Jonathan A Kropski
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Explore the profile of Jonathan A Kropski including associated specialties, affiliations and a list of published articles.
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111
Citations
5180
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Recent Articles
1.
Banaschewski B, Michki S, Sitaraman S, Pan R, Wang J, Stewart D, et al.
Commun Biol
. 2025 Feb;
8(1):284.
PMID: 39987372
The longitudinal cellular interactions that drive pulmonary fibrosis are not well understood. To investigate the disease underpinnings associated with fibrosis onset and progression, we generated a scRNA-seq atlas of lungs...
2.
Vannan A, Lyu R, Williams A, Negretti N, Mee E, Hirsh J, et al.
Nat Genet
. 2025 Feb;
57(3):647-658.
PMID: 39901013
Large-scale changes in the structure and cellular makeup of the distal lung are a hallmark of pulmonary fibrosis (PF), but the spatial contexts that contribute to disease pathogenesis have remained...
3.
Negretti N, Son Y, Crooke P, Plosa E, Benjamin J, Jetter C, et al.
JCI Insight
. 2025 Jan;
10(4).
PMID: 39773701
Determining how alveoli are formed and maintained is critical to understanding lung organogenesis and regeneration after injury. To study the cellular dynamics of this critical stage of lung development, we...
4.
McCall A, Gutor S, Tanjore H, Burman A, Sherrill T, Chapman M, et al.
Sci Transl Med
. 2025 Jan;
17(780):eadk8623.
PMID: 39772774
Idiopathic pulmonary fibrosis (IPF) is a progressive interstitial lung disease in which repetitive epithelial injury and incomplete alveolar repair result in accumulation of profibrotic intermediate/transitional "aberrant" epithelial cell states. The...
5.
Wang J, Michki S, Sitaraman S, Banaschewski B, Jamal R, Gokey J, et al.
JCI Insight
. 2024 Dec;
10(3).
PMID: 39699958
Hermansky-Pudlak syndrome (HPS) is a genetic disorder of endosomal protein trafficking associated with pulmonary fibrosis in specific subtypes, including HPS-1 and HPS-2. Single-mutant HPS1 and HPS2 mice display increased fibrotic...
6.
Bailin S, Ma S, Perry A, Terry J, Carr J, Nair S, et al.
J Infect Dis
. 2024 Dec;
231(2):e407-e418.
PMID: 39657693
Background: Persons with HIV (PWH) on contemporary antiretroviral therapy (ART) are at elevated risk for developing age-related cardiometabolic diseases. We hypothesized that integrative analysis of cross-tissue, multimodal data from PWH...
7.
McCall A, Singha U, Blackwell T, Gokey J, Kropski J
Am J Respir Cell Mol Biol
. 2024 Nov;
71(6):743-745.
PMID: 39601538
No abstract available.
8.
Blumhagen R, Humphries S, Peljto A, Lynch D, Cardwell J, Bang T, et al.
Ann Am Thorac Soc
. 2024 Nov;
PMID: 39591102
Rationale: Idiopathic pulmonary fibrosis (IPF) is a complex and heterogeneous disease. Given this, we reasoned that differences in genetic profiles may be associated with unique clinical and radiologic features. Computational...
9.
Alonso-Gonzalez A, Jaspez D, Lorenzo-Salazar J, Ma S, Strickland E, Mychaleckyj J, et al.
medRxiv
. 2024 Nov;
PMID: 39484282
Background: The clinical course of idiopathic pulmonary fibrosis (IPF) is highly variable and unpredictable, with multiple genetic variants influencing IPF outcomes. Notably, rare pathogenic variants in telomere-related genes are associated...
10.
Shirazi S, Negretti N, Jetter C, Sharkey A, Garg S, Kapp M, et al.
bioRxiv
. 2024 Sep;
PMID: 39253423
Lung injury in preterm infants leads to structural and functional respiratory deficits, with a risk for bronchopulmonary dysplasia (BPD) that in its most severe form is accompanied by pulmonary hypertension...