The DOI matches its Crossref record; 98 of the 98 references it cites were found in a registry or an index.
Idiopathic Pulmonary Fibrosis
Abstract
Idiopathic pulmonary fibrosis appears to be increasing in incidence. It requires early recognition and intervention with supportive care and pharmacologic agents to forestall its progression. Lung transplantation may be curative.
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In the citing paper
“marked by interstitial pneumonia, dyspnea and cough25, histologically characterized by fibroblast proliferation and extracellular matrix remodeling26–29.”
From A generative AI-discovered TNIK inhibitor for idiopathic pulmonary fibrosis: a randomized phase 2a trial (2025) · cites this paper as [25]
In the citing paper
“IPF is an age-related, progressive lung disease diagnosed by excluding other potential causes of interstitial lung disease (for example, environmental exposures, connective tissue disease, hypersensitivity pneumonitis or drug toxicities)24 and marked by interstitial pneumonia, dyspnea and cough25, histologically characterized by fibroblast proliferation and extracellular matrix remodeling26–29.”
From A generative AI-discovered TNIK inhibitor for idiopathic pulmonary fibrosis: a randomized phase 2a trial (2025) · cites this paper as [25]
In the citing paper
“Idiopathic pulmonary fibrosis (IPF) is a progressive, fatal, age-associated lung disease with poor survival1.”
From Inhaled LTI-03 for idiopathic pulmonary fibrosis: a randomized dose escalation study (2026) · cites this paper as [1]
In the citing paper
“IPF is a process that is characterized by epithelial cell injury, fibroblast expansion, augmented ECM remodeling, and lung architecture destruction (87, 141).”
From Aging and Lung Disease (2020) · cites this paper as [141]
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Raghu, G., Collard, H. R., Egan, J. J., Martinez, F. J., Behr, J., Brown, K. K., Colby, T. V., Cordier, J.-F., Flaherty, K. R., Lasky, J. A., et al. (2011) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.2009-040gl · Cited by 7,186
Efficacy and Safety of Nintedanib in Idiopathic Pulmonary Fibrosis
Richeldi, L., du Bois, R. M., Raghu, G., Azuma, A., Brown, K. K., Costabel, U., Cottin, V., Flaherty, K. R., Hansell, D. M., Inoue, Y., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1402584 · Cited by 4,654
A phase 3 trial of pirfenidone in patients with idiopathic pulmonary fibrosis.
King, T. E., Bradford, W. Z., Castro-Bernardini, S., Fagan, E. A., Glaspole, I., Glassberg, M. K., Gorina, E., Hopkins, P. M., Kardatzke, D., Lancaster, L., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1402582 · Cited by 3,975
Self-citationScreening for Lung Cancer: U.S. Preventive Services Task Force Recommendation Statement
Moyer, V. A., & on behalf of the U.S. Preventive Services Task Force* (2013) · Annals of Internal Medicine · doi:10.7326/m13-2771 · Cited by 2,642
MacMahon, H., Naidich, D. P., Goo, J. M., Lee, K. S., Leung, A. N. C., Mayo, J. R., Mehta, A. C., Ohno, Y., Powell, C. A., Prokop, M., et al. (2017) · Radiology · doi:10.1148/radiol.2017161659 · Cited by 2,491
Raghu, G., Rochwerg, B., Zhang, Y., Garcia, C. A. C., Azuma, A., Behr, J., Brozek, J. L., Collard, H. R., Cunningham, W., Homma, S., et al. (2015) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201506-1063st · Cited by 1,916
Prednisone, Azathioprine, and N -Acetylcysteine for Pulmonary Fibrosis
The Idiopathic Pulmonary Fibrosis Clinical Research Network (2012) · New England Journal of Medicine · doi:10.1056/nejmoa1113354 · Cited by 1,654
Acute Exacerbation of Idiopathic Pulmonary Fibrosis. An International Working Group Report
Collard, H. R., Ryerson, C. J., Corte, T. J., Jenkins, G., Kondoh, Y., Lederer, D. J., Lee, J. S., Maher, T. M., Wells, A. U., Antoniou, K. M., et al. (2016) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201604-0801ci · Cited by 1,444
Self-citationTelomerase Mutations in Families with Idiopathic Pulmonary Fibrosis
Armanios, M. Y., Chen, J. J.-L., Cogan, J. D., Alder, J. K., Ingersoll, R. G., Markin, C., Lawson, W. E., Xie, M., Vulto, I., Phillips, J. A., et al. (2007) · New England Journal of Medicine · doi:10.1056/nejmoa066157 · Cited by 1,357
Weill, D., Benden, C., Corris, P. A., Dark, J. H., Davis, R. D., Keshavjee, S., Lederer, D. J., Mulligan, M. J., Patterson, G. A., Singer, L. G., et al. (2015) · The Journal of Heart and Lung Transplantation · doi:10.1016/j.healun.2014.06.014 · Cited by 1,329
Self-citationA Common MUC5B Promoter Polymorphism and Pulmonary Fibrosis
Seibold, M. A., Wise, A. L., Speer, M. C., Steele, M. P., Brown, K. M., Loyd, J. E., Fingerlin, T. E., Zhang, W., Guðmundsson, G., Groshong, S. D., et al. (2011) · New England Journal of Medicine · doi:10.1056/nejmoa1013660 · Cited by 1,235
Monocyte-derived alveolar macrophages drive lung fibrosis and persist in the lung over the life span
Misharin, A. V., Morales-Nebreda, L., Reyfman, P. A., Cuda, C. M., Walter, J. M., McQuattie-Pimentel, A. C., Chen, C.-I., Anekalla, K. R., Joshi, N., Williams, K. J. N., et al. (2017) · Journal of Experimental Medicine · doi:10.1084/jem.20162152 · Cited by 1,133
Diagnostic criteria for idiopathic pulmonary fibrosis: a Fleischner Society White Paper
Lynch, D. A., Sverzellati, N., Travis, W. D., Brown, K. K., Colby, T. V., Galvin, J. R., Goldin, J. G., Hansell, D. M., Inoue, Y., Johkoh, T., et al. (2018) · The Lancet Respiratory Medicine · doi:10.1016/s2213-2600(17)30433-2 · Cited by 1,030
Global incidence and mortality of idiopathic pulmonary fibrosis: a systematic review
Hutchinson, J., Fogarty, A., Hubbard, R., & McKeever, T. M. (2015) · European Respiratory Journal · doi:10.1183/09031936.00185114 · Cited by 913
Adult-onset pulmonary fibrosis caused by mutations in telomerase
Tsakiri, K. D., Cronkhite, J. T., Kuan, P. J., Xing, C., Raghu, G., Weissler, J. C., Rosenblatt, R. L., Shay, J. W., & Garcia, C. K. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0701009104 · Cited by 894
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis
Fingerlin, T. E., Murphy, E., Zhang, W., Peljto, A. L., Brown, K. K., Steele, M. P., Loyd, J. E., Cosgrove, G. P., Lynch, D., Groshong, S., et al. (2013) · Nature Genetics · doi:10.1038/ng.2609 · Cited by 809
Short telomeres are a risk factor for idiopathic pulmonary fibrosis
Alder, J. K., Chen, J. J.-L., Lancaster, L., Danoff, S., Su, S.-C., Cogan, J. D., Vulto, I., Xie, M., Qi, X., Tuder, R. M., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804280105 · Cited by 805
Muc5b is required for airway defence
Roy, M. G., Livraghi-Butrico, A., Fletcher, A. A., McElwee, M. M., Evans, S. E., Boerner, R. M., Alexander, S. N., Bellinghausen, L. K., Song, A. S., Petrova, Y. M., et al. (2014) · Nature · doi:10.1038/nature12807 · Cited by 764
Raghu, G., Chen, S.-Y., Yeh, W.-S., Maroni, B., Li, Q., Lee, Y.-C., & Collard, H. R. (2014) · The Lancet Respiratory Medicine · doi:10.1016/s2213-2600(14)70101-8 · Cited by 716
Idiopathic Interstitial Pneumonia
Flaherty, K. R., King, T. E., Raghu, G., Lynch, J. P., Colby, T. V., Travis, W. D., Gross, B. H., Kazerooni, E. A., Toews, G. B., Long, Q., et al. (2004) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200402-147oc · Cited by 672
Noth, I., Zhang, Y., Ma, S., Flores, C., Barber, M., Huang, Y., Broderick, S. M., Wade, M. S., Hysi, P. G., Scuirba, J., et al. (2013) · The Lancet Respiratory Medicine · doi:10.1016/s2213-2600(13)70045-6 · Cited by 622
MMP1 and MMP7 as Potential Peripheral Blood Biomarkers in Idiopathic Pulmonary Fibrosis
Rosas, I. O., Richards, T. J., Konishi, K., Zhang, Y., Gibson, K., Lokshin, A. E., Lindell, K. O., Cisneros, J., MacDonald, S. D., Pardo, A., et al. (2008) · PLoS Medicine · doi:10.1371/journal.pmed.0050093 · Cited by 582
Increased Prevalence of Gastroesophageal Reflux in Patients with Idiopathic Pulmonary Fibrosis
Tobin, R. W., Pope, C. E., Pellegrini, C. A., Emond, M. J., Sillery, J. K., & Raghu, G. (1998) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.158.6.9804105 · Cited by 568
The role of bacteria in the pathogenesis and progression of idiopathic pulmonary fibrosis
Molyneaux, P. L., Cox, M. J., Willis-Owen, S. A. G., Mallia, P., Russell, K. E., Russell, A.-M., Murphy, E., Johnston, S. L., Schwartz, D. A., Wells, A. U., et al. (2014) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201403-0541oc · Cited by 567
Treatment of Idiopathic Pulmonary Fibrosis With Ambrisentan: A Parallel, Randomized Trial
Raghu, G., Behr, J., Brown, K. K., Egan, J. J., Kawut, S. M., Flaherty, K. R., Martinez, F. J., Nathan, S. D., Wells, A. U., Collard, H. R., et al. (2013) · Annals of Internal Medicine · doi:10.7326/0003-4819-158-9-201305070-00003 · Cited by 553
Self-citationKing, T. E., Albera, C., Bradford, W. Z., Costabel, U., Hormel, P., Lancaster, L., Noble, P. W., Sahn, S. A., Szwarcberg, J., Thomeer, M., et al. (2009) · The Lancet · doi:10.1016/s0140-6736(09)60551-1 · Cited by 531
Randomized Trial of Acetylcysteine in Idiopathic Pulmonary Fibrosis
The Idiopathic Pulmonary Fibrosis Clinical Research Network (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1401739 · Cited by 506
Abdulqawi, R., Dockry, R., Holt, K. J., Layton, G. R., McCarthy, B. G., Ford, A. P. D. W., & Smith, J. A. (2014) · The Lancet · doi:10.1016/s0140-6736(14)61255-1 · Cited by 488
Association Between Interstitial Lung Abnormalities and All-Cause Mortality
Putman, R. K., Hatabu, H., Araki, T., Guðmundsson, G., Gao, W. D., Nishino, M., Okajima, Y., Dupuis, J., Latourelle, J. C., Cho, M. H., et al. (2016) · JAMA · doi:10.1001/jama.2016.0518 · Cited by 480
Selman, M., & Pardo, A. (2014) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201312-2221pp · Cited by 472
Comorbidities in idiopathic pulmonary fibrosis patients: a systematic literature review
Raghu, G., Amatto, V. C., Behr, J., & Stowasser, S. (2015) · European Respiratory Journal · doi:10.1183/13993003.02316-2014 · Cited by 470
A Placebo-Controlled Randomized Trial of Warfarin in Idiopathic Pulmonary Fibrosis
Noth, I., Anstrom, K. J., Calvert, S. B., de Andrade, J., Flaherty, K. R., Glazer, C., Kaner, R. J., & Olman, M. A. (2012) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201202-0314oc · Cited by 463
MUC5B Promoter Polymorphism and Interstitial Lung Abnormalities
Hunninghake, G. M., Hatabu, H., Okajima, Y., Gao, W. D., Dupuis, J., Latourelle, J. C., Nishino, M., Araki, T., Zazueta, O. E., Kurugol, S., et al. (2013) · New England Journal of Medicine · doi:10.1056/nejmoa1216076 · Cited by 463
Richeldi, L., Cottin, V., du Bois, R. M., Selman, M., Kimura, T., Bailes, Z., Schlenker-Herceg, R., Stowasser, S., & Brown, K. K. (2016) · Respiratory Medicine · doi:10.1016/j.rmed.2016.02.001 · Cited by 463
Walsh, S. L. F., Wells, A. U., Desai, S. R., Poletti, V. E., Piciucchi, S., Dubini, A., Nunès, H., Valeyre, D., Brillet, P., Kambouchner, M., et al. (2016) · The Lancet Respiratory Medicine · doi:10.1016/s2213-2600(16)30033-9 · Cited by 461
Lee, J. S., Ryu, J. H., Elicker, B. M., Lydell, C. P., Jones, K. D., Wolters, P. J., King, T. E., & Collard, H. R. (2011) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201101-0138oc · Cited by 435
Han, M. K., Zhou, Y., Murray, S., Tayob, N., Noth, I., Lama, V. N., Moore, B. B., White, E. S., Flaherty, K. R., Hu, B., et al. (2014) · The Lancet Respiratory Medicine · doi:10.1016/s2213-2600(14)70069-4 · Cited by 419
Lee, J. S., Collard, H. R., Anstrom, K. J., Martínez, F. J., Noth, I., Roberts, R., Yow, E. S., & Raghu, G. (2013) · The Lancet Respiratory Medicine · doi:10.1016/s2213-2600(13)70105-x · Cited by 415
Baumgartner, K. B., Samet, J. M., Coultas, D., Stidley, C. A., Hunt, W. C., Colby, T. V., Waldron, J. A., & Centers, C. (2000) · American Journal of Epidemiology · doi:10.1093/aje/152.4.307 · Cited by 374
Incidence and prevalence of idiopathic pulmonary fibrosis in US adults 18–64 years old
Raghu, G., Chen, S., Hou, Q., Yeh, W., & Collard, H. R. (2016) · European Respiratory Journal · doi:10.1183/13993003.01653-2015 · Cited by 348
Oldham, J. M., Ma, S.-F., Martinez, F. J., Anstrom, K. J., Raghu, G., Schwartz, D. A., Valenzi, E., Witt, L., Lee, C., Vij, R., et al. (2015) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201505-1010oc · Cited by 341
Tomassetti, S., Wells, A. U., Costabel, U., Cavazza, A., Colby, T. V., Rossi, G., Sverzellati, N., Carloni, A., Carretta, E., Buccioli, M., et al. (2015) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201504-0711oc · Cited by 339
Nathan, S. D., Albera, C., Bradford, W. Z., Costabel, U., Glaspole, I., Glassberg, M. K., Kardatzke, D. R., Daigl, M., Kirchgaessler, K.-U., Lancaster, L. H., et al. (2017) · The Lancet Respiratory Medicine · doi:10.1016/s2213-2600(16)30326-5 · Cited by 335
Self-citationHerpesvirus DNA Is Consistently Detected in Lungs of Patients with Idiopathic Pulmonary Fibrosis
Tang, Y., Johnson, J. E., Browning, P. J., Cruz-Gervis, R. A., Davis, A., Graham, B. S., Brigham, K. L., Oates, J. A., Loyd, J. E., & Stecenko, A. A. (2003) · Journal of Clinical Microbiology · doi:10.1128/jcm.41.6.2633-2640.2003 · Cited by 310
Nintedanib with Add-on Pirfenidone in Idiopathic Pulmonary Fibrosis. Results of the INJOURNEY Trial
Vancheri, C., Kreuter, M., Richeldi, L., Ryerson, C. J., Valeyre, D., Grutters, J. C., Wiebe, S., Stansen, W., Quaresma, M., Stowasser, S., et al. (2018) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201706-1301oc · Cited by 305
Allen, R. J., Porte, J., Braybrooke, R., Flores, C., Fingerlin, T. E., Oldham, J. M., Guillen-Guio, B., Ma, S.-F., Okamoto, T., John, A. E., et al. (2017) · The Lancet Respiratory Medicine · doi:10.1016/s2213-2600(17)30387-9 · Cited by 297
The incidence of cancer in patients with idiopathic pulmonary fibrosis and sarcoidosis in the UK
Jeune, I. L., Gribbin, J., West, J., Smith, C., Cullinan, P., & Hubbard, R. (2007) · Respiratory Medicine · doi:10.1016/j.rmed.2007.07.012 · Cited by 295
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Marks, P. W., Witten, C. M., & Califf, R. M. (2016) · New England Journal of Medicine · doi:10.1056/nejmp1613723 · Cited by 294
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Costabel, U., Inoue, Y., Richeldi, L., Collard, H. R., Tschoepe, I., Stowasser, S., & Azuma, A. (2016) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201503-0562oc · Cited by 280
Dowman, L., McDonald, C. F., Hill, C. J., Lee, A. L., Barker, K., Boote, C., Glaspole, I., Goh, N. S. L., Southcott, A. M., Burge, A. T., et al. (2017) · Thorax · doi:10.1136/thoraxjnl-2016-208638 · Cited by 279
The need for randomization in the study of intended effects
Miettinen, O. S. (1983) · Statistics in Medicine · doi:10.1002/sim.4780020222 · Cited by 277
Nintedanib in patients with idiopathic pulmonary fibrosis and preserved lung volume
Kolb, M. R. J., Richeldi, L., Behr, J., Maher, T. M., Tang, W., Stowasser, S., Hallmann, C., & du Bois, R. M. (2016) · Thorax · doi:10.1136/thoraxjnl-2016-208710 · Cited by 242
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Kreuter, M., Wuyts, W. A., Renzoni, E. A., Koschel, D., Maher, T. M., Kolb, M. R. J., Weycker, D. A., Spagnolo, P., Kirchgaessler, K.-U., Herth, F. J. F., et al. (2016) · The Lancet Respiratory Medicine · doi:10.1016/s2213-2600(16)00067-9 · Cited by 219
Johannson, K. A., Marcoux, V. S., Ronksley, P. E., & Ryerson, C. J. (2016) · Annals of the American Thoracic Society · doi:10.1513/annalsats.201606-461sr · Cited by 216
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Hutchinson, J. P., McKeever, T. M., Fogarty, A., Navaratnam, V. V., & Hubbard, R. (2014) · Annals of the American Thoracic Society · doi:10.1513/annalsats.201404-145oc · Cited by 214
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Ley, B., Swigris, J. J., Day, B.-M., Stauffer, J. L., Raimundo, K., Chou, W., & Collard, H. R. (2017) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201701-0091oc · Cited by 212
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Horton, M. R., Santopietro, V., Mathew, L., Horton, K. M., Polito, A. J., Liu, M. C., Danoff, S. K., & Lechtzin, N. (2012) · Annals of Internal Medicine · doi:10.7326/0003-4819-157-6-201209180-00003 · Cited by 206
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Canestaro, W. J., Forrester, S. H., Raghu, G., Ho, L. A., & Devine, B. E. (2016) · CHEST Journal · doi:10.1016/j.chest.2015.11.013 · Cited by 188
Raghu, G., & Selman, M. (2015) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201411-2044ed · Cited by 184
White, E. S., Xia, M., Murray, S., Dyal, R., Flaherty, C. M., Flaherty, K. R., Moore, B. B., Cheng, L., Doyle, T. J., Villalba, J., et al. (2016) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201505-0862oc · Cited by 180
Albera, C., Costabel, U., Fagan, E., Glassberg, M. K., Gorina, E., LANCASTER, L. H., Lederer, D. J., Nathan, S. D., Spirig, D., & Swigris, J. J. (2016) · European Respiratory Journal · doi:10.1183/13993003.01966-2015 · Cited by 169
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Podolanczuk, A. J., Oelsner, E. C., Barr, R. G., Hoffman, E. A., Armstrong, H. F., Austin, J. H. M., Basner, R. C., Bartels, M. N., Christie, J. D., Enright, P., et al. (2016) · European Respiratory Journal · doi:10.1183/13993003.00129-2016 · Cited by 167
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Lindell, K. O., Liang, Z., Hoffman, L. A., Rosenzweig, M. Q., Saul, M. I., Pilewski, J. M., Gibson, K. F., & Kaminski, N. (2014) · CHEST Journal · doi:10.1378/chest.14-1127 · Cited by 166
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Valapour, M., Lehr, C. J., Skeans, M. A., Smith, J. M., Carrico, R., Uccellini, K., Lehman, R., Robinson, A., Israni, A. K., Snyder, J. J., et al. (2018) · American Journal of Transplantation · doi:10.1111/ajt.14562 · Cited by 163
Esposito, D. B., Lanes, S., Donneyong, M. M., Holick, C. N., Lasky, J. A., Lederer, D. J., Nathan, S. D., O’Quinn, S., Parker, J. M., & Tran, T. N. (2015) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201504-0818oc · Cited by 153
Self-citationMicrobes Are Associated with Host Innate Immune Response in Idiopathic Pulmonary Fibrosis
Huang, Y., Ma, S.-F., Espindola, M. S., Vij, R., Oldham, J. M., Huffnagle, G. B., Erb-Downward, J. R., Flaherty, K. R., Moore, B. B., White, E. S., et al. (2017) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201607-1525oc · Cited by 142
Kim, S. Y., Diggans, J., Pankratz, D., Huang, J., Pagan, M., Sindy, N., Tom, E., Anderson, J. D., Choi, Y., Lynch, D. A., et al. (2015) · The Lancet Respiratory Medicine · doi:10.1016/s2213-2600(15)00140-x · Cited by 137
Therapeutic targets in idiopathic pulmonary fibrosis
Kolb, M. R. J., Bonella, F., & Wollin, L. (2017) · Respiratory Medicine · doi:10.1016/j.rmed.2017.07.062 · Cited by 134
Brownell, R., Moua, T., Henry, T. S., Elicker, B. M., White, D. B., Vittinghoff, E., Jones, K. D., Urisman, A., Aravena, C., Johannson, K. A., et al. (2017) · Thorax · doi:10.1136/thoraxjnl-2016-209671 · Cited by 128
Sack, C. S., Vedal, S., Sheppard, L. A., Raghu, G., Barr, R. G., Podolanczuk, A. J., Doney, B. C., Hoffman, E. A., Gassett, A. J., Stukovsky, K. H., et al. (2017) · European Respiratory Journal · doi:10.1183/13993003.00559-2017 · Cited by 126
Self-citationBirring, S. S., Wijsenbeek, M. S., Agrawal, S., van den Berg, J. W., Stone, H., Maher, T. M., Tutuncu, A., & Morice, A. H. (2017) · The Lancet Respiratory Medicine · doi:10.1016/s2213-2600(17)30310-7 · Cited by 123
Han, Q., Luo, Q., Xie, J., Wu, L., Liao, L.-Y., Zhang, X., & Chen, R. (2015) · Journal of Thoracic and Cardiovascular Surgery · doi:10.1016/j.jtcvs.2014.12.057 · Cited by 117
Nakano, Y., Yang, I. V., Walts, A. D., Watson, A. M., Helling, B. A., Fletcher, A. A., Lara, A., Schwarz, M. I., Evans, C. M., & Schwartz, D. A. (2016) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201509-1872le · Cited by 113
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Cottin, V., Hansell, D. M., Sverzellati, N., Weycker, D. A., Antoniou, K. M., Atwood, M., Oster, G., Kirchgaessler, K.-U., Collard, H. R., & Wells, A. U. (2017) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201612-2492oc · Cited by 112
Singer, J. P., Katz, P., Soong, A., Shrestha, P., Huang, D., Ho, J., Mindo, M., Greenland, J. R., Hays, S. R., Golden, J. A., et al. (2016) · American Journal of Transplantation · doi:10.1111/ajt.14081 · Cited by 109
DiBardino, D. M., Haas, A. R., Lanfranco, A. R., Litzky, L. A., Sterman, D. H., & Bessich, J. L. (2017) · Annals of the American Thoracic Society · doi:10.1513/annalsats.201610-829oc · Cited by 108
Treatment of idiopathic pulmonary fibrosis: a network meta-analysis
Rochwerg, B., Neupane, B., Zhang, Y., Garcia, C. C., Raghu, G., Richeldi, L., Brozek, J., Beyene, J., & Schünemann, H. (2016) · BMC Medicine · doi:10.1186/s12916-016-0558-x · Cited by 101
Walsh, S. L. F., Maher, T. M., Kolb, M. R. J., Poletti, V. E., Nusser, R., Richeldi, L., Vancheri, C., WILSHER, M. L., Antoniou, K. M., Behr, J., et al. (2017) · European Respiratory Journal · doi:10.1183/13993003.00936-2017 · Cited by 100
Effect of pirfenidone on cough in patients with idiopathic pulmonary fibrosis
van Manen, M. J. G., Birring, S. S., Vancheri, C., Vindigni, V., Renzoni, E. A., Russell, A., Wapenaar, M., Cottin, V., & Wijsenbeek, M. S. (2017) · European Respiratory Journal · doi:10.1183/13993003.01157-2017 · Cited by 99
van den Blink, B., Dillingh, M. R., Ginns, L. C., Morrison, L. D., Moerland, M., Wijsenbeek, M. S., Trehu, E., Bartholmai, B. J., & Burggraaf, J. (2016) · European Respiratory Journal · doi:10.1183/13993003.00850-2015 · Cited by 98
Usual Interstitial Pneumonia Can Be Detected in Transbronchial Biopsies Using Machine Learning
Pankratz, D. G., Choi, Y., Imtiaz, U., Fedorowicz, G. M., Anderson, J. D., Colby, T. V., Myers, J. L., Lynch, D. A., Brown, K. K., Flaherty, K. R., et al. (2017) · Annals of the American Thoracic Society · doi:10.1513/annalsats.201612-947oc · Cited by 96
Yang, I. V., Luna, L. G., Cotter, J., Talbert, J. L., Leach, S. M., Kidd, R., Turner, J., Kummer, N., Kervitsky, D. J., Brown, K. K., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037708 · Cited by 94
Disease-Specific Survival Benefit of Lung Transplantation in Adults: A National Cohort Study
Titman, A., Rogers, C. A., Bonser, R. S., Banner, N. R., & Sharples, L. D. (2009) · American Journal of Transplantation · doi:10.1111/j.1600-6143.2009.02613.x · Cited by 90
Podolanczuk, A. J., Oelsner, E. C., Barr, R. G., Bernstein, E. J., Hoffman, E. A., Easthausen, I. J., Stukovsky, K. H., RoyChoudhury, A., Michos, E. D., Raghu, G., et al. (2017) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201703-0555oc · Cited by 83
Self-citationThe Increasing Secondary Care Burden of Idiopathic Pulmonary Fibrosis
Navaratnam, V. V., Fogarty, A., Glendening, R., McKeever, T. M., & Hubbard, R. (2013) · CHEST Journal · doi:10.1378/chest.12-0803 · Cited by 74
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Wiener, R. S., Ouellette, D. R., Diamond, E., Fan, V. S., MAURER, J. R., Mularski, R. A., Peters, J. I., & Halpern, S. D. (2014) · CHEST Journal · doi:10.1378/chest.14-0670 · Cited by 74
Dowman, L., Mcdonald, C., Bozinovski, S., Vlahos, R., Gillies, R., Pouniotis, D., Hill, C., Goh, N., & Holland, A. E. (2017) · Respirology (Carlton South. Print) · doi:10.1111/resp.13002 · Cited by 73
Kim, J. S., Podolanczuk, A. J., Borker, P. V., Kawut, S. M., Raghu, G., Kaufman, J. D., Stukovsky, K. H., Hoffman, E. A., Barr, R. G., Gottlieb, D. J., et al. (2017) · Annals of the American Thoracic Society · doi:10.1513/annalsats.201701-091oc · Cited by 66
Self-citationTiming of onset of symptoms in people with idiopathic pulmonary fibrosis
Hewson, T., McKeever, T. M., Gibson, J., Navaratnam, V. V., Hubbard, R., & Hutchinson, J. P. (2017) · Thorax · doi:10.1136/thoraxjnl-2017-210177 · Cited by 66
Salisbury, M. L., Xia, M., Murray, S., Bartholmai, B. J., Kazerooni, E. A., Meldrum, C. A., Martínez, F. J., & Flaherty, K. R. (2016) · Respiratory Medicine · doi:10.1016/j.rmed.2016.07.016 · Cited by 52
Kitsios, G. D., Rojas, M. M., Kass, D. J., Fitch, A. C., Sembrat, J., Qin, S., Veraldi, K. L., Gibson, K. F., Lindell, K. O., Pilewski, J. M., et al. (2017) · Thorax · doi:10.1136/thoraxjnl-2017-210537 · Cited by 50
Interstitial Lung Disease: NHLBI Workshop on the Primary Prevention of Chronic Lung Diseases
Rosas, I. O., Dellaripa, P. F., Lederer, D. J., Khanna, D., Young, L. R., & Martínez, F. J. (2014) · Annals of the American Thoracic Society · doi:10.1513/annalsats.201312-429ld · Cited by 46
Self-citationVenous thromboembolism in people with idiopathic pulmonary fibrosis: a population-based study
Dalleywater, W. J., Powell, H. A., Fogarty, A., Hubbard, R., & Navaratnam, V. V. (2014) · European Respiratory Journal · doi:10.1183/09031936.00099614 · Cited by 36
Morris, A., Gibson, K. F., & Collman, R. G. (2014) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201409-1626ed · Cited by 26
Cryobiopsy in the Diagnosis of Interstitial Lung Disease. A Step Forward or Back?
Patel, N. M., Borczuk, A., & Lederer, D. J. (2016) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201511-2313ed · Cited by 23
Self-citationHirani, N., Nicol, L. M., MacKinnon, A. C., Ford, P., Schambye, H. T., Pedersen, Nilsson, U., Leffler, H., Thomas, T., Knott, O., et al. (2016) · QJM · doi:10.1093/qjmed/hcw127.003 · Cited by 21
Gorina, E., Richeldi, L., Raghu, G., Pérez, E. R. F., Costabel, U., Albera, C., Lederer, D. J., Flaherty, K. R., Ettinger, N. A., Bercz, P. A., et al. (2017) · doi:10.1183/1393003.congress-2017.oa3400 · Cited by 19
Self-citation
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Research works printed but not linked: 2
- Philp CJ, Siebeke I, Clements D, et al. ECM crosslinking enhances fibroblast growth and protects against matrix proteolysis in lung fibrosis. Am J Respir Cell Mol Biol 2017 October 20 (Epub ahead of print).29053339
- Parker J, Sawtell R, Gagnon L, et al. PBI-4050 is safe and well tolerated and shows evidence of benefit in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2017;195:A7606-A7606. abstract.
Cited by
Sorted by citations
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Flaherty, K. R., Wells, A. U., Cottin, V., Devaraj, A., Walsh, S. L. F., Inoue, Y., Richeldi, L., Kolb, M., Tetzlaff, K., Stowasser, S., et al. (2019) · New England Journal of Medicine · doi:10.1056/nejmoa1908681 · Cited by 2,403
Adams, T. S., Schupp, J. C., Poli, S., Ayaub, E. A., Neumark, N., Ahangari, F., Chu, S. G., Raby, B. A., DeIuliis, G., Januszyk, M., et al. (2020) · Science Advances · doi:10.1126/sciadv.aba1983 · Cited by 1,420
Reyfman, P. A., Walter, J. M., Joshi, N., Anekalla, K. R., McQuattie-Pimentel, A. C., Chiu, S., Fernandez, R., Akbarpour, M., Chen, C.-I., Ren, Z., et al. (2019) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201712-2410oc · Cited by 1,203
New insights into TGF-β/Smad signaling in tissue fibrosis
Hu, H.-H., Chen, D., Wang, Y., Feng, Y., Cao, G., Vaziri, N. D., & Zhao, Y. (2018) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2018.07.008 · Cited by 1,205
Habermann, A. C., Gutierrez, A. J., Bui, L. T., Yahn, S. L., Winters, N. I., Calvi, C. L., Peter, L., Chung, M.-I., Taylor, C. J., Jetter, C., et al. (2020) · Science Advances · doi:10.1126/sciadv.aba1972 · Cited by 1,129
Metadata
- Authors
- Lederer, D. J., & Martinez, F. J.
- Affiliations
- Columbia University Irving Medical Center (US)
- From the Departments of Medicine and Epidemiology, Columbia University Irving Medical Center (D.J.L.), and the Department of Medicine, Weill Cornell Medical Center (F.J.M.) — both in New York.
- ORCID
- Lederer, David J.
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 2018-05-10
- Volume
- 378
- Issue
- 19
- Pages
- 1811-1823
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W2799479598
- Cited by
- 2,056
- References
- 98
- Citations by year
- 2026: 248 · 2025: 267 · 2024: 299 · 2023: 308 · 2022: 301 · 2021: 266 · 2020: 197 · 2019: 129 · 2018: 40
- FWCI
- 28.43
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- New England Journal of Medicine (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Occupational and environmental lung diseases
- Health Sciences › Medicine › Surgery › Transplantation: Methods and Outcomes
- Keywords
- idiopathic pulmonary fibrosis, incidence, early recognition, supportive care, pharmacotherapy, disease progression, lung transplantation
- MeSH terms
- Diagnosis, Differential, Dyspnea, Enzyme Inhibitors, Humans, Indoles, Lung, Oxygen Inhalation Therapy, Prognosis, Pyridones, Risk Factors, Tomography, X-Ray Computed, Transforming Growth Factor beta, Idiopathic Pulmonary Fibrosis
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