-
1
-
-
0030739458
-
Diabetic eye disease
-
Klein R, Klein BEK: Diabetic eye disease. Lancet 350:197-204, 1997
-
(1997)
Lancet
, vol.350
, pp. 197-204
-
-
Klein, R.1
Klein, B.E.K.2
-
2
-
-
6844241955
-
Glycaemic control and development of retinopathy in type 2 diabetes mellitus: A longitudinal study
-
Guillausseau PJ, Massin P, Charles MA, Allaguy H, Guvenli Z, Virally M, Tielmans D, Assayag M, Warnet A, Lubetzki J: Glycaemic control and development of retinopathy in type 2 diabetes mellitus: a longitudinal study. Diabet Med 15:151-155, 1998
-
(1998)
Diabet Med
, vol.15
, pp. 151-155
-
-
Guillausseau, P.J.1
Massin, P.2
Charles, M.A.3
Allaguy, H.4
Guvenli, Z.5
Virally, M.6
Tielmans, D.7
Assayag, M.8
Warnet, A.9
Lubetzki, J.10
-
3
-
-
0032511583
-
Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33)
-
UK Prospective Diabetes Study (UKPDS) Group
-
UK Prospective Diabetes Study (UKPDS) Group: Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). Lancet 352:837-853, 1998
-
(1998)
Lancet
, vol.352
, pp. 837-853
-
-
-
4
-
-
0035134120
-
UKPDS 50: Risk factors for incidence and progression of retinopathy in type II diabetes over 6 years from diagnosis
-
for the UKPDS Group
-
Stratton IM, Kohner EM, Aldington SJ, Turner RC, Holman RR, Manley SE, Matthews DR, for the UKPDS Group: UKPDS 50: risk factors for incidence and progression of retinopathy in type II diabetes over 6 years from diagnosis. Diabetologia 44:156-163, 2001
-
(2001)
Diabetologia
, vol.44
, pp. 156-163
-
-
Stratton, I.M.1
Kohner, E.M.2
Aldington, S.J.3
Turner, R.C.4
Holman, R.R.5
Manley, S.E.6
Matthews, D.R.7
-
5
-
-
0020042123
-
Diabetic retinopathy in identical twins
-
Leslie RD, Pyke DA: Diabetic retinopathy in identical twins. Diabetes 31:19-21, 1982
-
(1982)
Diabetes
, vol.31
, pp. 19-21
-
-
Leslie, R.D.1
Pyke, D.A.2
-
6
-
-
0036434422
-
Familial clustering of diabetic retinopathy in South Indian type 2 diabetic patients
-
Rema M, Saravanan G, Deepa R, Mohan V: Familial clustering of diabetic retinopathy in South Indian type 2 diabetic patients. Diabet Med 19:910-916, 2002
-
(2002)
Diabet Med
, vol.19
, pp. 910-916
-
-
Rema, M.1
Saravanan, G.2
Deepa, R.3
Mohan, V.4
-
7
-
-
0030725948
-
Clustering of long-term complications in families with diabetes in the Diabetes Control and Complications Trial
-
Diabetes Control and Complications Trial Research Group
-
Diabetes Control and Complications Trial Research Group: Clustering of long-term complications in families with diabetes in the Diabetes Control and Complications Trial. Diabetes 46:1829-1839, 1997
-
(1997)
Diabetes
, vol.46
, pp. 1829-1839
-
-
-
8
-
-
18144384717
-
Familial aggregation of severity of diabetic retinopathy in Mexican Americans from Starr County, Texas
-
Hallman DM, Huber JC Jr, Gonzalez VH, Klein BE, Klein R, Hanis CL: Familial aggregation of severity of diabetic retinopathy in Mexican Americans from Starr County, Texas. Diabetes Care 28:1163-1168, 2005
-
(2005)
Diabetes Care
, vol.28
, pp. 1163-1168
-
-
Hallman, D.M.1
Huber Jr, J.C.2
Gonzalez, V.H.3
Klein, B.E.4
Klein, R.5
Hanis, C.L.6
-
9
-
-
0037617928
-
Molecular genetics of microvascular disease in diabetic retinopathy
-
Warpeha KM, Chakravarthy U: Molecular genetics of microvascular disease in diabetic retinopathy. Eye 17:305-311, 2003
-
(2003)
Eye
, vol.17
, pp. 305-311
-
-
Warpeha, K.M.1
Chakravarthy, U.2
-
10
-
-
0029112492
-
n dinucleotide repeat polymorphic marker at the 5′ end of the aldose reductase gene is associated with early-onset diabetic retinopathy in NIDDM patients
-
n dinucleotide repeat polymorphic marker at the 5′ end of the aldose reductase gene is associated with early-onset diabetic retinopathy in NIDDM patients. Diabetes 44:727-732, 1995
-
(1995)
Diabetes
, vol.44
, pp. 727-732
-
-
Ko, B.C.1
Lam, K.S.2
Wat, N.M.3
Chung, S.S.4
-
11
-
-
0029898063
-
Chromosome 7q35 and susceptibility to diabetic microvascular complications
-
Patel A, Hibberd ML, Millward BA, Demaine AG: Chromosome 7q35 and susceptibility to diabetic microvascular complications. J Diabetes Complications 10:62-67, 1996
-
(1996)
J Diabetes Complications
, vol.10
, pp. 62-67
-
-
Patel, A.1
Hibberd, M.L.2
Millward, B.A.3
Demaine, A.G.4
-
12
-
-
0345161817
-
A novel polymorphism in the aldose reductase gene promoter region is strongly associated with diabetic retinopathy in adolescents with type 1 diabetes
-
Kao YL, Donaghue K, Chan A, Knight J, Silink M: A novel polymorphism in the aldose reductase gene promoter region is strongly associated with diabetic retinopathy in adolescents with type 1 diabetes. Diabetes 48:1338-1340, 1999
-
(1999)
Diabetes
, vol.48
, pp. 1338-1340
-
-
Kao, Y.L.1
Donaghue, K.2
Chan, A.3
Knight, J.4
Silink, M.5
-
13
-
-
0032711922
-
An aldose reductase intragenic polymorphism associated with diabetic retinopathy
-
Kao YL, Donaghue K, Chan A, Knight J, Silink M: An aldose reductase intragenic polymorphism associated with diabetic retinopathy. Diabetes Res Clin Pract 46:155-160, 1999
-
(1999)
Diabetes Res Clin Pract
, vol.46
, pp. 155-160
-
-
Kao, Y.L.1
Donaghue, K.2
Chan, A.3
Knight, J.4
Silink, M.5
-
14
-
-
0033390623
-
Length rather than a specific allele of dinucleotide repeat in the 5′ upstream region of the aldose reductase gene is associated with diabetic retinopathy
-
Fujisawa T, Ikegami H, Kawaguchi Y, Yamato E, Nakagawa Y, Shen GQ, Fukuda M, Ogihara T: Length rather than a specific allele of dinucleotide repeat in the 5′ upstream region of the aldose reductase gene is associated with diabetic retinopathy. Diabet Med 16:1044-1047, 1999
-
(1999)
Diabet Med
, vol.16
, pp. 1044-1047
-
-
Fujisawa, T.1
Ikegami, H.2
Kawaguchi, Y.3
Yamato, E.4
Nakagawa, Y.5
Shen, G.Q.6
Fukuda, M.7
Ogihara, T.8
-
15
-
-
0032886411
-
Association of an (A-C)n dinucleotide repeat polymorphic marker at the 5′-region of the aldose reductase gene with retinopathy but not with nephropathy or neuropathy in Japanese patients with type 2 diabetes mellitus
-
Ichikawa F, Yamada K, Ishiyama-Shigemoto S, Yuan X, Nonaka K: Association of an (A-C)n dinucleotide repeat polymorphic marker at the 5′-region of the aldose reductase gene with retinopathy but not with nephropathy or neuropathy in Japanese patients with type 2 diabetes mellitus. Diabet Med 16:744-748, 1999
-
(1999)
Diabet Med
, vol.16
, pp. 744-748
-
-
Ichikawa, F.1
Yamada, K.2
Ishiyama-Shigemoto, S.3
Yuan, X.4
Nonaka, K.5
-
16
-
-
0033536561
-
Z-4 allele upstream of the aldose reductase gene is associated with proliferative retinopathy in Japanese patients with NIDDM, and elevated luciferase gene transcription in vitro
-
Ikegishi Y, Tawata M, Aida K, Onaya T: Z-4 allele upstream of the aldose reductase gene is associated with proliferative retinopathy in Japanese patients with NIDDM, and elevated luciferase gene transcription in vitro. Life Sci 65:2061-2070, 1999
-
(1999)
Life Sci
, vol.65
, pp. 2061-2070
-
-
Ikegishi, Y.1
Tawata, M.2
Aida, K.3
Onaya, T.4
-
17
-
-
0033621849
-
23 [Z-2] polymorphism of the aldose reductase gene and fast progression of retinopathy in Chilean type 2 diabetics
-
23 [Z-2] polymorphism of the aldose reductase gene and fast progression of retinopathy in Chilean type 2 diabetics. Diabetes Res Clin Pract 47:169-176, 2000
-
(2000)
Diabetes Res Clin Pract
, vol.47
, pp. 169-176
-
-
Olmos, P.1
Futers, S.2
Acosta, A.M.3
Siegel, S.4
Maiz, A.5
Schiaffino, R.6
Morales, P.7
Díaz, R.8
Arriagada, P.9
Claro, J.C.10
Vega, R.11
Vollrath, V.12
Velasco, S.13
Emmerich, M.14
-
18
-
-
0032870334
-
ACE gene polymorphism and proliferative retinopathy in type 1 diabetes: Results of a case-control study
-
Rabensteiner D, Abrahamian H, Irsigler K, Hermann KM, Kiener HP, Mayer G, Kaider A, Prager R: ACE gene polymorphism and proliferative retinopathy in type 1 diabetes: results of a case-control study. Diabetes Care 22:1530-1535, 1999
-
(1999)
Diabetes Care
, vol.22
, pp. 1530-1535
-
-
Rabensteiner, D.1
Abrahamian, H.2
Irsigler, K.3
Hermann, K.M.4
Kiener, H.P.5
Mayer, G.6
Kaider, A.7
Prager, R.8
-
19
-
-
0033661751
-
Detection of the association between a deletion polymorphism in the gene encoding angiotensin I-converting enzyme and advanced diabetic retinopathy
-
Matsumoto A, Iwashima Y, Abiko A, Morikawa A, Sekiguchi M, Eto M, Makino I: Detection of the association between a deletion polymorphism in the gene encoding angiotensin I-converting enzyme and advanced diabetic retinopathy. Diabetes Res Clin Pract 50:195-202, 2000
-
(2000)
Diabetes Res Clin Pract
, vol.50
, pp. 195-202
-
-
Matsumoto, A.1
Iwashima, Y.2
Abiko, A.3
Morikawa, A.4
Sekiguchi, M.5
Eto, M.6
Makino, I.7
-
20
-
-
0031931515
-
Meta-analysis of association of insertion/deletion polymorphism of angiotensin I-converting enzyme gene with diabetic nephropathy and retinopathy
-
Fujisawa T, Ikegami H, Kawaguchi Y, Hamada Y, Ueda H, Shintani M, Fukuda M, Ogihara T: Meta-analysis of association of insertion/deletion polymorphism of angiotensin I-converting enzyme gene with diabetic nephropathy and retinopathy. Diabetologia 41:47-53, 1998
-
(1998)
Diabetologia
, vol.41
, pp. 47-53
-
-
Fujisawa, T.1
Ikegami, H.2
Kawaguchi, Y.3
Hamada, Y.4
Ueda, H.5
Shintani, M.6
Fukuda, M.7
Ogihara, T.8
-
21
-
-
0031942841
-
Sib-pair linkage analysis for susceptibility genes for microvascular complications among Pima Indians with type 2 diabetes: Pima Diabetes Genes Group
-
Imperatore G, Hanson RL, Pettitt DJ, Kobes S, Bennett PH, Knowler WC: Sib-pair linkage analysis for susceptibility genes for microvascular complications among Pima Indians with type 2 diabetes: Pima Diabetes Genes Group. Diabetes 47:821-830, 1998
-
(1998)
Diabetes
, vol.47
, pp. 821-830
-
-
Imperatore, G.1
Hanson, R.L.2
Pettitt, D.J.3
Kobes, S.4
Bennett, P.H.5
Knowler, W.C.6
-
22
-
-
18244379376
-
Multi-center genetic study of hypertension: The Family Blood Pressure Program (FBPP)
-
The FBPP Investigators
-
The FBPP Investigators: Multi-center genetic study of hypertension: the Family Blood Pressure Program (FBPP). Hypertension 39:3-9, 2002
-
(2002)
Hypertension
, vol.39
, pp. 3-9
-
-
-
23
-
-
0025845943
-
Grading diabetic retinopathy from stereoscopic color fundus photographs: An extension of the modified Airlie House classification
-
Early Treatment Diabetic Retinopathy Study Research Group
-
Early Treatment Diabetic Retinopathy Study Research Group: Grading diabetic retinopathy from stereoscopic color fundus photographs: an extension of the modified Airlie House classification. Ophthalmology 98 (Suppl.):786-806, 1991
-
(1991)
Ophthalmology
, vol.98
, Issue.SUPPL.
, pp. 786-806
-
-
-
24
-
-
0030728925
-
Allele-sharing models: LOD scores and accurate linkage tests
-
Kong A, Cox NJ: Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet 61:1179-1188, 1997
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1179-1188
-
-
Kong, A.1
Cox, N.J.2
-
25
-
-
3042513608
-
Ordered subset analysis in genetic linkage mapping of complex traits
-
Hauser ER, Watanabe RM, Duren WL, Bass MP, Langefeld CD, Boehnke M: Ordered subset analysis in genetic linkage mapping of complex traits. Genet Epidemiol 27:53-63, 2004
-
(2004)
Genet Epidemiol
, vol.27
, pp. 53-63
-
-
Hauser, E.R.1
Watanabe, R.M.2
Duren, W.L.3
Bass, M.P.4
Langefeld, C.D.5
Boehnke, M.6
-
26
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander E, Kruglyak L: Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet 11:241-247, 1995
-
(1995)
Nat Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
27
-
-
0027966026
-
A locus on chromosome 15q26 (IDDM3) produces susceptibility to insulin-dependent diabetes mellitus
-
Field LL, Tobias R, Magnus T: A locus on chromosome 15q26 (IDDM3) produces susceptibility to insulin-dependent diabetes mellitus. Nat Genet 8:189-194, 1994
-
(1994)
Nat Genet
, vol.8
, pp. 189-194
-
-
Field, L.L.1
Tobias, R.2
Magnus, T.3
-
28
-
-
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: 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
-
(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
-
29
-
-
0030907295
-
New susceptibility locus for NIDDM is localized to human chromosome 20q
-
Ji L, Malecki M, Warram JH, Yang Y, Rich SS, Krolewski AS: New susceptibility locus for NIDDM is localized to human chromosome 20q. Diabetes 46:876-881, 1997
-
(1997)
Diabetes
, vol.46
, pp. 876-881
-
-
Ji, L.1
Malecki, M.2
Warram, J.H.3
Yang, Y.4
Rich, S.S.5
Krolewski, A.S.6
-
30
-
-
0030766446
-
A susceptibility locus for early-onset non-insulin dependent (type 2) diabetes mellitus maps to chromosome 20q, proximal to the phosphoenolpyruvate carboxykinase gene
-
Zouali H, Hani EH, Philippi A, Vionnet N, Beckmann JS, Demenais F, Froguel P: A susceptibility locus for early-onset non-insulin dependent (type 2) diabetes mellitus maps to chromosome 20q, proximal to the phosphoenolpyruvate carboxykinase gene. Hum Mol Genet 6:1401-1408, 1997
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1401-1408
-
-
Zouali, H.1
Hani, E.H.2
Philippi, A.3
Vionnet, N.4
Beckmann, J.S.5
Demenais, F.6
Froguel, P.7
-
31
-
-
13044277561
-
-
Ghosh S, Watanabe RM, Hauser ER, Valle T, Magnuson VL, Erdos MR, Langefeld CD, Balow J Jr, Ally DS, Kohtamaki K, Chines P, Birznieks G, Kaleta H-S, Musick A, Te C, Tannenbaum J, Eldridge W, Shapiro S, Martin C, Witt A, So A, Chang J, Shurtleff B, Porter R, Kudelko K, Unni A, Segal L, Sharaf R, Blaschak-Harvan J, Eriksson J, Tenkula T, Vidgren G, Ehnholm C, Tuomilehto-Wolf E, Hagopian W, Buchanan TA, Tuomilehto J, Bergman RN, Collins FS, Boehnke M: Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs. Proc Natl Acad Sci U S A 96:2198-2203, 1999
-
Ghosh S, Watanabe RM, Hauser ER, Valle T, Magnuson VL, Erdos MR, Langefeld CD, Balow J Jr, Ally DS, Kohtamaki K, Chines P, Birznieks G, Kaleta H-S, Musick A, Te C, Tannenbaum J, Eldridge W, Shapiro S, Martin C, Witt A, So A, Chang J, Shurtleff B, Porter R, Kudelko K, Unni A, Segal L, Sharaf R, Blaschak-Harvan J, Eriksson J, Tenkula T, Vidgren G, Ehnholm C, Tuomilehto-Wolf E, Hagopian W, Buchanan TA, Tuomilehto J, Bergman RN, Collins FS, Boehnke M: Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs. Proc Natl Acad Sci U S A 96:2198-2203, 1999
-
-
-
-
32
-
-
0346096976
-
Transplantation of Schwann cell line clones secreting GDNF or BDNF into the retinas of dystrophic Royal College of Surgeons rats
-
Lawrence JM, Keegan DJ, Muir EM, Coffey PJ, Rogers JH, Wilby MJ, Fawcett JW, Lund RD: Transplantation of Schwann cell line clones secreting GDNF or BDNF into the retinas of dystrophic Royal College of Surgeons rats. Invest Ophthalmol Vis Sci 45:267-274, 2004
-
(2004)
Invest Ophthalmol Vis Sci
, vol.45
, pp. 267-274
-
-
Lawrence, J.M.1
Keegan, D.J.2
Muir, E.M.3
Coffey, P.J.4
Rogers, J.H.5
Wilby, M.J.6
Fawcett, J.W.7
Lund, R.D.8
-
33
-
-
0037406876
-
An early-onset autosomal dominant macular dystrophy (MCDR3) resembling North Carolina macular dystrophy maps to chromosome 5
-
Michaelides M, Johnson S, Tekriwal AK, Holder GE, Bellmann C, Kinning E, Woodruff G, Trembath RC, Hunt DM, Moore AT: An early-onset autosomal dominant macular dystrophy (MCDR3) resembling North Carolina macular dystrophy maps to chromosome 5. Invest Ophthalmol Vis Sci 44:2178-2183, 2003
-
(2003)
Invest Ophthalmol Vis Sci
, vol.44
, pp. 2178-2183
-
-
Michaelides, M.1
Johnson, S.2
Tekriwal, A.K.3
Holder, G.E.4
Bellmann, C.5
Kinning, E.6
Woodruff, G.7
Trembath, R.C.8
Hunt, D.M.9
Moore, A.T.10
-
34
-
-
13144267708
-
Functions of the two glutamate transporters GLAST and GLT-1 in the retina
-
Harada T, Harada C, Watanabe M, Inoue Y, Sakagawa T, Nakayama N, Sasaki S, Okuyama S, Watase K, Wada K, Tanaka K: Functions of the two glutamate transporters GLAST and GLT-1 in the retina. Proc Natl Acad Sci U S A 95:4663-4666, 1998
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 4663-4666
-
-
Harada, T.1
Harada, C.2
Watanabe, M.3
Inoue, Y.4
Sakagawa, T.5
Nakayama, N.6
Sasaki, S.7
Okuyama, S.8
Watase, K.9
Wada, K.10
Tanaka, K.11
-
35
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch N, Merikangas K: The future of genetic studies of complex human diseases. Science 273:1516-1517, 1996
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
36
-
-
0034753277
-
The genetic dissection of complex traits in a founder population
-
Ober C, Abney M, McPeek MS: The genetic dissection of complex traits in a founder population. Am J Hum Genet 69:1068-1079, 2001
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1068-1079
-
-
Ober, C.1
Abney, M.2
McPeek, M.S.3
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