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of 69
pro vyhledávání: '"Hu, Youna"'
Nowadays, with many e-commerce platforms conducting global business, e-commerce search systems are required to handle product retrieval under multilingual scenarios. Moreover, comparing with maintaining per-country specific e-commerce search systems,
Externí odkaz:
http://arxiv.org/abs/2105.02978
Understanding search queries is critical for shopping search engines to deliver a satisfying customer experience. Popular shopping search engines receive billions of unique queries yearly, each of which can depict any of hundreds of user preferences
Externí odkaz:
http://arxiv.org/abs/2001.04345
Autor:
Hu, Youna
This thesis investigates the effects of the earth's rotation on internal waves from two perspectives of nonlinear internal wave theory: near-resonant triads and weakly nonlinear models. We apply perturbation theory (multiple scale analysis) to the go
Externí odkaz:
http://hdl.handle.net/10012/3180
Understanding search queries is critical for shopping search engines to deliver a satisfying customer experience. Popular shopping search engines receive billions of unique queries yearly, each of which can depict any of hundreds of user preferences
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2d54d4021361e51ca205ff086ff8cf2
Autor:
Huusko, Johanna M., Karjalainen, Minna K., Graham, Britney E., Zhang, Ge, Farrow, Emily G., Miller, Neil A., Jacobsson, Bo, Eidem, Haley R., Murray, Jeffrey C., Bedell, Bruce, Breheny, Patrick, Brown, Noah W., Bødker, Frans L., Litterman, Nadia K., Jiang, Pan-Pan, Russell, Laura, Hinds, David A., Hu, Youna, Rokas, Antonis, Teramo, Kari, Christensen, Kaare, Williams, Scott M., Rämet, Mika, Kingsmore, Stephen F., Ryckman, Kelli K., Hallman, Mikko, Muglia, Louis J.
Publikováno v:
PLoS Genetics
Preterm birth is a leading cause of morbidity and mortality in infants. Genetic and environmental factors play a role in the susceptibility to preterm birth, but despite many investigations, the genetic basis for preterm birth remain largely unknown.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::46f42bea68bf73e3347c0c309cdd9d3a
http://europepmc.org/articles/PMC6042692
http://europepmc.org/articles/PMC6042692
Autor:
Jones, Samuel E., Tyrrell, Jessica, Wood, Andrew R., Beaumont, Robin N., Ruth, Katherine S., Tuke, Marcus A., Yaghootkar, Hanieh, Hu, Youna, Teder-Laving, Maris, Hayward, Caroline, Roenneberg, Till, Wilson, James F., Del Greco, Fabiola, Hicks, Andrew A., Shin, Chol, Yun, Chang-Ho, Lee, Seung Ku, Metspalu, Andres, Byrne, Enda M., Gehrman, Philip R., Tiemeier, Henning, Allebrandt, Karla V., Freathy, Rachel M., Murray, Anna, Hinds, David A., Frayling, Timothy M., Weedon, Michael N.
Publikováno v:
PLoS Genetics, Vol 12, Iss 8, p e1006125 (2016)
PLoS Genetics
PLoS Genetics (online), 12(8). Public Library of Science
Jones, S E, Tyrrell, J, Wood, A R, Beaumont, R N, Ruth, K S, Tuke, M A, Yaghootkar, H, Hu, Y, Teder-laving, M, Hayward, C, Roenneberg, T, Wilson, J F, Del Greco, F, Hicks, A A, Shin, C, Yun, C, Lee, S K, Metspalu, A, Byrne, E M, Gehrman, P R, Tiemeier, H, Allebrandt, K V, Freathy, R M, Murray, A, Hinds, D A, Frayling, T M, Weedon, M N & Shi, J (ed.) 2016, ' Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci ', PLoS Genetics, vol. 12, no. 8, e1006125 . https://doi.org/10.1371/journal.pgen.1006125
PLoS Genetics
PLoS Genetics (online), 12(8). Public Library of Science
Jones, S E, Tyrrell, J, Wood, A R, Beaumont, R N, Ruth, K S, Tuke, M A, Yaghootkar, H, Hu, Y, Teder-laving, M, Hayward, C, Roenneberg, T, Wilson, J F, Del Greco, F, Hicks, A A, Shin, C, Yun, C, Lee, S K, Metspalu, A, Byrne, E M, Gehrman, P R, Tiemeier, H, Allebrandt, K V, Freathy, R M, Murray, A, Hinds, D A, Frayling, T M, Weedon, M N & Shi, J (ed.) 2016, ' Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci ', PLoS Genetics, vol. 12, no. 8, e1006125 . https://doi.org/10.1371/journal.pgen.1006125
Disrupted circadian rhythms and reduced sleep duration are associated with several human diseases, particularly obesity and type 2 diabetes, but until recently, little was known about the genetic factors influencing these heritable traits. We perform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::936f931580b1284259d2fae906453156
http://europepmc.org/articles/PMC4975467?pdf=render
http://europepmc.org/articles/PMC4975467?pdf=render
Akademický článek
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Autor:
Lohmueller, Kirk E., Sparsø, Thomas, Li, Qibin, Andersson, Ehm, Korneliussen, Thorfinn, Albrechtsen, Anders, Banasik, Karina, Grarup, Niels, Hallgrimsdottir, Ingileif, Kiil, Kristoffer, Kilpeläinen, Tuomas O., Krarup, Nikolaj T., Pers, Tune H., Sanchez, Gaston, Hu, Youna, Degiorgio, Michael, Jørgensen, Torben, Sandbæk, Annelli, Lauritzen, Torsten, Brunak, Søren, Kristiansen, Karsten, Li, Yingrui, Hansen, Torben, Wang, Jun, Nielsen, Rasmus, Pedersen, Oluf
Publikováno v:
Lohmueller, K E, Sparsø, T, Li, Q, Andersson, E, Korneliussen, T, Albrechtsen, A, Banasik, K, Grarup, N, Hallgrimsdottir, I, Kiil, K, Kilpeläinen, T O, Krarup, N T, Pers, T H, Sanchez, G, Hu, Y, Degiorgio, M, Jørgensen, T, Sandbæk, A, Lauritzen, T, Brunak, S, Kristiansen, K, Li, Y, Hansen, T, Wang, J, Nielsen, R & Pedersen, O 2014, ' Erratum : Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes (The American Journal of Human Genetics (2013) 93 (1072-1086)) ', American Journal of Human Genetics, vol. 94, no. 3 . https://doi.org/10.1016/j.ajhg.2014.02.002
Lohmueller, K E, Sparsø, T, Li, Q, Andersson, E, Korneliussen, T, Albrechtsen, A, Banasik, K, Grarup, N, Hallgrimsdottir, I, Kiil, K, Kilpeläinen, T O, Krarup, N T, Pers, T H, Sanchez, G, Hu, Y, Degiorgio, M, Jørgensen, T, Sandbæk, A, Lauritzen, T, Brunak, S, Kristiansen, K, Li, Y, Hansen, T, Wang, J, Nielsen, R & Pedersen, O 2014, ' Erratum : Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes (The American Journal of Human Genetics (2013) 93 (1072-1086)) ', American Journal of Human Genetics, vol. 94, no. 3, pp. 479 . https://doi.org/10.1016/j.ajhg.2014.02.002
Lohmueller, K E, Sparsø, T, Li, Q, Andersson, E, Korneliussen, T, Albrechtsen, A, Banasik, K, Grarup, N, Hallgrimsdottir, I, Kiil, K, Kilpeläinen, T O, Krarup, N T, Pers, T H, Sanchez, G, Hu, Y, Degiorgio, M, Jørgensen, T, Sandbæk, A, Lauritzen, T, Brunak, S, Kristiansen, K, Li, Y, Hansen, T, Wang, J, Nielsen, R & Pedersen, O 2014, ' Erratum : Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes (The American Journal of Human Genetics (2013) 93 (1072-1086)) ', American Journal of Human Genetics, vol. 94, no. 3, pp. 479 . https://doi.org/10.1016/j.ajhg.2014.02.002
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4dec809ebf2d6c13623efe05fb72d19f
https://vbn.aau.dk/da/publications/1bee8b7d-9e9b-4b9a-87ca-44512b85e7cd
https://vbn.aau.dk/da/publications/1bee8b7d-9e9b-4b9a-87ca-44512b85e7cd
Autor:
Lange, Leslie A, Hu, Youna, Zhang, He, Xue, Chenyi, Schmidt, Ellen M, Tang, Zheng-Zheng, Bizon, Chris, Lange, Ethan M, Smith, Joshua D, Turner, Emily H, Jun, Goo, Kang, Hyun Min, Peloso, Gina, Auer, Paul, Li, Kuo-Ping, Flannick, Jason, Zhang, Ji, Fuchsberger, Christian, Gaulton, Kyle, Lindgren, Cecilia, Locke, Adam, Manning, Alisa, Sim, Xueling, Rivas, Manuel A, Holmen, Oddgeir L, Gottesman, Omri, Lu, Yingchang, Ruderfer, Douglas, Stahl, Eli A, Duan, Qing, Li, Yun, Durda, Peter, Jiao, Shuo, Isaacs, Aaron, Hofman, Albert, Bis, Joshua C, Correa, Adolfo, Griswold, Michael E, Jakobsdottir, Johanna, Smith, Albert V, Schreiner, Pamela J, Feitosa, Mary F, Zhang, Qunyuan, Huffman, Jennifer E, Crosby, Jacy, Wassel, Christina L, Do, Ron, Franceschini, Nora, Martin, Lisa W, Robinson, Jennifer G, Assimes, Themistocles L, Crosslin, David R, Rosenthal, Elisabeth A, Tsai, Michael, Rieder, Mark J, Farlow, Deborah N, Folsom, Aaron R, Lumley, Thomas, Fox, Ervin R, Carlson, Christopher S, Peters, Ulrike, Jackson, Rebecca D, van Duijn, Cornelia M, Uitterlinden, André G, Levy, Daniel, Rotter, Jerome I, Taylor, Herman A, Gudnason, Vilmundur, Siscovick, David S, Fornage, Myriam, Borecki, Ingrid B, Hayward, Caroline, Rudan, Igor, Chen, Y Eugene, Bottinger, Erwin P, Loos, Ruth JF, Sætrom, Pål, Hveem, Kristian, Boehnke, Michael, Groop, Leif, McCarthy, Mark, Meitinger, Thomas, Ballantyne, Christie M, Gabriel, Stacey B, O'Donnell, Christopher J, Post, Wendy S, North, Kari E, Reiner, Alexander P, Boerwinkle, Eric, Psaty, Bruce M, Altshuler, David, Kathiresan, Sekar, Lin, Dan-Yu, Jarvik, Gail P, Cupples, L Adrienne, Kooperberg, Charles, Wilson, James G, Nickerson, Deborah A, Abecasis, Goncalo R, Rich, Stephen S
Publikováno v:
American journal of human genetics, vol 94, iss 2
Elevated low-density lipoprotein cholesterol (LDL-C) is a treatable, heritable risk factor for cardiovascular disease. Genome-wide association studies (GWASs) have identified 157 variants associated with lipid levels but are not well suited to assess
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::b0c59997ecf5a9de491aa1cfc1960172
https://escholarship.org/uc/item/3w75q2zz
https://escholarship.org/uc/item/3w75q2zz
Autor:
Durda, Peter, Ruderfer, Douglas, Jun, Goo, Zhang, Ji, Li, Yun, Lange, Leslie A., Lindgren, Cecilia, Gaulton, Kyle, Flannick, Jason, Locke, Adam, Peloso, Gina, Xue, Chenyi, Holmen, Oddgeir L., Turner, Emily H., Tang, Zheng-Zheng, Auer, Paul, Smith, Joshua D., Manning, Alisa, Li, Kuo-ping, Bizon, Chris, Rivas, Manuel A., Zhang, He, Kang, Hyun Min, Schmidt, Ellen M., Hu, Youna, Stahl, Eli A., Lange, Ethan M., Fuchsberger, Christian, Sim, Xueling, Gottesman, Omri, Duan, Qing, Lu, Yingchang
Elevated low-density lipoprotein cholesterol (LDL-C) is a treatable, heritable risk factor for cardiovascular disease. Genome-wide association studies (GWASs) have identified 157 variants associated with lipid levels but are not well suited to assess
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abb6bc65c44511152a95a6b8de37602f