Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Bowler, Russell"'
Autor:
Li, Xihao, Li, Zilin, Zhou, Hufeng, Gaynor, Sheila M., Liu, Yaowu, Chen, Han, Sun, Ryan, Dey, Rounak, Arnett, Donna K., Aslibekyan, Stella, Ballantyne, Christie M., Bielak, Lawrence F., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Broome, Jai G., Conomos, Matthew P., Correa, Adolfo, Cupples, L. Adrienne, Curran, Joanne E., Freedman, Barry I., Guo, Xiuqing, Hindy, George, Irvin, Marguerite R., Kardia, Sharon L.R., Kathiresan, Sekar, Khan, Alyna T., Kooperberg, Charles L., Laurie, Cathy C., Liu, X. Shirley, Mahaney, Michael C., Manichaikul, Ani W., Martin, Lisa W., Mathias, Rasika A., McGarvey, Stephen T., Mitchell, Braxton D., Montasser, May E., Moore, Jill E., Morrison, Alanna C., O’Connell, Jeffrey R., Palmer, Nicholette D., Pampana, Akhil, Peralta, Juan M., Peyser, Patricia A., Psaty, Bruce M., Redline, Susan, Rice, Kenneth M., Rich, Stephen S., Smith, Jennifer A., Tiwari, Hemant K., Tsai, Michael Y., Vasan, Ramachandran S., Wang, Fei Fei, Weeks, Daniel E., Weng, Zhiping, Wilson, James G., Yanek, Lisa R., Abe, Namiko, Abecasis, Gonçalo R., Aguet, Francois, Albert, Christine, Almasy, Laura, Alonso, Alvaro, Ament, Seth, Anderson, Peter, Anugu, Pramod, Applebaum-Bowden, Deborah, Ardlie, Kristin, Arking, Dan, Ashley-Koch, Allison, Assimes, Tim, Auer, Paul, Avramopoulos, Dimitrios, Barnard, John, Barnes, Kathleen, Barr, R. Graham, Barron-Casella, Emily, Barwick, Lucas, Beaty, Terri, Beck, Gerald, Becker, Diane, Becker, Lewis, Beer, Rebecca, Beitelshees, Amber, Benjamin, Emelia, Benos, Takis, Bezerra, Marcos, Bis, Joshua, Blackwell, Thomas, Bowler, Russell, Brody, Jennifer, Broeckel, Ulrich, Bunting, Karen
Publikováno v:
Nature genetics
Large-scale whole-genome sequencing studies have enabled the analysis of rare variants (RVs) associated with complex phenotypes. Commonly used RV association tests have limited scope to leverage variant functions. We propose STAAR (variant-set test f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99f12714921c18f4c5508dca85d54088
https://hdl.handle.net/10576/17547
https://hdl.handle.net/10576/17547
Akademický článek
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Akademický článek
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Autor:
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., Batini, Chiara, Zhao, Jing Hua, Wielscher, Matthias, Weiss, Stefan, Kentistou, Katherine A., Cook, James P., Hui, Jennie, Karrasch, Stefan, Imboden, Medea, Harris, Sarah E., Marten, Jonathan, Enroth, Stefan, Kerr, Shona M., Surakka, Ida, Vitart, Veronique, Lehtimäki, Terho, Ewert, Ralf, Gieger, Christian, Homuth, Georg, Joshi, Peter K., Langenberg, Claudia, Lind, Lars, Luan, Jian’an, Mahajan, Anubha, Murray, Alison, Porteous, David J., Rawal, Rajesh, Smith, Blair H., Timmers, Paul R. H. J., 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, Hayward, Caroline, Morris, Andrew P., Agusti, Alvar, Anderson, Wayne, Bakerly, Nawar, Bals, Robert, Barnes, Kathleen C., Bleecker, Eugene R., Bowler, Russell, Brightling, Christopher, de Bruijne, Marleen, Castaldi, Peter J., Celli, Bartolome, Coxson, Harvey O., Crystal, Ron, de Jong, Pim, Dirksen, Asger, Dy, Jennifer, Foreman, Marilyn, Garcia-Aymerich, Judith, Gevenois, Pierre, Ghosh, Soumitra, Gietema, Hester, Hansel, Nadia, Hersh, Craig P., Hoffman, Eric, Kalsheker, Noor, Kauczor, Hans-Ulrich, Laitinen, Tarja, Lambrechts, Diether, Lee, Sang-Do, Litonjua, Augusto A., Loth, Daan W., Lutz, Sharon M., Lynch, David, MacNee, William, McDonald, Merry-Lynn, Newell, John D., Nordestgaard, Borge G., Oh, Yeon-Mok, Paré, Peter D., Pistolesi, Massimo, Postma, Dirkje S., Puhan, Milo, Regan, Elizabeth, Rich, Stephen S., Seo, Joon Beom, Short, Andrea, Stoel, Berend, Sverzellati, Nicola, ter Riet, Gerben, Van Beek, Edwin J. R., van Ginneken, Bram, Vogelmeier, Claus F., Wanner, Adam, Washko, George, Wauters, Els, Wouters, Emiel F. M., Young, Robert P., Zeigler-Heitbrock, Loems, SpiroMeta Consortium, Understanding Society Scientific Group, International COPD Genetics Consortium
Publikováno v:
International COPD Genetics Consortium & Vestbo, J 2019, ' Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations ', Nature Genetics . https://doi.org/10.1038/s41588-018-0342-2
Nature Genetics, 51, 494
Nature Genetics, 51(3), 494-505. Nature Publishing Group
Nat. Genet. 51, 494-505 (2019)
Nature genetics, 51(3), 494-505. Nature Publishing Group
Nature Genetics, 51(3), 494-+. NATURE PUBLISHING GROUP
Nature Genetics, 51, 3, pp. 494
Nature Genetics, 51(3), 494-+. Nature Publishing Group
NATURE GENETICS
Nature genetics
2019, ' Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations ', Nature Genetics, vol. 51, no. 3, pp. 494-+ . https://doi.org/10.1038/s41588-018-0342-2
Nature Genetics, 51, 494
Nature Genetics, 51(3), 494-505. Nature Publishing Group
Nat. Genet. 51, 494-505 (2019)
Nature genetics, 51(3), 494-505. Nature Publishing Group
Nature Genetics, 51(3), 494-+. NATURE PUBLISHING GROUP
Nature Genetics, 51, 3, pp. 494
Nature Genetics, 51(3), 494-+. Nature Publishing Group
NATURE GENETICS
Nature genetics
2019, ' Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations ', Nature Genetics, vol. 51, no. 3, pp. 494-+ . https://doi.org/10.1038/s41588-018-0342-2
Chronic obstructive pulmonary disease (COPD) is the leading cause of respiratory mortality worldwide. Genetic risk loci provide novel insights into disease pathogenesis. We performed a genome-wide association study in 35,735 cases and 222,076 control
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec099389f4fe41f794ef3134769ca9f2
http://hdl.handle.net/10138/313327
http://hdl.handle.net/10138/313327
Autor:
Chen, Han, Huffman, Jennifer E, Brody, Jennifer A, Wang, Chaolong, Lee, Seunggeun, Li, Zilin, Gogarten, Stephanie M, Sofer, Tamar, Bielak, Lawrence F, Bis, Joshua C, Blangero, John, Bowler, Russell P, Cade, Brian E, Cho, Michael H, Correa, Adolfo, Curran, Joanne E, de Vries, Paul S, Glahn, David C, Guo, Xiuqing, Johnson, Andrew D, Kardia, Sharon, Kooperberg, Charles, Lewis, Joshua P, Liu, Xiaoming, Mathias, Rasika A, Mitchell, Braxton D, O'Connell, Jeffrey R, Peyser, Patricia A, Post, Wendy S, Reiner, Alex P, Rich, Stephen S, Rotter, Jerome I, Silverman, Edwin K, Smith, Jennifer A, Vasan, Ramachandran S, Wilson, James G, Yanek, Lisa R, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Hematology and Hemostasis Working Group, Redline, Susan, Smith, Nicholas L, Boerwinkle, Eric, Borecki, Ingrid B, Cupples, L Adrienne, Laurie, Cathy C, Morrison, Alanna C, Rice, Kenneth M, Lin, Xihong
Publikováno v:
American journal of human genetics, vol 104, iss 2
With advances in whole-genome sequencing (WGS) technology, more advanced statistical methods for testing genetic association with rare variants are being developed. Methods in which variants are grouped for analysis are also known as variant-set, gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::e04981594ad18439135805d7f8a27f68
https://escholarship.org/uc/item/1918z4zr
https://escholarship.org/uc/item/1918z4zr
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Bowler, Russell P.1 (AUTHOR) bowlerr@njhealth.org
Publikováno v:
COPD: Journal of Chronic Obstructive Pulmonary Disease. Dec2012, Vol. 9 Issue 6, p651-653. 3p. 1 Chart.
Autor:
Fawzy, Ashraf, Putcha, Nirupama, Paulin, Laura M., Aaron, Carrie P., Labaki, Wassim W., Han, MeiLan K., Wise, Robert A., Kanner, Richard E., Bowler, Russell P., Barr, R. Graham, Hansel, Nadia N., SPIROMICS and COPDGene Investigators
Publikováno v:
Respiratory Research; 1/26/2018, Vol. 19, p1-N.PAG, 9p, 3 Diagrams, 3 Charts
Autor:
Reinhold, Dominik, Morrow, Jarrett D., Jacobson, Sean, Hu, Junxiao, Ringel, Benjamin, Seibold, Max A., Hersh, Craig P., Kechris, Katerina J., Bowler, Russell P.
Publikováno v:
PLoS ONE; 10/09/2017, Vol. 12 Issue 10, p1-20, 20p
Autor:
Sun, Wei, Kechris, Katerina, Jacobson, Sean, Drummond, M Bradley, Hawkins, Gregory A, Yang, Jenny, Chen, Ting-Huei, Quibrera, Pedro Miguel, Anderson, Wayne, Barr, R Graham, Basta, Patricia V, Bleecker, Eugene R, Beaty, Terri, Casaburi, Richard, Castaldi, Peter, Cho, Michael H, Comellas, Alejandro, Crapo, James D, Criner, Gerard, Demeo, Dawn, Christenson, Stephanie A, Couper, David J, Curtis, Jeffrey L, Doerschuk, Claire M, Freeman, Christine M, Gouskova, Natalia A, Han, MeiLan K, Hanania, Nicola A, Hansel, Nadia N, Hersh, Craig P, Hoffman, Eric A, Kaner, Robert J, Kanner, Richard E, Kleerup, Eric C, Lutz, Sharon, Martinez, Fernando J, Meyers, Deborah A, Peters, Stephen P, Regan, Elizabeth A, Rennard, Stephen I, Scholand, Mary Beth, Silverman, Edwin K, Woodruff, Prescott G, O'Neal, Wanda K, Bowler, Russell P, SPIROMICS Research Group, COPDGene Investigators
Publikováno v:
PLoS genetics, vol 12, iss 8
PLoS Genetics
PLoS Genetics, Vol 12, Iss 8, p e1006011 (2016)
PLoS Genetics
PLoS Genetics, Vol 12, Iss 8, p e1006011 (2016)
Implementing precision medicine for complex diseases such as chronic obstructive lung disease (COPD) will require extensive use of biomarkers and an in-depth understanding of how genetic, epigenetic, and environmental variations contribute to phenoty