Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 72 Records) |
Query Trace: Syndrome and LOXL1[original query] |
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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 |
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 |
Association of polymorphisms in APOE and LOXL1 with pseudoexfoliation syndrome and pseudoexfoliation glaucoma in a Turkish population. Ophthalmic genetics 2016 Mar 1-3. Tuncay Fulya Yaylacio?lu, Akta? Zeynep, Ergün Mehmet Ali, Ergün Sezin Güntekin, Hasanreiso?lu Murat, Hasanreiso?lu Bera |
Lysyl oxidase-like 1 polymorphisms in a southwestern Greek cataract population with pseudoexfoliation syndrome. Clinical ophthalmology (Auckland, N.Z.) 2016 10 161-6. Panoutsopoulos Alexios A, Gartaganis Vassiliki S, Giannakopoulos Marios P, Goumas Panos D, Anastassiou Evangelos D, Gartaganis Sotirios |
Association of Lysyl Oxidase-Like 1 Gene Polymorphism in Turkish Patients With Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma. Journal of glaucoma 2016 Oct . Asfuroglu Mahmut, Cavdarli Busranur, Koz Ozlem G, A Yarangumeli Ahmet, Ozdemir Emine |
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 |
Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1. Nature communications 2017 May 8 15466. Pasutto Francesca, Zenkel Matthias, Hoja Ursula, Berner Daniel, Uebe Steffen, Ferrazzi Fulvia, Schödel Johannes, Liravi Panah, Ozaki Mineo, Paoli Daniela, Frezzotti Paolo, Mizoguchi Takanori, Nakano Satoko, Kubota Toshiaki, Manabe Shinichi, Salvi Erika, Manunta Paolo, Cusi Daniele, Gieger Christian, Wichmann Heinz-Erich, Aung Tin, Khor Chiea Chuen, Kruse Friedrich E, Reis André, Schlötzer-Schrehardt Ursu |
GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma.
Experimental eye research 2017 Dec . Zagajewska Katarzyna, Pi?tkowska Magdalena, Goryca Krzysztof, Ba?abas Aneta, Kluska Anna, Paziewska Agnieszka, Po?piech Ewelina, Grabska-Liberek Iwona, Hennig Ewa |
Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population. European journal of ophthalmology 2019 Jul 29 (4): 431-436. Pandav Surinder Singh, Chakma Partha, Khera Alka, Chugh Neera, Gupta Parul Chawla, Thattaruthody Faisal, Seth Natasha Gautam, Raj Srishti, Kaushik Sushmita, Khullar Madhu, Ram Jag |
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 |
Three Single Nucleotide Polymorphisms of LOXL1' in a Turkish Population with Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma. Turkish journal of ophthalmology 2018 11 48 (5): 215-220. Yaz Yetkin, Y?ld?r?m Nilgün, Ayd?n Yaz Yasemin, Çilingir O?uz, Yüksel Zafer, Mutlu Fez |
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 |
De novo variants in an extracellular matrix protein coding gene, fibulin-5 (FBLN5) are associated with pseudoexfoliation. European journal of human genetics : EJHG 2019 Jul . Padhy Biswajit, Kapuganti Ramani Shyam, Hayat Bushra, Mohanty Pranjya Paramita, Alone Debasmita Pank |
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- |
The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome. Human molecular genetics 2019 4 28 (15): 2531-2548. Berner Daniel, Hoja Ursula, Zenkel Matthias, Ross James Julian, Uebe Steffen, Paoli Daniela, Frezzotti Paolo, Rautenbach Robyn M, Ziskind Ari, Williams Susan E, Carmichael Trevor R, Ramsay Michele, Topouzis Fotis, Chatzikyriakidou Anthi, Lambropoulos Alexandros, Sundaresan Periasamy, Ayub Humaira, Akhtar Farah, Qamar Raheel, Zenteno Juan C, Cruz-Aguilar Marisa, Astakhov Yury S, Dubina Michael, Wiggs Janey, Ozaki Mineo, Kruse Friedrich E, Aung Tin, Reis André, Khor Chiea Chuen, Pasutto Francesca, Schlötzer-Schrehardt Ursu |
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 of LOXL1 Gene Polymorphisms with Exfoliation Glaucoma Patients. Iranian journal of public health 2019 Oct 48 (10): 1827-1837. Taghavi Elham, Daneshvar Ramin, Noormohammadi Zahra, Modarresi Seyed Mohammad-Hossein, Sedaghat Mohammad Re |
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 |
Associations of polymorphisms in LOXL1 and copper chaperone genes with pseudoexfoliation-syndrome-related cataract in a Chinese Uygur population. International ophthalmology 2020 Apr . Jing Qinghe, Li Dan, Gao Wei, Zhang Fan, Lu Yi, Jiang Yongxia |
Prevalence of Pseudoexfoliation Glaucoma Risk-associated Variants Within Lysyl Oxidase-like 1 in an Irish Population. Journal of glaucoma 2020 Feb . Eivers Sarah B, Greene Alison G, Dervan Edward, O'Brien Colm, Wallace Debor |
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 |
Correlation of the intronic LOXL1 polymorphism rs11638944 with pseudoexfoliation syndrome and glaucoma in a Greek population. Ophthalmic genetics 2021 4 42 (4): 405-411. Papadopoulou Maria-Kyriaki, Chatziralli Irini, Tzika Konstantina, Chiras Dimitrios, Kitsos George, Kroupis Christ |
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 |
A Study on the Candidate Gene Association and Interaction with Measures of UV Exposure in Pseudoexfoliation Patients from India. Current eye research 2023 8 1-9. Suganya Kandeeban, Sureshkumar Ishwarya, R N Nareshkumar, Vaishaali Gunalan, P Porkodi, J Shyam Sundar, Rashima Asokan, R Sharada, Krishnamoorthy Sripriya, Ronnie George, Sarangapani Sripri |
Minimal phenotypes in transgenic mice with the human LOXL1/LOXL1-AS1 locus associated with exfoliation glaucoma. Vision research 2024 8 223 108464. Kacie J Meyer, Hannah E Mercer, Ben R Roos, John H Fingert, Michael G Anders |
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