Distinct Imprinting Signatures and Biased Differentiation of Human Androgenetic and Parthenogenetic Embryonic Stem Cells von Sagi, Ido, De Pinho, Joao C., Zuccaro, Michael V., Atzmon, Chen, Golan-Lev, Tamar, Yanuka, Ofra, Prosser, Robert, Sadowy, Alexandra, Perez, Gloria, Cabral, Thiago, Glaser, Benjamin, Tsang, Stephen H., Goland, Robin, Sauer, Mark V., Lobo, Rogerio, Benvenisty, Nissim, Egli, Dieter

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A structural variation reference for medical and population genetics von Collins, Ryan L., Brand, Harrison, Karczewski, Konrad J., Zhao, Xuefang, Alföldi, Jessica, Francioli, Laurent C., Khera, Amit V., Lowther, Chelsea, Gauthier, Laura D., Wang, Harold, Watts, Nicholas A., Solomonson, Matthew, O’Donnell-Luria, Anne, Baumann, Alexander, Munshi, Ruchi, Walker, Mark, Whelan, Christopher W., Huang, Yongqing, Brookings, Ted, Sharpe, Ted, Stone, Matthew R., Valkanas, Elise, Fu, Jack, Tiao, Grace, Laricchia, Kristen M., Ruano-Rubio, Valentin, Stevens, Christine, Gupta, Namrata, Cusick, Caroline, Margolin, Lauren, Taylor, Kent D., Lin, Henry J., Rich, Stephen S., Post, Wendy S., Chen, Yii-Der Ida, Rotter, Jerome I., Nusbaum, Chad, Philippakis, Anthony, Lander, Eric, Gabriel, Stacey, Neale, Benjamin M., Kathiresan, Sekar, Daly, Mark J., Banks, Eric, MacArthur, Daniel G., Talkowski, Michael E.

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Association of common genetic variation in the insulin/IGF1 signaling pathway with human longevity von Pawlikowska, Ludmila, Hu, Donglei, Huntsman, Scott, Sung, Andrew, Chu, Catherine, Chen, Justin, Joyner, Alexander H., Schork, Nicholas J., Hsueh, Wen‐Chi, Reiner, Alexander P., Psaty, Bruce M., Atzmon, Gil, Barzilai, Nir, Cummings, Steven R., Browner, Warren S., Kwok, Pui‐Yan, Ziv, Elad

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Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees von Jun, Goo, Manning, Alisa, Almeida, Marcio, Zawistowski, Matthew, Wood, Andrew R., Teslovich, Tanya M., Fuchsberger, Christian, Feng, Shuang, Cingolani, Pablo, Gaulton, Kyle J., Dyer, Thomas, Blackwell, Thomas W., Chen, Han, Chines, Peter S., Choi, Sungkyoung, Churchhouse, Claire, Fontanillas, Pierre, King, Ryan, Lee, SungYoung, Lincoln, Stephen E., Trubetskoy, Vasily, DePristo, Mark, Fingerlin, Tasha, Grossman, Robert, Grundstad, Jason, Heath, Alison, Kim, Jayoun, Kim, Young Jin, Laramie, Jason, Lee, Jaehoon, Li, Heng, Liu, Xuanyao, Livne, Oren, Locke, Adam E., Maller, Julian, Mazur, Alexander, Morris, Andrew P., Pollin, Toni I., Ragona, Derek, Reich, David, Rivas, Manuel A., Scott, Laura J., Sim, Xueling, Tearle, Rick G., Teo, Yik Ying, Williams, Amy L., Zöllner, Sebastian, Curran, Joanne E., Peralta, Juan, Akolkar, Beena, Bell, Graeme I., Burtt, Noël P., Cox, Nancy J., Florez, Jose C., Hanis, Craig L., McKeon, Catherine, Mohlke, Karen L., Seielstad, Mark, Wilson, James G., Atzmon, Gil, Below, Jennifer E., Dupuis, Josée, Nicolae, Dan L., Lehman, Donna, Park, Taesung, Won, Sungho, Sladek, Robert, Altshuler, David, McCarthy, Mark I., Duggirala, Ravindranath, Boehnke, Michael, Frayling, Timothy M., Abecasis, Gonçalo R., Blangero, John

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Author Correction: A structural variation reference for medical and population genetics von Collins, Ryan L., Brand, Harrison, Karczewski, Konrad J., Zhao, Xuefang, Alföldi, Jessica, Francioli, Laurent C., Khera, Amit V., Lowther, Chelsea, Gauthier, Laura D., Wang, Harold, Watts, Nicholas A., Solomonson, Matthew, O’Donnell-Luria, Anne, Baumann, Alexander, Munshi, Ruchi, Walker, Mark, Whelan, Christopher W., Huang, Yongqing, Brookings, Ted, Sharpe, Ted, Stone, Matthew R., Valkanas, Elise, Fu, Jack, Tiao, Grace, Laricchia, Kristen M., Ruano-Rubio, Valentin, Stevens, Christine, Gupta, Namrata, Cusick, Caroline, Margolin, Lauren, Taylor, Kent D., Lin, Henry J., Rich, Stephen S., Post, Wendy S., Chen, Yii-Der Ida, Rotter, Jerome I., Nusbaum, Chad, Philippakis, Anthony, Lander, Eric, Gabriel, Stacey, Neale, Benjamin M., Kathiresan, Sekar, Daly, Mark J., Banks, Eric, MacArthur, Daniel G., Talkowski, Michael E.

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Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms von Horikoshi, Momoko, Pasquali, Lorenzo, Wiltshire, Steven, Huyghe, Jeroen R, Mahajan, Anubha, Asimit, Jennifer L, Ferreira, Teresa, Locke, Adam E, Robertson, Neil R, Wang, Xu, Sim, Xueling, Fujita, Hayato, Hara, Kazuo, Young, Robin, Zhang, Weihua, Choi, Sungkyoung, Chen, Han, Kaur, Ismeet, Takeuchi, Fumihiko, Fontanillas, Pierre, Thuillier, Dorothée, Yengo, Loic, Below, Jennifer E, Tam, Claudia H T, Wu, Ying, Abecasis, Gonçalo, Altshuler, David, Bell, Graeme I, Blangero, John, Burtt, Noél P, Duggirala, Ravindranath, Florez, Jose C, Hanis, Craig L, Seielstad, Mark, Atzmon, Gil, Chan, Juliana C N, Ma, Ronald C W, Froguel, Philippe, Wilson, James G, Bharadwaj, Dwaipayan, Dupuis, Josee, Meigs, James B, Cho, Yoon Shin, Park, Taesung, Kooner, Jaspal S, Chambers, John C, Saleheen, Danish, Kadowaki, Takashi, Tai, E Shyong, Mohlke, Karen L, Cox, Nancy J, Ferrer, Jorge, Zeggini, Eleftheria, Kato, Norihiro, Teo, Yik Ying, Boehnke, Michael, McCarthy, Mark I, Morris, Andrew P

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A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data von Kim, Young Jin, Lee, Juyoung, Kim, Bong-Jo, Park, Taesung

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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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Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms von Horikoshi, Momoko, Pasquali, Lorenzo, Wiltshire, Steven, Huyghe, Jeroen R, Mahajan, Anubha, Asimit, Jennifer L, Ferreira, Teresa, Locke, Adam E, Robertson, Neil R, Wang, Xu, Sim, Xueling, Fujita, Hayato, Hara, Kazuo, Young, Robin, Zhang, Weihua, Choi, Sungkyoung, Chen, Han, Kaur, Ismeet, Takeuchi, Fumihiko, Fontanillas, Pierre, Thuillier, Dorothée, Yengo, Loic, Below, Jennifer E, Tam, Claudia H.T, Wu, Ying, Abecasis, Gonçalo, Altshuler, David, Bell, Graeme I, Blangero, John, Burtt, Noél P, Duggirala, Ravindranath, Florez, Jose C, Hanis, Craig L, Seielstad, Mark, Atzmon, Gil, Chan, Juliana C.N, Ma, Ronald C.W, Froguel, Philippe, Wilson, James G, Bharadwaj, Dwaipayan, Dupuis, Josee, Meigs, James B, Cho, Yoon Shin, Park, Taesung, Kooner, Jaspal S, Chambers, John C, Saleheen, Danish, Kadowaki, Takashi, Tai, E. Shyong, Mohlke, Karen L, Cox, Nancy J, Ferrer, Jorge, Zeggini, Eleftheria, Kato, Norihiro, Teo, Yik Ying, Boehnke, Michael, McCarthy, Mark I, Morris, Andrew P

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Edify Image: High-Quality Image Generation with Pixel Space Laplacian Diffusion Models von NVIDIA, :, Atzmon, Yuval, Bala, Maciej, Balaji, Yogesh, Cai, Tiffany, Cui, Yin, Fan, Jiaojiao, Ge, Yunhao, Gururani, Siddharth, Huffman, Jacob, Isaac, Ronald, Jannaty, Pooya, Karras, Tero, Lam, Grace, Lewis, J. P, Licata, Aaron, Lin, Yen-Chen, Liu, Ming-Yu, Ma, Qianli, Mallya, Arun, Martino-Tarr, Ashlee, Mendez, Doug, Nah, Seungjun, Pruett, Chris, Reda, Fitsum, Song, Jiaming, Wang, Ting-Chun, Wei, Fangyin, Zeng, Xiaohui, Zeng, Yu, Zhang, Qinsheng

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Edify Image: High-Quality Image Generation with Pixel Space Laplacian Diffusion Models von NVIDIA, Atzmon, Yuval, Bala, Maciej, Balaji, Yogesh, Cai, Tiffany, Cui, Yin, Fan, Jiaojiao, Ge, Yunhao, Gururani, Siddharth, Huffman, Jacob, Isaac, Ronald, Jannaty, Pooya, Karras, Tero, Lam, Grace, Lewis, J P, Licata, Aaron, Yen-Chen, Lin, Ming-Yu, Liu, Ma, Qianli, Mallya, Arun, Martino-Tarr, Ashlee, Mendez, Doug, Nah, Seungjun, Pruett, Chris, Fitsum Reda, Song, Jiaming, Ting-Chun, Wang, Fangyin Wei, Zeng, Xiaohui, Zeng, Yu, Zhang, Qinsheng

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Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease von Hui, KY, Fernandez-Hernandez, H, Hu, J, Schaffner, A, Pankratz, N, Hsu, N-Y, Chuang, L-S, Carmi, S, Villaverde, N, Li, X, Rivas, M, Levine, AP, Bao, X, Labrias, PR, Haritunians, T, Ruane, D, Gettler, K, Chen, E, Li, D, Schiff, ER, Pontikos, N, Barzilai, N, Brant, SR, Bressman, S, Cheifetz, AS, Clark, LN, Daly, MJ, Desnick, RJ, Duerr, RH, Katz, S, Lencz, T, Myers, RH, Ostrer, H, Ozelius, L, Payami, H, Peter, Y, Rioux, JD, Segal, AW, Scott, WK, Silverberg, MS, Vance, JM, Ubarretxena-Belandia, I, Foroud, T, Atzmon, G, Pe'er, I, Ioannou, Y, McGovern, DPB, Yue, Z, Schadt, EE, Cho, JH, Peter, I

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Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms von Horikoshi, Momoko, Pasquali, Lorenzo, Wiltshire, Steven, Huyghe, Jeroen R, Mahajan, Anubha, Asimit, Jennifer L, Ferreira, Teresa, Locke, Adam E, Robertson, Neil R, Wang, Xu, Sim, Xueling, Fujita, Hayato, Hara, Kazuo, Young, Robin, Zhang, Weihua, Choi, Sungkyoung, Chen, Han, Kaur, Ismeet, Takeuchi, Fumihiko, Fontanillas, Pierre, Thuillier, Dorothée, Yengo, Loic, Below, Jennifer E, Tam, Claudia HT, Wu, Ying, Abecasis, Gonçalo, Altshuler, David, Bell, Graeme I, Blangero, John, Burtt, Noél P, Duggirala, Ravindranath, Florez, Jose C, Hanis, Craig L, Seielstad, Mark, Atzmon, Gil, Chan, Juliana CN, Ma, Ronald CW, Froguel, Philippe, Wilson, James G, Bharadwaj, Dwaipayan, Dupuis, Josee, Meigs, James B, Cho, Yoon Shin, Park, Taesung, Kooner, Jaspal S, Chambers, John C, Saleheen, Danish, Kadowaki, Takashi, Tai, E Shyong, Mohlke, Karen L, Cox, Nancy J, Ferrer, Jorge, Zeggini, Eleftheria, Kato, Norihiro, Teo, Yik Ying, Boehnke, Michael, McCarthy, Mark I, Morris, Andrew P, T2D-GENES Consortium

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Abstracts of papers presented at the 2nd conference on agricultural entomology von Yathom, Shoshana, Halperin, J., Gol’Berg, ALLA M., Gamliel, B., Wolfovich, M., Sando, T., Almogi, Ahuva, Gerson, U., Gerling, D., Cohen, S., Keren, J., Harpaz, I., Bar-Joseph, Rachel, Berlinger, M. J., Dahan, R., Mordechi, Sara, Orkin-Shevach, Esther, Morag, Yorith, Tal, M., Pilowsky, M., Ucko, Orna, Dayan, R., Raccah, B., Klein, M., Purcell, A. H., Bar-Zakay, I., Hefetz, A., Sternlicht, M., Peleg, B. A., Gokkes, M., Singer, G., Geffen, D., Kronenberg, S., Dunkelblum, E., Ben-Dov, Y., Goldschmidt, Z., Wolk, J. L., Somekh, LILA, Or, R., Kehat, M., Chen, CH, Klein, Z., Fishler, G., Navon, A., Melamed-Madjar, Venezia, Keren, Sara, Tam, S., Broza, M., Sneh, B., Attoun, Y., Argov, Yael, Bar Shalom, O., Auerbach, Ofra, Podoler, H., Rosen, D., Rubin, A., Atzmon, R., Shabtay, S., Roessler, Y., Yizhar, Y., Ben-Avraham, Bracha, Palevsky, E., Steinberg, S., Falk, H., Yablonka, G., Navarro, S., Donahaye, E., Dias, R., Meisner, J., Ascher, K. R. S., Ishaaya, I., Yablonski, SARA, Gurevitz, E., Renneh, S., Sheinboim, Y., Ohali, Y., Tal, Susana, Nemny, Nadia E., Shahar, Y., Tadmor, U.

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