The MUC5B variant is associated with idiopathic pulmonary fibrosis but not with systemic sclerosis interstitial lung disease in the European Caucasian population by Borie, Raphael, Crestani, Bruno, Dieude, Philippe, Nunes, Hilario, Allanore, Yannick, Kannengiesser, Caroline, Airo, Paolo, Matucci-Cerinic, Marco, Wallaert, Benoit, Israel-Biet, Dominique, Cadranel, Jacques, Cottin, Vincent, Gazal, Steven, Peljto, Anna L, Varga, John, Schwartz, David A, Valeyre, Dominique, Grandchamp, Bernard

Get full text

Incidence and Progression of Fibrotic Lung Disease in an At-Risk Cohort by Steele, Mark P, Peljto, Anna L, Mathai, Susan K, Humphries, Stephen, Bang, Tami J, Oh, Andrea, Teague, Shawn, Cicchetti, Giuseppe, Sigakis, Christopher, Kropski, Jonathan A, Loyd, James E, Blackwell, Timothy S, Brown, Kevin K, Schwarz, Marvin I, Warren, Rachel A, Powers, Julia, Walts, Avram D, Markin, Cheryl, Fingerlin, Tasha E, Yang, Ivana V, Lynch, David A, Lee, Joyce S, Schwartz, David A

Get full text

Association Between the MUC5B Promoter Polymorphism and Survival in Patients With Idiopathic Pulmonary Fibrosis by Peljto, Anna L, Zhang, Yingze, Fingerlin, Tasha E, Ma, Shwu-Fan, Garcia, Joe G. N, Richards, Thomas J, Silveira, Lori J, Lindell, Kathleen O, Steele, Mark P, Loyd, James E, Gibson, Kevin F, Seibold, Max A, Brown, Kevin K, Talbert, Janet L, Markin, Cheryl, Kossen, Karl, Seiwert, Scott D, Murphy, Elissa, Noth, Imre, Schwarz, Marvin I, Kaminski, Naftali, Schwartz, David A

Get full text

Familial risk of epilepsy: a population-based study by PELJTO, Anna L, BARKER-CUMMINGS, Christie, VASOLI, Vincent M, LEIBSON, Cynthia L, HAUSER, W. Allen, BUCHHALTER, Jeffrey R, OTTMAN, Ruth

Get full text

Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants by 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, R 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 J, 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 G, 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

Get full text

Prospective Identification of Subclinical Interstitial Lung Disease in a Rheumatoid Arthritis Cohort Is Associated with the MUC5B Promoter Variant by Matson, Scott M, Deane, Kevin D, Peljto, Anna L, Bang, Tami J, Sachs, Peter B, Walts, Avram D, Collora, Christopher, Ye, Shuyu, Demoruelle, M Kristen, Humphries, Stephen M, Schwartz, David A, Lee, Joyce S

Get full text

A Polygenic Risk Score for Idiopathic Pulmonary Fibrosis and Interstitial Lung Abnormalities by Moll, Matthew, Peljto, Anna L, Kim, John S, Xu, Hanfei, Debban, Catherine L, Chen, Xianfeng, Menon, Aravind, Putman, Rachel K, Ghosh, Auyon J, Saferali, Aabida, Nishino, Mizuki, Hatabu, Hiroto, Hobbs, Brian D, Hecker, Julian, McDermott, Gregory, Sparks, Jeffrey A, Wain, Louise V, Allen, Richard J, Tobin, Martin D, Raby, Benjamin A, Chun, Sung, Silverman, Edwin K, Zamora, Ana C, Ortega, Victor E, Garcia, Christine K, Barr, R Graham, Bleecker, Eugene R, Meyers, Deborah A, Kaner, Robert J, Rich, Stephen S, Manichaikul, Ani, Rotter, Jerome I, Dupuis, Josée, O'Connor, George T, Fingerlin, Tasha E, Hunninghake, Gary M, Schwartz, David A, Cho, Michael H

Get full text

Multiple Subsampling of Dense SNP Data Localizes Disease Genes with Increased Precision by Stewart, William C. L., Peljto, Anna L., Greenberg, David A.

Get full text

Rare genetic variants explain missing heritability in smoking by Jang, Seon-Kyeong, Evans, Luke, Fialkowski, Allison, Arnett, Donna K., Ashley-Koch, Allison E., Barnes, Kathleen C., Becker, Diane M., Bis, Joshua C., Blangero, John, Bleecker, Eugene R., Boorgula, Meher Preethi, Bowden, Donald W., Brody, Jennifer A., Cade, Brian E., Jenkins, Brenda W. Campbell, Carson, April P., Chavan, Sameer, Cupples, L. Adrienne, Custer, Brian, Damrauer, Scott M., David, Sean P., de Andrade, Mariza, Dinardo, Carla L., Fingerlin, Tasha E., Fornage, Myriam, Freedman, Barry I., Garrett, Melanie E., Gharib, Sina A., Glahn, David C., Haessler, Jeffrey, Heckbert, Susan R., Hokanson, John E., Hou, Lifang, Hwang, Shih-Jen, Hyman, Matthew C., Judy, Renae, Justice, Anne E., Kaplan, Robert C., Kardia, Sharon L. R., Kelly, Shannon, Kim, Wonji, Kooperberg, Charles, Levy, Daniel, Lloyd-Jones, Donald M., Loos, Ruth J. F., Manichaikul, Ani W., Gladwin, Mark T., Martin, Lisa Warsinger, Nouraie, Mehdi, Melander, Olle, Meyers, Deborah A., Montgomery, Courtney G., North, Kari E., Oelsner, Elizabeth C., Palmer, Nicholette D., Payton, Marinelle, Peljto, Anna L., Peyser, Patricia A., Preuss, Michael, Psaty, Bruce M., Qiao, Dandi, Rader, Daniel J., Rafaels, Nicholas, Redline, Susan, Reed, Robert M., Reiner, Alexander P., Rich, Stephen S., Rotter, Jerome I., Schwartz, David A., Shadyab, Aladdin H., Silverman, Edwin K., Smith, Nicholas L., Smith, J. Gustav, Smith, Albert V., Smith, Jennifer A., Tang, Weihong, Taylor, Kent D., Telen, Marilyn J., Vasan, Ramachandran S., Gordeuk, Victor R., Wang, Zhe, Wiggins, Kerri L., Yanek, Lisa R., Yang, Ivana V., Young, Kendra A., Young, Kristin L., Zhang, Yingze, Liu, Dajiang J., Keller, Matthew C., Vrieze, Scott

Get full text

NOS1AP Is a Genetic Modifier of the Long-QT Syndrome by CROTTI, Lia, MONTI, Maria Cristina, INSOLIA, Roberto, PELJTO, Anna, GOOSEN, Althea, BRINK, Paul A, GREENBERG, David A, SCHWARTZ, Peter J, GEORGE, Alfred L

Get full text