-
1
-
-
33645767953
-
What is the global burden of visual impairment?
-
Available at: http://www.biomedcentral.com/1741-7015/4/6. Accessed July 31, 2007
-
Dandona L., and Dandona R. What is the global burden of visual impairment?. BMC Med [serial online] 4 (2006) 6. http://www.biomedcentral.com/1741-7015/4/6 Available at: http://www.biomedcentral.com/1741-7015/4/6. Accessed July 31, 2007
-
(2006)
BMC Med [serial online]
, vol.4
, pp. 6
-
-
Dandona, L.1
Dandona, R.2
-
3
-
-
0037129621
-
Myopia
-
Fredrick D.R. Myopia. BMJ 324 (2002) 1195-1199
-
(2002)
BMJ
, vol.324
, pp. 1195-1199
-
-
Fredrick, D.R.1
-
7
-
-
0024445992
-
Genetic linkage analysis of hereditary arthro-ophthalmopathy (Stickler syndrome) and the type II procollagen gene
-
Knowlton R.G., Weaver E.J., Struyk A.F., et al. Genetic linkage analysis of hereditary arthro-ophthalmopathy (Stickler syndrome) and the type II procollagen gene. Am J Hum Genet 45 (1989) 681-688
-
(1989)
Am J Hum Genet
, vol.45
, pp. 681-688
-
-
Knowlton, R.G.1
Weaver, E.J.2
Struyk, A.F.3
-
8
-
-
0025095962
-
X-linked myopia: Bornholm eye disease. Linkage to DNA markers on the distal part of Xq
-
Schwartz M., Haim M., and Skarsholm D. X-linked myopia: Bornholm eye disease. Linkage to DNA markers on the distal part of Xq. Clin Genet 38 (1990) 281-286
-
(1990)
Clin Genet
, vol.38
, pp. 281-286
-
-
Schwartz, M.1
Haim, M.2
Skarsholm, D.3
-
9
-
-
33745905223
-
Novel locus for X linked recessive high myopia maps to Xq23-q25 but outside MYP1
-
[electronic letter] Available at: http://jmg.bmj.com/cgi/content/abstract/43/5/e20. Accessed July 31, 2007
-
Zhang Q., Guo X., Xiao X., et al. Novel locus for X linked recessive high myopia maps to Xq23-q25 but outside MYP1. [electronic letter]. J Med Genet 43 (2006) e20. http://jmg.bmj.com/cgi/content/abstract/43/5/e20 Available at: http://jmg.bmj.com/cgi/content/abstract/43/5/e20. Accessed July 31, 2007
-
(2006)
J Med Genet
, vol.43
-
-
Zhang, Q.1
Guo, X.2
Xiao, X.3
-
10
-
-
2942534721
-
X-linked high myopia associated with cone dysfunction
-
Young T.L., Deeb S.S., Ronan S.M., et al. X-linked high myopia associated with cone dysfunction. Arch Ophthalmol 122 (2004) 897-908
-
(2004)
Arch Ophthalmol
, vol.122
, pp. 897-908
-
-
Young, T.L.1
Deeb, S.S.2
Ronan, S.M.3
-
11
-
-
0032231942
-
Evidence that a locus for familial high myopia maps to chromosome 18p
-
Young T.L., Ronan S.M., Drahozal L.A., et al. Evidence that a locus for familial high myopia maps to chromosome 18p. Am J Hum Genet 63 (1998) 109-119
-
(1998)
Am J Hum Genet
, vol.63
, pp. 109-119
-
-
Young, T.L.1
Ronan, S.M.2
Drahozal, L.A.3
-
12
-
-
0032231298
-
A second locus for familial high myopia maps to chromosome 12q
-
Young T.L., Ronan S.M., Alvear A.B., et al. A second locus for familial high myopia maps to chromosome 12q. Am J Hum Genet 63 (1998) 1419-1424
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1419-1424
-
-
Young, T.L.1
Ronan, S.M.2
Alvear, A.B.3
-
13
-
-
23244458724
-
Identification of a novel locus on 2q for autosomal dominant high-grade myopia
-
Paluru P.C., Nallasamy S., Devoto M., et al. Identification of a novel locus on 2q for autosomal dominant high-grade myopia. Invest Ophthalmol Vis Sci 46 (2005) 2300-2307
-
(2005)
Invest Ophthalmol Vis Sci
, vol.46
, pp. 2300-2307
-
-
Paluru, P.C.1
Nallasamy, S.2
Devoto, M.3
-
14
-
-
0242500304
-
New locus for autosomal dominant high myopia maps to the long arm of chromosome 17
-
Paluru P., Ronan S.M., Heon E., et al. New locus for autosomal dominant high myopia maps to the long arm of chromosome 17. Invest Ophthalmol Vis Sci 44 (2003) 1830-1836
-
(2003)
Invest Ophthalmol Vis Sci
, vol.44
, pp. 1830-1836
-
-
Paluru, P.1
Ronan, S.M.2
Heon, E.3
-
15
-
-
0036837879
-
Genetic loci for pathological myopia are not associated with juvenile myopia
-
Mutti D.O., Semina E., Marazita M., et al. Genetic loci for pathological myopia are not associated with juvenile myopia. Am J Med Genet 112 (2002) 355-360
-
(2002)
Am J Med Genet
, vol.112
, pp. 355-360
-
-
Mutti, D.O.1
Semina, E.2
Marazita, M.3
-
16
-
-
26244468175
-
A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612
-
Available at: http://www.molvis.org/molvis/v11/a65. Accessed July 31, 2007
-
Zhang Q., Guo X., Xiao X., et al. A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612. Mol Vis [serial online] 11 (2005) 554-560. http://www.molvis.org/molvis/v11/a65 Available at: http://www.molvis.org/molvis/v11/a65. Accessed July 31, 2007
-
(2005)
Mol Vis [serial online]
, vol.11
, pp. 554-560
-
-
Zhang, Q.1
Guo, X.2
Xiao, X.3
-
17
-
-
24044490682
-
Genome-wide scan for myopia in the Old Order Amish
-
Stambolian D., Ciner E.B., Reider L.C., et al. Genome-wide scan for myopia in the Old Order Amish. Am J Ophthalmol 140 (2005) 469-476
-
(2005)
Am J Ophthalmol
, vol.140
, pp. 469-476
-
-
Stambolian, D.1
Ciner, E.B.2
Reider, L.C.3
-
18
-
-
33645745403
-
Genomewide scan in Ashkenazi Jewish families demonstrates evidence of linkage of ocular refraction to a QTL on chromosome 1p36
-
Wojciechowski R., Moy C., Ciner E., et al. Genomewide scan in Ashkenazi Jewish families demonstrates evidence of linkage of ocular refraction to a QTL on chromosome 1p36. Hum Genet 119 (2006) 389-399
-
(2006)
Hum Genet
, vol.119
, pp. 389-399
-
-
Wojciechowski, R.1
Moy, C.2
Ciner, E.3
-
19
-
-
3242656225
-
A susceptibility locus for myopia in the normal population is linked to the PAX6 gene region on chromosome 11: a genomewide scan of dizygotic twins
-
Hammond C.J., Andrew T., Mak Y.T., and Spector T.D. A susceptibility locus for myopia in the normal population is linked to the PAX6 gene region on chromosome 11: a genomewide scan of dizygotic twins. Am J Hum Genet 75 (2004) 294-304
-
(2004)
Am J Hum Genet
, vol.75
, pp. 294-304
-
-
Hammond, C.J.1
Andrew, T.2
Mak, Y.T.3
Spector, T.D.4
-
20
-
-
4344599592
-
IQ and the association with myopia in children
-
Saw S.M., Tan S.B., Fung D., et al. IQ and the association with myopia in children. Invest Ophthalmol Vis Sci 45 (2004) 2943-2948
-
(2004)
Invest Ophthalmol Vis Sci
, vol.45
, pp. 2943-2948
-
-
Saw, S.M.1
Tan, S.B.2
Fung, D.3
-
21
-
-
0034921561
-
Academic achievement, close up work parameters, and myopia in Singapore military conscripts
-
Saw S.M., Wu H.M., Seet B., et al. Academic achievement, close up work parameters, and myopia in Singapore military conscripts. Br J Ophthalmol 85 (2001) 855-860
-
(2001)
Br J Ophthalmol
, vol.85
, pp. 855-860
-
-
Saw, S.M.1
Wu, H.M.2
Seet, B.3
-
22
-
-
0015877425
-
Modes of inheritance of errors of refraction
-
Sorsby A., and Benjamin B. Modes of inheritance of errors of refraction. J Med Genet 10 (1973) 161-164
-
(1973)
J Med Genet
, vol.10
, pp. 161-164
-
-
Sorsby, A.1
Benjamin, B.2
-
23
-
-
0017750306
-
Variation and heritability of ocular dimensions: a population study among adult Greenland Eskimos
-
Alsbirk P.H. Variation and heritability of ocular dimensions: a population study among adult Greenland Eskimos. Acta Ophthalmol (Copenh) 55 (1977) 443-456
-
(1977)
Acta Ophthalmol (Copenh)
, vol.55
, pp. 443-456
-
-
Alsbirk, P.H.1
-
24
-
-
0035671840
-
The importance of genes and environment for ocular refraction and its determiners: a population based study among 20-45 year old twins
-
Lyhne N., Sjolie A.K., Kyvik K.O., and Green A. The importance of genes and environment for ocular refraction and its determiners: a population based study among 20-45 year old twins. Br J Ophthalmol 85 (2001) 1470-1476
-
(2001)
Br J Ophthalmol
, vol.85
, pp. 1470-1476
-
-
Lyhne, N.1
Sjolie, A.K.2
Kyvik, K.O.3
Green, A.4
-
25
-
-
34147135789
-
Heritability of refractive error and ocular biometrics: the Genes in Myopia (GEM) twin study
-
Dirani M., Chamberlain M., Shekar S.N., et al. Heritability of refractive error and ocular biometrics: the Genes in Myopia (GEM) twin study. Invest Ophthalmol Vis Sci 47 (2006) 4756-4761
-
(2006)
Invest Ophthalmol Vis Sci
, vol.47
, pp. 4756-4761
-
-
Dirani, M.1
Chamberlain, M.2
Shekar, S.N.3
-
26
-
-
12944280869
-
Ocular refraction: heritability and genome-wide search for eye morphometry traits in an isolated Sardinian population
-
Biino G., Palmas M.A., Corona C., et al. Ocular refraction: heritability and genome-wide search for eye morphometry traits in an isolated Sardinian population. Hum Genet 116 (2005) 152-159
-
(2005)
Hum Genet
, vol.116
, pp. 152-159
-
-
Biino, G.1
Palmas, M.A.2
Corona, C.3
-
27
-
-
32944477174
-
Central corneal thickness is highly heritable: the twin eye studies
-
Toh T., Liew S.H., MacKinnon J.R., et al. Central corneal thickness is highly heritable: the twin eye studies. Invest Ophthalmol Vis Sci 46 (2005) 3718-3722
-
(2005)
Invest Ophthalmol Vis Sci
, vol.46
, pp. 3718-3722
-
-
Toh, T.1
Liew, S.H.2
MacKinnon, J.R.3
-
28
-
-
0032900220
-
Genetic and environmental contributions to size, color, shape, and other characteristics of melanocytic naevi in a sample of adolescent twins
-
McGregor B., Pfitzner J., Zhu G., et al. Genetic and environmental contributions to size, color, shape, and other characteristics of melanocytic naevi in a sample of adolescent twins. Genet Epidemiol 16 (1999) 40-53
-
(1999)
Genet Epidemiol
, vol.16
, pp. 40-53
-
-
McGregor, B.1
Pfitzner, J.2
Zhu, G.3
-
29
-
-
33645749049
-
On the probability of dizygotic twins being concordant for two alleles at multiple polymorphic loci
-
Nyholt D.R. On the probability of dizygotic twins being concordant for two alleles at multiple polymorphic loci. Twin Res Hum Genet 9 (2006) 194-197
-
(2006)
Twin Res Hum Genet
, vol.9
, pp. 194-197
-
-
Nyholt, D.R.1
-
30
-
-
11144355855
-
A genome scan for eye color in 502 twin families: most variation is due to a QTL on chromosome 15q
-
Zhu G., Evans D.M., Duffy D.L., et al. A genome scan for eye color in 502 twin families: most variation is due to a QTL on chromosome 15q. Twin Res 7 (2004) 197-210
-
(2004)
Twin Res
, vol.7
, pp. 197-210
-
-
Zhu, G.1
Evans, D.M.2
Duffy, D.L.3
-
31
-
-
23944505173
-
Genomewide significant linkage to migrainous headache on chromosome 5q21
-
Nyholt D.R., Morley K.I., Ferreira M.A., et al. Genomewide significant linkage to migrainous headache on chromosome 5q21. Am J Hum Genet 77 (2005) 500-512
-
(2005)
Am J Hum Genet
, vol.77
, pp. 500-512
-
-
Nyholt, D.R.1
Morley, K.I.2
Ferreira, M.A.3
-
32
-
-
0036338150
-
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis G.R., Cherny S.S., Cookson W.O., and Cardon L.R. Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 30 (2002) 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
-
33
-
-
18544381909
-
A high-resolution recombination map of the human genome
-
Kong A., Gudbjartsson D.F., Sainz J., et al. A high-resolution recombination map of the human genome. Nat Genet 31 (2002) 241-247
-
(2002)
Nat Genet
, vol.31
, pp. 241-247
-
-
Kong, A.1
Gudbjartsson, D.F.2
Sainz, J.3
-
34
-
-
0029049088
-
Genetic linkage of Wagner disease and erosive vitreoretinopathy to chromosome 5q13-14
-
Brown D.M., Graemiger R.A., Hergersberg M., et al. Genetic linkage of Wagner disease and erosive vitreoretinopathy to chromosome 5q13-14. Arch Ophthalmol 113 (1995) 671-675
-
(1995)
Arch Ophthalmol
, vol.113
, pp. 671-675
-
-
Brown, D.M.1
Graemiger, R.A.2
Hergersberg, M.3
-
35
-
-
33748103567
-
Erosive vitreoretinopathy and Wagner disease are caused by intronic mutations in CSPG2/Versican that result in an imbalance of splice variants
-
Mukhopadhyay A., Nikopoulos K., Maugeri A., et al. Erosive vitreoretinopathy and Wagner disease are caused by intronic mutations in CSPG2/Versican that result in an imbalance of splice variants. Invest Ophthalmol Vis Sci 47 (2006) 3565-3572
-
(2006)
Invest Ophthalmol Vis Sci
, vol.47
, pp. 3565-3572
-
-
Mukhopadhyay, A.1
Nikopoulos, K.2
Maugeri, A.3
-
36
-
-
1842452637
-
Microarray analysis of gene expression in human donor sclera
-
Available at: http://www.molvis.org/molvis/v10/a22. Accessed July 31, 2007
-
Young T.L., Scavello G.S., Paluru P.C., et al. Microarray analysis of gene expression in human donor sclera. Mol Vis [serial online] 10 (2004) 163-176. http://www.molvis.org/molvis/v10/a22 Available at: http://www.molvis.org/molvis/v10/a22. Accessed July 31, 2007
-
(2004)
Mol Vis [serial online]
, vol.10
, pp. 163-176
-
-
Young, T.L.1
Scavello, G.S.2
Paluru, P.C.3
-
37
-
-
0036775241
-
Versican: a versatile extracellular matrix proteoglycan in cell biology
-
Wight T.N. Versican: a versatile extracellular matrix proteoglycan in cell biology. Curr Opin Cell Biol 14 (2002) 617-623
-
(2002)
Curr Opin Cell Biol
, vol.14
, pp. 617-623
-
-
Wight, T.N.1
-
38
-
-
0031971589
-
A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32
-
Bessant D.A., Khaliq S., Hameed A., et al. A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32. Am J Hum Genet 62 (1998) 1113-1116
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1113-1116
-
-
Bessant, D.A.1
Khaliq, S.2
Hameed, A.3
|