Transcriptome analysis of cortical tissue reveals shared sets of downregulated genes in autism and schizophrenia von Ellis, S E, Panitch, R, West, A B, Arking, D E

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Novel gene variants predict serum levels of the cytokines IL-18 and IL-1ra in older adults von Matteini, A.M., Li, J., Lange, E.M., Tanaka, T., Lange, L.A., Tracy, R.P., Wang, Y., Biggs, M.L., Arking, D.E., Fallin, M.D., Chakravarti, A., Psaty, B.M., Bandinelli, S., Ferrucci, L., Reiner, A.P., Walston, J.D.

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GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium von Trampush, J W, Yang, M L Z, Yu, J, Knowles, E, Davies, G, Liewald, D C, Starr, J M, Djurovic, S, Melle, I, Sundet, K, Christoforou, A, Reinvang, I, DeRosse, P, Lundervold, A J, Steen, V M, Espeseth, T, Räikkönen, K, Widen, E, Palotie, A, Eriksson, J G, Giegling, I, Konte, B, Roussos, P, Giakoumaki, S, Burdick, K E, Payton, A, Ollier, W, Horan, M, Chiba-Falek, O, Attix, D K, Need, A C, Cirulli, E T, Voineskos, A N, Stefanis, N C, Avramopoulos, D, Hatzimanolis, A, Arking, D E, Smyrnis, N, Bilder, R M, Freimer, N A, Cannon, T D, London, E, Poldrack, R A, Sabb, F W, Congdon, E, Conley, E D, Scult, M A, Dickinson, D, Straub, R E, Donohoe, G, Morris, D, Corvin, A, Gill, M, Hariri, A R, Weinberger, D R, Pendleton, N, Bitsios, P, Rujescu, D, Lahti, J, Le Hellard, S, Keller, M C, Andreassen, O A, Deary, I J, Glahn, D C, Malhotra, A K, Lencz, T

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The association of genetic variants in interleukin-1 genes with cognition: Findings from the cardiovascular health study von Benke, K.S., Carlson, M.C., Doan, B.Q., Walston, J.D., Xue, Q.L., Reiner, A.P., Fried, L.P., Arking, D.E., Chakravarti, A., Fallin, M.D.

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Resting heart rate and incident atrial fibrillation: A stratified Mendelian randomization in the AFGen consortium von Siland, J E, Geelhoed, B, Roselli, C, Wang, B, Lin, H J, Weiss, S, Trompet, S, van den Berg, M E, Soliman, E Z, Chen, L Y, Ford, I, Jukema, J W, Macfarlane, P W, Kornej, J, Lin, H, Lunetta, K L, Kavousi, M, Kors, J A, Ikram, M A, Guo, X, Yao, J, Dörr, M, Felix, S B, Völker, U, Sotoodehnia, N, Arking, D E, Stricker, B H, Heckbert, S R, Lubitz, S A, Benjamin, E J, Alonso, A, Ellinor, P T, van der Harst, P, Rienstra, M

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Transcobalamin-II variants, decreased vitamin B12 availability and increased risk of frailty von Matteini, Amy M., Walston, J. D., Bandeen-Roche, K., Arking, D. E., Allen, R. H., Fried, L. P., Chakravarti, A., Stabler, S. P., Fallin, M. D.

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IL-6 gene variation is not associated with increased serum levels of IL-6, muscle, weakness, or frailty in older women von Walston, J., Arking, D.E., Fallin, D., Li, T., Beamer, B., Xue, Q., Ferrucci, L., Fried, L.P., Chakravarti, A.

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NOS1AP variant associated with incidence of type 2 diabetes in calcium channel blocker users in the Atherosclerosis Risk in Communities (ARIC) study von Chu, A. Y, Coresh, J, Arking, D. E, Pankow, J. S, Tomaselli, G. F, Chakravarti, A, Post, W. S, Spooner, P. H, Boerwinkle, E, Kao, W. H. L

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Exploring biologically relevant pathways in frailty von Ho, Yen-Yi, Matteini, Amy M, Beamer, Brock, Fried, Linda, Xue, Qian-li, Arking, Dan E, Chakravarti, Aravinda, Fallin, M Daniele, Walston, Jeremy

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Polygenic risk score associates with atherosclerosis severity at autopsy von Cornelissen, A, Gadhoke, N V, Ryan, K, Hodonsky, C J, Duong, T V, Dikongue, A, Sakamoto, A, Sato, Y, Miller, C L, Hong, C C, Arking, D E, Mitchell, B D, Guo, L, Virmani, R, Finn, A V

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A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism von Arking, Dan E., Cutler, David J., Brune, Camille W., Teslovich, Tanya M., West, Kristen, Ikeda, Morna, Rea, Alexis, Guy, Moltu, Lin, Shin, Cook, Edwin H., Chakravarti, Aravinda

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Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation von Longchamps, R. J., Yang, S. Y., Castellani, C. A., Shi, W., Lane, J., Grove, M. L., Bartz, T. M., Sarnowski, C., Liu, C., Burrows, K., Guyatt, A. L., Gaunt, T. R., Kacprowski, T., Yang, J., De Jager, P. L., Yu, L., Bergman, A., Xia, R., Fornage, M., Feitosa, M. F., Wojczynski, M. K., Kraja, A. T., Province, M. A., Amin, N., Rivadeneira, F., Tiemeier, H., Uitterlinden, A. G., Broer, L., Van Meurs, J. B. J., Van Duijn, C. M., Raffield, L. M., Lange, L., Rich, S. S., Lemaitre, R. N., Goodarzi, M. O., Sitlani, C. M., Mak, A. C. Y., Bennett, D. A., Rodriguez, S., Murabito, J. M., Lunetta, K. L., Sotoodehnia, N., Atzmon, G., Ye, K., Barzilai, N., Brody, J. A., Psaty, B. M., Taylor, K. D., Rotter, J. I., Boerwinkle, E., Pankratz, N., Arking, D. E.

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Association Between a Functional Variant of the KLOTHO Gene and High-Density Lipoprotein Cholesterol, Blood Pressure, Stroke, and Longevity von Arking, Dan E, Atzmon, Gil, Arking, Albert, Barzilai, Nir, Dietz, Harry C

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Understanding cardiovascular disease through the lens of genome-wide association studies von Arking, Dan E, Chakravarti, Aravinda

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Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation von Rienstra, Michiel, Roselli, Carolina, Yin, Xiaoyan, Geelhoed, Bastiaan, Lin, Honghuang, Arking, Dan E, Smith, Albert V, Albert, Christine M, Chaffin, Mark, Tucker, Nathan R, Li, Molong, Klarin, Derek, Low, Siew-Kee, Müller-Nurasyid, Martina, Dörr, Marcus, Trompet, Stella, Gustafsson, Stefan, Kleber, Marcus E, Lyytikäinen, Leo-Pekka, Seppälä, Ilkka, Malik, Rainer, Perez, Marco, Sinisalo, Juha, Thériault, Sébastien, Radmanesh, Farid, Teumer, Alexander, Weng, Lu-Chen, Deo, Rajat, Rader, Daniel J, Shah, Svati H, Yang, Qiong, Worrall, Bradford B, Kamatani, Yoichiro, Hagemeijer, Yanick P, Siland, Joylene E, Kubo, Michiaki, Smith, Jonathan D, Bis, Joshua C, Perz, Siegfried, Psaty, Bruce M, Ridker, Paul M, Magnani, Jared W, Harris, Tamara B, Launer, Lenore J, Shoemaker, M Benjamin, Padmanabhan, Sandosh, Haessler, Jeffrey, Kähönen, Mika, Risch, Lorenz, Mansur, Alfredo J, Smith, Blair H, Lu, Yingchang, Bottinger, Erwin B, Hernesniemi, Jussi, Lindgren, Cecilia M, Huang, Jie, Ford, Ian, Delgado, Graciela, Chen, Lin Y, Chen, Yii-Der Ida, Li, Man, Lannfelt, Lars, Rost, Natalia, Taylor, Kent D, Campbell, Archie, Porteous, David, Hocking, Lynne J, Nikus, Kjell, Orho-Melander, Marju, Hamsten, Anders, Denny, Joshua C, Kriebel, Jennifer, Newton-Cheh, Christopher, Shaffer, Christian, Macfarlane, Peter W, Heilmann-Heimbach, Stefanie, Huang, Paul L, Sotoodehnia, Nona, Soliman, Elsayed Z, Uitterlinden, Andre G, Hofman, Albert, Franco, Oscar H, Völker, Uwe, Lin, Henry J, Ingelsson, Erik, Kooperberg, Charles, Conen, David, Rosand, Jonathan, van der Harst, Pim, Kathiresan, Sekar, Stricker, Bruno H, Chung, Mina K, Felix, Stephan B, Gudnason, Vilmundur, Alonso, Alvaro, Kääb, Stefan, Chasman, Daniel I, Benjamin, Emelia J, Tanaka, Toshihiro, Lunetta, Kathryn L

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Resting heart rate and incident atrial fibrillation: A stratified Mendelian randomization in the AFGen consortium von Siland, J E, Geelhoed, B, Roselli, C, Wang, B, Lin, H J, Weiss, S, Trompet, S, van den Berg, M E, Soliman, E Z, Chen, L Y, Ford, I, Jukema, J W, Macfarlane, P W, Kornej, J, Lin, H, Lunetta, K L, Kavousi, M, Kors, J A, Ikram, M A, Guo, X, Yao, J, Dörr, M, Felix, S B, Völker, U, Sotoodehnia, N, Arking, D E, Stricker, B H, Heckbert, S R, Lubitz, S A, Benjamin, E J, Alonso, A, Ellinor, P T, van der Harst, P, Rienstra, M

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Association of Human Aging with a Functional Variant of Klotho von Arking, Dan E., Krebsova, Alice, Macek, Milan, Macek, Milan, Arking, Albert, Mian, I. Saira, Fried, Linda, Hamosh, Ada, Dey, Srabani, McIntosh, Iain, Dietz, Harry C.

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Dysregulation of TGF-β activation contributes to pathogenesis in Marfan syndrome von Neptune, Enid R., Frischmeyer, Pamela A., Arking, Dan E., Myers, Loretha, Bunton, Tracie E., Gayraud, Barbara, Ramirez, Francesco, Sakai, Lynn Y., Dietz, Harry C.

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Genome-wide association analysis identifies multiple loci related to resting heart rate von Eijgelsheim, Mark, Newton-Cheh, Christopher, Sotoodehnia, Nona, de Bakker, Paul I.W., Müller, Martina, Morrison, Alanna C., Smith, Albert V., Isaacs, Aaron, Sanna, Serena, Dörr, Marcus, Navarro, Pau, Fuchsberger, Christian, Nolte, Ilja M., de Geus, Eco J.C., Estrada, Karol, Hwang, Shih-Jen, Bis, Joshua C., Rückert, Ina-Maria, Alonso, Alvaro, Launer, Lenore J., Hottenga, Jouke Jan, Rivadeneira, Fernando, Noseworthy, Peter A., Rice, Kenneth M., Perz, Siegfried, Arking, Dan E., Spector, Tim D., Kors, Jan A., Aulchenko, Yurii S., Tarasov, Kirill V., Homuth, Georg, Wild, Sarah H., Marroni, Fabio, Gieger, Christian, Licht, Carmilla M., Prineas, Ronald J., Hofman, Albert, Rotter, Jerome I., Hicks, Andrew A., Ernst, Florian, Najjar, Samer S., Wright, Alan F., Peters, Annette, Fox, Ervin R., Oostra, Ben A., Kroemer, Heyo K., Couper, David, Völzke, Henry, Campbell, Harry, Meitinger, Thomas, Uda, Manuela, Witteman, Jacqueline C.M., Psaty, Bruce M., Wichmann, H-Erich, Harris, Tamara B., Kääb, Stefan, Siscovick, David S., Jamshidi, Yalda, Uitterlinden, André G., Folsom, Aaron R., Larson, Martin G., Wilson, James F., Penninx, Brenda W., Snieder, Harold, Pramstaller, Peter P., van Duijn, Cornelia M., Lakatta, Edward G., Felix, Stephan B., Gudnason, Vilmundur, Pfeufer, Arne, Heckbert, Susan R., Stricker, Bruno H.Ch, Boerwinkle, Eric, O'Donnell, Christopher J.

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Erratum: GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium von Trampush, J W, Yang, M L Z, Yu, J, Knowles, E, Davies, G, Liewald, D C, Starr, J M, Djurovic, S, Melle, I, Sundet, K, Christoforou, A, Reinvang, I, DeRosse, P, Lundervold, A J, Steen, V M, Espeseth, T, Räikkönen, K, Widen, E, Palotie, A, Eriksson, J G, Giegling, I, Konte, B, Roussos, P, Giakoumaki, S, Burdick, K E, Payton, A, Ollier, W, Horan, M, Chiba-Falek, O, Attix, D K, Need, A C, Cirulli, E T, Voineskos, A N, Stefanis, N C, Avramopoulos, D, Hatzimanolis, A, Arking, D E, Smyrnis, N, Bilder, R M, Freimer, N A, Cannon, T D, London, E, Poldrack, R A, Sabb, F W, Congdon, E, Conley, E D, Scult, M A, Dickinson, D, Straub, R E, Donohoe, G, Morris, D, Corvin, A, Gill, M, Hariri, A R, Weinberger, D R, Pendleton, N, Bitsios, P, Rujescu, D, Lahti, J, Le Hellard, S, Keller, M C, Andreassen, O A, Deary, I J, Glahn, D C, Malhotra, A K, Lencz, T

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