-
1
-
-
20444395829
-
Genetics of type 2 diabetes mellitus
-
Malecki MT. Genetics of type 2 diabetes mellitus. Diabetes Res Clin Pract 2005. 68)Suppl 1):S10-S21.
-
(2005)
Diabetes Res Clin Pract
, vol.68
, Issue.SUPPL. 1
-
-
Malecki, M.T.1
-
2
-
-
79551469699
-
Genetics of type 1 diabetes
-
Steck AK, Rewers MJ. Genetics of type 1 diabetes. Clin Chem 2011. 57(2):176-185.
-
(2011)
Clin Chem
, vol.57
, Issue.2
, pp. 176-185
-
-
Steck, A.K.1
Rewers, M.J.2
-
3
-
-
47149095990
-
Pancreatic alpha-cell dysfunction in diabetes
-
Burcelin R, Knauf C, Cani PD. Pancreatic alpha-cell dysfunction in diabetes. Diabetes Metab 2008. 34(Suppl 2):S49-S55.
-
(2008)
Diabetes Metab
, vol.34
, Issue.SUPPL. 2
-
-
Burcelin, R.1
Knauf, C.2
Cani, P.D.3
-
4
-
-
41149086669
-
Natural history of cardiovascular disease in patients with diabetes: Role of hyperglycemia
-
Milicevic Z, Raz I, Beattie SD, Campaigne BN, Sarwat S, Gromniak E, Kowalska I, Galic E, Tan M, Hanefeld M. Natural history of cardiovascular disease in patients with diabetes: role of hyperglycemia. Diabetes Care 2008. 31(Suppl 2):S155-S160.
-
(2008)
Diabetes Care
, vol.31
, Issue.SUPPL. 2
-
-
Milicevic, Z.1
Raz, I.2
Beattie, S.D.3
Campaigne, B.N.4
Sarwat, S.5
Gromniak, E.6
Kowalska, I.7
Galic, E.8
Tan, M.9
Hanefeld, M.10
-
5
-
-
58149328829
-
Metabolic and cardiovascular traits: An abundance of recently identified common genetic variants
-
Mohlke KL, Boehnke M, Abecasis GR. Metabolic and cardiovascular traits: an abundance of recently identified common genetic variants. Hum Mol Genet 2008. 17(R2):R102-R108.
-
(2008)
Hum Mol Genet
, vol.17
, Issue.R2
-
-
Mohlke, K.L.1
Boehnke, M.2
Abecasis, G.R.3
-
6
-
-
0034844049
-
Mortality and causes of death in the WHO Multinational Study of Vascular Disease in Diabetes
-
Morrish NJ, Wang SL, Stevens LK, Fuller JH, Keen H. Mortality and causes of death in the WHO Multinational Study of Vascular Disease in Diabetes. Diabetologia 2001. 44(Suppl 2):S14-S21.
-
(2001)
Diabetologia
, vol.44
, Issue.SUPPL. 2
-
-
Morrish, N.J.1
Wang, S.L.2
Stevens, L.K.3
Fuller, J.H.4
Keen, H.5
-
7
-
-
0027532914
-
Global estimates for prevalence of diabetes mellitus and impaired glucose tolerance in adults. WHO Ad Hoc Diabetes Reporting Group
-
King H, Rewers M. Global estimates for prevalence of diabetes mellitus and impaired glucose tolerance in adults. WHO Ad Hoc Diabetes Reporting Group. Diabetes Care 1993. 16(1):157-177.
-
(1993)
Diabetes Care
, vol.16
, Issue.1
, pp. 157-177
-
-
King, H.1
Rewers, M.2
-
8
-
-
17844373857
-
Genetics of type 2 diabetes
-
Barroso I. Genetics of type 2 diabetes. Diabet Med 2005. 22(5):517-535.
-
(2005)
Diabet Med
, vol.22
, Issue.5
, pp. 517-535
-
-
Barroso, I.1
-
9
-
-
0033645239
-
Parental transmission of type 2 diabetes: The Framingham Offspring Study
-
Meigs JB, Cupples LA, Wilson PW. Parental transmission of type 2 diabetes: the Framingham Offspring Study. Diabetes 2000. 49(12):2201-2207.
-
(2000)
Diabetes
, vol.49
, Issue.12
, pp. 2201-2207
-
-
Meigs, J.B.1
Cupples, L.A.2
Wilson, P.W.3
-
10
-
-
37849001441
-
Diabetes and impaired glucose regulation in first-degree relatives of patients with type 2 diabetes in Isfahan, Iran: Prevalence and risk factors
-
Amini M, Janghorbani M. Diabetes and impaired glucose regulation in first-degree relatives of patients with type 2 diabetes in Isfahan, Iran: prevalence and risk factors. Rev Diabet Stud 2007. 4(3):169-176.
-
(2007)
Rev Diabet Stud
, vol.4
, Issue.3
, pp. 169-176
-
-
Amini, M.1
Janghorbani, M.2
-
11
-
-
0032953097
-
Heritability of type II (non-insulin-dependent) diabetes mellitus and abnormal glucose tolerance-a population-based twin study
-
Poulsen P, Kyvik KO, Vaag A, Beck-Nielsen H. Heritability of type II (non-insulin-dependent) diabetes mellitus and abnormal glucose tolerance-a population-based twin study. Diabetologia 1999. 42(2):139-145.
-
(1999)
Diabetologia
, vol.42
, Issue.2
, pp. 139-145
-
-
Poulsen, P.1
Kyvik, K.O.2
Vaag, A.3
Beck-Nielsen, H.4
-
12
-
-
70849098773
-
Pathomechanisms of type 2 diabetes genes
-
Staiger H, Machicao F, Fritsche A, Haring HU. Pathomechanisms of type 2 diabetes genes. Endocr Rev 2009. 30(6):557-585.
-
(2009)
Endocr Rev
, vol.30
, Issue.6
, pp. 557-585
-
-
Staiger, H.1
Machicao, F.2
Fritsche, A.3
Haring, H.U.4
-
13
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 2007. 447(7145):661-678.
-
(2007)
Nature
, vol.447
, Issue.7145
, pp. 661-678
-
-
-
14
-
-
34249888775
-
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
-
Saxena R, Voight BF, Lyssenko V, Burtt NP, de Bakker PI, Chen H, Roix JJ, Kathiresan S, Hirschhorn JN, Daly MJ, et al. Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science 2007. 316(5829):1331-1336.
-
(2007)
Science
, vol.316
, Issue.5829
, pp. 1331-1336
-
-
Saxena, R.1
Voight, B.F.2
Lyssenko, V.3
Burtt, N.P.4
de Bakker, P.I.5
Chen, H.6
Roix, J.J.7
Kathiresan, S.8
Hirschhorn, J.N.9
Daly, M.J.10
-
15
-
-
34249885875
-
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants
-
Scott LJ, Mohlke KL, Bonnycastle LL, Willer CJ, Li Y, Duren WL, Erdos MR, Stringham HM, Chines PS, Jackson AU, et al. A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science 2007. 316(5829):1341-1345.
-
(2007)
Science
, vol.316
, Issue.5829
, pp. 1341-1345
-
-
Scott, L.J.1
Mohlke, K.L.2
Bonnycastle, L.L.3
Willer, C.J.4
Li, Y.5
Duren, W.L.6
Erdos, M.R.7
Stringham, H.M.8
Chines, P.S.9
Jackson, A.U.10
-
16
-
-
33847176604
-
A genome-wide association study identifies novel risk loci for type 2 diabetes
-
Sladek R, Rocheleau G, Rung J, Dina C, Shen L, Serre D, Boutin P, Vincent D, Belisle A, Hadjadj S, et al. A genome-wide association study identifies novel risk loci for type 2 diabetes. Nature 2007. 445(7130):881-885.
-
(2007)
Nature
, vol.445
, Issue.7130
, pp. 881-885
-
-
Sladek, R.1
Rocheleau, G.2
Rung, J.3
Dina, C.4
Shen, L.5
Serre, D.6
Boutin, P.7
Vincent, D.8
Belisle, A.9
Hadjadj, S.10
-
17
-
-
34249828965
-
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes
-
Steinthorsdottir V, Thorleifsson G, Reynisdottir I, Benediktsson R, Jonsdottir T, Walters GB, Styrkarsdottir U, Gretarsdottir S, Emilsson V, Ghosh S, et al. A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. Nat Genet 2007. 39(6):770-775.
-
(2007)
Nat Genet
, vol.39
, Issue.6
, pp. 770-775
-
-
Steinthorsdottir, V.1
Thorleifsson, G.2
Reynisdottir, I.3
Benediktsson, R.4
Jonsdottir, T.5
Walters, G.B.6
Styrkarsdottir, U.7
Gretarsdottir, S.8
Emilsson, V.9
Ghosh, S.10
-
18
-
-
42349106044
-
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
-
Zeggini E, Scott LJ, Saxena R, Voight BF, Marchini JL, Hu T, de Bakker PI, Abecasis GR, Almgren P, Andersen G, et al. Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nat Genet 2008. 40(5):638-645.
-
(2008)
Nat Genet
, vol.40
, Issue.5
, pp. 638-645
-
-
Zeggini, E.1
Scott, L.J.2
Saxena, R.3
Voight, B.F.4
Marchini, J.L.5
Hu, T.6
de Bakker, P.I.7
Abecasis, G.R.8
Almgren, P.9
Andersen, G.10
-
19
-
-
75749086085
-
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
-
Dupuis J, Langenberg C, Prokopenko I, Saxena R, Soranzo N, Jackson AU, Wheeler E, Glazer NL, Bouatia-Naji N, Gloyn AL, et al. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet. 42(2):105-116.
-
Nat Genet.
, vol.42
, Issue.2
, pp. 105-116
-
-
Dupuis, J.1
Langenberg, C.2
Prokopenko, I.3
Saxena, R.4
Soranzo, N.5
Jackson, A.U.6
Wheeler, E.7
Glazer, N.L.8
Bouatia-Naji, N.9
Gloyn, A.L.10
-
20
-
-
77958481810
-
Genetics of diabetes complications
-
Doria A. Genetics of diabetes complications. Curr Diab Rep 2010. 10(6):467-475.
-
(2010)
Curr Diab Rep
, vol.10
, Issue.6
, pp. 467-475
-
-
Doria, A.1
-
21
-
-
34249996115
-
A common allele on chromosome 9 associated with coronary heart disease
-
McPherson R, Pertsemlidis A, Kavaslar N, Stewart A, Roberts R, Cox DR, Hinds DA, Pennacchio LA, Tybjaerg-Hansen A, Folsom AR, et al. A common allele on chromosome 9 associated with coronary heart disease. Science 2007. 316(5830):1488-1491.
-
(2007)
Science
, vol.316
, Issue.5830
, pp. 1488-1491
-
-
McPherson, R.1
Pertsemlidis, A.2
Kavaslar, N.3
Stewart, A.4
Roberts, R.5
Cox, D.R.6
Hinds, D.A.7
Pennacchio, L.A.8
Tybjaerg-Hansen, A.9
Folsom, A.R.10
-
22
-
-
40549109924
-
Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p
-
Broadbent HM, Peden JF, Lorkowski S, Goel A, Ongen H, Green F, Clarke R, Collins R, Franzosi MG, Tognoni G, et al. Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p. Hum Mol Genet 2008. 17(6):806-814.
-
(2008)
Hum Mol Genet
, vol.17
, Issue.6
, pp. 806-814
-
-
Broadbent, H.M.1
Peden, J.F.2
Lorkowski, S.3
Goel, A.4
Ongen, H.5
Green, F.6
Clarke, R.7
Collins, R.8
Franzosi, M.G.9
Tognoni, G.10
-
23
-
-
61349177857
-
New susceptibility locus for coronary artery disease on chromosome 3q22.3
-
Erdmann J, Grosshennig A, Braund PS, Konig IR, Hengstenberg C, Hall AS, Linsel-Nitschke P, Kathiresan S, Wright B, Tregouet DA, et al. New susceptibility locus for coronary artery disease on chromosome 3q22.3. Nat Genet 2009. 41(3):280-282.
-
(2009)
Nat Genet
, vol.41
, Issue.3
, pp. 280-282
-
-
Erdmann, J.1
Grosshennig, A.2
Braund, P.S.3
Konig, I.R.4
Hengstenberg, C.5
Hall, A.S.6
Linsel-Nitschke, P.7
Kathiresan, S.8
Wright, B.9
Tregouet, D.A.10
-
24
-
-
70749096913
-
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
-
Kathiresan S, Voight BF, Purcell S, Musunuru K, Ardissino D, Mannucci PM, Anand S, Engert JC, Samani NJ, Schunkert H, et al. Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet 2009. 41(3):334-341.
-
(2009)
Nat Genet
, vol.41
, Issue.3
, pp. 334-341
-
-
Kathiresan, S.1
Voight, B.F.2
Purcell, S.3
Musunuru, K.4
Ardissino, D.5
Mannucci, P.M.6
Anand, S.7
Engert, J.C.8
Samani, N.J.9
Schunkert, H.10
-
25
-
-
34547623750
-
Genomewide association analysis of coronary artery disease
-
Samani NJ, Erdmann J, Hall AS, Hengstenberg C, Mangino M, Mayer B, Dixon RJ, Meitinger T, Braund P, Wichmann HE, et al. Genomewide association analysis of coronary artery disease. N Engl J Med 2007. 357(5):443-453.
-
(2007)
N Engl J Med
, vol.357
, Issue.5
, pp. 443-453
-
-
Samani, N.J.1
Erdmann, J.2
Hall, A.S.3
Hengstenberg, C.4
Mangino, M.5
Mayer, B.6
Dixon, R.J.7
Meitinger, T.8
Braund, P.9
Wichmann, H.E.10
-
26
-
-
61349137526
-
Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease
-
Tregouet DA, Konig IR, Erdmann J, Munteanu A, Braund PS, Hall AS, Grosshennig A, Linsel-Nitschke P, Perret C, DeSuremain M, et al. Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. Nat Genet 2009. 41(3):283-285.
-
(2009)
Nat Genet
, vol.41
, Issue.3
, pp. 283-285
-
-
Tregouet, D.A.1
Konig, I.R.2
Erdmann, J.3
Munteanu, A.4
Braund, P.S.5
Hall, A.S.6
Grosshennig, A.7
Linsel-Nitschke, P.8
Perret, C.9
DeSuremain, M.10
-
27
-
-
79960135936
-
Review of the Diabetes Heart Study (DHS) family of studies: A comprehensively examined sample for genetic and epidemiological studies of type 2 diabetes and its complications
-
Bowden DW, Cox AJ, Freedman BI, Hugenschimdt CE, Wagenknecht LE, Herrington D, Agarwal S, Register TD, Maldjian JA, Ng MC, et al. Review of the Diabetes Heart Study (DHS) family of studies: a comprehensively examined sample for genetic and epidemiological studies of type 2 diabetes and its complications. Rev Diabet Stud 2010. 7(3):188-201.
-
(2010)
Rev Diabet Stud
, vol.7
, Issue.3
, pp. 188-201
-
-
Bowden, D.W.1
Cox, A.J.2
Freedman, B.I.3
Hugenschimdt, C.E.4
Wagenknecht, L.E.5
Herrington, D.6
Agarwal, S.7
Register, T.D.8
Maldjian, J.A.9
Ng, M.C.10
-
28
-
-
0036310779
-
Heritability of carotid artery intima-medial thickness in type 2 diabetes
-
Lange LA, Bowden DW, Langefeld CD, Wagenknecht LE, Carr JJ, Rich SS, Riley WA, Freedman BI. Heritability of carotid artery intima-medial thickness in type 2 diabetes. Stroke 2002. 33(7):1876-1881.
-
(2002)
Stroke
, vol.33
, Issue.7
, pp. 1876-1881
-
-
Lange, L.A.1
Bowden, D.W.2
Langefeld, C.D.3
Wagenknecht, L.E.4
Carr, J.J.5
Rich, S.S.6
Riley, W.A.7
Freedman, B.I.8
-
29
-
-
0035078831
-
Familial aggregation of coronary artery calcium in families with type 2 diabetes
-
Wagenknecht LE, Bowden DW, Carr JJ, Langefeld CD, Freedman BI, Rich SS. Familial aggregation of coronary artery calcium in families with type 2 diabetes. Diabetes 2001. 50(4):861-866.
-
(2001)
Diabetes
, vol.50
, Issue.4
, pp. 861-866
-
-
Wagenknecht, L.E.1
Bowden, D.W.2
Carr, J.J.3
Langefeld, C.D.4
Freedman, B.I.5
Rich, S.S.6
-
30
-
-
34250010480
-
A common variant on chromosome 9p21 affects the risk of myocardial infarction
-
Helgadottir A, Thorleifsson G, Manolescu A, Gretarsdottir S, Blondal T, Jonasdottir A, Sigurdsson A, Baker A, Palsson A, Masson G, et al. A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science 2007. 316(5830):1491-1493.
-
(2007)
Science
, vol.316
, Issue.5830
, pp. 1491-1493
-
-
Helgadottir, A.1
Thorleifsson, G.2
Manolescu, A.3
Gretarsdottir, S.4
Blondal, T.5
Jonasdottir, A.6
Sigurdsson, A.7
Baker, A.8
Palsson, A.9
Masson, G.10
-
31
-
-
57049150338
-
Interaction between poor glycemic control and 9p21 locus on risk of coronary artery disease in type 2 diabetes
-
Doria A, Wojcik J, Xu R, Gervino EV, Hauser TH, Johnstone MT, Nolan D, Hu FB, Warram JH. Interaction between poor glycemic control and 9p21 locus on risk of coronary artery disease in type 2 diabetes. JAMA 2008; 300(20):2389-2397.
-
(2008)
JAMA
, vol.300
, Issue.20
, pp. 2389-2397
-
-
Doria, A.1
Wojcik, J.2
Xu, R.3
Gervino, E.V.4
Hauser, T.H.5
Johnstone, M.T.6
Nolan, D.7
Hu, F.B.8
Warram, J.H.9
-
32
-
-
18844432308
-
Adiponectin and adiponectin receptors
-
Kadowaki T, Yamauchi T. Adiponectin and adiponectin receptors. Endocr Rev 2005. 26(3):439-451.
-
(2005)
Endocr Rev
, vol.26
, Issue.3
, pp. 439-451
-
-
Kadowaki, T.1
Yamauchi, T.2
-
33
-
-
33745312587
-
Adiponectin genetic variability, plasma adiponectin, and cardiovascular risk in patients with type 2 diabetes
-
Qi L, Doria A, Manson JE, Meigs JB, Hunter D, Mantzoros CS, Hu FB. Adiponectin genetic variability, plasma adiponectin, and cardiovascular risk in patients with type 2 diabetes. Diabetes 2006. 55(5):1512-1516.
-
(2006)
Diabetes
, vol.55
, Issue.5
, pp. 1512-1516
-
-
Qi, L.1
Doria, A.2
Manson, J.E.3
Meigs, J.B.4
Hunter, D.5
Mantzoros, C.S.6
Hu, F.B.7
-
34
-
-
33750850125
-
Common haplotypes at the adiponectin receptor 1 (ADIPOR1) locus are associated with increased risk of coronary artery disease in type 2 diabetes
-
Soccio T, Zhang YY, Bacci S, Mlynarski W, Placha G, Raggio G, Di Paola R, Marucci A, Johnstone MT, Gervino EV, et al. Common haplotypes at the adiponectin receptor 1 (ADIPOR1) locus are associated with increased risk of coronary artery disease in type 2 diabetes. Diabetes 2006. 55(10):2763-2770.
-
(2006)
Diabetes
, vol.55
, Issue.10
, pp. 2763-2770
-
-
Soccio, T.1
Zhang, Y.Y.2
Bacci, S.3
Mlynarski, W.4
Placha, G.5
Raggio, G.6
di Paola, R.7
Marucci, A.8
Johnstone, M.T.9
Gervino, E.V.10
-
35
-
-
66249126304
-
Association between the adiponectin promoter rs266729 gene variant and oxidative stress in patients with diabetes mellitus
-
Prior SL, Gable DR, Cooper JA, Bain SC, Hurel SJ, Humphries SE, Stephens JW. Association between the adiponectin promoter rs266729 gene variant and oxidative stress in patients with diabetes mellitus. Eur Heart J 2009. 30(10):1263-1269.
-
(2009)
Eur Heart J
, vol.30
, Issue.10
, pp. 1263-1269
-
-
Prior, S.L.1
Gable, D.R.2
Cooper, J.A.3
Bain, S.C.4
Hurel, S.J.5
Humphries, S.E.6
Stephens, J.W.7
-
36
-
-
77957756358
-
Association between the rs4880 superoxide dismutase 2 (C>T) gene variant and coronary heart disease in diabetes mellitus
-
Jones DA, Prior SL, Tang TS, Bain SC, Hurel SJ, Humphries SE, Stephens JW. Association between the rs4880 superoxide dismutase 2 (C>T) gene variant and coronary heart disease in diabetes mellitus. Diabetes Res Clin Pract 2010. 90(2):196-201.
-
(2010)
Diabetes Res Clin Pract
, vol.90
, Issue.2
, pp. 196-201
-
-
Jones, D.A.1
Prior, S.L.2
Tang, T.S.3
Bain, S.C.4
Hurel, S.J.5
Humphries, S.E.6
Stephens, J.W.7
-
37
-
-
77955981820
-
Coronary artery calcification and its relationship to validated genetic variants for diabetes mellitus assessed in the Heinz Nixdorf recall cohort
-
Pechlivanis S, Scherag A, Muhleisen TW, Mohlenkamp S, Horsthemke B, Boes T, Brocker-Preuss M, Mann K, Erbel R, Jockel KH, Nothen MM, Moebus S. Coronary artery calcification and its relationship to validated genetic variants for diabetes mellitus assessed in the Heinz Nixdorf recall cohort. Arterioscler Thromb Vasc Biol. 30(9):1867-1872.
-
Arterioscler Thromb Vasc Biol.
, vol.30
, Issue.9
, pp. 1867-1872
-
-
Pechlivanis, S.1
Scherag, A.2
Muhleisen, T.W.3
Mohlenkamp, S.4
Horsthemke, B.5
Boes, T.6
Brocker-Preuss, M.7
Mann, K.8
Erbel, R.9
Jockel, K.H.10
Nothen, M.M.11
Moebus, S.12
-
38
-
-
54049144285
-
New gene variants alter type 2 diabetes risk predominantly through reduced beta-cell function
-
Perry JR, Frayling TM. New gene variants alter type 2 diabetes risk predominantly through reduced beta-cell function. Curr Opin Clin Nutr Metab Care 2008. 11(4):371-377.
-
(2008)
Curr Opin Clin Nutr Metab Care
, vol.11
, Issue.4
, pp. 371-377
-
-
Perry, J.R.1
Frayling, T.M.2
-
39
-
-
43049135122
-
TCF7L2 single nucleotide polymorphisms, cardiovascular disease and all-cause mortality: The Atherosclerosis Risk in Communities (ARIC) study
-
Bielinski SJ, Pankow JS, Folsom AR, North KE, Boerwinkle E. TCF7L2 single nucleotide polymorphisms, cardiovascular disease and all-cause mortality: the Atherosclerosis Risk in Communities (ARIC) study. Diabetologia 2008. 51(6):968-970.
-
(2008)
Diabetologia
, vol.51
, Issue.6
, pp. 968-970
-
-
Bielinski, S.J.1
Pankow, J.S.2
Folsom, A.R.3
North, K.E.4
Boerwinkle, E.5
-
40
-
-
70849088083
-
TCF7L2 polymorphism rs7903146 is associated with coronary artery disease severity and mortality
-
Sousa AG, Marquezine GF, Lemos PA, Martinez E, Lopes N, Hueb WA, Krieger JE, Pereira AC. TCF7L2 polymorphism rs7903146 is associated with coronary artery disease severity and mortality. PLoS One 2009. 4(11):e7697.
-
(2009)
PLoS One
, vol.4
, Issue.11
-
-
Sousa, A.G.1
Marquezine, G.F.2
Lemos, P.A.3
Martinez, E.4
Lopes, N.5
Hueb, W.A.6
Krieger, J.E.7
Pereira, A.C.8
-
41
-
-
79952662422
-
Single nucleotide polymorphisms of TCF7L2 are linked to diabetic coronary atherosclerosis
-
Muendlein A, Saely CH, Geller-Rhomberg S, Sonderegger G, Rein P, Winder T, Beer S, Vonbank A, Drexel H. Single nucleotide polymorphisms of TCF7L2 are linked to diabetic coronary atherosclerosis. PLoS One 2011. 6(3):e17978.
-
(2011)
PLoS One
, vol.6
, Issue.3
-
-
Muendlein, A.1
Saely, C.H.2
Geller-Rhomberg, S.3
Sonderegger, G.4
Rein, P.5
Winder, T.6
Beer, S.7
Vonbank, A.8
Drexel, H.9
-
42
-
-
79251650372
-
Genetic variants of diabetes risk and incident cardiovascular events in chronic coronary artery disease
-
Sousa AG, Lopes NH, Hueb WA, Krieger JE, Pereira AC. Genetic variants of diabetes risk and incident cardiovascular events in chronic coronary artery disease. PLoS One 2011. 6(1):e16341.
-
(2011)
PLoS One
, vol.6
, Issue.1
-
-
Sousa, A.G.1
Lopes, N.H.2
Hueb, W.A.3
Krieger, J.E.4
Pereira, A.C.5
-
43
-
-
83455258866
-
Role of BMI in the Association of the TCF7L2 rs7903146 Variant with Coronary Heart Disease: The Atherosclerosis Risk in Communities (ARIC) Study
-
Kucharska-Newton AM, Monda KL, Bielinski SJ, Boerwinkle E, Rea TD, Rosamond WD, Pankow JS, Kottgen A, Heiss G, North KE. Role of BMI in the Association of the TCF7L2 rs7903146 Variant with Coronary Heart Disease: The Atherosclerosis Risk in Communities (ARIC) Study. J Obes 2010. 2010: 651903.
-
(2010)
J Obes
, vol.2010
, pp. 651903
-
-
Kucharska-Newton, A.M.1
Monda, K.L.2
Bielinski, S.J.3
Boerwinkle, E.4
Rea, T.D.5
Rosamond, W.D.6
Pankow, J.S.7
Kottgen, A.8
Heiss, G.9
North, K.E.10
-
44
-
-
0037155050
-
A role for the beta-catenin/T-cell factor signaling cascade in vascular remodeling
-
Wang X, Xiao Y, Mou Y, Zhao Y, Blankesteijn WM, Hall JL. A role for the beta-catenin/T-cell factor signaling cascade in vascular remodeling. Circ Res 2002. 90(3):340-347.
-
(2002)
Circ Res
, vol.90
, Issue.3
, pp. 340-347
-
-
Wang, X.1
Xiao, Y.2
Mou, Y.3
Zhao, Y.4
Blankesteijn, W.M.5
Hall, J.L.6
-
45
-
-
78650818584
-
Pleiotropic effects of TCF7L2 gene variants and its modulation in the metabolic syndrome: From the LIPGENE study
-
Delgado-Lista J, Perez-Martinez P, Garcia-Rios A, Phillips CM, Williams CM, Gulseth HL, Helal O, Blaak EE, Kiec-Wilk B, Basu S, et al. Pleiotropic effects of TCF7L2 gene variants and its modulation in the metabolic syndrome: from the LIPGENE study. Atherosclerosis 2011. 214(1):110-116.
-
(2011)
Atherosclerosis
, vol.214
, Issue.1
, pp. 110-116
-
-
Delgado-Lista, J.1
Perez-Martinez, P.2
Garcia-Rios, A.3
Phillips, C.M.4
Williams, C.M.5
Gulseth, H.L.6
Helal, O.7
Blaak, E.E.8
Kiec-Wilk, B.9
Basu, S.10
-
46
-
-
78549272005
-
Potential role of TCF7L2 gene variants on cardiac sympathetic/parasympathetic activity
-
Boccardi V, Ambrosino I, Papa M, Fiore D, Rizzo MR, Paolisso G, Barbieri M. Potential role of TCF7L2 gene variants on cardiac sympathetic/parasympathetic activity. Eur J Hum Genet 2010. 18(12):1333-1338.
-
(2010)
Eur J Hum Genet
, vol.18
, Issue.12
, pp. 1333-1338
-
-
Boccardi, V.1
Ambrosino, I.2
Papa, M.3
Fiore, D.4
Rizzo, M.R.5
Paolisso, G.6
Barbieri, M.7
-
47
-
-
77958498526
-
From genetic association to molecular mechanism
-
van de Bunt M, Gloyn AL. From genetic association to molecular mechanism. Curr Diab Rep 2010. 10(6):452-466.
-
(2010)
Curr Diab Rep
, vol.10
, Issue.6
, pp. 452-466
-
-
van de Bunt, M.1
Gloyn, A.L.2
-
48
-
-
77951858557
-
Detailed physiologic characterization reveals diverse mechanisms for novel genetic Loci regulating glucose and insulin metabolism in humans
-
Ingelsson E, Langenberg C, Hivert MF, Prokopenko I, Lyssenko V, Dupuis J, Magi R, Sharp S, Jackson AU, Assimes TL, et al. Detailed physiologic characterization reveals diverse mechanisms for novel genetic Loci regulating glucose and insulin metabolism in humans. Diabetes 2010. 59(5):1266-1275.
-
(2010)
Diabetes
, vol.59
, Issue.5
, pp. 1266-1275
-
-
Ingelsson, E.1
Langenberg, C.2
Hivert, M.F.3
Prokopenko, I.4
Lyssenko, V.5
Dupuis, J.6
Magi, R.7
Sharp, S.8
Jackson, A.U.9
Assimes, T.L.10
-
49
-
-
77952888454
-
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci
-
Stahl EA, Raychaudhuri S, Remmers EF, Xie G, Eyre S, Thomson BP, Li Y, Kurreeman FA, Zhernakova A, Hinks A, et al. Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. Nat Genet 2010. 42(6):508-514.
-
(2010)
Nat Genet
, vol.42
, Issue.6
, pp. 508-514
-
-
Stahl, E.A.1
Raychaudhuri, S.2
Remmers, E.F.3
Xie, G.4
Eyre, S.5
Thomson, B.P.6
Li, Y.7
Kurreeman, F.A.8
Zhernakova, A.9
Hinks, A.10
-
50
-
-
79955841697
-
Evaluating the heritability explained by known susceptibility variants: A survey of ten complex diseases
-
So HC, Gui AH, Cherny SS, Sham PC. Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases. Genet Epidemiol 2011. 35(5):310-317.
-
(2011)
Genet Epidemiol
, vol.35
, Issue.5
, pp. 310-317
-
-
So, H.C.1
Gui, A.H.2
Cherny, S.S.3
Sham, P.C.4
-
51
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, McCarthy MI, Ramos EM, Cardon LR, Chakravarti A, et al. Finding the missing heritability of complex diseases. Nature 2009. 461(7265):747-753.
-
(2009)
Nature
, vol.461
, Issue.7265
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
Goldstein, D.B.4
Hindorff, L.A.5
Hunter, D.J.6
McCarthy, M.I.7
Ramos, E.M.8
Cardon, L.R.9
Chakravarti, A.10
-
52
-
-
79952795269
-
Diabetes mellitus, a microRNA-related disease?
-
Guay C, Roggli E, Nesca V, Jacovetti C, Regazzi R. Diabetes mellitus, a microRNA-related disease? Transl Res 2011. 157(4):253-264.
-
(2011)
Transl Res
, vol.157
, Issue.4
, pp. 253-264
-
-
Guay, C.1
Roggli, E.2
Nesca, V.3
Jacovetti, C.4
Regazzi, R.5
-
53
-
-
77950624912
-
Epigenetic mechanisms in the development of type 2 diabetes
-
Pinney SE, Simmons RA. Epigenetic mechanisms in the development of type 2 diabetes. Trends Endocrinol Metab 2010. 21(4):223-229.
-
(2010)
Trends Endocrinol Metab
, vol.21
, Issue.4
, pp. 223-229
-
-
Pinney, S.E.1
Simmons, R.A.2
-
54
-
-
79957487252
-
Epigenetic mechanisms in diabetic vascular complications
-
Reddy MA, Natarajan R. Epigenetic mechanisms in diabetic vascular complications. Cardiovasc Res 2011. 90(3):421-429.
-
(2011)
Cardiovasc Res
, vol.90
, Issue.3
, pp. 421-429
-
-
Reddy, M.A.1
Natarajan, R.2
-
55
-
-
29144453326
-
Intensive diabetes treatment and cardiovascular disease in patients with type 1 diabetes
-
Nathan DM, Cleary PA, Backlund JY, Genuth SM, Lachin JM, Orchard TJ, Raskin P, Zinman B. Intensive diabetes treatment and cardiovascular disease in patients with type 1 diabetes. N Engl J Med 2005. 353(25):2643-2653.
-
(2005)
N Engl J Med
, vol.353
, Issue.25
, pp. 2643-2653
-
-
Nathan, D.M.1
Cleary, P.A.2
Backlund, J.Y.3
Genuth, S.M.4
Lachin, J.M.5
Orchard, T.J.6
Raskin, P.7
Zinman, B.8
-
56
-
-
34247145010
-
Impact of inflammation on epigenetic DNA methylation-a novel risk factor for cardiovascular disease?
-
Stenvinkel P, Karimi M, Johansson S, Axelsson J, Suliman M, Lindholm B, Heimburger O, Barany P, Alvestrand A, Nordfors L, et al. Impact of inflammation on epigenetic DNA methylation-a novel risk factor for cardiovascular disease? J Intern Med 2007. 261(5):488-499.
-
(2007)
J Intern Med
, vol.261
, Issue.5
, pp. 488-499
-
-
Stenvinkel, P.1
Karimi, M.2
Johansson, S.3
Axelsson, J.4
Suliman, M.5
Lindholm, B.6
Heimburger, O.7
Barany, P.8
Alvestrand, A.9
Nordfors, L.10
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