-
1
-
-
0036338150
-
Merlin - Rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR. 2002. Merlin - Rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 30: 97-101.
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
2
-
-
0030897631
-
Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy
-
Bowden DW, Sale M, Howard TD, Qadri A, Spray BJ, Rothschild CB, Akots G, Rich SS, Freedman BI. 1997. Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy. Diabetes 46:882-886.
-
(1997)
Diabetes
, vol.46
, pp. 882-886
-
-
Bowden, D.W.1
Sale, M.2
Howard, T.D.3
Qadri, A.4
Spray, B.J.5
Rothschild, C.B.6
Akots, G.7
Rich, S.S.8
Freedman, B.I.9
-
3
-
-
10744230909
-
A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes
-
Demenais F, Kanninen T, Lindgren CM, Wiltshire S, Gaget S, Dandrieux C, Almgren P, Sjogren M, Hattersley A, Dina C, Tuomi T, McCarthy MI, Froguel P, Groop LC. 2003. A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes. Hum Mol Genet 12:1865-1873.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 1865-1873
-
-
Demenais, F.1
Kanninen, T.2
Lindgren, C.M.3
Wiltshire, S.4
Gaget, S.5
Dandrieux, C.6
Almgren, P.7
Sjogren, M.8
Hattersley, A.9
Dina, C.10
Tuomi, T.11
McCarthy, M.I.12
Froguel, P.13
Groop, L.C.14
-
4
-
-
0029845345
-
Maturity onset diabetes of the young (MODY)
-
Fajans SS, Bell GI, Bowden DW, Halter JB, Polonsky KS. 1996. Maturity onset diabetes of the young (MODY). Diabetes Med 13:S90-S95.
-
(1996)
Diabetes Med
, vol.13
-
-
Fajans, S.S.1
Bell, G.I.2
Bowden, D.W.3
Halter, J.B.4
Polonsky, K.S.5
-
5
-
-
34547947086
-
PSMD9 gene variants within NIDDM2 may rarely contribute to type 2 diabetes
-
Gragnoli C, Cronsell J. 2007. PSMD9 gene variants within NIDDM2 may rarely contribute to type 2 diabetes. J Cell Physiol 212:568-571.
-
(2007)
J Cell Physiol
, vol.212
, pp. 568-571
-
-
Gragnoli, C.1
Cronsell, J.2
-
6
-
-
16044374799
-
Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families [see comments]
-
Mahtani MM, Widen E, Lehto M, Thomas J, McCarthy M, Brayer J, Bryant B, Chan G, Daly M, Forsblom C, Kanninen T, Kirby A, Kruglyak L, Munnelly K, Parkkonen M, Reeve-Daly MP, Weaver A, Brettin T, Duyk G, Lander ES, Groop LC. 1996. Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families [see comments]. Nat Genet 14:90-94.
-
(1996)
Nat Genet
, vol.14
, pp. 90-94
-
-
Mahtani, M.M.1
Widen, E.2
Lehto, M.3
Thomas, J.4
McCarthy, M.5
Brayer, J.6
Bryant, B.7
Chan, G.8
Daly, M.9
Forsblom, C.10
Kanninen, T.11
Kirby, A.12
Kruglyak, L.13
Munnelly, K.14
Parkkonen, M.15
Reeve-Daly, M.P.16
Weaver, A.17
Brettin, T.18
Duyk, G.19
Lander, E.S.20
Groop, L.C.21
more..
-
7
-
-
0042666793
-
Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2
-
Reynisdottir I, Thorleifsson G, Benediktsson R, Sigurdsson G, Emilsson V, Einarsdottir AS, Hjorleifsdottir EE, Orlygsdottir GT, Bjornsdottir GT, Saemundsdottir J, Halldorsson S, Hrafnkelsdottir S, Sigurjonsdottir SB, Steinsdottir S, Martin M, Kochan JP, Rhees BK, Grant SF, Frigge ML, Kong A, Gudnason V, Stefansson K, Gulcher JR. 2003. Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2. Am J Hum Genet 73:323-335.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 323-335
-
-
Reynisdottir, I.1
Thorleifsson, G.2
Benediktsson, R.3
Sigurdsson, G.4
Emilsson, V.5
Einarsdottir, A.S.6
Hjorleifsdottir, E.E.7
Orlygsdottir, G.T.8
Bjornsdottir, G.T.9
Saemundsdottir, J.10
Halldorsson, S.11
Hrafnkelsdottir, S.12
Sigurjonsdottir, S.B.13
Steinsdottir, S.14
Martin, M.15
Kochan, J.P.16
Rhees, B.K.17
Grant, S.F.18
Frigge, M.L.19
Kong, A.20
Gudnason, V.21
Stefansson, K.22
Gulcher, J.R.23
more..
-
8
-
-
0031713870
-
Novel susceptibility gene for late-onset NIDDM is localized to human chromosome 12q
-
Shaw JT, Lovelock PK, Kesting JB, Cardinal J, Duffy D, Wainwright B, Cameron DP. 1998. Novel susceptibility gene for late-onset NIDDM is localized to human chromosome 12q. Diabetes 47:1793-1796.
-
(1998)
Diabetes
, vol.47
, pp. 1793-1796
-
-
Shaw, J.T.1
Lovelock, P.K.2
Kesting, J.B.3
Cardinal, J.4
Duffy, D.5
Wainwright, B.6
Cameron, D.P.7
-
9
-
-
0033499802
-
Bridge-1, a novel PDZ-domain coactivator of E2A-mediated regulation of insulin gene transcription
-
Thomas MKYK, Tenser MS, Wong GG, Habener JF. 1999. Bridge-1, a novel PDZ-domain coactivator of E2A-mediated regulation of insulin gene transcription. Mol Cell Biol 19:8492-8504.
-
(1999)
Mol Cell Biol
, vol.19
, pp. 8492-8504
-
-
Thomas, M.K.Y.K.1
Tenser, M.S.2
Wong, G.G.3
Habener, J.F.4
-
10
-
-
28044433467
-
Overexpression of the coactivator bridge-1 results in insulin deficiency and diabetes
-
Volinic JL, Lee JH, Eto K, Kaur V, Thomas MK. 2006. Overexpression of the coactivator bridge-1 results in insulin deficiency and diabetes. Mol Endocrinol 20:167-182.
-
(2006)
Mol Endocrinol
, vol.20
, pp. 167-182
-
-
Volinic, J.L.1
Lee, J.H.2
Eto, K.3
Kaur, V.4
Thomas, M.K.5
-
11
-
-
10744224697
-
Evidence from a large U.K. family collection that genes influencing age of onset of type 2 diabetes map to chromosome 12p and to the MODY3/NIDDM2 locus on 12q24
-
Wiltshire S, Frayling TM, Groves CJ, Levy JC, Hitman GA, Sampson M, Walker M, Menzel S, Hattersley AT, Cardon LR, McCarthy MI. 2004. Evidence from a large U.K. family collection that genes influencing age of onset of type 2 diabetes map to chromosome 12p and to the MODY3/NIDDM2 locus on 12q24. Diabetes 53:855-860.
-
(2004)
Diabetes
, vol.53
, pp. 855-860
-
-
Wiltshire, S.1
Frayling, T.M.2
Groves, C.J.3
Levy, J.C.4
Hitman, G.A.5
Sampson, M.6
Walker, M.7
Menzel, S.8
Hattersley, A.T.9
Cardon, L.R.10
McCarthy, M.I.11
-
12
-
-
23644442564
-
Association of common variation in the HNF1alpha gene region with risk of type 2 diabetes
-
Winckler W, Burtt NP, Holmkvist J, Cervin C, de Bakker PI, Sun M, Almgren P, Tuomi T, Gaudet D, Hudson TJ, Ardlie KG, Daly MJ, Hirschhorn JN, Altshuler D, Groop L. 2005. Association of common variation in the HNF1alpha gene region with risk of type 2 diabetes. Diabetes 54:2336-2342.
-
(2005)
Diabetes
, vol.54
, pp. 2336-2342
-
-
Winckler, W.1
Burtt, N.P.2
Holmkvist, J.3
Cervin, C.4
de Bakker, P.I.5
Sun, M.6
Almgren, P.7
Tuomi, T.8
Gaudet, D.9
Hudson, T.J.10
Ardlie, K.G.11
Daly, M.J.12
Hirschhorn, J.N.13
Altshuler, D.14
Groop, L.15
-
13
-
-
10544249874
-
Mutations in the hepatocyte nuclear factor-1alpha gene in maturity- onset diabetes of the young (MODY3) [see comments]
-
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, Bell GI, et al. 1996. Mutations in the hepatocyte nuclear factor-1alpha gene in maturity- onset diabetes of the young (MODY3) [see comments]. Nature 384:455-458.
-
(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
Bell, G.I.25
more..
|