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    Results: 6

    1.

    Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes.

    Bonnefond A, Clément N, Fawcett K, Yengo L, Vaillant E, Guillaume JL, Dechaume A, Payne F, Roussel R, Czernichow S, Hercberg S, Hadjadj S, Balkau B, Marre M, Lantieri O, Langenberg C, Bouatia-Naji N; Meta-Analysis of Glucose and Insulin-Related Traits Consortium (MAGIC), Charpentier G, Vaxillaire M, Rocheleau G, Wareham NJ, Sladek R, McCarthy MI, Dina C, Barroso I, Jockers R, Froguel P.

    Nat Genet. 2012 Jan 29;44(3):297-301. doi: 10.1038/ng.1053.

    PMID:
    22286214
    [PubMed - indexed for MEDLINE]
    2.

    Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians.

    Cho YS, Chen CH, Hu C, Long J, Ong RT, Sim X, Takeuchi F, Wu Y, Go MJ, Yamauchi T, Chang YC, Kwak SH, Ma RC, Yamamoto K, Adair LS, Aung T, Cai Q, Chang LC, Chen YT, Gao Y, Hu FB, Kim HL, Kim S, Kim YJ, Lee JJ, Lee NR, Li Y, Liu JJ, Lu W, Nakamura J, Nakashima E, Ng DP, Tay WT, Tsai FJ, Wong TY, Yokota M, Zheng W, Zhang R, Wang C, So WY, Ohnaka K, Ikegami H, Hara K, Cho YM, Cho NH, Chang TJ, Bao Y, Hedman ÅK, Morris AP, McCarthy MI; DIAGRAM Consortium; MuTHER Consortium, Takayanagi R, Park KS, Jia W, Chuang LM, Chan JC, Maeda S, Kadowaki T, Lee JY, Wu JY, Teo YY, Tai ES, Shu XO, Mohlke KL, Kato N, Han BG, Seielstad M.

    Nat Genet. 2011 Dec 11;44(1):67-72. doi: 10.1038/ng.1019.

    PMID:
    22158537
    [PubMed - indexed for MEDLINE]
    3.

    Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci.

    Kooner JS, Saleheen D, Sim X, Sehmi J, Zhang W, Frossard P, Been LF, Chia KS, Dimas AS, Hassanali N, Jafar T, Jowett JB, Li X, Radha V, Rees SD, Takeuchi F, Young R, Aung T, Basit A, Chidambaram M, Das D, Grundberg E, Hedman AK, Hydrie ZI, Islam M, Khor CC, Kowlessur S, Kristensen MM, Liju S, Lim WY, Matthews DR, Liu J, Morris AP, Nica AC, Pinidiyapathirage JM, Prokopenko I, Rasheed A, Samuel M, Shah N, Shera AS, Small KS, Suo C, Wickremasinghe AR, Wong TY, Yang M, Zhang F; DIAGRAM; MuTHER, Abecasis GR, Barnett AH, Caulfield M, Deloukas P, Frayling TM, Froguel P, Kato N, Katulanda P, Kelly MA, Liang J, Mohan V, Sanghera DK, Scott J, Seielstad M, Zimmet PZ, Elliott P, Teo YY, McCarthy MI, Danesh J, Tai ES, Chambers JC.

    Nat Genet. 2011 Aug 28;43(10):984-9. doi: 10.1038/ng.921.

    PMID:
    21874001
    [PubMed - indexed for MEDLINE]
    4.

    Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction.

    Shea J, Agarwala V, Philippakis AA, Maguire J, Banks E, Depristo M, Thomson B, Guiducci C, Onofrio RC, Kathiresan S, Gabriel S, Burtt NP, Daly MJ, Groop L, Altshuler D; Myocardial Infarction Genetics Consortium.

    Nat Genet. 2011 Jul 24;43(8):801-5. doi: 10.1038/ng.871.

    PMID:
    21775993
    [PubMed - indexed for MEDLINE]
    5.

    Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes.

    Small KS, Hedman AK, Grundberg E, Nica AC, Thorleifsson G, Kong A, Thorsteindottir U, Shin SY, Richards HB; GIANT Consortium; MAGIC Investigators; DIAGRAM Consortium, Soranzo N, Ahmadi KR, Lindgren CM, Stefansson K, Dermitzakis ET, Deloukas P, Spector TD, McCarthy MI; MuTHER Consortium.

    Nat Genet. 2011 Jun;43(6):561-4. Epub 2011 May 15. Erratum in: Nat Genet. 2011 Oct;43(10):1040.

    PMID:
    21572415
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    6.

    Error occurred: cannot get document summary

    PMID:
    21448178

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