Transcriptome analysis of cortical tissue reveals shared sets of downregulated genes in autism and schizophrenia by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by Arking, Dan E, Chakravarti, Aravinda

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Association of Human Aging with a Functional Variant of Klotho by 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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Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia by The Psychiatric Genomics Consortium, The Autism Spectrum Disorders Working Group Of, Anney, Richard J L, Ripke, Stephan, Anttila, Verneri, Grove, Jakob, Holmans, Peter, Huang, Hailiang, Klei, Lambertus, Lee, Phil H, Medland, Sarah E, Neale, Benjamin, Robinson, Elise, Weiss, Lauren A, Zwaigenbaum, Lonnie, Yu, Timothy W, Wittemeyer, Kerstin, Willsey, a Jeremy, Wijsman, Ellen M, Werge, Thomas, Wassink, Thomas H, Waltes, Regina, Walsh, Christopher A, Wallace, Simon, Vorstman, Jacob a S, Vieland, Veronica J, Vicente, Astrid M, Vanengeland, Herman, Tsang, Kathryn, Thompson, Ann P, Szatmari, Peter, Svantesson, Oscar, Steinberg, Stacy, Stefansson, Kari, Stefansson, Hreinn, State, Matthew W, Soorya, Latha, Silagadze, Teimuraz, Scherer, Stephen W, Schellenberg, Gerard D, Sandin, Sven, Sanders, Stephan J, Saemundsen, Evald, Rouleau, Guy A, Rogé, Bernadette, Roeder, Kathryn, Roberts, Wendy, Reichert, Jennifer, Reichenberg, Abraham, Rehnström, Karola, Regan, Regina, Poustka, Fritz, Poultney, Christopher S, Piven, Joseph, Pinto, Dalila, Pericak-Vance, Margaret A, Pejovic-Milovancevic, Milica, Pedersen, Marianne Giørtz, Pedersen, Carsten Bøcker, Paterson, Andrew D, Parr, Jeremy R, Pagnamenta, Alistair T, Oliveira, Guiomar, Nurnberger, John I, Nordentoft, Merete, Murtha, Michael T, Mouga, Susana, Mortensen, Preben Bo, Mors, Ole, Morrow, Eric M, Moreno-De-Luca, Daniel, Monaco, Anthony P, Minshew, Nancy, Merikangas, Alison, Mcmahon, William M, Mcgrew, Susan G, Mattheisen, Manuel, Martsenkovsky, Igor, Martin, Donna M, Mane, Shrikant M, Magnusson, Pall, Magalhaes, Tiago, Maestrini, Elena, Lowe, Jennifer K, Lord, Catherine, Levitt, Pat, Martin, Christa Lese, Ledbetter, David H, Leboyer, Marion, Lecouteur, Ann S, Ladd-Acosta, Christine, Kolevzon, Alexander, Klauck, Sabine M, Jacob, Suma, Iliadou, Bozenna, Hultman, Christina M, Hougaard, David M, Hertz-Picciotto, Irva, Hendren, Robert, Hansen, Christine Søholm, Haines, Jonathan L

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Genome-wide association analysis identifies multiple loci related to resting heart rate by 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 by 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 Genetics of Sudden Cardiac Death by Arking, Dan E, Sotoodehnia, Nona

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KLOTHO Allele Status and the Risk of Early-Onset Occult Coronary Artery Disease by Arking, Dan E., Becker, Diane M., Yanek, Lisa R., Fallin, Daniele, Judge, Daniel P., Moy, Taryn F., Becker, Lewis C., Dietz, Harry C.

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