A citation-based method for searching scientific literature

L M Nogee, A E Dunbar, S E Wert, F Askin, A Hamvas, J A Whitsett. N Engl J Med 2001
Times Cited: 576







List of co-cited articles
1170 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Telomerase mutations in families with idiopathic pulmonary fibrosis.
Mary Y Armanios, Julian J-L Chen, Joy D Cogan, Jonathan K Alder, Roxann G Ingersoll, Cheryl Markin, William E Lawson, Mingyi Xie, Irma Vulto, John A Phillips,[...]. N Engl J Med 2007
801
33

Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer.
Yongyu Wang, Phillip J Kuan, Chao Xing, Jennifer T Cronkhite, Fernando Torres, Randall L Rosenblatt, J Michael DiMaio, Lisa N Kinch, Nick V Grishin, Christine Kim Garcia. Am J Hum Genet 2009
286
30

A common MUC5B promoter polymorphism and pulmonary fibrosis.
Max A Seibold, Anastasia L Wise, Marcy C Speer, Mark P Steele, Kevin K Brown, James E Loyd, Tasha E Fingerlin, Weiming Zhang, Gunnar Gudmundsson, Steve D Groshong,[...]. N Engl J Med 2011
608
30

Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred.
Alan Q Thomas, Kirk Lane, John Phillips, Melissa Prince, Cheryl Markin, Marcy Speer, David A Schwartz, Radhika Gaddipati, Annis Marney, Joyce Johnson,[...]. Am J Respir Crit Care Med 2002
423
28

Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.
Tasha E Fingerlin, Elissa Murphy, Weiming Zhang, Anna L Peljto, Kevin K Brown, Mark P Steele, James E Loyd, Gregory P Cosgrove, David Lynch, Steve Groshong,[...]. Nat Genet 2013
414
28

Adult-onset pulmonary fibrosis caused by mutations in telomerase.
Kalliopi D Tsakiri, Jennifer T Cronkhite, Phillip J Kuan, Chao Xing, Ganesh Raghu, Jonathan C Weissler, Randall L Rosenblatt, Jerry W Shay, Christine Kim Garcia. Proc Natl Acad Sci U S A 2007
562
24

Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening.
Bridget D Stuart, Jungmin Choi, Samir Zaidi, Chao Xing, Brody Holohan, Rui Chen, Mihwa Choi, Pooja Dharwadkar, Fernando Torres, Carlos E Girod,[...]. Nat Genet 2015
242
23

Surfactant protein C mutations are the basis of a significant portion of adult familial pulmonary fibrosis in a dutch cohort.
Coline H M van Moorsel, Matthijs F M van Oosterhout, Nicole P Barlo, Pim A de Jong, Joanne J van der Vis, Henk J T Ruven, H Wouter van Es, Jules M M van den Bosch, Jan C Grutters. Am J Respir Crit Care Med 2010
169
23

Endoplasmic reticulum stress in alveolar epithelial cells is prominent in IPF: association with altered surfactant protein processing and herpesvirus infection.
William E Lawson, Peter F Crossno, Vasiliy V Polosukhin, Juan Roldan, Dong-Sheng Cheng, Kirk B Lane, Thomas R Blackwell, Carol Xu, Cheryl Markin, Lorraine B Ware,[...]. Am J Physiol Lung Cell Mol Physiol 2008
284
22

A surfactant protein C precursor protein BRICHOS domain mutation causes endoplasmic reticulum stress, proteasome dysfunction, and caspase 3 activation.
Surafel Mulugeta, Vu Nguyen, Scott J Russo, Madesh Muniswamy, Michael F Beers. Am J Respir Cell Mol Biol 2005
177
22

Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study.
Imre Noth, Yingze Zhang, Shwu-Fan Ma, Carlos Flores, Mathew Barber, Yong Huang, Steven M Broderick, Michael S Wade, Pirro Hysi, Joseph Scuirba,[...]. Lancet Respir Med 2013
304
21

An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management.
Ganesh Raghu, Harold R Collard, Jim J Egan, Fernando J Martinez, Juergen Behr, Kevin K Brown, Thomas V Colby, Jean-François Cordier, Kevin R Flaherty, Joseph A Lasky,[...]. Am J Respir Crit Care Med 2011
20

Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF.
W E Lawson, S W Grant, V Ambrosini, K E Womble, E P Dawson, K B Lane, C Markin, E Renzoni, P Lympany, A Q Thomas,[...]. Thorax 2004
171
19

Efficacy and safety of nintedanib in idiopathic pulmonary fibrosis.
Luca Richeldi, Roland M du Bois, Ganesh Raghu, Arata Azuma, Kevin K Brown, Ulrich Costabel, Vincent Cottin, Kevin R Flaherty, David M Hansell, Yoshikazu Inoue,[...]. N Engl J Med 2014
18

Expression of mutant Sftpc in murine alveolar epithelia drives spontaneous lung fibrosis.
Shin-Ichi Nureki, Yaniv Tomer, Alessandro Venosa, Jeremy Katzen, Scott J Russo, Sarita Jamil, Matthew Barrett, Vivian Nguyen, Meghan Kopp, Surafel Mulugeta,[...]. J Clin Invest 2018
74
24

Endoplasmic reticulum stress enhances fibrotic remodeling in the lungs.
William E Lawson, Dong-Sheng Cheng, Amber L Degryse, Harikrishna Tanjore, Vasiliy V Polosukhin, Xiaochuan C Xu, Dawn C Newcomb, Brittany R Jones, Juan Roldan, Kirk B Lane,[...]. Proc Natl Acad Sci U S A 2011
227
17

A phase 3 trial of pirfenidone in patients with idiopathic pulmonary fibrosis.
Talmadge E King, Williamson Z Bradford, Socorro Castro-Bernardini, Elizabeth A Fagan, Ian Glaspole, Marilyn K Glassberg, Eduard Gorina, Peter M Hopkins, David Kardatzke, Lisa Lancaster,[...]. N Engl J Med 2014
17

ABCA3 gene mutations in newborns with fatal surfactant deficiency.
Sergey Shulenin, Lawrence M Nogee, Tarmo Annilo, Susan E Wert, Jeffrey A Whitsett, Michael Dean. N Engl J Med 2004
417
16

Short telomeres are a risk factor for idiopathic pulmonary fibrosis.
Jonathan K Alder, Julian J-L Chen, Lisa Lancaster, Sonye Danoff, Shu-chih Su, Joy D Cogan, Irma Vulto, Mingyi Xie, Xiaodong Qi, Rubin M Tuder,[...]. Proc Natl Acad Sci U S A 2008
464
15

Rare variants in RTEL1 are associated with familial interstitial pneumonia.
Joy D Cogan, Jonathan A Kropski, Min Zhao, Daphne B Mitchell, Lynette Rives, Cheryl Markin, Errine T Garnett, Keri H Montgomery, Wendi R Mason, David F McKean,[...]. Am J Respir Crit Care Med 2015
107
15

An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias.
William D Travis, Ulrich Costabel, David M Hansell, Talmadge E King, David A Lynch, Andrew G Nicholson, Christopher J Ryerson, Jay H Ryu, Moisés Selman, Athol U Wells,[...]. Am J Respir Crit Care Med 2013
15

Exome sequencing identifies mutant TINF2 in a family with pulmonary fibrosis.
Jonathan K Alder, Susan E Stanley, Christa L Wagner, Makenzie Hamilton, Vidya Sagar Hanumanthu, Mary Armanios. Chest 2015
91
16

Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study.
Richard J Allen, Joanne Porte, Rebecca Braybrooke, Carlos Flores, Tasha E Fingerlin, Justin M Oldham, Beatriz Guillen-Guio, Shwu-Fan Ma, Tsukasa Okamoto, Alison E John,[...]. Lancet Respir Med 2017
114
15

Epithelial endoplasmic reticulum stress and apoptosis in sporadic idiopathic pulmonary fibrosis.
Martina Korfei, Clemens Ruppert, Poornima Mahavadi, Ingrid Henneke, Philipp Markart, Miriam Koch, Gyoergy Lang, Ludger Fink, Rainer-Maria Bohle, Werner Seeger,[...]. Am J Respir Crit Care Med 2008
335
14


Telomere dysfunction causes alveolar stem cell failure.
Jonathan K Alder, Christina E Barkauskas, Nathachit Limjunyawong, Susan E Stanley, Frant Kembou, Rubin M Tuder, Brigid L M Hogan, Wayne Mitzner, Mary Armanios. Proc Natl Acad Sci U S A 2015
167
14

Germline SFTPA1 mutation in familial idiopathic interstitial pneumonia and lung cancer.
Nadia Nathan, Violaine Giraud, Clément Picard, Hilario Nunes, Florence Dastot-Le Moal, Bruno Copin, Laurie Galeron, Alice De Ligniville, Nathalie Kuziner, Martine Reynaud-Gaubert,[...]. Hum Mol Genet 2016
62
22

Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis.
Anna L Peljto, Yingze Zhang, Tasha E Fingerlin, Shwu-Fan Ma, Joe G N Garcia, Thomas J Richards, Lori J Silveira, Kathleen O Lindell, Mark P Steele, James E Loyd,[...]. JAMA 2013
267
13

A common mutation in the surfactant protein C gene associated with lung disease.
H Scott Cameron, Marco Somaschini, Paola Carrera, Aaron Hamvas, Jeffrey A Whitsett, Susan E Wert, Gail Deutsch, Lawrence M Nogee. J Pediatr 2005
105
13

Type 2 alveolar cells are stem cells in adult lung.
Christina E Barkauskas, Michael J Cronce, Craig R Rackley, Emily J Bowie, Douglas R Keene, Barry R Stripp, Scott H Randell, Paul W Noble, Brigid L M Hogan. J Clin Invest 2013
733
13

SFTPA2 Mutations in Familial and Sporadic Idiopathic Interstitial Pneumonia.
Coline H M van Moorsel, Liesbeth Ten Klooster, Matthijs F M van Oosterhout, Pim A de Jong, Human Adams, H Wouter van Es, Henk J T Ruven, Joanne J van der Vis, Jan C Grutters. Am J Respir Crit Care Med 2015
41
31

Genotype alone does not predict the clinical course of SFTPC deficiency in paediatric patients.
Carolin Kröner, Simone Reu, Veronika Teusch, Andrea Schams, Ann-Christin Grimmelt, Michael Barker, Joerg Brand, Monika Gappa, Richard Kitz, Boris W Kramer,[...]. Eur Respir J 2015
32
37

Brief report: deficiency of pulmonary surfactant protein B in congenital alveolar proteinosis.
L M Nogee, D E de Mello, L P Dehner, H R Colten. N Engl J Med 1993
479
12

Surfactant protein A2 mutations associated with pulmonary fibrosis lead to protein instability and endoplasmic reticulum stress.
Meenakshi Maitra, Yongyu Wang, Robert D Gerard, Carole R Mendelson, Christine Kim Garcia. J Biol Chem 2010
94
12

Genotype-phenotype correlations for infants and children with ABCA3 deficiency.
Jennifer A Wambach, Alicia M Casey, Martha P Fishman, Daniel J Wegner, Susan E Wert, F Sessions Cole, Aaron Hamvas, Lawrence M Nogee. Am J Respir Crit Care Med 2014
87
13

Telomere shortening in familial and sporadic pulmonary fibrosis.
Jennifer T Cronkhite, Chao Xing, Ganesh Raghu, Kelly M Chin, Fernando Torres, Randall L Rosenblatt, Christine Kim Garcia. Am J Respir Crit Care Med 2008
318
12

Diagnosis of Idiopathic Pulmonary Fibrosis. An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline.
Ganesh Raghu, Martine Remy-Jardin, Jeffrey L Myers, Luca Richeldi, Christopher J Ryerson, David J Lederer, Juergen Behr, Vincent Cottin, Sonye K Danoff, Ferran Morell,[...]. Am J Respir Crit Care Med 2018
12


Surfactant protein C G100S mutation causes familial pulmonary fibrosis in Japanese kindred.
S Ono, T Tanaka, M Ishida, A Kinoshita, J Fukuoka, M Takaki, N Sakamoto, Y Ishimatsu, S Kohno, T Hayashi,[...]. Eur Respir J 2011
54
22

Telomere-related lung fibrosis is diagnostically heterogeneous but uniformly progressive.
Chad A Newton, Kiran Batra, Jose Torrealba, Julia Kozlitina, Craig S Glazer, Carlos Aravena, Keith Meyer, Ganesh Raghu, Harold R Collard, Christine Kim Garcia. Eur Respir J 2016
133
12

Genetic disorders of surfactant dysfunction.
Susan E Wert, Jeffrey A Whitsett, Lawrence M Nogee. Pediatr Dev Pathol 2009
131
11

A mutation in the surfactant protein B gene responsible for fatal neonatal respiratory disease in multiple kindreds.
L M Nogee, G Garnier, H C Dietz, L Singer, A M Murphy, D E deMello, H R Colten. J Clin Invest 1994
398
11

A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis.
T Mushiroda, S Wattanapokayakit, A Takahashi, T Nukiwa, S Kudoh, T Ogura, H Taniguchi, M Kubo, N Kamatani, Y Nakamura. J Med Genet 2008
146
11

Prednisone, azathioprine, and N-acetylcysteine for pulmonary fibrosis.
Ganesh Raghu, Kevin J Anstrom, Talmadge E King, Joseph A Lasky, Fernando J Martinez. N Engl J Med 2012
854
11

Clinical course and prediction of survival in idiopathic pulmonary fibrosis.
Brett Ley, Harold R Collard, Talmadge E King. Am J Respir Crit Care Med 2011
852
11

A novel dyskerin (DKC1) mutation is associated with familial interstitial pneumonia.
Jonathan A Kropski, Daphne B Mitchell, Cheryl Markin, Vasiliy V Polosukhin, Leena Choi, Joyce E Johnson, William E Lawson, John A Phillips, Joy D Cogan, Timothy S Blackwell,[...]. Chest 2014
77
14

Analysis of protein-altering variants in telomerase genes and their association with MUC5B common variant status in patients with idiopathic pulmonary fibrosis: a candidate gene sequencing study.
Amy Dressen, Alexander R Abbas, Christopher Cabanski, Janina Reeder, Thirumalai R Ramalingam, Margaret Neighbors, Tushar R Bhangale, Matthew J Brauer, Julie Hunkapiller, Jens Reeder,[...]. Lancet Respir Med 2018
63
17

PINK1 deficiency impairs mitochondrial homeostasis and promotes lung fibrosis.
Marta Bueno, Yen-Chun Lai, Yair Romero, Judith Brands, Claudette M St Croix, Christelle Kamga, Catherine Corey, Jose D Herazo-Maya, John Sembrat, Janet S Lee,[...]. J Clin Invest 2015
264
10

Characteristics of disorders associated with genetic mutations of surfactant protein C.
Guillaume Thouvenin, Rola Abou Taam, Florence Flamein, Loïc Guillot, Muriel Le Bourgeois, Philippe Reix, Mickael Fayon, François Counil, Ulrika Depontbriand, Delphine Feldmann,[...]. Arch Dis Child 2010
69
14

Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis.
Caroline Kannengiesser, Raphael Borie, Christelle Ménard, Marion Réocreux, Patrick Nitschké, Steven Gazal, Hervé Mal, Camille Taillé, Jacques Cadranel, Hilario Nunes,[...]. Eur Respir J 2015
86
11


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.