Integrative genomics identifies new genes associated with severe COPD and emphysema

gan Sakornsakolpat, Phuwanat, Morrow, Jarrett D., Castaldi, Peter J., Hersh, Craig P., Bossé, Yohan, Silverman, Edwin K., Manichaikul, Ani, Cho, Michael H.
Cyhoeddwyd yn Respir Res (2018)

Genome-Wide Association Analysis of Single-Breath Dl(CO)

gan Sakornsakolpat, Phuwanat, McCormack, Meredith, Bakke, Per, Gulsvik, Amund, Make, Barry J., Crapo, James D., Cho, Michael H., Silverman, Edwin K.
Cyhoeddwyd yn Am J Respir Cell Mol Biol (2019)

DSP variants may be associated with longitudinal change in quantitative emphysema

gan Kim, Woori, Cho, Michael H., Sakornsakolpat, Phuwanat, Lynch, David A., Coxson, Harvey O., Tal-Singer, Ruth, Silverman, Edwin K., Beaty, Terri H.
Cyhoeddwyd yn Respir Res (2019)

Relative contributions of family history and a polygenic risk score on COPD and related outcomes: COPDGene and ECLIPSE studies

gan Moll, Matthew, Lutz, Sharon M., Ghosh, Auyon J., Sakornsakolpat, Phuwanat, Hersh, Craig P., Beaty, Terri H., Dudbridge, Frank, Tobin, Martin D., Mittleman, Murray A., Silverman, Edwin K., Hobbs, Brian D., Cho, Michael H.
Cyhoeddwyd yn BMJ Open Respir Res (2020)

Genome-Wide Gene-by-Smoking Interaction Study of Chronic Obstructive Pulmonary Disease

gan Kim, Woori, Prokopenko, Dmitry, Sakornsakolpat, Phuwanat, Hobbs, Brian D, Lutz, Sharon M, Hokanson, John E, Wain, Louise V, Melbourne, Carl A, Shrine, Nick, Tobin, Martin D, Silverman, Edwin K, Cho, Michael H, Beaty, Terri H
Cyhoeddwyd yn Am J Epidemiol (2020)

Whole-Genome Sequencing in Severe Chronic Obstructive Pulmonary Disease

gan Prokopenko, Dmitry, Sakornsakolpat, Phuwanat, Fier, Heide Loehlein, Qiao, Dandi, Parker, Margaret M., McDonald, Merry-Lynn N., Manichaikul, Ani, Rich, Stephen S., Barr, R. Graham, Williams, Christopher J., Brantly, Mark L., Lange, Christoph, Beaty, Terri H., Crapo, James D., Silverman, Edwin K.
Cyhoeddwyd yn Am J Respir Cell Mol Biol (2018)

Integrative Genomics Analysis Identifies ACVR1B as a Candidate Causal Gene of Emphysema Distribution

gan Boueiz, Adel, Pham, Betty, Chase, Robert, Lamb, Andrew, Lee, Sool, Naing, Zun Zar Chi, Cho, Michael H., Parker, Margaret M., Sakornsakolpat, Phuwanat, Hersh, Craig P., Crapo, James D., Stergachis, Andrew B., Tal-Singer, Ruth, DeMeo, Dawn L., Silverman, Edwin K., Zhou, Xiaobo
Cyhoeddwyd yn Am J Respir Cell Mol Biol (2019)

Leveraging lung tissue transcriptome to uncover candidate causal genes in COPD genetic associations

gan Lamontagne, Maxime, Bérubé, Jean-Christophe, Obeidat, Ma’en, Cho, Michael H, Hobbs, Brian D, Sakornsakolpat, Phuwanat, de Jong, Kim, Boezen, H Marike, Nickle, David, Hao, Ke, Timens, Wim, van den Berge, Maarten, Joubert, Philippe, Laviolette, Michel, Sin, Don D, Paré, Peter D, Bossé, Yohan
Cyhoeddwyd yn Hum Mol Genet (2018)

GWAS and Systems Biology Analysis of Depressive Symptoms among Smokers from the COPDGene Cohort

gan Heinzman, Jonathan T., Hoth, Karin F., Cho, Michael H., Sakornsakolpat, Phuwanat, Regan, Elizabeth A., Make, Barry J., Kinney, Gregory L., Wamboldt, Frederick S., Holm, Kristen E., Bormann, Nicholas, Robles, Julian, Kim, Victor, Iyer, Anand S., Silverman, Edwin K., Crapo, James D., Han, Shizhong, Potash, James B., Shinozaki, Gen
Cyhoeddwyd yn J Affect Disord (2018)

Analysis of genetically driven alternative splicing identifies FBXO38 as a novel COPD susceptibility gene

gan Saferali, Aabida, Yun, Jeong H., Parker, Margaret M., Sakornsakolpat, Phuwanat, Chase, Robert P., Lamb, Andrew, Hobbs, Brian D., Boezen, Marike H., Dai, Xiangpeng, de Jong, Kim, Beaty, Terri H., Wei, Wenyi, Zhou, Xiaobo, Silverman, Edwin K., Cho, Michael H., Castaldi, Peter J., Hersh, Craig P.
Cyhoeddwyd yn PLoS Genet (2019)

A systematic analysis of protein-altering exonic variants in chronic obstructive pulmonary disease

gan Moll, Matthew, Jackson, Victoria E., Yu, Bing, Grove, Megan L., London, Stephanie J., Gharib, Sina A., Bartz, Traci M., Sitlani, Colleen M., Dupuis, Josée, O’Connor, George T., Xu, Hanfei, Cassano, Patricia A., Patchen, Bonnie Kaufmann, Kim, Woo Jin, Park, Jinkyeong, Kim, Kun Hee, Han, Buhm, Barr, R. Graham, Manichaikul, Ani, Nguyen, Jennifer N., Rich, Stephen S., Lahousse, Lies, Terzikhan, Natalie, Brusselle, Guy, Sakornsakolpat, Phuwanat, Liu, Jiangyuan, Benway, Christopher J., Hall, Ian P., Tobin, Martin D., Wain, Louise V., Silverman, Edwin K., Cho, Michael H., Hobbs, Brian D.
Cyhoeddwyd yn Am J Physiol Lung Cell Mol Physiol (2021)

Chronic obstructive pulmonary disease and related phenotypes: polygenic risk scores in population-based and case-control cohorts

gan Moll, Matthew, Sakornsakolpat, Phuwanat, Shrine, Nick, Hobbs, Brian D, DeMeo, Dawn L, John, Catherine, Guyatt, Anna L, McGeachie, Michael J, Gharib, Sina A, Obeidat, Ma'en, Lahousse, Lies, Wijnant, Sara R A, Brusselle, Guy, Meyers, Deborah A, Bleecker, Eugene R, Li, Xingnan, Tal-Singer, Ruth, Manichaikul, Ani, Rich, Stephen S, Won, Sungho, Kim, Woo Jin, Do, Ah Ra, Washko, George R, Barr, R Graham, Psaty, Bruce M, Bartz, Traci M, Hansel, Nadia N, Barnes, Kathleen, Hokanson, John E, Crapo, James D, Lynch, David, Bakke, Per, Gulsvik, Amund, Hall, Ian P, Wain, Louise, Weiss, Scott T, Silverman, Edwin K, Dudbridge, Frank, Tobin, Martin D, Cho, Michael H
Cyhoeddwyd yn Lancet Respir Med (2020)

Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell type and phenotype associations

gan Sakornsakolpat, Phuwanat, Prokopenko, Dmitry, Lamontagne, Maxime, Reeve, Nicola F., Guyatt, Anna L., Jackson, Victoria E., Shrine, Nick, Qiao, Dandi, Bartz, Traci M., Kim, Deog Kyeom, Lee, Mi Kyeong, Latourelle, Jeanne C., Li, Xingnan, Morrow, Jarrett D., Obeidat, Ma’en, Wyss, Annah B., Bakke, Per, Barr, R Graham, Beaty, Terri H., Belinsky, Steven A., Brusselle, Guy G., Crapo, James D., de Jong, Kim, DeMeo, Dawn L., Fingerlin, Tasha E., Gharib, Sina A., Gulsvik, Amund, Hall, Ian P., Hokanson, John E., Kim, Woo Jin, Lomas, David A., London, Stephanie J., Meyers, Deborah A., O’Connor, George T., Rennard, Stephen I., Schwartz, David A., Sliwinski, Pawel, Sparrow, David, Strachan, David P., Tal-Singer, Ruth, Tesfaigzi, Yohannes, Vestbo, Jørgen, Vonk, Judith M., Yim, Jae-Joon, Zhou, Xiaobo, Bossé, Yohan, Manichaikul, Ani, Lahousse, Lies, Silverman, Edwin K., Boezen, H. Marike, Wain, Louise V., Tobin, Martin D., Hobbs, Brian D., Cho, Michael H.
Cyhoeddwyd yn Nat Genet (2019)

Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis

gan Allen, Richard J., Guillen-Guio, Beatriz, Oldham, Justin M., Ma, Shwu-Fan, Dressen, Amy, Paynton, Megan L., Kraven, Luke M., Obeidat, Ma'en, Li, Xuan, Ng, Michael, Braybrooke, Rebecca, Molina-Molina, Maria, Hobbs, Brian D., Putman, Rachel K., Sakornsakolpat, Phuwanat, Booth, Helen L., Fahy, William A., Hart, Simon P., Hill, Mike R., Hirani, Nik, Hubbard, Richard B., McAnulty, Robin J., Millar, Ann B., Navaratnam, Vidyia, Oballa, Eunice, Parfrey, Helen, Saini, Gauri, Whyte, Moira K. B., Zhang, Yingze, Kaminski, Naftali, Adegunsoye, Ayodeji, Strek, Mary E., Neighbors, Margaret, Sheng, Xuting R., Gudmundsson, Gunnar, Gudnason, Vilmundur, Hatabu, Hiroto, Lederer, David J., Manichaikul, Ani, Newell, John D., O’Connor, George T., Ortega, Victor E., Xu, Hanfei, Fingerlin, Tasha E., Bossé, Yohan, Hao, Ke, Joubert, Philippe, Nickle, David C., Sin, Don D., Timens, Wim, Furniss, Dominic, Morris, Andrew P., Zondervan, Krina T., Hall, Ian P., Sayers, Ian, Tobin, Martin D., Maher, Toby M., Cho, Michael H., Hunninghake, Gary M., Schwartz, David A., Yaspan, Brian L., Molyneaux, Philip L., Flores, Carlos, Noth, Imre, Jenkins, R. Gisli, Wain, Louise V.
Cyhoeddwyd yn Am J Respir Crit Care Med (2019)

Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants

gan Zhao, Xutong, Qiao, Dandi, Yang, Chaojie, Kasela, Silva, Kim, Wonji, Ma, Yanlin, Shrine, Nick, Batini, Chiara, Sofer, Tamar, Taliun, Sarah A. Gagliano, Sakornsakolpat, Phuwanat, Balte, Pallavi P., Prokopenko, Dmitry, Yu, Bing, Lange, Leslie A., Dupuis, Josée, Cade, Brian E., Lee, Jiwon, Gharib, Sina A., Daya, Michelle, Laurie, Cecelia A., Ruczinski, Ingo, Cupples, L. Adrienne, Loehr, Laura R., Bartz, Traci M., Morrison, Alanna C., Psaty, Bruce M., Vasan, Ramachandran S., Wilson, James G., Taylor, Kent D., Durda, Peter, Johnson, W. Craig, Cornell, Elaine, Guo, Xiuqing, Liu, Yongmei, Tracy, Russell P., Ardlie, Kristin G., Aguet, François, VanDenBerg, David J., Papanicolaou, George J., Rotter, Jerome I., Barnes, Kathleen C., Jain, Deepti, Nickerson, Deborah A., Muzny, Donna M., Metcalf, Ginger A., Doddapaneni, Harshavardhan, Dugan-Perez, Shannon, Gupta, Namrata, Gabriel, Stacey, Rich, Stephen S., O’Connor, George T., Redline, Susan, Reed, Robert M., Laurie, Cathy C., Daviglus, Martha L., Preudhomme, Liana K., Burkart, Kristin M., Kaplan, Robert C., Wain, Louise V., Tobin, Martin D., London, Stephanie J., Lappalainen, Tuuli, Oelsner, Elizabeth C., Abecasis, Goncalo R., Silverman, Edwin K., Barr, R. Graham, Cho, Michael H., Manichaikul, Ani
Cyhoeddwyd yn Nat Commun (2020)

New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.

gan Shrine, Nick, Guyatt, Anna L, Erzurumluoglu, A Mesut, Jackson, Victoria E, Hobbs, Brian D, Melbourne, Carl A, Batini, Chiara, Fawcett, Katherine A, Song, Kijoung, Sakornsakolpat, Phuwanat, Li, Xingnan, Boxall, Ruth, Reeve, Nicola F, Obeidat, Ma’en, Zhao, Jing Hua, Wielscher, Matthias, Weiss, Stefan, Kentistou, Katherine A, Cook, James P, Sun, Benjamin B, Zhou, Jian, Hui, Jennie, Karrasch, Stefan, Imboden, Medea, Harris, Sarah E, Marten, Jonathan, Enroth, Stefan, Kerr, Shona M, Surakka, Ida, Vitart, Veronique, Lehtimäki, Terho, Allen, Richard J, Bakke, Per S, Beaty, Terri H, Bleecker, Eugene R, Bossé, Yohan, Brandsma, Corry-Anke, Chen, Zhengming, Crapo, James D, Danesh, John, DeMeo, Dawn L, Dudbridge, Frank, Ewert, Ralf, Gieger, Christian, Gulsvik, Amund, Hansell, Anna L, Hao, Ke, Hoffman, Joshua D, Hokanson, John E, Homuth, Georg, Joshi, Peter K, Joubert, Philippe, Langenberg, Claudia, Li, Xuan, Li, Liming, Lin, Kuang, Lind, Lars, Locantore, Nicholas, Luan, Jian’an, Mahajan, Anubha, Maranville, Joseph C, Murray, Alison, Nickle, David C, Packer, Richard, Parker, Margaret M, Paynton, Megan L, Porteous, David J, Prokopenko, Dmitry, Qiao, Dandi, Rawal, Rajesh, Runz, Heiko, Sayers, Ian, Sin, Don D, Smith, Blair H, Artigas, María Soler, Sparrow, David, Tal-Singer, Ruth, Timmers, Paul RHJ, Van den Berge, Maarten, Whittaker, John C, Woodruff, Prescott G, Yerges-Armstrong, Laura M, Troyanskaya, Olga G, Raitakari, Olli T, Kähönen, Mika, Polasek, Ozren, Gyllensten, Ulf, Rudan, Igor, Deary, Ian J, Probst-Hensch, Nicole M, Schulz, Holger, James, Alan L, Wilson, James F, Stubbe, Beate, Zeggini, Eleftheria, Jarvelin, Marjo-Riitta, Wareham, Nick, Silverman, Edwin K, Hayward, Caroline, Morris, Andrew P, Butterworth, Adam S, Scott, Robert A, Walters, Robin G, Meyers, Deborah A, Cho, Michael H, Strachan, David P, Hall, Ian P, Tobin, Martin D, Wain, Louise V
Cyhoeddwyd yn Nat Genet (2019)