Quality control and conduct of genome-wide association meta-analyses von Winkler, Thomas W, Day, Felix R, Croteau-Chonka, Damien C, Wood, Andrew R, Locke, Adam E, Mägi, Reedik, Ferreira, Teresa, Fall, Tove, Graff, Mariaelisa, Justice, Anne E, Luan, Jian'an, Gustafsson, Stefan, Randall, Joshua C, Vedantam, Sailaja, Workalemahu, Tsegaselassie, Kilpeläinen, Tuomas O, Scherag, André, Esko, Tonu, Kutalik, Zoltán, Heid, Iris M, Loos, Ruth J F

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Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia von Palmer, Duncan S., Howrigan, Daniel P., Chapman, Sinéad B., Adolfsson, Rolf, Bass, Nick, Blackwood, Douglas, Boks, Marco P. M., Chen, Chia-Yen, Churchhouse, Claire, Corvin, Aiden P., Craddock, Nicholas, Curtis, David, Di Florio, Arianna, Dickerson, Faith, Freimer, Nelson B., Goes, Fernando S., Jia, Xiaoming, Jones, Ian, Jones, Lisa, Jonsson, Lina, Kahn, Rene S., Landén, Mikael, Locke, Adam E., McIntosh, Andrew M., McQuillin, Andrew, Morris, Derek W., O’Donovan, Michael C., Ophoff, Roel A., Owen, Michael J., Pedersen, Nancy L., Posthuma, Danielle, Reif, Andreas, Risch, Neil, Schaefer, Catherine, Scott, Laura, Singh, Tarjinder, Smoller, Jordan W., Solomonson, Matthew, Clair, David St, Stahl, Eli A., Vreeker, Annabel, Walters, James T. R., Wang, Weiqing, Watts, Nicholas A., Yolken, Robert, Zandi, Peter P., Neale, Benjamin M.

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Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum von Ganna, Andrea, Satterstrom, F. Kyle, Zekavat, Seyedeh M., Das, Indraniel, Kurki, Mitja I., Churchhouse, Claire, Alfoldi, Jessica, Martin, Alicia R., Havulinna, Aki S., Byrnes, Andrea, Thompson, Wesley K., Nielsen, Philip R., Karczewski, Konrad J., Saarentaus, Elmo, Rivas, Manuel A., Gupta, Namrata, Pietiläinen, Olli, Emdin, Connor A., Lescai, Francesco, Bybjerg-Grauholm, Jonas, Flannick, Jason, Mercader, Josep M., Udler, Miriam, Laakso, Markku, Salomaa, Veikko, Hultman, Christina, Ripatti, Samuli, Hämäläinen, Eija, Moilanen, Jukka S., Körkkö, Jarmo, Kuismin, Outi, Nordentoft, Merete, Hougaard, David M., Mors, Ole, Werge, Thomas, Mortensen, Preben Bo, MacArthur, Daniel, Daly, Mark J., Sullivan, Patrick F., Locke, Adam E., Palotie, Aarno, Børglum, Anders D., Kathiresan, Sekar, Neale, Benjamin M.

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Population genetic differentiation of height and body mass index across Europe von Robinson, Matthew R, Hemani, Gibran, Medina-Gomez, Carolina, Mezzavilla, Massimo, Esko, Tonu, Shakhbazov, Konstantin, Powell, Joseph E, Vinkhuyzen, Anna, Berndt, Sonja I, Gustafsson, Stefan, Justice, Anne E, Kahali, Bratati, Locke, Adam E, Pers, Tune H, Vedantam, Sailaja, Wood, Andrew R, van Rheenen, Wouter, Andreassen, Ole A, Gasparini, Paolo, Metspalu, Andres, Berg, Leonard H van den, Veldink, Jan H, Rivadeneira, Fernando, Werge, Thomas M, Abecasis, Goncalo R, Boomsma, Dorret I, Chasman, Daniel I, de Geus, Eco J C, Frayling, Timothy M, Hirschhorn, Joel N, Hottenga, Jouke Jan, Ingelsson, Erik, Loos, Ruth J F, Magnusson, Patrik K E, Martin, Nicholas G, Montgomery, Grant W, North, Kari E, Pedersen, Nancy L, Spector, Timothy D, Speliotes, Elizabeth K, Goddard, Michael E, Yang, Jian, Visscher, Peter M

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Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder von Jia, Xiaoming, Goes, Fernando S., Locke, Adam E., Palmer, Duncan, Wang, Weiqing, Cohen-Woods, Sarah, Genovese, Giulio, Jackson, Anne U., Jiang, Chen, Kvale, Mark, Mullins, Niamh, Nguyen, Hoang, Pirooznia, Mehdi, Rivera, Margarita, Ruderfer, Douglas M., Shen, Ling, Thai, Khanh, Zawistowski, Matthew, Zhuang, Yongwen, Abecasis, Gonçalo, Akil, Huda, Bergen, Sarah, Burmeister, Margit, Chapman, Sinéad, DelaBastide, Melissa, Juréus, Anders, Kang, Hyun Min, Kwok, Pui-Yan, Li, Jun Z., Levy, Shawn E., Monson, Eric T., Moran, Jennifer, Sobell, Janet, Watson, Stanley, Willour, Virginia, Zöllner, Sebastian, Adolfsson, Rolf, Blackwood, Douglas, Boehnke, Michael, Breen, Gerome, Corvin, Aiden, Craddock, Nick, DiFlorio, Arianna, Hultman, Christina M., Landen, Mikael, Lewis, Cathryn, McCarroll, Steven A., Richard McCombie, W., McGuffin, Peter, McIntosh, Andrew, McQuillin, Andrew, Morris, Derek, Myers, Richard M., O’Donovan, Michael, Ophoff, Roel, Boks, Marco, Kahn, Rene, Ouwehand, Willem, Owen, Michael, Pato, Carlos, Pato, Michele, Posthuma, Danielle, Potash, James B., Reif, Andreas, Sklar, Pamela, Smoller, Jordan, Sullivan, Patrick F., Vincent, John, Walters, James, Neale, Benjamin, Purcell, Shaun, Risch, Neil, Schaefer, Catherine, Stahl, Eli A., Zandi, Peter P., Scott, Laura J.

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Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target von Roychowdhury, Tanmoy, Klarin, Derek, Levin, Michael G., Spin, Joshua M., Rhee, Yae Hyun, Deng, Alicia, Headley, Colwyn A., Tsao, Noah L., Gellatly, Corry, Zuber, Verena, Shen, Fred, Hornsby, Whitney E., Laursen, Ina Holst, Verma, Shefali S., Locke, Adam E., Einarsson, Gudmundur, Thorleifsson, Gudmar, Graham, Sarah E., Dikilitas, Ozan, Pattee, Jack W., Judy, Renae L., Pauls-Verges, Ferran, Nielsen, Jonas B., Wolford, Brooke N., Brumpton, Ben M., Dilmé, Jaume, Peypoch, Olga, Juscafresa, Laura Calsina, Edwards, Todd L., Li, Dadong, Banasik, Karina, Brunak, Søren, Jacobsen, Rikke L., Garcia-Barrio, Minerva T., Zhang, Jifeng, Rasmussen, Lars M., Lee, Regent, Handa, Ashok, Wanhainen, Anders, Mani, Kevin, Lindholt, Jes S., Obel, Lasse M., Strauss, Ewa, Oszkinis, Grzegorz, Nelson, Christopher P., Saxby, Katie L., van Herwaarden, Joost A., van der Laan, Sander W., van Setten, Jessica, Camacho, Mercedes, Davis, Frank M., Wasikowski, Rachael, Tsoi, Lam C., Gudjonsson, Johann E., Eliason, Jonathan L., Coleman, Dawn M., Henke, Peter K., Ganesh, Santhi K., Chen, Y. Eugene, Guan, Weihua, Pankow, James S., Pankratz, Nathan, Pedersen, Ole B., Erikstrup, Christian, Tang, Weihong, Hveem, Kristian, Gudbjartsson, Daniel, Gretarsdottir, Solveig, Thorsteinsdottir, Unnur, Holm, Hilma, Stefansson, Kari, Ferreira, Manuel A., Baras, Aris, Kullo, Iftikhar J., Ritchie, Marylyn D., Christensen, Alex H., Iversen, Kasper K., Eldrup, Nikolaj, Sillesen, Henrik, Ostrowski, Sisse R., Bundgaard, Henning, Ullum, Henrik, Burgess, Stephen, Gill, Dipender, Gallagher, Katherine, Sabater-Lleal, Maria, Surakka, Ida, Jones, Gregory T., Bown, Matthew J., Tsao, Philip S., Willer, Cristen J., Damrauer, Scott M.

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Gene-based meta-analysis of genome-wide association studies implicates new loci involved in obesity von Hägg, Sara, Ganna, Andrea, Van Der Laan, Sander W, Esko, Tonu, Pers, Tune H, Locke, Adam E, Berndt, Sonja I, Justice, Anne E, Kahali, Bratati, Siemelink, Marten A, Pasterkamp, Gerard, Strachan, David P, Speliotes, Elizabeth K, North, Kari E, Loos, Ruth J F, Hirschhorn, Joel N, Pawitan, Yudi, Ingelsson, Erik

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Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder von Jia, Xiaoming, Goes, Fernando S., Locke, Adam E., Palmer, Duncan, Wang, Weiqing, Cohen-Woods, Sarah, Genovese, Giulio, Jackson, Anne U., Jiang, Chen, Kvale, Mark, Mullins, Niamh, Nguyen, Hoang, Pirooznia, Mehdi, Rivera, Margarita, Ruderfer, Douglas M., Shen, Ling, Thai, Khanh, Zawistowski, Matthew, Zhuang, Yongwen, Abecasis, Gonçalo, Akil, Huda, Bergen, Sarah, Burmeister, Margit, Chapman, Sinéad, DelaBastide, Melissa, Juréus, Anders, Kang, Hyun Min, Kwok, Pui-Yan, Li, Jun Z., Levy, Shawn E., Monson, Eric T., Moran, Jennifer, Sobell, Janet, Watson, Stanley, Willour, Virginia, Zöllner, Sebastian, Adolfsson, Rolf, Blackwood, Douglas, Boehnke, Michael, Breen, Gerome, Corvin, Aiden, Craddock, Nick, DiFlorio, Arianna, Hultman, Christina M., Landen, Mikael, Lewis, Cathryn, McCarroll, Steven A., Richard McCombie, W., McGuffin, Peter, McIntosh, Andrew, McQuillin, Andrew, Morris, Derek, Myers, Richard M., O’Donovan, Michael, Ophoff, Roel, Boks, Marco, Kahn, Rene, Ouwehand, Willem, Owen, Michael, Pato, Carlos, Pato, Michele, Posthuma, Danielle, Potash, James B., Reif, Andreas, Sklar, Pamela, Smoller, Jordan, Sullivan, Patrick F., Vincent, John, Walters, James, Neale, Benjamin, Purcell, Shaun, Risch, Neil, Schaefer, Catherine, Stahl, Eli A., Zandi, Peter P., Scott, Laura J.

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Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (Jan, 10.1038/s41380-020-01006-9, 2021) von Jia, Xiaoming, Goes, Fernando S., Locke, Adam E., Palmer, Duncan, Wang, Weiqing, Cohen-Woods, Sarah, Genovese, Giulio, Jackson, Anne U., Jiang, Chen, Kvale, Mark, Mullins, Niamh, Nguyen, Hoang, Pirooznia, Mehdi, Rivera, Margarita, Ruderfer, Douglas M., Shen, Ling, Thai, Khanh, Zawistowski, Matthew, Zhuang, Yongwen, Abecasis, Goncalo, Akil, Huda, Bergen, Sarah, Burmeister, Margit, Chapman, Sinead, DelaBastide, Melissa, Jureus, Anders, Kang, Hyun Min, Kwok, Pui-Yan, Li, Jun Z., Levy, Shawn E., Monson, Eric T., Moran, Jennifer, Sobell, Janet, Watson, Stanley, Willour, Virginia, Zollner, Sebastian, Adolfsson, Rolf, Blackwood, Douglas, Boehnke, Michael, Breen, Gerome, Corvin, Aiden, Craddock, Nick, DiFlorio, Arianna, Hultman, Christina M., Landen, Mikael, Lewis, Cathryn, McCarroll, Steven A., Richard McCombie, W., McGuffin, Peter, McIntosh, Andrew, McQuillin, Andrew, Morris, Derek, Myers, Richard M., O'Donovan, Michael, Ophoff, Roel, Boks, Marco, Kahn, Rene, Ouwehand, Willem, Owen, Michael, Pato, Carlos, Pato, Michele, Posthuma, Danielle, Potash, James B., Reif, Andreas, Sklar, Pamela, Smoller, Jordan, Sullivan, Patrick F., Vincent, John, Walters, James, Neale, Benjamin, Purcell, Shaun, Risch, Neil, Schaefer, Catherine, Stahl, Eli A., Zandi, Peter P., Scott, Laura J.

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Author Correction: The power of genetic diversity in genome-wide association studies of lipids von Graham, SE, Clarke, SL, Wu, K-HH, Locke, AE, Poveda, A, Kurbasic, A, Forer, L, Scholz, M, Verweij, N, Delgado, GE, Leonard, HL, Arendt, M, Smyth, LJ, Hutri-Kahonen, N, Timmers, PRHJ, Lores-Motta, L, Long, J, Ekoru, K, Bollepalli, S, Verma, A, Chen, S, Gorski, M, Smith, JA, Chitrala, KN, Lin, S-Y, Couture, C, Lyytikainen, L-P, Zhu, X, Ichihara, S, Kovacs, P, Giardoglou, T, Helgadottir, A, De Kleijn, D, Gudbjartsson, DF, Bouchard, C, Holm, H, Heid, IM, Stark, KJ, Voelzke, H, Pasterkamp, G, Schmidt, R, Schmidt, H, Chen, YE, Kato, N, Mamakou, V, Kaprio, J, Wu, J-Y, Den Hollander, AI, Bharadwaj, D, Lind, L, Golightly, YM, Wilson, JF, Attia, J, Walker, M, Koistinen, HA, Mercader, JM, Orozco, L, Fornage, M, McKnight, AJ, Qu, J, Van der Harst, P, Loos, RJF, Brandslund, I, Rosenthal, EA, Linneberg, A, Jarvelin, M-R, Mook-Kanamori, DO, Watkins, H, Dantoft, TM, Karpe, F, Khor, CC, Pendergrass, SA, Cupples, LA, Gordon-Larsen, P, Chambers, JC, North, KE, Daviglus, M, Wei, W-Q, Okada, Y, Tsao, PS, Lin, K, Chang, K-M, Cho, K, O'Donnell, CJ, Van Heel, DA, Millwood, IY, Kim, B-J, Mohlke, KL, Kathiresan, S, Boehnke, M, Huang, H, Schmidt, EM, Gustafsson, S, Zhao, J-H, Yoon, K, Hottenga, JJ, Karhus, LL, Goel, A, Sabater-Lleal, M, McDaid, AF

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Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis von Kanoni, S, Locke, AE, Zajac, GJM, Wu, K-HH, Helgadottir, A, Han, S, Kanai, M, Zhou, W, Takayama, J, Martin, HC, Haessler, J, Giulianini, F, Miller, JE, Weir, DR, Graf, M, Sengupta, D, Mahajan, A, Zhang, W, Jang, H-M, Hottenga, JJ, Wood, AR, Karhus, LL, Mauro, P, Forer, L, Brody, JA, Benjamins, JW, Engmann, J, Kleber, ME, Huo, S, Ikeda, DD, Frank, M, Nakatochi, M, Hutri-Kahonen, N, Oldmeadow, C, Takeuchi, F, Wang, YX, Wei, WB, Nutile, T, Nardone, GG, Meidtner, K, Hebbar, P, Farmaki, A-E, Concas, MP, Rayner, NW, Wang, J-S, Hidalgo, B, Giannakopoulou, O, Terzikhan, N, Jackson, RD, Reiner, AP, Martin, LW, Chen, Z, Li, L, De Borst, GJ, Hansen, T, Mitchell, P, Lieb, W, Mellstrom, D, Rhee, SY, Evans, MK, Hoefer, IE, Redline, S, Schulze, MB, Girotto, G, De Jager, PL, Jonas, JB, Pajukanta, P, Wickremasinghe, AR, Hollander, AI, Hunt, SC, Fornage, M, McKnight, AJ, Jin, Z-B, Hishigaki, H, Elders, PJM, Kivimaki, M, Parra, EJ, Grant, SFA, De Graaf, J, Loefer, M, Mannikko, M, Grarup, N, Rotter, J, Peters, A, Gieger, C, Huang, W, Wareham, NJ, Langenberg, C, Abecasis, G, Kooner, JS, Kraft, P, Walters, RG, Yamamoto, M, Van Heel, DA, Kamatani, Y, Kim, B-J, Tsao, PS, Chang, K-M, Kathiresan, S, Peloso, GM

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Exome Sequencing of Familial Bipolar Disorder von Goes, Fernando S, Pirooznia, Mehdi, Parla, Jennifer S, Kramer, Melissa, Ghiban, Elena, Mavruk, Senem, Chen, Yun-Ching, Monson, Eric T, Willour, Virginia L, Karchin, Rachel, Flickinger, Matthew, Locke, Adam E, Levy, Shawn E, Scott, Laura J, Boehnke, Michael, Stahl, Eli, Moran, Jennifer L, Hultman, Christina M, Landén, Mikael, Purcell, Shaun M, Sklar, Pamela, Zandi, Peter P, McCombie, W. Richard, Potash, James B

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Exome sequencing of Finnish isolates enhances rare-variant association power von Locke, AE, Steinberg, KM, Chiang, CWK, Service, SK, Havulinna, AS, Stell, L, Pirinen, M, Abel, HJ, Chiang, CC, Fulton, RS, Jackson, AU, Kang, CJ, Kanchi, KL, Koboldt, DC, Larson, DE, Nelson, J, Nicholas, TJ, Pietila, A, Ramensky, V, Ray, D, Scott, LJ, Stringham, HM, Vangipurapu, J, Welch, R, Yajnik, P, Yin, X, Eriksson, JG, Ala-Korpela, M, Jarvelin, M-R, Mannikko, M, Laivuori, H, Dutcher, SK, Stitziel, NO, Wilson, RK, Hall, IM, Sabatti, C, Palotie, A, Salomaa, V, Laakso, M, Ripatti, S, Boehnke, M, Freimer, NB

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Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution von Karaderi, T, Highland, HM, Lu, Y, Fine, RS, Schurmann, C, Lempradl, A, Winkler, TW, Locke, AE, Medina-Gomez, C, Giri, A, Lo, KS, Alfred, T, Manning, AK, Sivapalaratnam, S, Amouyel, P, Balkau, B, Blüher, M, Brandslund, I, Burt, AA, Cesana, G, Christensen, C, Cook, JP, Danesh, J, Denus, SD, Mutsert, RD, Dedoussis, G, Demerath, EW, Angelantonio, ED, Drenos, F, Farmaki, A-E, Florez, JC, Fornage, M, Gan, W, Gasparini, P, Giedraitis, V, Girotto, G, Gorski, M, Grallert, H, Grove, ML, Haessler, J, Hansen, T, Hattersley, AT, Holmen, OL, Howson, JMM, Hveem, K, Jackson, AU, Jia, Y, Kardia, SLR, Karpe, F, Kooner, JS, Kuusisto, J, Laakso, M, Langenberg, C, Lee, NR, Lewis, CE, Li, J, Li-Gao, R, Lind, L, Liu, C-T, Lyytikäinen, L-P, Marenne, G, Masca, NGD, McCarthy, MI, Morris, AP, Müller-Nurasyid, M, Nelson, CP, Pennell, CE, Rasheed, A, Reilly, DF, Robino, A, Ruth, KS, Salomaa, V, Schreiner, PJ, Schulze, MB, Southam, L, Stirrups, KE, Sun, L, Surendran, P, Taylor, KD, Thompson, DJ, Thorleifsson, G, Tsafantakis, E, Vanhala, M, Vuckovic, D, Wagenknecht, LE, Wallentin, L, Wood, AR, Young, R, Zhao, W, Zheng, H, Zhou, W, CHD Exome+ Consortium, Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, ExomeBP Consortium, Frayling, TM, Lettre, G, Hirschhorn, JN, Cupples, LA, North, KE, Lindgren, CM

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Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity von Lu, Y, Highland, HM, Schurmann, C, Esko, T, Graff, M, Mahajan, A, Marouli, E, Sivapalaratnam, S, Feitosa, MF, Reiner, AP, Willems, SM, Allison, M, Auer, PL, Benn, M, Bottinger, EP, Bowden, DW, Caulfield, MJ, Chu, AY, Collins, FS, Crosslin, DS, Demerath, EW, Denny, JC, Farmaki, A-E, Faul, JD, Ferrieres, J, Florez, JC, Ford, I, Fornage, M, Friedrich, N, Gandin, I, Gordon-Larsen, P, Gorski, M, Grove, ML, Haessler, J, Hayward, C, Helgeland, O, Hovingh, GK, Jackson, AU, Jia, Y, Kahali, B, Kahn, RS, Kardia, SLR, Karpe, F, Kathiresan, S, Kiemeney, LA, Kim, E, Komulainen, P, Kuulasmaa, K, Kuusisto, J, Lange, EM, Lewis, CE, Lin, K-H, Lophatananon, A, Lotery, AJ, Luan, J, Meidtner, K, Mohlke, KL, Moitry, M, Moore, C, Mueller-Nurasyid, M, Narisu, N, Neville, M, Nikus, K, Nordestgaard, BG, Loohuis, LMO, Packard, CJ, Perry, JA, Peters, A, Petersen, ERB, Raitakari, OT, Rauramaa, R, Rheinberger, M, Rivas, MA, Robertson, NR, Saleheen, D, Sapkota, Y, Sheu, WH-H, Small, KS, Spector, TD, Starr, JM, Strauch, K, Stumvoll, M, Swift, AJ, Thorleifsson, G, Tuomilehto, J, Duijn, CM, Veronesi, G, Vuckovic, D, Wallentin, L, Wang, F, Wang, CA, Wareham, NJ, White, HD, Young, R, Zhan, X, Zhang, W, Zhao, JH, Zondervan, KT, North, KE, Lindgren, CM

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Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps von Mahajan, A, Taliun, D, Thurner, M, Robertson, NR, Torres, JM, Payne, AJ, Steinthorsdottir, V, Scott, RA, Grarup, N, Cook, JP, Wuttke, M, Sarnowski, C, Magill, R, Nano, J, Gieger, C, Trompet, S, Prins, BP, Guo, X, Bielak, LF, Below, JE, Bowden, DW, Chambers, JC, Kim, YJ, Ng, MCY, Petty, LE, Sim, X, Zhang, W, Brummett, CM, Kardt, K-UE, Kardia, SLR, Kronenberg, F, Lall, K, Liu, C-T, Locke, AE, Luan, J, Ntalla, L, Schoenherr, S, Schurmann, C, Yengo, L, Bottinger, EP, Brandslund, I, Christensen, C, Dedoussis, G, Florez, JC, Ford, I, France, OH, Frayling, TM, Giedraitis, V, Hackinger, S, Hattersley, AT, Herder, C, Jorgensen, ME, Jorgensen, T, Kriebel, J, Kuusisto, J, Ligthart, S, Linneberg, A, Mamakou, V, Meitinger, T, Mohlke, KL, Morris, AD, Nadkarni, G, Pankow, JS, Sattar, N, Stancakova, A, Strauch, K, Taylor, KD, Thorand, B, Thorleifsson, G, Tuomilehto, J, Witte, DR, Dupuis, J, Peyser, PA, Zeggini, E, Loos, RJF, Froguel, P, Ingelsson, E, Lind, L, Groop, L, Laakso, M, Collins, FS, Jukema, JW, Palmer, CNA, Grallert, H, Metspalu, A, Dehghan, A, Koettgen, A, Abecasis, GR, Meigs, JB, Rotter, J, Marchini, J, Pedersen, O, Hansen, T, Langenberg, C, Wareham, NJ, Stefansson, K, Gloyn, AL, Morris, AP, Boehnke, M, McCarthy, M

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A Low-Frequency Inactivating Akt2 Variant Enriched in the Finnish Population is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk von Fontanillas, P, Rivas, MA, Locke, AE, Isomaa, B, Meitinger, T, Deloukas, P, Stirrups, KE, Owen, KR, Frayling, TM, Levy, JC, Hodgkiss, D, Hattersley, AT, Kuulasmaa, T, Puppala, S, Teslovich, TM, Donnelly, PJ, Ebrahim, SB, Kumar, S, Jia, W, Ma, RC, Sandhu, M, Scott, J, Sladek, R, Tandon, N, Zeggini, E, Watanabe, RM, Koistinen, HA, Collins, FS, Karpe, F, Hansen, T, Kuusisto, J, Hale, DE, Duggirala, R, Hanis, CL, Mohlke, KL, Boehnke, M, Hartl, C, Gloyn, AL, Kumar, A, Ladenvall, C, Scott, LJ, Jula, A, Palotie, A, Jacobs, SB, Wessel, J, Buck, G, Buck, D, Gjesing, AP, Jackson, AU, Jun, G, Justesen, JM, Neville, M, Onofrio, R, Small, KS, Stringham, HM, Trakalo, J, Carneiro, MO, DePristo, M, Grant, G, Poplin, R, Purcell, S, Palmer, ND, Lakka, TA, Langenberg, C, Franks, PW, Ng, MC, Rolandsson, O, Bowden, DW, Mägi, R, Metspalu, A, Narisu, N, Kinnunen, L, Bonnycastle, LL, Pasko, D, Wood, AR, Fadista, J, Pollin, TI, Atzmon, G, Müller-Nurasyid, M, Wu, Y, Illig, T, Meisinger, C, Musani, SK, Taylor, HA, Correa, A, Oksa, H, Scott, WR, Afzal, U, Kooner, JS, Fuchsberger, C, Lee, JY, Huang, J, Melander, O, Below, JE, Lim, WY, Cheng, CY, Chan, E, Tai, ES, Gaulton, KJ, Linneberg, A

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Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms von Horikoshi, M, Pasquali, L, Wiltshire, S, Huyghe, JR, Mahajan, A, Asimit, JL, Ferreira, T, Locke, AE, Robertson, NR, Wang, X, Sim, X, Fujita, H, Hara, K, Young, R, Zhang, W, Choi, S, Chen, H, Kaur, I, Takeuchi, F, Fontanillas, P, Thuillier, D, Yengo, L, Below, JE, Tam, CH, Wu, Y, Abecasis, G, Altshuler, D, Bell, GI, Blangero, J, Burtt, NP, Duggirala, R, Florez, JC, Hanis, CL, Seielstad, M, Atzmon, G, Chan, JC, Ma, RC, Froguel, P, Wilson, JG, Bharadwaj, D, Dupuis, J, Meigs, JB, Cho, YS, Park, T, Kooner, JS, Chambers, JC, Saleheen, D, Kadowaki, T, Tai, ES, Mohlke, KL, Cox, NJ, Ferrer, J, Zeggini, E, Kato, N, Teo, YY, Boehnke, M, McCarthy, MI, Morris, AP

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The genetic architecture of type 2 diabetes von Mihailov, E, Blancher, C, Carneiro, MO, Poplin, R, Hrabé de Angelis, M, Deloukas, P, Onofrio, R, Thorand, B, Hansen, T, Tam, CH, Dupuis, J, Liang, L, O'Rahilly, SP, Watanabe, RM, Bottinger, EP, Cho, YS, Lindgren, CM, Elliott, P, Jablonski, KA, Arya, R, Ma, RC, Hartl, C, Teo, YY, Zeggini, E, DeFronzo, RA, Jackson, AU, Chan, E, Banks, E, Gieger, C, Ingelsson, E, Buck, G, Trakalo, J, Buck, D, Mägi, R, Owen, KR, Morris, AD, Bowden, DW, Atzmon, G, Laakso, M, Duggirala, R, McVean, G, Hanis, CL, Gabriel, S, Meitinger, T, Groop, L, Florez, JC, Altshuler, D, McCarthy, MI, Grarup, N, Stringham, HM, Gamazon, ER, Lee, J, Chen, Y, Below, JE, Huang, J, Pasko, D, Varga, TV, Green, T, Day-Williams, AG, Farook, VS, Fingerlin, T, Hu, C, Kim, BJ, Fowler, SP, Lin, KH, Barzilai, N, Kuusisto, J, Palmer, ND, Balkau, B, Abboud, HE, Griswold, M, Giedraitis, V, Smith, JD, Hale, DE, Lu, Y, Kwak, SH, Kumar, S, Thuillier, D, Musani, SK, Scott, WR, Blackwell, TW, Wong, TY, Bork-Jensen, J, Koistinen, HA, Rayner, NW, Kinnunen, L, Hodgkiss, D, Lyssenko, V, Hollensted, M, Cingolani, P, Jørgensen, T, Ladenvall, C, Justesen, JM, Kriebel, J, Lannfelt, L, Lauritzen, T, Linneberg, A, Locke, AE, Swift, A, Stirrups, K

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Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus von Mahajan, A, Sim, X, Ng, HJ, Manning, A, Rivas, MA, Highland, HM, Locke, AE, Grarup, N, Im, HK, Cingolani, P, Flannick, J, Fontanillas, P, Fuchsberger, C, Gaulton, KJ, Teslovich, TM, Rayner, NW, Robertson, NR, Beer, NL, Rundle, JK, Bork-Jensen, J, Ladenvall, C, Blancher, C, Buck, D, Buck, G, Burtt, NP, Gabriel, S, Gjesing, AP, Groves, CJ, Hollensted, M, Huyghe, JR, Jackson, AU, Jun, G, Justesen, JM, Mangino, M, Murphy, J, Neville, M, Onofrio, R, Small, KS, Stringham, HM, Syvanen, A-C, Trakalo, J, Abecasis, G, Bell, GI, Blangero, J, Cox, NJ, Duggirala, R, Hanis, CL, Seielstad, M, Wilson, JG, Christensen, C, Brandslund, I, Rauramaa, R, Surdulescu, GL, Doney, ASF, Lannfelt, L, Linneberg, A, Isomaa, B, Tuomi, T, Jorgensen, ME, Jorgensen, T, Kuusisto, J, Uusitupa, M, Salomaa, V, Spector, TD, Morris, AD, Palmer, CNA, Collins, FS, Mohlke, KL, Bergman, RN, Ingelsson, E, Lind, L, Tuomilehto, J, Hansen, T, Watanabe, RM, Prokopenko, I, Dupuis, J, Karpe, F, Groop, L, Laakso, M, Pedersen, O, Florez, JC, Morris, AP, Altshuler, D, Meigs, JB, Boehnke, M, McCarthy, MI, Lindgren, CM, Gloyn, AL

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