Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Anna L Peljto"'
Autor:
Raphael Borie, Bruno Crestani, Philippe Dieude, Hilario Nunes, Yannick Allanore, Caroline Kannengiesser, Paolo Airo, Marco Matucci-Cerinic, Benoit Wallaert, Dominique Israel-Biet, Jacques Cadranel, Vincent Cottin, Steven Gazal, Anna L Peljto, John Varga, David A Schwartz, Dominique Valeyre, Bernard Grandchamp
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e70621 (2013)
A polymorphism on the MUC5B promoter (rs35705950) has been associated with idiopathic pulmonary fibrosis (IPF) but not with systemic sclerosis (SSc) with interstitial lung disease (ILD). We genotyped the MUC5B promoter in the first 142 patients of th
Externí odkaz:
https://doaj.org/article/e4f3f0a63d2a4ce1aad9e5e92605ab27
Autor:
Mark P. Steele, Anna L. Peljto, Susan K. Mathai, Stephen Humphries, Tami J. Bang, Andrea Oh, Shawn Teague, Giuseppe Cicchetti, Christopher Sigakis, Jonathan A. Kropski, James E. Loyd, Timothy S. Blackwell, Kevin K. Brown, Marvin I. Schwarz, Rachel A. Warren, Julia Powers, Avram D. Walts, Cheryl Markin, Tasha E. Fingerlin, Ivana V. Yang, David A. Lynch, Joyce S. Lee, David A. Schwartz
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 207:587-593
Relatives of patients with familial interstitial pneumonia are at increased risk for pulmonary fibrosis, and develop preclinical pulmonary fibrosis (PrePF).We defined the incidence and progression of new onset PrePF; its relationship to survival amon
Autor:
Anna L. Peljto, Rachel Z. Blumhagen, Avram D. Walts, Jonathan Cardwell, Julia Powers, Tamera J. Corte, Joanne L. Dickinson, Ian Glaspole, Yuben P. Moodley, Martina Koziar Vasakova, Elisabeth Bendstrup, Jesper R. Davidsen, Raphael Borie, Bruno Crestani, Philippe Dieude, Francesco Bonella, Ulrich Costabel, Gunnar Gudmundsson, Seamas C. Donnelly, Jim Egan, Michael T. Henry, Michael P. Keane, Marcus P. Kennedy, Cormac McCarthy, Aoife N. McElroy, Joshua A. Olaniyi, Katherine M. A. O’Reilly, Luca Richeldi, Paolo M. Leone, Venerino Poletti, Francesco Puppo, Sara Tomassetti, Valentina Luzzi, Nurdan Kokturk, Nesrin Mogulkoc, Christine A. Fiddler, Nikhil Hirani, R. Gisli Jenkins, Toby M. Maher, Philip L. Molyneaux, Helen Parfrey, Rebecca Braybrooke, Timothy S. Blackwell, Peter D. Jackson, Steven D. Nathan, Mary K. Porteous, Kevin K. Brown, Jason D. Christie, Harold R. Collard, Oliver Eickelberg, Elena E. Foster, Kevin F. Gibson, Marilyn Glassberg, Daniel J. Kass, Jonathan A. Kropski, David Lederer, Angela L. Linderholm, Jim Loyd, Susan K. Mathai, Sydney B. Montesi, Imre Noth, Justin M. Oldham, Amy J. Palmisciano, Cristina A. Reichner, Mauricio Rojas, Jesse Roman, Neil Schluger, Barry S. Shea, Jeffrey J. Swigris, Paul J. Wolters, Yingze Zhang, Cecilia M. A. Prele, Juan I. Enghelmayer, Maria Otaola, Christopher J. Ryerson, Mauricio Salinas, Martina Sterclova, Tewodros H. Gebremariam, Marjukka Myllärniemi, Roberto G. Carbone, Haruhiko Furusawa, Masaki Hirose, Yoshikazu Inoue, Yasunari Miyazaki, Ken Ohta, Shin Ohta, Tsukasa Okamoto, Dong Soon Kim, Annie Pardo, Moises Selman, Alvaro U. Aranda, Moo Suk Park, Jong Sun Park, Jin Woo Song, Maria Molina-Molina, Lurdes Planas-Cerezales, Gunilla Westergren-Thorsson, Albert V. Smith, Ani W. Manichaikul, John S. Kim, Stephen S. Rich, Elizabeth C. Oelsner, R. Graham Barr, Jerome I. Rotter, Josee Dupuis, George O’Connor, Ramachandran S. Vasan, Michael H. Cho, Edwin K. Silverman, Marvin I. Schwarz, Mark P. Steele, Joyce S. Lee, Ivana V. Yang, Tasha E. Fingerlin, David A. Schwartz
Rationale: Idiopathic pulmonary fibrosis is a rare, irreversible, and progressive disease of the lungs. Common genetic variants, in addition to non-genetic factors, have been consistently associated with IPF. Rare variants identified by candidate gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0670c24aedc8efa23979477ed15d39b
http://hdl.handle.net/10044/1/101620
http://hdl.handle.net/10044/1/101620
Autor:
Scott M. Matson, Kevin D. Deane, Anna L. Peljto, Tami J. Bang, Peter B. Sachs, Avram D. Walts, Christopher Collora, Shuyu Ye, M. Kristen Demoruelle, Stephen M. Humphries, David A. Schwartz, Joyce S. Lee
Publikováno v:
Am J Respir Crit Care Med
Autor:
Seon-Kyeong Jang, Luke Evans, Allison Fialkowski, Donna K. Arnett, Allison E. Ashley-Koch, Kathleen C. Barnes, Diane M. Becker, Joshua C. Bis, John Blangero, Eugene R. Bleecker, Meher Preethi Boorgula, Donald W. Bowden, Jennifer A. Brody, Brian E. Cade, Brenda W. Campbell Jenkins, April P. Carson, Sameer Chavan, L. Adrienne Cupples, Brian Custer, Scott M. Damrauer, Sean P. David, Mariza de Andrade, Carla L. Dinardo, Tasha E. Fingerlin, Myriam Fornage, Barry I. Freedman, Melanie E. Garrett, Sina A. Gharib, David C. Glahn, Jeffrey Haessler, Susan R. Heckbert, John E. Hokanson, Lifang Hou, Shih-Jen Hwang, Matthew C. Hyman, Renae Judy, Anne E. Justice, Robert C. Kaplan, Sharon L. R. Kardia, Shannon Kelly, Wonji Kim, Charles Kooperberg, Daniel Levy, Donald M. Lloyd-Jones, Ruth J. F. Loos, Ani W. Manichaikul, Mark T. Gladwin, Lisa Warsinger Martin, Mehdi Nouraie, Olle Melander, Deborah A. Meyers, Courtney G. Montgomery, Kari E. North, Elizabeth C. Oelsner, Nicholette D. Palmer, Marinelle Payton, Anna L. Peljto, Patricia A. Peyser, Michael Preuss, Bruce M. Psaty, Dandi Qiao, Daniel J. Rader, Nicholas Rafaels, Susan Redline, Robert M. Reed, Alexander P. Reiner, Stephen S. Rich, Jerome I. Rotter, David A. Schwartz, Aladdin H. Shadyab, Edwin K. Silverman, Nicholas L. Smith, J. Gustav Smith, Albert V. Smith, Jennifer A. Smith, Weihong Tang, Kent D. Taylor, Marilyn J. Telen, Ramachandran S. Vasan, Victor R. Gordeuk, Zhe Wang, Kerri L. Wiggins, Lisa R. Yanek, Ivana V. Yang, Kendra A. Young, Kristin L. Young, Yingze Zhang, Dajiang J. Liu, Matthew C. Keller, Scott Vrieze
Publikováno v:
Nature human behaviour, vol 6, iss 11
Nat Hum Behav
Nat Hum Behav
Common genetic variants explain less variation in complex phenotypes than inferred from family-based studies, and there is a debate on the source of this 'missing heritability'. We investigated the contribution of rare genetic variants to tobacco use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30aa88d7690dcca16453c7af4c2f580f
https://escholarship.org/uc/item/3v26257d
https://escholarship.org/uc/item/3v26257d
Autor:
Haruhiko Furusawa, Anna L Peljto, Avram D Walts, Jonathan Cardwell, Philip L Molyneaux, Joyce S Lee, Evans R Fernández Pérez, Paul J Wolters, Ivana V Yang, David A Schwartz
Publikováno v:
Thorax
A subset of patients with hypersensitivity pneumonitis (HP) develop lung fibrosis that is clinically similar to idiopathic pulmonary fibrosis (IPF). To address the aetiological determinants of fibrotic HP, we investigated whether the common IPF genet
Autor:
Anne E. Justice, Ruth J. F. Loos, Robert C. Kaplan, Seon-Kyeong Jang, Matthew C. Keller, Daniel J. Rader, Nicholas L. Smith, Scott M. Damrauer, Joshua C. Bis, Dajiang J. Liu, Charles Kooperberg, Yingze Zhang, Elizabeth C. Oelsner, Kari E. North, Kerri L. Wiggins, David A. Schwartz, Renae Judy, Jeffrey Haessler, Olle Melander, Scott I. Vrieze, Kent D. Taylor, Daniel Levy, Victor Gordeuk, Kendra A. Young, Weihong Tang, Deborah A. Meyers, Mariza de Andrade, John E. Hokanson, Donna K. Arnett, Luke M. Evans, Jerome I. Rotter, Anna L. Peljto, Kristin L. Young, Dandi Qiao, Sean P. David, Allison Fialkowski, Susan R. Heckbert, Shih-Jen Hwang, Zhe Wang, Lisa W. Martin, Lisa R. Yanek, Wonji Kim, Matthew Hyman, Ramachandran S. Vasan, Mark T. Gladwin, Stephen S. Rich, Albert V. Smith, Mehdi Nouraie, Edwin K. Silverman, John Blangero, Eugene R. Bleecker, Tasha E. Fingerlin, Jennifer A. Brody, L. Adrienne Cupples, Ani Manichaikul, Diane M. Becker, Ivana V. Yang, Bruce M. Psaty, Aladdin Shadyab, David C. Glahn, Sina A. Gharib, Michael Preuss, Gustav Smith, Alexander P. Reiner, Robert M. Reed
Background Across complex traits, common variants explain only a modest amount of variance, with SNP-heritability consistently below heritability estimates from close relatives. Here, we examined the contribution of rare variant to tobacco use risk i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f05c3b86950c390a7509a69c132660b5
https://doi.org/10.21203/rs.3.rs-475149/v1
https://doi.org/10.21203/rs.3.rs-475149/v1
Autor:
David A. Schwartz, H. Furusawa, Carlyne D. Cool, Ivana V. Yang, Tami J. Bang, Jonathan Cardwell, Avram D Walts, Joyce S. Lee, Paul J. Wolters, Anna L. Peljto
Publikováno v:
TP65. TP065 ENVIRONMENTAL EXPOSURES AND LUNG DISEASE.
Autor:
Anna L. Peljto, Carlyne D. Cool, Kevin K. Brown, Jonathan H. Chung, Janet Talbert, David A. Lynch, David F. McKean, Steve D. Groshong, David A. Schwartz, Marvin I. Schwarz, Ashish Chawla, Tasha E. Fingerlin
Publikováno v:
Chest. 147:450-459
The current usual interstitial pneumonitis (UIP)/idiopathic pulmonary fibrosis CT scan classification system excludes probable UIP as a diagnostic category. We sought to determine the predictive effect of probable UIP on CT scan on histology and the
Autor:
Anna L. Peljto, Elissa Murphy, David A. Schwartz, Jung Su Lee, Annie Pardo, Wonjun Ji, Moisés Selman, Laura Tucker, Ivana V. Yang, Dong Soon Kim, Tasha E. Fingerlin, Marvin I. Schwarz
Publikováno v:
Chest. 147:460-464
BACKGROUND Polymorphisms in the MUC5B promoter, TOLLIP , and nine additional genetic loci have been associated with idiopathic pulmonary fibrosis (IPF) within non-Hispanic white populations. It is unknown whether these variants account for risk of IP