Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 38 Records) |
| Query Trace: Exfoliation Syndrome and LOXL1[original query] |
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| Evaluation of LOXL1 polymorphisms in eyes with exfoliation glaucoma in Japanese. Molecular vision 2008 14 1338-43. Fuse Nobuo, Miyazawa Akiko, Nakazawa Toru, Mengkegale Mingge, Otomo Takaaki, Nishida Koh |
| Evaluation of LOXL1 polymorphisms in primary open-angle glaucoma in southern and northern Chinese. Molecular vision 2008 14 2381-9. Gong Wei Fen, Chiang Sylvia W Y, Chen Li Jia, Tam Pancy O S, Jia Li Yun, Leung Dexter Y L, Geng Yi Qun, Tham Clement C Y, Lam Dennis S C, Ritch Robert, Wang Ningli, Pang Chi P |
| LOXL1 variants in elderly Japanese patients with exfoliation syndrome/glaucoma, primary open-angle glaucoma, normal tension glaucoma, and cataract. Molecular vision 2008 14 1898-905. Tanito Masaki, Minami Masayoshi, Akahori Masakazu, Kaidzu Sachiko, Takai Yasuyuki, Ohira Akihiro, Iwata Takes |
| Association of LOXL1 gene with Finnish exfoliation syndrome patients. Journal of human genetics 2009 May 54 (5): 289-97. Lemmelä Susanna, Forsman Eva, Onkamo Päivi, Nurmi Hanna, Laivuori Hannele, Kivelä Tero, Puska Päivi, Heger Martin, Eriksson Aldur, Forsius Henrik, Järvelä Ir |
| Evaluation of LOXL1 polymorphisms in exfoliation syndrome in a Chinese population. Molecular vision 2009 15 2349-57. Chen Ling, Jia Liyun, Wang Ningli, Tang Guangxian, Zhang Chun, Fan Sujie, Liu Wenru, Meng Hailin, Zeng Wotan, Liu Ningpu, Wang Huaizhou, Jia Hongy |
| LOXL1 gene sequence variants and vascular disease in exfoliation syndrome and exfoliative glaucoma. Journal of glaucoma 2011 Mar 20 (3): 143-7. Holló Gábor, Gál Anikó, Kóthy Péter, Molnár Judit |
| Ethnicity-based subgroup meta-analysis of the association of LOXL1 polymorphisms with glaucoma. Molecular vision 2010 16 167-77. Chen Haoyu, Chen Li Jia, Zhang Mingzhi, Gong Weifeng, Tam Pancy Oi Sin, Lam Dennis Shun Chiu, Pang Chi P |
| Evaluation of LOXL1 polymorphisms in exfoliation syndrome in the Uygur population. Molecular vision 2011 17 1734-44. Mayinu , Chen Xue |
| No association of LOXL1 gene polymorphisms with Alzheimer's disease. Neuromolecular medicine 2011 Jun 13 (2): 160-6. Abramsson Alexandra, Landgren Sara, Zetterberg Madeleine, Seibt Palmer Mona, Minthon Lennart, Gustafson Deborah R, Skoog Ingmar, Blennow Kaj, Zetterberg Henr |
| An investigation into LOXL1 variants in black South African individuals with exfoliation syndrome. Archives of ophthalmology (Chicago, Ill. : 1960) 2011 Feb 129 (2): 206-10. Rautenbach Robyn M, Bardien Soraya, Harvey Justin, Ziskind A |
| Association of lysyl oxidase-like 1 gene polymorphisms with exfoliation syndrome in Koreans. Molecular vision 2011 17 2808-17. Sagong Min, Gu Byoung Young, Cha Soon Che |
| LOXL1 promoter haplotypes are associated with exfoliation syndrome in a U.S. Caucasian population. Investigative ophthalmology & visual science 2011 Apr 52 (5): 2372-8. Fan Bao Jian, Pasquale Louis R, Rhee Douglas, Li Tiansen, Haines Jonathan L, Wiggs Janey |
| Development of novel LOXL1 genotyping method and evaluation of LOXL1, APOE and MTHFR polymorphisms in exfoliation syndrome/glaucoma in a Greek population. Molecular vision 2013 19 1006-16. Chiras Dimitrios, Tzika Konstantina, Kokotas Haris, Oliveira Samantha C, Grigoriadou Maria, Kastania Anastasia, Dima Kleanthi, Stefaniotou Maria, Aspiotis Miltiadis, Petersen Michael B, Kroupis Christos, Kitsos Geor |
| Association of LOXL1 gene polymorphisms with exfoliation syndrome/glaucoma and primary open angle glaucoma in a Turkish population. Molecular vision 2013 19 . Kas?m B, Irkeç M, Alika?ifo?lu M, Orhan M, Mocan MC, Akta? D |
| Lack of association of LOXL1 gene variants in Japanese patients with central retinal vein occlusion without clinically detectable pseudoexfoliation material deposits. Acta ophthalmologica 2015 May 93 (3): e214-7. Tanito Masaki, Hara Katsunori, Akahori Masakazu, Harata Ayano, Itabashi Takeshi, Takai Yasuyuki, Kaidzu Sachiko, Ohira Akihiro, Iwata Takes |
Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population.
Scientific reports 2014 4 5340. Nakano Masakazu, Ikeda Yoko, Tokuda Yuichi, Fuwa Masahiro, Ueno Morio, Imai Kojiro, Sato Ryuichi, Omi Natsue, Adachi Hiroko, Kageyama Masaaki, Mori Kazuhiko, Kinoshita Shigeru, Tashiro K |
| [Evaluation of LOXL1 polymorphisms in exfoliation syndrome in the Uygur population]. [Zhonghua yan ke za zhi] Chinese journal of ophthalmology 2014 Feb 50 (2): 126-32. Ma Yinu, Xie Tingyu, Zhu Guowei, Chen Xue |
| LOXL1 Gene Polymorphism With Exfoliation Syndrome/Exfoliation Glaucoma: A Meta-Analysis. Journal of glaucoma 2014 Oct . Wang Lin, Fu Songbin, Zhao Wencheng, Yu Yongbin, Liu Pi |
| Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus. Human molecular genetics 2015 Aug . Hauser Michael A, Aboobakar Inas F, Liu Yutao, Miura Shiroh, Whigham Benjamin T, Challa Pratap, Wheeler Joshua, Williams Andrew, Santiago-Turla Cecelia, Qin Xuejun, Rautenbach Robyn M, Ziskind Ari, Ramsay Michèle, Uebe Steffen, Song Lingyun, Safi Alexias, Vithana Eranga N, Mizoguchi Takanori, Nakano Satoko, Kubota Toshiaki, Hayashi Ken, Manabe Shin-Ichi, Kazama Shigeyasu, Mori Yosai, Miyata Kazunori, Yoshimura Nagahisa, Reis Andre, Crawford Gregory E, Pasutto Francesca, Carmichael Trevor R, Williams Susan E I, Ozaki Mineo, Aung Tin, Khor Chiea-Chuen, Stamer W Daniel, Ashley-Koch Allison E, Allingham R Ra |
| Association of clusterin (CLU) variants and exfoliation syndrome: An analysis in two Caucasian studies and a meta-analysis. Experimental eye research 2015 Aug . Fan Bao J, Pasquale Louis R, Kang Jae H, Levkovitch-Verbin Hani, Haines Jonathan L, Wiggs Janey |
| The association of LOXL1 polymorphisms with exfoliation syndrome/glaucoma: Meta-analysis. International journal of ophthalmology 2015 8 (1): 148-56. Ji Qing-Shan, Qi Bing, Wen Yue-Chun, Liu Lian, Guo Xiao-Ling, Yu Guo-Cheng, Zhong Jing-Xia |
| A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.
Nature genetics 2015 Apr 47 (4): 387-92. Aung Tin, Ozaki Mineo, Mizoguchi Takanori, Allingham R Rand, Li Zheng, Haripriya Aravind, Nakano Satoko, Uebe Steffen, Harder Jeffrey M, Chan Anita S Y, Lee Mei Chin, Burdon Kathryn P, Astakhov Yury S, Abu-Amero Khaled K, Zenteno Juan C, Nilgün Yildirim, Zarnowski Tomasz, Pakravan Mohammad, Safieh Leen Abu, Jia Liyun, Wang Ya Xing, Williams Susan, Paoli Daniela, Schlottmann Patricio G, Huang Lulin, Sim Kar Seng, Foo Jia Nee, Nakano Masakazu, Ikeda Yoko, Kumar Rajesh S, Ueno Morio, Manabe Shin-ichi, Hayashi Ken, Kazama Shigeyasu, Ideta Ryuichi, Mori Yosai, Miyata Kazunori, Sugiyama Kazuhisa, Higashide Tomomi, Chihara Etsuo, Inoue Kenji, Ishiko Satoshi, Yoshida Akitoshi, Yanagi Masahide, Kiuchi Yoshiaki, Aihara Makoto, Ohashi Tsutomu, Sakurai Toshiya, Sugimoto Takako, Chuman Hideki, Matsuda Fumihiko, Yamashiro Kenji, Gotoh Norimoto, Miyake Masahiro, Astakhov Sergei Y, Osman Essam A, Al-Obeidan Saleh A, Owaidhah Ohoud, Al-Jasim Leyla, Al Shahwan Sami, Fogarty Rhys A, Leo Paul, Yetkin Yaz, O?uz Çilingir, Kanavi Mozhgan Rezaei, Beni Afsaneh Nederi, Yazdani Shahin, Akopov Evgeny L, Toh Kai-Yee, Howell Gareth R, Orr Andrew C, Goh Yufen, Meah Wee Yang, Peh Su Qin, Kosior-Jarecka Ewa, Lukasik Urszula, Krumbiegel Mandy, Vithana Eranga N, Wong Tien Yin, Liu Yutao, Koch Allison E Ashley, Challa Pratap, Rautenbach Robyn M, Mackey David A, Hewitt Alex W, Mitchell Paul, Wang Jie Jin, Ziskind Ari, Carmichael Trevor, Ramakrishnan Rangappa, Narendran Kalpana, Venkatesh Rangaraj, Vijayan Saravanan, Zhao Peiquan, Chen Xueyi, Guadarrama-Vallejo Dalia, Cheng Ching Yu, Perera Shamira A, Husain Rahat, Ho Su-Ling, Welge-Luessen Ulrich-Christoph, Mardin Christian, Schloetzer-Schrehardt Ursula, Hillmer Axel M, Herms Stefan, Moebus Susanne, Nöthen Markus M, Weisschuh Nicole, Shetty Rohit, Ghosh Arkasubhra, Teo Yik Ying, Brown Matthew A, Lischinsky Ignacio, , , Crowston Jonathan G, Coote Michael, Zhao Bowen, Sang Jinghong, Zhang Nihong, You Qisheng, Vysochinskaya Vera, Founti Panayiota, Chatzikyriakidou Anthoula, Lambropoulos Alexandros, Anastasopoulos Eleftherios, Coleman Anne L, Wilson M Roy, Rhee Douglas J, Kang Jae Hee, May-Bolchakova Inna, Heegaard Steffen, Mori Kazuhiko, Alward Wallace L M, Jonas Jost B, Xu Liang, Liebmann Jeffrey M, Chowbay Balram, Schaeffeler Elke, Schwab Matthias, Lerner Fabian, Wang Ningli, Yang Zhenglin, Frezzotti Paolo, Kinoshita Shigeru, Fingert John H, Inatani Masaru, Tashiro Kei, Reis André, Edward Deepak P, Pasquale Louis R, Kubota Toshiaki, Wiggs Janey L, Pasutto Francesca, Topouzis Fotis, Dubina Michael, Craig Jamie E, Yoshimura Nagahisa, Sundaresan Periasamy, John Simon W M, Ritch Robert, Hauser Michael A, Khor Chiea-Chu |
| Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci. Nature genetics 2017 May . Aung Tin, Ozaki Mineo, Lee Mei Chin, Schlötzer-Schrehardt Ursula, Thorleifsson Gudmar, Mizoguchi Takanori, Igo Robert P, Haripriya Aravind, Williams Susan E, Astakhov Yury S, Orr Andrew C, Burdon Kathryn P, Nakano Satoko, Mori Kazuhiko, Abu-Amero Khaled, Hauser Michael, Li Zheng, Prakadeeswari Gopalakrishnan, Bailey Jessica N Cooke, Cherecheanu Alina Popa, Kang Jae H, Nelson Sarah, Hayashi Ken, Manabe Shin-Ichi, Kazama Shigeyasu, Zarnowski Tomasz, Inoue Kenji, Irkec Murat, Coca-Prados Miguel, Sugiyama Kazuhisa, Järvelä Irma, Schlottmann Patricio, Lerner S Fabian, Lamari Hasnaa, Nilgün Yildirim, Bikbov Mukharram, Park Ki Ho, Cha Soon Cheol, Yamashiro Kenji, Zenteno Juan C, Jonas Jost B, Kumar Rajesh S, Perera Shamira A, Chan Anita S Y, Kobakhidze Nino, George Ronnie, Vijaya Lingam, Do Tan, Edward Deepak P, de Juan Marcos Lourdes, Pakravan Mohammad, Moghimi Sasan, Ideta Ryuichi, Bach-Holm Daniella, Kappelgaard Per, Wirostko Barbara, Thomas Samuel, Gaston Daniel, Bedard Karen, Greer Wenda L, Yang Zhenglin, Chen Xueyi, Huang Lulin, Sang Jinghong, Jia Hongyan, Jia Liyun, Qiao Chunyan, Zhang Hui, Liu Xuyang, Zhao Bowen, Wang Ya-Xing, Xu Liang, Leruez Stéphanie, Reynier Pascal, Chichua George, Tabagari Sergo, Uebe Steffen, Zenkel Matthias, Berner Daniel, Mossböck Georg, Weisschuh Nicole, Hoja Ursula, Welge-Luessen Ulrich-Christoph, Mardin Christian, Founti Panayiota, Chatzikyriakidou Anthi, Pappas Theofanis, Anastasopoulos Eleftherios, Lambropoulos Alexandros, Ghosh Arkasubhra, Shetty Rohit, Porporato Natalia, Saravanan Vijayan, Venkatesh Rengaraj, Shivkumar Chandrashekaran, Kalpana Narendran, Sarangapani Sripriya, Kanavi Mozhgan R, Beni Afsaneh Naderi, Yazdani Shahin, Lashay Alireza, Naderifar Homa, Khatibi Nassim, Fea Antonio, Lavia Carlo, Dallorto Laura, Rolle Teresa, Frezzotti Paolo, Paoli Daniela, Salvi Erika, Manunta Paolo, Mori Yosai, Miyata Kazunori, Higashide Tomomi, Chihara Etsuo, Ishiko Satoshi, Yoshida Akitoshi, Yanagi Masahide, Kiuchi Yoshiaki, Ohashi Tsutomu, Sakurai Toshiya, Sugimoto Takako, Chuman Hideki, Aihara Makoto, Inatani Masaru, Miyake Masahiro, Gotoh Norimoto, Matsuda Fumihiko, Yoshimura Nagahisa, Ikeda Yoko, Ueno Morio, Sotozono Chie, Jeoung Jin Wook, Sagong Min, Park Kyu Hyung, Ahn Jeeyun, Cruz-Aguilar Marisa, Ezzouhairi Sidi M, Rafei Abderrahman, Chong Yaan Fun, Ng Xiao Yu, Goh Shuang Ru, Chen Yueming, Yong Victor H K, Khan Muhammad Imran, Olawoye Olusola O, Ashaye Adeyinka O, Ugbede Idakwo, Onakoya Adeola, Kizor-Akaraiwe Nkiru, Teekhasaenee Chaiwat, Suwan Yanin, Supakontanasan Wasu, Okeke Suhanya, Uche Nkechi J, Asimadu Ifeoma, Ayub Humaira, Akhtar Farah, Kosior-Jarecka Ewa, Lukasik Urszula, Lischinsky Ignacio, Castro Vania, Grossmann Rodolfo Perez, Megevand Gordana Sunaric, Roy Sylvain, Dervan Edward, Silke Eoin, Rao Aparna, Sahay Priti, Fornero Pablo, Cuello Osvaldo, Sivori Delia, Zompa Tamara, Mills Richard A, Souzeau Emmanuelle, Mitchell Paul, Wang Jie Jin, Hewitt Alex W, Coote Michael, Crowston Jonathan G, Astakhov Sergei Y, Akopov Eugeny L, Emelyanov Anton, Vysochinskaya Vera, Kazakbaeva Gyulli, Fayzrakhmanov Rinat, Al-Obeidan Saleh A, Owaidhah Ohoud, Aljasim Leyla Ali, Chowbay Balram, Foo Jia Nee, Soh Raphael Q, Sim Kar Seng, Xie Zhicheng, Cheong Augustine W O, Mok Shi Qi, Soo Hui Meng, Chen Xiao Yin, Peh Su Qin, Heng Khai Koon, Husain Rahat, Ho Su-Ling, Hillmer Axel M, Cheng Ching-Yu, Escudero-Domínguez Francisco A, González-Sarmiento Rogelio, Martinon-Torres Frederico, Salas Antonio, Pathanapitoon Kessara, Hansapinyo Linda, Wanichwecharugruang Boonsong, Kitnarong Naris, Sakuntabhai Anavaj, Nguyn Hip X, Nguyn Giang T T, Nguyn Trình V, Zenz Werner, Binder Alexander, Klobassa Daniela S, Hibberd Martin L, Davila Sonia, Herms Stefan, Nöthen Markus M, Moebus Susanne, Rautenbach Robyn M, Ziskind Ari, Carmichael Trevor R, Ramsay Michele, Álvarez Lydia, García Montserrat, González-Iglesias Héctor, Rodríguez-Calvo Pedro P, Cueto Luis Fernández-Vega, Oguz Çilingir, Tamcelik Nevbahar, Atalay Eray, Batu Bilge, Aktas Dilek, Kas?m Burcu, Wilson M Roy, Coleman Anne L, Liu Yutao, Challa Pratap, Herndon Leon, Kuchtey Rachel W, Kuchtey John, Curtin Karen, Chaya Craig J, Crandall Alan, Zangwill Linda M, Wong Tien Yin, Nakano Masakazu, Kinoshita Shigeru, den Hollander Anneke I, Vesti Eija, Fingert John H, Lee Richard K, Sit Arthur J, Shingleton Bradford J, Wang Ningli, Cusi Daniele, Qamar Raheel, Kraft Peter, Pericak-Vance Margaret A, Raychaudhuri Soumya, Heegaard Steffen, Kivelä Tero, Reis André, Kruse Friedrich E, Weinreb Robert N, Pasquale Louis R, Haines Jonathan L, Thorsteinsdottir Unnur, Jonasson Fridbert, Allingham R Rand, Milea Dan, Ritch Robert, Kubota Toshiaki, Tashiro Kei, Vithana Eranga N, Micheal Shazia, Topouzis Fotis, Craig Jamie E, Dubina Michael, Sundaresan Periasamy, Stefansson Kari, Wiggs Janey L, Pasutto Francesca, Khor Chiea Chu |
| Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report. Arquivos brasileiros de oftalmologia 2018 9 81 (5): 437-439. Takitani Guilherme Eiichi da Silva, Azevedo Alexandre Gomes Bortoloti de, Motta Fabiana Louise, Teixeira Sérgio Henrique, Sallum Juliana Maria Ferraz, Vessani Roberto Mur |
| Association of LOXL1 gene common sequence variants in Jordanian patients with exfoliation syndrome and exfoliative glaucoma. International journal of ophthalmology 2018 11 (10): 1583-1587. Shihadeh Wisam, Khabour Omar, Khalil Mohammed Bilal, Al-Dabbagh Alaa, Al-Hashimi Musta |
| Multiple Gene Polymorphisms Associated with Exfoliation Syndrome in the Uygur Population. Journal of ophthalmology 2019 2019 9687823. Ma Yi-Nu, Xie Ting-Yu, Chen Xue- |
| LOXL1 GENE VARIANTS IN ASSOCIATION WITH EXFOLIATION SYNDROME IN GEORGIAN POPULATION. Georgian medical news 2019 Jan (286): 32-36. Kobakhidze N, Tabagari S, Chichua |
| Association between Chronic Obstructive Pulmonary Disease and Exfoliation Syndrome: The Utah Project on Exfoliation Syndrome. Ophthalmology. Glaucoma 2020 7 2 (1): 3-10. Taylor Samuel C, Bernhisel Ashlie A, Curtin Karen, Allingham R Rand, Ritch Robert, Wirostko Barbara |
| LOXL1 gene polymorphisms are associated with exfoliation syndrome/exfoliation glaucoma risk: An updated meta-analysis. PloS one 2021 16 (4): e0250772. Li Xiaoyan, He Jie, Sun Ji |
| DNA Polymorphism of the LOXL1 Promoter Region in Exfoliation Syndrome in Uygur Individuals in XinJiang, China. Journal of ophthalmology 2022 2022 9342635. Ma Yinu, Yang Mengting, Chen Xueyi, Yi Xianglo |
- Page last reviewed:Oct 1, 2023
- Page last updated:Dec 11, 2023
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