-
1
-
-
33751265737
-
Identification of chromosomal regions linked to premature myocardial infarction: a meta-analysis of whole-genome searches
-
10.1007/s10038-006-0053-x, 17024316
-
Zintzaras E, Kitsios G. Identification of chromosomal regions linked to premature myocardial infarction: a meta-analysis of whole-genome searches. J Hum Genet 2006, 51:1015. 10.1007/s10038-006-0053-x, 17024316.
-
(2006)
J Hum Genet
, vol.51
, pp. 1015
-
-
Zintzaras, E.1
Kitsios, G.2
-
2
-
-
61349089164
-
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction
-
10.1038/ng.323, 19198610
-
Gudbjartsson DF, Bjornsdottir US, Halapi E, Helgadottir A, Sulem P, Jonsdottir GM, Thorleifsson G, Helgadottir H, Steinthorsdottir V, Stefansson H, Williams C, Hui J, Beilby J, Warrington NM, James A, Palmer LJ, Koppelman GH, Heinzmann A, Krueger M, Boezen HM, Wheatley A, Altmuller J, Shin HD, Uh ST, Cheong HS, Jonsdottir B, Gislason D, Park CS, Rasmussen LM, Porsbjerg C, Hansen JW, Backer V, Werge T, Janson C, Jonsson UB, Ng MC, Chan J, So WY, Ma R, Shah SH, Granger CB, Quyyumi AA, Levey AI, Vaccarino V, Reilly MP, Rader DJ, Williams MJ, van Rij AM, Jones GT, Trabetti E, Malerba G, Pignatti PF, Boner A, Pescollderungg L, Girelli D, Olivieri O, Martinelli N, Ludviksson BR, Ludviksdottir D, Eyjolfsson GI, Arnar D, Thorgeirsson G, Deichmann K, Thompson PJ, Wjst M, Hall IP, Postma DS, Gislason T, Gulcher J, Kong A, Jonsdottir I, Thorsteinsdottir U, Stefansson K. Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. Nat Genet 2009, 41:342. 10.1038/ng.323, 19198610.
-
(2009)
Nat Genet
, vol.41
, pp. 342
-
-
Gudbjartsson, D.F.1
Bjornsdottir, U.S.2
Halapi, E.3
Helgadottir, A.4
Sulem, P.5
Jonsdottir, G.M.6
Thorleifsson, G.7
Helgadottir, H.8
Steinthorsdottir, V.9
Stefansson, H.10
Williams, C.11
Hui, J.12
Beilby, J.13
Warrington, N.M.14
James, A.15
Palmer, L.J.16
Koppelman, G.H.17
Heinzmann, A.18
Krueger, M.19
Boezen, H.M.20
Wheatley, A.21
Altmuller, J.22
Shin, H.D.23
Uh, S.T.24
Cheong, H.S.25
Jonsdottir, B.26
Gislason, D.27
Park, C.S.28
Rasmussen, L.M.29
Porsbjerg, C.30
Hansen, J.W.31
Backer, V.32
Werge, T.33
Janson, C.34
Jonsson, U.B.35
Ng, M.C.36
Chan, J.37
So, W.Y.38
Ma, R.39
Shah, S.H.40
Granger, C.B.41
Quyyumi, A.A.42
Levey, A.I.43
Vaccarino, V.44
Reilly, M.P.45
Rader, D.J.46
Williams, M.J.47
van Rij, A.M.48
Jones, G.T.49
Trabetti, E.50
Malerba, G.51
Pignatti, P.F.52
Boner, A.53
Pescollderungg, L.54
Girelli, D.55
Olivieri, O.56
Martinelli, N.57
Ludviksson, B.R.58
Ludviksdottir, D.59
Eyjolfsson, G.I.60
Arnar, D.61
Thorgeirsson, G.62
Deichmann, K.63
Thompson, P.J.64
Wjst, M.65
Hall, I.P.66
Postma, D.S.67
Gislason, T.68
Gulcher, J.69
Kong, A.70
Jonsdottir, I.71
Thorsteinsdottir, U.72
Stefansson, K.73
more..
-
3
-
-
41149152464
-
A whole-genome scan for stroke or myocardial infarction in family blood pressure program families
-
10.1161/STROKEAHA.107.490433, 18323513
-
Sherva R, Miller MB, Pankow JS, Hunt SC, Boerwinkle E, Mosley TH, Weder AB, Curb JD, Luke A, Morrison AC, Fornage M, Arnett DK. A whole-genome scan for stroke or myocardial infarction in family blood pressure program families. Stroke 2008, 39:1115. 10.1161/STROKEAHA.107.490433, 18323513.
-
(2008)
Stroke
, vol.39
, pp. 1115
-
-
Sherva, R.1
Miller, M.B.2
Pankow, J.S.3
Hunt, S.C.4
Boerwinkle, E.5
Mosley, T.H.6
Weder, A.B.7
Curb, J.D.8
Luke, A.9
Morrison, A.C.10
Fornage, M.11
Arnett, D.K.12
-
4
-
-
34547947086
-
PSMD9 gene variants within NIDDM2 may rarely contribute to type 2 diabetes
-
10.1002/jcp.21127, 17516568
-
Gragnoli C, Cronsell J. PSMD9 gene variants within NIDDM2 may rarely contribute to type 2 diabetes. J Cell Physiol 2007, 212:568. 10.1002/jcp.21127, 17516568.
-
(2007)
J Cell Physiol
, vol.212
, pp. 568
-
-
Gragnoli, C.1
Cronsell, J.2
-
5
-
-
73349131734
-
PSMD9 gene in the NIDDM2 locus is linked to type 2 diabetes in Italians
-
10.1002/jcp.21954, 19877155
-
Gragnoli C. PSMD9 gene in the NIDDM2 locus is linked to type 2 diabetes in Italians. J Cell Physiol 2010, 222:265. 10.1002/jcp.21954, 19877155.
-
(2010)
J Cell Physiol
, vol.222
, pp. 265
-
-
Gragnoli, C.1
-
6
-
-
75749121855
-
PSMD9 is linked to MODY3
-
Gragnoli C. PSMD9 is linked to MODY3. J Cell Physiol 2010, 223:1.
-
(2010)
J Cell Physiol
, vol.223
, pp. 1
-
-
Gragnoli, C.1
-
7
-
-
0033499802
-
Bridge-1, a novel PDZ-domain coactivator of E2A-mediated regulation of insulin gene transcription
-
84960, 10567574
-
Thomas MKYK, Tenser MS, Wong GG, Habener JF. Bridge-1, a novel PDZ-domain coactivator of E2A-mediated regulation of insulin gene transcription. Mol Cell Biol 1999, 19:8492. 84960, 10567574.
-
(1999)
Mol Cell Biol
, vol.19
, pp. 8492
-
-
Thomas, M.K.Y.K.1
Tenser, M.S.2
Wong, G.G.3
Habener, J.F.4
-
8
-
-
33846539155
-
NEUROG3 variants and type 2 diabetes in Italians
-
Milord E, Gragnoli C. NEUROG3 variants and type 2 diabetes in Italians. Minerva Med 2006, 97:373.
-
(2006)
Minerva Med
, vol.97
, pp. 373
-
-
Milord, E.1
Gragnoli, C.2
-
9
-
-
0036338150
-
Merlin--rapid analysis of dense genetic maps using sparse gene flow trees
-
10.1038/ng786, 11731797
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR. Merlin--rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 2002, 30:97. 10.1038/ng786, 11731797.
-
(2002)
Nat Genet
, vol.30
, pp. 97
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
10
-
-
16044374799
-
Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families
-
10.1038/ng0996-90, 8782826
-
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. Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families. Nat Genet 1996, 14:90. 10.1038/ng0996-90, 8782826.
-
(1996)
Nat Genet
, vol.14
, pp. 90
-
-
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..
-
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
-
10.2337/diabetes.53.3.855, 14988275
-
Wiltshire SFT, Groves CJ, Levy JC, Hitman GA, Sampson M, Walker M, Menzel S, Hattersley AT, Cardon LRMM. 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 2004, 53:855. 10.2337/diabetes.53.3.855, 14988275.
-
(2004)
Diabetes
, vol.53
, pp. 855
-
-
Wiltshire, S.F.T.1
Groves, C.J.2
Levy, J.C.3
Hitman, G.A.4
Sampson, M.5
Walker, M.6
Menzel, S.7
Hattersley, A.T.8
Cardon, L.R.M.M.9
-
12
-
-
79958001279
-
T2D-Nephropathy Linkage within 12q24 Locus Diabetes
-
Gragnoli C. T2D-Nephropathy Linkage within 12q24 Locus Diabetes. Res Clin Pract 2011,
-
(2011)
Res Clin Pract
-
-
Gragnoli, C.1
-
13
-
-
0030897631
-
Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy
-
10.2337/diabetes.46.5.882, 9133559
-
Bowden DW, Sale M, Howard TD, Qadri A, Spray BJ, Rothschild CB, Akots G, Rich SS, Freedman BI. Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy. Diabetes 1997, 46:882. 10.2337/diabetes.46.5.882, 9133559.
-
(1997)
Diabetes
, vol.46
, pp. 882
-
-
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
|