270 related articles for article (PubMed ID: 25706626)
61. Association of Lysyl Oxidase-Like 1 Gene Polymorphism in Turkish Patients With Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma.
Asfuroglu M; Cavdarli B; Koz OG; A Yarangumeli A; Ozdemir EY
J Glaucoma; 2017 Feb; 26(2):e54-e57. PubMed ID: 27753755
[TBL] [Abstract][Full Text] [Related]
62. Association of LOXL1 polymorphisms with pseudoexfoliation, glaucoma, intraocular pressure, and systemic diseases in a Greek population. The Thessaloniki eye study.
Anastasopoulos E; Coleman AL; Wilson MR; Sinsheimer JS; Yu F; Katafigiotis S; Founti P; Salonikiou A; Pappas T; Koskosas A; Katopodi T; Lambropoulos A; Topouzis F
Invest Ophthalmol Vis Sci; 2014 Jun; 55(7):4238-43. PubMed ID: 24917141
[TBL] [Abstract][Full Text] [Related]
63. 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; Santiago-Turla C; Wiggs JL; Budenz DL; Akafo S; Challa P; Herndon LW; Hauser MA; Allingham RR
Invest Ophthalmol Vis Sci; 2008 Aug; 49(8):3465-8. PubMed ID: 18421074
[TBL] [Abstract][Full Text] [Related]
64. Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1.
Pasutto F; Zenkel M; Hoja U; Berner D; Uebe S; Ferrazzi F; Schödel J; Liravi P; Ozaki M; Paoli D; Frezzotti P; Mizoguchi T; Nakano S; Kubota T; Manabe S; Salvi E; Manunta P; Cusi D; Gieger C; Wichmann HE; Aung T; Khor CC; Kruse FE; Reis A; Schlötzer-Schrehardt U
Nat Commun; 2017 May; 8():15466. PubMed ID: 28534485
[TBL] [Abstract][Full Text] [Related]
65. Correlation of the intronic
Papadopoulou MK; Chatziralli I; Tzika K; Chiras D; Kitsos G; Kroupis C
Ophthalmic Genet; 2021 Aug; 42(4):405-411. PubMed ID: 33792495
[TBL] [Abstract][Full Text] [Related]
66. Genetic Risk Factors for Glaucoma and Exfoliation Syndrome Identified by Genome-wide Association Studies.
Sakurada Y; Mabuchi F
Curr Neuropharmacol; 2018; 16(7):933-941. PubMed ID: 28721823
[TBL] [Abstract][Full Text] [Related]
67. Lack of association of LOXL1 gene variants in Japanese patients with central retinal vein occlusion without clinically detectable pseudoexfoliation material deposits.
Tanito M; Hara K; Akahori M; Harata A; Itabashi T; Takai Y; Kaidzu S; Ohira A; Iwata T
Acta Ophthalmol; 2015 May; 93(3):e214-7. PubMed ID: 25130441
[TBL] [Abstract][Full Text] [Related]
68. Evaluation of MMP1 and MMP3 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma.
Tsironi EE; Pefkianaki M; Tsezou A; Kotoula MG; Dardiotis E; Almpanidou P; Papathanasiou AA; Rodopoulou P; Chatzoulis DZ; Hadjigeorgiou GM
Mol Vis; 2009 Dec; 15():2890-5. PubMed ID: 20038976
[TBL] [Abstract][Full Text] [Related]
69. The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome.
Berner D; Hoja U; Zenkel M; Ross JJ; Uebe S; Paoli D; Frezzotti P; Rautenbach RM; Ziskind A; Williams SE; Carmichael TR; Ramsay M; Topouzis F; Chatzikyriakidou A; Lambropoulos A; Sundaresan P; Ayub H; Akhtar F; Qamar R; Zenteno JC; Cruz-Aguilar M; Astakhov YS; Dubina M; Wiggs J; Ozaki M; Kruse FE; Aung T; Reis A; Khor CC; Pasutto F; Schlötzer-Schrehardt U
Hum Mol Genet; 2019 Aug; 28(15):2531-2548. PubMed ID: 30986821
[TBL] [Abstract][Full Text] [Related]
70. Association between Chronic Obstructive Pulmonary Disease and Exfoliation Syndrome: The Utah Project on Exfoliation Syndrome.
Taylor SC; Bernhisel AA; Curtin K; Allingham RR; Ritch R; Wirostko BM
Ophthalmol Glaucoma; 2019; 2(1):3-10. PubMed ID: 32672555
[TBL] [Abstract][Full Text] [Related]
71. Ethnicity-Based Differences in the Association of LOXL1 Polymorphisms with Pseudoexfoliation/Pseudoexfoliative Glaucoma: A Meta-Analysis.
Founti P; Haidich AB; Chatzikyriakidou A; Salonikiou A; Anastasopoulos E; Pappas T; Lambropoulos A; Viswanathan AC; Topouzis F
Ann Hum Genet; 2015 Nov; 79(6):431-50. PubMed ID: 26404116
[TBL] [Abstract][Full Text] [Related]
72. Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry.
; Hauser MA; Allingham RR; Aung T; Van Der Heide CJ; Taylor KD; Rotter JI; Wang SJ; Bonnemaijer PWM; Williams SE; Abdullahi SM; Abu-Amero KK; Anderson MG; Akafo S; Alhassan MB; Asimadu I; Ayyagari R; Bakayoko S; Nyamsi PB; Bowden DW; Bromley WC; Budenz DL; Carmichael TR; Challa P; Chen YI; Chuka-Okosa CM; Cooke Bailey JN; Costa VP; Cruz DA; DuBiner H; Ervin JF; Feldman RM; Flamme-Wiese M; Gaasterland DE; Garnai SJ; Girkin CA; Guirou N; Guo X; Haines JL; Hammond CJ; Herndon L; Hoffmann TJ; Hulette CM; Hydara A; Igo RP; Jorgenson E; Kabwe J; Kilangalanga NJ; Kizor-Akaraiwe N; Kuchtey RW; Lamari H; Li Z; Liebmann JM; Liu Y; Loos RJF; Melo MB; Moroi SE; Msosa JM; Mullins RF; Nadkarni G; Napo A; Ng MCY; Nunes HF; Obeng-Nyarkoh E; Okeke A; Okeke S; Olaniyi O; Olawoye O; Oliveira MB; Pasquale LR; Perez-Grossmann RA; Pericak-Vance MA; Qin X; Ramsay M; Resnikoff S; Richards JE; Schimiti RB; Sim KS; Sponsel WE; Svidnicki PV; Thiadens AAHJ; Uche NJ; van Duijn CM; de Vasconcellos JPC; Wiggs JL; Zangwill LM; Risch N; Milea D; Ashaye A; Klaver CCW; Weinreb RN; Ashley Koch AE; Fingert JH; Khor CC
JAMA; 2019 Nov; 322(17):1682-1691. PubMed ID: 31688885
[TBL] [Abstract][Full Text] [Related]
73. Evaluation of CNTNAP2 gene polymorphisms for exfoliation syndrome in Japanese.
Shimizu A; Takano Y; Shi D; Yokokura S; Yokoyama Y; Zheng X; Shiraishi A; Ohashi Y; Nakazawa T; Fuse N
Mol Vis; 2012; 18():1395-401. PubMed ID: 22690117
[TBL] [Abstract][Full Text] [Related]
74. [Study of the functional significance of polymorphic loci of the LOXL1 gene associated with glaucoma according to genome-wide studies (in silico analysis)].
Eliseeva NV; Ponomarenko IV; Churnosov MI
Vestn Oftalmol; 2021; 137(5):22-30. PubMed ID: 34726854
[TBL] [Abstract][Full Text] [Related]
75. GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma.
Zagajewska K; Piątkowska M; Goryca K; Bałabas A; Kluska A; Paziewska A; Pośpiech E; Grabska-Liberek I; Hennig EE
Exp Eye Res; 2018 Mar; 168():138-148. PubMed ID: 29278698
[TBL] [Abstract][Full Text] [Related]
76. Lysyl oxidase-like 1 gene in the reversal of promoter risk allele in pseudoexfoliation syndrome.
Dubey SK; Hejtmancik JF; Krishnadas SR; Sharmila R; Haripriya A; Sundaresan P
JAMA Ophthalmol; 2014 Aug; 132(8):949-55. PubMed ID: 24809751
[TBL] [Abstract][Full Text] [Related]
77. Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese.
Rong SS; Lu SY; Matsushita K; Huang C; Leung CKS; Kawashima R; Usui S; Tam POS; Young AL; Tsujikawa M; Zhang M; Nishida K; Wiggs JL; Tham CC; Pang CP; Chen LJ
Exp Eye Res; 2019 Mar; 180():129-136. PubMed ID: 30586556
[TBL] [Abstract][Full Text] [Related]
78. LOXL1 mutations are associated with exfoliation syndrome in patients from the midwestern United States.
Fingert JH; Alward WL; Kwon YH; Wang K; Streb LM; Sheffield VC; Stone EM
Am J Ophthalmol; 2007 Dec; 144(6):974-975. PubMed ID: 18036875
[No Abstract] [Full Text] [Related]
79. Lack of association between the C677T single nucleotide polymorphism of the MTHFR gene and glaucoma in Iranian patients.
Nilforoushan N; Aghapour S; Raoofian R; Saee Rad S; Greene WK; Fakhraie G; Heidari M
Acta Med Iran; 2012; 50(3):208-12. PubMed ID: 22418991
[TBL] [Abstract][Full Text] [Related]
80. Prospects for gene-environment interactions in exfoliation syndrome.
Pasquale LR; Kang JH; Wiggs JL
J Glaucoma; 2014; 23(8 Suppl 1):S64-7. PubMed ID: 25275911
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
