Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 37 Records) |
Query Trace: SIX1[original query] |
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CDKN2B polymorphism is associated with primary open-angle glaucoma (POAG) in the Afro-Caribbean population of Barbados, West Indies. PloS one 2012 7 (6): e39278. Cao Dan, Jiao Xiaodong, Liu Xing, Hennis Anselm, Leske M Cristina, Nemesure Barbara, Hejtmancik J Fieldi |
Genetic investigation into the endophenotypic status of central corneal thickness and optic disc parameters in relation to open-angle glaucoma. American journal of ophthalmology 2012 Jul . Dimasi DP, Burdon KP, Hewitt AW, Fitzgerald J, Wang JJ, Healey PR, Mitchell P, Mackey DA, Craig JE |
Genome-wide association study and meta-analysis of intraocular pressure.
Human genetics 2014 Jan 133 (1): 41-57. Ozel A Bilge, Moroi Sayoko E, Reed David M, Nika Melisa, Schmidt Caroline M, Akbari Sara, Scott Kathleen, Rozsa Frank, Pawar Hemant, Musch David C, Lichter Paul R, Gaasterland Doug, Branham Kari, Gilbert Jesse, Garnai Sarah J, Chen Wei, Othman Mohammad, Heckenlively John, Swaroop Anand, Abecasis Gonçalo, Friedman David S, Zack Don, Ashley-Koch Allison, Ulmer Megan, Kang Jae H, , Liu Yutao, Yaspan Brian L, Haines Jonathan, Allingham R Rand, Hauser Michael A, Pasquale Louis, Wiggs Janey, Richards Julia E, Li Jun |
Investigation of known genetic risk factors for primary open angle glaucoma in two populations of African ancestry. Investigative ophthalmology & visual science 2013 54 (9): 6248-54. Liu Yutao, Hauser Michael A, Akafo Stephen K, Qin Xuejun, Miura Shiroh, Gibson Jason R, Wheeler Joshua, Gaasterland Douglas E, Challa Pratap, Herndon Leon W, , Ritch Robert, Moroi Sayoko E, Pasquale Louis R, Girkin Christopher A, Budenz Donald L, Wiggs Janey L, Richards Julia E, Ashley-Koch Allison E, Allingham R Ra |
Genome-wide copy number variation analysis of a Branchio-oto-renal syndrome cohort identifies a recombination hotspot and implicates new candidate genes. Human genetics 2013 Dec 132 (12): 1339-50. Brophy Patrick D, Alasti Fatemeh, Darbro Benjamin W, Clarke Jason, Nishimura Carla, Cobb Bryan, Smith Richard J, Manak J Robe |
Association of open-angle glaucoma loci with incident glaucoma in the Blue Mountains Eye Study. American journal of ophthalmology 2015 Jan 159 (1): 31-6.e1. Burdon Kathryn P, Mitchell Paul, Lee Anne, Healey Paul R, White Andrew J R, Rochtchina Elena, Thomas Peter B M, Wang Jie Jin, Craig Jamie |
Involvement of genetic variants associated with primary open-angle glaucoma in pathogenic mechanisms and family history of glaucoma. American journal of ophthalmology 2015 Mar 159 (3): 437-44.e2. Mabuchi Fumihiko, Sakurada Yoichi, Kashiwagi Kenji, Yamagata Zentaro, Iijima Hiroyuki, Tsukahara Shig |
Association of known common genetic variants with primary open angle, primary angle closure, and pseudoexfoliation glaucoma in Pakistani cohorts. Molecular vision 2014 20 1471-9. Micheal Shazia, Ayub Humaira, Khan Muhammad Imran, Bakker Bjorn, Schoenmaker-Koller Frederieke E, Ali Mahmood, Akhtar Farah, Khan Wajid Ali, Qamar Raheel, den Hollander Anneke |
DNA copy number variants of known glaucoma genes in relation to primary open-angle glaucoma. Investigative ophthalmology & visual science 2014 Dec 55 (12): 8251-8. Liu Yutao, Garrett Melanie E, Yaspan Brian L, Bailey Jessica Cooke, Loomis Stephanie J, Brilliant Murray, Budenz Donald L, Christen William G, Fingert John H, Gaasterland Douglas, Gaasterland Terry, Kang Jae H, Lee Richard K, Lichter Paul, Moroi Sayoko E, Realini Anthony, Richards Julia E, Schuman Joel S, Scott William K, Singh Kuldev, Sit Arthur J, Vollrath Douglas, Weinreb Robert, Wollstein Gadi, Zack Donald J, Zhang Kang, Pericak-Vance Margaret A, Haines Jonathan L, Pasquale Louis R, Wiggs Janey L, Allingham R Rand, Ashley-Koch Allison E, Hauser Michael |
A Genetic Variant in TGFBR3-CDC7 Is Associated with Visual Field Progression in Primary Open-Angle Glaucoma Patients from Singapore. Ophthalmology 2015 Sep . Trikha Sameer, Saffari Ehsan, Nongpiur Monisha, Baskaran Mani, Ho Henrietta, Li Zheng, Tan Peng-Yi, Allen John, Khor Chiea-Chuen, Perera Shamira A, Cheng Ching-Yu, Aung Tin, Vithana Eran |
Genetic association of SNPs near ATOH7, CARD10, CDKN2B, CDC7 and SIX1/SIX6 with the endophenotypes of primary open angle glaucoma in Indian population. PloS one 2015 10 (3): e0119703. Philomenadin Ferdinamarie Sharmila, Asokan Rashima, N Viswanathan, George Ronnie, Lingam Vijaya, Sarangapani Sripri |
Genetic Variants Associated With Different Risks for High Tension Glaucoma and Normal Tension Glaucoma in a Chinese Population. Investigative ophthalmology & visual science 2015 Apr 56 (4): 2595-600. Chen Yuhong, Hughes Guy, Chen Xueli, Qian Shaohong, Cao Wenjun, Wang Li, Wang Min, Sun Xinghu |
Association of three single nucleotide polymorphisms at the SIX1-SIX6 locus with primary open angle glaucoma in the Chinese population. Science China. Life sciences 2016 Jun . Sang Jinghong, Jia Liyun, Zhao Bowen, Wang Huaizhou, Zhang Nihong, Wang Ning |
Association of SIX1/SIX6 locus polymorphisms with regional circumpapillary retinal nerve fibre layer thickness: The Nagahama study. Scientific reports 2017 Jun 7 (1): 4393. Yoshikawa Munemitsu, Yamashiro Kenji, Nakanishi Hideo, Miyata Manabu, Miyake Masahiro, Hosoda Yoshikatsu, Tabara Yasuharu, Matsuda Fumihiko, Yoshimura Nagahisa, |
Association of Glaucoma-Susceptible Genes to Regional Circumpapillary Retinal Nerve Fiber Layer Thickness and Visual Field Defects. Investigative ophthalmology & visual science 2017 05 58 (5): 2510-2519. Yoshikawa Munemitsu, Nakanishi Hideo, Yamashiro Kenji, Miyake Masahiro, Akagi Tadamichi, Gotoh Norimoto, Ikeda Hanako O, Suda Kenji, Yamada Hiroshi, Hasegawa Tomoko, Iida Yuto, Yamada Ryo, Matsuda Fumihiko, Yoshimura Nagahisa, |
Copy number variants in Ebstein anomaly. PloS one 2017 12 (12): e0188168. Giannakou Andreas, Sicko Robert J, Zhang Wei, Romitti Paul, Browne Marilyn L, Caggana Michele, Brody Lawrence C, Jelliffe-Pawlowski Laura, Shaw Gary M, Kay Denise M, Mills James |
Polymorphism rs10483727 in the SIX1/SIX6 Gene Locus Is a Risk Factor for Primary Open Angle Glaucoma in a Saudi Cohort. Genetic testing and molecular biomarkers 2018 Jan 22 (1): 74-78. Kondkar Altaf A, Azad Taif A, Almobarak Faisal A, Kalantan Hatem, Sultan Tahira, Alsabaani Nasser A, Al-Obeidan Saleh A, Abu-Amero Khaled |
STRC Deletion is a Frequent Cause of Slight to Moderate Congenital Hearing Impairment in the Czech Republic. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2017 10 38 (10): e393-e400. Plevova Pavlina, Paprskarova Martina, Tvrda Petra, Turska Petra, Slavkovsky Rastislav, Mrazkova E |
Identification and genotype phenotype correlation of novel mutations in SIX6 gene in primary open angle glaucoma. Ophthalmic genetics 2018 Feb 1-7. Mohanty Kuldeep, Dada Rima, Dada Tan |
Lack of Association of rs1192415 in TGFBR3-CDC7 With Visual Field Progression: A Cohort Study in Chinese Open Angle Glaucoma Patients. Frontiers in genetics 2018 9 488. Chen Yuhong, Qiu Chen, Qian Shaohong, Chen Junyi, Chen Xueli, Wang Li, Sun Xinghu |
Association of Polymorphisms at the SIX1-SIX6 Locus With Primary Open-Angle Glaucoma. Investigative ophthalmology & visual science 2019 Jul 60 (8): 2914-2924. Lu Shi Yao, He Zong Ze, Xu Jia Xin, Yang Chen, Chen Li Jia, Gong |
Genetic analysis of primary open-angle glaucoma-related risk alleles in a Korean population: the GLAU-GENDISK study. The British journal of ophthalmology 2020 Sep . Kim Yong Woo, Lee Yun Hwan, Kim Jin-Soo, Lee Jinho, Kim Yu Jeong, Cheong Hyun Sub, Kim Seok Hwan, Park Ki Ho, Kim Dong Myung, Choi Hyuk Jin, Jeoung Jin Wo |
Age-dependent regional retinal nerve fibre changes in SIX1/SIX6 polymorphism. Scientific reports 2020 Jul 10 (1): 12485. Charng Jason, Simcoe Mark, Sanfilippo Paul G, Allingham R Rand, Hewitt Alex W, Hammond Chris J, Mackey David A, Yazar Seyh |
Analysis of the mutational status of SIX1/2 and microRNA processing genes in paired primary and relapsed Wilms tumors and association with relapse. Cancer gene therapy 2020 12 28 (9): 1016-1024. Ciceri Sara, Montalvão-de-Azevedo Rafaela, Tajbakhsh Amir, Bertolotti Alessia, Spagnuolo Rosalin Dolores, Boschetti Luna, Capasso Maria, D'Angelo Paolo, Serra Annalisa, Diomedi-Camassei Francesca, Meli Mariaclaudia, Nantron Marilina, Quarello Paola, Buccoliero Anna Maria, Tamburini Angela, Ciniselli Chiara Maura, Verderio Paolo, Collini Paola, Radice Paolo, Spreafico Filippo, Perotti Danie |
Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders. Journal of medical genetics 2021 1 59 (2): 165-169. Calpena Eduardo, Wurmser Maud, McGowan Simon J, Atique Rodrigo, Bertola Débora R, Cunningham Michael L, Gustafson Jonas A, Johnson David, Morton Jenny E V, Passos-Bueno Maria Rita, Timberlake Andrew T, Lifton Richard P, Wall Steven A, Twigg Stephen R F, Maire Pascal, Wilkie Andrew O |
The Cochlea in Branchio-Oto-Renal Syndrome: An Objective Method for the Diagnosis of Offset Cochlear Turns. AJNR. American journal of neuroradiology 2022 9 43 (11): 1646-1652. Juliano A F, D'Arco F, Pao J, Picariello S, Clement E, Moonis G, Robson C |
Association of Polymorphisms at the SIX1/SIX6 Locus With Normal Tension Glaucoma in a Korean Population. Journal of glaucoma 2022 Jun . Shin Hye-Young, Lee Young Chun, Lee Mee Y |
Re-Examining the Cochlea in Branchio-Oto-Renal Syndrome: Genotype-Phenotype Correlation. AJNR. American journal of neuroradiology 2022 Feb 43 (2): 309-314. Pao J, D'Arco F, Clement E, Picariello S, Moonis G, Robson C D, Juliano A |
Association of SIX1-SIX6 polymorphisms with peripapillary retinal nerve fibre layer thickness in children. The British journal of ophthalmology 2022 1 . Lu Shi Yao, Zhang Xiu Juan, Wang Yu Meng, Yuan Nan, Kam Ka Wai, Chan Poemen P, Tam Pancy Os, Yip Wilson Wk, Young Alvin L, Tham Clement C, Pang Chi Pui, Yam Jason C, Chen Li J |
Lack of association between SIX1/SIX6 locus polymorphisms and pseudoexfoliation syndrome in a population from the Republic of Korea. Medicine 2023 1 101 (52): e31542. Lee Young Chun, Lee Mee Yon, Shin Hye-You |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
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