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Autor:
Yengo, Loïc, Vedantam, Sailaja, Marouli, Eirini, Sidorenko, Julia, Bartell, Eric, Sakaue, Saori, Graff, Marielisa, Eliasen, Anders U, Jiang, Yunxuan, Raghavan, Sridharan, Miao, Jenkai, Arias, Joshua D, Graham, Sarah E, Mukamel, Ronen E, Spracklen, Cassandra N, Yin, Xianyong, Chen, Shyh-Huei, Ferreira, Teresa, Highland, Heather H, Ji, Yingjie, Karaderi, Tugce, Lin, Kuang, Lüll, Kreete, Malden, Deborah E, Medina-Gomez, Carolina, Machado, Moara, Moore, Amy, Rüeger, Sina, Sim, Xueling, Vrieze, Scott, Ahluwalia, Tarunveer S, Akiyama, Masato, Allison, Matthew A, Alvarez, Marcus, Andersen, Mette K, Ani, Alireza, Appadurai, Vivek, Arbeeva, Liubov, Bhaskar, Seema, Bielak, Lawrence F, Bollepalli, Sailalitha, Bonnycastle, Lori L, Bork-Jensen, Jette, Bradfield, Jonathan P, Bradford, Yuki, Braund, Peter S, Brody, Jennifer A, Burgdorf, Kristoffer S, Cade, Brian E, Cai, Hui, Cai, Qiuyin, Campbell, Archie, Cañadas-Garre, Marisa, Catamo, Eulalia, Chai, Jin-Fang, Chai, Xiaoran, Chang, Li-Ching, Chang, Yi-Cheng, Chen, Chien-Hsiun, Chesi, Alessandra, Choi, Seung Hoan, Chung, Ren-Hua, Cocca, Massimiliano, Concas, Maria Pina, Couture, Christian, Cuellar-Partida, Gabriel, Danning, Rebecca, Daw, E Warwick, Degenhard, Frauke, Delgado, Graciela E, Delitala, Alessandro, Demirkan, Ayse, Deng, Xuan, Devineni, Poornima, Dietl, Alexander, Dimitriou, Maria, Dimitrov, Latchezar, Dorajoo, Rajkumar, Ekici, Arif B, Engmann, Jorgen E, Fairhurst-Hunter, Zammy, Farmaki, Aliki-Eleni, Faul, Jessica D, Fernandez-Lopez, Juan-Carlos, Forer, Lukas, Francescatto, Margherita, Freitag-Wolf, Sandra, Fuchsberger, Christian, Galesloot, Tessel E, Gao, Yan, Gao, Zishan, Geller, Frank, Giannakopoulou, Olga, Giulianini, Franco, Gjesing, Anette P, Goel, Anuj, Gordon, Scott D, Gorski, Mathias, Grove, Jakob, Guo, Xiuqing, Gustafsson, Stefan, Haessler, Jeffrey, Hansen, Thomas F, Havulinna, Aki S, Haworth, Simon J, He, Jing, Heard-Costa, Nancy, Hebbar, Prashantha, Hindy, George, Ho, Yuk-Lam A, Hofer, Edith, Holliday, Elizabeth, Horn, Katrin, Hornsby, Whitney E, Hottenga, Jouke-Jan, Huang, Hongyan, Huang, Jie, Huerta-Chagoya, Alicia, Huffman, Jennifer E, Hung, Yi-Jen, Huo, Shaofeng, Hwang, Mi Yeong, Iha, Hiroyuki, Ikeda, Daisuke D, Isono, Masato, Jackson, Anne U, Jäger, Susanne, Jansen, Iris E, Johansson, Ingegerd, Jonas, Jost B, Jonsson, Anna, Jørgensen, Torben, Kalafati, Ioanna-Panagiota, Kanai, Masahiro, Kanoni, Stavroula, Kårhus, Line L, Kasturiratne, Anuradhani, Katsuya, Tomohiro, Kawaguchi, Takahisa, Kember, Rachel L, Kentistou, Katherine A, Kim, Han-Na, Kim, Young Jin, Kleber, Marcus E, Knol, Maria J, Kurbasic, Azra, Lauzon, Marie, Le, Phuong, Lea, Rodney, Lee, Jong-Young, Leonard, Hampton L, Li, Shengchao A, Li, Xiaohui, Li, Xiaoyin, Liang, Jingjing, Lin, Honghuang, Lin, Shih-Yi, Liu, Jun, Liu, Xueping, Lo, Ken Sin, Long, Jirong, Lores-Motta, Laura, Luan, Jian'an, Lyssenko, Valeriya, Lyytikäinen, Leo-Pekka, Mahajan, Anubha, Mamakou, Vasiliki, Mangino, Massimo, Manichaikul, Ani, Marten, Jonathan, Mattheisen, Manuel, Mavarani, Laven, McDaid, Aaron F, Meidtner, Karina, Melendez, Tori L, Mercader, Josep M, Milaneschi, Yuri, Miller, Jason E, Millwood, Iona Y, Mishra, Pashupati P, Mitchell, Ruth E, Møllehave, Line T, Morgan, Anna, Mucha, Soeren, Munz, Matthias, Nakatochi, Masahiro, Nelson, Christopher P, Nethander, Maria, Nho, Chu Won, Nielsen, Aneta A, Nolte, Ilja M, Nongmaithem, Suraj S, Noordam, Raymond, Ntalla, Ioanna, Nutile, Teresa, Pandit, Anita, Christofidou, Paraskevi, Pärna, Katri, Pauper, Marc, Petersen, Eva RB, Petersen, Liselotte V, Pitkänen, Niina, Polašek, Ozren, Poveda, Alaitz, Preuss, Michael H, Pyarajan, Saiju, Raffield, Laura M, Rakugi, Hiromi, Ramirez, Julia, Rasheed, Asif, Raven, Dennis, Rayner, Nigel W, Riveros, Carlos, Rohde, Rebecca, Ruggiero, Daniela, Ruotsalainen, Sanni E, Ryan, Kathleen A, Sabater-Lleal, Maria, Saxena, Richa, Scholz, Markus, Sendamarai, Anoop, Shen, Botong, Shi, Jingchunzi, Shin, Jae Hun, Sidore, Carlo, Sitlani, Colleen M, Slieker, Roderick C, Smit, Roelof AJ, Smith, Albert V, Smith, Jennifer A, Smyth, Laura J, Southam, Lorraine, Steinthorsdottir, Valgerdur, Sun, Liang, Takeuchi, Fumihiko, Tallapragada, Divya Sri Priyanka, Taylor, Kent D, Tayo, Bamidele O, Tcheandjieu, Catherine, Terzikhan, Natalie, Tesolin, Paola, Teumer, Alexander, Theusch, Elizabeth, Thompson, Deborah J, Thorleifsson, Gudmar, Timmers, Paul RHJ, Trompet, Stella, Turman, Constance, Vaccargiu, Simona, Van Der Laan, Sander W, Van Der Most, Peter J, Van Klinken, Jan B, Van Setten, Jessica, Verma, Shefali S, Verweij, Niek, Veturi, Yogasudha, Wang, Carol A, Wang, Chaolong, Wang, Lihua, Wang, Zhe, Warren, Helen R, Bin Wei, Wen, Wickremasinghe, Ananda R, Wielscher, Matthias, Wiggins, Kerri L, Winsvold, Bendik S, Wong, Andrew, Wu, Yang, Wuttke, Matthias, Xia, Rui, Xie, Tian, Yamamoto, Ken, Yang, Jingyun, Yao, Jie, Young, Hannah, Yousri, Noha A, Yu, Lei, Zeng, Lingyao, Zhang, Weihua, Zhang, Xinyuan, Zhao, Jing-Hua, Zhao, Wei, Zhou, Wei, Zimmermann, Martina E, Zoledziewska, Magdalena, Adair, Linda S, Adams, Hieab HH, Aguilar-Salinas, Carlos A, Al-Mulla, Fahd, Arnett, Donna K, Asselbergs, Folkert W, Åsvold, Bjørn Olav, Attia, John, Banas, Bernhard, Bandinelli, Stefania, Bennett, David A, Bergler, Tobias, Bharadwaj, Dwaipayan, Biino, Ginevra, Bisgaard, Hans, Boerwinkle, Eric, Böger, Carsten A, Bønnelykke, Klaus, Boomsma, Dorret I, Børglum, Anders D, Borja, Judith B, Bouchard, Claude, Bowden, Donald W, Brandslund, Ivan, Brumpton, Ben, Buring, Julie E, Caulfield, Mark J, Chambers, John C, Chandak, Giriraj R, Chanock, Stephen J, Chaturvedi, Nish, Chen, Yii-Der Ida, Chen, Zhengming, Cheng, Ching-Yu, Christophersen, Ingrid E, Ciullo, Marina, Cole, John W, Collins, Francis S, Cooper, Richard S, Cruz, Miguel, Cucca, Francesco, Cupples, L Adrienne, Cutler, Michael J, Damrauer, Scott M, Dantoft, Thomas M, De Borst, Gert J, De Groot, Lisette CPGM, De Jager, Philip L, De Kleijn, Dominique PV, Janaka De Silva, H, Dedoussis, George V, Den Hollander, Anneke I, Du, Shufa, Easton, Douglas F, Elders, Petra JM, Eliassen, A Heather, Ellinor, Patrick T, Elmståhl, Sölve, Erdmann, Jeanette, Evans, Michele K, Fatkin, Diane, Feenstra, Bjarke, Feitosa, Mary F, Ferrucci, Luigi, Ford, Ian, Fornage, Myriam, Franke, Andre, Franks, Paul W, Freedman, Barry I, Gasparini, Paolo, Gieger, Christian, Girotto, Giorgia, Goddard, Michael E, Golightly, Yvonne M, Gonzalez-Villalpando, Clicerio, Gordon-Larsen, Penny, Grallert, Harald, Grant, Struan FA, Grarup, Niels, Griffiths, Lyn, Gudnason, Vilmundur, Haiman, Christopher, Hakonarson, Hakon, Hansen, Torben, Hartman, Catharina A, Hattersley, Andrew T, Hayward, Caroline, Heckbert, Susan R, Heng, Chew-Kiat, Hengstenberg, Christian, Hewitt, Alex W, Hishigaki, Haretsugu, Hoyng, Carel B, Huang, Paul L, Huang, Wei, Hunt, Steven C, Hveem, Kristian, Hyppönen, Elina, Iacono, William G, Ichihara, Sahoko, Ikram, M Arfan, Isasi, Carmen R, Jackson, Rebecca D, Jarvelin, Marjo-Riitta, Jin, Zi-Bing, Jöckel, Karl-Heinz, Joshi, Peter K, Jousilahti, Pekka, Jukema, J Wouter, Kähönen, Mika, Kamatani, Yoichiro, Kang, Kui Dong, Kaprio, Jaakko, Kardia, Sharon LR, Karpe, Fredrik, Kato, Norihiro, Kee, Frank, Kessler, Thorsten, Khera, Amit V, Khor, Chiea Chuen, Kiemeney, Lambertus ALM, Kim, Bong-Jo, Kim, Eung Kweon, Kim, Hyung-Lae, Kirchhof, Paulus, Kivimaki, Mika, Koh, Woon-Puay, Koistinen, Heikki A, Kolovou, Genovefa D, Kooner, Jaspal S, Kooperberg, Charles, Köttgen, Anna, Kovacs, Peter, Kraaijeveld, Adriaan, Kraft, Peter, Krauss, Ronald M, Kumari, Meena, Kutalik, Zoltan, Laakso, Markku, Lange, Leslie A, Langenberg, Claudia, Launer, Lenore J, Le Marchand, Loic, Lee, Hyejin, Lee, Nanette R, Lehtimäki, Terho, Li, Huaixing, Li, Liming, Lieb, Wolfgang, Lin, Xu, Lind, Lars, Linneberg, Allan, Liu, Ching-Ti, Liu, Jianjun, Loeffler, Markus, London, Barry, Lubitz, Steven A, Lye, Stephen J, Mackey, David A, Mägi, Reedik, Magnusson, Patrik KE, Marcus, Gregory M, Vidal, Pedro Marques, Martin, Nicholas G, März, Winfried, Matsuda, Fumihiko, McGarrah, Robert W, McGue, Matt, McKnight, Amy Jayne, Medland, Sarah E, Mellström, Dan, Metspalu, Andres, Mitchell, Braxton D, Mitchell, Paul, Mook-Kanamori, Dennis O, Morris, Andrew D, Mucci, Lorelei A, Munroe, Patricia B, Nalls, Mike A, Nazarian, Saman, Nelson, Amanda E, Neville, Matt J, Newton-Cheh, Christopher, Nielsen, Christopher S, Nöthen, Markus M, Ohlsson, Claes, Oldehinkel, Albertine J, Orozco, Lorena, Pahkala, Katja, Pajukanta, Päivi, Palmer, Colin NA, Parra, Esteban J, Pattaro, Cristian, Pedersen, Oluf, Pennell, Craig E, Penninx, Brenda WJH, Perusse, Louis, Peters, Annette, Peyser, Patricia A, Porteous, David J, Posthuma, Danielle, Power, Chris, Pramstaller, Peter P, Province, Michael A, Qi, Qibin, Qu, Jia, Rader, Daniel J, Raitakari, Olli T, Ralhan, Sarju, Rallidis, Loukianos S, Rao, Dabeeru C, Redline, Susan, Reilly, Dermot F, Reiner, Alexander P, Rhee, Sang Youl, Ridker, Paul M, Rienstra, Michiel, Ripatti, Samuli, Ritchie, Marylyn D, Roden, Dan M, Rosendaal, Frits R, Rotter, Jerome I, Rudan, Igor, Rutters, Femke, Sabanayagam, Charumathi, Saleheen, Danish, Salomaa, Veikko, Samani, Nilesh J, Sanghera, Dharambir K, Sattar, Naveed, Schmidt, Börge, Schmidt, Helena, Schmidt, Reinhold, Schulze, Matthias B, Schunkert, Heribert, Scott, Laura J, Scott, Rodney J, Sever, Peter, Shiroma, Eric J, Shoemaker, M Benjamin, Shu, Xiao-Ou, Simonsick, Eleanor M, Sims, Mario, Singh, Jai Rup, Singleton, Andrew B, Sinner, Moritz F, Smith, J Gustav, Snieder, Harold, Spector, Tim D, Stampfer, Meir J, Stark, Klaus J, Strachan, David P, 'T Hart, Leen M, Tabara, Yasuharu, Tang, Hua, Tardif, Jean-Claude, Thanaraj, Thangavel A, Timpson, Nicholas J, Tönjes, Anke, Tremblay, Angelo, Tuomi, Tiinamaija, Tuomilehto, Jaakko, Tusié-Luna, Maria-Teresa, Uitterlinden, Andre G, Van Dam, Rob M, Van Der Harst, Pim, Van Der Velde, Nathalie, Van Duijn, Cornelia M, Van Schoor, Natasja M, Vitart, Veronique, Völker, Uwe, Vollenweider, Peter, Völzke, Henry, Wacher-Rodarte, Niels H, Walker, Mark, Wang, Ya Xing, Wareham, Nicholas J, Watanabe, Richard M, Watkins, Hugh, Weir, David R, Werge, Thomas M, Widen, Elisabeth, Wilkens, Lynne R, Willemsen, Gonneke, Willett, Walter C, Wilson, James F, Wong, Tien-Yin, Woo, Jeong-Taek, Wright, Alan F, Wu, Jer-Yuarn, Xu, Huichun, Yajnik, Chittaranjan S, Yokota, Mitsuhiro, Yuan, Jian-Min, Zeggini, Eleftheria, Zemel, Babette S, Zheng, Wei, Zhu, Xiaofeng, Zmuda, Joseph M, Zonderman, Alan B, Zwart, John-Anker, 23andMe Research Team, VA Million Veteran Program, DiscovEHR (DiscovEHR And MyCode Community Health Initiative), EMERGE (Electronic Medical Records And Genomics Network), Lifelines Cohort Study, PRACTICAL Consortium, Understanding Society Scientific Group, Chasman, Daniel I, Cho, Yoon Shin, Heid, Iris M, McCarthy, Mark I, Ng, Maggie CY, O'Donnell, Christopher J, Rivadeneira, Fernando, Thorsteinsdottir, Unnur, Sun, Yan V, Tai, E Shyong, Boehnke, Michael, Deloukas, Panos, Justice, Anne E, Lindgren, Cecilia M, Loos, Ruth JF, Mohlke, Karen L, North, Kari E, Stefansson, Kari, Walters, Robin G, Winkler, Thomas W, Young, Kristin L, Loh, Po-Ru, Yang, Jian, Esko, Tõnu, Assimes, Themistocles L, Auton, Adam, Abecasis, Goncalo R, Willer, Cristen J, Locke, Adam E, Berndt, Sonja I, Lettre, Guillaume, Frayling, Timothy M, Okada, Yukinori, Wood, Andrew R, Visscher, Peter M, Hirschhorn, Joel N
Publikováno v:
Nature
Nature, 610(7933), 704-712. Nature Publishing Group
Nature, 610. Nature Publishing Group
Nature 610, 704–712 (2022)
23Andme Research Team 2022, ' A saturated map of common genetic variants associated with human height ', Nature, vol. 610, no. 7933, pp. 704-712 . https://doi.org/10.1038/s41586-022-05275-y, https://doi.org/10.1038/s41586-022-05275-y
NATURE
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Yengo, L, Vedantam, S, Marouli, E, Sidorenko, J, Bartell, E, Sakaue, S, Graff, M, Eliasen, A U, Jiang, Y, Raghavan, S, Miao, J, Arias, J D, Graham, S E, Mukamel, R E, Spracklen, C N, Yin, X, Chen, S-H, Ferreira, T, Highland, H H, Ji, Y, Karaderi, T, Lin, K, Lull, K, Malden, D E, Andersen, M K, Appadurai, V, Bork-Jensen, J, Burgdorf, K S, Hansen, T F, Jonsson, A, Jorgensen, T, Liu, J, Mollehave, L T, Smit, R A J, Zhao, J-H, Bisgaard, H, Bonnelykke, K, Dantoft, T M, Grarup, N, Hansen, T, Jackson, R D, Karpe, F, Kovacs, P, Lind, L, Linneberg, A, Pedersen, O, Werge, T M, Sun, Y, Loos, R J F, Winkler, T W, 23andMe Res Team, VA Million Vet Program, DiscovEHR DiscovEHR MyCode Communi, eEMERGE Elect Med Records Genomics, LifeLines Cohort Study, PRACTICAL consortium & Understanding Soc Sci Grp 2022, ' A saturated map of common genetic variants associated with human height ', Nature, vol. 610, pp. 704–712 . https://doi.org/10.1038/s41586-022-05275-y
23andMe Research Team, Yengo, L, Vedantam, S, Marouli, E, Sidorenko, J, Bartell, E, Sakaue, S, Graff, M, Eliasen, A U, Jiang, Y, Raghavan, S, Miao, J, Arias, J D, Graham, S E, Mukamel, R E, Spracklen, C N, Yin, X, Chen, S-H, Ferreira, T, Highland, H H, Ji, Y, Karaderi, T, Lin, K, Lüll, K, Malden, D E, Medina-Gomez, C, Machado, M, Moore, A, Rüeger, S, Sim, X, Vrieze, S, Ahluwalia, T S, Akiyama, M, Allison, M A, Alvarez, M, Andersen, M K, Ani, A, Appadurai, V, Arbeeva, L, Cai, H, Cañadas-Garre, M, Li, X, Nelson, C P, Smyth, L J, Sun, L, Wang, Z, Cole, J W, Cooper, R S, Kee, F, McKnight, A J & Weir, D R 2022, ' A saturated map of common genetic variants associated with human height ', Nature . https://doi.org/10.1038/s41586-022-05275-y
2022, ' A saturated map of common genetic variants associated with human height ', Nature, vol. 610, no. 7933, pp. 704-712 . https://doi.org/10.1038/s41586-022-05275-y
23andMe Research Team, VA Million Veteran Program, DiscovEHR (DiscovEHR and MyCode Community Health Initiative), eMERGE (Electronic Medical Records and Genomics Network), Lifelines Cohort Study, The PRACTICAL Consortium & Understanding Society Scientific Group 2022, ' A saturated map of common genetic variants associated with human height ', Nature, vol. 610, pp. 704–712 . https://doi.org/10.1038/s41586-022-05275-y
Nature, 610(7933), 704-712
Nature, 610, 704-712. Nature Publishing Group
Nature, 610, 7933, pp. 704-712
Nature 610 (2022)
Yengo, L, Vedantam, S, Marouli, E, Sidorenko, J, Bartell, E, Sakaue, S, Graff, M, Eliasen, A U, Jiang, Y, Raghavan, S, Miao, J, Arias, J D, Graham, S E, Mukamel, R E, Spracklen, C N, Yin, X, Chen, S-H, Ferreira, T, Highland, H H, Ji, Y, Karaderi, T, Lin, K, Lüll, K, Malden, D E, Medina-Gomez, C, Machado, M, Moore, A, Rüeger, S, Sim, X, Vrieze, S, Ahluwalia, T S, Akiyama, M, Andersen, M K, Grove, J, Hansen, T F, Jørgensen, T, Mattheisen, M, Petersen, L V, Wang, Z, Børglum, A D, Dantoft, T M, Grarup, N, Hansen, T, Huang, W, Nielsen, C S, Pedersen, O, Ng, M C Y, Sun, Y V, Winkler, T W, Yang, J, 23andMe Research Team, VA Million Vet Program, DiscovEHR Collaboration, eMERGE Consortium, Lifelines Cohort Study, The PRACTICAL Consortium & Understanding Society Scientific Group 2022, ' A saturated map of common genetic variants associated with human height ', Nature, vol. 610, no. 7933, pp. 704–712 . https://doi.org/10.1038/s41586-022-05275-y
Nature, 610, 704-712
Nature, vol. 610, no. 7933, pp. 704-712
eMERGE (Electronic Medical Records and Genomics Network), The PRACTICAL consortium, Lifelines Cohort Study, 23andMe Research team, Understanding Society Scientific group, VA Million Veteran Program & DiscovEHR (DiscovEHR and MyCode Community Health Initiative) 2022, ' A saturated map of common genetic variants associated with human height ', Nature, vol. 610, pp. 704-712 . https://doi.org/10.1038/s41586-022-05275-y
Nature, 610(7933), 704-712. Nature Publishing Group
Nature, 610. Nature Publishing Group
Nature 610, 704–712 (2022)
23Andme Research Team 2022, ' A saturated map of common genetic variants associated with human height ', Nature, vol. 610, no. 7933, pp. 704-712 . https://doi.org/10.1038/s41586-022-05275-y, https://doi.org/10.1038/s41586-022-05275-y
NATURE
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Yengo, L, Vedantam, S, Marouli, E, Sidorenko, J, Bartell, E, Sakaue, S, Graff, M, Eliasen, A U, Jiang, Y, Raghavan, S, Miao, J, Arias, J D, Graham, S E, Mukamel, R E, Spracklen, C N, Yin, X, Chen, S-H, Ferreira, T, Highland, H H, Ji, Y, Karaderi, T, Lin, K, Lull, K, Malden, D E, Andersen, M K, Appadurai, V, Bork-Jensen, J, Burgdorf, K S, Hansen, T F, Jonsson, A, Jorgensen, T, Liu, J, Mollehave, L T, Smit, R A J, Zhao, J-H, Bisgaard, H, Bonnelykke, K, Dantoft, T M, Grarup, N, Hansen, T, Jackson, R D, Karpe, F, Kovacs, P, Lind, L, Linneberg, A, Pedersen, O, Werge, T M, Sun, Y, Loos, R J F, Winkler, T W, 23andMe Res Team, VA Million Vet Program, DiscovEHR DiscovEHR MyCode Communi, eEMERGE Elect Med Records Genomics, LifeLines Cohort Study, PRACTICAL consortium & Understanding Soc Sci Grp 2022, ' A saturated map of common genetic variants associated with human height ', Nature, vol. 610, pp. 704–712 . https://doi.org/10.1038/s41586-022-05275-y
23andMe Research Team, Yengo, L, Vedantam, S, Marouli, E, Sidorenko, J, Bartell, E, Sakaue, S, Graff, M, Eliasen, A U, Jiang, Y, Raghavan, S, Miao, J, Arias, J D, Graham, S E, Mukamel, R E, Spracklen, C N, Yin, X, Chen, S-H, Ferreira, T, Highland, H H, Ji, Y, Karaderi, T, Lin, K, Lüll, K, Malden, D E, Medina-Gomez, C, Machado, M, Moore, A, Rüeger, S, Sim, X, Vrieze, S, Ahluwalia, T S, Akiyama, M, Allison, M A, Alvarez, M, Andersen, M K, Ani, A, Appadurai, V, Arbeeva, L, Cai, H, Cañadas-Garre, M, Li, X, Nelson, C P, Smyth, L J, Sun, L, Wang, Z, Cole, J W, Cooper, R S, Kee, F, McKnight, A J & Weir, D R 2022, ' A saturated map of common genetic variants associated with human height ', Nature . https://doi.org/10.1038/s41586-022-05275-y
2022, ' A saturated map of common genetic variants associated with human height ', Nature, vol. 610, no. 7933, pp. 704-712 . https://doi.org/10.1038/s41586-022-05275-y
23andMe Research Team, VA Million Veteran Program, DiscovEHR (DiscovEHR and MyCode Community Health Initiative), eMERGE (Electronic Medical Records and Genomics Network), Lifelines Cohort Study, The PRACTICAL Consortium & Understanding Society Scientific Group 2022, ' A saturated map of common genetic variants associated with human height ', Nature, vol. 610, pp. 704–712 . https://doi.org/10.1038/s41586-022-05275-y
Nature, 610(7933), 704-712
Nature, 610, 704-712. Nature Publishing Group
Nature, 610, 7933, pp. 704-712
Nature 610 (2022)
Yengo, L, Vedantam, S, Marouli, E, Sidorenko, J, Bartell, E, Sakaue, S, Graff, M, Eliasen, A U, Jiang, Y, Raghavan, S, Miao, J, Arias, J D, Graham, S E, Mukamel, R E, Spracklen, C N, Yin, X, Chen, S-H, Ferreira, T, Highland, H H, Ji, Y, Karaderi, T, Lin, K, Lüll, K, Malden, D E, Medina-Gomez, C, Machado, M, Moore, A, Rüeger, S, Sim, X, Vrieze, S, Ahluwalia, T S, Akiyama, M, Andersen, M K, Grove, J, Hansen, T F, Jørgensen, T, Mattheisen, M, Petersen, L V, Wang, Z, Børglum, A D, Dantoft, T M, Grarup, N, Hansen, T, Huang, W, Nielsen, C S, Pedersen, O, Ng, M C Y, Sun, Y V, Winkler, T W, Yang, J, 23andMe Research Team, VA Million Vet Program, DiscovEHR Collaboration, eMERGE Consortium, Lifelines Cohort Study, The PRACTICAL Consortium & Understanding Society Scientific Group 2022, ' A saturated map of common genetic variants associated with human height ', Nature, vol. 610, no. 7933, pp. 704–712 . https://doi.org/10.1038/s41586-022-05275-y
Nature, 610, 704-712
Nature, vol. 610, no. 7933, pp. 704-712
eMERGE (Electronic Medical Records and Genomics Network), The PRACTICAL consortium, Lifelines Cohort Study, 23andMe Research team, Understanding Society Scientific group, VA Million Veteran Program & DiscovEHR (DiscovEHR and MyCode Community Health Initiative) 2022, ' A saturated map of common genetic variants associated with human height ', Nature, vol. 610, pp. 704-712 . https://doi.org/10.1038/s41586-022-05275-y
Common single-nucleotide polymorphisms (SNPs) are predicted to collectively explain 40-50% of phenotypic variation in human height, but identifying the specific variants and associated regions requires huge sample sizes(1). Here, using data from a ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe30ce8ab0d3d1860e1c661db7ddbbe9
http://hdl.handle.net/10852/97480
http://hdl.handle.net/10852/97480
Autor:
Mikhaylova, Anna V, McHugh, Caitlin P, Polfus, Linda M, Raffield, Laura M, Boorgula, Meher Preethi, Blackwell, Thomas W, Brody, Jennifer A, Broome, Jai, Chami, Nathalie, Chen, Ming-Huei, Conomos, Matthew P, Cox, Corey, Curran, Joanne E, Daya, Michelle, Ekunwe, Lynette, Glahn, David C, Heard-Costa, Nancy, Highland, Heather M, Hobbs, Brian D, Ilboudo, Yann, Jain, Deepti, Lange, Leslie A, Miller-Fleming, Tyne W, Min, Nancy, Moon, Jee-Young, Preuss, Michael H, Rosen, Jonathon, Ryan, Kathleen, Smith, Albert V, Sun, Quan, Surendran, Praveen, de Vries, Paul S, Walter, Klaudia, Wang, Zhe, Wheeler, Marsha, Yanek, Lisa R, Zhong, Xue, Abecasis, Goncalo R, Almasy, Laura, Barnes, Kathleen C, Beaty, Terri H, Becker, Lewis C, Blangero, John, Boerwinkle, Eric, Butterworth, Adam S, Chavan, Sameer, Cho, Michael H, Choquet, Hélène, Correa, Adolfo, Cox, Nancy, DeMeo, Dawn L, Faraday, Nauder, Fornage, Myriam, Gerszten, Robert E, Hou, Lifang, Johnson, Andrew D, Jorgenson, Eric, Kaplan, Robert, Kooperberg, Charles, Kundu, Kousik, Laurie, Cecelia A, Lettre, Guillaume, Lewis, Joshua P, Li, Bingshan, Li, Yun, Lloyd-Jones, Donald M, Loos, Ruth JF, Manichaikul, Ani, Meyers, Deborah A, Mitchell, Braxton D, Morrison, Alanna C, Ngo, Debby, Nickerson, Deborah A, Nongmaithem, Suraj, North, Kari E, O'Connell, Jeffrey R, Ortega, Victor E, Pankratz, Nathan, Perry, James A, Psaty, Bruce M, Rich, Stephen S, Soranzo, Nicole, Rotter, Jerome I, Silverman, Edwin K, Smith, Nicholas L, Tang, Hua, Tracy, Russell P, Thornton, Timothy A, Vasan, Ramachandran S, Zein, Joe, Mathias, Rasika A, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Reiner, Alexander P, Auer, Paul L
Publikováno v:
American journal of human genetics, vol 108, iss 10
Many common and rare variants associated with hematologic traits have been discovered through imputation on large-scale reference panels. However, the majority of genome-wide association studies (GWASs) have been conducted in Europeans, and determini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::1f3a94426432e7d8d437082d4c6c39d7
https://escholarship.org/uc/item/6432c6xx
https://escholarship.org/uc/item/6432c6xx
Akademický článek
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Akademický článek
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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
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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