A citation-based method for searching scientific literature

Bridget D Stuart, Jungmin Choi, Samir Zaidi, Chao Xing, Brody Holohan, Rui Chen, Mihwa Choi, Pooja Dharwadkar, Fernando Torres, Carlos E Girod, Jonathan Weissler, John Fitzgerald, Corey Kershaw, Julia Klesney-Tait, Yolanda Mageto, Jerry W Shay, Weizhen Ji, Kaya Bilguvar, Shrikant Mane, Richard P Lifton, Christine Kim Garcia. Nat Genet 2015
Times Cited: 230



Caroline Kannengiesser, Raphael Borie, Christelle Ménard, Marion Réocreux, Patrick Nitschké, Steven Gazal, Hervé Mal, Camille Taillé, Jacques Cadranel, Hilario Nunes, Dominique Valeyre, Jean François Cordier, Isabelle Callebaut, Catherine Boileau, Vincent Cottin, Bernard Grandchamp, Patrick Revy, Bruno Crestani. Eur Respir J 2015
Times Cited: 85




List of shared articles



Times cited

Whole-exome sequencing identifies susceptibility genes and pathways for idiopathic pulmonary fibrosis in the Chinese population.
Chuling Fang, Hui Huang, Yujia Feng, Qian Zhang, Na Wang, Xiaoyan Jing, Jian Guo, Martin Ferianc, Zuojun Xu. Sci Rep 2021
1


Telomeres in Interstitial Lung Disease.
Carmel J W Stock, Elisabetta A Renzoni. J Clin Med 2021
0

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
40

NHP2 deficiency impairs rRNA biogenesis and causes pulmonary fibrosis and Høyeraal-Hreidarsson syndrome.
Maname Benyelles, Marie-Françoise O'Donohue, Laëtitia Kermasson, Elodie Lainey, Raphael Borie, Chantal Lagresle-Peyrou, Hilario Nunes, Clarisse Cazelles, Cécile Fourrage, Emmanuelle Ollivier,[...]. Hum Mol Genet 2020
6

Alveolar Epithelial Type II Cells as Drivers of Lung Fibrosis in Idiopathic Pulmonary Fibrosis.
Tanyalak Parimon, Changfu Yao, Barry R Stripp, Paul W Noble, Peter Chen. Int J Mol Sci 2020
28

Familial Interstitial Lung Disease.
Jonathan A Kropski. Semin Respir Crit Care Med 2020
1

Impact of genetic factors on fibrosing interstitial lung diseases. Incidence and clinical presentation in adults.
Raphael Borie, Caroline Kannengiesser, Clairelyne Dupin, Marie-Pierre Debray, Aurélie Cazes, Bruno Crestani. Presse Med 2020
1

Telomere biology disorder prevalence and phenotypes in adults with familial hematologic and/or pulmonary presentations.
Simone Feurstein, Ayodeji Adegunsoye, Danijela Mojsilovic, Rekha Vij, Allison H West DePersia, Padma Sheila Rajagopal, Afaf Osman, Robert H Collins, Raymond H Kim, Steven D Gore,[...]. Blood Adv 2020
1

DNA helicases and their roles in cancer.
Srijita Dhar, Arindam Datta, Robert M Brosh. DNA Repair (Amst) 2020
2

Extrahematopoietic manifestations of the short telomere syndromes.
Kristen E Schratz. Hematology Am Soc Hematol Educ Program 2020
0

Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing.
Elodie Girard, Séverine Eon-Marchais, Robert Olaso, Anne-Laure Renault, Francesca Damiola, Marie-Gabrielle Dondon, Laure Barjhoux, Didier Goidin, Vincent Meyer, Dorothée Le Gal,[...]. Int J Cancer 2019
18

Regulator of telomere length 1 (RTEL1) mutations are associated with heterogeneous pulmonary and extra-pulmonary phenotypes.
Raphael Borie, Diane Bouvry, Vincent Cottin, Clement Gauvain, Aurélie Cazes, Marie-Pierre Debray, Jacques Cadranel, Philippe Dieude, Tristan Degot, Stephane Dominique,[...]. Eur Respir J 2019
15

Existing and emerging biomarkers for disease progression in idiopathic pulmonary fibrosis.
Riccardo Inchingolo, Francesco Varone, Giacomo Sgalla, Luca Richeldi. Expert Rev Respir Med 2019
10

Telomere Length and Use of Immunosuppressive Medications in Idiopathic Pulmonary Fibrosis.
Chad A Newton, David Zhang, Justin M Oldham, Julia Kozlitina, Shwu-Fan Ma, Fernando J Martinez, Ganesh Raghu, Imre Noth, Christine Kim Garcia. Am J Respir Crit Care Med 2019
30

Telomere length and genetic variant associations with interstitial lung disease progression and survival.
Chad A Newton, Justin M Oldham, Brett Ley, Vikram Anand, Ayodeji Adegunsoye, Gabrielle Liu, Kiran Batra, Jose Torrealba, Julia Kozlitina, Craig Glazer,[...]. Eur Respir J 2019
42

Progress in Understanding and Treating Idiopathic Pulmonary Fibrosis.
Jonathan A Kropski, Timothy S Blackwell. Annu Rev Med 2019
27

Translational research in pulmonary fibrosis.
Susan K Mathai, David A Schwartz. Transl Res 2019
5

A novel germline mutation of the SFTPA1 gene in familial interstitial pneumonia.
Martina Doubková, Kateřina Staňo Kozubík, Lenka Radová, Michaela Pešová, Jakub Trizuljak, Karol Pál, Klára Svobodová, Kamila Réblová, Hana Svozilová, Zuzana Vrzalová,[...]. Hum Genome Var 2019
6

Lung Transplant Outcomes in Patients With Pulmonary Fibrosis With Telomere-Related Gene Variants.
Aparna C Swaminathan, Megan L Neely, Courtney W Frankel, Fran L Kelly, Slavé Petrovski, Michael T Durheim, Erika Bush, Laurie Snyder, David B Goldstein, Jamie L Todd,[...]. Chest 2019
17

Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes.
Elena G Arias-Salgado, Eva Galvez, Lurdes Planas-Cerezales, Laura Pintado-Berninches, Elena Vallespin, Pilar Martinez, Jaime Carrillo, Laura Iarriccio, Anna Ruiz-Llobet, Albert Catalá,[...]. Orphanet J Rare Dis 2019
7

Fatal Acute Exacerbation of Familial Interstitial Pneumonia Complicated with Dyskeratosis Congenita after Influenza Virus B Infection.
Takashi Tachiwada, Keishi Oda, Masahiro Tahara, Konomi Sennari, Kazuki Nemoto, Shingo Noguchi, Toshinori Kawanami, Takashi Kido, Hiroki Yamaguchi, Kazuhiro Yatera. Intern Med 2019
0

Rare Protein-Altering Telomere-related Gene Variants in Patients with Chronic Hypersensitivity Pneumonitis.
Brett Ley, Dara G Torgerson, Justin M Oldham, Ayodeji Adegunsoye, Shuo Liu, Jie Li, Brett M Elicker, Travis S Henry, Jeffrey A Golden, Kirk D Jones,[...]. Am J Respir Crit Care Med 2019
28

From incomplete penetrance with normal telomere length to severe disease and telomere shortening in a family with monoallelic and biallelic PARN pathogenic variants.
Lois M Dodson, Alessandro Baldan, Mikael Nissbeck, Sethu M R Gunja, Penelope E Bonnen, Geraldine Aubert, Sherri Birchansky, Anders Virtanen, Alison A Bertuch. Hum Mutat 2019
6