Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: Idiopathic Pulmonary Fibrosis 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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, |
| 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, |
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- Page last updated:Sep 29, 2023
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