Genetic invalidation of Lp-PLA(2) as a therapeutic target: Large-scale study of five functional Lp-PLA(2)-lowering alleles

by Gregson, J.M., Freitag, D.F., Surendran, P., Stitziel, N.O., Chowdhury, R., Burgess, S., Kaptoge, S., Gao, P., Staley, J.R., Willeit, P., Nielsen, S.F., Caslake, M., Trompet, S., Polfus, L.M., Kuulasmaa, K., Kontto, J., Perola, M., Blankenberg, S., Veronesi, G., Gianfagna, F., Mannisto, S., Kimura, A., Lin, H.H., Reilly, D.F., Gorski, M., Mijatovic, V., Munroe, P.B., Ehret, G.B., Thompson, A., Uria-Nickelsen, M., Malarstig, A., Dehghan, A., Vogt, T.F., Sasaoka, T., Takeuchi, F., Kato, N., Yamada, Y., Kee, F., Muller-Nurasyid, M., Ferrieres, J., Arveiler, D., Amouyel, P., Salomaa, V., Boerwinkle, E., Thompson, S.G., Ford, I., Jukema, J.W., Sattar, N., Packard, C.J., Majumder, A.A., Alam, D.S., Deloukas, P., Schunkert, H., Samani, N.J., Kathiresan, S., Nordestgaard, B.G., Saleheen, D., Howson, J.M.M., Angelantonio, E. di, Butterworth, A.S., Danesh, J., CKDGen Consortium, Int Consortium Blood Pressure, CHARGE Inflammation Working Grp, MICAD Exome Consortium, EPIC-CVD Consortium, CHD Exome Consortium
Published 2017

Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease

by Webb, T.R., Erdmann, J., Stirrups, K.E., Stitziel, N.O., Masca, N.G.D., Jansen, H., Kanoni, S., Nelson, C.P., Ferrario, P.G., Konig, I.R., Eicher, J.D., Johnson, A.D., Hamby, S.E., Betsholtz, C., Ruusalepp, A., Franzen, O., Schadt, E.E., Bjorkegren, J.L.M., Weeke, P.E., Auer, P.L., Schick, U.M., Lu, Y.C., Zhang, H., Dube, M.P., Goel, A., Farrall, M., Peloso, G.M., Won, H.H., , R. do, Iperen, E. van, Kruppa, J., Mahajan, A., Scott, R.A., Willenborg, C., Braund, P.S., Capelleveen, J.C. van, Doney, A.S.F., Donnelly, L.A., Asselta, R., Merlini, P.A., Duga, S., Marziliano, N., Denny, J.C., Shaffer, C., El-Mokhtari, N.E., Franke, A., Heilmann, S., Hengstenberg, C., Hoffmann, P., Holmen, O.L., Hveem, K., Jansson, J.H., Jockel, K.H., Kessler, T., Kriebel, J., Laugwitz, K.L., Marouli, E., Martinelli, N., McCarthy, M.I., Zuydam, N.R. van, Meisinger, C., Esko, T., Mihailov, E., Escher, S.A., Alver, M., Moebus, S., Morris, A.D., Virtamo, J., Nikpay, M., Olivieri, O., Provost, S., AlQarawi, A., Robertson, N.R., Akinsansya, K.O., Reilly, D.F., Vogt, T.F., Yin, W., Asselbergs, F.W., Kooperberg, C., Jackson, R.D., Stahl, E., Muller-Nurasyid, M., Strauch, K., Varga, T.V., Waldenberger, M., Zeng, L.Y., Chowdhury, R., Salomaa, V., Ford, I., Jukema, J.W., Amouyel, P., Kontto, J., Nordestgaard, B.G., Ferrieres, J., Saleheen, D., Sattar, N., Surendran, P., Wagner, A., Young, R., Howson, J.M.M., Butterworth, A.S., Danesh, J., Ardissino, D., Bottinger, E.P., Erbel, R., Franks, P.W., Girelli, D., Hall, A.S., Hovingh, G.K., Kastrati, A., Lieb, W., Meitinger, T., Kraus, W.E., Shah, S.H., McPherson, R., Orho-Melander, M., Melander, O., Metspalu, A., Palmer, C.N.A., Peters, A., Rader, D.J., Reilly, M.P., Loos, R.J.F., Reiner, A.P., Roden, D.M., Tardif, J.C., Thompson, J.R., Wareham, N.J., Watkins, H., Willer, C.J., Samani, N.J., Schunkert, H., Deloukas, P., Kathiresan, S., Wellcome Trust Case Control, MORGAM Investigators, Myocardial Infarction Genetics
Published 2017

Genetic invalidation of Lp-PLA$_{2}$ as a therapeutic target: Large-scale study of five functional Lp-PLA$_{2}$-lowering alleles

by Gregson, JM, Freitag, DF, Surendran, P, Stitziel, NO, Chowdhury, R, Burgess, S, Kaptoge, S, Gao, P, Staley, JR, Willeit, P, Nielsen, SF, Caslake, M, Trompet, S, Polfus, LM, Kuulasmaa, K, Kontto, J, Perola, M, Blankenberg, S, Veronesi, G, Gianfagna, F, Männistö, S, Kimura, A, Lin, H, Reilly, DF, Gorski, M, Mijatovic, V, CKDGen consortium, Munroe, PB, Ehret, GB, International Consortium for Blood Pressure, Thompson, A, Uria-Nickelsen, M, Malarstig, A, Dehghan, A, CHARGE inflammation working group, Vogt, TF, Sasaoka, T, Takeuchi, F, Kato, N, Yamada, Y, Kee, F, Müller-Nurasyid, M, Ferrières, J, Arveiler, D, Amouyel, P, Salomaa, V, Boerwinkle, E, Thompson, SG, Ford, I, Wouter Jukema, J, Sattar, N, Packard, CJ, Shafi Majumder, AA, Alam, DS, Deloukas, P, Schunkert, H, Samani, NJ, Kathiresan, S, MICAD Exome consortium, Nordestgaard, BG, Saleheen, D, Howson, JM, Di Angelantonio, E, Butterworth, AS, Danesh, J, EPIC-CVD consortium and the CHD Exome+ consortium
Published 2017

Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

by Surendran, P., Drenos, F., Young, R., Warren, H., Cook, J.P., Manning, A.K., Grarup, N., Sim, X., Barnes, D.R., Witkowska, K., Staley, J.R., Tragante, V., Tukiainen, T., Yaghootkar, H., Masca, N., Freitag, D.F., Ferreira, T., Giannakopoulou, O., Tinker, A., Harakalova, M., Mihailov, E., Liu, C., Kraja, A.T., Nielsen, S.F., Rasheed, A., Samue, M., Zhao, W., Bonnycastle, L.L., Jackson, A.U., Narisu, N., Swift, A.J., Southam, L., Marten, J., Huyghe, J.R., Stancakova, A., Fava, C., Ohlsson, T., Matchan, A., Stirrups, K.E., Bork-Jensen, J., Gjesing, A.P., Kontto, J., Perola, M., Shaw-Hawkins, S., Havulinna, A.S., Zhang, H., Donnelly, L.A., Groves, C.J., Rayner, N.W., Neville, M.J., Robertson, N.R., Yiorkas, A.M., Herzig, K.H., Kajantie, E., Zhang, W., Willems, S.M., Lannfelt, L., Malerba, G., Soranzo, N., Trabetti, E., Verweij, N., Evangelou, E., Moayyeri, A., Vergnaud, A.C., Nelson, C.P., Poveda, A., Varga, T.V., Caslake, M., Craen, A.J.M. de, Trompet, S., Luan, J., Scott, R.A., Harris, S.E., Liewald, D.C.M., Marioni, R., Menni, C., Farmaki, A.E., Hallmans, G., Renstrom, F., Huffman, J.E., Hassinen, M., Burgess, S., Vasan, R.S., Felix, J.F., Uria-Nickelsen, M., Malarstign, A., Reilly, D.F., Hoek, M., Vogt, T.F., Lin, H.H., Lieb, W., Traylor, M., Markus, H.S., Highland, H.M., Justice, A.E., Marouli, E., Lindstrom, J., Uusitupa, M., Komulainen, P., Lakka, T.A., Rauramaa, R., Polasek, O., Rudan, I., Rolandsson, O., Franks, P.W., Dedoussis, G., Spector, T.D., Jousilahti, P., Mannisto, S., Deary, I.J., Starr, J.M., Langenberg, C., Wareham, N.J., Brown, M.J., Dominiczak, A.F., Connell, J.M., Jukema, J.W., Sattar, N., Ford, I., Packard, C.J., Esko, T., Magi, R., Metspalu, A., Boer, R.A. de, Meer, P. van der, Harst, P. van der, Gambaro, G., Ingelsson, E., Lind, L., Bakker, P.I.W. de, Numans, M.E., Brandslund, I., Christensen, C., Petersen, E.R.B., Korpi-Hyovalti, E., Oksa, H., Chambers, J.C., Kooner, J.S., Blakemore, A.I.F., Franks, S., Jarvelin, M.R., Husemoen, L.L., Linneberg, A., Skaaby, T., Thuesen, B., Karpe, F., Tuomilehto, J., Doney, A.S.F., Morris, A.D., Palmer, C.N.A., Holmen, O.L., Hveem, K., Willer, C.J., Tuomi, T., Groop, L., Karajamaki, A., Palotie, A., Ripatti, S., Salomaa, V., Alam, D.S., Majmnder, A.A.S., Angelantonio, E. di, Chowdhury, R., McCarthy, M.I., Poulter, N., Stanton, A.V., Sever, P., Amouyel, P., Arveiler, D., Blankenberg, S., Ferrieres, J., Kee, F., Kuulasmaa, K., Muller-Nurasyid, M., Veronesi, G., Virtamo, J., Deloukas, P., Elliott, P., Zeggini, E., Kathiresan, S., Melander, O., Kuusisto, J., Laakso, M., Padmanabhan, S., Porteous, D.J., Hayward, C., Scotland, G., Collins, F.S., Mohlke, K.L., Hansen, T., Pedersen, O., Boehnke, M., Stringham, H.M., Frossard, P., Newton-Cheh, C., Tobin, M.D., Nordestgaard, B.G., Caulfield, M.J., Mahajan, A., Morris, A.P., Tomaszewski, M., Samani, N.J., Saleheen, D., Asselbergs, F.W., Lindgren, C.M., Danesh, J., Wain, L.V., Butterworth, A.S., Howson, J.M.M., Munroe, P.B., CHARGE Heart Failure Consortiumm, EchoGen Consortiumm, Metastroke Consortiumm, Giant Consortiumm, EPIC-InterAct Consortium, Lifelines Cohort Study, Wellcome Trust Case Control Consor, Understanding Soc Sci Grp, EPIC-CVD Consortium, CHARGE Exome Chip Blood Pressure C, T2D-GENES Consortium, GoT2DGenes Consortium, ExomeBP Consortium, CHD Exome Consortium
Published 2016

Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

by Justice, A.E., Karaderi, T., Highland, H.M., Young, K.L., Graff, M., Lu, Y.C., Turcot, V., Auer, P.L., Fine, R.S., Guo, X.Q., Schurmann, C., Lempradl, A., Marouli, E., Mahajan, A., Winkler, T.W., Locke, A.E., Medina-Gomez, C., Esko, T., Vedantam, S., Giri, A., , K.S. lo, Alfred, T., Mudgal, P., Ng, M.C.Y., Heard-Costa, N.L., Feitosa, M.F., Manning, A.K., Willems, S.M., Sivapalaratnam, S., Abecasis, G., Alam, D.S., Allison, M., Amouyel, P., Arzumanyanm, Z., Balkau, B., Bastarache, L., Bergmann, S., Bielak, L.F., Blueher, M., Boehnke, M., Boeing, H., Boerwinkle, E., Boger, C.A., Bork-Jensen, J., Bottinger, E.P., Bowden, D.W., Brandslund, I., Broer, L., Burt, A.A., Butterworth, A.S., Caulfield, M., Cesana, G., Chambers, J.C., Chasman, D.I., Chen, Y.D.I., Chowdhury, R., Christensen, C., Chu, A., Collins, F.S., Cook, J.P., Cox, A.J., Crosslin, D.S., Danesh, J., Bakker, P.I.W. de, Denus, S. de, Mutsert, R. de, Dedoussis, G., Demerath, E.W., Dennis, J.G., Denny, J.C., Angelantonio, E. di, Dorr, M., Drenos, F., Dube, M.P., Dunning, A.M., Easton, D.F., Elliott, P., Evangelou, E., Farmaki, A.E., Feng, S., Ferrannini, E., Ferrieres, J., Florez, J.C., Fornage, M., Fox, C.S., Franks, P.W., Friedrich, N., Gan, W., Gandin, I., Gasparini, P., Giedraitis, V., Girotto, G., Gorski, M., Grallert, H., Grarup, N., Groves, M.L., Gustafsson, S., Haessler, J., Hansen, T., Hattersley, A.T., Hayward, C., Heid, I.M., Holmen, O.L., Hovingh, G.K., Howson, J.M.M., Hu, Y., Hung, Y.J., Hveem, K., Ikram, M.A., Ingelsson, E., Jackson, A.U., Jarvik, G.P., Jia, Y.C., Jorgensen, T., Jousilahti, P., Justesen, J.M., Kahali, B., Karaleftheri, M., Kardia, S.L.R., Karpe, F., Kee, F., Kitajima, H., Komulainen, P., Kooner, J.S., Kovacs, P., Kramer, B.K., Kuulasmaa, K., Kuusisto, J., Laakso, M., Lakka, T.A., Lamparter, D., Nge, L.A. la, Langenberg, C., Larson, E.B., Lee, N.R., Lee, W.J., Lehtimaki, T., Lewis, C.E., Li, H.X., Li, J., RuifangLi-Gao, Lin, L.A., Lin, X., Lind, L., Lindstrom, J., Linneberg, A., Liu, C.T., Liu, D.J.J., Luan, J., Lyytikainen, L.P., MacGregor, S., Magi, R., Mannisto, S., Marenne, G., Marten, J., Mascal, N.G.D., McCarthy, M.I., Meidtner, K., Mihailov, E., Moilanen, L., Moitry, M., Mook-Kanamori, D.O., Morgan, A., Morris, A.P., Muller-Nurasyid, M., Munroe, P.B., Narisu, N., Nelson, C.P., Neville, M., Ntalla, I., Owen, K.R., Pedersen, O., Peloso, G.M., Pennell, C.E., Perola, M., James, A., Perry, J.R.B., Pers, T.H., Ewing, A., Polasek, O., Rasheed, A., Raulerson, C.K., Rauramaa, R., Reilly, D.F., Reiner, A.P., Ridker, P.M., Rivas, M.A., Robertson, N.R., Robino, A., Rudan, I., Ruth, K.S., Saleheen, D., Salomaa, V., Samani, N.J., Schreiner, P.J., Schulze, M.B., Scott, R.A., Segura-Lepe, M., Sim, X.L., Slater, A.J., Small, K.S., Smith, B.H., Smith, J.A., Southam, L., Spector, T.D., Speliotes, E.K., Stefansson, K., Steinthorsdottir, V., Stirrups, K.E., Strauch, K., Stringham, H.M., Stumvoll, M., Sun, L., Surendran, P., Swart, K.M.A., Tardif, J.C., Taylor, K.D., Teumer, A., Thompson, D.J., Thorleifsson, G., Thorsteinsdottir, U., Thuesen, B.H., Tonjes, A., Torres, M., Tsafantakis, E., Tuomilehto, J., Uitterlinden, A.G., Uusitupa, M., Duijn, C.M. van, Vanhala, M., Varma, R., Vermeulen, S.H., Vestergaard, H., Vitart, V., Vogt, T.F., Vuckovic, D., Wagenknecht, L.E., Walker, M., Wallentin, L., Wang, F.J., Wang, C.A., Wang, S., Wareham, N.I.J., Warren, H.R., Waterworth, D.M., Wessel, J., White, H.D., Willer, C.J., Wilson, J.G., Wood, A.R., Wu, Y., Yaghootkar, H., Yao, J., Verges-Armstrong, L.M., Young, R., Zeggini, E., Zhan, X.W., Zhang, W.H., Zhao, J.H., Zhao, W., Zheng, H., Zhou, W., Zillikens, M.C., Rivadeneira, F., Borecki, I.B., Pospisilik, J.A., Deloukas, P., Frayling, T.M., Lettre, G., Mohlke, K.L., Rotter, J.I., Kutalik, Z., Hirschhorn, J.N., Cupples, L.A., Loos, R.J.F., North, K.E., Lindgren, C.M., O'Connell, J.R., Raitakari, O.T., Cupples
Published 2019

Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease

by Webb, TR, Erdmann, J, Stirrups, KE, Stitziel, NO, Masca, NGD, Jansen, H, Kanoni, S, Nelson, CP, Ferrario, PG, König, IR, Eicher, JD, Johnson, AD, Hamby, SE, Betsholtz, C, Ruusalepp, A, Franzén, O, Schadt, EE, Björkegren, JLM, Weeke, PE, Auer, PL, Schick, UM, Lu, Y, Zhang, H, Dube, M-P, Goel, A, Farrall, M, Peloso, GM, Won, H-H, Do, R, van Iperen, E, Kruppa, J, Mahajan, A, Scott, RA, Willenborg, C, Braund, PS, van Capelleveen, JC, Doney, ASF, Donnelly, LA, Asselta, R, Merlini, PA, Duga, S, Marziliano, N, Denny, JC, Shaffer, C, El-Mokhtari, NE, Franke, A, Heilmann, S, Hengstenberg, C, Hoffmann, P, Holmen, OL, Hveem, K, Jansson, J-H, Jöckel, K-H, Kessler, T, Kriebel, J, Laugwitz, KL, Marouli, E, Martinelli, N, McCarthy, MI, Van Zuydam, NR, Meisinger, C, Esko, T, Mihailov, E, Escher, SA, Alver, M, Moebus, S, Morris, AD, Virtamo, J, Nikpay, M, Olivieri, O, Provost, S, AlQarawi, A, Robertson, NR, Akinsansya, KO, Reilly, DF, Vogt, TF, Yin, W, Asselbergs, FW, Kooperberg, C, Jackson, RD, Stahl, E, Müller-Nurasyid, M, Strauch, K, Varga, TV, Waldenberger, M, Wellcome Trust Case Control Consortium, Zeng, L, Chowdhury, R, Salomaa, V, Ford, I, Jukema, JW, Amouyel, P, Kontto, J, MORGAM Investigators, Nordestgaard, BG, Ferrières, J, Saleheen, D, Sattar, N, Surendran, P, Wagner, A, Young, R, Howson, JMM, Butterworth, AS, Danesh, J, Ardissino, D, Bottinger, EP, Erbel, R, Franks, PW, Girelli, D, Hall, AS, Hovingh, GK, Kastrati, A, Lieb, W, Meitinger, T, Kraus, WE, Shah, SH, McPherson, R, Orho-Melander, M, Melander, O, Metspalu, A, Palmer, CNA, Peters, A, Rader, DJ, Reilly, MP, Loos, RJF, Reiner, AP, Roden, DM, Tardif, J-C, Thompson, JR, Wareham, NJ, Watkins, H, Willer, CJ, Samani, NJ, Schunkert, H, Deloukas, P, Kathiresan, S, Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators
Published 2017