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Published in partnership with the
European Association for the Study of Diabetes
Research Letter
Y. Liu, L. Yu, D. Zhang, Z. Chen, D. Z. Zhou, T. Zhao, S. Li, T. Wang, X. Hu and G. Y. Feng, et al.
Journal Article
Variants in KCNQ1 are associated with susceptibility to type 2 diabetes in the population of mainland China
Y. Liu, D. Z. Zhou, D. Zhang, Z. Chen and T. Zhao, et al.
Diabetologia, 2009, Volume 52, Number 7, Pages 1315-1321
Association of GCKR rs780094, alone or in combination with GCK rs1799884, with type 2 diabetes and related traits in a Han Chinese population
Q. Qi, Y. Wu, H. Li, R. J. F. Loos and F. B. Hu, et al.
Diabetologia, 2009, Volume 52, Number 5, Pages 834-843
Association study of genetic variants in eight genes/loci with type 2 diabetes in a Han Chinese population
Ying Lin, Pengqiu Li, Li Cai, Ben Zhang and Xin Tang, et al.
BMC Medical Genetics, 2010, Volume 11, Number 1, 97
Association between polymorphisms in SLC30A8 , HHEX , CDKN2A/B , IGF2BP2 , FTO , WFS1 , CDKAL1 , KCNQ1 and type 2 diabetes in the Korean population
Yong-Ho Lee, Eun Seok Kang, So Hun Kim, Seung Jin Han and Chul Hoon Kim, et al.
Journal of Human Genetics, 2008, Volume 53, Numbers 11-12, Pages 991-998
Replication study for the association of new meta-analysis-derived risk loci with susceptibility to type 2 diabetes in 6,244 Japanese individuals
S. Omori, Y. Tanaka, M. Horikoshi, A. Takahashi and K. Hara, et al.
Diabetologia, 2009, Volume 52, Number 8, Pages 1554-1560
Genetic analysis of recently identified type 2 diabetes loci in 1,638 unselected patients with type 2 diabetes and 1,858 control participants from a Norwegian population-based cohort (the HUNT study)
J. K. Hertel, S. Johansson, H. Ræder, K. Midthjell and V. Lyssenko, et al.
Diabetologia, 2008, Volume 51, Number 6, Pages 971-977
Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2, KCNQ1, and WFS1 in Type 2 Diabetes in a Chinese population
Xueyao Han, Yingying Luo, Qian Ren, Xiuying Zhang and Fang Wang, et al.
BMC Medical Genetics, 2010, Volume 11, Number 1, 81
Beta cell glucose sensitivity is decreased by 39% in non-diabetic individuals carrying multiple diabetes-risk alleles compared with those with no risk alleles
L. Pascoe, T. M. Frayling, M. N. Weedon, A. Mari and A. Tura, et al.
Diabetologia, 2008, Volume 51, Number 11, Pages 1989-1992
Variations in the HHEX gene are associated with increased risk of type 2 diabetes in the Japanese population
M. Horikoshi, K. Hara, C. Ito, N. Shojima and R. Nagai, et al.
Diabetologia, 2007, Volume 50, Number 12, Pages 2461-2466
A common variant in MTNR1B, encoding melatonin receptor 1B, is associated with type 2 diabetes and fasting plasma glucose in Han Chinese individuals
T. Rönn, J. Wen, Z. Yang, B. Lu and Y. Du, et al.
Diabetologia, 2009, Volume 52, Number 5, Pages 830-833
Keywords Association study - Genetic variations - Type 2 diabetes
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