-
1
-
-
79952781248
-
-
Health at a Glance: Europe 2012. OECD Publishing; 2012. doi: 10.1787/9789264183896-en Available: http://www.oecd-ilibrary.org/social-issues-migration-health/health-at-a-glance-europe-2012-9789264183896-en.
-
(2012)
OECD Publishing 2012
-
-
Health at a Glance: Europe1
-
2
-
-
0031848442
-
Cloning of the promoters for the beta-cell ATP-sensitive K-channel subunits Kir6.2 and SUR1
-
PMID: 9703328
-
Ashfield R, Ashcroft SJ. Cloning of the promoters for the beta-cell ATP-sensitive K-channel subunits Kir6.2 and SUR1. Diabetes. 1998; 47: 1274-1280. PMID: 9703328
-
(1998)
Diabetes
, vol.47
, pp. 1274-1280
-
-
Ashfield, R.1
Ashcroft, S.J.2
-
3
-
-
0030996141
-
Association and stoichiometry of K(ATP) channel subunits
-
PMID: 9182806
-
Clement JP, Kunjilwar K, Gonzalez G, Schwanstecher M, Panten U, Aguilar-Bryan L, et al. Association and stoichiometry of K(ATP) channel subunits. Neuron. 1997; 18: 827-838. PMID: 9182806
-
(1997)
Neuron.
, vol.18
, pp. 827-838
-
-
Clement, J.P.1
Kunjilwar, K.2
Gonzalez, G.3
Schwanstecher, M.4
Panten, U.5
Aguilar-Bryan, L.6
-
4
-
-
0029021696
-
Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy
-
PMID: 7716548
-
Thomas PM, Cote GJ, Wohllk N, Haddad B, Mathew PM, Rabl W, et al. Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy. Science. 1995; 268: 426-429. PMID: 7716548
-
(1995)
Science
, vol.268
, pp. 426-429
-
-
Thomas, P.M.1
Cote, G.J.2
Wohllk, N.3
Haddad, B.4
Mathew, P.M.5
Rabl, W.6
-
5
-
-
0029836983
-
Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy
-
PMID: 8923010
-
Thomas P, Ye Y, Lightner E. Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy. Hum Mol Genet. 1996; 5: 1809-1812. PMID: 8923010
-
(1996)
Hum Mol Genet.
, vol.5
, pp. 1809-1812
-
-
Thomas, P.1
Ye, Y.2
Lightner, E.3
-
6
-
-
0036314298
-
KIR6.2 polymorphism predisposes to type 2 diabetes by inducing overactivity of pancreatic-cell ATP-sensitive K+ channels
-
PMID: 11872696
-
Schwanstecher C, Meyer U, Schwanstecher M. KIR6.2 Polymorphism Predisposes to Type 2 Diabetes by Inducing Overactivity of Pancreatic-Cell ATP-Sensitive K+ Channels. Diabetes. 2002; 51: 875-879. doi: 10.2337/diabetes.51.3.875 PMID: 11872696
-
(2002)
Diabetes
, vol.51
, pp. 875-879
-
-
Schwanstecher, C.1
Meyer, U.2
Schwanstecher, M.3
-
7
-
-
79952022272
-
Gene-gene interactions lead to higher risk for development of type 2 diabetes in an Ashkenazi Jewish population
-
PMID: 20361036
-
Neuman RJ, Wasson J, Atzmon G, Wainstein J, Yerushalmi Y, Cohen J, et al. Gene-gene interactions lead to higher risk for development of type 2 diabetes in an Ashkenazi Jewish population. PLoS One. 2010; 5: e9903. doi: 10.1371/journal.pone.0009903 PMID: 20361036
-
(2010)
PLoS One
, vol.5
, pp. e9903
-
-
Neuman, R.J.1
Wasson, J.2
Atzmon, G.3
Wainstein, J.4
Yerushalmi, Y.5
Cohen, J.6
-
8
-
-
84865325543
-
Genetic variants in potassium channels are associated with type 2 diabetes in a Mongolian population
-
PMID: 22151254
-
Odgerel Z, Lee HS, Erdenebileg N, Gandbold S, Luvsanjamba M, Sambuuqhin N, et al. Genetic variants in potassium channels are associated with type 2 diabetes in a Mongolian population. J Diabetes. 2012; 4: 238-242. doi: 10.1111/j.1753-0407.2011.00177.x PMID: 22151254
-
(2012)
J Diabetes
, vol.4
, pp. 238-242
-
-
Odgerel, Z.1
Lee, H.S.2
Erdenebileg, N.3
Gandbold, S.4
Luvsanjamba, M.5
Sambuuqhin, N.6
-
9
-
-
47749128415
-
Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala) IGF2BP2 TCF7L2 and FTO variants confer a significant risk
-
PMID: 18598350
-
Sanghera DK, Ortega L, Han S, Singh J, Ralhan SK, Wander GS, et al. Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk. BMC Med Genet. 2008; 9: 59. doi: 10.1186/1471-2350-9-59 PMID: 18598350
-
(2008)
BMC Med Genet
, vol.9
, pp. 59
-
-
Sanghera, D.K.1
Ortega, L.2
Han, S.3
Singh, J.4
Ralhan, S.K.5
Wander, G.S.6
-
10
-
-
80155133645
-
Association of variants in genes involved in pancreatic β-cell development and function with type 2 diabetes in North Indians
-
PMID: 21814221
-
Chavali S, Mahajan A, Tabassum R, Dwivedi OP, Chauhan G, Ghosh S, et al. Association of variants in genes involved in pancreatic β-cell development and function with type 2 diabetes in North Indians. J Hum Genet. 2011; 56: 695-700. doi: 10.1038/jhg.2011.83 PMID: 21814221
-
(2011)
J Hum Genet
, vol.56
, pp. 695-700
-
-
Chavali, S.1
Mahajan, A.2
Tabassum, R.3
Dwivedi, O.P.4
Chauhan, G.5
Ghosh, S.6
-
11
-
-
70349648967
-
Coexpression of the type 2 diabetes susceptibility gene variants KCNJ11 E23K and ABCC8 S1369A alter the ATP and sulfonylurea sensitivities of the ATP-sensitive K(+) channel
-
PMID: 19587354
-
Hamming KSC, Soliman D, Matemisz LC, Niazi O, Lang Y, Gloyn AL, et al. Coexpression of the type 2 diabetes susceptibility gene variants KCNJ11 E23K and ABCC8 S1369A alter the ATP and sulfonylurea sensitivities of the ATP-sensitive K(+) channel. Diabetes. 2009; 58: 2419-2424. doi: 10.2337/db09-0143 PMID: 19587354
-
(2009)
Diabetes
, vol.58
, pp. 2419-2424
-
-
Ksc, H.1
Soliman, D.2
Matemisz, L.C.3
Niazi, O.4
Lang, Y.5
Gloyn, A.L.6
-
12
-
-
59449083573
-
Genetic variations in the pancreatic ATP-sensitive potassium channel, beta-cell dysfunction, and susceptibility to type 2 diabetes
-
PMID: 18758683
-
Chistiakov DA, Potapov VA, Khodirev DC, Shamkhalova MS, Shestakova MV, Nosikov VV.Genetic variations in the pancreatic ATP-sensitive potassium channel, beta-cell dysfunction, and susceptibility to type 2 diabetes. Acta Diabetol. 2009; 46: 43-49. doi: 10.1007/s00592-008-0056-5 PMID: 18758683
-
(2009)
Acta Diabetol
, vol.46
, pp. 43-49
-
-
Chistiakov, D.A.1
Potapov, V.A.2
Khodirev, D.C.3
Shamkhalova, M.S.4
Shestakova, M.V.5
Nosikov, V.V.6
-
13
-
-
0031851293
-
Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: Diagnosis and classification of diabetes mellitus provisional report of a WHO consultation
-
PMID: 9686693
-
Alberti KG, Zimmet PZ (1998) Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: diagnosis and classification of diabetes mellitus provisional report of a WHO consultation. Diabet Med 15: 539-553. PMID: 9686693
-
(1998)
Diabet Med
, vol.15
, pp. 539-553
-
-
Alberti, K.G.1
Zimmet, P.Z.2
-
14
-
-
15144338831
-
Sequence variants in the pancreatic islet beta-cell inwardly rectifying K+ channel Kir6.2 (Bir) gene: Identification and lack of role in Caucasian patients with NIDDM
-
PMID: 9032109
-
Inoue H, Ferrer J, Warren-Perry M, Zhang Y, Millns H, Turner RC, et al. Sequence variants in the pancreatic islet beta-cell inwardly rectifying K+ channel Kir6.2 (Bir) gene: identification and lack of role in Caucasian patients with NIDDM. Diabetes. 1997; 46: 502-507. PMID: 9032109
-
(1997)
Diabetes
, vol.46
, pp. 502-507
-
-
Inoue, H.1
Ferrer, J.2
Warren-Perry, M.3
Zhang, Y.4
Millns, H.5
Turner, R.C.6
-
15
-
-
75849160547
-
Replication of association between polymorphisms of the pancreatic ATP-sensitive potassium channel and susceptibility to type 2 diabetes in two Russian urban populations
-
Chistiakov D a, Potapov V a, Khodirev DS, Shamkhalova MS, Shestakova MV, Nosikov VV Replication of association between polymorphisms of the pancreatic ATP-sensitive potassium channel and susceptibility to type 2 diabetes in two Russian urban populations. Cent Eur J Biol. 2009; 5: 67-77.
-
(2009)
Cent Eur J Biol.
, vol.5
, pp. 67-77
-
-
Chistiakov, D.1
Potapov, V.2
Khodirev, D.S.3
Shamkhalova, M.S.4
Shestakova, M.V.5
Nosikov, V.V.6
-
16
-
-
33846608291
-
Polymorphisms of KCNJ11 (Kir6.2 gene) are associated with Type 2 diabetes and hypertension in the Korean population
-
PMID: 17257281
-
Koo BK, Cho YM, Park BL, Cheong HS, Shin HD, Jang HC, et al. Polymorphisms of KCNJ11 (Kir6.2 gene) are associated with Type 2 diabetes and hypertension in the Korean population. Diabet Med. 2007; 24: 178-186. PMID: 17257281
-
(2007)
Diabet Med.
, vol.24
, pp. 178-186
-
-
Koo, B.K.1
Cho, Y.M.2
Park, B.L.3
Cheong, H.S.4
Shin, H.D.5
Jang, H.C.6
-
17
-
-
34948819195
-
Variants of the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in an African-American population enriched for nephropathy
-
PMID: 17601994
-
Sale MM, Smith SG, Mychaleckyj JC, Keene KL, Langefeld CD, Leak TC, et al. Variants of the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in an African-American population enriched for nephropathy. Diabetes. 2007; 56: 2638-2642. PMID: 17601994
-
(2007)
Diabetes
, vol.56
, pp. 2638-2642
-
-
Sale, M.M.1
Smith, S.G.2
Mychaleckyj, J.C.3
Keene, K.L.4
Langefeld, C.D.5
Leak, T.C.6
-
18
-
-
46949088755
-
Type 2 diabetes susceptibility loci in the Ashkenazi Jewish population
-
PMID: 18516622
-
Bronstein M, Pisanté A, Yakir B, Darvasi A. Type 2 diabetes susceptibility loci in the Ashkenazi Jewish population. Hum Genet. 2008; 124: 101-104. doi: 10.1007/s00439-008-0520-x PMID: 18516622
-
(2008)
Hum Genet
, vol.124
, pp. 101-104
-
-
Bronstein, M.1
Pisanté, A.2
Yakir, B.3
Darvasi, A.4
-
19
-
-
84882782303
-
Search of Kir6.2 transgenic in Japanese non-insulin dependent diabetes mellitus
-
Keiko K, Keiko A, Hiroto B TM. Search of Kir6.2 transgenic in Japanese non-insulin dependent diabetes mellitus. Ann Rep Kansai Coll Acupunct Med. 1999; 14: 58-61.
-
(1999)
Ann Rep Kansai Coll Acupunct Med.
, vol.14
, pp. 58-61
-
-
Keiko, K.1
Keiko, A.2
Hiroto, B.T.M.3
-
20
-
-
0029740428
-
Sequence variations in the human Kir6.2 gene, a subunit of the beta-cell ATP-sensitive K-channel: No association with NIDDM in while Caucasian subjects or evidence of abnormal function when expressed in vitro
-
PMID: 8897013
-
Sakura H, Wat N, Horton V, Millns H, Turner RC, Ashcroft FM. Sequence variations in the human Kir6.2 gene, a subunit of the beta-cell ATP-sensitive K-channel: no association with NIDDM in while Caucasian subjects or evidence of abnormal function when expressed in vitro. Diabetologia. 1996; 39: 1233-1236. PMID: 8897013
-
(1996)
Diabetologia
, vol.39
, pp. 1233-1236
-
-
Sakura, H.1
Wat, N.2
Horton, V.3
Millns, H.4
Turner, R.C.5
Ashcroft, F.M.6
-
21
-
-
0031051534
-
Amino acid polymorphisms in the ATP-regulatable inward rectifier Kir6.2 and their relationships to glucose- and tolbutamide-induced insulin secretion, the insulin sensitivity index, and NIDDM
-
PMID: 9032110
-
Hansen L, Echwald SM, Hansen T, Urhammer SA, Clausen JO, Pedersen O. Amino acid polymorphisms in the ATP-regulatable inward rectifier Kir6.2 and their relationships to glucose- and tolbutamide-induced insulin secretion, the insulin sensitivity index, and NIDDM. Diabetes. 1997; 46: 508-512. PMID: 9032110
-
(1997)
Diabetes
, vol.46
, pp. 508-512
-
-
Hansen, L.1
Echwald, S.M.2
Hansen, T.3
Urhammer, S.A.4
Clausen, J.O.5
Pedersen, O.6
-
22
-
-
0035043009
-
Association studies of variants in promoter and coding regions of beta-cell ATP-sensitive K-channel genes SUR1 and Kir6.2 with Type 2 diabetes mellitus (UKPDS 53)
-
PMID: 11318841
-
Gloyn AL, Hashim Y, Ashcroft SJ, Ashfield R, Wiltshire S, Turner RC, et al. Association studies of variants in promoter and coding regions of beta-cell ATP-sensitive K-channel genes SUR1 and Kir6.2 with Type 2 diabetes mellitus (UKPDS 53). Diabet Med. 2001; 18: 206-212. PMID: 11318841
-
(2001)
Diabet Med
, vol.18
, pp. 206-212
-
-
Gloyn, A.L.1
Hashim, Y.2
Ashcroft, S.J.3
Ashfield, R.4
Wiltshire, S.5
Turner, R.C.6
-
23
-
-
0037312864
-
The E23K variant of Kir6.2 associates with impaired post-OGTT serum insulin response and increased risk of type 2 diabetes
-
PMID: 12540638
-
Nielsen ED, Hansen L, Carstensen B, Echwald SM, Drivsholm T, Glumer C, et al. The E23K variant of Kir6.2 associates with impaired post-OGTT serum insulin response and increased risk of type 2 diabetes. Diabetes. 2003; 52: 573-577. PMID: 12540638
-
(2003)
Diabetes
, vol.52
, pp. 573-577
-
-
Nielsen, E.D.1
Hansen, L.2
Carstensen, B.3
Echwald, S.M.4
Drivsholm, T.5
Glumer, C.6
-
24
-
-
66249089500
-
Construction of a prediction model for type 2 diabetes mellitus in the Japanese population based on 11 genes with strong evidence of the association
-
PMID: 19247372
-
Miyake K, Yang W, Hara K, Yasuda K, Horikawa Y, Osawa H, et al. Construction of a prediction model for type 2 diabetes mellitus in the Japanese population based on 11 genes with strong evidence of the association. J Hum Genet.2009; 54: 236-241. doi: 10.1038/jhg.2009.17 PMID: 19247372
-
(2009)
J Hum Genet
, vol.54
, pp. 236-241
-
-
Miyake, K.1
Yang, W.2
Hara, K.3
Yasuda, K.4
Horikawa, Y.5
Osawa, H.6
-
25
-
-
35848945259
-
Variations in the HHEX gene are associated with increased risk of type 2 diabetes in the Japanese population
-
PMID: 17928989
-
Horikoshi M, Hara K, Ito C, Shojima N, Nagai R, Ueki K, et al. Variations in the HHEX gene are associated with increased risk of type 2 diabetes in the Japanese population. Diabetologia. 2007; 50: 2461-2466. PMID: 17928989
-
(2007)
Diabetologia
, vol.50
, pp. 2461-2466
-
-
Horikoshi, M.1
Hara, K.2
Ito, C.3
Shojima, N.4
Nagai, R.5
Ueki, K.6
-
26
-
-
33749351977
-
Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects
-
PMID: 16873704
-
Yokoi N, Kanamori M, Horikawa Y, Takeda J, Sanke T, Furuta H, et al. Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects. Diabetes. 2006; 55: 2379-2386. doi: 10.2337/db05-1203 PMID: 16873704
-
(2006)
Diabetes
, vol.55
, pp. 2379-2386
-
-
Yokoi, N.1
Kanamori, M.2
Horikawa, Y.3
Takeda, J.4
Sanke, T.5
Furuta, H.6
-
27
-
-
0033624575
-
The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
-
PMID: 10973253
-
Altshuler D, Hirschhorn JN, Klannemark M, Lindgren CM, Vohl MC, Nemesh J et al. The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes. Nat Genet. 2000; 26: 76-80. PMID: 10973253
-
(2000)
Nat Genet
, vol.26
, pp. 76-80
-
-
Altshuler, D.1
Hirschhorn, J.N.2
Klannemark, M.3
Lindgren, C.M.4
Vohl, M.C.5
Nemesh, J.6
-
28
-
-
0037280761
-
E23K single nucleotide polymorphism in the islet ATP-sensitive potassium channel gene (Kir6.2) contributes as much to the risk of Type II diabetes in Caucasians as the PPARgamma Pro12Ala variant
-
PMID: 12643262
-
Love-Gregory L, Wasson J, Lin J, Skolnick G, Suarez B, Permutt MA. E23K single nucleotide polymorphism in the islet ATP-sensitive potassium channel gene (Kir6.2) contributes as much to the risk of Type II diabetes in Caucasians as the PPARgamma Pro12Ala variant. Diabetologia. 2003. 46: 136-137. PMID: 12643262
-
(2003)
Diabetologia
, vol.46
, pp. 136-137
-
-
Love-Gregory, L.1
Wasson, J.2
Lin, J.3
Skolnick, G.4
Suarez, B.5
Ma, P.6
-
29
-
-
33847176604
-
A genome-wide association study identifies novel risk loci for type 2 diabetes
-
PMID: 17293876
-
Sladek R, Rocheleau G, Rung J, Dina C, Shen L, Serre D, et al. A genome-wide association study identifies novel risk loci for type 2 diabetes. Nature. 2007; 445: 881-885. PMID: 17293876
-
(2007)
Nature
, vol.445
, pp. 881-885
-
-
Sladek, R.1
Rocheleau, G.2
Rung, J.3
Dina, C.4
Shen, L.5
Serre, D.6
-
30
-
-
34249828965
-
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes
-
PMID: 17460697
-
Steinthorsdottir V, Thorleifsson G, Reynisdottir I, Benediktsson R, Jonsdottir T, Walters GB, et al. A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. Nat Genet. 2007; 39: 770-775. PMID: 17460697
-
(2007)
Nat Genet
, vol.39
, pp. 770-775
-
-
Steinthorsdottir, V.1
Thorleifsson, G.2
Reynisdottir, I.3
Benediktsson, R.4
Jonsdottir, T.5
Walters, G.B.6
-
31
-
-
34547755055
-
Type 2 diabetes wholegenome association study in four populations: The DiaGen consortium
-
PMID: 17668382
-
Salonen JT, Uimari P, Aalto J- M, Pirskanen M, Kaikkonen J, Todorova B, et al. Type 2 diabetes wholegenome association study in four populations: the DiaGen consortium. Am J Hum Genet. 2007; 81: 338-345. PMID: 17668382
-
(2007)
Am J Hum Genet
, vol.81
, pp. 338-345
-
-
Salonen, J.T.1
Uimari, P.2
Aalto, J.-M.3
Pirskanen, M.4
Kaikkonen, J.5
Todorova, B.6
-
32
-
-
36849029819
-
A search for variants associated with young-onset type 2 diabetes in American Indians in a 100K genotyping array
-
PMID: 17846125
-
Hanson RL, Bogardus C, Duggan D, Kobes S, Knowlton M, Infante AM, et al. A search for variants associated with young-onset type 2 diabetes in American Indians in a 100K genotyping array. Diabetes. 2007; 56: 3045-3052. PMID: 17846125
-
(2007)
Diabetes
, vol.56
, pp. 3045-3052
-
-
Hanson, R.L.1
Bogardus, C.2
Duggan, D.3
Kobes, S.4
Knowlton, M.5
Infante, A.M.6
-
33
-
-
36849081967
-
Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies
-
PMID: 17846124
-
Hayes MG, Pluzhnikov A, Miyake K, Sun Y, Ng MC, Roe CA, et al. Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies. Diabetes. 2007; 56: 3033-3044. PMID: 17846124
-
(2007)
Diabetes
, vol.56
, pp. 3033-3044
-
-
Hayes, M.G.1
Pluzhnikov, A.2
Miyake, K.3
Sun, Y.4
Ng, M.C.5
Roe, C.A.6
-
34
-
-
36849023376
-
Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: Evidence for replication from diabetes-related quantitative traits and from independent populations
-
PMID: 17846126
-
Rampersaud E, Damcott CM, Fu M, Shen H, McArdle P, Shi X, et al. Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations. Diabetes. 2007; 56: 3053-3062. PMID: 17846126
-
(2007)
Diabetes
, vol.56
, pp. 3053-3062
-
-
Rampersaud, E.1
Damcott, C.M.2
Fu, M.3
Shen, H.4
McArdle, P.5
Shi, X.6
-
35
-
-
77149143848
-
KCNJ11 Lys23Glu and TCF7L2 rs290487(C/T) polymorphisms affect therapeutic efficacy of repaglinide in Chinese patients with type 2 diabetes
-
PMID: 20054294
-
Yu M, Xu X-J, Yin J-Y, Wu J, Chen X, Gong ZC, et al. KCNJ11 Lys23Glu and TCF7L2 rs290487(C/T) polymorphisms affect therapeutic efficacy of repaglinide in Chinese patients with type 2 diabetes. Clin Pharmacol Ther. 2010; 87: 330-335. doi: 10.1038/clpt.2009.242 PMID: 20054294
-
(2010)
Clin Pharmacol Ther
, vol.87
, pp. 330-335
-
-
Yu, M.1
Xu, X.-J.2
Yin, J.-Y.3
Wu, J.4
Chen, X.5
Gong, Z.C.6
-
36
-
-
84898926505
-
Gender-dependent associations of CDKN2A/2B, KCNJ11, POLI, SLC30A8, and TCF7L2 variants with type 2 diabetes in (North African) Tunisian Arabs
-
PMID: 24485399
-
Turki A, Al-Zaben GS, Khirallah M, Marmouch H, Mahjoub T, Almawi WY. Gender-dependent associations of CDKN2A/2B, KCNJ11, POLI, SLC30A8, and TCF7L2 variants with type 2 diabetes in (North African) Tunisian Arabs. Diabetes Res Clin Pract. 2014; 103: e40-3. doi: 10.1016/j.diabres.2013.12.040 PMID: 24485399
-
(2014)
Diabetes Res Clin Pract
, vol.103
, pp. e40-e43
-
-
Turki, A.1
Al-Zaben, G.S.2
Khirallah, M.3
Marmouch, H.4
Mahjoub, T.5
Almawi, W.Y.6
-
37
-
-
65649086047
-
Comparison of genetic risk in three candidate genes (TCF7L2, PPARG, KCNJ11) with traditional risk factors for type 2 diabetes in a population-based study - The HUNT study
-
PMID: 18972257
-
Thorsby PM, Midthjell K, Gjerlaugsen N, Holmen J, Hanssen KF, Birkeland KI, et al. Comparison of genetic risk in three candidate genes (TCF7L2, PPARG, KCNJ11) with traditional risk factors for type 2 diabetes in a population-based study - the HUNT study. Scand J Clin Lab Invest. 2009; 69: 282-287. doi: 10.1080/00365510802538188 PMID: 18972257
-
(2009)
Scand J Clin Lab Invest
, vol.69
, pp. 282-287
-
-
Thorsby, P.M.1
Midthjell, K.2
Gjerlaugsen, N.3
Holmen, J.4
Hanssen, K.F.5
Birkeland, K.I.6
-
38
-
-
77957553197
-
A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B
-
PMID: 20818381
-
Yamauchi T, Hara K, Maeda S, Yasuda K, Takahashi A, Horikoshi M, et al. A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B. Nat Genet. 2010; 42: 864-868. doi: 10.1038/ng.660 PMID: 20818381
-
(2010)
Nat Genet
, vol.42
, pp. 864-868
-
-
Yamauchi, T.1
Hara, K.2
Maeda, S.3
Yasuda, K.4
Takahashi, A.5
Horikoshi, M.6
-
39
-
-
55649105963
-
Clinical risk factors, DNA variants, and the development of type 2 diabetes
-
PMID: 19020324
-
Lyssenko V, Jonsson A, Almgren P, Pulizzi N, Isomaa B, Tuomi T, et al. Clinical risk factors, DNA variants, and the development of type 2 diabetes. N Engl J Med. 2008; 359: 2220-2232. doi: 10.1056/NEJMoa0801869 PMID: 19020324
-
(2008)
N Engl J Med
, vol.359
, pp. 2220-2232
-
-
Lyssenko, V.1
Jonsson, A.2
Almgren, P.3
Pulizzi, N.4
Isomaa, B.5
Tuomi, T.6
-
40
-
-
44649133311
-
The genetic susceptibility to type 2 diabetes may be modulated by obesity status: Implications for association studies
-
PMID: 18498634
-
Cauchi S, Nead KT, Choquet H, Horber F, Potoczna N, Balkau B, et al. The genetic susceptibility to type 2 diabetes may be modulated by obesity status: implications for association studies. BMC Med Genet. 2008; 9: 45. doi: 10.1186/1471-2350-9-45 PMID: 18498634
-
(2008)
BMC Med Genet
, vol.9
, pp. 45
-
-
Cauchi, S.1
Nead, K.T.2
Choquet, H.3
Horber, F.4
Potoczna, N.5
Balkau, B.6
-
41
-
-
80052517091
-
Replication of 13 genomewide association (GWA)-validated risk variants for type 2 diabetes in Pakistani populations
-
PMID: 21350842
-
Rees SD, Hydrie MZI, Shera a S, Kumar S, O'Hare JP, Barnett AH, et al. Replication of 13 genomewide association (GWA)-validated risk variants for type 2 diabetes in Pakistani populations. Diabetologia. 2011; 54: 1368-1374. doi: 10.1007/s00125-011-2063-2 PMID: 21350842
-
(2011)
Diabetologia
, vol.54
, pp. 1368-1374
-
-
Rees, S.D.1
Hydrie, M.Z.I.2
Shera, S.3
Kumar, S.4
O'Hare, J.P.5
Barnett, A.H.6
-
42
-
-
84899450126
-
Quantitative assessment of the effect of KCNJ11 gene polymorphism on the risk of type 2 diabetes
-
PMID: 24710510
-
Qiu L, Na R, Xu R, Wang S, Sheng H, Wu W, et al. Quantitative Assessment of the Effect of KCNJ11 Gene Polymorphism on the Risk of Type 2 Diabetes. PLoS One. 2014; 9: e93961. doi: 10.1371/journal.pone.0093961 PMID: 24710510
-
(2014)
PLoS One
, vol.9
, pp. e93961
-
-
Qiu, L.1
Na, R.2
Xu, R.3
Wang, S.4
Sheng, H.5
Wu, W.6
-
43
-
-
0023615785
-
Meta-analysis in clinical research
-
PMID: 3300460
-
L'Abbé KA, Detsky AS, O'Rourke K. Meta-analysis in clinical research. Ann Intern Med. 1987; 107: 224-233. PMID: 3300460
-
(1987)
Ann Intern Med
, vol.107
, pp. 224-233
-
-
L'Abbé, K.A.1
Detsky, A.S.2
O'Rourke, K.3
-
44
-
-
0031684712
-
Clinical characterization of polymorphisms in the sulphonylurea receptor 1 gene in Japanese subjects with Type 2 diabetes mellitus
-
PMID: 9796882
-
Ishiyama-Shigemoto S, Yamada K, Yuan X, Koyama W, Nonaka K. Clinical characterization of polymorphisms in the sulphonylurea receptor 1 gene in Japanese subjects with Type 2 diabetes mellitus. Diabet Med. 1998; 15: 826-829. PMID: 9796882
-
(1998)
Diabet Med
, vol.15
, pp. 826-829
-
-
Ishiyama-Shigemoto, S.1
Yamada, K.2
Yuan, X.3
Koyama, W.4
Nonaka, K.5
-
45
-
-
0031773333
-
Missense mutations in the pancreatic islet beta cell inwardly rectifying K+ channel gene (KIR6.2/BIR): A meta-analysis suggests a role in the polygenic basis of Type II diabetes mellitus in Caucasians
-
PMID: 9867219
-
Hani EH, Boutin P, Durand E, Inoue H, Permutt MA, Velho G, et al. Missense mutations in the pancreatic islet beta cell inwardly rectifying K+ channel gene (KIR6.2/BIR): a meta-analysis suggests a role in the polygenic basis of Type II diabetes mellitus in Caucasians. Diabetologia. 1998; 41: 1511-1515. PMID: 9867219
-
(1998)
Diabetologia
, vol.41
, pp. 1511-1515
-
-
Hani, E.H.1
Boutin, P.2
Durand, E.3
Inoue, H.4
Permutt, M.A.5
Velho, G.6
-
46
-
-
0031915309
-
Identification and functional analysis of sulfonylurea receptor 1 variants in Japanese patients with NIDDM
-
PMID: 9519757
-
Ohta Y, Tanizawa Y, Inoue H, Hosaka T, Ueda K, Matsutani A, et al. Identification and functional analysis of sulfonylurea receptor 1 variants in Japanese patients with NIDDM. Diabetes. 1998; 47: 476-481. PMID: 9519757
-
(1998)
Diabetes
, vol.47
, pp. 476-481
-
-
Ohta, Y.1
Tanizawa, Y.2
Inoue, H.3
Hosaka, T.4
Ueda, K.5
Matsutani, A.6
-
47
-
-
39649085581
-
Genetic study of Saudi diabetes (GSSD): Significant association of the KCNJ11 E23K polymorphism with type 2 diabetes
-
PMID: 17922473
-
Alsmadi O, Al-Rubeaan K, Wakil SM, Imtiaz F, Mohamed G, Al-Saud H, et al. Genetic study of Saudi diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes. Diabetes Metab Res Rev. 2008; 24: 137-140. PMID: 17922473
-
(2008)
Diabetes Metab Res Rev.
, vol.24
, pp. 137-140
-
-
Alsmadi, O.1
Al-Rubeaan, K.2
Wakil, S.M.3
Imtiaz, F.4
Mohamed, G.5
Al-Saud, H.6
-
48
-
-
2342561802
-
Haplotype structure and genotype- phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region
-
PMID: 15111507
-
Florez JC, Burtt N, de Bakker PIW, Almgren P, Tuomi T, Holmkvist J, et al. Haplotype structure and genotype- phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region. Diabetes. 2004; 53: 1360-1368. PMID: 15111507
-
(2004)
Diabetes
, vol.53
, pp. 1360-1368
-
-
Florez, J.C.1
Burtt, N.2
De Bakker3
Almgren, P.4
Tuomi, T.5
Holmkvist, J.6
-
49
-
-
0034933966
-
Genomic variation in pancreatic ion channel genes in Japanese type 2 diabetic patients
-
PMID: 11424233
-
Yamada Y, Kuroe A, Li Q, Someya Y, Kubota A, Ihara Y, et al. Genomic variation in pancreatic ion channel genes in Japanese type 2 diabetic patients. Diabetes Metab Res Rev 2001; 17: 213-216. PMID: 11424233
-
(2001)
Diabetes Metab Res Rev
, vol.17
, pp. 213-216
-
-
Yamada, Y.1
Kuroe, A.2
Li, Q.3
Someya, Y.4
Kubota, A.5
Ihara, Y.6
-
50
-
-
0037317981
-
Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes
-
PMID: 12540637
-
Gloyn AL, Weedon MN, Owen KR, Turner MJ, Knight BA, Hitman G, et al. Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes. Diabetes 2003; 52: 568-572. PMID: 12540637
-
(2003)
Diabetes
, vol.52
, pp. 568-572
-
-
Gloyn, A.L.1
Weedon, M.N.2
Owen, K.R.3
Turner, M.J.4
Knight, B.A.5
Hitman, G.6
-
51
-
-
4243062602
-
Candidate gene association study in type 2 diabetes indicates a role for genes involved in beta-cell function as well as insulin action
-
PMID: 14551916
-
Barroso I, Luan J, Middelberg RPS, Harding A-H, Franks PW, Jakes RW, et al. Candidate gene association study in type 2 diabetes indicates a role for genes involved in beta-cell function as well as insulin action. PLoS Biol. 2003; 1: E20. PMID: 14551916
-
(2003)
PLoS Biol.
, vol.1
, pp. E20
-
-
Barroso, I.1
Luan, J.2
Rps, M.3
Harding, A.-H.4
Franks, P.W.5
Jakes, R.W.6
-
52
-
-
21244439539
-
Analysis of separate and combined effects of common variation in KCNJ11 and PPARG on risk of type 2 diabetes
-
PMID: 15797964
-
Hansen SK, Nielsen E- MD, Ek J, Andersen G, Glümer C, Carstensen B, et al. Analysis of separate and combined effects of common variation in KCNJ11 and PPARG on risk of type 2 diabetes. J Clin Endocrinol Metab. 2005; 90: 3629-3637. PMID: 15797964
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 3629-3637
-
-
Hansen, S.K.1
Nielsen, E.-M.D.2
Ek, J.3
Andersen, G.4
Glümer, C.5
Carstensen, B.6
-
53
-
-
17844410419
-
Common variants in the ATP-sensitive K+ channel genes KCNJ11 (Kir6.2) and ABCC8 (SUR1) in relation to glucose intolerance: Population-based studies and meta-analyses
-
PMID: 15842514
-
Van Dam RM, Hoebee B, Seidell JC, Schaap MM, de Bruin TW, Feskens EJ. Common variants in the ATP-sensitive K+ channel genes KCNJ11 (Kir6.2) and ABCC8 (SUR1) in relation to glucose intolerance: population-based studies and meta-analyses. Diabet Med 2005; 22: 590-598. PMID: 15842514
-
(2005)
Diabet Med
, vol.22
, pp. 590-598
-
-
Van Dam, R.M.1
Hoebee, B.2
Seidell, J.C.3
Schaap, M.M.4
De Bruin, T.W.5
Feskens, E.J.6
-
54
-
-
33750876203
-
Combining information from common type 2 diabetes risk polymorphisms improves disease prediction
-
PMID: 17020404
-
Weedon MN, McCarthy MI, Hitman G, Walker M, Groves CJ, Zeggini E, et al. Combining information from common type 2 diabetes risk polymorphisms improves disease prediction. PLoS Med. 2006; 3: e374. PMID: 17020404
-
(2006)
PLoS Med
, vol.3
, pp. e374
-
-
Weedon, M.N.1
McCarthy, M.I.2
Hitman, G.3
Walker, M.4
Groves, C.J.5
Zeggini, E.6
-
55
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. (2007)
-
PMID: 17554300
-
Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. (2007). Nature. 2007; 447: 661-678. PMID: 17554300
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
Wellcome Trust Case Control Consortium1
-
56
-
-
34249888775
-
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
-
PMID: 17463246
-
Saxena R, Voight BF, Lyssenko V, Burtt NP, de Bakker PI, Chen H, et al. Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science. 2007; 316: 1331-1336. PMID: 17463246
-
(2007)
Science
, vol.316
, 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
-
57
-
-
34249885875
-
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants
-
PMID: 17463248
-
Scott LJ, Mohlke KL, Bonnycastle LL, Willer CJ, Li Y, Duren WL, et al. A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science. 2007; 316: 1341-1345. PMID: 17463248
-
(2007)
Science
, vol.316
, 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
-
58
-
-
35448944056
-
Gene-gene interactions between HNF4A and KCNJ11 in predicting Type 2 diabetes in women
-
PMID: 17894829
-
Qi L, van Dam RM, Asselbergs FW, Hu FB. Gene-gene interactions between HNF4A and KCNJ11 in predicting Type 2 diabetes in women. Diabet Med. 2007; 24: 1187-1191. PMID: 17894829
-
(2007)
Diabet Med
, vol.24
, pp. 1187-1191
-
-
Qi, L.1
Van Dam, R.M.2
Asselbergs, F.W.3
Hu, F.B.4
-
59
-
-
35848945259
-
Variations in the HHEX gene are associated with increased risk of type 2 diabetes in the Japanese population
-
PMID: 17928989
-
Horikoshi M, Hara K, Ito C, Shojima N, Nagai R, Ueki K, et al. Variations in the HHEX gene are associated with increased risk of type 2 diabetes in the Japanese population. Diabetologia. 2007; 50: 2461-2466. PMID: 17928989
-
(2007)
Diabetologia
, vol.50
, pp. 2461-2466
-
-
Horikoshi, M.1
Hara, K.2
Ito, C.3
Shojima, N.4
Nagai, R.5
Ueki, K.6
-
60
-
-
34848895423
-
SNPs in the KCNJ11-ABCC8 gene locus are associated with type 2 diabetes and blood pressure levels in the Japanese population
-
PMID: 17823772
-
Sakamoto Y, Inoue H, Keshavarz P, Miyawaki K, Yamaguchi Y, Moritani M, et al. SNPs in the KCNJ11-ABCC8 gene locus are associated with type 2 diabetes and blood pressure levels in the Japanese population. J Hum Genet. 2007; 52: 781-793. PMID: 17823772
-
(2007)
J Hum Genet
, vol.52
, pp. 781-793
-
-
Sakamoto, Y.1
Inoue, H.2
Keshavarz, P.3
Miyawaki, K.4
Yamaguchi, Y.5
Moritani, M.6
-
61
-
-
35748940314
-
Impact of Kir6.2 E23K polymorphism on the development of type 2 diabetes in a general Japanese population: The Hisayama Study
-
PMID: 17965318
-
Doi Y, Kubo M, Ninomiya T, Yonemoto K, Iwase M, Arima H, et al. Impact of Kir6.2 E23K polymorphism on the development of type 2 diabetes in a general Japanese population: The Hisayama Study. Diabetes. 2007; 56: 2829-2833. PMID: 17965318
-
(2007)
Diabetes
, vol.56
, pp. 2829-2833
-
-
Doi, Y.1
Kubo, M.2
Ninomiya, T.3
Yonemoto, K.4
Iwase, M.5
Arima, H.6
-
62
-
-
35248887041
-
KCNJ11 E23K polymorphism and diabetes mellitus with adult onset in Czech patients
-
PMID: 17976307
-
Cejková P, Novota P, Cerná M, Kolostová K, Nováková D, Kucera P, et al. KCNJ11 E23K polymorphism and diabetes mellitus with adult onset in Czech patients. Folia Biol (Praha). 2007; 53: 173-175. PMID: 17976307
-
(2007)
Folia Biol (Praha)
, vol.53
, pp. 173-175
-
-
Cejková, P.1
Novota, P.2
Cerná, M.3
Kolostová, K.4
Nováková, D.5
Kucera, P.6
-
63
-
-
33847022334
-
Screening of 134 single nucleotide polymorphisms (SNPs) previously associated with type 2 diabetes replicates association with 12 SNPs in nine genes
-
PMID: 17192490
-
Willer CJ, Bonnycastle LL, Conneely KN, Duren WL, Jackson AU, Scott LJ, et al. Screening of 134 single nucleotide polymorphisms (SNPs) previously associated with type 2 diabetes replicates association with 12 SNPs in nine genes. Diabetes. 2007; 56: 256-264. PMID: 17192490
-
(2007)
Diabetes
, vol.56
, pp. 256-264
-
-
Willer, C.J.1
Bonnycastle, L.L.2
Conneely, K.N.3
Duren, W.L.4
Jackson, A.U.5
Scott, L.J.6
-
64
-
-
40949087723
-
Association of CDKAL1, IGF2BP2, CDKN2A/B, HHEX, SLC30A8, and KCNJ11 with susceptibility to type 2 diabetes in a Japanese population
-
PMID: 18162508
-
Omori S, Tanaka Y, Takahashi A, Hirose H, Kashiwagi A, Kaku K, et al. Association of CDKAL1, IGF2BP2, CDKN2A/B, HHEX, SLC30A8, and KCNJ11 with susceptibility to type 2 diabetes in a Japanese population. Diabetes. 2008; 57: 791-795. PMID: 18162508
-
(2008)
Diabetes
, vol.57
, pp. 791-795
-
-
Omori, S.1
Tanaka, Y.2
Takahashi, A.3
Hirose, H.4
Kashiwagi, A.5
Kaku, K.6
-
65
-
-
38449118682
-
Impact of common type 2 diabetes risk polymorphisms in the DESIR prospective study
-
PMID: 17977958
-
Vaxillaire M, Veslot J, Dina C, Proença C, Cauchi S, Charpentier G, et al. Impact of common type 2 diabetes risk polymorphisms in the DESIR prospective study. Diabetes. 2008; 57: 244-254. PMID: 17977958
-
(2008)
Diabetes
, vol.57
, pp. 244-254
-
-
Vaxillaire, M.1
Veslot, J.2
Dina, C.3
Proença, C.4
Cauchi, S.5
Charpentier, G.6
-
66
-
-
67650248695
-
Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population
-
PMID: 19401414
-
Takeuchi F, Serizawa M, Yamamoto K, Fujisawa T, Nakashima E, Ohnaka K, et al. Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. Diabetes. 2009; 58: 1690-1699. doi: 10.2337/db08-1494 PMID: 19401414
-
(2009)
Diabetes
, vol.58
, pp. 1690-1699
-
-
Takeuchi, F.1
Serizawa, M.2
Yamamoto, K.3
Fujisawa, T.4
Nakashima, E.5
Ohnaka, K.6
-
67
-
-
70449433016
-
PPARG, KCNJ11, CDKAL1, CDKN2A-CDKN2B, IDE-KIF11-HHEX, IGF2BP2 and SLC30A8 are associated with type 2 diabetes in a Chinese population
-
PMID: 19862325
-
Hu C, Zhang R, Wang C, Wang J, Ma X, Lu J, et al. PPARG, KCNJ11, CDKAL1, CDKN2A-CDKN2B, IDE-KIF11-HHEX, IGF2BP2 and SLC30A8 are associated with type 2 diabetes in a Chinese population. PLoS One. 2009; 4: e7643. doi: 10.1371/journal.pone.0007643 PMID: 19862325
-
(2009)
PLoS One
, vol.4
, pp. e7643
-
-
Hu, C.1
Zhang, R.2
Wang, C.3
Wang, J.4
Ma, X.5
Lu, J.6
-
68
-
-
63249118012
-
Replication study of candidate genes associated with type 2 diabetes based on genome-wide screening
-
PMID: 19033397
-
Tabara Y, Osawa H, Kawamoto R, Onuma H, Shimizu I, Miki T, et al. Replication Study of Candidate Genes Associated With Type 2 Diabetes Based On Genome-Wide Screening. Diabetes. 2009; 58: 493-498. doi: 10.2337/db07-1785 PMID: 19033397
-
(2009)
Diabetes
, vol.58
, pp. 493-498
-
-
Tabara, Y.1
Osawa, H.2
Kawamoto, R.3
Onuma, H.4
Shimizu, I.5
Miki, T.6
-
69
-
-
68449086849
-
The E23K variation in the KCNJ11 gene is associated with type 2 diabetes in Chinese and East Asian population
-
PMID: 19498446
-
Zhou D, Zhang D, Liu Y, Zhao T, Chen Z, Liu Z, et al. The E23K variation in the KCNJ11 gene is associated with type 2 diabetes in Chinese and East Asian population. J Hum Genet. 2009; 54: 433-435. doi: 10.1038/jhg.2009.54 PMID: 19498446
-
(2009)
J Hum Genet
, vol.54
, pp. 433-435
-
-
Zhou, D.1
Zhang, D.2
Liu, Y.3
Zhao, T.4
Chen, Z.5
Liu, Z.6
-
70
-
-
70350702970
-
Effect of genetic variants in KCNJ11, ABCC8, PPARG and HNF4A loci on the susceptibility of type 2 diabetes in Chinese Han population
-
PMID: 20079163
-
Wang F, Han X, Ren Q, Zhang X, Han L, luo YY, et al. Effect of genetic variants in KCNJ11, ABCC8, PPARG and HNF4A loci on the susceptibility of type 2 diabetes in Chinese Han population. Chin Med J (Engl). 2009; 122: 2477-2482. PMID: 20079163
-
(2009)
Chin Med J (Engl)
, vol.122
, pp. 2477-2482
-
-
Wang, F.1
Han, X.2
Ren, Q.3
Zhang, X.4
Han, L.5
Luo, Y.Y.6
-
71
-
-
65549152213
-
Contribution of type 2 diabetes associated loci in the Arabic population from Tunisia: A case-control study
-
PMID: 19368707
-
Ezzidi I, Mtiraoui N, Cauchi S, Vaillant E, Dechaume A, Chaieb M, et al. Contribution of type 2 diabetes associated loci in the Arabic population from Tunisia: a case-control study. BMC Med Genet. 2009; 10: 33. doi: 10.1186/1471-2350-10-33 PMID: 19368707
-
(2009)
BMC Med Genet
, vol.10
, pp. 33
-
-
Ezzidi, I.1
Mtiraoui, N.2
Cauchi, S.3
Vaillant, E.4
Dechaume, A.5
Chaieb, M.6
-
72
-
-
65349192772
-
Joint effects of common genetic variants on the risk for type 2 diabetes in U.S. Men and women of European ancestry
-
PMID: 19380854
-
Cornelis MC, Qi L, Zhang C, Kraft P, Manson J, Cai T, et al. Joint effects of common genetic variants on the risk for type 2 diabetes in U.S. men and women of European ancestry. Ann Intern Med. 2009; 150: 541-550. PMID: 19380854
-
(2009)
Ann Intern Med
, vol.150
, pp. 541-550
-
-
Cornelis, M.C.1
Qi, L.2
Zhang, C.3
Kraft, P.4
Manson, J.5
Cai, T.6
-
73
-
-
77949346987
-
Investigation of type 2 diabetes risk alleles support CDKN2A/B CDKAL1 and TCF7L2 as susceptibility genes in a Han Chinese cohort
-
PMID: 20161779
-
Wen J, Rönn T, Olsson A, Yang Z, Lu B, Du Y, et al. Investigation of type 2 diabetes risk alleles support CDKN2A/B, CDKAL1, and TCF7L2 as susceptibility genes in a Han Chinese cohort. PLoS One. 2010; 5: e9153. doi: 10.1371/journal.pone.0009153 PMID: 20161779
-
(2010)
PLoS One
, vol.5
, pp. e9153
-
-
Wen, J.1
Rönn, T.2
Olsson, A.3
Yang, Z.4
Lu, B.5
Du, Y.6
-
74
-
-
77955411524
-
Impact of common variants of PPARG, KCNJ11, TCF7L2, SLC30A8, HHEX, CDKN2A, IGF2BP2, and CDKAL1 on the risk of type 2 diabetes in 5,164 Indians
-
PMID: 20424228
-
Chauhan G, Spurgeon CJ, Tabassum R, Bhaskar S, Kulkarni SR, Mahajan A, et al. Impact of common variants of PPARG, KCNJ11, TCF7L2, SLC30A8, HHEX, CDKN2A, IGF2BP2, and CDKAL1 on the risk of type 2 diabetes in 5,164 Indians. Diabetes. 2010; 59: 2068-2074. doi: 10.2337/db09-1386 PMID: 20424228
-
(2010)
Diabetes
, vol.59
, pp. 2068-2074
-
-
Chauhan, G.1
Spurgeon, C.J.2
Tabassum, R.3
Bhaskar, S.4
Kulkarni, S.R.5
Mahajan, A.6
-
75
-
-
77952804503
-
Identification of susceptibility genes loci associated with type 2 diabetes
-
Liu L, Lei J, Liu H, Zou Q, Sun Y, et al. Identification of susceptibility genes loci associated with type 2 diabetes. Wuhan Univ J Nat Sci. 2010; 15: 171-175.
-
(2010)
Wuhan Univ J Nat Sci.
, vol.15
, pp. 171-175
-
-
Liu, L.1
Lei, J.2
Liu, H.3
Zou, Q.4
Sun, Y.5
-
76
-
-
84855188457
-
Association between KCNJ11 gene polymorphisms and risk of type 2 diabetes mellitus in East Asian populations: A meta-analysis in 42,573 individuals
-
PMID: 21573802
-
Yang L, Zhou X, Luo Y, Sun X, Tang Y, Guo W, et al. Association between KCNJ11 gene polymorphisms and risk of type 2 diabetes mellitus in East Asian populations: a meta-analysis in 42,573 individuals. Mol Biol Rep. 2012; 39: 645-659. doi: 10.1007/s11033-011-0782-6 PMID: 21573802
-
(2012)
Mol Biol Rep.
, vol.39
, pp. 645-659
-
-
Yang, L.1
Zhou, X.2
Luo, Y.3
Sun, X.4
Tang, Y.5
Guo, W.6
-
77
-
-
84869144898
-
Contribution of common variants of ENPP1, IGF2BP2, KCNJ11, MLXIPL, PPARγ, SLC30A8 and TCF7L2 to the risk of type 2 diabetes in Lebanese and Tunisian Arabs
-
PMID: 22749234
-
Mtiraoui N, Turki A, Nemr R, Echtay A, Izzidi I, Al-Zaben GS, et al. Contribution of common variants of ENPP1, IGF2BP2, KCNJ11, MLXIPL, PPARγ, SLC30A8 and TCF7L2 to the risk of type 2 diabetes in Lebanese and Tunisian Arabs. Diabetes Metab. 2012; 38: 444-449. doi: 10.1016/j.diabet.2012.05.002 PMID: 22749234
-
(2012)
Diabetes Metab
, vol.38
, pp. 444-449
-
-
Mtiraoui, N.1
Turki, A.2
Nemr, R.3
Echtay, A.4
Izzidi, I.5
Al-Zaben, G.S.6
-
78
-
-
84861374437
-
The effect of KCNJ11 polymorphism on the risk of type 2 diabetes: A global meta-analysis based on 49 case-control studies
-
PMID: 22082043
-
Gong B, Yu J, Li H, Li W, Tong X. The effect of KCNJ11 polymorphism on the risk of type 2 diabetes: a global meta-analysis based on 49 case-control studies. DNA Cell Biol. 2012; 31: 801-810. doi: 10.1089/dna.2011.1445 PMID: 22082043
-
(2012)
DNA Cell Biol
, vol.31
, pp. 801-810
-
-
Gong, B.1
Yu, J.2
Li, H.3
Li, W.4
Tong, X.5
-
79
-
-
84884376592
-
The TCF7L2 rs7903146 (T) allele is associated with type 2 diabetes in urban Ghana: A hospital-based case-control study
-
PMID: 24059590
-
Danquah I, Othmer T, Frank LK, Bedu-Addo G, Schulze MB, Mockenhaupt FP. The TCF7L2 rs7903146 (T) allele is associated with type 2 diabetes in urban Ghana: a hospital-based case-control study. BMC Med Genet. 2013; 14: 96. doi: 10.1186/1471-2350-14-96 PMID: 24059590
-
(2013)
BMC Med Genet
, vol.14
, pp. 96
-
-
Danquah, I.1
Othmer, T.2
Frank, L.K.3
Bedu-Addo, G.4
Schulze, M.B.5
Mockenhaupt, F.P.6
-
80
-
-
84882748780
-
Meta-analysis of association of common variants in the KCNJ11-ABCC8 region with type 2 diabetes
-
PMID: 24065655
-
Qin LJ, Lv Y, Huang QY. Meta-analysis of association of common variants in the KCNJ11-ABCC8 region with type 2 diabetes. Genet Mol Res. 2013; 12: 2990-3002. doi: 10.4238/2013.August.20.1 PMID: 24065655
-
(2013)
Genet Mol Res
, vol.12
, pp. 2990-3002
-
-
Qin, L.J.1
Lv, Y.2
Huang, Q.Y.3
-
81
-
-
15844366738
-
Sequence variants in the sulfonylurea receptor (SUR) gene are associated with NIDDM in Caucasians
-
PMID: 8635661
-
Inoue H, Ferrer J, Welling CM, Elbein SC, Hoffman M, Mayorga R, et al. Sequence variants in the sulfonylurea receptor (SUR) gene are associated with NIDDM in Caucasians. Diabetes. 1996; 45: 825-831. PMID: 8635661
-
(1996)
Diabetes
, vol.45
, pp. 825-831
-
-
Inoue, H.1
Ferrer, J.2
Welling, C.M.3
Elbein, S.C.4
Hoffman, M.5
Mayorga, R.6
-
82
-
-
0033625771
-
Sulfonylurea receptor 1 gene variants are associated with gestational diabetes and type 2 diabetes but not with altered secretion of insulin
-
2000. PMID: 10857971
-
Rissanen J, Markkanen A, Kärkkäinen P, Pihlajamäki J, Kekäläinen P, Mykkänen L, et al. (2000) Sulfonylurea receptor 1 gene variants are associated with gestational diabetes and type 2 diabetes but not with altered secretion of insulin. Diabetes Care. 2000; 23: 70-73. PMID: 10857971
-
(2000)
Diabetes Care
, vol.23
, pp. 70-73
-
-
Rissanen, J.1
Markkanen, A.2
Kärkkäinen, P.3
Pihlajamäki, J.4
Kekäläinen, P.5
Mykkänen, L.6
|