A citation-based method for searching scientific literature

Martina Doubková, Kateřina Staňo Kozubík, Lenka Radová, Michaela Pešová, Jakub Trizuljak, Karol Pál, Klára Svobodová, Kamila Réblová, Hana Svozilová, Zuzana Vrzalová, Šárka Pospíšilová, Michael Doubek. Hum Genome Var 2019
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


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
282
85

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
57
71

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
39
71

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
63
71

A homozygous SFTPA1 mutation drives necroptosis of type II alveolar epithelial cells in patients with idiopathic pulmonary fibrosis.
Akio Takezaki, Shin-Ichi Tsukumo, Yasuhiro Setoguchi, Julie G Ledford, Hisatsugu Goto, Kazuyoshi Hosomichi, Hisanori Uehara, Yasuhiko Nishioka, Koji Yasutomo. J Exp Med 2019
16
71

Idiopathic Pulmonary Fibrosis.
David J Lederer, Fernando J Martinez. N Engl J Med 2018
382
57

An official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancy.
Geoffrey Kurland, Robin R Deterding, James S Hagood, Lisa R Young, Alan S Brody, Robert G Castile, Sharon Dell, Leland L Fan, Aaron Hamvas, Bettina C Hilman,[...]. Am J Respir Crit Care Med 2013
189
57

Combined pulmonary fibrosis and emphysema syndrome associated with ABCA3 mutations.
Ralph Epaud, Céline Delestrain, Malek Louha, Stéphanie Simon, Pascale Fanen, Abdellatif Tazi. Eur Respir J 2014
41
57

Sequencing of idiopathic pulmonary fibrosis-related genes reveals independent single gene associations.
Meghan A Coghlan, Adrian Shifren, Howard J Huang, Tonya D Russell, Robi D Mitra, Qunyuan Zhang, Daniel J Wegner, F Sessions Cole, Aaron Hamvas. BMJ Open Respir Res 2014
45
57

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
172
57

Genetic causes and clinical management of pediatric interstitial lung diseases.
Nadia Nathan, Keren Borensztajn, Annick Clement. Curr Opin Pulm Med 2018
14
57

Heterogeneity of lung disease associated with NK2 homeobox 1 mutations.
Elodie Nattes, Stephanie Lejeune, Ania Carsin, Raphael Borie, Isabelle Gibertini, Juan Balinotti, Nadia Nathan, Sylvain Marchand-Adam, Caroline Thumerelle, Brigitte Fauroux,[...]. Respir Med 2017
23
57

Lung disease caused by ABCA3 mutations.
Carolin Kröner, Thomas Wittmann, Simone Reu, Veronika Teusch, Mathias Klemme, Daniela Rauch, Meike Hengst, Matthias Kappler, Nazan Cobanoglu, Tugba Sismanlar,[...]. Thorax 2017
48
42

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
415
42

Diffuse lung disease in young children: application of a novel classification scheme.
Gail H Deutsch, Lisa R Young, Robin R Deterding, Leland L Fan, Sharon D Dell, Judy A Bean, Alan S Brody, Lawrence M Nogee, Bruce C Trapnell, Claire Langston,[...]. Am J Respir Crit Care Med 2007
254
42

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
42

COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis.
Levi B Watkin, Birthe Jessen, Wojciech Wiszniewski, Timothy J Vece, Max Jan, Youbao Sha, Maike Thamsen, Regie L P Santos-Cortez, Kwanghyuk Lee, Tomasz Gambin,[...]. Nat Genet 2015
132
42

Combined pulmonary fibrosis and emphysema syndrome associated with familial SFTPC mutation.
Vincent Cottin, Philippe Reix, Chahéra Khouatra, Françoise Thivolet-Béjui, Delphine Feldmann, Jean-François Cordier. Thorax 2011
60
42

IPF, comorbidities and management implications.
Carlo Vancheri, Vincent Cottin, Michael Kreuter, Ole Hilberg. Sarcoidosis Vasc Diffuse Lung Dis 2015
19
42

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
996
42

Familial interstitial disease with I73T mutation: A mid- and long-term study.
Rola Abou Taam, Francis Jaubert, Sophie Emond, Muriel Le Bourgeois, Ralph Epaud, Chantal Karila, Delphine Feldmann, Pierre Scheinmann, Jacques de Blic. Pediatr Pulmonol 2009
44
42

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
165
42

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
52
42

European protocols for the diagnosis and initial treatment of interstitial lung disease in children.
Andrew Bush, Steve Cunningham, Jacques de Blic, Angelo Barbato, Annick Clement, Ralph Epaud, Meike Hengst, Nural Kiper, Andrew G Nicholson, Martin Wetzke,[...]. Thorax 2015
93
42

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
791
42

Biomarkers in Interstitial lung diseases.
Nadia Nathan, Harriet Corvol, Serge Amselem, Annick Clement. Paediatr Respir Rev 2015
13
42

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
42

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
587
42

Genetic studies provide clues on the pathogenesis of idiopathic pulmonary fibrosis.
Jonathan A Kropski, William E Lawson, Lisa R Young, Timothy S Blackwell. Dis Model Mech 2013
87
42

Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis.
Richard J Allen, Beatriz Guillen-Guio, Justin M Oldham, Shwu-Fan Ma, Amy Dressen, Megan L Paynton, Luke M Kraven, Ma'en Obeidat, Xuan Li, Michael Ng,[...]. Am J Respir Crit Care Med 2020
46
42

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
42

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
125
42

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
414
42

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
88
42

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
169
42

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
235
42

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
403
42

A non-BRICHOS SFTPC mutant (SP-CI73T) linked to interstitial lung disease promotes a late block in macroautophagy disrupting cellular proteostasis and mitophagy.
Arie Hawkins, Susan H Guttentag, Robin Deterding, William K Funkhouser, Jennifer L Goralski, Shampa Chatterjee, Surafel Mulugeta, Michael F Beers. Am J Physiol Lung Cell Mol Physiol 2015
46
42

Heterogeneous pulmonary phenotypes associated with mutations in the thyroid transcription factor gene NKX2-1.
Aaron Hamvas, Robin R Deterding, Susan E Wert, Frances V White, Megan K Dishop, Danielle N Alfano, Ann C Halbower, Benjamin Planer, Mark J Stephan, Derek A Uchida,[...]. Chest 2013
80
42

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
75
42

Persistent Lung Disease in Adults with NKX2.1 Mutation and Familial Neuroendocrine Cell Hyperplasia of Infancy.
Rebekah J Nevel, Errine T Garnett, John A Worrell, Ronald L Morton, Lawrence M Nogee, Timothy S Blackwell, Lisa R Young. Ann Am Thorac Soc 2016
18
42

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
566
42

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
68
42

Management of suspected monogenic lung fibrosis in a specialised centre.
Raphael Borie, Caroline Kannengiesser, Flore Sicre de Fontbrune, Laurent Gouya, Nadia Nathan, Bruno Crestani. Eur Respir Rev 2017
20
42

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
454
28

Alveolar surfactant homeostasis and the pathogenesis of pulmonary disease.
Jeffrey A Whitsett, Susan E Wert, Timothy E Weaver. Annu Rev Med 2010
230
28

Activated STING in a vascular and pulmonary syndrome.
Y Liu, A A Jesus, B Marrero, D Yang, S E Ramsey, G A Montealegre Sanchez, K Tenbrock, H Wittkowski, O Y Jones, H S Kuehn,[...]. N Engl J Med 2014
593
28

Interstitial lung diseases in children.
Annick Clement, Nadia Nathan, Ralph Epaud, Brigitte Fauroux, Harriet Corvol. Orphanet J Rare Dis 2010
66
28

Health-related quality of life in infants and children with interstitial lung disease.
Clara Lauby, Pierre-Yves Boelle, Rola Abou Taam, Katia Bessaci, Jacques Brouard, Marie-Laure Dalphin, Christophe Delacourt, Céline Delestrain, Antoine Deschildre, Jean-Christophe Dubus,[...]. Pediatr Pulmonol 2019
4
50

Chronic interstitial lung diseases in children: diagnosis approaches.
Nadia Nathan, Laura Berdah, Keren Borensztajn, Annick Clement. Expert Rev Respir Med 2018
5
40


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.