trait Locus Mapping in Pulmonary Arterial Hypertension.
Ulrich A, Otero-Núñez P, Wharton J, Swietlik EM, Gräf S, Morrell NW, Wang D, Lawrie A, Wilkins MR, Prokopenko I, Rhodes CJ, Consortium OBOTNBD, Consortium UPCS. Ulrich A, et al. Genes (Basel). 2020 Oct 22;11(11):1247. doi: 10.3390/genes11111247. Genes (Basel). 2020. PMID: 33105808 Free PMC article.
83 results