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Comparing Power for Gene-based and Low-frequency SNP Tests in Quantitative Traits (a GoT2D Study) by Manning, A, Sim, X, Locke, A, Agarwala, V, Moutsianas, L, Weyant, R, McCarthy, M, Altshuler, D, Boehnke, M

Muscle dysfunction caused by a KATP channel mutation in neonatal diabetes is neuronal in origin. by Clark, R, McTaggart, J, Webster, R, Mannikko, R, Iberl, M, Sim, X, Rorsman, P, Glitsch, M, Beeson, D, Ashcroft, F

The oldest plesiosaur (Reptilia, Sauropterygia) from Antarctica by Alexander Wilhelm Armin Kellner, Tiago Rodrigues Simões, Douglas Riff, Orlando Grillo, Pedro Romano, Helder de Paula, Renato Ramos, Marcelo Carvalho, Juliana Sayão, Gustavo Oliveira, Taissa Rodrigues

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Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci by Kooner, J, Saleheen, D, Sim, X, Sehmi, J, Zhang, W, Frossard, P, Been, L, Chia, K, Dimas, A, Hassanali, N, Jafar, T, Jowett, J, Li, X, Radha, V, Rees, S, Takeuchi, F, Young, R, Aung, T, Basit, A, Chidambaram, M, Das, D, Grunberg, E, Hedman, A, Hydrie, Z, Islam, M

Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians. by Cho, Y, Chen, C, Hu, C, Long, J, Ong, RT, Sim, X, Takeuchi, F, Wu, Y, Go, M, Yamauchi, T, Chang, Y, Kwak, S, Ma, R, Yamamoto, K, Adair, L, Aung, T, Cai, Q, Chang, L, Chen, Y, Gao, Y, Hu, F, Kim, H, Kim, S, Kim, Y, Lee, J

Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India. by Saxena, R, Saleheen, D, Been, L, Garavito, M, Braun, T, Bjonnes, A, Young, R, Ho, W, Rasheed, A, Frossard, P, Sim, X, Hassanali, N, Radha, V, Chidambaram, M, Liju, S, Rees, S, Ng, D, Wong, T, Yamauchi, T, Hara, K, Tanaka, Y, Hirose, H, McCarthy, M, Morris, A, Basit, A

Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci. by Kooner, J, Saleheen, D, Sim, X, Sehmi, J, Zhang, W, Frossard, P, Been, L, Chia, K, Dimas, A, Hassanali, N, Jafar, T, Jowett, J, Li, X, Radha, V, Rees, S, Takeuchi, F, Young, R, Aung, T, Basit, A, Chidambaram, M, Das, D, Grundberg, E, Hedman, A, Hydrie, Z, Islam, M

Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians by Cho, Y, Chen, C, Hu, C, Long, J, Hee Ong, RT, Sim, X, Takeuchi, F, Wu, Y, Go, M, Yamauchi, T, Chang, Y, Kwak, S, Ma, R, Yamamoto, K, Adair, L, Aung, T, Cai, Q, Chang, L, Chen, Y, Gao, Y, Hu, F, Kim, H, Kim, S, Kim, Y, Lee, J

Genetic associations of type 2 diabetes with islet amyloid polypeptide processing and degrading pathways in asian populations by Lam, V, Ma, R, Lee, H, Hu, C, Park, K, Furuta, H, Wang, Y, Tam, C, Sim, X, Ng, D, Liu, J, Wong, T, Tai, E, Morris, A, Tang, N, Woo, J, Leung, P, Kong, A, Ozaki, R, Jia, W, Lee, H, Nanjo, K, Xu, G, Ng, M, So, W, Chan, J

Gene-age interactions in blood pressure regulation: A large-scale investigation with the CHARGE, global BPgen, and ICBP consortia by Simino, J, Shi, G, Bis, J, Chasman, D, Ehret, G, Gu, X, Guo, X, Hwang, S, Sijbrands, E, Smith, A, Verwoert, G, Bragg-Gresham, J, Cadby, G, Chen, P, Cheng, C, Corre, T, De Boer, R, Goel, A, Johnson, T, Khor, C, Lluís-Ganella, C, Luan, J, Lyytikäinen, L, Nolte, I, Sim, X

Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4. by Ma, R, Hu, C, Tam, C, Zhang, R, Kwan, P, Leung, T, Thomas, G, Go, M, Hara, K, Sim, X, Ho, J, Wang, C, Li, H, Lu, L, Wang, Y, Li, J, Wang, Y, Lam, V, Wang, J, Yu, W, Kim, Y, Ng, D, Fujita, H, Panoutsopoulou, K, Day-Williams, A

Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. by Simino, J, Shi, G, Bis, J, Chasman, D, Ehret, G, Gu, X, Guo, X, Hwang, S, Sijbrands, E, Smith, A, Verwoert, G, Bragg-Gresham, J, Cadby, G, Chen, P, Cheng, C, Corre, T, de Boer, R, Goel, A, Johnson, T, Khor, C, Lluís-Ganella, C, Luan, J, Lyytikäinen, L, Nolte, I, Sim, X

Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4 by Ma, R, Hu, C, Tam, C, Zhang, R, Kwan, P, Leung, T, Thomas, G, Go, M, Hara, K, Sim, X, Ho, J, Wang, C, Li, H, Lu, L, Wang, Y, Li, J, Lam, V, Wang, J, Yu, W, Kim, Y, Ng, D, Fujita, H, Panoutsopoulou, K, Day-Williams, A, Lee, H

Distribution and medical impact of loss-of-function variants in the Finnish founder population by Lim, E, Würtz, P, Havulinna, A, Palta, P, Tukiainen, T, Rehnström, K, Esko, T, Mägi, R, Inouye, M, Lappalainen, T, Chan, Y, Salem, R, Lek, M, Flannick, J, Sim, X, Manning, A, Ladenvall, C, Bumpstead, S, Hämäläinen, E, Aalto, K, Maksimow, M, Salmi, M, Blankenberg, S, Ardissino, D, Shah, S, Horne, B, McPherson, R, Hovingh, G, Reilly, M, Watkins, H, Goel, A, Farrall, M, Girelli, D, Reiner, A, Stitziel, N, Kathiresan, S, Gabriel, S, Barrett, J, Lehtimäki, T, Laakso, M, Groop, L, Kaprio, J, Perola, M, McCarthy, M, Boehnke, M, Altshuler, D, Lindgren, C, Hirschhorn, J, Metspalu, A, Freimer, N, Zeller, T, Jalkanen, S, Koskinen, S, Raitakari, O, Durbin, R, Macarthur, D, Salomaa, V, Ripatti, S, Daly, M, Palotie, A

Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees by Jun, G, Manning, A, Almeida, M, Zawistowski, M, Wood, AR, Teslovich, TM, Fuchsberger, C, Feng, S, Cingolani, P, Gaulton, KJ, Dyer, T, Blackwell, TW, Chen, H, Chines, PS, Choi, S, Churchhouse, C, Fontanillas, P, King, R, Lee, S, Lincoln, SE, Trubetskoy, V, DePristo, M, Fingerlin, T, Grossman, R, Grundstad, J, Heath, A, Kim, J, Kim, YJ, Laramie, J, Lee, J, Li, H, Liu, X, Livne, O, Locke, AE, Maller, J, Mazur, A, Morris, AP, Pollin, TI, Ragona, D, Reich, D, Rivas, MA, Scott, LJ, Sim, X, Tearle, RG, Teo, YY, Williams, AL, Zöllner, S, Curran, JE, Peralta, J, Akolkar, B, Bell, GI, Burtt, NP, Cox, NJ, Florez, JC, Hanis, CL, McKeon, C, Mohlke, KL, Seielstad, M, Wilson, JG, Atzmon, G, Below, JE, Dupuis, J, Nicolae, DL, Lehman, D, Park, T, Won, S, Sladek, R, Altshuler, D, McCarthy, MI, Duggirala, R, Boehnke, M, Frayling, TM, Abecasis, GR, Blangero, J

Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma. by Vithana, E, Khor, C, Qiao, C, Nongpiur, M, George, R, Chen, L, Do, T, Abu-Amero, K, Huang, C, Low, S, Tajudin, L, Perera, SA, Cheng, C, Xu, L, Jia, H, Ho, C, Sim, K, Wu, R, Tham, C, Chew, P, Su, D, Oen, F, Sarangapani, S, Soumittra, N, Osman, E, Wong, H, Tang, G, Fan, S, Meng, H, Huong, D, Wang, H, Feng, B, Baskaran, M, Shantha, B, Ramprasad, V, Kumaramanickavel, G, Iyengar, S, How, A, Lee, K, Sivakumaran, T, Yong, V, Ting, S, Li, Y, Wang, Y, Tay, W, Sim, X, Lavanya, R, Cornes, B, Zheng, Y, Wong, T, Loon, S, Yong, V, Waseem, N, Yaakub, A, Chia, K, Allingham, R, Hauser, M, Lam, D, Hibberd, M, Bhattacharya, S, Zhang, M, Teo, Y, Tan, D, Jonas, J, Tai, E, Saw, S, Hon, D, Al-Obeidan, SA, Liu, J, Chau, T, Simmons, C, Bei, J, Zeng, Y, Foster, P, Vijaya, L, Wong, T, Pang, C, Wang, N, Aung, T

Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma by Vithana, E, Khor, C, Qiao, C, Nongpiur, M, George, R, Chen, L, Do, T, Abu-Amero, K, Huang, C, Low, S, Tajudin, L, Perera, S, Cheng, C, Xu, L, Jia, H, Ho, C, Sim, K, Wu, R, Tham, C, Chew, P, Su, D, Oen, F, Sarangapani, S, Soumittra, N, Osman, E, Wong, H, Tang, G, Fan, S, Meng, H, Huong, D, Wang, H, Feng, B, Baskaran, M, Shantha, B, Ramprasad, V, Kumaramanickavel, G, Iyengar, S, How, A, Lee, K, Sivakumaran, T, Yong, V, Ting, S, Li, Y, Wang, Y, Tay, W, Sim, X, Lavanya, R, Cornes, B, Zheng, Y, Wong, T, Loon, S, Yong, V, Waseem, N, Yaakub, A, Chia, K, Allingham, R, Hauser, M, Lam, D, Hibberd, M, Bhattacharya, S, Zhang, M, Teo, Y, Tan, D, Jonas, J, Tai, E, Saw, S, Hon, D, Al-Obeidan, S, Liu, J, Chau, T, Simmons, C, Bei, J, Zeng, Y, Foster, P, Vijaya, L, Wong, T, Pang, C, Wang, N, Aung, T

A genome-wide association study of diabetic kidney disease in subjects with type 2 diabetes by van Zuydam, NR, Ahlqvist, E, Sandholm, N, Deshmukh, H, Rayner, NW, Abdalla, M, Ladenvall, C, Ziemek, D, Fauman, E, Robertson, NR, McKeigue, PM, Valo, E, Forsblom, C, Harjutsalo, V, Perna, A, Rurali, E, Marcovecchio, ML, Igo, RP, Salem, RM, Perico, N, Lajer, M, Käräjämäki, A, Imamura, M, Kubo, M, Takahashi, A, Sim, X, Liu, J, van Dam, RM, Jiang, G, Tam, CHT, Luk, AOY, Lee, HM, Lim, CKP, Szeto, CC, So, WY, Chan, JCN, Ang, SF, Dorajoo, R, Wang, L, Clara, TS, McKnight, A-J, Duffy, S, Pezzolesi, MG, Consortium, G, Marre, M, Gyorgy, B, Hadjadj, S, Hiraki, LT, Ahluwalia, TS, Almgren, P, Schulz, C-A, Orho-Melander, M, Linneberg, A, Christensen, C, Witte, DR, Grarup, N, Brandslund, I, Melander, O, Paterson, AD, Tregouet, D, Maxwell, AP, Lim, SC, Ma, RCW, Tai, ES, Maeda, S, Lyssenko, V, Tuomi, T, Krolewski, AS, Rich, SS, Hirschhorn, JN, Florez, JC, Dunger, D, Pedersen, O, Hansen, T, Rossing, P, Remuzzi, G, Brosnan, MJ, Palmer, CNA, Groop, P-H, Colhoun, HM, Groop, LC, McCarthy, MI

Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma by Vithana, E, Vithana, E, Khor, C, Khor, C, Khor, C, Khor, C, Khor, C, Khor, C, Qiao, C, Nongpiur, M, Nongpiur, M, George, R, Chen, L, Do, T, Abu-Amero, K, Abu-Amero, K, Huang, C, Low, S, Tajudin, L, Perera, SA, Cheng, C, Cheng, C, Cheng, C, Xu, L, Jia, H, Ho, C, Sim, K, Wu, R, Wu, R, Tham, C, Chew, P, Su, D, Oen, F, Sarangapani, S, Soumittra, N, Osman, E, Wong, H, Tang, G, Fan, S, Meng, H, Huong, D, Wang, H, Feng, B, Baskaran, M, Shantha, B, Ramprasad, V, Kumaramanickavel, G, Iyengar, S, How, A, Lee, K, Sivakumaran, T, Yong, V, Ting, S, Li, Y, Wang, Y, Tay, W, Sim, X, Lavanya, R, Cornes, B, Zheng, Y, Zheng, Y, Wong, T, Loon, S, Yong, V, Waseem, N, Yaakub, A, Chia, K, Rand Allingham, R, Hauser, M, Lam, D, Hibberd, M, Hibberd, M, Bhattacharya, S, Zhang, M, Teo, Y, Teo, Y, Teo, Y, Tan, D, Tan, D, Jonas, J, Tai, E, Tai, E, Tai, E, Saw, S, Saw, S, Hon, D, Al-Obeidan, SA, Liu, J, Liu, J, Chau, T, Simmons, C, Simmons, C, Bei, J, Bei, J, Zeng, Y, Zeng, Y, Zeng, Y, Foster, P, Vijaya, L, Wong, T