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Allen, Richard J. and Porte, Joanne and Braybrooke, Rebecca and Flores, Carlos and Fingerlin, Tasha E. and Oldham, Justin M. and Guillen-Guio, Beatriz and Ma, Shwu-Fan and Okamoto, Tsukasa and John, Alison E. and Obeidat, Ma'en and Yang, Ivana V. and Henry, Amanda and Hubbard, Richard B. and Navaratnam, Vidya and Saini, Gauri and Thompson, Norma and Booth, Helen L. and Hart, Simon P. and Hill, Mike R. and Hirani, Nik and Maher, Toby M. and McAnulty, Robin J. and Millar, Ann B. and Molyneaux, Philip L. and Parfrey, Helen and Rassl, Doris M. and Whyte, Moira K.B. and Fahy, William A. and Marshall, Richard P. and Oballa, Eunice and Bossé, Yohan and Nickle, David C. and Sin, Don D. and Timens, Wim and Shrine, Nick and Sayers, Ian and Hall, Ian P. and Noth, Imre and Schwartz, David A. and Tobin, Martin D. and Wain, Louise V. and Jenkins, R. Gisli (2017) Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study. Lancet Respiratory Medicine, 5 (11). pp. 869-880. ISSN 2213-2619

Hobbs, Brian D. and de Jong, Kim and Lamontagne, Maxime and Bossé, Yohan and Shrine, Nick and Artigas, María Soler and Wain, Louise V. and Hall, Ian P. and Jackson, Victoria E. and Wyss, Annah B. and London, Stephanie J. and North, Kari E. and Franceschini, Nora and Strachan, David P. and Beaty, Terri H. and Hokanson, John E. and Crapo, James D. and Castaldi, Peter J. and Chase, Robert P. and Bartz, Traci M. and Heckbert, Susan R. and Psaty, Bruce M. and Gharib, Sina A. and Zanen, Pieter and Lammers, Jan W. and Oudkerk, Matthijs and Groen, H.J. and Locantore, Nicholas and Tal-Singer, Ruth and Rennard, Stephen I. and Vestbo, Jørgen and Timens, Wim and Paré, Peter D. and Latourelle, Jeanne C. and Dupuis, Josée and O'Connor, George T. and Wilk, Jemma B. and Kim, Woo Jin and Lee, Mi Kyeong and Oh, Yeon-Mok and Vonk, Judith M. and de Koning, Harry J. and Leng, Shuguang and Belinsky, Steven A. and Tesfaigzi, Yohannes and Manichaikul, Ani and Wang, Xin-Qun and Rich, Stephen S. and Barr, R. Graham and Sparrow, David and Litonjua, Augusto A. and Bakke, Per and Gulsvik, Amund and Lahousse, Lies and Brusselle, Guy G. and Stricker, Bruno H. and Uitterlinden, André G. and Ampleford, Elizabeth J. and Bleecker, Eugene R. and Woodruff, Prescott G. and Meyers, Deborah A. and Qiao, Dandi and Lomas, David A. and Yim, Jae-Joon and Kim, Deog Kyeom and Hawrylkiewicz, Iwona and Sliwinski, Pawel and Hardin, Megan and Fingerlin, Tasha E. and Schwartz, David A. and Postma, Dirkje S. and MacNee, William and Tobin, Martin D. and Silverman, Edwin K. and Boezen, H. Marike and Cho, Michael H. (2017) Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis. Nature Genetics, 49 (3). pp. 426-432. ISSN 1546-1718

Ierodiakonou, Despo and Portelli, Michael A. and Postma, Dirkje S. and Koppelman, Gerard H. and Gerritsen, Jorrit and ten Hacken, Nick H.T. and Timens, Wim and Boezen, H. Marike and Vonk, Judith M. and Sayers, Ian (2016) Urokinase plasminogen activator receptor polymorphisms and airway remodelling in asthma. European Respiratory Journal, 47 (5). pp. 1568-1571. ISSN 1399-3003

Obeidat, Ma'en and Hao, Ke and Bossé, Yohan and Nickle, David C. and Nie, Yunlong and Postma, Dirkje S. and Laviolette, Michel and Sandford, Andrew J. and Daley, Denise D. and Hogg, James C. and Elliott, W. Mark and Fishbane, Nick and Timens, Wim and Hysi, Pirro G. and Kaprio, Jaakko and Wilson, James F. and Hui, Jennie and Rawal, Rajesh and Schulz, Holger and Stubbe, Beate and Hayward, Caroline and Polasek, Ozren and Järvelin, Marjo-Riitta and Zhao, Jing Hua and Jarvis, Deborah and Kähönen, Mika and Franceschini, Nora and North, Kari E. and Loth, Daan W. and Brusselle, Guy G. and Smith, Albert Vernon and Gudnason, Vilmundur and Bartz, Traci M and Wilk, Jemma B. and O'Connor, George T. and Cassano, Patricia A. and Tang, Wenbo and Wain, Louise V. and Artigas, María Soler and Gharib, Sina A. and Strachan, David P. and Sin, Don D. and Tobin, Martin D. and London, Stephanie J. and Hall, Ian P. and Paré, Peter D. (2015) Molecular mechanisms underlying variations in lung function: a systems genetics analysis. Lancet Respiratory Medicine, 3 (10). pp. 782-795. ISSN 2213-2619