Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 34 Records) |
| Query Trace: Disease and RTEL1[original query] |
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Identification of seven loci affecting mean telomere length and their association with disease.
Nature genetics 2013 Apr 45 (4): 422-7, 427e1-2. Codd Veryan, Nelson Christopher P, Albrecht Eva, Mangino Massimo, Deelen Joris, Buxton Jessica L, Hottenga Jouke Jan, Fischer Krista, Esko Tõnu, Surakka Ida, Broer Linda, Nyholt Dale R, Mateo Leach Irene, Salo Perttu, Hägg Sara, Matthews Mary K, Palmen Jutta, Norata Giuseppe D, O'Reilly Paul F, Saleheen Danish, Amin Najaf, Balmforth Anthony J, Beekman Marian, de Boer Rudolf A, Böhringer Stefan, Braund Peter S, Burton Paul R, de Craen Anton J M, Denniff Matthew, Dong Yanbin, Douroudis Konstantinos, Dubinina Elena, Eriksson Johan G, Garlaschelli Katia, Guo Dehuang, Hartikainen Anna-Liisa, Henders Anjali K, Houwing-Duistermaat Jeanine J, Kananen Laura, Karssen Lennart C, Kettunen Johannes, Klopp Norman, Lagou Vasiliki, van Leeuwen Elisabeth M, Madden Pamela A, Mägi Reedik, Magnusson Patrik K E, Männistö Satu, McCarthy Mark I, Medland Sarah E, Mihailov Evelin, Montgomery Grant W, Oostra Ben A, Palotie Aarno, Peters Annette, Pollard Helen, Pouta Anneli, Prokopenko Inga, Ripatti Samuli, Salomaa Veikko, Suchiman H Eka D, Valdes Ana M, Verweij Niek, Viñuela Ana, Wang Xiaoling, Wichmann H-Erich, Widen Elisabeth, Willemsen Gonneke, Wright Margaret J, Xia Kai, Xiao Xiangjun, van Veldhuisen Dirk J, Catapano Alberico L, Tobin Martin D, Hall Alistair S, Blakemore Alexandra I F, van Gilst Wiek H, Zhu Haidong, Consortium Cardiogram, Erdmann Jeanette, Reilly Muredach P, Kathiresan Sekar, Schunkert Heribert, Talmud Philippa J, Pedersen Nancy L, Perola Markus, Ouwehand Willem, Kaprio Jaakko, Martin Nicholas G, van Duijn Cornelia M, Hovatta Iiris, Gieger Christian, Metspalu Andres, Boomsma Dorret I, Jarvelin Marjo-Riitta, Slagboom P Eline, Thompson John R, Spector Tim D, van der Harst Pim, Samani Nilesh |
| Association between previously identified loci affecting telomere length and coronary heart disease (CHD) in Han Chinese population. Clinical interventions in aging 2014 9 857-61. Ding Hui, Yan Fen, Zhou Lin-Lin, Ji Xiu-Hai, Gu Xin-Nan, Tang Zhi-Wei, Chen Ru-H |
| Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening. Nature genetics 2015 May 47 (5): 512-7. Stuart Bridget D, Choi Jungmin, Zaidi Samir, Xing Chao, Holohan Brody, Chen Rui, Choi Mihwa, Dharwadkar Pooja, Torres Fernando, Girod Carlos E, Weissler Jonathan, Fitzgerald John, Kershaw Corey, Klesney-Tait Julia, Mageto Yolanda, Shay Jerry W, Ji Weizhen, Bilguvar Kaya, Mane Shrikant, Lifton Richard P, Garcia Christine K |
| Rare variants in RTEL1 are associated with familial interstitial pneumonia. American journal of respiratory and critical care medicine 2015 Mar 191 (6): 646-55. Cogan Joy D, Kropski Jonathan A, Zhao Min, Mitchell Daphne B, Rives Lynette, Markin Cheryl, Garnett Errine T, Montgomery Keri H, Mason Wendi R, McKean David F, Powers Julia, Murphy Elissa, Olson Lana M, Choi Leena, Cheng Dong-Sheng, Blue Elizabeth Marchani, Young Lisa R, Lancaster Lisa H, Steele Mark P, Brown Kevin K, Schwarz Marvin I, Fingerlin Tasha E, Schwartz David A, Lawson William E, Loyd James E, Zhao Zhongming, Phillips John A, Blackwell Timothy |
| 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 |
| Genetic Variation Associated with Longer Telomere Length Increases Risk of Chronic Lymphocytic Leukemia. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2016 May . Ojha Juhi, Codd Veryan, Nelson Christopher P, Samani Nilesh J, Smirnov Ivan V, Madsen Nils R, Hansen Helen M, de Smith Adam J, Bracci Paige M, Wiencke John K, Wrensch Margaret R, Wiemels Joseph L, Walsh Kyle |
| 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 |
| Association between RTEL1 gene polymorphisms and COPD susceptibility in a Chinese Han population. International journal of chronic obstructive pulmonary disease 2017 12 931-936. Ding Yipeng, Xu Heping, Yao Jinjian, Xu Dongchuan, He Ping, Yi Shengyang, Li Quanni, Liu Yuanshui, Wu Cibing, Tian Zhongj |
| Genome-wide association study of telomere length among South Asians identifies a second RTEL1 association signal.
Journal of medical genetics 2017 Nov . Delgado Dayana A, Zhang Chenan, Chen Lin S, Gao Jianjun, Roy Shantanu, Shinkle Justin, Sabarinathan Mekala, Argos Maria, Tong Lin, Ahmed Alauddin, Islam Tariqul, Rakibuz-Zaman Muhammad, Sarwar Golam, Shahriar Hasan, Rahman Mahfuzar, Yunus Mohammad, Jasmine Farzana, Kibriya Muhammad G, Ahsan Habibul, Pierce Brandon |
| 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 |
| Analysis of protein-altering variants in telomerase genes and their association with MUC5B common variant status in patients with idiopathic pulmonary fibrosis: a candidate gene sequencing study. The Lancet. Respiratory medicine 2018 Jun . Dressen Amy, Abbas Alexander R, Cabanski Christopher, Reeder Janina, Ramalingam Thirumalai R, Neighbors Margaret, Bhangale Tushar R, Brauer Matthew J, Hunkapiller Julie, Reeder Jens, Mukhyala Kiran, Cuenco Karen, Tom Jennifer, Cowgill Amy, Vogel Jan, Forrest William F, Collard Harold R, Wolters Paul J, Kropski Jonathan A, Lancaster Lisa H, Blackwell Timothy S, Arron Joseph R, Yaspan Brian |
| 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 |
| Heterozygous RTEL1 variants in bone marrow failure and myeloid neoplasms. Blood advances 2018 Jan 2 (1): 36-48. Marsh Judith C W, Gutierrez-Rodrigues Fernanda, Cooper James, Jiang Jie, Gandhi Shreyans, Kajigaya Sachiko, Feng Xingmin, Ibanez Maria Del Pilar F, Donaires Flávia S, Lopes da Silva João P, Li Zejuan, Das Soma, Ibanez Maria, Smith Alexander E, Lea Nicholas, Best Steven, Ireland Robin, Kulasekararaj Austin G, McLornan Donal P, Pagliuca Anthony, Callebaut Isabelle, Young Neal S, Calado Rodrigo T, Townsley Danielle M, Mufti Ghulam |
| Telomere length and aging-related outcomes in humans: A Mendelian randomization study in 261,000 older participants. Aging cell 2019 8 18 (6): e13017. Kuo Chia-Ling, Pilling Luke C, Kuchel George A, Ferrucci Luigi, Melzer Dav |
| Resequencing Study Confirms That Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis. American journal of respiratory and critical care medicine 2019 Apr . Moore Camille, Blumhagen Rachel Z, Yang Ivana V, Walts Avram, Powers Julie, Walker Tarik, Bishop Makenna, Russell Pamela, Vestal Brian, Cardwell Jonathan, Markin Cheryl R, Mathai Susan K, Schwarz Marvin I, Steele Mark P, Lee Joyce, Brown Kevin K, Loyd James E, Crapo James D, Silverman Edwin K, Cho Michael H, James Judith A, Guthridge Joel M, Cogan Joy D, Kropski Jonathan A, Swigris Jeffrey J, Bair Carol, Kim Dong Soon, Ji Wonjun, Kim Hocheol, Song Jin Woo, Maier Lisa A, Pacheco Karin A, Hirani Nikhil, Poon Azin S, Li Feng, Jenkins R Gisli, Braybrooke Rebecca, Saini Gauri, Maher Toby M, Molyneaux Philip L, Saunders Peter, Zhang Yingze, Gibson Kevin F, Kass Daniel J, Rojas Mauricio, Sembrat John, Wolters Paul J, Collard Harold R, Sundy John S, O'Riordan Thomas, Strek Mary E, Noth Imre, Ma Shwu-Fan, Porteous Mary K, Kreider Maryl E, Patel Namrata B, Inoue Yoshikazu, Hirose Masaki, Arai Toru, Akagawa Shinobu, Eickelberg Oliver, Fernandez Isis Enlil, Behr Jürgen, Mogulkoc Nesrin, Corte Tamera J, Glaspole Ian, Tomassetti Sara, Ravaglia Claudia, Poletti Venerino, Crestani Bruno, Borie Raphael, Kannengiesser Caroline, Parfrey Helen, Fiddler Christine, Rassl Doris, Molina-Molina Maria, Machahua Carlos, Worboys Ana Montes, Gudmundsson Gunnar, Isaksson Helgi J, Lederer David J, Podolanczuk Anna J, Montesi Sydney B, Bendstrup Elisabeth, Danchel Vivi, Selman Moises, Pardo Annie, Henry Michael T, Keane Michael P, Doran Peter, Vašáková Martina, Sterclova Martina, Ryerson Christopher J, Wilcox Pearce G, Okamoto Tsukasa, Furusawa Haruhiko, Miyazaki Yasunari, Laurent Geoffrey, Baltic Svetlana, Prele Cecilia, Moodley Yuben, Shea Barry S, Ohta Ken, Suzukawa Maho, Narumoto Osamu, Nathan Steven D, Venuto Drew C, Woldehanna Merte L, Kokturk Nurdan, de Andrade Joao A, Luckhardt Tracy, Kulkarni Tejaswini, Bonella Francesco, Donnelly Seamus C, McElroy Aoife, Armstong Michelle E, Aranda Alvaro, Carbone Roberto G, Puppo Francesco, Beckman Kenneth B, Nickerson Deborah A, Fingerlin Tasha E, Schwartz David |
| Lung Transplant Outcomes in Patients With Pulmonary Fibrosis With Telomere-Related Gene Variants. Chest 2019 4 156 (3): 477-485. Swaminathan Aparna C, Neely Megan L, Frankel Courtney W, Kelly Fran L, Petrovski Slavé, Durheim Michael T, Bush Erika, Snyder Laurie, Goldstein David B, Todd Jamie L, Palmer Scott |
| Telomerase Variants in Patients with Cirrhosis Awaiting Liver Transplantation. Hepatology (Baltimore, Md.) 2019 Feb . Chiu Victor, Hogen Rachel, Sher Linda, Wadé Niquelle, Conti David, Martynova Anastasia, Li Hongtao, Liang Gangning, O'Connell Cas |
| Genetic variants in RTEL1 influencing telomere length are associated with prostate cancer risk. Journal of Cancer 2019 10 (24): 6170-6174. Gu Cheng-Yuan, Jin Sheng-Ming, Qin Xiao-Jian, Zhu Yao, Bo Dai, Lin Guo-Wen, Shi Guo-Hai, Ye Ding-W |
| Genetic analysis of the relation of telomere length-related gene (RTEL1) and coronary heart disease risk. Molecular genetics & genomic medicine 2019 1 7 (3): e550. Lu Shijuan, Zhong Jianghua, Wu Miao, Huang Kang, Zhou Yilei, Zhong Zanrui, Li Qiang, Zhou Hongh |
| Exome Sequencing Analysis Identifies Rare Variants in ATM and RPL8 That Are Associated With Shorter Telomere Length. Frontiers in genetics 2020 11 337. van der Spek Ashley, Warner Sophie C, Broer Linda, Nelson Christopher P, Vojinovic Dina, Ahmad Shahzad, Arp Pascal P, Brouwer Rutger W W, Denniff Matthew, van den Hout Mirjam C G N, van Rooij Jeroen G J, Kraaij Robert, van IJcken Wilfred F J, Samani Nilesh J, Ikram M Arfan, Uitterlinden André G, Codd Veryan, Amin Najaf, van Duijn Cornelia |
| Determinants of survival after lung transplantation in telomerase-related gene mutation carriers: A retrospective cohort. American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons 2021 Dec . Phillips-Houlbracq Mathilde, Mal Hervé, Cottin Vincent, Gauvain Clément, Beier Fabian, Sicre de Fontbrune Flore, Sidali Sabrina, Mornex Jean François, Hirschi Sandrine, Roux Antoine, Weisenburger Gaelle, Roussel Arnaud, Wémeau-Stervinou Lidwine, Le Pavec Jérôme, Pison Christophe, Marchand Adam Sylvain, Froidure Antoine, Lazor Romain, Naccache Jean-Marc, Jouneau Stéphane, Nunes Hilario, Reynaud-Gaubert Martine, Le Borgne Aurélie, Boutboul David, Ba Ibrahima, Boileau Catherine, Crestani Bruno, Kannengiesser Caroline, Borie Raphaël, |
| [Telomeres and lung]. Revue des maladies respiratoires 2022 6 39 (7): 595-606. Guérin C, Crestani B, Dupin C, Kawano-Dourado L, Ba I, Kannengiesser C, Borie |
| Rare and Common Variants in KIF15 Contribute to Genetic Risk of Idiopathic Pulmonary Fibrosis. American journal of respiratory and critical care medicine 2022 4 206 (1): 56-69. Zhang David, Povysil Gundula, Kobeissy Philippe H, Li Qi, Wang Binhan, Amelotte Mason, Jaouadi Hager, Newton Chad A, Maher Toby M, Molyneaux Philip L, Noth Imre, Martinez Fernando J, Raghu Ganesh, Todd Jamie L, Palmer Scott M, Haefliger Carolina, Platt Adam, Petrovski Slavé, Garcia Joseph A, Goldstein David B, Garcia Christine K |
| Genotype-Phenotype Relationships in Inheritable Idiopathic Pulmonary Fibrosis: A Greek National Cohort Study. Respiration; international review of thoracic diseases 2022 1 101 (6): 531-543. Manali Effrosyni D, Kannengiesser Caroline, Borie Raphael, Ba Ibrahima, Bouros Demosthenes, Markopoulou Aikaterini, Antoniou Katerina, Kolilekas Lykourgos, Papaioannou Andriana I, Tzilas Vasileios, Tzouvelekis Argyrios, Daniil Zoe, Fouka Evangelia, Papakosta Despoina, Xyfteri Areti, Karakatsani Anna, Loukides Stylianos, Korbila Ioanna, Tomos Ioannis P, Konstantinidis Athanasios K, Gogali Athina, Steiropoulos Paschalis, Papanikolaou Ilias C, Bazaka Chrysa, Haritou Aggeliki, Vassilakopoulos Theodoros, Maniati Maria, Kagouridis Konstantinos, Markozannes Evangelos, Bouros Evangelos, Rampiadou Christina, Kounti Georgia, Trachalaki Athina, Dimeas Ilias, Karampitsakos Theodoros, Lyberopoulos Panagiotis, Malamadakis Nikolaos, Spyropoulou Sofia, Revy Patrick, Lainey Elodie, Dieudé Philippe, Rebah Khedidja, Ménard Christelle, Oudin Claire, Masson Cécile, Plessier Aurélie, Legendre Marie, Nathan Nadia, Coulomb-L'Hermine Aurore, Clement Annick, Amselem Serge, Boileau Catherine, Crestani Bruno, Papiris Spyros, |
| Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder. Respiratory research 2023 6 24 (1): 158. Laura Bergantini, Margherita Baldassarri, Miriana d'Alessandro, Giulia Brunelli, Gaia Fabbri, Kristina Zguro, Andrea Degl'Innocenti, , Chiara Fallerini, Elena Bargagli, Alessandra Renie |
| Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants. American journal of respiratory and critical care medicine 2023 1 . Peljto Anna L, Blumhagen Rachel Z, Walts Avram D, Cardwell Jonathan, Powers Julia, Corte Tamera J, Dickinson Joanne L, Glaspole Ian, Moodley Yuben P, Vasakova Martina Koziar, Bendstrup Elisabeth, Davidsen Jesper R, Borie Raphael, Crestani Bruno, Dieude Philippe, Bonella Francesco, Costabel Ulrich, Gudmundsson Gunnar, Donnelly Seamas C, Egan Jim, Henry Michael T, Keane Michael P, Kennedy Marcus P, McCarthy Cormac, McElroy Aoife N, Olaniyi Joshua A, O'Reilly Katherine M A, Richeldi Luca, Leone Paolo M, Poletti Venerino, Puppo Francesco, Tomassetti Sara, Luzzi Valentina, Kokturk Nurdan, Mogulkoc Nesrin, Fiddler Christine A, Hirani Nikhil, Jenkins Gisli, Maher Toby M, Molyneaux Philip L, Parfrey Helen, Braybrooke Rebecca, Blackwell Timothy S, Jackson Peter D, Nathan Steven D, Porteous Mary K, Brown Kevin K, Christie Jason D, Collard Harold R, Eickelberg Oliver, Foster Elena E, Gibson Kevin F, Glassberg Marilyn, Kass Daniel, Kropski Jonathan A, Lederer David, Linderholm Angela L, Loyd Jim, Mathai Susan K, Montesi Sydney B, Noth Imre, Oldham Justin M, Palmisciano Amy J, Reichner Cristina A, Rojas Mauricio, Roman Jesse, Schluger Neil, Shea Barry S, Swigris Jeffrey J, Wolters Paul J, Zhang Yingze, Prele Cecilia M A, Enghelmayer Juan I, Otaola Maria, Ryerson Christopher J, Salinas Mauricio, Sterclova Martina, Gebremariam Tewodros H, Myllärniemi Marjukka, Carbone Roberto, Furusawa Haruhiko, Hirose Masaki, Inoue Yoshikazu, Miyazaki Yasunari, Ohta Ken, Ohta Shin, Okamoto Tsukasa, Kim Dong Soon, Pardo Annie, Selman Moises, Aranda Alvaro U, Park Moo Suk, Park Jong Sun, Song Jin Woo, Molina-Molina Maria, Planas-Cerezales Lurdes, Westergren-Thorsson Gunilla, Smith Albert V, Manichaikul Ani W, Kim John S, Rich Stephen S, Oelsner Elizabeth C, Barr R Graham, Rotter Jerome I, Dupuis Josee, O'Connor George, Vasan Ramachandran S, Cho Michael H, Silverman Edwin K, Schwarz Marvin I, Steele Mark P, Lee Joyce S, Yang Ivana V, Fingerlin Tasha E, Schwartz David A, |
| Germline RTEL1 Variants in Telomere Biology Disorders. American journal of medical genetics. Part A 2024 9 e63882. Ashley S Thompson, Marena R Niewisch, Neelam Giri, Lisa J McReynolds, Sharon A Sava |
| Genetic architecture of telomere length in 462,666 UK Biobank whole-genome sequences. Nature genetics 2024 8 . Oliver S Burren, Ryan S Dhindsa, Sri V V Deevi, Sean Wen, Abhishek Nag, Jonathan Mitchell, Fengyuan Hu, Douglas P Loesch, Katherine R Smith, Neetu Razdan, Henric Olsson, Adam Platt, Dimitrios Vitsios, Qiang Wu, , Veryan Codd, Christopher P Nelson, Nilesh J Samani, Ruth E March, Sebastian Wasilewski, Keren Carss, Margarete Fabre, Quanli Wang, Menelas N Pangalos, Slavé Petrovs |
| A tiered strategy to identify relevant genetic variants in familial pulmonary fibrosis: a proof of concept for the clinical practice. European journal of human genetics : EJHG 2025 1 . Aitana Alonso-González, Ibrahim Véliz-Flores, Eva Tosco-Herrera, Silvia González-Barbuzano, Alejandro Mendoza-Alvarez, Helena Galván-Fernández, Leandro Sastre, Beatriz Fernández-Varas, Almudena Corrales, Luis A Rubio-Rodríguez, David Jáspez, José M Lorenzo-Salazar, Maria Molina-Molina, Felipe Rodríguez-de-Castro, Rafaela González-Montelongo, Carlos Flor |
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