Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Abecasis, Goncalo"'
Autor:
Ramdas, Shweta, Judd, Jonathan, Graham, Sarah E, Kanoni, Stavroula, Wang, Yuxuan, Surakka, Ida, Wenz, Brandon, Clarke, Shoa L, Chesi, Alessandra, Wells, Andrew, Bhatti, Konain Fatima, Vedantam, Sailaja, Winkler, Thomas W, Locke, Adam E, Marouli, Eirini, Zajac, Greg J M, Wu, Kuan-Han H, Ntalla, Ioanna, Hui, Qin, Klarin, Derek, Hilliard, Austin T, Wang, Zeyuan, Xue, Chao, Thorleifsson, Gudmar, Helgadottir, Anna, Gudbjartsson, Daniel F, Holm, Hilma, Olafsson, Isleifur, Hwang, Mi Yeong, Han, Sohee, Akiyama, Masato, Sakaue, Saori, Terao, Chikashi, Kanai, Masahiro, Zhou, Wei, Brumpton, Ben M, Rasheed, Humaira, Havulinna, Aki S, Veturi, Yogasudha, Pacheco, Jennifer Allen, Rosenthal, Elisabeth A, Lingren, Todd, Feng, QiPing, Kullo, Iftikhar J, Narita, Akira, Takayama, Jun, Martin, Hilary C, Hunt, Karen A, Trivedi, Bhavi, Haessler, Jeffrey, Giulianini, Franco, Bradford, Yuki, Miller, Jason E, Campbell, Archie, Lin, Kuang, Millwood, Iona Y, Rasheed, Asif, Hindy, George, Faul, Jessica D, Zhao, Wei, Weir, David R, Turman, Constance, Huang, Hongyan, Graff, Mariaelisa, Choudhury, Ananyo, Sengupta, Dhriti, Mahajan, Anubha, Brown, Michael R, Zhang, Weihua, Yu, Ketian, Schmidt, Ellen M, Pandit, Anita, Gustafsson, Stefan, Yin, Xianyong, Luan, Jian'an, Zhao, Jing-Hua, Matsuda, Fumihiko, Jang, Hye-Mi, Yoon, Kyungheon, Medina-Gomez, Carolina, Pitsillides, Achilleas, Hottenga, Jouke Jan, Wood, Andrew R, Ji, Yingji, Gao, Zishan, Haworth, Simon, Mitchell, Ruth E, Chai, Jin Fang, Aadahl, Mette, Bjerregaard, Anne A, Yao, Jie, Manichaikul, Ani, Lee, Wen-Jane, Hsiung, Chao Agnes, Warren, Helen R, Ramirez, Julia, Bork-Jensen, Jette, Kårhus, Line L, Goel, Anuj, Sabater-Lleal, Maria, Noordam, Raymond, Mauro, Pala, Matteo, Floris, McDaid, Aaron F, Marques-Vidal, Pedro, Wielscher, Matthias, Trompet, Stella, Sattar, Naveed, Møllehave, Line T, Munz, Matthias, Zeng, Lingyao, Huang, Jianfeng, Yang, Bin, Poveda, Alaitz, Kurbasic, Azra, Schönherr, Sebastian, Forer, Lukas, Scholz, Markus, Galesloot, Tessel E, Bradfield, Jonathan P, Ruotsalainen, Sanni E, Daw, E Warwick, Zmuda, Joseph M, Mitchell, Jonathan S, Fuchsberger, Christian, Christensen, Henry, Brody, Jennifer A, Le, Phuong, Feitosa, Mary F, Wojczynski, Mary K, Hemerich, Daiane, Preuss, Michael, Mangino, Massimo, Christofidou, Paraskevi, Verweij, Niek, Benjamins, Jan W, Engmann, Jorgen, Noah, Tsao L, Verma, Anurag, Slieker, Roderick C, Lo, Ken Sin, Zilhao, Nuno R, Kleber, Marcus E, Delgado, Graciela E, Huo, Shaofeng, Ikeda, Daisuke D, Iha, Hiroyuki, Yang, Jian, Liu, Jun, Demirkan, Ayşe, Leonard, Hampton L, Marten, Jonathan, Emmel, Carina, Schmidt, Börge, Smyth, Laura J, Cañadas-Garre, Marisa, Wang, Chaolong, Nakatochi, Masahiro, Wong, Andrew, Hutri-Kähönen, Nina, Sim, Xueling, Xia, Rui, Huerta-Chagoya, Alicia, Fernandez-Lopez, Juan Carlos, Lyssenko, Valeriya, Nongmaithem, Suraj S, Sankareswaran, Alagu, Irvin, Marguerite R, Oldmeadow, Christopher, Kim, Han-Na, Ryu, Seungho, Timmers, Paul R H J, Arbeeva, Liubov, Dorajoo, Rajkumar, Lange, Leslie A, Prasad, Gauri, Lorés-Motta, Laura, Pauper, Marc, Long, Jirong, Li, Xiaohui, Theusch, Elizabeth, Takeuchi, Fumihiko, Spracklen, Cassandra N, Loukola, Anu, Bollepalli, Sailalitha, Warner, Sophie C, Wang, Ya Xing, Wei, Wen B, Nutile, Teresa, Ruggiero, Daniela, Sung, Yun Ju, Chen, Shufeng, Liu, Fangchao, Yang, Jingyun, Kentistou, Katherine A, Banas, Bernhard, Morgan, Anna, Meidtner, Karina, Bielak, Lawrence F, Smith, Jennifer A, Hebbar, Prashantha, Farmaki, Aliki-Eleni, Hofer, Edith, Lin, Maoxuan, Concas, Maria Pina, Vaccargiu, Simona, van der Most, Peter J, Pitkänen, Niina, Cade, Brian E, van der Laan, Sander W, Chitrala, Kumaraswamy Naidu, Weiss, Stefan, Bentley, Amy R, Doumatey, Ayo P, Adeyemo, Adebowale A, Lee, Jong Young, Petersen, Eva R B, Nielsen, Aneta A, Choi, Hyeok Sun, Nethander, Maria, Freitag-Wolf, Sandra, Southam, Lorraine, Rayner, Nigel W, Wang, Carol A, Lin, Shih-Yi, Wang, Jun-Sing, Couture, Christian, Lyytikäinen, Leo-Pekka, Nikus, Kjell, Cuellar-Partida, Gabriel, Vestergaard, Henrik, Hidalgo, Bertha, Giannakopoulou, Olga, Cai, Qiuyin, Obura, Morgan O, van Setten, Jessica, He, Karen Y, Tang, Hua, Terzikhan, Natalie, Shin, Jae Hun, Jackson, Rebecca D, Reiner, Alexander P, Martin, Lisa Warsinger, Chen, Zhengming, Li, Liming, Kawaguchi, Takahisa, Thiery, Joachim, Bis, Joshua C, Launer, Lenore J, Li, Huaixing, Nalls, Mike A, Raitakari, Olli T, Ichihara, Sahoko, Wild, Sarah H, Nelson, Christopher P, Campbell, Harry, Jäger, Susanne, Nabika, Toru, Al-Mulla, Fahd, Niinikoski, Harri, Braund, Peter S, Kolcic, Ivana, Kovacs, Peter, Giardoglou, Tota, Katsuya, Tomohiro, de Kleijn, Dominique, de Borst, Gert J, Kim, Eung Kweon, Adams, Hieab H H, Ikram, M Arfan, Zhu, Xiaofeng, Asselbergs, Folkert W, Kraaijeveld, Adriaan O, Beulens, Joline W J, Shu, Xiao-Ou, Rallidis, Loukianos S, Pedersen, Oluf, Hansen, Torben, Mitchell, Paul, Hewitt, Alex W, Kähönen, Mika, Pérusse, Louis, Bouchard, Claude, Tönjes, Anke, Ida Chen, Yii-Der, Pennell, Craig E, Mori, Trevor A, Lieb, Wolfgang, Franke, Andre, Ohlsson, Claes, Mellström, Dan, Cho, Yoon Shin, Lee, Hyejin, Yuan, Jian-Min, Koh, Woon-Puay, Rhee, Sang Youl, Woo, Jeong-Taek, Heid, Iris M, Stark, Klaus J, Zimmermann, Martina E, Völzke, Henry, Homuth, Georg, Evans, Michele K, Zonderman, Alan B, Polasek, Ozren, Pasterkamp, Gerard, Hoefer, Imo E, Redline, Susan, Pahkala, Katja, Oldehinkel, Albertine J, Snieder, Harold, Biino, Ginevra, Schmidt, Reinhold, Schmidt, Helena, Bandinelli, Stefania, Dedoussis, George, Thanaraj, Thangavel Alphonse, Peyser, Patricia A, Kato, Norihiro, Schulze, Matthias B, Girotto, Giorgia, Böger, Carsten A, Jung, Bettina, Joshi, Peter K, Bennett, David A, De Jager, Philip L, Lu, Xiangfeng, Mamakou, Vasiliki, Brown, Morris, Caulfield, Mark J, Munroe, Patricia B, Guo, Xiuqing, Ciullo, Marina, Jonas, Jost B, Samani, Nilesh J, Kaprio, Jaakko, Pajukanta, Päivi, Tusié-Luna, Teresa, Aguilar-Salinas, Carlos A, Adair, Linda S, Bechayda, Sonny Augustin, de Silva, H Janaka, Wickremasinghe, Ananda R, Krauss, Ronald M, Wu, Jer-Yuarn, Zheng, Wei, den Hollander, Anneke I, Bharadwaj, Dwaipayan, Correa, Adolfo, Wilson, James G, Lind, Lars, Heng, Chew-Kiat, Nelson, Amanda E, Golightly, Yvonne M, Wilson, James F, Penninx, Brenda, Kim, Hyung-Lae, Attia, John, Scott, Rodney J, Rao, D C, Arnett, Donna K, Walker, Mark, Scott, Laura J, Koistinen, Heikki A, Chandak, Giriraj R, Mercader, Josep M, Villalpando, Clicerio Gonzalez, Orozco, Lorena, Fornage, Myriam, Tai, E Shyong, van Dam, Rob M, Lehtimäki, Terho, Chaturvedi, Nish, Yokota, Mitsuhiro, Liu, Jianjun, Reilly, Dermot F, McKnight, Amy Jayne, Kee, Frank, Jöckel, Karl-Heinz, McCarthy, Mark I, Palmer, Colin N A, Vitart, Veronique, Hayward, Caroline, Simonsick, Eleanor, van Duijn, Cornelia M, Jin, Zi-Bing, Lu, Fan, Hishigaki, Haretsugu, Lin, Xu, März, Winfried, Gudnason, Vilmundur, Tardif, Jean-Claude, Lettre, Guillaume, T Hart, Leen M, Elders, Petra J M, Rader, Daniel J, Damrauer, Scott M, Kumari, Meena, Kivimaki, Mika, van der Harst, Pim, Spector, Tim D, Loos, Ruth J F, Province, Michael A, Parra, Esteban J, Cruz, Miguel, Psaty, Bruce M, Brandslund, Ivan, Pramstaller, Peter P, Rotimi, Charles N, Christensen, Kaare, Ripatti, Samuli, Widén, Elisabeth, Hakonarson, Hakon, Grant, Struan F A, Kiemeney, Lambertus, de Graaf, Jacqueline, Loeffler, Markus, Kronenberg, Florian, Gu, Dongfeng, Erdmann, Jeanette, Schunkert, Heribert, Franks, Paul W, Linneberg, Allan, Jukema, J Wouter, Khera, Amit V, Männikkö, Minna, Jarvelin, Marjo-Riitta, Kutalik, Zoltan, Francesco, Cucca, Mook-Kanamori, Dennis O, Willems van Dijk, Ko, Watkins, Hugh, Strachan, David P, Grarup, Niels, Sever, Peter, Poulter, Neil, Huey-Herng Sheu, Wayne, Rotter, Jerome I, Dantoft, Thomas M, Karpe, Fredrik, Neville, Matt J, Timpson, Nicholas J, Cheng, Ching-Yu, Wong, Tien-Yin, Khor, Chiea Chuen, Li, Hengtong, Sabanayagam, Charumathi, Peters, Annette, Gieger, Christian, Hattersley, Andrew T, Pedersen, Nancy L, Magnusson, Patrik K E, Boomsma, Dorret I, de Geus, Eco J C, Cupples, L Adrienne, van Meurs, Joyce B J, Ikram, Arfan, Ghanbari, Mohsen, Gordon-Larsen, Penny, Huang, Wei, Kim, Young Jin, Tabara, Yasuharu, Wareham, Nicholas J, Langenberg, Claudia, Zeggini, Eleftheria, Tuomilehto, Jaakko, Kuusisto, Johanna, Laakso, Markku, Ingelsson, Erik, Abecasis, Goncalo, Chambers, John C, Kooner, Jaspal S, de Vries, Paul S, Morrison, Alanna C, Hazelhurst, Scott, Ramsay, Michèle, North, Kari E, Daviglus, Martha, Kraft, Peter, Martin, Nicholas G, Whitfield, John B, Abbas, Shahid, Saleheen, Danish, Walters, Robin G, Holmes, Michael V, Black, Corri, Smith, Blair H, Baras, Aris, Justice, Anne E, Buring, Julie E, Ridker, Paul M, Chasman, Daniel I, Kooperberg, Charles, Tamiya, Gen, Yamamoto, Masayuki, van Heel, David A, Trembath, Richard C, Wei, Wei-Qi, Jarvik, Gail P, Namjou, Bahram, Hayes, M Geoffrey, Ritchie, Marylyn D, Jousilahti, Pekka, Salomaa, Veikko, Hveem, Kristian, Åsvold, Bjørn Olav, Kubo, Michiaki, Kamatani, Yoichiro, Okada, Yukinori, Murakami, Yoshinori, Kim, Bong-Jo, Thorsteinsdottir, Unnur, Stefansson, Kari, Zhang, Jifeng, Chen, Y Eugene, Ho, Yuk-Lam, Lynch, Julie A, Tsao, Philip S, Chang, Kyong-Mi, Cho, Kelly, O'Donnell, Christopher J, Gaziano, John M, Wilson, Peter, Mohlke, Karen L, Frayling, Timothy M, Hirschhorn, Joel N, Kathiresan, Sekar, Boehnke, Michael, Million Veterans Program, Global Lipids Genetics Consortium, Struan Grant, Natarajan, Pradeep, Sun, Yan V, Morris, Andrew P, Deloukas, Panos, Peloso, Gina, Assimes, Themistocles L, Willer, Cristen J, Zhu, Xiang, Brown, Christopher D
Publikováno v:
American Journal of Human Genetics, 109(8), 1366-1387. CELL PRESS
Million Veterans Program, Ramdas, S, Judd, J, Graham, S E, Kanoni, S, Wang, Y, Surakka, I, Wenz, B, Clarke, S L, Chesi, A, Wells, A, Bhatti, K F, Vedantam, S, Winkler, T W, Locke, A E, Marouli, E, Zajac, G J M, Wu, K-H H, Ntalla, I, Hui, Q, Klarin, D, Hilliard, A T, Wang, Z, Xue, C, Thorleifsson, G, Helgadottir, A, Gudbjartsson, D F, Holm, H, Olafsson, I, Hwang, M Y, Han, S, Akiyama, M, Sakaue, S, Terao, C, Kanai, M, Zhou, W, Brumpton, B M, Rasheed, H, Havulinna, A S, Veturi, Y, Pacheco, J A, Weir, D R, Brown, M R, Smyth, L J, Cañadas-Garre, M, Li, X, Nelson, C P, McKnight, A J, Kee, F, Wilson, P & Brown, C D 2022, ' A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids ', The American Journal of Human Genetics, vol. 109, no. 8, pp. 1366-1387 . https://doi.org/10.1016/j.ajhg.2022.06.012
Ramdas, S, Judd, J, Graham, S E, Hottenga, J J, Penninx, B, Boomsma, D I, de Geus, E J C, Million Veterans Program & Global Lipids Genetics Consortium 2022, ' A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids ', American Journal of Human Genetics, vol. 109, no. 8, pp. 1366-1387 . https://doi.org/10.1016/j.ajhg.2022.06.012
Million Veterans Program & Global Lipids Genetics Consortium 2022, ' A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids ', American journal of human genetics, vol. 109, no. 8, pp. 1366-1387 . https://doi.org/10.1016/j.ajhg.2022.06.012
Am J Hum Genet
American journal of human genetics, vol 109, iss 8
AMERICAN JOURNAL OF HUMAN GENETICS
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
American Journal of Human Genetics
American journal of human genetics, 109(8), 1366-1387. Cell Press
American journal of human genetics, vol. 109, no. 8, pp. 1366-1387
Ramdas, S, Judd, J, Graham, S E, Kanoni, S, Wang, Y, Surakka, I, Wenz, B, Clarke, S L, Brumpton, B M, Rasheed, H, Haworth, S J, Mitchell, R E, Zhu, X & Brown, C D & et, A 2022, ' A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids ', American Journal of Human Genetics, vol. 109, no. 8, pp. 1366-1387 . https://doi.org/10.1016/j.ajhg.2022.06.012
2022, ' A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids ', American Journal of Human Genetics, vol. 109, no. 8, pp. 1366-1387 . https://doi.org/10.1016/j.ajhg.2022.06.012
American Journal of Human Genetics, 109, 8, pp. 1366-1387
American Journal of Human Genetics, 109, 1366-1387
American Journal of Human Genetics, 109(8), 1366-1387. Cell Press
Million Veterans Program, Ramdas, S, Judd, J, Graham, S E, Kanoni, S, Wang, Y, Surakka, I, Wenz, B, Clarke, S L, Chesi, A, Wells, A, Bhatti, K F, Vedantam, S, Winkler, T W, Locke, A E, Marouli, E, Zajac, G J M, Wu, K-H H, Ntalla, I, Hui, Q, Klarin, D, Hilliard, A T, Wang, Z, Xue, C, Thorleifsson, G, Helgadottir, A, Gudbjartsson, D F, Holm, H, Olafsson, I, Hwang, M Y, Han, S, Akiyama, M, Sakaue, S, Terao, C, Kanai, M, Zhou, W, Brumpton, B M, Rasheed, H, Havulinna, A S, Veturi, Y, Pacheco, J A, Weir, D R, Brown, M R, Smyth, L J, Cañadas-Garre, M, Li, X, Nelson, C P, McKnight, A J, Kee, F, Wilson, P & Brown, C D 2022, ' A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids ', The American Journal of Human Genetics, vol. 109, no. 8, pp. 1366-1387 . https://doi.org/10.1016/j.ajhg.2022.06.012
Ramdas, S, Judd, J, Graham, S E, Hottenga, J J, Penninx, B, Boomsma, D I, de Geus, E J C, Million Veterans Program & Global Lipids Genetics Consortium 2022, ' A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids ', American Journal of Human Genetics, vol. 109, no. 8, pp. 1366-1387 . https://doi.org/10.1016/j.ajhg.2022.06.012
Million Veterans Program & Global Lipids Genetics Consortium 2022, ' A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids ', American journal of human genetics, vol. 109, no. 8, pp. 1366-1387 . https://doi.org/10.1016/j.ajhg.2022.06.012
Am J Hum Genet
American journal of human genetics, vol 109, iss 8
AMERICAN JOURNAL OF HUMAN GENETICS
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
American Journal of Human Genetics
American journal of human genetics, 109(8), 1366-1387. Cell Press
American journal of human genetics, vol. 109, no. 8, pp. 1366-1387
Ramdas, S, Judd, J, Graham, S E, Kanoni, S, Wang, Y, Surakka, I, Wenz, B, Clarke, S L, Brumpton, B M, Rasheed, H, Haworth, S J, Mitchell, R E, Zhu, X & Brown, C D & et, A 2022, ' A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids ', American Journal of Human Genetics, vol. 109, no. 8, pp. 1366-1387 . https://doi.org/10.1016/j.ajhg.2022.06.012
2022, ' A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids ', American Journal of Human Genetics, vol. 109, no. 8, pp. 1366-1387 . https://doi.org/10.1016/j.ajhg.2022.06.012
American Journal of Human Genetics, 109, 8, pp. 1366-1387
American Journal of Human Genetics, 109, 1366-1387
American Journal of Human Genetics, 109(8), 1366-1387. Cell Press
A major challenge of genome-wide association studies (GWASs) is to translate phenotypic associations into biological insights. Here, we integrate a large GWAS on blood lipids involving 1.6 million individuals from five ancestries with a wide array of
Autor:
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 JF, 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, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Publikováno v:
Science advances, vol 9, iss 17
Nononcogenic somatic mutations are thought to be uncommon and inconsequential. To test this, we analyzed 43,693 National Heart, Lung and Blood Institute Trans-Omics for Precision Medicine blood whole genomes from 37 cohorts and identified 7131 non-mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::9065bc0faf2d3ecc58a098ed4c436645
https://escholarship.org/uc/item/1496g128
https://escholarship.org/uc/item/1496g128
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
Autor:
Akbari, Parsa, Gilani, Ankit, Sosina, Olukayode, Kosmicki, Jack A, Khrimian, Lori, Fang, Yi-Ya, Persaud, Trikaldarshi, Garcia, Victor, Sun, Dylan, Li, Alexander, Mbatchou, Joelle, Locke, Adam E, Benner, Christian, Verweij, Niek, Lin, Nan, Hossain, Sakib, Agostinucci, Kevin, Pascale, Jonathan V, Dirice, Ercument, Dunn, Michael, Regeneron Genetics Center, DiscovEHR Collaboration, Kraus, William E, Shah, Svati H, Chen, Yii-Der I, Rotter, Jerome I, Rader, Daniel J, Melander, Olle, Still, Christopher D, Mirshahi, Tooraj, Carey, David J, Berumen-Campos, Jaime, Kuri-Morales, Pablo, Alegre-Díaz, Jesus, Torres, Jason M, Emberson, Jonathan R, Collins, Rory, Balasubramanian, Suganthi, Hawes, Alicia, Jones, Marcus, Zambrowicz, Brian, Murphy, Andrew J, Paulding, Charles, Coppola, Giovanni, Overton, John D, Reid, Jeffrey G, Shuldiner, Alan R, Cantor, Michael, Kang, Hyun M, Abecasis, Goncalo R, Karalis, Katia, Economides, Aris N, Marchini, Jonathan, Yancopoulos, George D, Sleeman, Mark W, Altarejos, Judith, Della Gatta, Giusy, Tapia-Conyer, Roberto, Schwartzman, Michal L, Baras, Aris, Ferreira, Manuel AR, Lotta, Luca A
Publikováno v:
Science (New York, N.Y.), vol 373, iss 6550
Large-scale human exome sequencing can identify rare protein-coding variants with a large impact on complex traits such as body adiposity. We sequenced the exomes of 645,626 individuals from the United Kingdom, the United States, and Mexico and estim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::ed8f1b9c84a53fab21f4ae18c7c8d7e2
https://escholarship.org/uc/item/78525869
https://escholarship.org/uc/item/78525869
Autor:
Nachun, Daniel, Lu, Ake T, Bick, Alexander G, Natarajan, Pradeep, Weinstock, Joshua, Szeto, Mindy D, Kathiresan, Sekar, Abecasis, Goncalo, Taylor, Kent D, Guo, Xiuqing, Tracy, Russ, Durda, Peter, Liu, Yongmei, Johnson, Craig, Rich, Stephen S, Van Den Berg, David, Laurie, Cecilia, Blackwell, Tom, Papanicolaou, George J, Correa, Adolfo, Raffield, Laura M, Johnson, Andrew D, Murabito, Joanne, Manson, JoAnn E, Desai, Pinkal, Kooperberg, Charles, Assimes, Themistocles L, Levy, Daniel, Rotter, Jerome I, Reiner, Alex P, Whitsel, Eric A, Wilson, James G, Horvath, Steve, Jaiswal, Siddhartha, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Publikováno v:
Aging cell, vol 20, iss 6
Clonal hematopoiesis of indeterminate potential (CHIP) is a common precursor state for blood cancers that most frequently occurs due to mutations in the DNA-methylation modifying enzymes DNMT3A or TET2. We used DNA-methylation array and whole-genome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::1e3574502fa7b59723b5f5791bdeced2
https://escholarship.org/uc/item/1m81d33g
https://escholarship.org/uc/item/1m81d33g
Autor:
Hu, Yao, Stilp, Adrienne M, McHugh, Caitlin P, Rao, Shuquan, Jain, Deepti, Zheng, Xiuwen, Lane, John, Méric de Bellefon, Sébastian, Raffield, Laura M, Chen, Ming-Huei, Yanek, Lisa R, Wheeler, Marsha, Yao, Yao, Ren, Chunyan, Broome, Jai, Moon, Jee-Young, de Vries, Paul S, Hobbs, Brian D, Sun, Quan, Surendran, Praveen, Brody, Jennifer A, Blackwell, Thomas W, Choquet, Hélène, Ryan, Kathleen, Duggirala, Ravindranath, Heard-Costa, Nancy, Wang, Zhe, Chami, Nathalie, Preuss, Michael H, Min, Nancy, Ekunwe, Lynette, Lange, Leslie A, Cushman, Mary, Faraday, Nauder, Curran, Joanne E, Almasy, Laura, Kundu, Kousik, Smith, Albert V, Gabriel, Stacey, Rotter, Jerome I, Fornage, Myriam, Lloyd-Jones, Donald M, Vasan, Ramachandran S, Smith, Nicholas L, North, Kari E, Boerwinkle, Eric, Becker, Lewis C, Lewis, Joshua P, Abecasis, Goncalo R, Hou, Lifang, O'Connell, Jeffrey R, Morrison, Alanna C, Beaty, Terri H, Kaplan, Robert, Correa, Adolfo, Blangero, John, Jorgenson, Eric, Psaty, Bruce M, Kooperberg, Charles, Walton, Russell T, Kleinstiver, Benjamin P, Tang, Hua, Loos, Ruth JF, Soranzo, Nicole, Butterworth, Adam S, Nickerson, Debbie, Rich, Stephen S, Mitchell, Braxton D, Johnson, Andrew D, Auer, Paul L, Li, Yun, Mathias, Rasika A, Lettre, Guillaume, Pankratz, Nathan, Laurie, Cathy C, Laurie, Cecelia A, Bauer, Daniel E, Conomos, Matthew P, Reiner, Alexander P, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Publikováno v:
American journal of human genetics, vol 108, iss 5
Whole-genome sequencing (WGS), a powerful tool for detecting novel coding and non-coding disease-causing variants, has largely been applied to clinical diagnosis of inherited disorders. Here we leveraged WGS data in up to 62,653 ethnically diverse pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::445eb02b1c412ec0c77798d591b7420a
https://escholarship.org/uc/item/24j6v92r
https://escholarship.org/uc/item/24j6v92r
Autor:
Ferreira, Manuel A R, Vonk, Judith M., Baurecht, Hansjörg, Marenholz, Ingo, Tian, Chao, Hoffman, Joshua D., Helmer, Quinta, Tillander, Annika, Ullemar, Vilhelmina, Lu, Yi, Grosche, Sarah, Ruschendorf, Franz, Granell, Raquel, Brumpton, Ben Michael, Fritsche, Lars, Bhatta, Laxmi, Gabrielsen, Maiken Elvestad, Nielsen, Jonas Bille, Zhou, Wei, Hveem, Kristian, Langhammer, Arnulf, Holmen, Oddgeir, Løset, Mari, Abecasis, Goncalo, Willer, Cristen J., Emami, Nima C., Cavazos, Taylor B., Witte, John S., Szwajda, Agnieszka, 23andMe Research Team,, collaborators of SHARE study,, Hinds, David A., Hubner, Norbert, Weidinger, Stephan, Magnusson, Patrik KE, Jorgenson, Eric, Karlsson, Robert, Paternoster, Lavinia, Boomsma, Dorret I., Almqvist, Catarina, Lee, Young-Ae, Koppelman, Gerard H., Esparza-Gordillo, Jorge, Hummel, Oliver, Hottenga, Jouke-Jan, Willemsen, Gonneke, Rodríguez, Elke, Hotze, Melanie, Franke, Andre, Matheson, Melanie C., Dharmage, Shyamali Chandrika, Arnold, Andreas, Homuth, Georg, Schmidt, Carsten O, Thompson, Philip J., Martin, Nicholas G, Duffy, David L., Novak, Natalija, Schulz, Holger, Karrasch, Stefan, Gieger, Christian, Strauch, Konstantin, Melles, Ronald B
Publikováno v:
Ferreira, M A R, Granell, R, Brumpton, B M, Paternoster, L & al., E 2020, ' Age-of-onset information helps identify 76 genetic variants associated with allergic disease ', PLoS Genetics . https://doi.org/10.1371/journal.pgen.1008725
PLoS Genetics
PLoS Genetics, Vol 16, Iss 6, p e1008725 (2020)
PLoS genetics, vol 16, iss 6
PLoS Genetics, 16(6):e1008725, 1-30. Public Library of Science
Ferreira, M A R, Helmer, Q, Boomsma, D I, Koppelman, G H, 23Andme Research Team & collaborators of the SHARE study 2020, ' Age-of-onset information helps identify 76 genetic variants associated with allergic disease ', PLoS Genetics, vol. 16, no. 6, e1008725, pp. 1-30 . https://doi.org/10.1371/journal.pgen.1008725
PLoS genetics, 16(6):e1008725. PUBLIC LIBRARY SCIENCE
PLoS Genetics
PLoS Genetics, Vol 16, Iss 6, p e1008725 (2020)
PLoS genetics, vol 16, iss 6
PLoS Genetics, 16(6):e1008725, 1-30. Public Library of Science
Ferreira, M A R, Helmer, Q, Boomsma, D I, Koppelman, G H, 23Andme Research Team & collaborators of the SHARE study 2020, ' Age-of-onset information helps identify 76 genetic variants associated with allergic disease ', PLoS Genetics, vol. 16, no. 6, e1008725, pp. 1-30 . https://doi.org/10.1371/journal.pgen.1008725
PLoS genetics, 16(6):e1008725. PUBLIC LIBRARY SCIENCE
Risk factors that contribute to inter-individual differences in the age-of-onset of allergic diseases are poorly understood. The aim of this study was to identify genetic risk variants associated with the age at which symptoms of allergic disease fir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef083f37bdedb51ecd1abbf93f78c33e
https://research-information.bris.ac.uk/ws/files/246941687/untitled.pdf
https://research-information.bris.ac.uk/ws/files/246941687/untitled.pdf
Autor:
Justice, Anne E, Karaderi, Tugce, Highland, Heather M, Young, Kristin L, Graff, Mariaelisa, Lu, Yingchang, Turcot, Valérie, Auer, Paul L, Fine, Rebecca S, Guo, Xiuqing, Schurmann, Claudia, Lempradl, Adelheid, Marouli, Eirini, Mahajan, Anubha, Winkler, Thomas W, Locke, Adam E, Medina-Gomez, Carolina, Esko, Tõnu, Vedantam, Sailaja, Giri, Ayush, Lo, Ken Sin, Alfred, Tamuno, Mudgal, Poorva, Ng, Maggie CY, Heard-Costa, Nancy L, Feitosa, Mary F, Manning, Alisa K, Willems, Sara M, Sivapalaratnam, Suthesh, Abecasis, Goncalo, Alam, Dewan S, Allison, Matthew, Amouyel, Philippe, Arzumanyan, Zorayr, Balkau, Beverley, Bastarache, Lisa, Bergmann, Sven, Bielak, Lawrence F, Blüher, Matthias, Boehnke, Michael, Boeing, Heiner, Boerwinkle, Eric, Böger, Carsten A, Bork-Jensen, Jette, Bottinger, Erwin P, Bowden, Donald W, Brandslund, Ivan, Broer, Linda, Burt, Amber A, Butterworth, Adam S, Caulfield, Mark J, Cesana, Giancarlo, Chambers, John C, Chasman, Daniel I, Chen, Yii-Der Ida, Chowdhury, Rajiv, Christensen, Cramer, Chu, Audrey Y, Collins, Francis S, Cook, James P, Cox, Amanda J, Crosslin, David S, Danesh, John, de Bakker, Paul IW, Denus, Simon de, Mutsert, Renée de, Dedoussis, George, Demerath, Ellen W, Dennis, Joe G, Denny, Josh C, Di Angelantonio, Emanuele, Dörr, Marcus, Drenos, Fotios, Dubé, Marie-Pierre, Dunning, Alison M, Easton, Douglas F, Elliott, Paul, Evangelou, Evangelos, Farmaki, Aliki-Eleni, Feng, Shuang, Ferrannini, Ele, Ferrieres, Jean, Florez, Jose C, Fornage, Myriam, Fox, Caroline S, Franks, Paul W, Friedrich, Nele, Gan, Wei, Gandin, Ilaria, Gasparini, Paolo, Giedraitis, Vilmantas, Girotto, Giorgia, Gorski, Mathias, Grallert, Harald, Grarup, Niels, Grove, Megan L, Gustafsson, Stefan, Haessler, Jeff, Hansen, Torben, Hattersley, Andrew T
Publikováno v:
Nature genetics, vol 51, iss 3
Body-fat distribution is a risk factor for adverse cardiovascular health consequences. We analyzed the association of body-fat distribution, assessed by waist-to-hip ratio adjusted for body mass index, with 228,985 predicted coding and splice site va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::44e9320cc018881e9ec908bf4c8015fe
https://escholarship.org/uc/item/1fv3j0h9
https://escholarship.org/uc/item/1fv3j0h9
Autor:
Marouli, Eirini, Graff, Mariaelisa, Medina-Gomez, Carolina, Lo, Ken Sin, Wood, Andrew R, Kjaer, Troels R, Fine, Rebecca S, Lu, Yingchang, Schurmann, Claudia, Highland, Heather M, Rueger, Sina, Thorleifsson, Gudmar, Justice, Anne E, Lamparter, David, Stirrups, Kathleen E, Turcot, Valerie, Young, Kristin L, Winkler, Thomas W, Esko, Tonu, Karaderi, Tugce, Locke, Adam E, Masca, Nicholas GD, Ng, Maggie CY, Mudgal, Poorva, Rivas, Manuel A, Vedantam, Sailaja, Mahajan, Anubha, Guo, Xiuqing, Abecasis, Goncalo, Aben, Katja K, Adair, Linda S, Alam, Dewan S, Albrecht, Eva, Allin, Kristine H, Allison, Matthew, Amouyel, Philippe, Appel, Emil V, Arveiler, Dominique, Asselbergs, Folkert W, Auer, Paul L, Balkau, Beverley, Banas, Bernhard, Bang, Lia E, Benn, Marianne, Bergmann, Sven, Bielak, Lawrence F, Blueher, Matthias, Boeing, Heiner, Boerwinkle, Eric, Boeger, Carsten A, Bonnycastle, Lori L, Bork-Jensen, Jette, Bots, Michiel L, Bottinger, Erwin P, Bowden, Donald W, Brandslund, Ivan, Breen, Gerome, Brilliant, Murray H, Broer, Linda, Burt, Amber A, Butterworth, Adam S, Carey, David J, Caulfield, Mark J, Chambers, John C, Chasman, Daniel I, Chen, Yii-Der Ida, Chowdhury, Rajiv, Christensen, Cramer, Chu, Audrey Y, Cocca, Massimiliano, Collins, Francis S, Cook, James P, Corley, Janie, Galbany, Jordi Corominas, Cox, Amanda J, Cuellar-Partida, Gabriel, Danesh, John, Davies, Gail, de Bakker, Paul IW, de Borst, Gert J, de Denus, Simon, de Groot, Mark CH, de Mutsert, Renee, Deary, Ian J, Dedoussis, George, Demerath, Ellen W, den Hollander, Anneke I, Dennis, Joe G, Di Angelantonio, Emanuele, Drenos, Fotios, Du, Mengmeng, Dunning, Alison M, Easton, Douglas F, Ebeling, Tapani, Edwards, Todd L, Ellinor, Patrick T, Elliott, Paul, Evangelou, Evangelos, Farmaki, Aliki-Eleni, Faul, Jessica D, Feitosa, Mary F, Feng, Shuang, Ferrannini, Ele, Ferrario, Marco M, Ferrieres, Jean, Florez, Jose C, Ford, Ian, Fornage, Myriam, Franks, Paul W, Frikke-Schmidt, Ruth, Galesloot, Tessel E, Gan, Wei, Gandin, Ilaria, Gasparini, Paolo, Giedraitis, Vilmantas, Giri, Ayush, Girotto, Giorgia, Gordon, Scott D, Gordon-Larsen, Penny, Gorski, Mathias, Grarup, Niels, Grove, Megan L, Gudnason, Vilmundur, Gustafsson, Stefan, Hansen, Torben, Harris, Kathleen Mullan, Harris, Tamara B, Hattersley, Andrew T, Hayward, Caroline, He, Liang, Heid, Iris M, Heikkila, Kauko, Helgeland, Oyvind, Hernesniemi, Jussi, Hewitt, Alex W, Hocking, Lynne J, Hollensted, Mette, Holmen, Oddgeir L, Hovingh, G Kees, Howson, Joanna MM, Hoyng, Carel B, Huang, Paul L, Hveem, Kristian, Ikram, M Arfan, Ingelsson, Erik, Jackson, Anne U, Jansson, Jan-Hakan, Jarvik, Gail P, Jensen, Gorm B, Jhun, Min A, Jia, Yucheng, Jiang, Xuejuan, Johansson, Stefan, Jorgensen, Marit E, Jorgensen, Torben, Jousilahti, Pekka, Jukema, J Wouter, Kahali, Bratati, Kahn, Rene S, Kahonen, Mika, Kamstrup, Pia R, Kanoni, Stavroula, Kaprio, Jaakko, Karaleftheri, Maria, Kardia, Sharon LR, Karpe, Fredrik, Kee, Frank, Keeman, Renske, Kiemeney, Lambertus A, Kitajima, Hidetoshi, Kluivers, Kirsten B, Kocher, Thomas, Komulainen, Pirjo, Kontto, Jukka, Kooner, Jaspal S, Kooperberg, Charles, Kovacs, Peter, Kriebel, Jennifer, Kuivaniemi, Helena, Kury, Sebastien, Kuusisto, Johanna, La Bianca, Martina, Laakso, Markku, Lakka, Timo A, Lange, Ethan M, Lange, Leslie A, Langefeld, Carl D, Langenberg, Claudia, Larson, Eric B, Lee, I-Te, Lehtimaki, Terho, Lewis, Cora E, Li, Huaixing, Li, Jin, Li-Gao, Ruifang, Lin, Honghuang, Lin, Li-An, Lin, Xu, Lind, Lars, Lindstrom, Jaana, Linneberg, Allan, Liu, Yeheng, Liu, Yongmei, Lophatananon, Artitaya, Luan, Jian'an, Lubitz, Steven A, Lyytikainen, Leo-Pekka, Mackey, David A, Madden, Pamela AF, Manning, Alisa K, Mannisto, Satu, Marenne, Gaelle, Marten, Jonathan, Martin, Nicholas G, Mazul, Angela L, Meidtner, Karina, Metspalu, Andres, Mitchell, Paul, Mohlke, Karen L, Mook-Kanamori, Dennis O, Morgan, Anna, Morris, Andrew D, Morris, Andrew P, Mueller-Nurasyid, Martina, Munroe, Patricia B, Nalls, Mike A, Nauck, Matthias, Nelson, Christopher P, Neville, Matt, Nielsen, Sune F, Nikus, Kjell, Njolstad, Pal R, Nordestgaard, Borge G, Ntalla, Ioanna, O'Connel, Jeffrey R, Oksa, Heikki, Loohuis, Loes M Olde, Ophoff, Roel A, Owen, Katharine R, Packard, Chris J, Padmanabhan, Sandosh, Palmer, Colin NA, Pasterkamp, Gerard, Patel, Aniruddh P, Pattie, Alison, Pedersen, Oluf, Peissig, Peggy L, Peloso, Gina M, Pennell, Craig E, Perola, Markus, Perry, James A, Perry, John RB, Person, Thomas N, Pirie, Ailith, Polasek, Ozren, Posthuma, Danielle, Raitakari, Olli T, Rasheed, Asif, Rauramaa, Rainer, Reilly, Dermot F, Reiner, Alex P, Renstrom, Frida, Ridker, Paul M, Rioux, John D, Robertson, Neil, Robino, Antonietta, Rolandsson, Olov, Rudan, Igor, Ruth, Katherine S, Saleheen, Danish, Salomaa, Veikko, Samani, Nilesh J, Sandow, Kevin, Sapkota, Yadav, Sattar, Naveed, Schmidt, Marjanka K, Schreiner, Pamela J, Schulze, Matthias B, Scott, Robert A, Segura-Lepe, Marcelo P, Shah, Svati, Sim, Xueling, Sivapalaratnam, Suthesh, Small, Kerrin S, Smith, Albert Vernon, Smith, Jennifer A, Southam, Lorraine, Spector, Timothy D, Speliotes, Elizabeth K, Starr, John M, Steinthorsdottir, Valgerdur, Stringham, Heather M, Stumvoll, Michael, Surendran, Praveen, 't Hart, Leen M, Tansey, Katherine E, Tardif, Jean-Claude, Taylor, Kent D, Teumer, Alexander, Thompson, Deborah J, Thorsteinsdottir, Unnur, Thuesen, Betina H, Toenjes, Anke, Tromp, Gerard, Trompet, Stella, Tsafantakis, Emmanouil, Tuomilehto, Jaakko, Tybjaerg-Hansen, Anne, Tyrer, Jonathan P, Uher, Rudolf, Uitterlinden, Andre G, Ulivi, Sheila, van der Laan, Sander W, Van Der Leij, Andries R, van Duijn, Cornelia M, van Schoor, Natasja M, van Setten, Jessica, Varbo, Anette, Varga, Tibor V, Varma, Rohit, Edwards, Digna R Velez, Vermeulen, Sita H, Vestergaard, Henrik, Vitart, Veronique, Vogt, Thomas F, Vozzi, Diego, Walker, Mark, Wang, Feijie, Wang, Carol A, Wang, Shuai, Wang, Yiqin, Wareham, Nicholas J, Warren, Helen R, Wessel, Jennifer, Willems, Sara M, Wilson, James G, Witte, Daniel R, Woods, Michael O, Wu, Ying, Yaghootkar, Hanieh, Yao, Jie, Yao, Pang, Yerges-Armstrong, Laura M, Young, Robin, Zeggini, Eleftheria, Zhan, Xiaowei, Zhang, Weihua, Zhao, Jing Hua, Zhao, Wei, Zheng, He, Zhou, Wei, Rotter, Jerome I, Boehnke, Michael, Kathiresan, Sekar, McCarthy, Mark I, Willer, Cristen J, Stefansson, Kari, Borecki, Ingrid B, Liu, Dajiang J, North, Kari E, Heard-Costa, Nancy L, Pers, Tune H, Lindgren, Cecilia M, Oxvig, Claus, Kutalik, Zoltan, Rivadeneira, Fernando, Loos, Ruth JF, Frayling, Timothy M, Hirschhorn, Joel N, Deloukas, Panos, Lettre, Guillaume, Consortium, EPIC-InterAct, Consortium, EPIC-CVD, Consortium, CHD Exome, Consortium, ExomeBP, Consortium, T2D-Genes, Consortium, GoT2D Genes, Consortium, Global Lipids Genetics, Consortium, ReproGen, Investigators, MAGIC
Publikováno v:
Nature, 542, 186-190
Marouli, E, Graff, M, Medina-Gomez, C, Lo, K S, Wood, A R, Kjaer, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M, Amouyel, P, Appel, E V, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S, Bielak, L F, Blüher, M, Li, J, Posthuma, D, van Schoor, N M & EPIC-InterAct Consortium 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
Marouli, E, Graff, M, Medina-Gomez, C, Lo, K S, Wood, A R, Kjær, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G R, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M A, Amouyel, P, Appel, E V, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S, Bielak, L F, Blüher, M, Boeing, H, Boerwinkle, E, Jørgensen, T & EPIC-InterAct Consortium 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
Marouli, E, Graff, M, Medina-Gomez, C, Lo, K S, Wood, A R, Kjaer, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M, Amouyel, P, Appel, E V, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S, Bielak, L F, Blüher, M, Boeing, H, Boerwinkle, E, Posthuma, D & EPIC-InterAct Consortium 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
NATURE
Nature, 542(7640), 186-190. Nature Publishing Group
Nature 542, 186-190 (2017)
Nature
Nature, vol 542, iss 7640
Marouli, E, Graff, M, Medina-Gómez, C, Lo, K S, Wood, A R, Kjaer, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G R, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M A, Amouyel, P, Appel, E V R, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S, Brandslund, I, Christensen, C, Hansen, T, Jensen, G B, Jørgensen, M E & EPIC-InterAct Consortium 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
Marouli, E, Graff, M, Medina-Gómez, C, Lo, K S, Wood, A R, Kjaer, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G R, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M A, Amouyel, P, Appel, E V, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S M, Bielak, L F, Blüher, M, Boeing, H, Boerwinkle, E, Oxvig, C & EPIC InterAct Consortium 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
Marouli, E, Graff, M, Medina-gomez, C, Lo, K S, Wood, A R, Kjaer, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M, Amouyel, P, Appel, E V, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S, Bielak, L F, Blüher, M, Boeing, H, Boerwinkle, E, Böger, C A, Bonnycastle, L L, Bork-jensen, J, Bots, M L, Bottinger, E P, Bowden, D W, Brandslund, I, Breen, G, Brilliant, M H, Broer, L, Burt, A A, Butterworth, A S, Carey, D J, Caulfield, M J, Chambers, J C, Chasman, D I, Chen, Y I, Chowdhury, R, Christensen, C, Chu, A Y, Cocca, M, Collins, F S, Cook, J P, Corley, J, Galbany, J C, Cox, A J, Cuellar-partida, G, Danesh, J, Davies, G, De Bakker, P I W, De Borst, G J, De Denus, S, De Groot, M C H, De Mutsert, R, Deary, I J, Dedoussis, G, Demerath, E W, Den Hollander, A I, Dennis, J G, Di Angelantonio, E, Drenos, F, Du, M, Dunning, A M, Easton, D F, Ebeling, T, Edwards, T L, Ellinor, P T, Elliott, P, Evangelou, E, Farmaki, A, Faul, J D, Feitosa, M F, Feng, S, Ferrannini, E, Ferrario, M M, Ferrieres, J, Florez, J C, Ford, I, Fornage, M, Franks, P W, Frikke-schmidt, R, Galesloot, T E, Gan, W, Gandin, I, Gasparini, P, Giedraitis, V, Giri, A, Girotto, G, Gordon, S D, Gordon-larsen, P, Gorski, M, Grarup, N, Grove, M L, Gudnason, V, Gustafsson, S, Hansen, T, Harris, K M, Harris, T B, Hattersley, A T, Hayward, C, He, L, Heid, I M, Heikkilä, K, Helgeland, Ø, Hernesniemi, J, Hewitt, A W, Hocking, L J, Hollensted, M, Holmen, O L, Hovingh, G K, Howson, J M M, Hoyng, C B, Huang, P L, Hveem, K, Ikram, M A, Ingelsson, E, Jackson, A U, Jansson, J, Jarvik, G P, Jensen, G B, Jhun, M A, Jia, Y, Jiang, X, Johansson, S, Jørgensen, M E, Jørgensen, T, Jousilahti, P, Jukema, J W, Kahali, B, Kahn, R S, Kähönen, M, Kamstrup, P R, Kanoni, S, Kaprio, J, Karaleftheri, M, Kardia, S L R, Karpe, F, Kee, F, Keeman, R, Kiemeney, L A, Kitajima, H, Kluivers, K B, Kocher, T, Komulainen, P, Kontto, J, Kooner, J S, Kooperberg, C, Kovacs, P, Kriebel, J, Kuivaniemi, H, Küry, S, Kuusisto, J, La Bianca, M, Laakso, M, Lakka, T A, Lange, E M, Lange, L A, Langefeld, C D, Langenberg, C, Larson, E B, Lee, I, Lehtimäki, T, Lewis, C E, Li, H, Li, J, Li-gao, R, Lin, H, Lin, L, Lin, X, Lind, L, Lindström, J, Linneberg, A, Liu, Y, Liu, Y, Lophatananon, A, Luan, J, Lubitz, S A, Lyytikäinen, L, Mackey, D A, Madden, P A F, Manning, A K, Männistö, S, Marenne, G, Marten, J, Martin, N G, Mazul, A L, Meidtner, K, Metspalu, A, Mitchell, P, Mohlke, K L, Mook-kanamori, D O, Morgan, A, Morris, A D, Morris, A P, Müller-nurasyid, M, Munroe, P B, Nalls, M A, Nauck, M, Nelson, C P, Neville, M, Nielsen, S F, Nikus, K, Njølstad, P R, Nordestgaard, B G, Ntalla, I, O'connel, J R, Oksa, H, Loohuis, L M O, Ophoff, R A, Owen, K R, Packard, C J, Padmanabhan, S, Palmer, C N A, Pasterkamp, G, Patel, A P, Pattie, A, Pedersen, O, Peissig, P L, Peloso, G M, Pennell, C E, Perola, M, Perry, J A, Perry, J R B, Person, T N, Pirie, A, Polasek, O, Posthuma, D, Raitakari, O T, Rasheed, A, Rauramaa, R, Reilly, D F, Reiner, A P, Renström, F, Ridker, P M, Rioux, J D, Robertson, N, Robino, A, Rolandsson, O, Rudan, I, Ruth, K S, Saleheen, D, Salomaa, V, Samani, N J, Sandow, K, Sapkota, Y, Sattar, N, Schmidt, M K, Schreiner, P J, Schulze, M B, Scott, R A, Segura-lepe, M P, Shah, S, Sim, X, Sivapalaratnam, S, Small, K S, Smith, A V, Smith, J A, Southam, L, Spector, T D, Speliotes, E K, Starr, J M, Steinthorsdottir, V, Stringham, H M, Stumvoll, M, Surendran, P, ‘t Hart, L M, Tansey, K E, Tardif, J, Taylor, K D, Teumer, A, Thompson, D J, Thorsteinsdottir, U, Thuesen, B H, Tönjes, A, Tromp, G, Trompet, S, Tsafantakis, E, Tuomilehto, J, Tybjaerg-hansen, A, Tyrer, J P, Uher, R, Uitterlinden, A G, Ulivi, S, Van Der Laan, S W, Van Der Leij, A R, Van Duijn, C M, Van Schoor, N M, Van Setten, J, Varbo, A, Varga, T V, Varma, R, Edwards, D R V, Vermeulen, S H, Vestergaard, H, Vitart, V, Vogt, T F, Vozzi, D, Walker, M, Wang, F, Wang, C A, Wang, S, Wang, Y, Wareham, N J, Warren, H R, Wessel, J, Willems, S M, Wilson, J G, Witte, D R, Woods, M O, Wu, Y, Yaghootkar, H, Yao, J, Yao, P, Yerges-armstrong, L M, Young, R, Zeggini, E, Zhan, X, Zhang, W, Zhao, J H, Zhao, W, Zhao, W, Zheng, H, Zhou, W, Rotter, J I, Boehnke, M, Kathiresan, S, Mccarthy, M I, Willer, C J, Stefansson, K, Borecki, I B, Liu, D J, North, K E, Heard-costa, N L, Pers, T H, Lindgren, C M, Oxvig, C, Kutalik, Z, Rivadeneira, F, Loos, R J F, Frayling, T M, Hirschhorn, J N, Deloukas, P & Lettre, G 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
Nature, 542(7640), 186-190
Marouli, E, Graff, M, Medina-Gomez, C, Lo, K S, Wood, A R, Kjaer, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M, Amouyel, P, Appel, E V, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S, Bielak, L F, Blüher, M, Boeing, H, Boerwinkle, E, Lophatananon, A & EPIC-InterAct Consortium 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
Nature, 542, 7640, pp. 186-190
Nature, 542(7640), 186. Nature Research
Nature, vol. 542, no. 7640, pp. 186-190
Marouli, E; Graff, M; Medina-Gomez, C; Lo, KS; Wood, AR; Kjaer, TR; et al.(2017). Rare and low-frequency coding variants alter human adult height. Nature, 542(7640), 186-190. doi: 10.1038/nature21039. UCLA: Retrieved from: http://www.escholarship.org/uc/item/1sq5r8fb
Nature, 542, 186. Nature Publishing Group
Marouli, E, Graff, M, Medina-Gomez, C, Lo, K S, Wood, A R, Kjaer, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M, Amouyel, P, Appel, E V, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S, Bielak, L F, Blüher, M, Li, J, Posthuma, D, van Schoor, N M & EPIC-InterAct Consortium 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
Marouli, E, Graff, M, Medina-Gomez, C, Lo, K S, Wood, A R, Kjær, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G R, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M A, Amouyel, P, Appel, E V, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S, Bielak, L F, Blüher, M, Boeing, H, Boerwinkle, E, Jørgensen, T & EPIC-InterAct Consortium 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
Marouli, E, Graff, M, Medina-Gomez, C, Lo, K S, Wood, A R, Kjaer, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M, Amouyel, P, Appel, E V, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S, Bielak, L F, Blüher, M, Boeing, H, Boerwinkle, E, Posthuma, D & EPIC-InterAct Consortium 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
NATURE
Nature, 542(7640), 186-190. Nature Publishing Group
Nature 542, 186-190 (2017)
Nature
Nature, vol 542, iss 7640
Marouli, E, Graff, M, Medina-Gómez, C, Lo, K S, Wood, A R, Kjaer, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G R, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M A, Amouyel, P, Appel, E V R, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S, Brandslund, I, Christensen, C, Hansen, T, Jensen, G B, Jørgensen, M E & EPIC-InterAct Consortium 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
Marouli, E, Graff, M, Medina-Gómez, C, Lo, K S, Wood, A R, Kjaer, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G R, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M A, Amouyel, P, Appel, E V, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S M, Bielak, L F, Blüher, M, Boeing, H, Boerwinkle, E, Oxvig, C & EPIC InterAct Consortium 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
Marouli, E, Graff, M, Medina-gomez, C, Lo, K S, Wood, A R, Kjaer, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M, Amouyel, P, Appel, E V, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S, Bielak, L F, Blüher, M, Boeing, H, Boerwinkle, E, Böger, C A, Bonnycastle, L L, Bork-jensen, J, Bots, M L, Bottinger, E P, Bowden, D W, Brandslund, I, Breen, G, Brilliant, M H, Broer, L, Burt, A A, Butterworth, A S, Carey, D J, Caulfield, M J, Chambers, J C, Chasman, D I, Chen, Y I, Chowdhury, R, Christensen, C, Chu, A Y, Cocca, M, Collins, F S, Cook, J P, Corley, J, Galbany, J C, Cox, A J, Cuellar-partida, G, Danesh, J, Davies, G, De Bakker, P I W, De Borst, G J, De Denus, S, De Groot, M C H, De Mutsert, R, Deary, I J, Dedoussis, G, Demerath, E W, Den Hollander, A I, Dennis, J G, Di Angelantonio, E, Drenos, F, Du, M, Dunning, A M, Easton, D F, Ebeling, T, Edwards, T L, Ellinor, P T, Elliott, P, Evangelou, E, Farmaki, A, Faul, J D, Feitosa, M F, Feng, S, Ferrannini, E, Ferrario, M M, Ferrieres, J, Florez, J C, Ford, I, Fornage, M, Franks, P W, Frikke-schmidt, R, Galesloot, T E, Gan, W, Gandin, I, Gasparini, P, Giedraitis, V, Giri, A, Girotto, G, Gordon, S D, Gordon-larsen, P, Gorski, M, Grarup, N, Grove, M L, Gudnason, V, Gustafsson, S, Hansen, T, Harris, K M, Harris, T B, Hattersley, A T, Hayward, C, He, L, Heid, I M, Heikkilä, K, Helgeland, Ø, Hernesniemi, J, Hewitt, A W, Hocking, L J, Hollensted, M, Holmen, O L, Hovingh, G K, Howson, J M M, Hoyng, C B, Huang, P L, Hveem, K, Ikram, M A, Ingelsson, E, Jackson, A U, Jansson, J, Jarvik, G P, Jensen, G B, Jhun, M A, Jia, Y, Jiang, X, Johansson, S, Jørgensen, M E, Jørgensen, T, Jousilahti, P, Jukema, J W, Kahali, B, Kahn, R S, Kähönen, M, Kamstrup, P R, Kanoni, S, Kaprio, J, Karaleftheri, M, Kardia, S L R, Karpe, F, Kee, F, Keeman, R, Kiemeney, L A, Kitajima, H, Kluivers, K B, Kocher, T, Komulainen, P, Kontto, J, Kooner, J S, Kooperberg, C, Kovacs, P, Kriebel, J, Kuivaniemi, H, Küry, S, Kuusisto, J, La Bianca, M, Laakso, M, Lakka, T A, Lange, E M, Lange, L A, Langefeld, C D, Langenberg, C, Larson, E B, Lee, I, Lehtimäki, T, Lewis, C E, Li, H, Li, J, Li-gao, R, Lin, H, Lin, L, Lin, X, Lind, L, Lindström, J, Linneberg, A, Liu, Y, Liu, Y, Lophatananon, A, Luan, J, Lubitz, S A, Lyytikäinen, L, Mackey, D A, Madden, P A F, Manning, A K, Männistö, S, Marenne, G, Marten, J, Martin, N G, Mazul, A L, Meidtner, K, Metspalu, A, Mitchell, P, Mohlke, K L, Mook-kanamori, D O, Morgan, A, Morris, A D, Morris, A P, Müller-nurasyid, M, Munroe, P B, Nalls, M A, Nauck, M, Nelson, C P, Neville, M, Nielsen, S F, Nikus, K, Njølstad, P R, Nordestgaard, B G, Ntalla, I, O'connel, J R, Oksa, H, Loohuis, L M O, Ophoff, R A, Owen, K R, Packard, C J, Padmanabhan, S, Palmer, C N A, Pasterkamp, G, Patel, A P, Pattie, A, Pedersen, O, Peissig, P L, Peloso, G M, Pennell, C E, Perola, M, Perry, J A, Perry, J R B, Person, T N, Pirie, A, Polasek, O, Posthuma, D, Raitakari, O T, Rasheed, A, Rauramaa, R, Reilly, D F, Reiner, A P, Renström, F, Ridker, P M, Rioux, J D, Robertson, N, Robino, A, Rolandsson, O, Rudan, I, Ruth, K S, Saleheen, D, Salomaa, V, Samani, N J, Sandow, K, Sapkota, Y, Sattar, N, Schmidt, M K, Schreiner, P J, Schulze, M B, Scott, R A, Segura-lepe, M P, Shah, S, Sim, X, Sivapalaratnam, S, Small, K S, Smith, A V, Smith, J A, Southam, L, Spector, T D, Speliotes, E K, Starr, J M, Steinthorsdottir, V, Stringham, H M, Stumvoll, M, Surendran, P, ‘t Hart, L M, Tansey, K E, Tardif, J, Taylor, K D, Teumer, A, Thompson, D J, Thorsteinsdottir, U, Thuesen, B H, Tönjes, A, Tromp, G, Trompet, S, Tsafantakis, E, Tuomilehto, J, Tybjaerg-hansen, A, Tyrer, J P, Uher, R, Uitterlinden, A G, Ulivi, S, Van Der Laan, S W, Van Der Leij, A R, Van Duijn, C M, Van Schoor, N M, Van Setten, J, Varbo, A, Varga, T V, Varma, R, Edwards, D R V, Vermeulen, S H, Vestergaard, H, Vitart, V, Vogt, T F, Vozzi, D, Walker, M, Wang, F, Wang, C A, Wang, S, Wang, Y, Wareham, N J, Warren, H R, Wessel, J, Willems, S M, Wilson, J G, Witte, D R, Woods, M O, Wu, Y, Yaghootkar, H, Yao, J, Yao, P, Yerges-armstrong, L M, Young, R, Zeggini, E, Zhan, X, Zhang, W, Zhao, J H, Zhao, W, Zhao, W, Zheng, H, Zhou, W, Rotter, J I, Boehnke, M, Kathiresan, S, Mccarthy, M I, Willer, C J, Stefansson, K, Borecki, I B, Liu, D J, North, K E, Heard-costa, N L, Pers, T H, Lindgren, C M, Oxvig, C, Kutalik, Z, Rivadeneira, F, Loos, R J F, Frayling, T M, Hirschhorn, J N, Deloukas, P & Lettre, G 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
Nature, 542(7640), 186-190
Marouli, E, Graff, M, Medina-Gomez, C, Lo, K S, Wood, A R, Kjaer, T R, Fine, R S, Lu, Y, Schurmann, C, Highland, H M, Rüeger, S, Thorleifsson, G, Justice, A E, Lamparter, D, Stirrups, K E, Turcot, V, Young, K L, Winkler, T W, Esko, T, Karaderi, T, Locke, A E, Masca, N G D, Ng, M C Y, Mudgal, P, Rivas, M A, Vedantam, S, Mahajan, A, Guo, X, Abecasis, G, Aben, K K, Adair, L S, Alam, D S, Albrecht, E, Allin, K H, Allison, M, Amouyel, P, Appel, E V, Arveiler, D, Asselbergs, F W, Auer, P L, Balkau, B, Banas, B, Bang, L E, Benn, M, Bergmann, S, Bielak, L F, Blüher, M, Boeing, H, Boerwinkle, E, Lophatananon, A & EPIC-InterAct Consortium 2017, ' Rare and low-frequency coding variants alter human adult height ', Nature, vol. 542, no. 7640, pp. 186-190 . https://doi.org/10.1038/nature21039
Nature, 542, 7640, pp. 186-190
Nature, 542(7640), 186. Nature Research
Nature, vol. 542, no. 7640, pp. 186-190
Marouli, E; Graff, M; Medina-Gomez, C; Lo, KS; Wood, AR; Kjaer, TR; et al.(2017). Rare and low-frequency coding variants alter human adult height. Nature, 542(7640), 186-190. doi: 10.1038/nature21039. UCLA: Retrieved from: http://www.escholarship.org/uc/item/1sq5r8fb
Nature, 542, 186. Nature Publishing Group
Contains fulltext : 169801.pdf (Publisher’s version ) (Closed access) Height is a highly heritable, classic polygenic trait with approximately 700 common associated variants identified through genome-wide association studies so far. Here, we report
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https://doi.org/10.1038/nature21039
https://doi.org/10.1038/nature21039
Autor:
Savage, Jeanne E, Jansen, Philip R, Stringer, Sven, Watanabe, Kyoko, Bryois, Julien, de Leeuw, Christiaan A, Nagel, Mats, Awasthi, Swapnil, Barr, Peter B, Coleman, Jonathan RI, Grasby, Katrina L, Hammerschlag, Anke R, Kaminski, Jakob A, Karlsson, Robert, Krapohl, Eva, Lam, Max, Nygaard, Marianne, Reynolds, Chandra A, Trampush, Joey W, Young, Hannah, Zabaneh, Delilah, Hägg, Sara, Hansell, Narelle K, Karlsson, Ida K, Linnarsson, Sten, Montgomery, Grant W, Muñoz-Manchado, Ana B, Quinlan, Erin B, Schumann, Gunter, Skene, Nathan G, Webb, Bradley T, White, Tonya, Arking, Dan E, Avramopoulos, Dimitrios, Bilder, Robert M, Bitsios, Panos, Burdick, Katherine E, Cannon, Tyrone D, Chiba-Falek, Ornit, Christoforou, Andrea, Cirulli, Elizabeth T, Congdon, Eliza, Corvin, Aiden, Davies, Gail, Deary, Ian J, DeRosse, Pamela, Dickinson, Dwight, Djurovic, Srdjan, Donohoe, Gary, Conley, Emily Drabant, Eriksson, Johan G, Espeseth, Thomas, Freimer, Nelson A, Giakoumaki, Stella, Giegling, Ina, Gill, Michael, Glahn, David C, Hariri, Ahmad R, Hatzimanolis, Alex, Keller, Matthew C, Knowles, Emma, Koltai, Deborah, Konte, Bettina, Lahti, Jari, Le Hellard, Stephanie, Lencz, Todd, Liewald, David C, London, Edythe, Lundervold, Astri J, Malhotra, Anil K, Melle, Ingrid, Morris, Derek, Need, Anna C, Ollier, William, Palotie, Aarno, Payton, Antony, Pendleton, Neil, Poldrack, Russell A, Räikkönen, Katri, Reinvang, Ivar, Roussos, Panos, Rujescu, Dan, Sabb, Fred W, Scult, Matthew A, Smeland, Olav B, Smyrnis, Nikolaos, Starr, John M, Steen, Vidar M, Stefanis, Nikos C, Straub, Richard E, Sundet, Kjetil, Tiemeier, Henning, Voineskos, Aristotle N, Weinberger, Daniel R, Widen, Elisabeth, Yu, Jin, Abecasis, Goncalo, Andreassen, Ole A, Breen, Gerome, Christiansen, Lene
Publikováno v:
Nature genetics, vol 50, iss 7
Intelligence is highly heritable1 and a major determinant of human health and well-being2. Recent genome-wide meta-analyses have identified 24 genomic loci linked to variation in intelligence3-7, but much about its genetic underpinnings remains to be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::82860e64d5a6c4d94b1c261b4f60387c
https://escholarship.org/uc/item/869275xx
https://escholarship.org/uc/item/869275xx