A citation-based method for searching scientific literature

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, Julia Powers, Elissa Murphy, Lana M Olson, Leena Choi, Dong-Sheng Cheng, Elizabeth Marchani Blue, Lisa R Young, Lisa H Lancaster, Mark P Steele, Kevin K Brown, Marvin I Schwarz, Tasha E Fingerlin, David A Schwartz, William E Lawson, James E Loyd, Zhongming Zhao, John A Phillips, Timothy S Blackwell. Am J Respir Crit Care Med 2015
Times Cited: 107







List of co-cited articles
1029 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
807
78

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
243
78

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
564
63

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
93
58

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
465
50

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
612
49

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
87
56

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
416
47

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
59

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
43

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
306
42

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
288
40

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
319
37

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
268
34

Telomere lengths, pulmonary fibrosis and telomerase (TERT) mutations.
Alberto Diaz de Leon, Jennifer T Cronkhite, Anna-Luise A Katzenstein, J David Godwin, Ganesh Raghu, Craig S Glazer, Randall L Rosenblatt, Carlos E Girod, Edward R Garrity, Chao Xing,[...]. PLoS One 2010
214
34

Lung transplantation in telomerase mutation carriers with pulmonary fibrosis.
Leann L Silhan, Pali D Shah, Daniel C Chambers, Laurie D Snyder, Gerdt C Riise, Christa L Wagner, Eva Hellström-Lindberg, Jonathan B Orens, Juliette F Mewton, Sonye K Danoff,[...]. Eur Respir J 2014
103
32

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
31

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
30

Effect of telomere length on survival in patients with idiopathic pulmonary fibrosis: an observational cohort study with independent validation.
Bridget D Stuart, Joyce S Lee, Julia Kozlitina, Imre Noth, Megan S Devine, Craig S Glazer, Fernando Torres, Vaidehi Kaza, Carlos E Girod, Kirk D Jones,[...]. Lancet Respir Med 2014
145
30

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
29

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
170
29

A mutation in the surfactant protein C gene associated with familial interstitial lung disease.
L M Nogee, A E Dunbar, S E Wert, F Askin, A Hamvas, J A Whitsett. N Engl J Med 2001
579
29

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
29

Clinical and pathologic features of familial interstitial pneumonia.
Mark P Steele, Marcy C Speer, James E Loyd, Kevin K Brown, Aretha Herron, Susan H Slifer, Lauranell H Burch, Momen M Wahidi, John A Phillips, Thomas A Sporn,[...]. Am J Respir Crit Care Med 2005
260
27

Telomere phenotypes in females with heterozygous mutations in the dyskeratosis congenita 1 (DKC1) gene.
Jonathan K Alder, Erin M Parry, Srinivasan Yegnasubramanian, Christa L Wagner, Lawrence M Lieblich, Robert Auerbach, Arleen D Auerbach, Sarah J Wheelan, Mary Armanios. Hum Mutat 2013
58
44

MUC5B promoter polymorphism and interstitial lung abnormalities.
Gary M Hunninghake, Hiroto Hatabu, Yuka Okajima, Wei Gao, Josée Dupuis, Jeanne C Latourelle, Mizuki Nishino, Tetsuro Araki, Oscar E Zazueta, Sila Kurugol,[...]. N Engl J Med 2013
232
25

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
135
25

Loss-of-function mutations in the RNA biogenesis factor NAF1 predispose to pulmonary fibrosis-emphysema.
Susan E Stanley, Dustin L Gable, Christa L Wagner, Thomas M Carlile, Vidya Sagar Hanumanthu, Joshua D Podlevsky, Sara E Khalil, Amy E DeZern, Maria F Rojas-Duran, Carolyn D Applegate,[...]. Sci Transl Med 2016
100
25

An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis.
Slavé Petrovski, Jamie L Todd, Michael T Durheim, Quanli Wang, Jason W Chien, Fran L Kelly, Courtney Frankel, Caroline M Mebane, Zhong Ren, Joshua Bridgers,[...]. Am J Respir Crit Care Med 2017
97
25

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
424
24

Extensive phenotyping of individuals at risk for familial interstitial pneumonia reveals clues to the pathogenesis of interstitial lung disease.
Jonathan A Kropski, Jason M Pritchett, Donald F Zoz, Peter F Crossno, Cheryl Markin, Errine T Garnett, Amber L Degryse, Daphne B Mitchell, Vasiliy V Polosukhin, Otis B Rickman,[...]. Am J Respir Crit Care Med 2015
93
24

The MUC5B variant is associated with idiopathic pulmonary fibrosis but not with systemic sclerosis interstitial lung disease in the European Caucasian population.
Raphael Borie, Bruno Crestani, Philippe Dieude, Hilario Nunes, Yannick Allanore, Caroline Kannengiesser, Paolo Airo, Marco Matucci-Cerinic, Benoit Wallaert, Dominique Israel-Biet,[...]. PLoS One 2013
102
22

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
22

Mucin 5B promoter polymorphism is associated with idiopathic pulmonary fibrosis but not with development of lung fibrosis in systemic sclerosis or sarcoidosis.
Carmel J Stock, Hiroe Sato, Carmen Fonseca, Winston A S Banya, Philip L Molyneaux, Huzaifa Adamali, Anne-Marie Russell, Christopher P Denton, David J Abraham, David M Hansell,[...]. Thorax 2013
135
22

The telomere syndromes.
Mary Armanios, Elizabeth H Blackburn. Nat Rev Genet 2012
568
22

The MUC5B promoter polymorphism is associated with idiopathic pulmonary fibrosis in a Mexican cohort but is rare among Asian ancestries.
Anna L Peljto, Moises Selman, Dong Soon Kim, Elissa Murphy, Laura Tucker, Annie Pardo, Jung Su Lee, Wonjun Ji, Marvin I Schwarz, Ivana V Yang,[...]. Chest 2015
56
37

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
21

Constitutional mutations in RTEL1 cause severe dyskeratosis congenita.
Amanda J Walne, Tom Vulliamy, Michael Kirwan, Vincent Plagnol, Inderjeet Dokal. Am J Hum Genet 2013
133
20

MUC5B promoter polymorphism in Japanese patients with idiopathic pulmonary fibrosis.
Yasushi Horimasu, Shinichiro Ohshimo, Francesco Bonella, Sonosuke Tanaka, Nobuhisa Ishikawa, Noboru Hattori, Nobuoki Kohno, Josune Guzman, Ulrich Costabel. Respirology 2015
66
30

A variant in the promoter of MUC5B and idiopathic pulmonary fibrosis.
Yingze Zhang, Imre Noth, Joe G N Garcia, Naftali Kaminski. N Engl J Med 2011
136
20

Severe hematologic complications after lung transplantation in patients with telomerase complex mutations.
Raphael Borie, Caroline Kannengiesser, Sandrine Hirschi, Jérôme Le Pavec, Hervé Mal, Emmanuel Bergot, Stéphane Jouneau, Jean-Marc Naccache, Patrick Revy, David Boutboul,[...]. J Heart Lung Transplant 2015
62
30

TOLLIP, MUC5B, and the Response to N-Acetylcysteine among Individuals with Idiopathic Pulmonary Fibrosis.
Justin M Oldham, Shwu-Fan Ma, Fernando J Martinez, Kevin J Anstrom, Ganesh Raghu, David A Schwartz, Eleanor Valenzi, Leah Witt, Cathryn Lee, Rekha Vij,[...]. Am J Respir Crit Care Med 2015
156
19

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
286
18


A large kindred of pulmonary fibrosis associated with a novel ABCA3 gene variant.
Ilaria Campo, Michele Zorzetto, Francesca Mariani, Zamir Kadija, Patrizia Morbini, Roberto Dore, Eva Kaltenborn, Sabrina Frixel, Ralf Zarbock, Gerhard Liebisch,[...]. Respir Res 2014
64
28

Syndrome complex of bone marrow failure and pulmonary fibrosis predicts germline defects in telomerase.
Erin M Parry, Jonathan K Alder, Xiaodong Qi, Julian J-L Chen, Mary Armanios. Blood 2011
101
18

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
28

Telomerase mutations in smokers with severe emphysema.
Susan E Stanley, Julian J L Chen, Joshua D Podlevsky, Jonathan K Alder, Nadia N Hansel, Rasika A Mathias, Xiaodong Qi, Nicholas M Rafaels, Robert A Wise, Edwin K Silverman,[...]. J Clin Invest 2015
102
17

Human RTEL1 deficiency causes Hoyeraal-Hreidarsson syndrome with short telomeres and genome instability.
Tangui Le Guen, Laurent Jullien, Fabien Touzot, Michael Schertzer, Laetitia Gaillard, Mylène Perderiset, Wassila Carpentier, Patrick Nitschke, Capucine Picard, Gérard Couillault,[...]. Hum Mol Genet 2013
101
17

Poly(A)-specific ribonuclease deficiency impacts telomere biology and causes dyskeratosis congenita.
Hemanth Tummala, Amanda Walne, Laura Collopy, Shirleny Cardoso, Josu de la Fuente, Sarah Lawson, James Powell, Nicola Cooper, Alison Foster, Shehla Mohammed,[...]. J Clin Invest 2015
107
17


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.