A citation-based method for searching scientific literature

Sergey Shulenin, Lawrence M Nogee, Tarmo Annilo, Susan E Wert, Jeffrey A Whitsett, Michael Dean. N Engl J Med 2004
Times Cited: 418







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



Times Cited
  Times     Co-cited
Similarity


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
89
40

ABCA3 mutations associated with pediatric interstitial lung disease.
Janine E Bullard, Susan E Wert, Jeffrey A Whitsett, Michael Dean, Lawrence M Nogee. Am J Respir Crit Care Med 2005
193
33

ABCA3 as a lipid transporter in pulmonary surfactant biogenesis.
Nobuhiro Ban, Yoshihiro Matsumura, Hiromichi Sakai, Yasukazu Takanezawa, Mayumi Sasaki, Hiroyuki Arai, Nobuya Inagaki. J Biol Chem 2007
147
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
580
26

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
52
50

Clinical, radiological and pathological features of ABCA3 mutations in children.
M L Doan, R P Guillerman, M K Dishop, L M Nogee, C Langston, G B Mallory, M M Sockrider, L L Fan. Thorax 2008
126
23

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
480
22

Alteration of the pulmonary surfactant system in full-term infants with hereditary ABCA3 deficiency.
Frank Brasch, Sven Schimanski, Christian Mühlfeld, Stefan Barlage, Thomas Langmann, Charalampos Aslanidis, Alfred Boettcher, Ashraf Dada, Horst Schroten, Eva Mildenberger,[...]. Am J Respir Crit Care Med 2006
103
22

Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome.
Jennifer A Wambach, Daniel J Wegner, Kelcey Depass, Hillary Heins, Todd E Druley, Robi D Mitra, Ping An, Qunyuan Zhang, Lawrence M Nogee, F Sessions Cole,[...]. Pediatrics 2012
53
39

ABCA3 is critical for lamellar body biogenesis in vivo.
Naeun Cheong, Huayan Zhang, Muniswamy Madesh, Ming Zhao, Kevin Yu, Chandra Dodia, Aron B Fisher, Rashmin C Savani, Henry Shuman. J Biol Chem 2007
100
21

ABCA3 is a lamellar body membrane protein in human lung alveolar type II cells.
G Yamano, H Funahashi, O Kawanami, L X Zhao, N Ban, Y Uchida, T Morohoshi, J Ogawa, S Shioda, N Inagaki. FEBS Lett 2001
201
19

The biology of the ABCA3 lipid transporter in lung health and disease.
Michael F Beers, Surafel Mulugeta. Cell Tissue Res 2017
41
46

Functional and trafficking defects in ATP binding cassette A3 mutants associated with respiratory distress syndrome.
Naeun Cheong, Muniswamy Madesh, Linda W Gonzales, Ming Zhao, Kevin Yu, Philip L Ballard, Henry Shuman. J Biol Chem 2006
141
17

Molecular and cellular characteristics of ABCA3 mutations associated with diffuse parenchymal lung diseases in children.
Florence Flamein, Laure Riffault, Céline Muselet-Charlier, Julie Pernelle, Delphine Feldmann, Laurence Jonard, Anne-Marie Durand-Schneider, Aurore Coulomb, Michèle Maurice, Lawrence M Nogee,[...]. Hum Mol Genet 2012
57
29

Characterization and classification of ATP-binding cassette transporter ABCA3 mutants in fatal surfactant deficiency.
Yoshihiro Matsumura, Nobuhiro Ban, Kazumitsu Ueda, Nobuya Inagaki. J Biol Chem 2006
77
22

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
201
16

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
82
19

ABCA3 inactivation in mice causes respiratory failure, loss of pulmonary surfactant, and depletion of lung phosphatidylglycerol.
Michael L Fitzgerald, Ramnik Xavier, Kathleen J Haley, Ruth Welti, Julie L Goss, Cari E Brown, Debbie Z Zhuang, Susan A Bell, Naifang Lu, Mary McKee,[...]. J Lipid Res 2007
109
16

Genetic disorders of surfactant dysfunction.
Susan E Wert, Jeffrey A Whitsett, Lawrence M Nogee. Pediatr Dev Pathol 2009
134
16

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
25

Functional Characterization of ATP-Binding Cassette Transporter A3 Mutations from Infants with Respiratory Distress Syndrome.
Jennifer A Wambach, Ping Yang, Daniel J Wegner, Hillary B Heins, Lyudmila N Kaliberova, Sergey A Kaliberov, David T Curiel, Frances V White, Aaron Hamvas, Brian P Hackett,[...]. Am J Respir Cell Mol Biol 2016
24
66

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
261
14

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
96
14

Outcomes of Lung Transplantation for Infants and Children with Genetic Disorders of Surfactant Metabolism.
Whitney B Eldridge, Qunyuan Zhang, Albert Faro, Stuart C Sweet, Pirooz Eghtesady, Aaron Hamvas, F Sessions Cole, Jennifer A Wambach. J Pediatr 2017
30
46

Population and disease-based prevalence of the common mutations associated with surfactant deficiency.
Tami H Garmany, Jennifer A Wambach, Hillary B Heins, Julie M Watkins-Torry, Daniel J Wegner, Kate Bennet, Ping An, Garland Land, Ola D Saugstad, Howard Henderson,[...]. Pediatr Res 2008
54
24

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
13


Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
13

Diseases of pulmonary surfactant homeostasis.
Jeffrey A Whitsett, Susan E Wert, Timothy E Weaver. Annu Rev Pathol 2015
112
12

Identification of LBM180, a lamellar body limiting membrane protein of alveolar type II cells, as the ABC transporter protein ABCA3.
Surafel Mulugeta, Joseph M Gray, Kathleen L Notarfrancesco, Linda W Gonzales, Michael Koval, Sheldon I Feinstein, Philip L Ballard, Aron B Fisher, Henry Shuman. J Biol Chem 2002
148
12

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
289
12

ABCA3 missense mutations causing surfactant dysfunction disorders have distinct cellular phenotypes.
Ulrike Schindlbeck, Thomas Wittmann, Stefanie Höppner, Susanna Kinting, Gerhard Liebisch, Jan Hegermann, Matthias Griese. Hum Mutat 2018
12
100

Surfactant composition and function in patients with ABCA3 mutations.
Tami H Garmany, Michael A Moxley, Frances V White, Michael Dean, William M Hull, Jeffrey A Whitsett, Lawrence M Nogee, Aaron Hamvas. Pediatr Res 2006
78
14

Conditional deletion of Abca3 in alveolar type II cells alters surfactant homeostasis in newborn and adult mice.
Valérie Besnard, Yohei Matsuzaki, Jean Clark, Yan Xu, Susan E Wert, Machiko Ikegami, Mildred T Stahlman, Timothy E Weaver, Alan N Hunt, Anthony D Postle,[...]. Am J Physiol Lung Cell Mol Physiol 2010
42
26

Some ABCA3 mutations elevate ER stress and initiate apoptosis of lung epithelial cells.
Nina Weichert, Eva Kaltenborn, Andreas Hector, Markus Woischnik, Andrea Schams, Andreas Holzinger, Sunčana Kern, Matthias Griese. Respir Res 2011
64
17

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
43
25

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
179
10

Genetic testing in children with surfactant dysfunction.
Simona Turcu, Emma Ashton, Lucy Jenkins, Atul Gupta, Quen Mok. Arch Dis Child 2013
38
26

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
47
21

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
287
10

Unexplained neonatal respiratory distress due to congenital surfactant deficiency.
Marco Somaschini, Lawrence M Nogee, Isabella Sassi, Olivier Danhaive, Silvia Presi, Renata Boldrini, Cristina Montrasio, Maurizio Ferrari, Susan E Wert, Paola Carrera. J Pediatr 2007
47
21

Functional rescue of misfolding ABCA3 mutations by small molecular correctors.
Susanna Kinting, Stefanie Höppner, Ulrike Schindlbeck, Maria E Forstner, Jacqueline Harfst, Thomas Wittmann, Matthias Griese. Hum Mol Genet 2018
15
66

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
45
20


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
49
18

Genetic Basis of Children's Interstitial Lung Disease.
Lawrence M Nogee. Pediatr Allergy Immunol Pulmonol 2010
42
21

Natural history of five children with surfactant protein C mutations and interstitial lung disease.
Avraham Avital, Avigdor Hevroni, Simon Godfrey, Shlomo Cohen, Channa Maayan, Samir Nusair, Lawrence M Nogee, Chaim Springer. Pediatr Pulmonol 2014
38
23

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
106
9


Ultrastructure of lamellar bodies in congenital surfactant deficiency.
V Edwards, E Cutz, S Viero, A M Moore, L Nogee. Ultrastruct Pathol 2005
47
19


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.