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Volumn 115, Issue 6, 2008, Pages

Genetic Dissection of Myopia. Evidence for Linkage of Ocular Axial Length to Chromosome 5q

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUSTRALIA; CHILD; CHROMOSOME 10; CHROMOSOME 14; CHROMOSOME 5Q; CHROMOSOME 6; CONTROLLED STUDY; DIZYGOTIC TWINS; ENVIRONMENTAL FACTOR; EYE AXIS LENGTH; FEMALE; GENETIC ANALYSIS; GENETIC LINKAGE; GENOME; HERITABILITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MICROSATELLITE MARKER; MONOZYGOTIC TWINS; MYOPIA; PRIORITY JOURNAL; QUANTITATIVE TRAIT LOCUS; SEX DIFFERENCE;

EID: 44349100253     PISSN: 01616420     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ophtha.2007.08.013     Document Type: Article
Times cited : (49)

References (38)
  • 1
    • 33645767953 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • Myopia
    • Fredrick D.R. Myopia. BMJ 324 (2002) 1195-1199
    • (2002) BMJ , vol.324 , pp. 1195-1199
    • Fredrick, D.R.1
  • 5
    • 0034942777 scopus 로고    scopus 로고
    • The increasing prevalence of myopia: implications for Australia
    • Rose K., Smith W., Morgan I., and Mitchell P. The increasing prevalence of myopia: implications for Australia. Clin Experiment Ophthalmol 29 (2001) 116-120
    • (2001) Clin Experiment Ophthalmol , vol.29 , pp. 116-120
    • Rose, K.1    Smith, W.2    Morgan, I.3    Mitchell, P.4
  • 6
    • 33846061148 scopus 로고    scopus 로고
    • Complex trait genetics of refractive error
    • Young T.L., Metlapally R., and Shay A.E. Complex trait genetics of refractive error. Arch Ophthalmol 125 (2007) 38-48
    • (2007) Arch Ophthalmol , vol.125 , pp. 38-48
    • Young, T.L.1    Metlapally, R.2    Shay, A.E.3
  • 7
    • 0024445992 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


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