-
1
-
-
0026583193
-
Linkage of type 2 diabetes to the glucokinase gene
-
Hattersley AT, Turner RC, Permutt MA, Patel P, Tanizawa Y, Chiu KC, O'Rahilly S, Watkins PJ, Wainscoat JS: Linkage of type 2 diabetes to the glucokinase gene. Lancet 339:1307-1310, 1992
-
(1992)
Lancet
, vol.339
, pp. 1307-1310
-
-
Hattersley, A.T.1
Turner, R.C.2
Permutt, M.A.3
Patel, P.4
Tanizawa, Y.5
Chiu, K.C.6
O'Rahilly, S.7
Watkins, P.J.8
Wainscoat, J.S.9
-
2
-
-
10544249874
-
Mutations in the hepatocyte nuclear factor-1α gene in maturity-onset diabetes of the young (MODY3)
-
Yamagata K, Oda N, Kaisaki PJ, Menzel S, Furuta H, Vaxillaire M, Southam L, Cox RD, Lathrop GM, Boriraj VV, Chen X, Cox NJ, Oda Y, Yano H, Le Beau MM, Yamada S, Nishigori H, Takeda J, Fajans SS, Hattersley AT, Iwasaki N, Hansen T, Pedersen O, Polonsky KS, Turner RC, Velho G, Chévre J-C, Froguel P, Bell GI: Mutations in the hepatocyte nuclear factor-1α gene in maturity-onset diabetes of the young (MODY3). Nature 384:455-458, 1996
-
(1996)
Nature
, vol.384
, pp. 455-458
-
-
Yamagata, K.1
Oda, N.2
Kaisaki, P.J.3
Menzel, S.4
Furuta, H.5
Vaxillaire, M.6
Southam, L.7
Cox, R.D.8
Lathrop, G.M.9
Boriraj, V.V.10
Chen, X.11
Cox, N.J.12
Oda, Y.13
Yano, H.14
Le Beau, M.M.15
Yamada, S.16
Nishigori, H.17
Takeda, J.18
Fajans, S.S.19
Hattersley, A.T.20
Iwasaki, N.21
Hansen, T.22
Pedersen, O.23
Polonsky, K.S.24
Turner, R.C.25
Velho, G.26
Chévre, J.-C.27
Froguel, P.28
Bell, G.I.29
more..
-
3
-
-
10544236911
-
Mutations in the hepatocyte nuclear factor-4α gene in maturity-onset diabetes of the young (MODY1)
-
Yamagata K, Furuta H, Oda N, Kaisaki PJ, Menzel S, Cox NJ, Fajans SS, Signorini S, Stoffel M, Bell GI: Mutations in the hepatocyte nuclear factor-4α gene in maturity-onset diabetes of the young (MODY1). Nature 384:458-460, 1996
-
(1996)
Nature
, vol.384
, pp. 458-460
-
-
Yamagata, K.1
Furuta, H.2
Oda, N.3
Kaisaki, P.J.4
Menzel, S.5
Cox, N.J.6
Fajans, S.S.7
Signorini, S.8
Stoffel, M.9
Bell, G.I.10
-
4
-
-
0031453186
-
Mutation in hepatocyte nuclear factor-1β gene (TCF2) associated with MODY
-
Horikawa Y, Iwasaki N, Hara M, Furuta H, Hinokio Y, Cockburn BN, Lindner T, Yamagata K, Ogata M, Tomonaga O, Kuroki H, Kasahara T, Iwamoto Y, Bell GI: Mutation in hepatocyte nuclear factor-1β gene (TCF2) associated with MODY. Nat Genet 17:384-385, 1997
-
(1997)
Nat Genet
, vol.17
, pp. 384-385
-
-
Horikawa, Y.1
Iwasaki, N.2
Hara, M.3
Furuta, H.4
Hinokio, Y.5
Cockburn, B.N.6
Lindner, T.7
Yamagata, K.8
Ogata, M.9
Tomonaga, O.10
Kuroki, H.11
Kasahara, T.12
Iwamoto, Y.13
Bell, G.I.14
-
5
-
-
0031253820
-
Early-onset type-II diabetes mellitus (MODY4) linked to IPF1
-
Stoffers DA, Ferrer J, Clarke WL, Habener JF: Early-onset type-II diabetes mellitus (MODY4) linked to IPF1. Nat Genet 17:138-139, 1997
-
(1997)
Nat Genet
, vol.17
, pp. 138-139
-
-
Stoffers, D.A.1
Ferrer, J.2
Clarke, W.L.3
Habener, J.F.4
-
6
-
-
0032700272
-
Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus
-
Malecki MT, Jhala US, Antonellis A, Fields L, Doria A, Orban T, Saad M, Warram JH, Montminy M, Krolewski AS: Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus. Nat Genet 23:323-328, 1999
-
(1999)
Nat Genet
, vol.23
, pp. 323-328
-
-
Malecki, M.T.1
Jhala, U.S.2
Antonellis, A.3
Fields, L.4
Doria, A.5
Orban, T.6
Saad, M.7
Warram, J.H.8
Montminy, M.9
Krolewski, A.S.10
-
7
-
-
0035204024
-
MODY in Iceland is associated with mutations in HNF-1α and a novel mutation in NeuroD1
-
Kristinsson SY, Thorolfsdottir ET, Talseth B, Steingrimsson E, Thorsson AV, Helgason T, Hreidarsson AB, Arngrimsson R: MODY in Iceland is associated with mutations in HNF-1α and a novel mutation in NeuroD1. Diabetologia 44:2098-2103, 2001
-
(2001)
Diabetologia
, vol.44
, pp. 2098-2103
-
-
Kristinsson, S.Y.1
Thorolfsdottir, E.T.2
Talseth, B.3
Steingrimsson, E.4
Thorsson, A.V.5
Helgason, T.6
Hreidarsson, A.B.7
Arngrimsson, R.8
-
8
-
-
15144347575
-
Mutation screening in 18 Caucasian families suggest the existence of other MODY genes
-
Chévre J-C, Hani EH, Boutin P, Vaxillaire M, Blanche H, Vionnet N, Pardini VC, Timsit J, Larger E, Charpentier G, Beckers D, Maes M, Bellanné-Chancelot C, Velho G, Froguel P: Mutation screening in 18 Caucasian families suggest the existence of other MODY genes. Diabetologia 41:1017-1023, 1998
-
(1998)
Diabetologia
, vol.41
, pp. 1017-1023
-
-
Chévre, J.-C.1
Hani, E.H.2
Boutin, P.3
Vaxillaire, M.4
Blanche, H.5
Vionnet, N.6
Pardini, V.C.7
Timsit, J.8
Larger, E.9
Charpentier, G.10
Beckers, D.11
Maes, M.12
Bellanné-Chancelot, C.13
Velho, G.14
Froguel, P.15
-
9
-
-
0032857518
-
High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes
-
Lehto M, Wipemo C, Ivarsson S-A, Lindgren C, Lipsanen-Nyman M, Weng J, Wibell L, Widén E, Tuomi T, Groop L: High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes. Diabetologia 42:1131-1137, 1999
-
(1999)
Diabetologia
, vol.42
, pp. 1131-1137
-
-
Lehto, M.1
Wipemo, C.2
Ivarsson, S.-A.3
Lindgren, C.4
Lipsanen-Nyman, M.5
Weng, J.6
Wibell, L.7
Widén, E.8
Tuomi, T.9
Groop, L.10
-
10
-
-
0037300839
-
Genetic epidemiology of MODY in the Czech republic: New mutations in the MODY genes HNF-4α, GCK and HNF-1α
-
Pruhova S, Ek J, Lebl J, Sumnik Z, Saudek F, Andel M, Pedersen O, Hansen T: Genetic epidemiology of MODY in the Czech republic: new mutations in the MODY genes HNF-4α, GCK and HNF-1α. Diabetologia 46:291-295, 2003
-
(2003)
Diabetologia
, vol.46
, pp. 291-295
-
-
Pruhova, S.1
Ek, J.2
Lebl, J.3
Sumnik, Z.4
Saudek, F.5
Andel, M.6
Pedersen, O.7
Hansen, T.8
-
11
-
-
3242657911
-
Absence of a reductase, NCB5OR, causes insulin-deficient diabetes
-
Xie J, Zhu H, Larade K, Ladoux A, Seguritan A, Chu M, Ito S, Bronson RT, Leiter EH, Zhang C-Y, Rosen ED, Bunn HF: Absence of a reductase, NCB5OR, causes insulin-deficient diabetes. Proc Natl Acad Sci U S A 101: 10750-10755, 2004
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, pp. 10750-10755
-
-
Xie, J.1
Zhu, H.2
Larade, K.3
Ladoux, A.4
Seguritan, A.5
Chu, M.6
Ito, S.7
Bronson, R.T.8
Leiter, E.H.9
Zhang, C.-Y.10
Rosen, E.D.11
Bunn, H.F.12
-
12
-
-
0033592866
-
Identification of a cytochrome b-type NAD(P)H oxidoreductase ubiquitously expressed in human cells
-
Zhu H, Qui H, Yoon H-WP, Huang S, Bunn HF: Identification of a cytochrome b-type NAD(P)H oxidoreductase ubiquitously expressed in human cells. Proc Natl Acad Sci U S A 96:14742-14747, 1999
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 14742-14747
-
-
Zhu, H.1
Qui, H.2
Yoon, H.-W.P.3
Huang, S.4
Bunn, H.F.5
-
13
-
-
0344837809
-
A genome-wide scan in families with maturity-onset diabetes of the young: Evidence for further genetic heterogeneity
-
Frayling TM, Lindgren CM, Chevre JC, Menzel S, Wishart M, Benmezroua Y, Brown A, Evans JC, Rao PS, Dina C, Lecoeur C, Kanninen T, Almgren P, Bulman MP, Wang Y, Mills J, Wright-Pascoe R, Mahtani MM, Prisco F, Costa A, Cognet I, Hansen T, Pedersen O, Ellard S, Tuomi T, Groop LC, Froguel P, Hattersley AT, Vaxillaire M: A genome-wide scan in families with maturity-onset diabetes of the young: evidence for further genetic heterogeneity. Diabetes 52:872-881, 2003
-
(2003)
Diabetes
, vol.52
, pp. 872-881
-
-
Frayling, T.M.1
Lindgren, C.M.2
Chevre, J.C.3
Menzel, S.4
Wishart, M.5
Benmezroua, Y.6
Brown, A.7
Evans, J.C.8
Rao, P.S.9
Dina, C.10
Lecoeur, C.11
Kanninen, T.12
Almgren, P.13
Bulman, M.P.14
Wang, Y.15
Mills, J.16
Wright-Pascoe, R.17
Mahtani, M.M.18
Prisco, F.19
Costa, A.20
Cognet, I.21
Hansen, T.22
Pedersen, O.23
Ellard, S.24
Tuomi, T.25
Groop, L.C.26
Froguel, P.27
Hattersley, A.T.28
Vaxillaire, M.29
more..
-
14
-
-
10744226236
-
A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14
-
Silander K, Scott LJ, Valle TT, Mohlke KL, Stringham HM, Wiles KR, Duren WL, Doheny KF, Pugh EW, Chines P, Narisu N, White PP, Fingerlin TE, Jackson AU, Li C, Ghosh S, Magnuson VL, Colby K, Erdos MR, Hill JE, Hollstein P, Humphreys KM, Kasad RA, Lambert J, Lazaridis KN, Lin G, Morales-Mena A, Patzkowski K, Pfahl C, Porter R, Rha D, Segal L, Suh YD, Tovar J, Unni A, Welch C, Douglas JA, Epstein MP, Hauser ER, Hagopian W, Buchanan TA, Watanabe RM, Bergman RN, Tuomilehto J, Collins FS, Boehnke M: A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14. Diabetes 53:821-829, 2004
-
(2004)
Diabetes
, vol.53
, pp. 821-829
-
-
Silander, K.1
Scott, L.J.2
Valle, T.T.3
Mohlke, K.L.4
Stringham, H.M.5
Wiles, K.R.6
Duren, W.L.7
Doheny, K.F.8
Pugh, E.W.9
Chines, P.10
Narisu, N.11
White, P.P.12
Fingerlin, T.E.13
Jackson, A.U.14
Li, C.15
Ghosh, S.16
Magnuson, V.L.17
Colby, K.18
Erdos, M.R.19
Hill, J.E.20
Hollstein, P.21
Humphreys, K.M.22
Kasad, R.A.23
Lambert, J.24
Lazaridis, K.N.25
Lin, G.26
Morales-Mena, A.27
Patzkowski, K.28
Pfahl, C.29
Porter, R.30
Rha, D.31
Segal, L.32
Suh, Y.D.33
Tovar, J.34
Unni, A.35
Welch, C.36
Douglas, J.A.37
Epstein, M.P.38
Hauser, E.R.39
Hagopian, W.40
Buchanan, T.A.41
Watanabe, R.M.42
Bergman, R.N.43
Tuomilehto, J.44
Collins, F.S.45
Boehnke, M.46
more..
-
15
-
-
1242292305
-
Epidemiology of gestational diabetes mellitus and its association with type 2 diabetes
-
Ben-Haroush A, Yogev Y, Hod M: Epidemiology of gestational diabetes mellitus and its association with type 2 diabetes. Diabet Med 21:103-113, 2004
-
(2004)
Diabet Med
, vol.21
, pp. 103-113
-
-
Ben-Haroush, A.1
Yogev, Y.2
Hod, M.3
-
16
-
-
0036130398
-
Diabetic family history is an isolated risk factor for gestational diabetes after 30 years of age
-
Chan LY-S, Wong SF, Ho LC: Diabetic family history is an isolated risk factor for gestational diabetes after 30 years of age. Acta Obstet Gynecol Scand 81:115-117, 2002
-
(2002)
Acta Obstet Gynecol Scand
, vol.81
, pp. 115-117
-
-
Chan, L.Y.-S.1
Wong, S.F.2
Ho, L.C.3
-
17
-
-
18144452590
-
Defective insulin secretion in hepatocyte nuclear factor 1α-deficient mice
-
Pontoglio M, Sreenan S, Roe M, Pugh W, Ostrega D, Doyen A, Pick AJ, Baldwin A, Velho G, Froguel P, Levisetti M, Bonner-Weir S, Bell GI, Yaniv M, Polonsky KS: Defective insulin secretion in hepatocyte nuclear factor 1α-deficient mice. J Clin Invest 101:2215-2222, 1998
-
(1998)
J Clin Invest
, vol.101
, pp. 2215-2222
-
-
Pontoglio, M.1
Sreenan, S.2
Roe, M.3
Pugh, W.4
Ostrega, D.5
Doyen, A.6
Pick, A.J.7
Baldwin, A.8
Velho, G.9
Froguel, P.10
Levisetti, M.11
Bonner-Weir, S.12
Bell, G.I.13
Yaniv, M.14
Polonsky, K.S.15
-
18
-
-
0030943465
-
A prevalent amino acid polymorphism at codon 98 in the hepatocyte nuclear factor-1α gene is associated with reduced serum C-peptide and insulin responses to an oral glucose challenge
-
Urhammer SA, Fridberg M, Hansen T, Rasmussen SK, Møller AM, Clausen JO, Pedersen O: A prevalent amino acid polymorphism at codon 98 in the hepatocyte nuclear factor-1α gene is associated with reduced serum C-peptide and insulin responses to an oral glucose challenge. Diabetes 46:912-916, 1997
-
(1997)
Diabetes
, vol.46
, pp. 912-916
-
-
Urhammer, S.A.1
Fridberg, M.2
Hansen, T.3
Rasmussen, S.K.4
Møller, A.M.5
Clausen, J.O.6
Pedersen, O.7
-
19
-
-
0032217152
-
The Ala/Val98 polymorphism of the hepatocyte nuclear factor-1α gene contributes to the interindividual variation in serum C-peptide response during an oral glucose tolerance test: Evidence from studies of 231 glucose-tolerant first degree relatives of type 2 diabetic probands
-
Urhammer SA, Hansen T, Ekstrom CT, Eiberg H, Pedersen O: The Ala/Val98 polymorphism of the hepatocyte nuclear factor-1α gene contributes to the interindividual variation in serum C-peptide response during an oral glucose tolerance test: evidence from studies of 231 glucose-tolerant first degree relatives of type 2 diabetic probands. J Clin Endocrinol Metab 83:4506-4509, 1998
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 4506-4509
-
-
Urhammer, S.A.1
Hansen, T.2
Ekstrom, C.T.3
Eiberg, H.4
Pedersen, O.5
-
20
-
-
0035085146
-
Increasing prevalence of diabetes mellitus and impaired glucose tolerance among 60-year-old Danes
-
Drivsholm T, Ibsen H, Schroll M, Davidsen M, Borch-Johnsen K: Increasing prevalence of diabetes mellitus and impaired glucose tolerance among 60-year-old Danes. Diabet Med 18:126-132, 2001
-
(2001)
Diabet Med
, vol.18
, pp. 126-132
-
-
Drivsholm, T.1
Ibsen, H.2
Schroll, M.3
Davidsen, M.4
Borch-Johnsen, K.5
-
21
-
-
7044234168
-
Studies of the ala/val98 polymorphism of the hepatocyte nuclear factor-1α gene and the relationship to β-cell function during an OGTT in glucose tolerant women with and without previous gestational diabetes mellitus
-
In press
-
Lauenborg J, Damm P, Ek J, Glümer C, Jørgensen T, Borch-Johnsen K, Vestergaard H, Hornnes P, Pedersen O, Hansen T: Studies of the ala/val98 polymorphism of the hepatocyte nuclear factor-1α gene and the relationship to β-cell function during an OGTT in glucose tolerant women with and without previous gestational diabetes mellitus. Diabet Med (In press)
-
Diabet Med
-
-
Lauenborg, J.1
Damm, P.2
Ek, J.3
Glümer, C.4
Jørgensen, T.5
Borch-Johnsen, K.6
Vestergaard, H.7
Hornnes, P.8
Pedersen, O.9
Hansen, T.10
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