4158The association of physical activity with plasma lipoproteins and inflammation measured by NMR-metabolomics: evidence from the China Kadoorie Biobank study von Pang, Y., Bennett, D.A., Holmes, M.V., Kartsonaki, C., Du, H., Millwood, I.Y., Guo, Y., Bian, Z., Chen, J., Li, L., Chen, Z.

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Understanding the genetic complexity of puberty timing across the allele frequency spectrum von Stankovic, S, Vaudel, M, Walters, R.G, Helgason, H, Thompson, D.J, Santoni, F, Zouaghi, Y, Huang-Doran, I, Bratland, E, Lin, K, Zhao, Y, Riggan, M.J, Bolla, M.K, Yazdanpanah, M, Broer, L, Chasman, D.I, Girotto, G, Kamatani, Y, Lunetta, K.L, Mägi, R, Mangino, M, Medland, S.E, Polašek, O, Sala, C, Smith, A.V, Anton-Culver, H, Antoniou, A.C, Barnes, C.L.K, Beckmann, M.W, Brenner, H, Couch, F.J, Cox, A, Czene, K, Daly, M.B, Devilee, P, De Vivo, I, Dörk, T, Dunning, A.M, Dwek, M, Fernandez-Rhodes, L, González-Neira, A, Grallert, H, Haiman, C.A, Hamann, U, Hooning, M.J, Hoppe, R, Hopper, J.L, Hunter, D.J, Lacey, J.V, Lambrechts, D, Magnusson, P.K.E, Meitinger, T, Michailidou, K, Nyholt, D.R, Offit, K, Ostrowski, S.R, Pedersen, O.B, Pianigiani, G, Pozarickij, A, Rosendaal, F.R, Schipf, S, Schmidt, C.O, Spedicati, B, Stone, J, Tamimi, R.M, Teras, L.R, Tikkanen, E, Vachon, C.M, Winqvist, R, Wolk, A, Zemel, B.S, van Dijk, K.W, Alizadeh, B.Z, Boerwinkle, E, Ciullo, M, Cucca, F, Esko, T, Hayward, C, Kraft, P, Lawlor, D.A, Pennell, C.E, Robino, A, Snieder, H, Sovio, U, Timpson, N.J, Völzke, H, Wareham, N.J, Widen, E, Sulem, P, Murabito, J.M, Murray, A, Manousaki, D, Juul, A, Stefansson, K, Chen, Z, Pitteloud, N, Johansson, S, Day, F.R, Perry, J.R.B, Ong, K.K

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The power of genetic diversity in genome-wide association studies of lipids (vol 600, pg 675, 2021) von Kanoni, S., Ramdas, S., Surakka, I., Winkler, T.W., Marouli, E., Hwang, M.Y., Hunt, K.A., Helgadottir, A., Olafsson, I., Terao, C., Zhou, W., Veturi, Y., Haessler, J., Giulianini, F., Miller, J.E., Campbell, A., Rasheed, A., Turman, C., Schmidt, E.M., Yin, X.Y., Luan, J.A., Medina-Gomez, C., Wood, A.R., Ji, Y.J., Haworth, S., Mitchell, R.E., Warren, H.R., Bork-Jensen, J., Noordam, R., Fiorillo, E., Mollehave, L.T., Munz, M., Yang, B., Scholz, M., Galesloot, T.E., Zmuda, J.M., Fuchsberger, C., Feitosa, M.F., Preuss, M., Verweij, N., Kember, R.L., Slieker, R.C., Delgado, G.E., Huo, S.F., Iha, H., Marten, J., Schmidt, B., Xia, R., Fernandez-Lopez, J.C., Ahmed, M., Yousri, N.A., Ryu, S., Timmers, P.R.H.J., Arbeeva, L., Pauper, M., Loukola, A., Warner, S.C., Wei, W.B., Ruggiero, D., Chen, S.F., Liu, F.C., Yang, J.Y., Bielak, L.F., Farmaki, A.E., Lin, M.X., Zhang, J.F., Vaccargiu, S., Most, P.J. van der, Pitkänen, N., Cade, B.E., Laan, S.W. van der, Weiss, S., Zimmermann, M.E., Nethander, M., Freitag-Wolf, S., Wang, J.S., Cuellar-Partida, G., Vestergaard, H., Hildalgo, B., Jackson, R.D., Martin, L.W., Chen, Z.M., Thiery, J., Bis, J.C., Launer, L.J., Nalls, M.A., Raitakari, O.T., Ichihara, S., Campbell, H., Braund, P.S., Kolcic, I., Kovacs, P., Katsuya, T., Adams, H.H.H., Zhu, X.F., Kähönen, M., Mori, T.A., Franke, A., Lee, H., Heid, I.M.

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Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk von Izquierdo, A.G., Chen, J., Batini, C., Pavuluri, C., Hobbs, B.D., Moll, M., Tal-Singer, R., Bakke, P., Fawcett, K.A., Coley, K., Pozarickij, A., Li, L.M., Wijnant, S.R.A., Lahousse, L., Uitterlinden, A.G., Oelsner, E.C., Rich, S.S., Barr, R.G., Kerr, S.M., Brown, M.R., Wielscher, M., Jeong, A., Gharib, S.A., Flexeder, C., Karrasch, S., Meyers, D.A., Bleecker, E.R., Gabriel, S.B., Smith, A.V., Luan, J.A., Smith, B.H., Campbell, A., Sofer, T., Lee, J., Daviglus, M.L., Albagha, O.M.E., Al-Muftah, W., Mbarek, H., Yasin, H., Abdellatif, R., Alkuwari, F., Alvi, M., Al-Sarraj, Y., Saad, C., Qafoud, F., Tomei, S., Liu, W., Syed, N., Almabrazi, H., Vempalli, F.R., Temanni, R., Abu Saqri, T., Khatib, M., Abu Zaid, T., Khouly, A. el, Pathare, T., Poolat, S., Puthen, J., Tatari, Z., Suhre, K., Granell, R., Hiemstra, P.S., Beilby, J., Patasova, K., Hysi, P., Lee, M., May-Wilson, S., Pirastu, N., Kentistou, K.A., Free, R.C., Wang, X.Y., Morrison, J.L., Wang, C.A., Foong, R.E., Harris, S.E., Taylor, A., Mahajan, A., Lind, L., Palviainen, T., Lehtimäki, T., Kaprio, J., Rantanen, T., Pietiläinen, K.H., Pennell, C.E., Brightling, C., Vasankari, T., Laitinen, T., Hayward, C., Weiss, S., Homuth, G., Schmidt, C.O., Probst-Hensch, N., Morrison, A.C., Polasek, O., Lee, J.H., Silverman, E.K., Walters, R.G., Morris, A.P., London, S.J., Hall, I.P.

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Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis von Clarke, S.L., Winkler, T.W., Marouli, E., Klarin, D., Wang, Z.Y., Xue, C., Helgadottir, A., Sakaue, S., Kanai, M., Veturi, Y., Pacheco, J.A., Lingren, T., Narita, A., Hunt, K.A., Trivedi, B., Miller, J.E., Rasheed, A., Hindy, G., Faul, J.D., Brown, M.R., Yu, K.T., Pandit, A., Luan, J.A., Matsuda, F., Wood, A.R., Ji, Y.J., Yousri, N.A., Chai, J.F., Manichaikul, A., Bork-Jensen, J., Sabater-Lleal, M., Noordam, R., Mauro, P., Matteo, F., Trompet, S., Sattar, N., Munz, M., Kurbasic, A., Scholz, M., Galesloot, T.E., Bradfeld, J.P., Daw, E., Zmuda, J.M., Fuchsberger, C., Feitosa, M.F., Wang, Z., Preuss, M.H., Engmann, J., Tsao, N.L., Slieker, R.C., , K.S. lo, , P. le, Ikeda, D.D., Yang, J., Liu, J., Schmidt, B., Wang, C.L., Wong, A., Sim, X.L., Xia, R., Nongmaithem, S.S., Irvin, M.R., Timmers, P.R.H.J., Lange, L.A., Prasad, G., Lores-Motta, L., Long, J.R., Takeuchi, F., Spracklen, C.N., Loukola, A., Bollepalli, S., Nutile, T., Ruggiero, D., Sung, Y.J., Chen, S.F., Yang, J.Y., Bielak, L.F., Adeyemo, A.A., Choi, H.S., Southam, L., Wang, C.A., Setten, J. van, Li, X.Y., Liang, J.J., Jackson, R.D., Chen, Z.M., Li, L.M., Thiery, J., Wild, S.H., Nelson, C.P., Jager, S., Asselbergs, F.W., Beulens, J.W.J., Pedersen, O., Hewitt, A.W., Kahonen, M., Pennell, C.E., Mori, T.A., Lieb, W., Mellstrom, D.

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A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids von Ramdas, S., Kanoni, S., Surakka, I., Wenz, B., Chesi, A., Vedantam, S., Holm, H., Hwang, M.Y., Han, S., Terao, C., Zhou, W., Rosenthal, E.A., Kullo, I.J., Narita, A., Takayama, J., Bradford, Y., Zhao, W., Weir, D.R., Huang, H.Y., Choudhury, A., Mahajan, A., Schmidt, E.M., Pandit, A., Yin, X.Y., Luan, J.A., Yoon, K., Medina-Gomez, C., Mitchell, R.E., Yao, J., Lee, W.J., Warren, H.R., Karhus, L.L., Sabater-Lleal, M., McDaid, A.F., Marques-Vidal, P., Wielscher, M., Scholz, M., Daw, E.W., Zmuda, J.M., Mitchell, J.S., Brody, J.A., Verweij, N., Benjamins, J.W., Verma, A., Kleber, M.E., Yang, J., Liu, J., Marten, J., Canadas-Garre, M., Hutri-Kahonen, N., Sim, X.L., Xia, R., Fernandez-Lopez, J.C., Lyssenko, V., Oldmeadow, C., Ryu, S., Timmers, P.R.H.J., Arbeeva, L., Dorajoo, R., Lange, L.A., Spracklen, C.N., Bollepalli, S., Sung, Y.J., Chen, S.F., Liu, F.C., Kentistou, K.A., Banas, B., Bielak, L.F., Hebbar, P., Hofer, E., Vaccargiu, S., Most, P.J. van der, Chitrala, K.N., Doumatey, A.P., Petersen, E.R.B., Freitag-Wolf, S., Rayner, N.W., Nikus, K., Hidalgo, B., Obura, M.O., Setten, J. van, Jackson, R.D., Chen, Z.M., Li, L.M., Thiery, J., Bis, J.C., Wild, S.H., Nelson, C.P., Jager, S., Asselbergs, F.W., Beulens, J.W.J., Shu, X.O., Pedersen, O., Hewitt, A.W., Kahonen, M., Pennell, C.E., Mori, T.A., Lieb, W., Mellstrom, D., Cho, Y.S.

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A saturated map of common genetic variants associated with human height von Yengo, L., Eliasen, A.U., Raghavan, S., Arias, J.D., Mukamel, R.E., Yin, X.Y., Lull, K., Malden, D.E., Vrieze, S., Andersen, M.K., Arbeeva, L., Brody, J.A., Cai, Q.Y., Chang, L.C., Chang, Y.C., Chen, C.H., Chesi, A., Chung, R.H., Cocca, M., Degenhard, F., Delitala, A., Demirkan, A., Devineni, P., Dorajoo, R., Ekici, A.B., Engmann, J.E., Fernandez-Lopez, J.C., Freitag-Wolf, S., Geller, F., Giulianini, F., Gorski, M., Havulinna, A.S., Haworth, S.J., Heard-Costa, N., Holliday, E., Horn, K., Jonas, J.B., Jonsson, A., Kanoni, S., Karhus, L.L., Katsuya, T., Kentistou, K.A., , P. le, Li, X.H., Liang, J.J., Lin, S.Y., Liu, X.P., Long, J.R., Mamakou, V., Mangino, M., Manichaikul, A., Mattheisen, M., Mavarani, L., McDaid, A.F., Melendez, T.L., Miller, J.E., Mitchell, R.E., Mollehave, L.T., Munz, M., Pandit, A., Christofidou, P., Pauper, M., Petersen, E.R.B., Petersen, L.V., Polasek, O., Pyarajan, S., Raffield, L.M., Rakugi, H., Ramirez, J., Raven, D., Riveros, C., Ruggiero, D., Ryan, K.A., Saxena, R., Sidore, C., Sitlani, C.M., Slieker, R.K.C., Smit, R.A.J., Smith, J.A., Smyth, L.J., Steinthorsdottir, V., Terzikhan, N., Tesolin, P., Laan, S.W. van der, Verma, S.S., Veturi, Y., Wang, Z., Wickremasinghe, A.R., Wiggins, K.L., Wong, A., Xia, R., Yao, J., Young, H., Yousri, N.A., Yu, L., Zeng, L.Y., Zimmermann, M.E., Adair, L.S., Aguilar-Salinas, C.A., Al-Mulla, F.

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A Gene-Based Genetic Linkage and Comparative Map of the Rat X Chromosome von Millwood, Iona Y., Bihoreau, Marie-Therese, Gauguier, Dominique, Hyne, Gina, Levy, Elaine R., Kreutz, Reinhold, Lathrop, G.Mark, Monaco, Anthony P.

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Metabolomic Consequences of Genetic Inhibition of PCSK9 Compared With Statin Treatment von Sliz, E., Kettunen, J., Holmes, M.V., Williams, C.O., Boachie, C., Wang, Q., Mannikko, M., Sebert, S., Walters, R., Lin, K., Millwood, I.Y., Clarke, R., Li, L., Rankin, N., Welsh, P., Delles, C., Jukema, J.W., Trompet, S., Ford, I., Perola, M., Salomaa, V., Jarvelin, M.R., Chen, Z., Lawlor, D.A., Ala-Korpela, M., Danesh, J., Davey Smith, G., Sattar, N., Butterworth, A., Wurtz, P.

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