PubMed

Lack of association of genetic variation in chromosome region 15q14-22.1 with type 2 diabetes in a Japanese population.

Yamaguchi Y, Moritani M, Tanahashi T, Osabe D, Nomura K, Fujita Y, Keshavarz P, Kunika K, Nakamura N, Yoshikawa T, Ichiishi E, Shiota H, Yasui N, Inoue H, Itakura M.

BMC Med Genet. 2008 Mar 27;9:22.PMID: 18366806 [PubMed - indexed for MEDLINE]Related articlesFree article

Genetic association of single nucleotide polymorphisms in endonuclease G-like 1 gene with type 2 diabetes in a Japanese population.

Moritani M, Nomura K, Tanahashi T, Osabe D, Fujita Y, Shinohara S, Yamaguchi Y, Keshavarz P, Kudo E, Nakamura N, Yoshikawa T, Ichiishi E, Takata Y, Yasui N, Shiota H, Kunika K, Inoue H, Itakura M.

Diabetologia. 2007 Jun;50(6):1218-27. Epub 2007 Apr 6.PMID: 17415550 [PubMed - indexed for MEDLINE]Related articles

Association study on chromosome 20q11.21-13.13 locus and its contribution to type 2 diabetes susceptibility in Japanese.

Tanahashi T, Osabe D, Nomura K, Shinohara S, Kato H, Ichiishi E, Nakamura N, Yoshikawa T, Takata Y, Miyamoto T, Shiota H, Keshavarz P, Yamaguchi Y, Kunika K, Moritani M, Inoue H, Itakura M.

Hum Genet. 2006 Nov;120(4):527-42. Epub 2006 Sep 6.PMID: 16955255 [PubMed - indexed for MEDLINE]Related articles

Analysis of common PTPN1 gene variants in type 2 diabetes, obesity and associated phenotypes in the French population.

Cheyssac C, Lecoeur C, Dechaume A, Bibi A, Charpentier G, Balkau B, Marre M, Froguel P, Gibson F, Vaxillaire M.

BMC Med Genet. 2006 May 5;7:44.PMID: 16677372 [PubMed - indexed for MEDLINE]Related articlesFree article

Association between single-nucleotide polymorphisms in the SEC8L1 gene, which encodes a subunit of the exocyst complex, and rheumatoid arthritis in a Japanese population.

Hamada D, Takata Y, Osabe D, Nomura K, Shinohara S, Egawa H, Nakano S, Shinomiya F, Scafe CR, Reeve VM, Miyamoto T, Moritani M, Kunika K, Inoue H, Yasui N, Itakura M.

Arthritis Rheum. 2005 May;52(5):1371-80.PMID: 15880602 [PubMed - indexed for MEDLINE]Related articlesFree article

Evaluation of a SNP map of 6q24-27 confirms diabetic nephropathy loci and identifies novel associations in type 2 diabetes patients with nephropathy from an African-American population.

Leak TS, Mychaleckyj JC, Smith SG, Keene KL, Gordon CJ, Hicks PJ, Freedman BI, Bowden DW, Sale MM.

Hum Genet. 2008 Aug;124(1):63-71. Epub 2008 Jun 17.PMID: 18560894 [PubMed - indexed for MEDLINE]Related articlesFree article

CHOP T/C and C/T haplotypes contribute to early-onset type 2 diabetes in Italians.

Gragnoli C.

J Cell Physiol. 2008 Nov;217(2):291-5.PMID: 18680108 [PubMed - indexed for MEDLINE]Related articles

Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population.

Takeuchi F, Serizawa M, Yamamoto K, Fujisawa T, Nakashima E, Ohnaka K, Ikegami H, Sugiyama T, Katsuya T, Miyagishi M, Nakashima N, Nawata H, Nakamura J, Kono S, Takayanagi R, Kato N.

Diabetes. 2009 Jul;58(7):1690-9. Epub 2009 Apr 28.PMID: 19401414 [PubMed - indexed for MEDLINE]Related articlesFree article

Genetic association study of synphilin-1 in idiopathic Parkinson's disease.

Myhre R, Klungland H, Farrer MJ, Aasly JO.

BMC Med Genet. 2008 Mar 21;9:19.PMID: 18366718 [PubMed - indexed for MEDLINE]Related articlesFree article

The association of genetic variants in Krüppel-like factor 11 and Type 2 diabetes in the Japanese population.

Tanahashi T, Shinohara K, Keshavarz P, Yamaguchi Y, Miyawaki K, Kunika K, Moritani M, Nakamura N, Yoshikawa T, Shiota H, Inoue H, Itakura M.

Diabet Med. 2008 Jan;25(1):19-26.PMID: 18199129 [PubMed - indexed for MEDLINE]Related articlesFree article

Linkage disequilibrium mapping of the replicated type 2 diabetes linkage signal on chromosome 1q.

Prokopenko I, Zeggini E, Hanson RL, Mitchell BD, Rayner NW, Akan P, Baier L, Das SK, Elliott KS, Fu M, Frayling TM, Groves CJ, Gwilliam R, Scott LJ, Voight BF, Hattersley AT, Hu C, Morris AD, Ng M, Palmer CN, Tello-Ruiz M, Vaxillaire M, Wang CR, Stein L, Chan J, Jia W, Froguel P, Elbein SC, Deloukas P, Bogardus C, Shuldiner AR, McCarthy MI; International Type 2 Diabetes 1q Consortium.

Diabetes. 2009 Jul;58(7):1704-9. Epub 2009 Apr 23.PMID: 19389826 [PubMed - indexed for MEDLINE]Related articlesFree article

Evaluating the association of common PBX1 variants with type 2 diabetes.

Duesing K, Charpentier G, Marre M, Tichet J, Hercberg S, Balkau B, Froguel P, Gibson F.

BMC Med Genet. 2008 Feb 29;9:14.PMID: 18312624 [PubMed - indexed for MEDLINE]Related articlesFree article

ATRIUM: testing untyped SNPs in case-control association studies with related individuals.

Wang Z, McPeek MS.

Am J Hum Genet. 2009 Nov;85(5):667-78.PMID: 19913122 [PubMed - indexed for MEDLINE]Related articles

Role of STAT4 polymorphisms in systemic lupus erythematosus in a Japanese population: a case-control association study of the STAT1-STAT4 region.

Kawasaki A, Ito I, Hikami K, Ohashi J, Hayashi T, Goto D, Matsumoto I, Ito S, Tsutsumi A, Koga M, Arinami T, Graham RR, Hom G, Takasaki Y, Hashimoto H, Behrens TW, Sumida T, Tsuchiya N.

Arthritis Res Ther. 2008;10(5):R113. Epub 2008 Sep 19.PMID: 18803832 [PubMed - indexed for MEDLINE]Related articlesFree article

Association of single-nucleotide polymorphisms in the suppressor of cytokine signaling 2 (SOCS2) gene with type 2 diabetes in the Japanese.

Kato H, Nomura K, Osabe D, Shinohara S, Mizumori O, Katashima R, Iwasaki S, Nishimura K, Yoshino M, Kobori M, Ichiishi E, Nakamura N, Yoshikawa T, Tanahashi T, Keshavarz P, Kunika K, Moritani M, Kudo E, Tsugawa K, Takata Y, Hamada D, Yasui N, Miyamoto T, Shiota H, Inoue H, Itakura M.

Genomics. 2006 Apr;87(4):446-58. Epub 2006 Jan 10.PMID: 16406727 [PubMed - indexed for MEDLINE]Related articles

SNPs in the KCNJ11-ABCC8 gene locus are associated with type 2 diabetes and blood pressure levels in the Japanese population.

Sakamoto Y, Inoue H, Keshavarz P, Miyawaki K, Yamaguchi Y, Moritani M, Kunika K, Nakamura N, Yoshikawa T, Yasui N, Shiota H, Tanahashi T, Itakura M.

J Hum Genet. 2007;52(10):781-93. Epub 2007 Sep 6.PMID: 17823772 [PubMed - indexed for MEDLINE]Related articles

Genetic association between the PRKCH gene encoding protein kinase Ceta isozyme and rheumatoid arthritis in the Japanese population.

Takata Y, Hamada D, Miyatake K, Nakano S, Shinomiya F, Scafe CR, Reeve VM, Osabe D, Moritani M, Kunika K, Kamatani N, Inoue H, Yasui N, Itakura M.

Arthritis Rheum. 2007 Jan;56(1):30-42.PMID: 17195206 [PubMed - indexed for MEDLINE]Related articlesFree article

Calsquestrin 1 (CASQ1) gene polymorphisms under chromosome 1q21 linkage peak are associated with type 2 diabetes in Northern European Caucasians.

Das SK, Chu W, Zhang Z, Hasstedt SJ, Elbein SC.

Diabetes. 2004 Dec;53(12):3300-6.PMID: 15561963 [PubMed - indexed for MEDLINE]Related articlesFree article

Single nucleotide polymorphisms in genes encoding LKB1 (STK11), TORC2 (CRTC2) and AMPK alpha2-subunit (PRKAA2) and risk of type 2 diabetes.

Keshavarz P, Inoue H, Nakamura N, Yoshikawa T, Tanahashi T, Itakura M.

Mol Genet Metab. 2008 Feb;93(2):200-9. Epub 2007 Oct 18.PMID: 17950019 [PubMed - indexed for MEDLINE]Related articles

Haplotype construction of the FRDA gene and evaluation of its role in type II diabetes.

Holmkvist J, Almgren P, Parikh H, Zucchelli M, Kere J, Groop L, Lindgren CM.

Eur J Hum Genet. 2005 Jul;13(7):849-55.PMID: 15827563 [PubMed - indexed for MEDLINE]Related articlesFree article