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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 12 (of 12 Records)

Query Trace: Pneumonia and TERT[original query]
Telomere shortening in familial and sporadic pulmonary fibrosis.
American journal of respiratory and critical care medicine 2008 Oct 178 (7): 729-37.
Cronkhite Jennifer T, Xing Chao, Raghu Ganesh, Chin Kelly M, Torres Fernando, Rosenblatt Randall L, Garcia Christine K
Telomere-related lung fibrosis is diagnostically heterogeneous but uniformly progressive.
The European respiratory journal 2016 Aug .
Newton Chad A, Batra Kiran, Torrealba Jose, Kozlitina Julia, Glazer Craig S, Aravena Carlos, Meyer Keith, Raghu Ganesh, Collard Harold R, Garcia Christine K
Prevalence and characteristics of TERT and TERC mutations in suspected genetic pulmonary fibrosis.
The European respiratory journal 2016 Dec 48 (6): 1721-1731.
Borie Raphael, Tabèze Laure, Thabut Gabriel, Nunes Hilario, Cottin Vincent, Marchand-Adam Sylvain, Prevot Grégoire, Tazi Abdellatif, Cadranel Jacques, Mal Herve, Wemeau-Stervinou Lidwine, Bergeron Lafaurie Anne, Israel-Biet Dominique, Picard Clement, Reynaud Gaubert Martine, Jouneau Stephane, Naccache Jean-Marc, Mankikian Julie, Ménard Christelle, Cordier Jean-François, Valeyre Dominique, Reocreux Marion, Grandchamp Bernard, Revy Patrick, Kannengiesser Caroline, Crestani Bru
Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis.
The European respiratory journal 2017 May 49 (5): .
Juge Pierre-Antoine, Borie Raphaël, Kannengiesser Caroline, Gazal Steven, Revy Patrick, Wemeau-Stervinou Lidwine, Debray Marie-Pierre, Ottaviani Sébastien, Marchand-Adam Sylvain, Nathan Nadia, Thabut Gabriel, Richez Christophe, Nunes Hilario, Callebaut Isabelle, Justet Aurélien, Leulliot Nicolas, Bonnefond Amélie, Salgado David, Richette Pascal, Desvignes Jean-Pierre, Lioté Huguette, Froguel Philippe, Allanore Yannick, Sand Olivier, Dromer Claire, Flipo René-Marc, Clément Annick, Béroud Christophe, Sibilia Jean, Coustet Baptiste, Cottin Vincent, Boissier Marie-Christophe, Wallaert Benoit, Schaeverbeke Thierry, Dastot le Moal Florence, Frazier Aline, Ménard Christelle, Soubrier Martin, Saidenberg Nathalie, Valeyre Dominique, Amselem Serge, , Boileau Catherine, Crestani Bruno, Dieudé Philip
An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis.
American journal of respiratory and critical care medicine 2017 07 196 (1): 82-93.
Petrovski Slavé, Todd Jamie L, Durheim Michael T, Wang Quanli, Chien Jason W, Kelly Fran L, Frankel Courtney, Mebane Caroline M, Ren Zhong, Bridgers Joshua, Urban Thomas J, Malone Colin D, Finlen Copeland Ashley, Brinkley Christie, Allen Andrew S, O'Riordan Thomas, McHutchison John G, Palmer Scott M, Goldstein David
IDIOPATHIC PULMONARY FIBROSIS IS A COMPLEX GENETIC DISORDER.
Transactions of the American Clinical and Climatological Association 2016 127 34-45.
Schwartz David
Regulator of telomere length 1 (RTEL1) mutations are associated with heterogeneous pulmonary and extra-pulmonary phenotypes.
The European respiratory journal 2018 12 53 (2): .
Borie Raphael, Bouvry Diane, Cottin Vincent, Gauvain Clement, Cazes Aurélie, Debray Marie-Pierre, Cadranel Jacques, Dieude Philippe, Degot Tristan, Dominique Stephane, Gamez Anne Sophie, Jaillet Madeleine, Juge Pierre-Antoine, Londono-Vallejo Arturo, Mailleux Arnaud, Mal Hervé, Boileau Catherine, Menard Christelle, Nunes Hilario, Prevot Gregoire, Quetant Sebastien, Revy Patrick, Traclet Julie, Wemeau-Stervinou Lidwine, Wislez Marie, Kannengiesser Caroline, Crestani Bru
MUC5B variant is associated with visually and quantitatively detected preclinical pulmonary fibrosis.
Thorax 2019 9 74 (12): 1131-1139.
Mathai Susan K, Humphries Stephen, Kropski Jonathan A, Blackwell Timothy S, Powers Julia, Walts Avram D, Markin Cheryl, Woodward Julia, Chung Jonathan H, Brown Kevin K, Steele Mark P, Loyd James E, Schwarz Marvin I, Fingerlin Tasha, Yang Ivana V, Lynch David A, Schwartz David
Integrating Genomics Into Management of Fibrotic Interstitial Lung Disease.
Chest 2019 1 155 (5): 1026-1040.
Adegunsoye Ayodeji, Vij Rekha, Noth Im
Pulmonary fibrosis in dyskeratosis congenita: a case report with a PRISMA-compliant systematic review.
BMC pulmonary medicine 2021 9 21 (1): 279.
Wang Ping, Xu Zuoj
Association of a Single Nucleotide Variant in TERT with Airway Disease in Japanese Rheumatoid Arthritis Patients.
Genes 2023 11 14 (11): .
Takashi Higuchi, Shomi Oka, Hiroshi Furukawa, Kota Shimada, Shinichiro Tsunoda, Satoshi Ito, Akira Okamoto, Misuzu Fujimori, Tadashi Nakamura, Masao Katayama, Koichiro Saisho, Satoshi Shinohara, Toshihiro Matsui, Kiyoshi Migita, Shouhei Nagaoka, Shigeto Toh
A cross-trait study of lung cancer and its related respiratory diseases based on large-scale exome sequencing population.
Translational lung cancer research 2024 4 13 (3): 512-525.
Yunke Jiang, Hongru Li, Zaiming Li, Sha Du, Ruyang Zhang, Yang Zhao, David C Christiani, Sipeng Shen, Feng Ch
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