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



Jonathan K Alder, Vidya Sagar Hanumanthu, Margaret A Strong, Amy E DeZern, Susan E Stanley, Clifford M Takemoto, Ludmila Danilova, Carolyn D Applegate, Stephen G Bolton, David W Mohr, Robert A Brodsky, James F Casella, Carol W Greider, J Brooks Jackson, Mary Armanios. Proc Natl Acad Sci U S A 2018
Times Cited: 67




List of shared articles



Times cited

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

Regulation of human telomerase in homeostasis and disease.
Caitlin M Roake, Steven E Artandi. Nat Rev Mol Cell Biol 2020
39

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

Synonymous Mutation in DKC1 Causes Telomerase RNA Insufficiency Manifesting as Familial Pulmonary Fibrosis.
Valeriya Gaysinskaya, Susan E Stanley, Soheir Adam, Mary Armanios. Chest 2020
2


Determinants of telomere length across human tissues.
Kathryn Demanelis, Farzana Jasmine, Lin S Chen, Meytal Chernoff, Lin Tong, Dayana Delgado, Chenan Zhang, Justin Shinkle, Mekala Sabarinathan, Hannah Lin,[...]. Science 2020
30

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

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

Understanding the evolving phenotype of vascular complications in telomere biology disorders.
Cecilia Higgs, Yanick J Crow, Denise M Adams, Emmanuel Chang, Don Hayes, Utz Herbig, James N Huang, Ryan Himes, Kunal Jajoo, F Brad Johnson,[...]. Angiogenesis 2019
24

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

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

Telomere Abnormalities in the Pathobiology of Idiopathic Pulmonary Fibrosis.
Hasancan Bilgili, Adam J Białas, Paweł Górski, Wojciech J Piotrowski. J Clin Med 2019
8

GDF15 is an epithelial-derived biomarker of idiopathic pulmonary fibrosis.
Yingze Zhang, Mao Jiang, Mehdi Nouraie, Mark G Roth, Tracy Tabib, Spencer Winters, Xiaoping Chen, John Sembrat, Yanxia Chu, Nayra Cardenes,[...]. Am J Physiol Lung Cell Mol Physiol 2019
17

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


ZCCHC8, the nuclear exosome targeting component, is mutated in familial pulmonary fibrosis and is required for telomerase RNA maturation.
Dustin L Gable, Valeriya Gaysinskaya, Christine C Atik, C Conover Talbot, Byunghak Kang, Susan E Stanley, Elizabeth W Pugh, Nuria Amat-Codina, Kara M Schenk, Murat O Arcasoy,[...]. Genes Dev 2019
27