-
1
-
-
33644655886
-
The number of people with glaucoma worldwide in 2010 and 2020
-
Quigley HA, Broman AT. The number of people with glaucoma worldwide in 2010 and 2020. Br J Ophthalmol 2006; 90:262-7.
-
(2006)
Br J Ophthalmol
, vol.90
, pp. 262-267
-
-
Quigley, H.A.1
Broman, A.T.2
-
2
-
-
9644283089
-
Global data on visual impairment in the year 2002
-
Resnikoff S, Pascolini D, Etya'ale D, Kocur I, Pararajasegaram R, Pokharel GP, Mariotti SP. Global data on visual impairment in the year 2002. Bull World Health Organ 2004; 82:844-51.
-
(2004)
Bull World Health Organ
, vol.82
, pp. 844-851
-
-
Resnikoff, S.1
Pascolini, D.2
Etya'ale, D.3
Kocur, I.4
Pararajasegaram, R.5
Pokharel, G.P.6
Mariotti, S.P.7
-
3
-
-
78049241108
-
Myocilin and optineurin coding variants in Hispanics of Mexican descent with POAG
-
McDonald KK, Abramson K, Beltran MA, Ramirez MG, Alvarez M, Ventura A, Santiago-Turla C, Schmidt S, Hauser MA, Allingham RR. Myocilin and optineurin coding variants in Hispanics of Mexican descent with POAG. J Hum Genet 2010; 55:697-700.
-
(2010)
J Hum Genet
, vol.55
, pp. 697-700
-
-
McDonald, K.K.1
Abramson, K.2
Beltran, M.A.3
Ramirez, M.G.4
Alvarez, M.5
Ventura, A.6
Santiago-Turla, C.7
Schmidt, S.8
Hauser, M.A.9
Allingham, R.R.10
-
4
-
-
34648840351
-
Genetic contributions to glaucoma: Heritability of intraocular pressure, retinal nerve fiber layer thickness, and optic disc morphology
-
van Koolwijk LM, Despriet DD, van Duijn CM, Pardo Cortes LM, Vingerling JR, Aulchenko YS, Oostra BA, Klaver CC, Lemij HG. Genetic contributions to glaucoma: heritability of intraocular pressure, retinal nerve fiber layer thickness, and optic disc morphology. Invest Ophthalmol Vis Sci 2007; 48:3669-76.
-
(2007)
Invest Ophthalmol Vis Sci
, vol.48
, pp. 3669-3676
-
-
van Koolwijk, L.M.1
Despriet, D.D.2
van Duijn, C.M.3
Pardo Cortes, L.M.4
Vingerling, J.R.5
Aulchenko, Y.S.6
Oostra, B.A.7
Klaver, C.C.8
Lemij, H.G.9
-
5
-
-
14444283397
-
Identification of a gene that causes primary open angle glaucoma
-
Stone EM, Fingert JH, Alward WL, Nguyen TD, Polansky JR, Sunden SL, Nishimura D, Clark AF, Nystuen A, Nichols BE, Mackey DA, Ritch R, Kalenak JW, Craven ER, Sheffield VC. Identification of a gene that causes primary open angle glaucoma. Science 1997; 275:668-70.
-
(1997)
Science
, vol.275
, pp. 668-670
-
-
Stone, E.M.1
Fingert, J.H.2
Alward, W.L.3
Nguyen, T.D.4
Polansky, J.R.5
Sunden, S.L.6
Nishimura, D.7
Clark, A.F.8
Nystuen, A.9
Nichols, B.E.10
Mackey, D.A.11
Ritch, R.12
Kalenak, J.W.13
Craven, E.R.14
Sheffield, V.C.15
-
6
-
-
77957603164
-
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
-
Thorleifsson G, Walters GB, Hewitt AW, Masson G, Helgason A, DeWan A, Sigurdsson A, Jonasdottir A, Gudjonsson SA, Magnusson KP, Stefansson H, Lam DS, Tam PO, Gudmundsdottir GJ, Southgate L, Burdon KP, Gottfredsdottir MS, Aldred MA, Mitchell P, St Clair D, Collier DA, Tang N, Sveinsson O, Macgregor S, Martin NG, Cree AJ, Gibson J, Macleod A, Jacob A, Ennis S, Young TL, Chan JC, Karwatowski WS, Hammond CJ, Thordarson K, Zhang M, Wadelius C, Lotery AJ, Trembath RC, Pang CP, Hoh J, Craig JE, Kong A, Mackey DA, Jonasson F, Thorsteinsdottir U, Stefansson K. Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. Nat Genet 2010; 42:906-9.
-
(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
Dewan, A.6
Sigurdsson, A.7
Jonasdottir, A.8
Gudjonsson, S.A.9
Magnusson, K.P.10
Stefansson, H.11
Lam, D.S.12
Tam, P.O.13
Gudmundsdottir, G.J.14
Southgate, L.15
Burdon, K.P.16
Gottfredsdottir, M.S.17
Aldred, M.A.18
Mitchell, P.19
St Clair, D.20
Collier, D.A.21
Tang, N.22
Sveinsson, O.23
Macgregor, S.24
Martin, N.G.25
Cree, A.J.26
Gibson, J.27
Macleod, A.28
Jacob, A.29
Ennis, S.30
Young, T.L.31
Chan, J.C.32
Karwatowski, W.S.33
Hammond, C.J.34
Thordarson, K.35
Zhang, M.36
Wadelius, C.37
Lotery, A.J.38
Trembath, R.C.39
Pang, C.P.40
Hoh, J.41
Craig, J.E.42
Kong, A.43
Mackey, D.A.44
Jonasson, F.45
Thorsteinsdottir, U.46
Stefansson, K.47
more..
-
7
-
-
18244385269
-
Adult-onset primary open-angle glaucoma caused by mutations in optineurin
-
Rezaie T, Child A, Hitchings R, Brice G, Miller L, Coca-Prados M, Heon E, Krupin T, Ritch R, Kreutzer D, Crick RP, Sarfarazi M. Adult-onset primary open-angle glaucoma caused by mutations in optineurin. Science 2002; 295:1077-9.
-
(2002)
Science
, vol.295
, pp. 1077-1079
-
-
Rezaie, T.1
Child, A.2
Hitchings, R.3
Brice, G.4
Miller, L.5
Coca-Prados, M.6
Heon, E.7
Krupin, T.8
Ritch, R.9
Kreutzer, D.10
Crick, R.P.11
Sarfarazi, M.12
-
8
-
-
79955983465
-
Primary open-angle glaucoma genes
-
Fingert JH. Primary open-angle glaucoma genes. Eye (Lond) 2011; 25:587-95.
-
(2011)
Eye (Lond)
, vol.25
, pp. 587-595
-
-
Fingert, J.H.1
-
9
-
-
34248578241
-
Inherited familial and sporadic primary openangle glaucoma
-
Gong G, Kosoko-Lasaki S, Haynatzki G, Lynch HT, Lynch JA, Wilson MR. Inherited, familial and sporadic primary openangle glaucoma. J Natl Med Assoc 2007; 99:559-63.
-
(2007)
J Natl Med Assoc
, vol.99
, pp. 559-563
-
-
Gong, G.1
Kosoko-Lasaki, S.2
Haynatzki, G.3
Lynch, H.T.4
Lynch, J.A.5
Wilson, M.R.6
-
10
-
-
84863230548
-
Current concepts on primary open-angle glaucoma genetics: A contribution to disease pathophysiology and future treatment
-
Gemenetzi M, Yang Y, Lotery AJ. Current concepts on primary open-angle glaucoma genetics: a contribution to disease pathophysiology and future treatment. Eye (Lond) 2012; 26:355-69.
-
(2012)
Eye (Lond)
, vol.26
, pp. 355-369
-
-
Gemenetzi, M.1
Yang, Y.2
Lotery, A.J.3
-
12
-
-
20144382615
-
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, Liebmann J, Ritch R, Heon E, Crick RP, Child A, Sarfarazi M. Identification of a novel adult-onset primary open-angle glaucoma (POAG) gene on 5q22.1. Hum Mol Genet 2005; 14:725-33.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 725-733
-
-
Monemi, S.1
Spaeth, G.2
Dasilva, A.3
Popinchalk, S.4
Ilitchev, E.5
Liebmann, J.6
Ritch, R.7
Heon, E.8
Crick, R.P.9
Child, A.10
Sarfarazi, M.11
-
13
-
-
70350500461
-
Heterozygous NTF4 mutations impairing neurotrophin-4 signaling in patients with primary open-angle glaucoma
-
Pasutto F, Matsumoto T, Mardin CY, Sticht H, Brandstatter JH, Michels-Rautenstrauss K, Weisschuh N, Gramer E, Ramdas WD, van Koolwijk LM, Klaver CC, Vingerling JR, Weber BH, Kruse FE, Rautenstrauss B, Barde YA, Reis A. Heterozygous NTF4 mutations impairing neurotrophin-4 signaling in patients with primary open-angle glaucoma. Am J Hum Genet 2009; 85:447-56.
-
(2009)
Am J Hum Genet
, vol.85
, pp. 447-456
-
-
Pasutto, F.1
Matsumoto, T.2
Mardin, C.Y.3
Sticht, H.4
Brandstatter, J.H.5
Michels-Rautenstrauss, K.6
Weisschuh, N.7
Gramer, E.8
Ramdas, W.D.9
van Koolwijk, L.M.10
Klaver, C.C.11
Vingerling, J.R.12
Weber, B.H.13
Kruse, F.E.14
Rautenstrauss, B.15
Barde, Y.A.16
Reis, A.17
-
14
-
-
77956970117
-
Identification of a novel mutation in the NTF4 gene that causes primary open-angle glaucoma in a Chinese population
-
Vithana EN, Nongpiur ME, Venkataraman D, Chan SH, Mavinahalli J, Aung T. Identification of a novel mutation in the NTF4 gene that causes primary open-angle glaucoma in a Chinese population. Mol Vis 2010; 16:1640-5.
-
(2010)
Mol Vis
, vol.16
, pp. 1640-1645
-
-
Vithana, E.N.1
Nongpiur, M.E.2
Venkataraman, D.3
Chan, S.H.4
Mavinahalli, J.5
Aung, T.6
-
15
-
-
33745672351
-
Distribution of WDR36 DNA sequence variants in patients with primary open-angle glaucoma
-
Hauser MA, Allingham RR, Linkroum K, Wang J, LaRocque- Abramson K, Figueiredo D, Santiago-Turla C, del Bono EA, Haines JL, Pericak-Vance MA, Wiggs JL. Distribution of WDR36 DNA sequence variants in patients with primary open-angle glaucoma. Invest Ophthalmol Vis Sci 2006; 47:2542-6.
-
(2006)
Invest Ophthalmol Vis Sci
, vol.47
, pp. 2542-2546
-
-
Hauser, M.A.1
Allingham, R.R.2
Linkroum, K.3
Wang, J.4
LaRocque-Abramson, K.5
Figueiredo, D.6
Santiago-Turla, C.7
del Bono, E.A.8
Haines, J.L.9
Pericak-Vance, M.A.10
Wiggs, J.L.11
-
16
-
-
40749089626
-
Structural variation of chromosomes in autism spectrum disorder
-
Marshall CR, Noor A, Vincent JB, Lionel AC, Feuk L, Skaug J, Shago M, Moessner R, Pinto D, Ren Y, Thiruvahindrapduram B, Fiebig A, Schreiber S, Friedman J, Ketelaars CE, Vos YJ, Ficicioglu C, Kirkpatrick S, Nicolson R, Sloman L, Summers A, Gibbons CA, Teebi A, Chitayat D, Weksberg R, Thompson A, Vardy C, Crosbie V, Luscombe S, Baatjes R, Zwaigenbaum L, Roberts W, Fernandez B, Szatmari P, Scherer SW. Structural variation of chromosomes in autism spectrum disorder. Am J Hum Genet 2008; 82:477-88.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 477-488
-
-
Marshall, C.R.1
Noor, A.2
Vincent, J.B.3
Lionel, A.C.4
Feuk, L.5
Skaug, J.6
Shago, M.7
Moessner, R.8
Pinto, D.9
Ren, Y.10
Thiruvahindrapduram, B.11
Fiebig, A.12
Schreiber, S.13
Friedman, J.14
Ketelaars, C.E.15
Vos, Y.J.16
Ficicioglu, C.17
Kirkpatrick, S.18
Nicolson, R.19
Sloman, L.20
Summers, A.21
Gibbons, C.A.22
Teebi, A.23
Chitayat, D.24
Weksberg, R.25
Thompson, A.26
Vardy, C.27
Crosbie, V.28
Luscombe, S.29
Baatjes, R.30
Zwaigenbaum, L.31
Roberts, W.32
Fernandez, B.33
Szatmari, P.34
Scherer, S.W.35
more..
-
17
-
-
67349182343
-
Autism genomewide copy number variation reveals ubiquitin and neuronal genes
-
Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, Zhang H, Estes A, Brune CW, Bradfield JP, Imielinski M, Frackelton EC, Reichert J, Crawford EL, Munson J, Sleiman PM, Chiavacci R, Annaiah K, Thomas K, Hou C, Glaberson W, Flory J, Otieno F, Garris M, Soorya L, Klei L, Piven J, Meyer KJ, Anagnostou E, Sakurai T, Game RM, Rudd DS, Zurawiecki D, McDougle CJ, Davis LK, Miller J, Posey DJ, Michaels S, Kolevzon A, Silverman JM, Bernier R, Levy SE, Schultz RT, Dawson G, Owley T, McMahon WM, Wassink TH, Sweeney JA, Nurnberger JI, Coon H, Sutcliffe JS, Minshew NJ, Grant SF, Bucan M, Cook EH, Buxbaum JD, Devlin B, Schellenberg GD, Hakonarson H. Autism genomewide copy number variation reveals ubiquitin and neuronal genes. Nature 2009; 459:569-73.
-
(2009)
Nature
, vol.459
, pp. 569-573
-
-
Glessner, J.T.1
Wang, K.2
Cai, G.3
Korvatska, O.4
Kim, C.E.5
Wood, S.6
Zhang, H.7
Estes, A.8
Brune, C.W.9
Bradfield, J.P.10
Imielinski, M.11
Frackelton, E.C.12
Reichert, J.13
Crawford, E.L.14
Munson, J.15
Sleiman, P.M.16
Chiavacci, R.17
Annaiah, K.18
Thomas, K.19
Hou, C.20
Glaberson, W.21
Flory, J.22
Otieno, F.23
Garris, M.24
Soorya, L.25
Klei, L.26
Piven, J.27
Meyer, K.J.28
Anagnostou, E.29
Sakurai, T.30
Game, R.M.31
Rudd, D.S.32
Zurawiecki, D.33
McDougle, C.J.34
Davis, L.K.35
Miller, J.36
Posey, D.J.37
Michaels, S.38
Kolevzon, A.39
Silverman, J.M.40
Bernier, R.41
Levy, S.E.42
Schultz, R.T.43
Dawson, G.44
Owley, T.45
McMahon, W.M.46
Wassink, T.H.47
Sweeney, J.A.48
Nurnberger, J.I.49
Coon, H.50
Sutcliffe, J.S.51
Minshew, N.J.52
Grant, S.F.53
Bucan, M.54
Cook, E.H.55
Buxbaum, J.D.56
Devlin, B.57
Schellenberg, G.D.58
Hakonarson, H.59
more..
-
18
-
-
57049132697
-
Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome
-
Bassett AS, Marshall CR, Lionel AC, Chow EW, Scherer SW. Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome. Hum Mol Genet 2008; 17:4045-53.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 4045-4053
-
-
Bassett, A.S.1
Marshall, C.R.2
Lionel, A.C.3
Chow, E.W.4
Scherer, S.W.5
-
19
-
-
33748558056
-
A chromosome 8 genecluster polymorphism with low human beta-defensin 2 gene copy number predisposes to Crohn disease of the colon
-
Fellermann K, Stange DE, Schaeffeler E, Schmalzl H, Wehkamp J, Bevins CL, Reinisch W, Teml A, Schwab M, Lichter P, Radlwimmer B, Stange EF. A chromosome 8 genecluster polymorphism with low human beta-defensin 2 gene copy number predisposes to Crohn disease of the colon. Am J Hum Genet 2006; 79:439-48.
-
(2006)
Am J Hum Genet
, vol.79
, pp. 439-448
-
-
Fellermann, K.1
Stange, D.E.2
Schaeffeler, E.3
Schmalzl, H.4
Wehkamp, J.5
Bevins, C.L.6
Reinisch, W.7
Teml, A.8
Schwab, M.9
Lichter, P.10
Radlwimmer, B.11
Stange, E.F.12
-
20
-
-
4444315011
-
CYP1B1 mutations in French patients with early-onset primary openangle glaucoma
-
Melki R, Colomb E, Lefort N, Brezin AP, Garchon HJ. CYP1B1 mutations in French patients with early-onset primary openangle glaucoma. J Med Genet 2004; 41:647-51.
-
(2004)
J Med Genet
, vol.41
, pp. 647-651
-
-
Melki, R.1
Colomb, E.2
Lefort, N.3
Brezin, A.P.4
Garchon, H.J.5
-
21
-
-
0036157114
-
Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene
-
Vincent AL, Billingsley G, Buys Y, Levin AV, Priston M, Trope G, Williams-Lyn D, Heon E. Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene. Am J Hum Genet 2002; 70:448-60.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 448-460
-
-
Vincent, A.L.1
Billingsley, G.2
Buys, Y.3
Levin, A.V.4
Priston, M.5
Trope, G.6
Williams-Lyn, D.7
Heon, E.8
-
22
-
-
75749114183
-
Heterozygous loss-of-function variants in CYP1B1 predispose to primary open-angle glaucoma
-
Pasutto F, Chavarria-Soley G, Mardin CY, Michels- Rautenstrauss K, Ingelman-Sundberg M, Fernandez- Martinez L, Weber BH, Rautenstrauss B, Reis A. Heterozygous loss-of-function variants in CYP1B1 predispose to primary open-angle glaucoma. Invest Ophthalmol Vis Sci 2010; 51:249-54.
-
(2010)
Invest Ophthalmol Vis Sci
, vol.51
, pp. 249-254
-
-
Pasutto, F.1
Chavarria-Soley, G.2
Mardin, C.Y.3
Michels-Rautenstrauss, K.4
Ingelman-Sundberg, M.5
Fernandez-Martinez, L.6
Weber, B.H.7
Rautenstrauss, B.8
Reis, A.9
-
23
-
-
34248212139
-
Role of CYP1B1, MYOC, OPTN, and OPTC genes in adult-onset primary open-angle glaucoma: Predominance of CYP1B1 mutations in Indian patients
-
Kumar A, Basavaraj MG, Gupta SK, Qamar I, Ali AM, Bajaj V, Ramesh TK, Prakash DR, Shetty JS, Dorairaj SK. Role of CYP1B1, MYOC, OPTN, and OPTC genes in adult-onset primary open-angle glaucoma: predominance of CYP1B1 mutations in Indian patients. Mol Vis 2007; 13:667-76.
-
(2007)
Mol Vis
, vol.13
, pp. 667-676
-
-
Kumar, A.1
Basavaraj, M.G.2
Gupta, S.K.3
Qamar, I.4
Ali, A.M.5
Bajaj, V.6
Ramesh, T.K.7
Prakash, D.R.8
Shetty, J.S.9
Dorairaj, S.K.10
-
24
-
-
38549084181
-
Glaucomaassociated CYP1B1 mutations share similar haplotype backgrounds in POAG and PACG phenotypes
-
Chakrabarti S, Devi KR, Komatireddy S, Kaur K, Parikh RS, Mandal AK, Chandrasekhar G, Thomas R. Glaucomaassociated CYP1B1 mutations share similar haplotype backgrounds in POAG and PACG phenotypes. Invest Ophthalmol Vis Sci 2007; 48:5439-44.
-
(2007)
Invest Ophthalmol Vis Sci
, vol.48
, pp. 5439-5444
-
-
Chakrabarti, S.1
Devi, K.R.2
Komatireddy, S.3
Kaur, K.4
Parikh, R.S.5
Mandal, A.K.6
Chandrasekhar, G.7
Thomas, R.8
-
25
-
-
58049113515
-
Screening of common CYP1B1 mutations in Iranian POAG patients using a microarray-based PrASE protocol
-
Suri F, Kalhor R, Zargar SJ, Nilforooshan N, Yazdani S, Nezari H, Paylakhi SH, Narooie-Nejhad M, Bayat B, Sedaghati T, Ahmadian A, Elahi E. Screening of common CYP1B1 mutations in Iranian POAG patients using a microarray-based PrASE protocol. Mol Vis 2008; 14:2349-56.
-
(2008)
Mol Vis
, vol.14
, pp. 2349-2356
-
-
Suri, F.1
Kalhor, R.2
Zargar, S.J.3
Nilforooshan, N.4
Yazdani, S.5
Nezari, H.6
Paylakhi, S.H.7
Narooie-Nejhad, M.8
Bayat, B.9
Sedaghati, T.10
Ahmadian, A.11
Elahi, E.12
-
26
-
-
33745925304
-
Heterozygous CYP1B1 gene mutations in Spanish patients with primary open-angle glaucoma
-
López-Garrido MP, Sanchez-Sanchez F, Lopez-Martinez F, Aroca-Aguilar JD, Blanco-Marchite C, Coca-Prados M, Escribano J. Heterozygous CYP1B1 gene mutations in Spanish patients with primary open-angle glaucoma. Mol Vis 2006; 12:748-55.
-
(2006)
Mol Vis
, vol.12
, pp. 748-755
-
-
López-Garrido, M.P.1
Sanchez-Sanchez, F.2
Lopez-Martinez, F.3
Aroca-Aguilar, J.D.4
Blanco-Marchite, C.5
Coca-Prados, M.6
Escribano, J.7
-
27
-
-
77955593629
-
Screening of CYP1B1 and MYOC in Moroccan families with primary congenital glaucoma: Three novel mutations in CYP1B1
-
Hilal L, Boutayeb S, Serrou A, Refass-Buret L, Shisseh H, Bencherifa F, El Mzibri M, Benazzouz B, Berraho A. Screening of CYP1B1 and MYOC in Moroccan families with primary congenital glaucoma: three novel mutations in CYP1B1. Mol Vis 2010; 16:1215-26.
-
(2010)
Mol Vis
, vol.16
, pp. 1215-1226
-
-
Hilal, L.1
Boutayeb, S.2
Serrou, A.3
Refass-Buret, L.4
Shisseh, H.5
Bencherifa, F.6
El Mzibri, M.7
Benazzouz, B.8
Berraho, A.9
-
28
-
-
73049105367
-
Functional analysis of CYP1B1 mutations and association of heterozygous hypomorphic alleles with primary open-angle glaucoma
-
López-Garrido MP, Blanco-Marchite C, Sanchez-Sanchez F, Lopez-Sanchez E, Chaques-Alepuz V, Campos-Mollo E, Salinas-Sanchez AS, Escribano J. Functional analysis of CYP1B1 mutations and association of heterozygous hypomorphic alleles with primary open-angle glaucoma. Clin Genet 2010; 77:70-8.
-
(2010)
Clin Genet
, vol.77
, pp. 70-78
-
-
López-Garrido, M.P.1
Blanco-Marchite, C.2
Sanchez-Sanchez, F.3
Lopez-Sanchez, E.4
Chaques-Alepuz, V.5
Campos-Mollo, E.6
Salinas-Sanchez, A.S.7
Escribano, J.8
-
29
-
-
84859448041
-
Screening glaucoma genes in adult glaucoma suggests a multiallelic contribution of CYP1B1 to open angle glaucoma phenotypes
-
Patel HY, Richards AJ, De Karolyi B, Best SJ, Danesh-Meyer HV, Vincent AL. Screening glaucoma genes in adult glaucoma suggests a multiallelic contribution of CYP1B1 to open angle glaucoma phenotypes. Clin Experiment Ophthalmol. 2011
-
(2011)
Clin Experiment Ophthalmol
-
-
Patel, H.Y.1
Richards, A.J.2
de Karolyi, B.3
Best, S.J.4
Danesh-Meyer, H.V.5
Vincent, A.L.6
-
30
-
-
33645860816
-
Primary role of CYP1B1 in Indian juvenile-onset POAG patients
-
Acharya M, Mookherjee S, Bhattacharjee A, Bandyopadhyay AK, Daulat Thakur SK, Bhaduri G, Sen A, Ray K. Primary role of CYP1B1 in Indian juvenile-onset POAG patients. Mol Vis 2006; 12:399-404.
-
(2006)
Mol Vis
, vol.12
, pp. 399-404
-
-
Acharya, M.1
Mookherjee, S.2
Bhattacharjee, A.3
Bandyopadhyay, A.K.4
Daulat Thakur, S.K.5
Bhaduri, G.6
Sen, A.7
Ray, K.8
-
31
-
-
44149120064
-
Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucoma
-
Bhattacharjee A, Banerjee D, Mookherjee S, Acharya M, Banerjee A, Ray A, Sen A, Ray K. Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucoma. Mol Vis 2008; 14:841-50.
-
(2008)
Mol Vis
, vol.14
, pp. 841-850
-
-
Bhattacharjee, A.1
Banerjee, D.2
Mookherjee, S.3
Acharya, M.4
Banerjee, A.5
Ray, A.6
Sen, A.7
Ray, K.8
-
32
-
-
78149479800
-
Tag SNPs detect association of the CYP1B1 gene with primary open angle glaucoma
-
Burdon KP, Hewitt AW, Mackey DA, Mitchell P, Craig JE. Tag SNPs detect association of the CYP1B1 gene with primary open angle glaucoma. Mol Vis 2010; 16:2286-93.
-
(2010)
Mol Vis
, vol.16
, pp. 2286-2293
-
-
Burdon, K.P.1
Hewitt, A.W.2
Mackey, D.A.3
Mitchell, P.4
Craig, J.E.5
-
33
-
-
77955890933
-
Association of polymorphisms of tumor necrosis factor and tumor protein p53 with primary open-angle glaucoma
-
Fan BJ, Liu K, Wang DY, Tham CC, Tam PO, Lam DS, Pang CP. Association of polymorphisms of tumor necrosis factor and tumor protein p53 with primary open-angle glaucoma. Invest Ophthalmol Vis Sci 2010; 51:4110-6.
-
(2010)
Invest Ophthalmol Vis Sci
, vol.51
, pp. 4110-4116
-
-
Fan, B.J.1
Liu, K.2
Wang, D.Y.3
Tham, C.C.4
Tam, P.O.5
Lam, D.S.6
Pang, C.P.7
-
34
-
-
27944470375
-
Association of a common coding polymorphism (N453S) of the cytochrome P450 1B1 (CYP1B1) gene with optic disc cupping and visual field alteration in French patients with primary open-angle glaucoma
-
Melki R, Lefort N, Brezin AP, Garchon HJ. Association of a common coding polymorphism (N453S) of the cytochrome P450 1B1 (CYP1B1) gene with optic disc cupping and visual field alteration in French patients with primary open-angle glaucoma. Mol Vis 2005; 11:1012-7.
-
(2005)
Mol Vis
, vol.11
, pp. 1012-1017
-
-
Melki, R.1
Lefort, N.2
Brezin, A.P.3
Garchon, H.J.4
-
35
-
-
84864290527
-
Genetic variants in FTO associated with metabolic syndrome: A meta- and genebased analysis
-
Wang H, Dong S, Xu H, Qian J, Yang J. Genetic variants in FTO associated with metabolic syndrome: a meta- and genebased analysis. Mol Biol Rep. 2011
-
(2011)
Mol Biol Rep
-
-
Wang, H.1
Dong, S.2
Xu, H.3
Qian, J.4
Yang, J.5
-
36
-
-
0032513020
-
Gene structure and properties of TIGR, an olfactomedinrelated glycoprotein cloned from glucocorticoid-induced trabecular meshwork cells
-
Nguyen TD, Chen P, Huang WD, Chen H, Johnson D, Polansky JR. Gene structure and properties of TIGR, an olfactomedinrelated glycoprotein cloned from glucocorticoid-induced trabecular meshwork cells. J Biol Chem 1998; 273:6341-50.
-
(1998)
J Biol Chem
, vol.273
, pp. 6341-6350
-
-
Nguyen, T.D.1
Chen, P.2
Huang, W.D.3
Chen, H.4
Johnson, D.5
Polansky, J.R.6
-
37
-
-
33751106672
-
Expression of mutated mouse myocilin induces open-angle glaucoma in transgenic mice
-
Senatorov V, Malyukova I, Fariss R, Wawrousek EF, Swaminathan S, Sharan SK, Tomarev S. Expression of mutated mouse myocilin induces open-angle glaucoma in transgenic mice. J Neurosci 2006; 26:11903-14.
-
(2006)
J Neurosci
, vol.26
, pp. 11903-11914
-
-
Senatorov, V.1
Malyukova, I.2
Fariss, R.3
Wawrousek, E.F.4
Swaminathan, S.5
Sharan, S.K.6
Tomarev, S.7
-
38
-
-
44649105940
-
Transgenic mice expressing the Tyr437His mutant of human myocilin protein develop glaucoma
-
Zhou Y, Grinchuk O, Tomarev SI. Transgenic mice expressing the Tyr437His mutant of human myocilin protein develop glaucoma. Invest Ophthalmol Vis Sci 2008; 49:1932-9.
-
(2008)
Invest Ophthalmol Vis Sci
, vol.49
, pp. 1932-1939
-
-
Zhou, Y.1
Grinchuk, O.2
Tomarev, S.I.3
-
39
-
-
34249048046
-
Cyp1b1 protein in the mouse eye during development: An immunohistochemical study
-
Choudhary D, Jansson I, Rezaul K, Han DK, Sarfarazi M, Schenkman JB. Cyp1b1 protein in the mouse eye during development: an immunohistochemical study. Drug Metab Dispos 2007; 35:987-94.
-
(2007)
Drug Metab Dispos
, vol.35
, pp. 987-994
-
-
Choudhary, D.1
Jansson, I.2
Rezaul, K.3
Han, D.K.4
Sarfarazi, M.5
Schenkman, J.B.6
-
40
-
-
0030942553
-
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. 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 1997; 6:641-7.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 641-647
-
-
Stoilov, I.1
Akarsu, A.N.2
Sarfarazi, M.3
-
42
-
-
41549137836
-
Contributions of MYOC and CYP1B1 mutations to JOAG
-
Bayat B, Yazdani S, Alavi A, Chiani M, Chitsazian F, Tusi BK, Suri F, Narooie-Nejhad M, Sanati MH, Elahi E. Contributions of MYOC and CYP1B1 mutations to JOAG. Mol Vis 2008; 14:508-17.
-
(2008)
Mol Vis
, vol.14
, pp. 508-517
-
-
Bayat, B.1
Yazdani, S.2
Alavi, A.3
Chiani, M.4
Chitsazian, F.5
Tusi, B.K.6
Suri, F.7
Narooie-Nejhad, M.8
Sanati, M.H.9
Elahi, E.10
-
43
-
-
0037423886
-
Modification of ocular defects in mouse developmental glaucoma models by tyrosinase
-
Libby RT, Smith RS, Savinova OV, Zabaleta A, Martin JE, Gonzalez FJ, John SW. Modification of ocular defects in mouse developmental glaucoma models by tyrosinase. Science 2003; 299:1578-81.
-
(2003)
Science
, vol.299
, pp. 1578-1581
-
-
Libby, R.T.1
Smith, R.S.2
Savinova, O.V.3
Zabaleta, A.4
Martin, J.E.5
Gonzalez, F.J.6
John, S.W.7
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