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4. Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci. Aung T; Ozaki M; Lee MC; Schlötzer-Schrehardt U; Thorleifsson G; Mizoguchi T; Igo RP; Haripriya A; Williams SE; Astakhov YS; Orr AC; Burdon KP; Nakano S; Mori K; Abu-Amero K; Hauser M; Li Z; Prakadeeswari G; Bailey JNC; Cherecheanu AP; Kang JH; Nelson S; Hayashi K; Manabe SI; Kazama S; Zarnowski T; Inoue K; Irkec M; Coca-Prados M; Sugiyama K; Järvelä I; Schlottmann P; Lerner SF; Lamari H; Nilgün Y; Bikbov M; Park KH; Cha SC; Yamashiro K; Zenteno JC; Jonas JB; Kumar RS; Perera SA; Chan ASY; Kobakhidze N; George R; Vijaya L; Do T; Edward DP; de Juan Marcos L; Pakravan M; Moghimi S; Ideta R; Bach-Holm D; Kappelgaard P; Wirostko B; Thomas S; Gaston D; Bedard K; Greer WL; Yang Z; Chen X; Huang L; Sang J; Jia H; Jia L; Qiao C; Zhang H; Liu X; Zhao B; Wang YX; Xu L; Leruez S; Reynier P; Chichua G; Tabagari S; Uebe S; Zenkel M; Berner D; Mossböck G; Weisschuh N; Hoja U; Welge-Luessen UC; Mardin C; Founti P; Chatzikyriakidou A; Pappas T; Anastasopoulos E; Lambropoulos A; Ghosh A; Shetty R; Porporato N; Saravanan V; Venkatesh R; Shivkumar C; Kalpana N; Sarangapani S; Kanavi MR; Beni AN; Yazdani S; Lashay A; Naderifar H; Khatibi N; Fea A; Lavia C; Dallorto L; Rolle T; Frezzotti P; Paoli D; Salvi E; Manunta P; Mori Y; Miyata K; Higashide T; Chihara E; Ishiko S; Yoshida A; Yanagi M; Kiuchi Y; Ohashi T; Sakurai T; Sugimoto T; Chuman H; Aihara M; Inatani M; Miyake M; Gotoh N; Matsuda F; Yoshimura N; Ikeda Y; Ueno M; Sotozono C; Jeoung JW; Sagong M; Park KH; Ahn J; Cruz-Aguilar M; Ezzouhairi SM; Rafei A; Chong YF; Ng XY; Goh SR; Chen Y; Yong VHK; Khan MI; Olawoye OO; Ashaye AO; Ugbede I; Onakoya A; Kizor-Akaraiwe N; Teekhasaenee C; Suwan Y; Supakontanasan W; Okeke S; Uche NJ; Asimadu I; Ayub H; Akhtar F; Kosior-Jarecka E; Lukasik U; Lischinsky I; Castro V; Grossmann RP; Sunaric Megevand G; Roy S; Dervan E; Silke E; Rao A; Sahay P; Fornero P; Cuello O; Sivori D; Zompa T; Mills RA; Souzeau E; Mitchell P; Wang JJ; Hewitt AW; Coote M; Crowston JG; Astakhov SY; Akopov EL; Emelyanov A; Vysochinskaya V; Kazakbaeva G; Fayzrakhmanov R; Al-Obeidan SA; Owaidhah O; Aljasim LA; Chowbay B; Foo JN; Soh RQ; Sim KS; Xie Z; Cheong AWO; Mok SQ; Soo HM; Chen XY; Peh SQ; Heng KK; Husain R; Ho SL; Hillmer AM; Cheng CY; Escudero-Domínguez FA; González-Sarmiento R; Martinon-Torres F; Salas A; Pathanapitoon K; Hansapinyo L; Wanichwecharugruang B; Kitnarong N; Sakuntabhai A; Nguyn HX; Nguyn GTT; Nguyn TV; Zenz W; Binder A; Klobassa DS; Hibberd ML; Davila S; Herms S; Nöthen MM; Moebus S; Rautenbach RM; Ziskind A; Carmichael TR; Ramsay M; Álvarez L; García M; González-Iglesias H; Rodríguez-Calvo PP; Fernández-Vega Cueto L; Oguz Ç; Tamcelik N; Atalay E; Batu B; Aktas D; Kasım B; Wilson MR; Coleman AL; Liu Y; Challa P; Herndon L; Kuchtey RW; Kuchtey J; Curtin K; Chaya CJ; Crandall A; Zangwill LM; Wong TY; Nakano M; Kinoshita S; den Hollander AI; Vesti E; Fingert JH; Lee RK; Sit AJ; Shingleton BJ; Wang N; Cusi D; Qamar R; Kraft P; Pericak-Vance MA; Raychaudhuri S; Heegaard S; Kivelä T; Reis A; Kruse FE; Weinreb RN; Pasquale LR; Haines JL; Thorsteinsdottir U; Jonasson F; Allingham RR; Milea D; Ritch R; Kubota T; Tashiro K; Vithana EN; Micheal S; Topouzis F; Craig JE; Dubina M; Sundaresan P; Stefansson K; Wiggs JL; Pasutto F; Khor CC Nat Genet; 2017 Jul; 49(7):993-1004. PubMed ID: 28553957 [TBL] [Abstract][Full Text] [Related]
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13. Exfoliation Syndrome: A Disease of Autophagy and LOXL1 Proteopathy. Bernstein AM; Ritch R; Wolosin JM J Glaucoma; 2018 Jul; 27 Suppl 1(Suppl 1):S44-S53. PubMed ID: 29547474 [TBL] [Abstract][Full Text] [Related]
14. Extracellular Matrix Regulation and Dysregulation in Exfoliation Syndrome. Zenkel M J Glaucoma; 2018 Jul; 27 Suppl 1():S24-S28. PubMed ID: 29432335 [TBL] [Abstract][Full Text] [Related]
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19. Prevalence of high-risk alleles in the LOXL1 gene and its association with pseudoexfoliation syndrome and exfoliation glaucoma in a Latin American population. Jaimes M; Rivera-Parra D; Miranda-Duarte A; Valdés G; Zenteno JC Ophthalmic Genet; 2012 Mar; 33(1):12-7. PubMed ID: 21970694 [TBL] [Abstract][Full Text] [Related]
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