Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Barnes, Kathleen"'
Autor:
Daya, Michelle, Cox, Corey, Acevedo, Nathalie, Boorgula, Meher P, Campbell, Monica, Chavan, Sameer, Cho, Michael H, David, Gloria L, Kachroo, Priyadarshini, Lasky-Su, Jessica, Li, Xingnan, McHugh, Caitlin P, Qiao, Dandi, Rafaels, Nicholas, Beck, Lisa A, Bleecker, Eugene R, Caraballo, Luis, Cupples, Adrienne L, Figueiredo, Camila A, Gallo, Richard L, Hanifin, Jon, Hansel, Nadia N, Hata, Tissa R, Hersh, Craig P, Knight-Madden, Jennifer, Leung, Donald YM, Guttman-Yassky, Emma, Meyers, Deborah A, O'Connor, George, Ober, Carole, Ong, Peck Y, Ortega, Victor E, Paller, Amy S, Putcha, Nirupama, Reed, Robert M, Schneider, Lynda C, Silverman, Edwin K, Slifka, Mark K, Spergel, Jonathan M, Vasan, Ramachandran S, Viaud-Martinez, Karine A, Watson, Harold, Weiss, Scott T, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Ruczinski, Ingo, Beaty, Terri H, Mathias, Rasika A, Barnes, Kathleen C
Publikováno v:
The Journal of allergy and clinical immunology, vol 148, iss 6
BackgroundTotal serum IgE (tIgE) is an important intermediate phenotype of allergic disease. Whole genome genetic association studies across ancestries may identify important determinants of IgE.ObjectiveWe aimed to increase understanding of genetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::46df25ec3f8a0180fb0189f24bd8deb9
https://escholarship.org/uc/item/6k5046vq
https://escholarship.org/uc/item/6k5046vq
Autor:
Bick, Alexander G, Weinstock, Joshua S, Nandakumar, Satish K, Fulco, Charles P, Bao, Erik L, Zekavat, Seyedeh M, Szeto, Mindy D, Liao, Xiaotian, Leventhal, Matthew J, Nasser, Joseph, Chang, Kyle, Laurie, Cecelia, Burugula, Bala Bharathi, Gibson, Christopher J, Lin, Amy E, Taub, Margaret A, Aguet, Francois, Ardlie, Kristin, Mitchell, Braxton D, Barnes, Kathleen C, Moscati, Arden, Fornage, Myriam, Redline, Susan, Psaty, Bruce M, Silverman, Edwin K, Weiss, Scott T, Palmer, Nicholette D, Vasan, Ramachandran S, Burchard, Esteban G, Kardia, Sharon LR, He, Jiang, Kaplan, Robert C, Smith, Nicholas L, Arnett, Donna K, Schwartz, David A, Correa, Adolfo, de Andrade, Mariza, Guo, Xiuqing, Konkle, Barbara A, Custer, Brian, Peralta, Juan M, Gui, Hongsheng, Meyers, Deborah A, McGarvey, Stephen T, Chen, Ida Yii-Der, Shoemaker, M Benjamin, Peyser, Patricia A, Broome, Jai G, Gogarten, Stephanie M, Wang, Fei Fei, Wong, Quenna, Montasser, May E, Daya, Michelle, Kenny, Eimear E, North, Kari E, Launer, Lenore J, Cade, Brian E, Bis, Joshua C, Cho, Michael H, Lasky-Su, Jessica, Bowden, Donald W, Cupples, L Adrienne, Mak, Angel CY, Becker, Lewis C, Smith, Jennifer A, Kelly, Tanika N, Aslibekyan, Stella, Heckbert, Susan R, Tiwari, Hemant K, Yang, Ivana V, Heit, John A, Lubitz, Steven A, Johnsen, Jill M, Curran, Joanne E, Wenzel, Sally E, Weeks, Daniel E, Rao, Dabeeru C, Darbar, Dawood, Moon, Jee-Young, Tracy, Russell P, Buth, Erin J, Rafaels, Nicholas, Loos, Ruth JF, Durda, Peter, Liu, Yongmei, Hou, Lifang, Lee, Jiwon, Kachroo, Priyadarshini, Freedman, Barry I, Levy, Daniel, Bielak, Lawrence F, Hixson, James E, Floyd, James S, Whitsel, Eric A, Ellinor, Patrick T, Irvin, Marguerite R, Fingerlin, Tasha E, Raffield, Laura M, Armasu, Sebastian M, Wheeler, Marsha M
Publikováno v:
Nature, vol 586, iss 7831
Age is the dominant risk factor for most chronic human diseases, but the mechanisms through which ageing confers this risk are largely unknown1. The age-related acquisition of somatic mutations that lead to clonal expansion in regenerating haematopoi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::7a0a8f97539e2476439614239fdd3d58
https://escholarship.org/uc/item/7w16b34n
https://escholarship.org/uc/item/7w16b34n
Autor:
Kessler, Michael D, Loesch, Douglas P, Perry, James A, Heard-Costa, Nancy L, Taliun, Daniel, Cade, Brian E, Wang, Heming, Daya, Michelle, Ziniti, John, Datta, Soma, Celedón, Juan C, Soto-Quiros, Manuel E, Avila, Lydiana, Weiss, Scott T, Barnes, Kathleen, Redline, Susan S, Vasan, Ramachandran S, Johnson, Andrew D, Mathias, Rasika A, Hernandez, Ryan, Wilson, James G, Nickerson, Deborah A, Abecasis, Goncalo, Browning, Sharon R, Zöllner, Sebastian, O'Connell, Jeffrey R, Mitchell, Braxton D, National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Population Genetics Working Group, O'Connor, Timothy D
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, vol 117, iss 5
De novo mutations (DNMs), or mutations that appear in an individual despite not being seen in their parents, are an important source of genetic variation whose impact is relevant to studies of human evolution, genetics, and disease. Utilizing high-co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5778ea52629dd4de661d77f184f9d3c2
https://escholarship.org/uc/item/4ms3s7pr
https://escholarship.org/uc/item/4ms3s7pr
Autor:
Kowalski, Madeline H, Qian, Huijun, Hou, Ziyi, Rosen, Jonathan D, Tapia, Amanda L, Shan, Yue, Jain, Deepti, Argos, Maria, Arnett, Donna K, Avery, Christy, Barnes, Kathleen C, Becker, Lewis C, Bien, Stephanie A, Bis, Joshua C, Blangero, John, Boerwinkle, Eric, Bowden, Donald W, Buyske, Steve, Cai, Jianwen, Cho, Michael H, Choi, Seung Hoan, Choquet, Hélène, Cupples, L Adrienne, Cushman, Mary, Daya, Michelle, de Vries, Paul S, Ellinor, Patrick T, Faraday, Nauder, Fornage, Myriam, Gabriel, Stacey, Ganesh, Santhi K, Graff, Misa, Gupta, Namrata, He, Jiang, Heckbert, Susan R, Hidalgo, Bertha, Hodonsky, Chani J, Irvin, Marguerite R, Johnson, Andrew D, Jorgenson, Eric, Kaplan, Robert, Kardia, Sharon LR, Kelly, Tanika N, Kooperberg, Charles, Lasky-Su, Jessica A, Loos, Ruth JF, Lubitz, Steven A, Mathias, Rasika A, McHugh, Caitlin P, Montgomery, Courtney, Moon, Jee-Young, Morrison, Alanna C, Palmer, Nicholette D, Pankratz, Nathan, Papanicolaou, George J, Peralta, Juan M, Peyser, Patricia A, Rich, Stephen S, Rotter, Jerome I, Silverman, Edwin K, Smith, Jennifer A, Smith, Nicholas L, Taylor, Kent D, Thornton, Timothy A, Tiwari, Hemant K, Tracy, Russell P, Wang, Tao, Weiss, Scott T, Weng, Lu-Chen, Wiggins, Kerri L, Wilson, James G, Yanek, Lisa R, Zöllner, Sebastian, North, Kari E, Auer, Paul L, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Hematology & Hemostasis Working Group, Raffield, Laura M, Reiner, Alexander P, Li, Yun
Publikováno v:
PLoS genetics, vol 15, iss 12
Most genome-wide association and fine-mapping studies to date have been conducted in individuals of European descent, and genetic studies of populations of Hispanic/Latino and African ancestry are limited. In addition, these populations have more com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::bab8b5c8e78cd50e0e0fef9bcbda665e
https://escholarship.org/uc/item/1h98c4b1
https://escholarship.org/uc/item/1h98c4b1
Autor:
Kachroo, Priyadarshini, Hecker, Julian, Chawes, Bo L, Ahluwalia, Tarunveer S, Cho, Michael H, Qiao, Dandi, Kelly, Rachel S, Chu, Su H, Virkud, Yamini V, Huang, Mengna, Barnes, Kathleen C, Burchard, Esteban G, Eng, Celeste, Hu, Donglei, Celedón, Juan C, Daya, Michelle, Levin, Albert M, Gui, Hongsheng, Williams, L Keoki, Forno, Erick, Mak, Angel CY, Avila, Lydiana, Soto-Quiros, Manuel E, Cloutier, Michelle M, Acosta-Pérez, Edna, Canino, Glorisa, Bønnelykke, Klaus, Bisgaard, Hans, Raby, Benjamin A, Lange, Christoph, Weiss, Scott T, Lasky-Su, Jessica A, National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Consortium
Publikováno v:
Chest, vol 156, iss 6
BackgroundAsthma is a common respiratory disorder with a highly heterogeneous nature that remains poorly understood. The objective was to use whole genome sequencing (WGS) data to identify regions of common genetic variation contributing to lung func
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::0381a72d3f90c0d778febeca2923744b
https://escholarship.org/uc/item/9m92f03v
https://escholarship.org/uc/item/9m92f03v
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:
Obeidat, Ma'en, Li, Xuan, Burgess, Stephen, Zhou, Guohai, Fishbane, Nick, Hansel, Nadia N, Bossé, Yohan, Joubert, Philippe, Hao, Ke, Nickle, David C, Van Den Berge, Maarten, Timens, Wim, Cho, Michael H, Hobbs, Brian D, De Jong, Kim, Boezen, Marike, Hung, Rayjean J, Rafaels, Nicholas, Mathias, Rasika, Ruczinski, Ingo, Beaty, Terri H, Barnes, Kathleen C, Paré, Peter D, Sin, Don D, International COPD Genetics Consortium, Lung EQTL Consortium
Surfactant protein D (SP-D) is produced primarily in the lung and is involved in regulating pulmonary surfactants, lipid homeostasis and innate immunity. Circulating SP-D levels in blood are associated with chronic obstructive pulmonary disease (COPD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b75e424ee5db88225e2312d2816e57a
Autor:
Elmasri, Mary, Romero Rivero, Karina Maribel, Gilman, Robert Hugh, Hansel, Nadia N., Robinson, Colin L., Baumann, Lauren M., Cabrera, Lilia, Hamilton, Robert G., Checkley, William, Combe, Juan, Gomez, Alfonso, Gonzalvez, Guillermo, Barnes, Kathleen, Wise, Robert, Breysse, Patrick, Williams, D'Ann
Publikováno v:
Lung. 192:305-312
Purpose: Fractional exhaled nitric oxide (FeNO) has emerged as an important biomarker in asthma. Increasing evidence points to atopy as a confounding factor in the interpretation of elevated FeNO. We conducted a longitudinal study to understand the c
Autor:
Pino-Yanes, Maria, Gignoux, Christopher R, Galanter, Joshua M, Levin, Albert M, Campbell, Catarina D, Eng, Celeste, Huntsman, Scott, Nishimura, Katherine K, Gourraud, Pierre-Antoine, Mohajeri, Kiana, O'Roak, Brian J, Hu, Donglei, Mathias, Rasika A, Nguyen, Elizabeth A, Roth, Lindsey A, Padhukasahasram, Badri, Moreno-Estrada, Andres, Sandoval, Karla, Winkler, Cheryl A, Lurmann, Fred, Davis, Adam, Farber, Harold J, Meade, Kelley, Avila, Pedro C, Serebrisky, Denise, Chapela, Rocio, Ford, Jean G, Lenoir, Michael A, Thyne, Shannon M, Brigino-Buenaventura, Emerita, Borrell, Luisa N, Rodriguez-Cintron, William, Sen, Saunak, Kumar, Rajesh, Rodriguez-Santana, Jose R, Bustamante, Carlos D, Martinez, Fernando D, Raby, Benjamin A, Weiss, Scott T, Nicolae, Dan L, Ober, Carole, Meyers, Deborah A, Bleecker, Eugene R, Mack, Steven J, Hernandez, Ryan D, Eichler, Evan E, Barnes, Kathleen C, Williams, L Keoki, Torgerson, Dara G, Burchard, Esteban G
Publikováno v:
The Journal of allergy and clinical immunology, vol 135, iss 6
BackgroundIgE is a key mediator of allergic inflammation, and its levels are frequently increased in patients with allergic disorders.ObjectiveWe sought to identify genetic variants associated with IgE levels in Latinos.MethodsWe performed a genome-w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::29b9326c5262a148c0a18946da00e825
https://escholarship.org/uc/item/95s67401
https://escholarship.org/uc/item/95s67401
Autor:
Hunninghake, Gary M., Soto-Quirós, Manuel E., Avila, Lydiana, Kim, Hong P., Lasky-Su, Jessica, Rafaels, Nicholas, Ruczinski, Ingo, Beaty, Terry H., Mathias, Rasika A., Barnes, Kathleen C., Wilk, Jemma B., O’Connor, George T., Gauderman, W. James, Vora, Hita, Baurley, James W., Gilliland, Frank, Liang, Catherine, Sylvia, Jody S., Klanderman, Barbara J., Sharma, Sunita S., Himes, Blanca E., Bossley, Cara J., Israel, Elliot, Raby, Benjamin A., Bush, Andrew, Choi, Augustine M., Weiss, Scott T., Celedón, Juan C.
Single nucleotide polymorphisms (SNPs) in thymic stromal lymphopoietin (TSLP) have been associated with IgE (in girls) and asthma (in general). We sought to determine whether TSLP SNPs are associated with asthma in a sex-specific fashion.We conducted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::72b45f496ff2196a68c86b2dd0a25a86
https://europepmc.org/articles/PMC2970693/
https://europepmc.org/articles/PMC2970693/