The behavior of money and other economic variables: Two natural experiments von Lothian, James R., McCarthy, Cornelia H.

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Money and monetary policy von Dwyer, G P, Lothian, J R, Boyer, R S, Dellas, H, Tavlas, G S, Fischer, B, Lenza, M, Pill, H, Reichlin, L, Hofmann, B, Basco, E, D'Amato, L, Garegnani, L, McCarthy, C H, Fisher, M

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Editorial Perspectives on the financial crisis in Asia von Edison, H J, McCarthy, C H

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A roadmap for child health research in Europe von Ottová, V, Staines, A, Rigby, MJ, Hjern, A, Leonardi, M, Bourek, A, Blair, M, Tamburlini, G, Gaspar de Matos, M, Alexander, D, Rasche, C, Rossi, G, Ravens-Sieberer, U

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Real Exchange Rate Behaviour under Fixed and Floating Exchange Rate Regimes von Lothian, James R., McCarthy, Cornelia H.

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Perspectives on the financial crisis in Asia von Edison, Hali J, McCarthy, Cornelia H

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A Imunidade De Jurisdição Penal Das Familias De Diplomatas von McCarthy, H. C.

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Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium von Lemaitre, Rozenn N, Tanaka, Toshiko, Tang, Weihong, Manichaikul, Ani, Foy, Millennia, Kabagambe, Edmond K, Nettleton, Jennifer A, King, Irena B, Weng, Lu-Chen, Bhattacharya, Sayanti, Bandinelli, Stefania, Bis, Joshua C, Rich, Stephen S, Jacobs, Jr, David R, Cherubini, Antonio, McKnight, Barbara, Liang, Shuang, Gu, Xiangjun, Rice, Kenneth, Laurie, Cathy C, Lumley, Thomas, Browning, Brian L, Psaty, Bruce M, Chen, Yii-Der I, Friedlander, Yechiel, Djousse, Luc, Wu, Jason H Y, Siscovick, David S, Uitterlinden, André G, Arnett, Donna K, Ferrucci, Luigi, Fornage, Myriam, Tsai, Michael Y, Mozaffarian, Dariush, Steffen, Lyn M

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Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits von Speliotes, Elizabeth K, Yerges-Armstrong, Laura M, Wu, Jun, Hernaez, Ruben, Kim, Lauren J, Palmer, Cameron D, Gudnason, Vilmundur, Eiriksdottir, Gudny, Garcia, Melissa E, Launer, Lenore J, Nalls, Michael A, Clark, Jeanne M, Mitchell, Braxton D, Shuldiner, Alan R, Butler, Johannah L, Tomas, Marta, Hoffmann, Udo, Hwang, Shih-Jen, Massaro, Joseph M, O'Donnell, Christopher J, Sahani, Dushyant V, Salomaa, Veikko, Schadt, Eric E, Schwartz, Stephen M, Siscovick, David S, Voight, Benjamin F, Carr, J Jeffrey, Feitosa, Mary F, Harris, Tamara B, Fox, Caroline S, Smith, Albert V, Kao, W H Linda, Hirschhorn, Joel N, Borecki, Ingrid B

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A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function von Porcu, Eleonora, Medici, Marco, Pistis, Giorgio, Volpato, Claudia B, Wilson, Scott G, Cappola, Anne R, Bos, Steffan D, Deelen, Joris, den Heijer, Martin, Freathy, Rachel M, Lahti, Jari, Liu, Chunyu, Lopez, Lorna M, Nolte, Ilja M, O'Connell, Jeffrey R, Tanaka, Toshiko, Trompet, Stella, Arnold, Alice, Bandinelli, Stefania, Beekman, Marian, Böhringer, Stefan, Brown, Suzanne J, Buckley, Brendan M, Camaschella, Clara, de Craen, Anton J M, Davies, Gail, de Visser, Marieke C H, Ford, Ian, Forsen, Tom, Frayling, Timothy M, Fugazzola, Laura, Gögele, Martin, Hattersley, Andrew T, Hermus, Ad R, Hofman, Albert, Houwing-Duistermaat, Jeanine J, Jensen, Richard A, Kajantie, Eero, Kloppenburg, Margreet, Lim, Ee M, Masciullo, Corrado, Mariotti, Stefano, Minelli, Cosetta, Mitchell, Braxton D, Nagaraja, Ramaiah, Netea-Maier, Romana T, Palotie, Aarno, Persani, Luca, Piras, Maria G, Psaty, Bruce M, Räikkönen, Katri, Richards, J Brent, Rivadeneira, Fernando, Sala, Cinzia, Sabra, Mona M, Sattar, Naveed, Shields, Beverley M, Soranzo, Nicole, Starr, John M, Stott, David J, Sweep, Fred C G J, Usala, Gianluca, van der Klauw, Melanie M, van Heemst, Diana, van Mullem, Alies, Vermeulen, Sita H, Visser, W Edward, Walsh, John P, Westendorp, Rudi G J, Widen, Elisabeth, Zhai, Guangju, Cucca, Francesco, Deary, Ian J, Eriksson, Johan G, Ferrucci, Luigi, Fox, Caroline S, Jukema, J Wouter, Kiemeney, Lambertus A, Pramstaller, Peter P, Schlessinger, David, Shuldiner, Alan R, Slagboom, Eline P, Uitterlinden, André G, Vaidya, Bijay, Visser, Theo J, Wolffenbuttel, Bruce H R, Meulenbelt, Ingrid, Rotter, Jerome I, Spector, Tim D, Hicks, Andrew A, Toniolo, Daniela, Sanna, Serena, Peeters, Robin P, Naitza, Silvia

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Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis von Kiryluk, Krzysztof, Li, Yifu, Sanna-Cherchi, Simone, Rohanizadegan, Mersedeh, Suzuki, Hitoshi, Eitner, Frank, Snyder, Holly J, Choi, Murim, Hou, Ping, Scolari, Francesco, Izzi, Claudia, Gigante, Maddalena, Gesualdo, Loreto, Savoldi, Silvana, Amoroso, Antonio, Cusi, Daniele, Zamboli, Pasquale, Julian, Bruce A, Novak, Jan, Wyatt, Robert J, Mucha, Krzysztof, Perola, Markus, Kristiansson, Kati, Viktorin, Alexander, Magnusson, Patrik K, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Stefansson, Kari, Boland, Anne, Metzger, Marie, Thibaudin, Lise, Wanner, Christoph, Jager, Kitty J, Goto, Shin, Maixnerova, Dita, Karnib, Hussein H, Nagy, Judit, Panzer, Ulf, Xie, Jingyuan, Chen, Nan, Tesar, Vladimir, Narita, Ichiei, Berthoux, Francois, Floege, Jürgen, Stengel, Benedicte, Zhang, Hong, Lifton, Richard P, Gharavi, Ali G

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Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases von Gudbjartsson, Daniel F, Holm, Hilma, Indridason, Olafur S, Thorleifsson, Gudmar, Edvardsson, Vidar, Sulem, Patrick, de Vegt, Femmie, d'Ancona, Frank C H, den Heijer, Martin, Wetzels, Jack F M, Franzson, Leifur, Rafnar, Thorunn, Kristjansson, Kristleifur, Bjornsdottir, Unnur S, Eyjolfsson, Gudmundur I, Kiemeney, Lambertus A, Kong, Augustine, Palsson, Runolfur, Thorsteinsdottir, Unnur, Stefansson, Kari

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Genetic effects on the timing of parturition and links to fetal birth weight von Solé-Navais, Pol, Flatley, Christopher, Steinthorsdottir, Valgerdur, Vaudel, Marc, Juodakis, Julius, Chen, Jing, Laisk, Triin, LaBella, Abigail L., Westergaard, David, Bacelis, Jonas, Brumpton, Ben, Skotte, Line, Borges, Maria C., Helgeland, Øyvind, Mahajan, Anubha, Wielscher, Matthias, Lin, Frederick, Briggs, Catherine, Wang, Carol A., Moen, Gunn-Helen, Beaumont, Robin N., Bradfield, Jonathan P., Abraham, Abin, Thorleifsson, Gudmar, Gabrielsen, Maiken E., Ostrowski, Sisse R., Modzelewska, Dominika, Nohr, Ellen A., Hypponen, Elina, Srivastava, Amit, Talbot, Octavious, Allard, Catherine, Williams, Scott M., Menon, Ramkumar, Shields, Beverley M., Sveinbjornsson, Gardar, Xu, Huan, Melbye, Mads, Lowe, William, Bouchard, Luigi, Oken, Emily, Pedersen, Ole B., Gudbjartsson, Daniel F., Erikstrup, Christian, Sørensen, Erik, Lie, Rolv T., Teramo, Kari, Hallman, Mikko, Juliusdottir, Thorhildur, Hakonarson, Hakon, Ullum, Henrik, Hattersley, Andrew T., Sletner, Line, Merialdi, Mario, Rifas-Shiman, Sheryl L., Steingrimsdottir, Thora, Scholtens, Denise, Power, Christine, West, Jane, Nyegaard, Mette, Capra, John A., Skogholt, Anne H., Magnus, Per, Andreassen, Ole A., Thorsteinsdottir, Unnur, Grant, Struan F. A., Qvigstad, Elisabeth, Pennell, Craig E., Hivert, Marie-France, Hayes, Geoffrey M., Jarvelin, Marjo-Riitta, McCarthy, Mark I., Lawlor, Deborah A., Nielsen, Henriette S., Mägi, Reedik, Rokas, Antonis, Hveem, Kristian, Stefansson, Kari, Feenstra, Bjarke, Njolstad, Pål, Muglia, Louis J., Freathy, Rachel M., Johansson, Stefan, Zhang, Ge, Jacobsson, Bo

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Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1 von Winkelmann, Juliane, Czamara, Darina, Schormair, Barbara, Knauf, Franziska, Schulte, Eva C, Trenkwalder, Claudia, Dauvilliers, Yves, Polo, Olli, Högl, Birgit, Berger, Klaus, Fuhs, Andrea, Gross, Nadine, Stiasny-Kolster, Karin, Oertel, Wolfgang, Bachmann, Cornelius G, Paulus, Walter, Xiong, Lan, Montplaisir, Jacques, Rouleau, Guy A, Fietze, Ingo, Vávrová, Jana, Kemlink, David, Sonka, Karel, Nevsimalova, Sona, Lin, Siong-Chi, Wszolek, Zbigniew, Vilariño-Güell, Carles, Farrer, Matthew J, Gschliesser, Viola, Frauscher, Birgit, Falkenstetter, Tina, Poewe, Werner, Allen, Richard P, Earley, Christopher J, Ondo, William G, Le, Wei-Dong, Spieler, Derek, Kaffe, Maria, Zimprich, Alexander, Kettunen, Johannes, Perola, Markus, Silander, Kaisa, Cournu-Rebeix, Isabelle, Francavilla, Marcella, Fontenille, Claire, Fontaine, Bertrand, Vodicka, Pavel, Prokisch, Holger, Lichtner, Peter, Peppard, Paul, Faraco, Juliette, Mignot, Emmanuel, Gieger, Christian, Illig, Thomas, Wichmann, H-Erich, Müller-Myhsok, Bertram, Meitinger, Thomas

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A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architectu... von Peters, Ulrike, North, Kari E, Sethupathy, Praveen, Buyske, Steve, Haessler, Jeff, Jiao, Shuo, Fesinmeyer, Megan D, Jackson, Rebecca D, Kuller, Lew H, Rajkovic, Aleksandar, Lim, Unhee, Cheng, Iona, Schumacher, Fred, Wilkens, Lynne, Li, Rongling, Monda, Keri, Ehret, Georg, Nguyen, Khanh-Dung H, Cooper, Richard, Lewis, Cora E, Leppert, Mark, Irvin, Marguerite R, Gu, C Charles, Houston, Denise, Buzkova, Petra, Ritchie, Marylyn, Matise, Tara C, Le Marchand, Loic, Hindorff, Lucia A, Crawford, Dana C, Haiman, Christopher A, Kooperberg, Charles

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Gene Ontology Consortium: going forward

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MicroRNA-3148 modulates allelic expression of toll-like receptor 7 variant associated with systemic lupus erythematosus von Deng, Yun, Zhao, Jian, Sakurai, Daisuke, Kaufman, Kenneth M, Edberg, Jeffrey C, Kimberly, Robert P, Kamen, Diane L, Gilkeson, Gary S, Jacob, Chaim O, Scofield, R Hal, Langefeld, Carl D, Kelly, Jennifer A, Ramsey-Goldman, Rosalind, Petri, Michelle A, Reveille, John D, Vilá, Luis M, Alarcón, Graciela S, Vyse, Timothy J, Pons-Estel, Bernardo A, Freedman, Barry I, Gaffney, Patrick M, Sivils, Kathy Moser, James, Judith A, Gregersen, Peter K, Anaya, Juan-Manuel, Niewold, Timothy B, Merrill, Joan T, Criswell, Lindsey A, Stevens, Anne M, Boackle, Susan A, Cantor, Rita M, Chen, Weiling, Grossman, Jeniffer M, Hahn, Bevra H, Harley, John B, Alarcόn-Riquelme, Marta E, Brown, Elizabeth E, Tsao, Betty P

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Author Correction: Genetic effects on the timing of parturition and links to fetal birth weight von Solé-Navais, Pol, Flatley, Christopher, Steinthorsdottir, Valgerdur, Vaudel, Marc, Juodakis, Julius, Chen, Jing, Laisk, Triin, LaBella, Abigail L., Westergaard, David, Bacelis, Jonas, Brumpton, Ben, Skotte, Line, Borges, Maria C., Helgeland, Øyvind, Mahajan, Anubha, Wielscher, Matthias, Lin, Frederick, Briggs, Catherine, Wang, Carol A., Moen, Gunn-Helen, Beaumont, Robin N., Bradfield, Jonathan P., Abraham, Abin, Thorleifsson, Gudmar, Gabrielsen, Maiken E., Ostrowski, Sisse R., Modzelewska, Dominika, Nohr, Ellen A., Hypponen, Elina, Srivastava, Amit, Talbot, Octavious, Allard, Catherine, Williams, Scott M., Menon, Ramkumar, Shields, Beverley M., Sveinbjornsson, Gardar, Xu, Huan, Melbye, Mads, Lowe, William, Bouchard, Luigi, Oken, Emily, Pedersen, Ole B., Gudbjartsson, Daniel F., Erikstrup, Christian, Sørensen, Erik, Lie, Rolv T., Teramo, Kari, Hallman, Mikko, Juliusdottir, Thorhildur, Hakonarson, Hakon, Ullum, Henrik, Hattersley, Andrew T., Sletner, Line, Merialdi, Mario, Rifas-Shiman, Sheryl L., Steingrimsdottir, Thora, Scholtens, Denise, Power, Christine, West, Jane, Nyegaard, Mette, Capra, John A., Skogholt, Anne H., Magnus, Per, Andreassen, Ole A., Thorsteinsdottir, Unnur, Grant, Struan F. A., Qvigstad, Elisabeth, Pennell, Craig E., Hivert, Marie-France, Hayes, Geoffrey M., Jarvelin, Marjo-Riitta, McCarthy, Mark I., Lawlor, Deborah A., Nielsen, Henriette S., Mägi, Reedik, Rokas, Antonis, Hveem, Kristian, Stefansson, Kari, Feenstra, Bjarke, Njolstad, Pål, Muglia, Louis J., Freathy, Rachel M., Johansson, Stefan, Zhang, Ge, Jacobsson, Bo

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Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes von Prescott, Natalie J, Lehne, Benjamin, Stone, Kristina, Lee, James C, Taylor, Kirstin, Knight, Jo, Papouli, Efterpi, Mirza, Muddassar M, Simpson, Michael A, Spain, Sarah L, Lu, Grace, Fraternali, Franca, Bumpstead, Suzannah J, Gray, Emma, Amar, Ariella, Bye, Hannah, Green, Peter, Chung-Faye, Guy, Hayee, Bu'Hussain, Pollok, Richard, Satsangi, Jack, Parkes, Miles, Barrett, Jeffrey C, Mansfield, John C, Sanderson, Jeremy, Lewis, Cathryn M, Weale, Michael E, Schlitt, Thomas, Mathew, Christopher G

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Coronary heart disease-associated variation in TCF21 disrupts a miR-224 binding site and miRNA-mediated regulation von Miller, Clint L, Haas, Ulrike, Diaz, Roxanne, Leeper, Nicholas J, Kundu, Ramendra K, Patlolla, Bhagat, Assimes, Themistocles L, Kaiser, Frank J, Perisic, Ljubica, Hedin, Ulf, Maegdefessel, Lars, Schunkert, Heribert, Erdmann, Jeanette, Quertermous, Thomas, Sczakiel, Georg

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