-
1
-
-
0029561974
-
Molecular dissection of quantitative traits: Progress and prospects
-
Paterson AH. Molecular dissection of quantitative traits: progress and prospects. Genome Res 1995;5:321-33.
-
(1995)
Genome Res
, vol.5
, pp. 321-333
-
-
Paterson, A.H.1
-
2
-
-
0005813632
-
The epidemiology of blindness
-
Miller S, ed. Bristol: Wright
-
Cullinan TM. The epidemiology of blindness. In: Miller S, ed. Clinical ophthalmology. Bristol: Wright, 1987:571-8.
-
(1987)
Clinical Ophthalmology
, pp. 571-578
-
-
Cullinan, T.M.1
-
3
-
-
0030027775
-
Is the incidence of registrable age-related macular degeneration increasing?
-
Evans J, Wormald R. Is the incidence of registrable age-related macular degeneration increasing? Br J Ophthalmol 1996;80:9-14.
-
(1996)
Br J Ophthalmol
, vol.80
, pp. 9-14
-
-
Evans, J.1
Wormald, R.2
-
4
-
-
0028934221
-
An international classification and grading system for age-related maculopathy and age-related macular degeneration
-
The International ARM Epidemiological Study Group. An international classification and grading system for age-related maculopathy and age-related macular degeneration. Surv Ophthalmol 1995;39:367-74.
-
(1995)
Surv Ophthalmol
, vol.39
, pp. 367-374
-
-
-
7
-
-
0026739091
-
Monozygotic twin brothers with age-related macular degeneration
-
Dosso AA, Bovet J. Monozygotic twin brothers with age-related macular degeneration. Ophthalmologies 1992;205:24-8.
-
(1992)
Ophthalmologies
, vol.205
, pp. 24-28
-
-
Dosso, A.A.1
Bovet, J.2
-
8
-
-
0028610188
-
A twin study on age-related macular degeneration
-
Meyers SM. A twin study on age-related macular degeneration. Trans Am Ophthalmol Soc 1994;92:775-843.
-
(1994)
Trans Am Ophthalmol Soc
, vol.92
, pp. 775-843
-
-
Meyers, S.M.1
-
9
-
-
0028244159
-
Heredity and age-related macular degeneration. Observations in monozygotic twins
-
Klein ML, Maudlin WM, Stoumbos VD. Heredity and age-related macular degeneration. Observations in monozygotic twins. Arch Ophthalmol 1995;112:932-7.
-
(1995)
Arch Ophthalmol
, vol.112
, pp. 932-937
-
-
Klein, M.L.1
Maudlin, W.M.2
Stoumbos, V.D.3
-
10
-
-
0028033697
-
Is genetic predisposition an important risk factor in age-related macular degeneration?
-
Silvestri G, Johnson PB, Hughes AE. Is genetic predisposition an important risk factor in age-related macular degeneration? Eye 1994;8:564-8.
-
(1994)
Eye
, vol.8
, pp. 564-568
-
-
Silvestri, G.1
Johnson, P.B.2
Hughes, A.E.3
-
11
-
-
0027201976
-
Age-related Bruch's membrane change: A clinical study of the relative role of heredity and environment
-
Piguet B, Wells JA, Palmvang IB, Wormald R, Chisholm IH, Bird AC. Age-related Bruch's membrane change: a clinical study of the relative role of heredity and environment. Br J Ophthalmol 1993;77:400-3.
-
(1993)
Br J Ophthalmol
, vol.77
, pp. 400-403
-
-
Piguet, B.1
Wells, J.A.2
Palmvang, I.B.3
Wormald, R.4
Chisholm, I.H.5
Bird, A.C.6
-
12
-
-
0019215047
-
The Framingham Eye Study monograph
-
Leibowitz H, Krueger D, Maunder L, Milton RC, Kini MM, Kahn HA, et al. The Framingham Eye Study monograph. Surv Ophthalmol 1980; 24(suppl):428-35.
-
(1980)
Surv Ophthalmol
, vol.24
, Issue.SUPPL.
, pp. 428-435
-
-
Leibowitz, H.1
Krueger, D.2
Maunder, L.3
Milton, R.C.4
Kini, M.M.5
Kahn, H.A.6
-
13
-
-
0028945839
-
Racial/ethnic differences in age-related maculopathy: Third National Health and nutritional examination survey
-
Klein R, Rowland ML, Harris MI. Racial/ethnic differences in age-related maculopathy: Third National Health and nutritional examination survey. Ophthalmology 1995;102:317-81.
-
(1995)
Ophthalmology
, vol.102
, pp. 317-381
-
-
Klein, R.1
Rowland, M.L.2
Harris, M.I.3
-
15
-
-
0027955814
-
Decreasing stromal iris pigmentation as a risk factor for age-related macular degeneration
-
Holz FG, Piguet B, Minassian DC, Bird AC, Weale RA. Decreasing stromal iris pigmentation as a risk factor for age-related macular degeneration. Am J Ophthalmol 1994 117:19-23.
-
(1994)
Am J Ophthalmol
, vol.117
, pp. 19-23
-
-
Holz, F.G.1
Piguet, B.2
Minassian, D.C.3
Bird, A.C.4
Weale, R.A.5
-
16
-
-
0028298094
-
Sibling correlations and segregation analysis of age-related maculopathy: The Beaver Dam Eye Study
-
Heiba IM, Elston RC, Klein BEK, Klein R. Sibling correlations and segregation analysis of age-related maculopathy: the Beaver Dam Eye Study. Gen Epidemiol 1994;11:51-67.
-
(1994)
Gen Epidemiol
, vol.11
, pp. 51-67
-
-
Heiba, I.M.1
Elston, R.C.2
Bek, K.3
Klein, R.4
-
17
-
-
0029035306
-
Retinal photoreceptor dystrophies. L1. Edward Jackson Memorial Lecture
-
Bird AC. Retinal photoreceptor dystrophies. L1. Edward Jackson Memorial Lecture. Am J Ophthalmol 1995;118:543-62.
-
(1995)
Am J Ophthalmol
, vol.118
, pp. 543-562
-
-
Bird, A.C.1
-
18
-
-
9044250844
-
Linkage of autosomal dominant radial drusen (malattia levantinese) to chromosome 2p16-21
-
Héon E, Piguet B, Munier F, Sneed SR, Morgan CM, Forni S, et al. Linkage of autosomal dominant radial drusen (malattia levantinese) to chromosome 2p16-21. Nature Genet 1996;114:193-8.
-
(1996)
Nature Genet
, vol.114
, pp. 193-198
-
-
Héon, E.1
Piguet, B.2
Munier, F.3
Sneed, S.R.4
Morgan, C.M.5
Forni, S.6
-
19
-
-
0028900170
-
Extensive intrafamilial and interfamilial phenotypic variation among patients with autosomal dominant retinal dystrophy and muations in the human RDS/peripherin gene
-
Apfelstedt-Sylla E, Theischen M, Ruther K, Wedemann H, Gal A, Zrenner E. Extensive intrafamilial and interfamilial phenotypic variation among patients with autosomal dominant retinal dystrophy and muations in the human RDS/peripherin gene. Br J Ophthalmol 1995;79:28-34.
-
(1995)
Br J Ophthalmol
, vol.79
, pp. 28-34
-
-
Apfelstedt-Sylla, E.1
Theischen, M.2
Ruther, K.3
Wedemann, H.4
Gal, A.5
Zrenner, E.6
-
20
-
-
0028097367
-
Mutations in the tissue inhibitor of metalloproteinases-3 (TTMP3) in patients with Sorsby's fundus dystrophy
-
Weber, BHF, Vogt G, Pruett RC, Stohr H, Felbor U. Mutations in the tissue inhibitor of metalloproteinases-3 (TTMP3) in patients with Sorsby's fundus dystrophy. Nature Genet 1994;8:352-6.
-
(1994)
Nature Genet
, vol.8
, pp. 352-356
-
-
Weber, B.H.F.1
Vogt, G.2
Pruett, R.C.3
Stohr, H.4
Felbor, U.5
-
21
-
-
0017654306
-
The Framingham Eye Study II. Association of ophthalmic pathology with single variables previously measured in the Framlingham Heart Study
-
Khan H, Leibowitz H, Ganley J, Kini MM, Colton T, Nickerson RS, et al. The Framingham Eye Study II. Association of ophthalmic pathology with single variables previously measured in the Framlingham Heart Study. Am J Epidemiol 1977;106:33-11.
-
(1977)
Am J Epidemiol
, vol.106
, pp. 33-111
-
-
Khan, H.1
Leibowitz, H.2
Ganley, J.3
Kini, M.M.4
Colton, T.5
Nickerson, R.S.6
-
22
-
-
0029084456
-
Age-related macular degeneration is accociated with atherosclerosis - The Rotterdam study
-
Vingerling JR, Dielemans I, Bots ML, Hofman A, Grobbee DE, DeJong PTVM. Age-related macular degeneration is accociated with atherosclerosis - the Rotterdam study. Am J Epidemiol 1995;142:404-9.
-
(1995)
Am J Epidemiol
, vol.142
, pp. 404-409
-
-
Vingerling, J.R.1
Dielemans, I.2
Bots, M.L.3
Hofman, A.4
Grobbee, D.E.5
DeJong, P.T.V.M.6
-
23
-
-
0029093734
-
Alcohol use and age-related maculopathy in the Beaver Dam Eye Study
-
Ritter LL, Klein R, Klein BE Mares-Pelman JA, Jensen SC. Alcohol use and age-related maculopathy in the Beaver Dam Eye Study. Am J Ophthalmol 1995;120:190-6.
-
(1995)
Am J Ophthalmol
, vol.120
, pp. 190-196
-
-
Ritter, L.L.1
Klein, R.2
Klein, B.E.3
Mares-Pelman, J.A.4
Jensen, S.C.5
-
24
-
-
0029064313
-
Macular degeneration and early menopause: A case-control study
-
Vingerling JR, Dielemans I, Witteman JCM, Hofman A, Grobbee DE, De Jong PTVM. Macular degeneration and early menopause: a case-control study. BMJ 1995;310:1570-1.
-
(1995)
BMJ
, vol.310
, pp. 1570-1571
-
-
Vingerling, J.R.1
Dielemans, I.2
Witteman, J.C.M.3
Hofman, A.4
Grobbee, D.E.5
De Jong, P.T.V.M.6
-
25
-
-
0027450026
-
The Beaver Dam Eye Study: The relation of age-related maculopathy to smoking
-
Klein R, Klein BEK, Linton KLP, Demets DL. The Beaver Dam Eye Study: the relation of age-related maculopathy to smoking. Am J Epidemiol 1993; 137:190-200.
-
(1993)
Am J Epidemiol
, vol.137
, pp. 190-200
-
-
Klein, R.1
Klein, B.E.K.2
Linton, K.L.P.3
Demets, D.L.4
-
26
-
-
0025764557
-
Doyne lecture: Pathogenesis of retinal pigment epithelial detachment in the elderly; the relevance of Bruch's membrane change
-
Bird AC. Doyne lecture: Pathogenesis of retinal pigment epithelial detachment in the elderly; the relevance of Bruch's membrane change. Eye 1991;5:1-12.
-
(1991)
Eye
, vol.5
, pp. 1-12
-
-
Bird, A.C.1
-
27
-
-
0029017808
-
Nutritional supplement use and age-related macular degeneration
-
Chew EY. Nutritional supplement use and age-related macular degeneration. Curr Opin Ophthalmol 1995;6:19-24.
-
(1995)
Curr Opin Ophthalmol
, vol.6
, pp. 19-24
-
-
Chew, E.Y.1
-
28
-
-
0028082441
-
Are antioxidants or supplements protective for age-related macular degeneration
-
West S, Vitale S, Hallfrisch J, Munoz B, Muller D, Bressler S, et al. Are antioxidants or supplements protective for age-related macular degeneration. Arch Ophthalmol 1994;112:222-7.
-
(1994)
Arch Ophthalmol
, vol.112
, pp. 222-227
-
-
West, S.1
Vitale, S.2
Hallfrisch, J.3
Munoz, B.4
Muller, D.5
Bressler, S.6
-
29
-
-
0028786898
-
Serum antioxidants and age-related macular degeneration in a population based case-control study
-
Mares-Pelman JA, Brady WE, Klein R, Klein BEK, Bowen P, Stecewicz-Apuntzakis M, et al. Serum antioxidants and age-related macular degeneration in a population based case-control study. Arch Ophthalmol 1995;113:1518-23.
-
(1995)
Arch Ophthalmol
, vol.113
, pp. 1518-1523
-
-
Mares-Pelman, J.A.1
Brady, W.E.2
Klein, R.3
Klein, B.E.K.4
Bowen, P.5
Stecewicz-Apuntzakis, M.6
-
30
-
-
0023736201
-
-
Klein R, Klein BEK, Moss SE, Davis MD, DeMets DL. Glycosylated hemoglobin predicts the incidence and progression of diabetic retinopathy. JAMA 1988;268:2864-71.
-
(1988)
Glycosylated Hemoglobin Predicts the Incidence and Progression of Diabetic Retinopathy. JAMA
, vol.268
, pp. 2864-2871
-
-
Klein, R.1
Klein, B.E.K.2
Moss, S.E.3
Davis, M.D.4
DeMets, D.L.5
-
31
-
-
0028833239
-
The effect of intensive diabetes treatment on the progression of diabetic retinopathy in insulin-dependent diabetes
-
Diabetes Control and Complications Trial Research Group. The effect of intensive diabetes treatment on the progression of diabetic retinopathy in insulin-dependent diabetes. Arch Ophthalmol 1995;113:36-51.
-
(1995)
Arch Ophthalmol
, vol.113
, pp. 36-51
-
-
-
33
-
-
0029045820
-
Extra-pancreatic manifestations in diabetes secondary to mitochondrial-DNA point mutations within the tRNA (Leu)UUR gene
-
Vialettes B, Paquisfluchinger V, Silvestreailland P, Bendaham D, Pelissier JF, Etcharybouyx F, et al. Extra-pancreatic manifestations in diabetes secondary to mitochondrial-DNA point mutations within the tRNA (Leu)UUR gene. Diabetes Care 1995;18:1023-8.
-
(1995)
Diabetes Care
, vol.18
, pp. 1023-1028
-
-
Vialettes, B.1
Paquisfluchinger, V.2
Silvestreailland, P.3
Bendaham, D.4
Pelissier, J.F.5
Etcharybouyx, F.6
-
34
-
-
0030046495
-
Mitochondria and diabetes - Genetic, biochemical and clinical implications of the cellular energy circuit
-
Gerbitz KD, Gempel K, Bradiczka D. Mitochondria and diabetes - genetic, biochemical and clinical implications of the cellular energy circuit. Diabetes 1996;45:113-26.
-
(1996)
Diabetes
, vol.45
, pp. 113-126
-
-
Gerbitz, K.D.1
Gempel, K.2
Bradiczka, D.3
-
35
-
-
0021136256
-
The Wisconsin epidemiologic study of diabetic retinopathy II. Prevalence and risk of diabetic retinopathy when age at diagnosis is less that 30 years
-
Klein R, Klein BEK, Moss SE, Davis MD, DeMets DL. The Wisconsin epidemiologic study of diabetic retinopathy II. Prevalence and risk of diabetic retinopathy when age at diagnosis is less that 30 years. Arch Ophthalmol 1984;102:520-6.
-
(1984)
Arch Ophthalmol
, vol.102
, pp. 520-526
-
-
Klein, R.1
Klein, B.E.K.2
Moss, S.E.3
Davis, M.D.4
DeMets, D.L.5
-
36
-
-
0021191759
-
The Wisconsin epidemiologic study of diabetic retinopathy III. Prevalence and risk of diabetic retinopathy when age at diagnosis is 30 or more years
-
Klein R, Klein BEK, Moss SE, Davis MD, DeMets DL. The Wisconsin epidemiologic study of diabetic retinopathy III. Prevalence and risk of diabetic retinopathy when age at diagnosis is 30 or more years. Arch Ophthalmol 1984;102:527-32.
-
(1984)
Arch Ophthalmol
, vol.102
, pp. 527-532
-
-
Klein, R.1
Klein, B.E.K.2
Moss, S.E.3
Davis, M.D.4
DeMets, D.L.5
-
37
-
-
0022365329
-
Multiple factors in the prediction of risk of proliferative diabetic retinopathy
-
Rand LI, Krolewski AS, Aiello LM, Warram JH, Baker RS, Maki T. Multiple factors in the prediction of risk of proliferative diabetic retinopathy. N Engl J Med 1985;313:1433-8.
-
(1985)
N Engl J Med
, vol.313
, pp. 1433-1438
-
-
Rand, L.I.1
Krolewski, A.S.2
Aiello, L.M.3
Warram, J.H.4
Baker, R.S.5
Maki, T.6
-
39
-
-
0028009661
-
The emperor's new genes: 1993 RD Lawrence lecture
-
Todd JA. The emperor's new genes: 1993 RD Lawrence lecture. Diabetic Med 1994;11:6-16.
-
(1994)
Diabetic Med
, vol.11
, pp. 6-16
-
-
Todd, J.A.1
-
40
-
-
0028829170
-
Multifactorial inheritance in type 1 diabetes
-
Cordell HJ, Todd JA. Multifactorial inheritance in type 1 diabetes. TIGS 1995;11:499-504.
-
(1995)
TIGS
, vol.11
, pp. 499-504
-
-
Cordell, H.J.1
Todd, J.A.2
-
41
-
-
0028881617
-
The minisatellite in the diabetes susceptibility locus IDDM2 regulates insulin transcription
-
Kennedy GC, German MS, Rutter WJ. The minisatellite in the diabetes susceptibility locus IDDM2 regulates insulin transcription. Nature Genet 1995;9:293-8.
-
(1995)
Nature Genet
, vol.9
, pp. 293-298
-
-
Kennedy, G.C.1
German, M.S.2
Rutter, W.J.3
-
42
-
-
0023201498
-
Concordance for type 2 (non-insulin-dependent) diabetes mellitus in male twins
-
Newman B, Selby J, King M-C, Slemenda C, Fabsitz R, Friedman G. Concordance for type 2 (non-insulin-dependent) diabetes mellitus in male twins). Diabetologia 1987;30:763-8.
-
(1987)
Diabetologia
, vol.30
, pp. 763-768
-
-
Newman, B.1
Selby, J.2
King, M.-C.3
Slemenda, C.4
Fabsitz, R.5
Friedman, G.6
-
43
-
-
0026641354
-
Concordance for type 1 (insulin-dependent) and type 2 (non-insulin-dependent) diabetes mellitus in a population-based cohort of twins in Finland
-
Kaprio J, Tuomilehto J, Koshenvuo M, Romanov K, Reuanen A, Eriksson J, et al. Concordance for type 1 (insulin-dependent) and type 2 (non-insulin-dependent) diabetes mellitus in a population-based cohort of twins in Finland. Diabetologia 1992;35:1060-7.
-
(1992)
Diabetologia
, vol.35
, pp. 1060-1067
-
-
Kaprio, J.1
Tuomilehto, J.2
Koshenvuo, M.3
Romanov, K.4
Reuanen, A.5
Eriksson, J.6
-
44
-
-
0025094344
-
Mapping genes in diabetes. Genetic epidemiological perspective
-
Rich SS. Mapping genes in diabetes. Genetic epidemiological perspective. Diabetes 1990;39:1315-9.
-
(1990)
Diabetes
, vol.39
, pp. 1315-1319
-
-
Rich, S.S.1
-
45
-
-
0029269383
-
Probability and complex disease genes
-
Ghosh S. Probability and complex disease genes. Nature Genet 1995;9: 223-4.
-
(1995)
Nature Genet
, vol.9
, pp. 223-224
-
-
Ghosh, S.1
-
46
-
-
0028848010
-
A missense mutation in the glucagon receptor gene is associated with non-insulin dependent diabetes mellitus
-
Hager J, Hansen L, Vaiisse C, Vionnet N, Pilippi A, Poller W, et al. A missense mutation in the glucagon receptor gene is associated with non-insulin dependent diabetes mellitus. Nature Genet 1995;9:299-304.
-
(1995)
Nature Genet
, vol.9
, pp. 299-304
-
-
Hager, J.1
Hansen, L.2
Vaiisse, C.3
Vionnet, N.4
Pilippi, A.5
Poller, W.6
-
47
-
-
0030058877
-
Genetic analysis of non-insulin dependent diabetes mellitus in the GK rat
-
Galli J, Luo-Sheng L, Glaser A, Claes-Göran Ö, Jiao H, Fakhari-Rad H, et al. Genetic analysis of non-insulin dependent diabetes mellitus in the GK rat. Nature Genet 1996;12:31-7.
-
(1996)
Nature Genet
, vol.12
, pp. 31-37
-
-
Galli, J.1
Luo-Sheng, L.2
Glaser, A.3
Claes-Göran, Ö.4
Jiao, H.5
Fakhari-Rad, H.6
-
48
-
-
9044247460
-
Chromosomal mapping of genetic loci associated with non-insulin dependent diabetes in the GK rat
-
Gauguier D, Froguel P, Parent V, Bernard C, Bihoreau M-T, Portha B, et al. Chromosomal mapping of genetic loci associated with non-insulin dependent diabetes in the GK rat. Nature Genet 1996;12:38-43.
-
(1996)
Nature Genet
, vol.12
, pp. 38-43
-
-
Gauguier, D.1
Froguel, P.2
Parent, V.3
Bernard, C.4
Bihoreau, M.-T.5
Portha, B.6
-
49
-
-
0029689364
-
Rat model contributes new loci for NIDDM susceptibility in man
-
Permutt MA, Ghosh S. Rat model contributes new loci for NIDDM susceptibility in man. Nature Genet 1996;12:4-6.
-
(1996)
Nature Genet
, vol.12
, pp. 4-6
-
-
Permutt, M.A.1
Ghosh, S.2
-
50
-
-
0025234860
-
The Swedish childhood diabetes study. An analysis of the temporal variation in diabetes incidence 1978-1987
-
Nystrom L, Dahlquist G, Rewers M, Wall S. The Swedish childhood diabetes study. An analysis of the temporal variation in diabetes incidence 1978-1987. Int J Epidemiol 1990;1:141-6.
-
(1990)
Int J Epidemiol
, vol.1
, pp. 141-146
-
-
Nystrom, L.1
Dahlquist, G.2
Rewers, M.3
Wall, S.4
-
51
-
-
0028803464
-
Spatial clustering in childhood diabetes: Evidence of an environmental cause
-
Bedingten MJ, Muzulu SI, Burden AC. Spatial clustering in childhood diabetes: evidence of an environmental cause. Diabetic Med 1995;12:865-7.
-
(1995)
Diabetic Med
, vol.12
, pp. 865-867
-
-
Bedingten, M.J.1
Muzulu, S.I.2
Burden, A.C.3
-
52
-
-
0023757321
-
Significance of the concordance rate in type 1 (insulin-dependent) diabetes in identical twins
-
Olmos P, A'Hern R, Heaton DA, Millward BA, Risley D, Pyke DA, et al. Significance of the concordance rate in type 1 (insulin-dependent) diabetes in identical twins. Diabitologia 1988;31:747-50.
-
(1988)
Diabitologia
, vol.31
, pp. 747-750
-
-
Olmos, P.1
A'Hern, R.2
Heaton, D.A.3
Millward, B.A.4
Risley, D.5
Pyke, D.A.6
-
53
-
-
0023950172
-
Association of cytomegalovirus infection with autoimmune type 1 diabetes
-
Pak CY, Hyone-Myong E, McArthur RG, Yoon JW. Association of cytomegalovirus infection with autoimmune type 1 diabetes. Lancet 1988;ii:1-4.
-
(1988)
Lancet
, vol.2
, pp. 1-4
-
-
Pak, C.Y.1
Hyone-Myong, E.2
McArthur, R.G.3
Yoon, J.W.4
-
54
-
-
0025787852
-
A protective role of the environment in the development of type 1 diabetes ?
-
Todd JA. A protective role of the environment in the development of type 1 diabetes ? Diabetic Med 1991;8:906-10.
-
(1991)
Diabetic Med
, vol.8
, pp. 906-910
-
-
Todd, J.A.1
-
55
-
-
0001900504
-
Etiologic mechanisms in diabetic retinopathy
-
Ryan SJ, ed. St Louis: CV Mosby
-
Frank RN. Etiologic mechanisms in diabetic retinopathy. In: Ryan SJ, ed. Retina. II Medical retina. St Louis: CV Mosby, 1994.
-
(1994)
Retina. II Medical Retina
-
-
Frank, R.N.1
-
56
-
-
0024388554
-
Epidemiology and genetics of primary congenital glaucoma in Slovakia. Description of a form of primary congenital glaucoma in gypsies with autosomal recessive inheritance and complete penetrance
-
Gencik A. Epidemiology and genetics of primary congenital glaucoma in Slovakia. Description of a form of primary congenital glaucoma in gypsies with autosomal recessive inheritance and complete penetrance. Dev Ophthalmol 1989;16:76-115.
-
(1989)
Dev Ophthalmol
, vol.16
, pp. 76-115
-
-
Gencik, A.1
-
58
-
-
0022386973
-
Hereditary glaucomas: A report of two pedigrees
-
Lee DA, Brubaker RF, Hruska L. Hereditary glaucomas: a report of two pedigrees. Ann Ophthalmol 1985;17:739-41.
-
(1985)
Ann Ophthalmol
, vol.17
, pp. 739-741
-
-
Lee, D.A.1
Brubaker, R.F.2
Hruska, L.3
-
59
-
-
0027419893
-
Clinical features and linkage analysis of a family with autosomal dominant juvenile glaucoma
-
Johnson AT, Drack AV, Kwite AE, Cannon RL, Stone EM, Alward WLM. Clinical features and linkage analysis of a family with autosomal dominant juvenile glaucoma. Ophthalmology 1993;100:524-9.
-
(1993)
Ophthalmology
, vol.100
, pp. 524-529
-
-
Johnson, A.T.1
Drack, A.V.2
Kwite, A.E.3
Cannon, R.L.4
Stone, E.M.5
Alward, W.L.M.6
-
60
-
-
0024148639
-
Un exemple d'hérédité dominante pour la transmission du glaucome primitif à angle ouvert dans une région du nordouest de la Grèce
-
Kitsos G, Cote G, Psilas K. Un exemple d'hérédité dominante pour la transmission du glaucome primitif à angle ouvert dans une région du nordouest de la Grèce. J Fr Ophtalmol 1988;11:859-64.
-
(1988)
J Fr Ophtalmol
, vol.11
, pp. 859-864
-
-
Kitsos, G.1
Cote, G.2
Psilas, K.3
-
61
-
-
0013898525
-
Genetics and primary open-angle glaucoma
-
François J. Genetics and primary open-angle glaucoma. Am J Ophthalmol 1966,61:652-65.
-
(1966)
Am J Ophthalmol
, vol.61
, pp. 652-665
-
-
François, J.1
-
62
-
-
0017027908
-
Survey of first degree relatives of glaucoma patients
-
Leighton DA. Survey of first degree relatives of glaucoma patients. Trans Ophthalmol Soc UK 1976,96:28-32.
-
(1976)
Trans Ophthalmol Soc UK
, vol.96
, pp. 28-32
-
-
Leighton, D.A.1
-
63
-
-
0019520746
-
Multivariate analysis in glaucoma. Use of discriminant analysis in predicting glaucomatous visual field loss
-
Drance SM, Schulzer M, Thomas B, Douglas GR. Multivariate analysis in glaucoma. Use of discriminant analysis in predicting glaucomatous visual field loss. Arch Ophthalmol 1981;99:1019-22.
-
(1981)
Arch Ophthalmol
, vol.99
, pp. 1019-1022
-
-
Drance, S.M.1
Schulzer, M.2
Thomas, B.3
Douglas, G.R.4
-
64
-
-
0016301283
-
Family studies in glaucoma
-
Perkins ES. Family studies in glaucoma. Br J Ophthalmol 1974;58:529-35.
-
(1974)
Br J Ophthalmol
, vol.58
, pp. 529-535
-
-
Perkins, E.S.1
-
65
-
-
0023544319
-
Genetic factors in open-angle (simple and capsular) glaucoma. A population-based twin study
-
Teikari T. Genetic factors in open-angle (simple and capsular) glaucoma. A population-based twin study. Acta Ophthalmol (C) 1987;65:715-20.
-
(1987)
Acta Ophthalmol (C)
, vol.65
, pp. 715-720
-
-
Teikari, T.1
-
66
-
-
0028905218
-
The effect of lifestyle on the relative risk to develop open-angle glaucoma
-
Stewart WC. The effect of lifestyle on the relative risk to develop open-angle glaucoma. Curr Opin Ophthalmol 1995;6:3-9.
-
(1995)
Curr Opin Ophthalmol
, vol.6
, pp. 3-9
-
-
Stewart, W.C.1
-
67
-
-
0028880039
-
Assignment of a locus (GLC3A) for primary congenital glaucoma (buphthalmos) to 2p21 and evidence for genetic heterogeneity
-
Sarfarazi M, Akarsu AN, Hossain A, Turacli E, Aktan SG, Barsoum-Homsy MB, et al. Assignment of a locus (GLC3A) for primary congenital glaucoma (buphthalmos) to 2p21 and evidence for genetic heterogeneity. Genomics 1995;30:171-7.
-
(1995)
Genomics
, vol.30
, pp. 171-177
-
-
Sarfarazi, M.1
Akarsu, A.N.2
Hossain, A.3
Turacli, E.4
Aktan, S.G.5
Barsoum-Homsy, M.B.6
-
68
-
-
0027972492
-
Mapping of a gene for autosomal dominant juvenile-onset open-angle glaucoma to chromosome 1q
-
Richards JE, Lichter PR, Boehnke M, Uro JLA, Torrez D, Wong D, et al. Mapping of a gene for autosomal dominant juvenile-onset open-angle glaucoma to chromosome 1q. Am J Hum Genet 1994;54:62-70.
-
(1994)
Am J Hum Genet
, vol.54
, pp. 62-70
-
-
Richards, J.E.1
Lichter, P.R.2
Boehnke, M.3
Uro, J.L.A.4
Torrez, D.5
Wong, D.6
-
69
-
-
0028332417
-
Genetic linkage analysis of autosomal dominant juvenile glaucoma to 1q21-q31 in three affected pedigrees
-
Wiggs JL, Hains JL, Paglinauan C, Fine A, Sporn C, Lou D. Genetic linkage analysis of autosomal dominant juvenile glaucoma to 1q21-q31 in three affected pedigrees. Genomics 1994;21:299-303.
-
(1994)
Genomics
, vol.21
, pp. 299-303
-
-
Wiggs, J.L.1
Hains, J.L.2
Paglinauan, C.3
Fine, A.4
Sporn, C.5
Lou, D.6
-
70
-
-
0029003117
-
A common gene for juvenile and adult onset primary open-angle glaucomas confined on chromosome 1q
-
Morissette J, Côte G, Anctil J-L, Plante M, Amyot M, Héon E, et al. A common gene for juvenile and adult onset primary open-angle glaucomas confined on chromosome 1q. Am J Hum Genet 1995;56:1431-42.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 1431-1442
-
-
Morissette, J.1
Côte, G.2
Anctil, J.-L.3
Plante, M.4
Amyot, M.5
Héon, E.6
-
71
-
-
0029595371
-
Genetic-analysis of disease susceptibility (disease susceptibility)
-
Foot S. Genetic-analysis of disease susceptibility (disease susceptibility). Aust NZ J Med 1995;25:757-60.
-
(1995)
Aust NZ J Med
, vol.25
, pp. 757-760
-
-
Foot, S.1
-
72
-
-
0027715021
-
Mutations in the PAX6 gene in patients with hereditary aniridia
-
Dans A, Cowell JK. Mutations in the PAX6 gene in patients with hereditary aniridia. Hum Mol Genet 1993;2:2093-7.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 2093-2097
-
-
Dans, A.1
Cowell, J.K.2
-
73
-
-
10544225762
-
Background to molecular genetic principles and techniques
-
Wright AF, Jay B, eds. Switzerland: Harwood Academic Press
-
Gorin MB, Wright AF. Background to molecular genetic principles and techniques. In: Wright AF, Jay B, eds. Molecular genetics of inherited eye disorders. Switzerland: Harwood Academic Press, 1994:1-28.
-
(1994)
Molecular Genetics of Inherited Eye Disorders
, pp. 1-28
-
-
Gorin, M.B.1
Wright, A.F.2
-
74
-
-
0028857007
-
Polygenic disease: Methods for mapping complex disease traits
-
Weeks DE, Lathrop GM. Polygenic disease: methods for mapping complex disease traits. TIGS 1995;11:513-9.
-
(1995)
TIGS
, vol.11
, pp. 513-519
-
-
Weeks, D.E.1
Lathrop, G.M.2
-
75
-
-
0025019555
-
Linkage strategies for genetically complex traits I. Multilocus models
-
Risch N. Linkage strategies for genetically complex traits I. Multilocus models. Am J Hum Genet 1990a;46:222-8.
-
(1990)
Am J Hum Genet
, vol.46
, pp. 222-228
-
-
Risch, N.1
-
76
-
-
0025008677
-
Linkage strategies for genetically complex traits H. the power of affected relative pairs
-
Risch N. Linkage strategies for genetically complex traits H. The power of affected relative pairs. Am J Hum Genet 1990b;46:229-41.
-
(1990)
Am J Hum Genet
, vol.46
, pp. 229-241
-
-
Risch, N.1
-
77
-
-
0025020461
-
Linkage strategies for genetically complex traits III. The effect of marker polymorphism on analysis of affected relative pairs
-
Risch N. Linkage strategies for genetically complex traits III. The effect of marker polymorphism on analysis of affected relative pairs. Am J Hum Genet 1990c;46:242-53.
-
(1990)
Am J Hum Genet
, vol.46
, pp. 242-253
-
-
Risch, N.1
-
78
-
-
0029001682
-
Extreme discordant sib pairs for mapping quantitative trait loci in humans
-
Risch N, Zhang H. Extreme discordant sib pairs for mapping quantitative trait loci in humans. Science 1995;268:1584-9.
-
(1995)
Science
, vol.268
, pp. 1584-1589
-
-
Risch, N.1
Zhang, H.2
-
79
-
-
0028843796
-
Prevalence of age-related maculopathy in Australia. The Blue Mountains Eye Study
-
Mitchell P, Smith W, Attebo K, Wang JJ. Prevalence of age-related maculopathy in Australia. The Blue Mountains Eye Study. Ophthalmology 1995;102:1450-60.
-
(1995)
Ophthalmology
, vol.102
, pp. 1450-1460
-
-
Mitchell, P.1
Smith, W.2
Attebo, K.3
Wang, J.J.4
-
80
-
-
0027933734
-
A genome-wide search for human type 1 diabetes susceptibility genes
-
Davies JL, Kawaguchi Y, Bennett ST, Copeman JB, Cordell HJ, Pritchard LE, et al. A genome-wide search for human type 1 diabetes susceptibility genes. Nature 1994;371:130-6.
-
(1994)
Nature
, vol.371
, pp. 130-136
-
-
Davies, J.L.1
Kawaguchi, Y.2
Bennett, S.T.3
Copeman, J.B.4
Cordell, H.J.5
Pritchard, L.E.6
-
81
-
-
0029134874
-
Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error-a twin and family history study of autism
-
Pickles A, Bolton P, MacDonald H Bailey A, Lecouteur A, Sim CH, et al. Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error-a twin and family history study of autism. Am J Hum Genet 1995;57:717-26.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 717-726
-
-
Pickles, A.1
Bolton, P.2
Bailey A, M.H.3
Lecouteur, A.4
Sim, C.H.5
-
82
-
-
0027529253
-
Asymptotic properties of affected-sib-pair linkage analysis
-
Holmans P. Asymptotic properties of affected-sib-pair linkage analysis. Am J Hum Genet 1993;52:362-74.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 362-374
-
-
Holmans, P.1
-
83
-
-
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. Nature Genet 1995;11:241-7.
-
(1995)
Nature Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
84
-
-
0028338710
-
Sequential-analysis and case-control candidate gene association studies-reply
-
Sham P. Sequential-analysis and case-control candidate gene association studies-reply. Am J Med Genet 1994;54:154-5.
-
(1994)
Am J Med Genet
, vol.54
, pp. 154-155
-
-
Sham, P.1
-
85
-
-
0028090099
-
Interactive effect of two candidate genes in a disease: Extension of the marker-association-segregation 2 method
-
Dizier MH, Babron M-C, Clerget-Darpoux F. Interactive effect of two candidate genes in a disease: extension of the marker-association-segregation 2 method. Am J Hum Genet 1994;55:1042-9.
-
(1994)
Am J Hum Genet
, vol.55
, pp. 1042-1049
-
-
Dizier, M.H.1
Babron, M.-C.2
Clerget-Darpoux, F.3
-
86
-
-
0028840092
-
The HOXDS locus (2q31) is linked to type 1 diabetes-interaction with chromosome 6 and chromosome 11 disease susceptibility genes
-
Owerbach D, Gabbay KH. The HOXDS locus (2q31) is linked to type 1 diabetes-interaction with chromosome 6 and chromosome 11 disease susceptibility genes. Diabetes 1995;44:132-6.
-
(1995)
Diabetes
, vol.44
, pp. 132-136
-
-
Owerbach, D.1
Gabbay, K.H.2
-
87
-
-
0029112753
-
Two-locus maximum lod score analysis of a multifactorial trait: Joint consideration of IDDM2 and IDDM4 with IDDM1 in type 1 diabetes
-
Cordell HJ, Todd JA, Bennett ST, Kawaguchi Y, Farrall M. Two-locus maximum lod score analysis of a multifactorial trait: joint consideration of IDDM2 and IDDM4 with IDDM1 in type 1 diabetes. Am J Hum Genet 1995;57:920-34.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 920-934
-
-
Cordell, H.J.1
Todd, J.A.2
Bennett, S.T.3
Kawaguchi, Y.4
Farrall, M.5
-
88
-
-
0027430716
-
Two-trait-locus linkage analysis: A powerful strategy for mapping complex genetic traits
-
Schock NJ, Boehnke M, Terwilliger JD, Ott J. Two-trait-locus linkage analysis: a powerful strategy for mapping complex genetic traits. Am J Hum Genet 1993;53:1127-36.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 1127-1136
-
-
Schock, N.J.1
Boehnke, M.2
Terwilliger, J.D.3
Ott, J.4
-
89
-
-
0024453308
-
Identification of the cystic fibrosis gene: Chromosome walking and jumping
-
Rommens HM, Iannuzzi MC, Kerem B, Drumm ML, Melmer G, Dean N, et al. Identification of the cystic fibrosis gene: chromosome walking and jumping. Science 1989;245:1059-65.
-
(1989)
Science
, vol.245
, pp. 1059-1065
-
-
Rommens, H.M.1
Iannuzzi, M.C.2
Kerem, B.3
Drumm, M.L.4
Melmer, G.5
Dean, N.6
-
90
-
-
0024423668
-
Identification of the cystic fibrosis gene: Genetic analysis
-
Kerem B, Rommens JM, Buchanan JA, Markiewicz D, Cox TK, Chakravarti A, et al. Identification of the cystic fibrosis gene: genetic analysis. Science 1989;245:1073-80.
-
(1989)
Science
, vol.245
, pp. 1073-1080
-
-
Kerem, B.1
Rommens, J.M.2
Buchanan, J.A.3
Markiewicz, D.4
Cox, T.K.5
Chakravarti, A.6
-
91
-
-
0029150074
-
A comparison of linkage disequilibrium measures for fine scale mapping
-
Devlin B, Risch N. A comparison of linkage disequilibrium measures for fine scale mapping. Genomics 1995;29:311-22.
-
(1995)
Genomics
, vol.29
, pp. 311-322
-
-
Devlin, B.1
Risch, N.2
-
92
-
-
0027978110
-
The diastrophic dysplasia gene encodes a novel sulphate transporter; positional cloning by fine-structure linkage disequilibrium mapping
-
Hästbacka J, de la Chapelle A, Mahanti MM, Clines G, Reeves-Daly MP, Daly M, et al. The diastrophic dysplasia gene encodes a novel sulphate transporter; positional cloning by fine-structure linkage disequilibrium mapping. Cell 1994;78:1073-87.
-
(1994)
Cell
, vol.78
, pp. 1073-1087
-
-
Hästbacka, J.1
De La Chapelle, A.2
Mahanti, M.M.3
Clines, G.4
Reeves-Daly, M.P.5
Daly, M.6
-
93
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
Spielman RS, McGinnis RE, Ewens WJ. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet 1993;52:506-16.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
94
-
-
0029101985
-
A YAC contig spanning the dominant retinitis pigmentosa locus (RP9) on chromosome 7p
-
Keen TJ, Inglehearn CF, Green ED, Cunningham AF, Patel RJ, Peacock RE, et al. A YAC contig spanning the dominant retinitis pigmentosa locus (RP9) on chromosome 7p. Genomics 1995;28:383-8.
-
(1995)
Genomics
, vol.28
, pp. 383-388
-
-
Keen, T.J.1
Inglehearn, C.F.2
Green, E.D.3
Cunningham, A.F.4
Patel, R.J.5
Peacock, R.E.6
-
95
-
-
0027518279
-
Current methods of mutation detection
-
Cotton RGH. Current methods of mutation detection. Mutation Res 1993; 285:125-14.
-
(1993)
Mutation Res
, vol.285
, pp. 125-214
-
-
Cotton, R.G.H.1
-
97
-
-
0024756969
-
Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction
-
Orita M, Suzuki Y, Sekity AT, Hyashi K. Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction. Genomics 1989;5:874-9.
-
(1989)
Genomics
, vol.5
, pp. 874-879
-
-
Orita, M.1
Suzuki, Y.2
Sekity, A.T.3
Hyashi, K.4
-
98
-
-
0027401094
-
Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene
-
Nichols BE, Sheffield VC, Vandenburgh K, Drack AV, Kimura AE, Stone EM. Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene. Nature Genet 1993;3:202-6.
-
(1993)
Nature Genet
, vol.3
, pp. 202-206
-
-
Nichols, B.E.1
Sheffield, V.C.2
Vandenburgh, K.3
Drack, A.V.4
Kimura, A.E.5
Stone, E.M.6
-
99
-
-
0028096060
-
Retinal pattern dystrophy associated with a 4 bp insertion at codon 140 in the RDS-peripherin gene
-
Keen TJ, Inglehearn CF, Kim R, Bird AC, Bhattacharya S. Retinal pattern dystrophy associated with a 4 bp insertion at codon 140 in the RDS-peripherin gene. Hum Mol Genet 1994;3:367-8.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 367-368
-
-
Keen, T.J.1
Inglehearn, C.F.2
Kim, R.3
Bird, A.C.4
Bhattacharya, S.5
-
100
-
-
0024021305
-
Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxamine and osmium tetroxide and its application to the study of mutations
-
Cotton RGH, Rodrigues NR, Campbell DR. Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxamine and osmium tetroxide and its application to the study of mutations. Proc Natl Acad Sci USA 1988;85:4397-401.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 4397-4401
-
-
Cotton, R.G.H.1
Rodrigues, N.R.2
Campbell, D.R.3
-
101
-
-
0022353404
-
Detection of single base substitutions by ribonuclease cleavage at mismatches in RNA-DNA duplexes
-
Myers RM, Larin Z, Maniatis T. Detection of single base substitutions by ribonuclease cleavage at mismatches in RNA-DNA duplexes. Science 1985; 230:1242-6.
-
(1985)
Science
, vol.230
, pp. 1242-1246
-
-
Myers, R.M.1
Larin, Z.2
Maniatis, T.3
-
102
-
-
0028876575
-
Detection of mutations by cleavage of DNA heteroduplexes with bacteriophage resolvases
-
Mashal RD, Koontz J, Sklar J. Detection of mutations by cleavage of DNA heteroduplexes with bacteriophage resolvases. Nature Genet 1995;9:177-83.
-
(1995)
Nature Genet
, vol.9
, pp. 177-183
-
-
Mashal, R.D.1
Koontz, J.2
Sklar, J.3
-
103
-
-
0025242793
-
Automated DNA diagnostics using an ELISA-based oligonucleotide ligation assay
-
Nickerson DA, Kaisser R, Lappin S, Stewart J, Hood L, Landegren U. Automated DNA diagnostics using an ELISA-based oligonucleotide ligation assay. Proc Natl Acad Sci USA 1990;87:8923-7.
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 8923-8927
-
-
Nickerson, D.A.1
Kaisser, R.2
Lappin, S.3
Stewart, J.4
Hood, L.5
Landegren, U.6
-
104
-
-
0025777873
-
Genetic analysis of autoimmune type 1 diabetes mellitus in mice
-
Todd JA, Aitman TJ, Cornall RJ, Ghosh S, Hall RJS, Hearne CM, et al. Genetic analysis of autoimmune type 1 diabetes mellitus in mice. Nature 1991;351:542-7.
-
(1991)
Nature
, vol.351
, pp. 542-547
-
-
Todd, J.A.1
Aitman, T.J.2
Cornall, R.J.3
Ghosh, S.4
Hall, R.J.S.5
Hearne, C.M.6
|