메뉴 건너뛰기




Volumn 6, Issue 11, 2011, Pages

Correction: GALC deletions increase the risk of primary open-angle glaucoma: The role of mendelian variants in complex disease (PLoS ONE (2011) 6, 11 (e27134) DOI: 10.1371/journal.pone.0027134);GALC deletions increase the risk of primary Open-Angle Glaucoma: The role of mendelian variants in complex disease

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE DEHYDROGENASE 1 FAMILY MEMBER A2; CELL PROTEIN; CILIARY ROOTLET COILED COIL ROOTLLETIN PROTEIN; EYES ABSENT 1 HOMOLOG 1 PROTEIN; GALACTOSYLCERAMIDASE; RAS P21 PROTEIN ACTIVATOR 4; UNCLASSIFIED DRUG;

EID: 80455150254     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0103197     Document Type: Erratum
Times cited : (37)

References (39)
  • 1
    • 33644655886 scopus 로고    scopus 로고
    • The number of people with glaucoma worldwide in 2010 and 2020
    • Quigley HA, Broman AT, (2006) The number of people with glaucoma worldwide in 2010 and 2020. Br J Ophthalmol 90: 262-267.
    • (2006) Br J Ophthalmol , vol.90 , pp. 262-267
    • Quigley, H.A.1    Broman, A.T.2
  • 6
    • 64249096137 scopus 로고    scopus 로고
    • The genetics of primary open-angle glaucoma: a review
    • Allingham RR, Liu Y, Rhee DJ, (2009) The genetics of primary open-angle glaucoma: a review. Exp Eye Res 88: 837-844.
    • (2009) Exp Eye Res , vol.88 , pp. 837-844
    • Allingham, R.R.1    Liu, Y.2    Rhee, D.J.3
  • 7
    • 18244385269 scopus 로고    scopus 로고
    • Adult-onset primary open-angle glaucoma caused by mutations in optineurin
    • Rezaie T, Child A, Hitchings R, Brice G, Miller L, et al. (2002) Adult-onset primary open-angle glaucoma caused by mutations in optineurin. Science 295: 1077-1079.
    • (2002) Science , vol.295 , pp. 1077-1079
    • Rezaie, T.1    Child, A.2    Hitchings, R.3    Brice, G.4    Miller, L.5
  • 9
    • 20144382615 scopus 로고    scopus 로고
    • Identification of a novel adult-onset primary open-angle glaucoma (POAG) gene on 5q22.1
    • Monemi S, Spaeth G, DaSilva A, Popinchalk S, Ilitchev E, et al. (2005) Identification of a novel adult-onset primary open-angle glaucoma (POAG) gene on 5q22.1. Hum Mol Genet 14: 725-733.
    • (2005) Hum Mol Genet , vol.14 , pp. 725-733
    • Monemi, S.1    Spaeth, G.2    DaSilva, A.3    Popinchalk, S.4    Ilitchev, E.5
  • 10
    • 0030942553 scopus 로고    scopus 로고
    • Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21
    • Stoilov I, Akarsu AN, Sarfarazi M, (1997) Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21. Hum Mol Genet 6: 641-647.
    • (1997) Hum Mol Genet , vol.6 , pp. 641-647
    • Stoilov, I.1    Akarsu, A.N.2    Sarfarazi, M.3
  • 12
    • 77951745194 scopus 로고    scopus 로고
    • Genetic bases for glaucoma
    • Fuse N, (2010) Genetic bases for glaucoma. Tohoku J Exp Med 221: 1-10.
    • (2010) Tohoku J Exp Med , vol.221 , pp. 1-10
    • Fuse, N.1
  • 13
    • 79957611419 scopus 로고    scopus 로고
    • Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1
    • Burdon KP, Macgregor S, Hewitt AW, Sharma S, Chidlow G, et al. (2011) Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1. Nat Genet 43: 574-578.
    • (2011) Nat Genet , vol.43 , pp. 574-578
    • Burdon, K.P.1    Macgregor, S.2    Hewitt, A.W.3    Sharma, S.4    Chidlow, G.5
  • 14
    • 77951468653 scopus 로고    scopus 로고
    • The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions
    • Cornelis MC, Agrawal A, Cole JW, Hansel NN, Barnes KC, et al. (2010) The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions. Genet Epidemiol 34: 364-372.
    • (2010) Genet Epidemiol , vol.34 , pp. 364-372
    • Cornelis, M.C.1    Agrawal, A.2    Cole, J.W.3    Hansel, N.N.4    Barnes, K.C.5
  • 15
    • 77953226403 scopus 로고    scopus 로고
    • Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness
    • Lu Y, Dimasi DP, Hysi PG, Hewitt AW, Burdon KP, et al. (2010) Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. PLoS Genet 6: e1000947.
    • (2010) PLoS Genet , vol.6
    • Lu, Y.1    Dimasi, D.P.2    Hysi, P.G.3    Hewitt, A.W.4    Burdon, K.P.5
  • 16
    • 77954168341 scopus 로고    scopus 로고
    • Genome-wide association identifies ATOH7 as a major gene determining human optic disc size
    • Macgregor S, Hewitt AW, Hysi PG, Ruddle JB, Medland SE, et al. (2010) Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. Hum Mol Genet 19: 2716-2724.
    • (2010) Hum Mol Genet , vol.19 , pp. 2716-2724
    • Macgregor, S.1    Hewitt, A.W.2    Hysi, P.G.3    Ruddle, J.B.4    Medland, S.E.5
  • 17
    • 77954349639 scopus 로고    scopus 로고
    • Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility
    • Meguro A, Inoko H, Ota M, Mizuki N, Bahram S, (2010) Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility. Ophthalmology 117: 1331-1338 e1335.
    • (2010) Ophthalmology , vol.117
    • Meguro, A.1    Inoko, H.2    Ota, M.3    Mizuki, N.4    Bahram, S.5
  • 19
    • 77957603164 scopus 로고    scopus 로고
    • Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
    • Thorleifsson G, Walters GB, Hewitt AW, Masson G, Helgason A, et al. (2010) Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. Nat Genet 42: 906-909.
    • (2010) Nat Genet , vol.42 , pp. 906-909
    • Thorleifsson, G.1    Walters, G.B.2    Hewitt, A.W.3    Masson, G.4    Helgason, A.5
  • 22
    • 68949155297 scopus 로고    scopus 로고
    • High-resolution analysis of DNA copy number alterations in patients with primary open-angle glaucoma
    • Abu-Amero KK, Hellani A, Bender P, Spaeth GL, Myers J, et al. (2009) High-resolution analysis of DNA copy number alterations in patients with primary open-angle glaucoma. Mol Vis 15: 1594-1598.
    • (2009) Mol Vis , vol.15 , pp. 1594-1598
    • Abu-Amero, K.K.1    Hellani, A.2    Bender, P.3    Spaeth, G.L.4    Myers, J.5
  • 24
    • 79956006929 scopus 로고    scopus 로고
    • Copy number variations on chromosome 12q14 in patients with normal tension glaucoma
    • Fingert JH, Robin AL, Stone JL, Roos BR, Davis LK, et al. (2011) Copy number variations on chromosome 12q14 in patients with normal tension glaucoma. Hum Mol Genet 20: 2482-2494.
    • (2011) Hum Mol Genet , vol.20 , pp. 2482-2494
    • Fingert, J.H.1    Robin, A.L.2    Stone, J.L.3    Roos, B.R.4    Davis, L.K.5
  • 25
    • 69749121852 scopus 로고    scopus 로고
    • High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications
    • Shaikh TH, Gai X, Perin JC, Glessner JT, Xie H, et al. (2009) High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications. Genome Res 19: 1682-1690.
    • (2009) Genome Res , vol.19 , pp. 1682-1690
    • Shaikh, T.H.1    Gai, X.2    Perin, J.C.3    Glessner, J.T.4    Xie, H.5
  • 26
    • 0028827824 scopus 로고
    • Characterization of the large deletion in the GALC gene found in patients with Krabbe disease
    • Luzi P, Rafi MA, Wenger DA, (1995) Characterization of the large deletion in the GALC gene found in patients with Krabbe disease. Hum Mol Genet 4: 2335-2338.
    • (1995) Hum Mol Genet , vol.4 , pp. 2335-2338
    • Luzi, P.1    Rafi, M.A.2    Wenger, D.A.3
  • 27
    • 0029156759 scopus 로고
    • A large deletion together with a point mutation in the GALC gene is a common mutant allele in patients with infantile Krabbe disease
    • Rafi MA, Luzi P, Chen YQ, Wenger DA, (1995) A large deletion together with a point mutation in the GALC gene is a common mutant allele in patients with infantile Krabbe disease. Hum Mol Genet 4: 1285-1289.
    • (1995) Hum Mol Genet , vol.4 , pp. 1285-1289
    • Rafi, M.A.1    Luzi, P.2    Chen, Y.Q.3    Wenger, D.A.4
  • 28
    • 0028958549 scopus 로고
    • Structure and organization of the human galactocerebrosidase (GALC) gene
    • Luzi P, Rafi MA, Wenger DA, (1995) Structure and organization of the human galactocerebrosidase (GALC) gene. Genomics 26: 407-409.
    • (1995) Genomics , vol.26 , pp. 407-409
    • Luzi, P.1    Rafi, M.A.2    Wenger, D.A.3
  • 29
    • 0030964590 scopus 로고    scopus 로고
    • Molecular genetics of Krabbe disease (globoid cell leukodystrophy): diagnostic and clinical implications
    • Wenger DA, Rafi MA, Luzi P, (1997) Molecular genetics of Krabbe disease (globoid cell leukodystrophy): diagnostic and clinical implications. Hum Mutat 10: 268-279.
    • (1997) Hum Mutat , vol.10 , pp. 268-279
    • Wenger, D.A.1    Rafi, M.A.2    Luzi, P.3
  • 31
  • 32
    • 52949141845 scopus 로고    scopus 로고
    • Integrated detection and population-genetic analysis of SNPs and copy number variation
    • McCarroll SA, Kuruvilla FG, Korn JM, Cawley S, Nemesh J, et al. (2008) Integrated detection and population-genetic analysis of SNPs and copy number variation. Nat Genet 40: 1166-1174.
    • (2008) Nat Genet , vol.40 , pp. 1166-1174
    • McCarroll, S.A.1    Kuruvilla, F.G.2    Korn, J.M.3    Cawley, S.4    Nemesh, J.5
  • 33
    • 33751329250 scopus 로고    scopus 로고
    • Global variation in copy number in the human genome
    • Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, et al. (2006) Global variation in copy number in the human genome. Nature 444: 444-454.
    • (2006) Nature , vol.444 , pp. 444-454
    • Redon, R.1    Ishikawa, S.2    Fitch, K.R.3    Feuk, L.4    Perry, G.H.5
  • 34
    • 58849106627 scopus 로고    scopus 로고
    • Identification of common genetic variants that account for transcript isoform variation between human populations
    • Zhang W, Duan S, Bleibel WK, Wisel SA, Huang RS, et al. (2009) Identification of common genetic variants that account for transcript isoform variation between human populations. Hum Genet 125: 81-93.
    • (2009) Hum Genet , vol.125 , pp. 81-93
    • Zhang, W.1    Duan, S.2    Bleibel, W.K.3    Wisel, S.A.4    Huang, R.S.5
  • 35
    • 33846631884 scopus 로고    scopus 로고
    • Common genetic variants account for differences in gene expression among ethnic groups
    • Spielman RS, Bastone LA, Burdick JT, Morley M, Ewens WJ, et al. (2007) Common genetic variants account for differences in gene expression among ethnic groups. Nat Genet 39: 226-231.
    • (2007) Nat Genet , vol.39 , pp. 226-231
    • Spielman, R.S.1    Bastone, L.A.2    Burdick, J.T.3    Morley, M.4    Ewens, W.J.5
  • 36
    • 48949109588 scopus 로고    scopus 로고
    • Lack of association between LOXL1 variants and primary open-angle glaucoma in three different populations
    • Liu Y, Schmidt S, Qin X, Gibson J, Hutchins K, et al. (2008) Lack of association between LOXL1 variants and primary open-angle glaucoma in three different populations. Invest Ophthalmol Vis Sci 49: 3465-3468.
    • (2008) Invest Ophthalmol Vis Sci , vol.49 , pp. 3465-3468
    • Liu, Y.1    Schmidt, S.2    Qin, X.3    Gibson, J.4    Hutchins, K.5
  • 37
    • 67349182343 scopus 로고    scopus 로고
    • Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
    • Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, et al. (2009) Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature 459: 569-573.
    • (2009) Nature , vol.459 , pp. 569-573
    • Glessner, J.T.1    Wang, K.2    Cai, G.3    Korvatska, O.4    Kim, C.E.5
  • 38
    • 35948984173 scopus 로고    scopus 로고
    • PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
    • Wang K, Li M, Hadley D, Liu R, Glessner J, et al. (2007) PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. Genome Res 17: 1665-1674.
    • (2007) Genome Res , vol.17 , pp. 1665-1674
    • Wang, K.1    Li, M.2    Hadley, D.3    Liu, R.4    Glessner, J.5
  • 39
    • 72949118299 scopus 로고    scopus 로고
    • Transformation of chronic lymphocytic leukemia/small lymphocytic lymphoma to interdigitating dendritic cell sarcoma: evidence for transdifferentiation of the lymphoma clone
    • Fraser CR, Wang W, Gomez M, Zhang T, Mathew S, et al. (2009) Transformation of chronic lymphocytic leukemia/small lymphocytic lymphoma to interdigitating dendritic cell sarcoma: evidence for transdifferentiation of the lymphoma clone. Am J Clin Pathol 132: 928-939.
    • (2009) Am J Clin Pathol , vol.132 , pp. 928-939
    • Fraser, C.R.1    Wang, W.2    Gomez, M.3    Zhang, T.4    Mathew, S.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.