Cheryl R Markin
Overview
Explore the profile of Cheryl R Markin including associated specialties, affiliations and a list of published articles.
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Articles
8
Citations
619
Followers
0
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Recent Articles
1.
Salisbury M, Markin C, Fadely T, Guttentag A, Kropski J, Blackwell T
Am J Respir Crit Care Med
. 2024 May;
210(5):669-672.
PMID: 38762792
No abstract available.
2.
Liu Q, Zhou Y, Cogan J, Mitchell D, Sheng Q, Zhao S, et al.
Am J Respir Crit Care Med
. 2023 Jan;
207(10):1345-1357.
PMID: 36622818
Up to 20% of idiopathic interstitial lung disease is familial, referred to as familial pulmonary fibrosis (FPF). An integrated analysis of FPF genetic risk was performed by comprehensively evaluating for...
3.
Salisbury M, Markin C, Wu P, Cogan J, Mitchell D, Liu Q, et al.
Am J Respir Crit Care Med
. 2022 Aug;
207(2):208-211.
PMID: 36036734
No abstract available.
4.
Copeland C, Donnelly E, Mehrad M, Ding G, Markin C, Douglas K, et al.
Ann Am Thorac Soc
. 2022 Jul;
19(12):2003-2012.
PMID: 35877079
Heterogeneous characteristics are observed in familial pulmonary fibrosis (FPF), suggesting that nongenetic factors contribute to disease manifestations. To determine the relationship between environmental exposures and disease characteristics of FPF, including...
5.
Salisbury M, Hewlett J, Ding G, Markin C, Douglas K, Mason W, et al.
Am J Respir Crit Care Med
. 2020 Feb;
201(10):1230-1239.
PMID: 32011901
The preclinical natural history of progressive lung fibrosis is poorly understood. Our goals were to identify risk factors for interstitial lung abnormalities (ILA) on high-resolution computed tomography (HRCT) scans and...
6.
Moore C, Blumhagen R, Yang I, Walts A, Powers J, Walker T, et al.
Am J Respir Crit Care Med
. 2019 Apr;
200(2):199-208.
PMID: 31034279
Several common and rare genetic variants have been associated with idiopathic pulmonary fibrosis, a progressive fibrotic condition that is localized to the lung. To develop an integrated understanding of the...
7.
Fingerlin T, Zhang W, Yang I, Ainsworth H, Russell P, Blumhagen R, et al.
BMC Genet
. 2016 Jun;
17(1):74.
PMID: 27266705
Background: Fibrotic idiopathic interstitial pneumonias (fIIP) are a group of fatal lung diseases with largely unknown etiology and without definitive treatment other than lung transplant to prolong life. There is...
8.
Fingerlin T, Murphy E, Zhang W, Peljto A, Brown K, Steele M, et al.
Nat Genet
. 2013 Apr;
45(6):613-20.
PMID: 23583980
We performed a genome-wide association study of non-Hispanic, white individuals with fibrotic idiopathic interstitial pneumonias (IIPs; n = 1,616) and controls (n = 4,683), with follow-up replication analyses in 876...