Handling the data management needs of high-throughput sequencing data: SpeedGene, a compression algorithm for the efficient storage of genetic data

por Qiao, Dandi, Yip, Wai-Ki, Lange, Christoph
Publicado 2012

WISARD: workbench for integrated superfast association studies for related datasets

por Lee, Sungyoung, Choi, Sungkyoung, Qiao, Dandi, Cho, Michael, Silverman, Edwin K., Park, Taesung, Won, Sungho
Publicado 2018

metaFARVAT: An Efficient Tool for Meta-Analysis of Family-Based, Case-Control, and Population-Based Rare Variant Association Studies

por Wang, Longfei, Lee, Sungyoung, Qiao, Dandi, Cho, Michael H., Silverman, Edwin K., Lange, Christoph, Won, Sungho
Publicado 2019

Tempo-spatial regulation of the Wnt pathway by FAM13A modulates the stemness of alveolar epithelial progenitors

por Lin, Xin, Li, Yujun, Gong, Lu, Yun, Jeong H., Xu, Shuang, Tesfaigzi, Yohannes, Qiao, Dandi, Zhou, Xiaobo
Publicado 2021

A statistical physics approach for disease module detection

por Wang, Xu-Wen, Qiao, Dandi, Cho, Michael H., DeMeo, Dawn L., Silverman, Edwin K., Liu, Yang-Yu
Publicado 2022

A comparative analysis of family-based and population-based association tests using whole genome sequence data

por Zhou, Jin J, Yip, Wai-Ki, Cho, Michael H, Qiao, Dandi, McDonald, Merry-Lynn N, Laird, Nan M
Publicado 2014

Heterozygosity of the Alpha 1‐Antitrypsin Pi*Z Allele and Risk of Liver Disease

por Hakim, Aaron, Moll, Matthew, Qiao, Dandi, Liu, Jiangyuan, Lasky‐Su, Jessica A., Silverman, Edwin K., Vilarinho, Silvia, Jiang, Z. Gordon, Hobbs, Brian D., Cho, Michael H.
Publicado 2021

Genome-wide assessment of gene-by-smoking interactions in COPD

por Park, Boram, Koo, So-My, An, Jaehoon, Lee, MoonGyu, Kang, Hae Yeon, Qiao, Dandi, Cho, Michael H., Sung, Joohon, Silverman, Edwin K., Yang, Hyeon-Jong, Won, Sungho
Publicado 2018

Interaction of Cigarette Smoking and Polygenic Risk Score on Reduced Lung Function

por Kim, Woori, Moll, Matthew, Qiao, Dandi, Hobbs, Brian D., Shrine, Nick, Sakornsakolpat, Phuwanat, Tobin, Martin D., Dudbridge, Frank, Wain, Louise V., Ladd-Acosta, Christine, Chatterjee, Nilanjan, Silverman, Edwin K., Cho, Michael H., Beaty, Terri H.
Publicado 2021

A linear prognostic score based on the ratio of interleukin-6 to interleukin-10 predicts outcomes in COVID-19

por McElvaney, Oliver J, Hobbs, Brian D, Qiao, Dandi, McElvaney, Oisín F, Moll, Matthew, McEvoy, Natalie L, Clarke, Jennifer, O'Connor, Eoin, Walsh, Seán, Cho, Michael H, Curley, Gerard F, McElvaney, Noel G
Publicado 2020

Corrigendum to ‘A linear prognostic score based on the ratio of interleukin-6 to interleukin-10 predicts outcomes in COVID-19’

por McElvaney, Oliver J, Hobbs, Brian D, Qiao, Dandi, McElvaney, Oisín F, Moll, Matthew, McEvoy, Natalie L, Clarke, Jennifer, O'Connor, Eoin, Walsh, Sean, Cho, Michael H, Curley, Gerard F, McElvaney, Noel G
Publicado 2020

FAM13A Represses AMPK Activity and Regulates Hepatic Glucose and Lipid Metabolism

por Lin, Xin, Liou, Yae-Huei, Li, Yujun, Gong, Lu, Li, Yan, Hao, Yuan, Pham, Betty, Xu, Shuang, Jiang, Zhiqiang, Li, Lijia, Peng, Yifan, Qiao, Dandi, Lin, Honghuang, Liu, Pengda, Wei, Wenyi, Zhang, Guo, Lee, Chih-Hao, Zhou, Xiaobo
Publicado 2020

A robust and adaptive framework for interaction testing in quantitative traits between multiple genetic loci and exposure variables

por Hecker, Julian, Prokopenko, Dmitry, Moll, Matthew, Lee, Sanghun, Kim, Wonji, Qiao, Dandi, Voorhies, Kirsten, Kim, Woori, Vansteelandt, Stijn, Hobbs, Brian D., Cho, Michael H., Silverman, Edwin K., Lutz, Sharon M., DeMeo, Dawn L., Weiss, Scott T., Lange, Christoph
Publicado 2022

A Genome-Wide Linkage Study for Chronic Obstructive Pulmonary Disease in a Dutch Genetic Isolate Identifies Novel Rare Candidate Variants

por Nedeljkovic, Ivana, Terzikhan, Natalie, Vonk, Judith M., van der Plaat, Diana A., Lahousse, Lies, van Diemen, Cleo C., Hobbs, Brian D., Qiao, Dandi, Cho, Michael H., Brusselle, Guy G., Postma, Dirkje S., Boezen, H. M., van Duijn, Cornelia M., Amin, Najaf
Publicado 2018

Association of clonal hematopoiesis with chronic obstructive pulmonary disease

por Miller, Peter G., Qiao, Dandi, Rojas-Quintero, Joselyn, Honigberg, Michael C., Sperling, Adam S., Gibson, Christopher J., Bick, Alexander G., Niroula, Abhishek, McConkey, Marie E., Sandoval, Brittany, Miller, Brian C., Shi, Weiwei, Viswanathan, Kaushik, Leventhal, Matthew, Werner, Lillian, Moll, Matthew, Cade, Brian E., Barr, R. Graham, Correa, Adolfo, Cupples, L. Adrienne, Gharib, Sina A., Jain, Deepti, Gogarten, Stephanie M., Lange, Leslie A., London, Stephanie J., Manichaikul, Ani, O’Connor, George T., Oelsner, Elizabeth C., Redline, Susan, Rich, Stephen S., Rotter, Jerome I., Ramachandran, Vasan, Yu, Bing, Sholl, Lynette, Neuberg, Donna, Jaiswal, Siddhartha, Levy, Bruce D., Owen, Caroline A., Natarajan, Pradeep, Silverman, Edwin K., van Galen, Peter, Tesfaigzi, Yohannes, Cho, Michael H., Ebert, Benjamin L.
Publicado 2022

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

por 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.
Publicado 2019

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

por 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
Publicado 2020

The genetic determinants of recurrent somatic mutations in 43,693 blood genomes

por Weinstock, Joshua S., Laurie, Cecelia A., Broome, Jai G., Taylor, Kent D., Guo, Xiuqing, Shuldiner, Alan R., O’Connell, Jeffrey R., Lewis, Joshua P., Boerwinkle, Eric, Barnes, Kathleen C., Chami, Nathalie, Kenny, Eimear E., Loos, Ruth J. F., Fornage, Myriam, Redline, Susan, Cade, Brian E., Gilliland, Frank D., Chen, Zhanghua, Gauderman, W. James, Kumar, Rajesh, Grammer, Leslie, Schleimer, Robert P., Psaty, Bruce M., Bis, Joshua C., Brody, Jennifer A., Silverman, Edwin K., Yun, Jeong H., Qiao, Dandi, Weiss, Scott T., Lasky-Su, Jessica, DeMeo, Dawn L., Palmer, Nicholette D., Freedman, Barry I., Bowden, Donald W., Cho, Michael H., Vasan, Ramachandran S., Johnson, Andrew D., Yanek, Lisa R., Becker, Lewis C., Kardia, Sharon, He, Jiang, Kaplan, Robert, Heckbert, Susan R., Smith, Nicholas L., Wiggins, Kerri L., Arnett, Donna K., Irvin, Marguerite R., Tiwari, Hemant, Correa, Adolfo, Raffield, Laura M., Gao, Yan, de Andrade, Mariza, Rotter, Jerome I., Rich, Stephen S., Manichaikul, Ani W., Konkle, Barbara A., Johnsen, Jill M., Wheeler, Marsha M., Custer, Brian S., Duggirala, Ravindranath, Curran, Joanne E., Blangero, John, Gui, Hongsheng, Xiao, Shujie, Williams, L. Keoki, Meyers, Deborah A., Li, Xingnan, Ortega, Victor, McGarvey, Stephen, Gu, C. Charles, Chen, Yii-Der Ida, Lee, Wen-Jane, Shoemaker, M. Benjamin, Darbar, Dawood, Roden, Dan, Albert, Christine, Kooperberg, Charles, Desai, Pinkal, Blackwell, Thomas W., Abecasis, Goncalo R., Smith, Albert V., Kang, Hyun M., Mathias, Rasika, Natarajan, Pradeep, Jaiswal, Siddhartha, Reiner, Alexander P., Bick, Alexander G.
Publicado 2023

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

por 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
Publicado 2019

Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential

por Nakao, Tetsushi, Bick, Alexander G., Taub, Margaret A., Zekavat, Seyedeh M., Uddin, Md M., Niroula, Abhishek, Carty, Cara L., Lane, John, Honigberg, Michael C., Weinstock, Joshua S., Pampana, Akhil, Gibson, Christopher J., Griffin, Gabriel K., Clarke, Shoa L., Bhattacharya, Romit, Assimes, Themistocles L., Emery, Leslie S., Stilp, Adrienne M., Wong, Quenna, Broome, Jai, Laurie, Cecelia A., Khan, Alyna T., Smith, Albert V., Blackwell, Thomas W., Codd, Veryan, Nelson, Christopher P., Yoneda, Zachary T., Peralta, Juan M., Bowden, Donald W., Irvin, Marguerite R., Boorgula, Meher, Zhao, Wei, Yanek, Lisa R., Wiggins, Kerri L., Hixson, James E., Gu, C. Charles, Peloso, Gina M., Roden, Dan M., Reupena, Muagututi’a S., Hwu, Chii-Min, DeMeo, Dawn L., North, Kari E., Kelly, Shannon, Musani, Solomon K., Bis, Joshua C., Lloyd-Jones, Donald M., Johnsen, Jill M., Preuss, Michael, Tracy, Russell P., Peyser, Patricia A., Qiao, Dandi, Desai, Pinkal, Curran, Joanne E., Freedman, Barry I., Tiwari, Hemant K., Chavan, Sameer, Smith, Jennifer A., Smith, Nicholas L., Kelly, Tanika N., Hidalgo, Bertha, Cupples, L. Adrienne, Weeks, Daniel E., Hawley, Nicola L., Minster, Ryan L., Deka, Ranjan, Naseri, Take T., de las Fuentes, Lisa, Raffield, Laura M., Morrison, Alanna C., Vries, Paul S., Ballantyne, Christie M., Kenny, Eimear E., Rich, Stephen S., Whitsel, Eric A., Cho, Michael H., Shoemaker, M. Benjamin, Pace, Betty S., Blangero, John, Palmer, Nicholette D., Mitchell, Braxton D., Shuldiner, Alan R., Barnes, Kathleen C., Redline, Susan, Kardia, Sharon L.R., Abecasis, Gonçalo R., Becker, Lewis C., Heckbert, Susan R., He, Jiang, Post, Wendy, Arnett, Donna K., Vasan, Ramachandran S., Darbar, Dawood, Weiss, Scott T., McGarvey, Stephen T., de Andrade, Mariza, Chen, Yii-Der Ida, Kaplan, Robert C., Meyers, Deborah A., Custer, Brian S., Correa, Adolfo, Psaty, Bruce M., Fornage, Myriam, Manson, JoAnn E., Boerwinkle, Eric, Konkle, Barbara A., Loos, Ruth J.F., Rotter, Jerome I., Silverman, Edwin K., Kooperberg, Charles, Danesh, John, Samani, Nilesh J., Jaiswal, Siddhartha, Libby, Peter, Ellinor, Patrick T., Pankratz, Nathan, Ebert, Benjamin L., Reiner, Alexander P., Mathias, Rasika A., Do, Ron, Natarajan, Pradeep
Publicado 2022