The genomic psychiatry cohort: Partners in discovery by Pato, Michele T., Sobell, Janet L., Medeiros, Helena, Abbott, Colony, Sklar, Brooke M., Buckley, Peter F., Bromet, Evelyn J., Escamilla, Michael A., Fanous, Ayman H., Lehrer, Douglas S., Macciardi, Fabio, Malaspina, Dolores, McCarroll, Steve A., Marder, Stephen R., Moran, Jennifer, Morley, Christopher P., Nicolini, Humberto, Perkins, Diana O., Purcell, Shaun M., Rapaport, Mark H., Sklar, Pamela, Smoller, Jordan W., Knowles, James A., Pato, Carlos N.

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Characterization of bipolar disorder patient-specific induced pluripotent stem cells from a family reveals neurodevelopmental and mRNA expression abnormalities by Madison, J M, Zhou, F, Nigam, A, Hussain, A, Barker, D D, Nehme, R, van der Ven, K, Hsu, J, Wolf, P, Fleishman, M, O'Dushlaine, C, Rose, S, Chambert, K, Lau, F H, Ahfeldt, T, Rueckert, E H, Sheridan, S D, Fass, D M, Nemesh, J, Mullen, T E, Daheron, L, McCarroll, S, Sklar, P, Perlis, R H, Haggarty, S J

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Variation and taphonomic implications of composition in modern and fossil malacostracan cuticles (Decapoda: Malacostraca) by Plotnick, Roy E, McCarroll, Steve

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41. CHARACTERIZING FUNCTIONAL CONVERGENCE OF COMMON POLYGENIC VARIATION IN NEUROPSYCHIATRIC DISORDER RISK GENES by Kuo, Susan, Weiner, Daniel, Ling, Emi, Fu, Jack, Satterstrom, F. Kyle, Talkowski, Michael, McCarroll, Steve, Robinson, Elise

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The Lin28/let-7 Axis Regulates Glucose Metabolism by Zhu, Hao, Shyh-Chang, Ng, Segrè, Ayellet V., Shinoda, Gen, Shah, Samar P., Einhorn, William S., Takeuchi, Ayumu, Engreitz, Jesse M., Hagan, John P., Kharas, Michael G., Urbach, Achia, Thornton, James E., Triboulet, Robinson, Gregory, Richard I., Altshuler, David, Daley, George Q.

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Role of complement C4A in developmental synaptic pruning by Presumey, Jessy, Bialas, Allison, Stevens, Beth, McCarroll, Steve, Carroll, Michael

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Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors by Andreassen, Ole A., Djurovic, Srdjan, Thompson, Wesley K., Schork, Andrew J., Kendler, Kenneth S., O’Donovan, Michael C., Rujescu, Dan, Werge, Thomas, van de Bunt, Martijn, Morris, Andrew P., McCarthy, Mark I., Roddey, J. Cooper, McEvoy, Linda K., Desikan, Rahul S., Dale, Anders M.

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T30. LEVERAGING WHOLE GENOME SEQUENCING OF FAMILIES TO DISCOVER RARE VARIANTS ASSOCIATED WITH BIPOLAR DISORDER by Kazemi, Hamed, Drake, John, Bigdeli, Tim, Bacanu, Silviu, Benke, Kelly, Maher, Brion, Pato, Michele, Knowles, James, McCarroll, Steve, Carvalho, Celia, Medeiros, Helena, Ferreira, Rute, Vladimirov, Vladimir, Fanous, Ayman

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30. IDENTIFICATION OF HUB GENES INVOLVED IN EARLY-ONSET SCHIZOPHRENIA USING GENETICALLY PREDICTED REGULATED GENE-EXPRESSION RISK SCORE FOR SCHIZOPHRENIA by Jen, Yawen, Yu, Sung-Liang, Hsiao, Po-Chang, Liu, Chih-Min, Liu, Chen-Chung, Hwang, Tzung-Jeng, Hsieh, Ming H., Huang, Hailiang, Chandler, Sharon D., Faraone, Stephen, Neale, Benjamin, McCarroll, Steve, Tsuang, Ming T., Hwu, Hai-Gwo, Chen, Wei J.

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A genome-wide association search for type 2 diabetes genes in African Americans by Palmer, Nicholette D, McDonough, Caitrin W, Hicks, Pamela J, Roh, Bong H, Wing, Maria R, An, S Sandy, Hester, Jessica M, Cooke, Jessica N, Bostrom, Meredith A, Rudock, Megan E, Talbert, Matthew E, Lewis, Joshua P, Ferrara, Assiamira, Lu, Lingyi, Ziegler, Julie T, Sale, Michele M, Divers, Jasmin, Shriner, Daniel, Adeyemo, Adebowale, Rotimi, Charles N, Ng, Maggie C Y, Langefeld, Carl D, Freedman, Barry I, Bowden, Donald W, Voight, Benjamin F, Scott, Laura J, Steinthorsdottir, Valgerdur, Morris, Andrew P, Dina, Christian, Welch, Ryan P, Zeggini, Eleftheria, Huth, Cornelia, Aulchenko, Yurii S, Thorleifsson, Gudmar, McCulloch, Laura J, Ferreira, Teresa, Grallert, Harald, Amin, Najaf, Wu, Guanming, Willer, Cristen J, Raychaudhuri, Soumya, McCarroll, Steve A, Langenberg, Claudia, Hofmann, Oliver M, Dupuis, Josée, Qi, Lu, Segrè, Ayellet V, van Hoek, Mandy, Navarro, Pau, Ardlie, Kristin, Balkau, Beverley, Benediktsson, Rafn, Bennett, Amanda J, Blagieva, Roza, Boerwinkle, Eric, Bonnycastle, Lori L, Boström, Kristina Bengtsson, Bravenboer, Bert, Bumpstead, Suzannah, Burtt, Noël P, Charpentier, Guillaume, Chines, Peter S, Cornelis, Marilyn, Couper, David J, Crawford, Gabe, Doney, Alex S F, Elliott, Katherine S, Elliott, Amanda L, Erdos, Michael R, Fox, Caroline S, Franklin, Christopher S, Ganser, Martha, Gieger, Christian, Grarup, Niels, Green, Todd, Griffin, Simon, Groves, Christopher J, Guiducci, Candace, Hadjadj, Samy, Hassanali, Neelam, Herder, Christian, Isomaa, Bo, Jackson, Anne U, Johnson, Paul R V, Jørgensen, Torben, Kao, Wen H L, Klopp, Norman, Kong, Augustine, Kraft, Peter, Kuusisto, Johanna, Lauritzen, Torsten, Li, Man, Lieverse, Aloysius, Lindgren, Cecilia M, Lyssenko, Valeriya, Marre, Michel, Meitinger, Thomas, Midthjell, Kristian, Morken, Mario A, Narisu, Narisu

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Parental origin of sequence variants associated with complex diseases by Gudjonsson, Sigurjon A, Sigurdsson, Helgi, Kristinsson, Kari Th, Sigurdsson, Asgeir, Hreidarsson, Astradur B, Masson, Gisli, Ferguson-Smith, Anne C, Frigge, Michael L, Jonsson, Thorvaldur, Stacey, Simon N, Olafsson, Jon H, Benediktsdottir, Kristrun R, Gudbjartsson, Daniel F, Besenbacher, Soren, Gylfason, Arnaldur, Sigurgeirsson, Bardur, Olason, Pall I, Sverrisson, Sverrir, Stefansson, Kari, Johannsson, Oskar Th, Thorsteinsdottir, Unnur, Benediktsson, Rafn, Thorleifsson, Gudmar, Kong, Augustine, Steinthorsdottir, Valgerdur, Sulem, Patrick, Jonasdottir, Aslaug, Jonasdottir, Adalbjorg, Sigurdsson, Gunnar

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Genome-wide association study identifies three novel loci for type 2 diabetes by Hara, Kazuo, Fujita, Hayato, Johnson, Todd A, Yamauchi, Toshimasa, Yasuda, Kazuki, Horikoshi, Momoko, Peng, Chen, Hu, Cheng, Ma, Ronald C W, Imamura, Minako, Iwata, Minoru, Tsunoda, Tatsuhiko, Morizono, Takashi, Shojima, Nobuhiro, So, Wing Yee, Leung, Ting Fan, Kwan, Patrick, Zhang, Rong, Wang, Jie, Yu, Weihui, Maegawa, Hiroshi, Hirose, Hiroshi, Kaku, Kohei, Ito, Chikako, Watada, Hirotaka, Tanaka, Yasushi, Tobe, Kazuyuki, Kashiwagi, Atsunori, Kawamori, Ryuzo, Jia, Weiping, Chan, Juliana C N, Teo, Yik Ying, Shyong, Tai E, Kamatani, Naoyuki, Kubo, Michiaki, Maeda, Shiro, Kadowaki, Takashi

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38. COMMON AND RARE GENETIC RISK FACTORS FOR SCHIZOPHRENIA AT CHROMOSOME 22Q INDUCE CONVERGENT, DISPERSED CHANGES IN GENE EXPRESSION by Nadig, Ajay, Tegtmeyer, Matthew, Weiner, Daniel J., Ling, Emi, Gordon, Aaron, O'Connor, Luke J., Aryee, Martin J., Bearden, Carrie E., Geschwind, Daniel, McCarroll, Steve A., Nehme, Ralda, Robinson, Elise B.

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STATISTICAL AND FUNCTIONAL CONVERGENCE OF COMMON AND RARE VARIANT RISK FOR AUTISM SPECTRUM DISORDERS AT CHROMOSOME 16P by Weiner, Daniel, Ling, Emi, Erdin, Serkan, Tai, Derek, Yadav, Rachita, Grove, Jakob, Fu, Jack, Nadig, Ajay, Sebat, Jonathan, O'Connor, Luke, Hougaard, David, Børglum, Anders, Talkowski, Michael, McCarroll, Steve, Robinson, Elise

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A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder by Duan, Jubao, Shi, Jianxin, Fiorentino, Alessia, Leites, Catherine, Chen, Xiangning, Moy, Winton, Chen, Jingchun, Alexandrov, Boian S., Usheva, Anny, He, Deli, Freda, Jessica, O’Brien, Niamh L., Gejman, Pablo V., Sanders, Alan R., Duan, Jubao, Levinson, Douglas F., Shi, Jianxin, Buccola, Nancy G., Mowry, Bryan J., Freedman, Robert, Olincy, Ann, Amin, Farooq, Black, Donald W., Silverman, Jeremy M., Byerley, William F., Svrakic, Dragan M., Cloninger, C. Robert, Pato, Michele T., Sobell, Janet L., Medeiros, Helena, Abbott, Colony, Skar, Brooke, Buckley, Peter F., Bromet, Evelyn J., Escamilla, Michael A., Fanous, Ayman H., Lehrer, Douglas S., Macciardi, Fabio, Malaspina, Dolores, McCarroll, Steve A., Marder, Stephen R., Moran, Jennifer, Morley, Christopher P., Nicolini, Humberto, Perkins, Diana O., Purcell, Shaun M., Rapaport, Mark H., Sklar, Pamela, Smoller, Jordan W., Knowles, James A., Pato, Carlos N., McQuillin, Andrew, Sanders, Alan R., Gershon, Elliot S., DeLisi, Lynn E., Bishop, Alan R., Gurling, Hugh M.D., Pato, Michele T., Levinson, Douglas F., Kendler, Kenneth S., Pato, Carlos N., Gejman, Pablo V.

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Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations by Demirkan, Ayşe, van Duijn, Cornelia M, Ugocsai, Peter, Isaacs, Aaron, Pramstaller, Peter P, Liebisch, Gerhard, Wilson, James F, Johansson, Åsa, Rudan, Igor, Aulchenko, Yurii S, Kirichenko, Anatoly V, Janssens, A Cecile J W, Jansen, Ritsert C, Gnewuch, Carsten, Domingues, Francisco S, Pattaro, Cristian, Wild, Sarah H, Jonasson, Inger, Polasek, Ozren, Zorkoltseva, Irina V, Hofman, Albert, Karssen, Lennart C, Struchalin, Maksim, Floyd, James, Igl, Wilmar, Biloglav, Zrinka, Broer, Linda, Pfeufer, Arne, Pichler, Irene, Campbell, Susan, Zaboli, Ghazal, Kolcic, Ivana, Rivadeneira, Fernando, Huffman, Jennifer, Hastie, Nicholas D, Uitterlinden, Andre, Franke, Lude, Franklin, Christopher S, Vitart, Veronique, Nelson, Christopher P, Preuss, Michael, Bis, Joshua C, O'Donnell, Christopher J, Franceschini, Nora, Witteman, Jacqueline C M, Axenovich, Tatiana, Oostra, Ben A, Meitinger, Thomas, Hicks, Andrew A, Hayward, Caroline, Wright, Alan F, Gyllensten, Ulf, Campbell, Harry, Schmitz, Gerd

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Clonal hematopoiesis and risk of chronic liver disease by Wong, Waihay J., Emdin, Connor, Bick, Alexander G., Zekavat, Seyedeh M., Niroula, Abhishek, Pirruccello, James P., Dichtel, Laura, Griffin, Gabriel, Uddin, Md Mesbah, Gibson, Christopher J., Kovalcik, Veronica, Lin, Amy E., McConkey, Marie E, Vromman, Amelie, Sellar, Rob S., Kim, Peter G., Agrawal, Mridul, Weinstock, Joshua, Long, Michelle T., Yu, Bing, Banerjee, Rajarshi, Nicholls, Rowan C., Dennis, Andrea, Kelly, Matt, Loh, Po-Ru, McCarroll, Steve, Boerwinkle, Eric, Vasan, Ramachandran S., Jaiswal, Siddhartha, Johnson, Andrew D., Chung, Raymond T., Corey, Kathleen, Levy, Daniel, Ballantyne, Christie, Ebert, Benjain L., Natarajan, Pradeep

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Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes by Albrechtsen, A., Grarup, N., Li, Y., Sparsø, T., Cao, H., Jiang, T., Kim, S. Y., Korneliussen, T., Li, Q., Nie, C., Wu, R., Morris, A. P., Ladenvall, C., Cauchi, S., Stančáková, A., Andersen, G., Astrup, A., Banasik, K., Bennett, A. J., Bolund, L., Charpentier, G., Chen, Y., Dekker, J. M., Doney, A. S. F., Dorkhan, M., Forsen, T., Frayling, T. M., Gui, Y., Hallmans, G., Hattersley, A. T., He, K., Hitman, G. A., Holmkvist, J., Huang, S., Jiang, H., Jin, X., Justesen, J. M., Kristiansen, K., Kuusisto, J., Lajer, M., Lantieri, O., Li, W., Liao, Q., Liu, X., Ma, T., Ma, X., Marre, M., Mokrosiński, J., Morris, A. D., Mu, B., Nielsen, A. A., Nijpels, G., Nilsson, P., Palmer, C. N. A., Rayner, N. W., Renström, F., Ribel-Madsen, R., Robertson, N., Rolandsson, O., Rossing, P., Schwartz, T. W., Slagboom, P. E., Sterner, M., Tang, M., Tarnow, L., Tuomi, T., van’t Riet, E., van Leeuwen, N., Varga, T. V., Vestmar, M. A., Walker, M., Wang, B., Wang, Y., Wu, H., Xi, F., Yengo, L., Yu, C., Zhang, J., Zhang, Q., Zhang, W., Zheng, H., Zhou, Y., Altshuler, D., ‘t Hart, L. M., Franks, P. W., Balkau, B., Froguel, P., McCarthy, M. I., Laakso, M., Groop, L., Christensen, C., Brandslund, I., Lauritzen, T., Witte, D. R., Linneberg, A., Jørgensen, T., Hansen, T., Wang, J., Nielsen, R., Pedersen, O.

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Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms by Dankel, Simon N., Klocke, Bernward, Grallert, Harald, Glunk, Viktoria, Lee, Heekyoung, Ehlers, Kerstin, Wahl, Simone, Hoffmann, Christoph, Qian, Kun, Riess, Helene, Schroeder, Timm, Horsthemke, Bernhard, Voight, Benjamin F., Welch, Ryan P., Zeggini, Eleftheria, Huth, Cornelia, Aulchenko, Yurii S., McCulloch, Laura J., Ferreira, Teresa, Amin, Najaf, McCarroll, Steve A., Qi, Lu, Navarro, Pau, Ardlie, Kristin, Benediktsson, Rafn, Bennett, Amanda J., Boström, Kristina Bengtsson, Burtt, Noël P., Charpentier, Guillaume, Crawford, Gabe, Erdos, Michael R., Fox, Caroline S., Franklin, Christopher S., Gieger, Christian, Grarup, Niels, Griffin, Simon, Groves, Christopher J., Hadjadj, Samy, Johnson, Paul R.V., Klopp, Norman, Kong, Augustine, Kraft, Peter, Lauritzen, Torsten, Li, Man, Lyssenko, Valeriya, Marre, Michel, Morken, Mario A., Narisu, Narisu, Nilsson, Peter, Owen, Katharine R., Payne, Felicity, Perry, John R.B., Petersen, Ann-Kristin, Shields, Beverley M., Shrader, Peter, Sigurdsson, Gunnar, Strassburger, Klaus, Stringham, Heather M., Sun, Qi, Tichet, Jean, van Dam, Rob M., van Haeften, Timon W., van Herpt, Thijs, van Vliet-Ostaptchouk, Jana V., Weedon, Michael N., Wijmenga, Cisca, Bergman, Richard N., Cauchi, Stephane, Collins, Francis S., Gyllensten, Ulf, Hansen, Torben, Hitman, Graham A., Hofman, Albert, Laakso, Markku, Rudan, Igor, Stein, Lincoln D., Tuomilehto, Jaakko, Uitterlinden, Andre, Walker, Mark, Wareham, Nicholas J., Daly, Mark J., Hu, Frank B., Pankow, James S., Pedersen, Oluf, Florez, Jose C., Frayling, Timothy M., Groop, Leif, Wilson, James F., Illig, Thomas, van Duijn, Cornelia M., Stefansson, Kari, Boehnke, Michael, Spieler, Derek, Klingenspor, Martin, Dahlman, Ingrid, Hauck, Stefanie M., Blüher, Matthias, Hsu, Yi-Hsiang, Mellgren, Gunnar, Hauner, Hans

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A single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations by IMAMURA, Minako, MAEDA, Shiro, TSUNODA, Tatsuhiko, KUBO, Michiaki, WATADA, Hirotaka, MAEGAWA, Hiroshi, OKADA-IWABU, Miki, IWABU, Masato, SHOJIMA, Nobuhiro, OHSHIGE, Toshihiko, OMORI, Shintaro, IWATA, Minoru, YAMAUCHI, Toshimasa, HIROSE, Hiroshi, KAKU, Kohei, ITO, Chikako, TANAKA, Yasushi, TOBE, Kazuyuki, KASHIWAGI, Atsunori, KAWAMORI, Ryuzo, KASUGA, Masato, KAMATANI, Naoyuki, GENETICS REPLICATION, Diabetes, HARA, Kazuo, CONSORTIUM, Meta-Analysis (diagram), NAKAMURA, Yusuke, KADOWAKI, Takashi, YASUDA, Kazuki, MORIZONO, Takashi, TAKAHASHI, Atsushi, HORIKOSHI, Momoko, NAKAMURA, Masahiro, FUJITA, Hayato

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