Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: ELOVL4[original query] |
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Evaluation of the ELOVL4 gene in patients with age-related macular degeneration. Ophthalmic genetics 2001 Dec 22 (4): 233-9. Ayyagari R, Zhang K, Hutchinson A, Yu Z, Swaroop A, Kakuk L E, Seddon J M, Bernstein P S, Lewis R A, Tammur J, Yang Z, Li Y, Zhang H, Yashar B M, Liu J, Petrukhin K, Sieving P A, Allikmets |
Candidate gene analysis suggests a role for fatty acid biosynthesis and regulation of the complement system in the etiology of age-related maculopathy. Human molecular genetics 2005 Jul 14 (14): 1991-2002. Conley Yvette P, Thalamuthu Anbupalam, Jakobsdottir Johanna, Weeks Daniel E, Mah Tammy, Ferrell Robert E, Gorin Michael |
CFH, ELOVL4, PLEKHA1 and LOC387715 genes and susceptibility to age-related maculopathy: AREDS and CHS cohorts and meta-analyses. Human molecular genetics 2006 Nov 15 (21): 3206-18. Conley Yvette P, Jakobsdottir Johanna, Mah Tammy, Weeks Daniel E, Klein Ronald, Kuller Lewis, Ferrell Robert E, Gorin Michael |
Analysis of variants in the complement factor H, the elongation of very long chain fatty acids-like 4 and the hemicentin 1 genes of age-related macular degeneration in the Finnish population. Molecular vision 2006 12 (): 796-801. Seitsonen Sanna, Lemmelä Susanna, Holopainen Juha, Tommila Petri, Ranta Päivi, Kotamies Antti, Moilanen Jukka, Palosaari Tapani, Kaarniranta Kai, Meri Seppo, Immonen Ilkka, Järvelä Ir |
Cigarette smoking, CFH, APOE, ELOVL4, and risk of neovascular age-related macular degeneration. Archives of ophthalmology (Chicago, Ill. : 1960) 2007 Jan 125 (1): 49-54. DeAngelis Margaret M, Ji Fei, Kim Ivana K, Adams Scott, Capone Antonio, Ott Jurg, Miller Joan W, Dryja Thaddeus |
[Association of M299V variant in ELOVL4 gene with exudative age-related macular degeneration in a Chinese population]. [Zhonghua yan ke za zhi] Chinese journal of ophthalmology 2010 Feb 46 (2): 125-8. Gu Hong, Cui Lei, Liu Ning- |
Genetic variation in fatty acid elongases is not associated with intermediate cardiovascular phenotypes or myocardial infarction. European journal of clinical nutrition 2012 Mar 66 (3): 353-9. Aslibekyan S, Jensen M K, Campos H, Linkletter C D, Loucks E B, Ordovas J M, Deka R, Rimm E B, Baylin |
Molecular diagnostic testing by eyeGENE: analysis of patients with hereditary retinal dystrophy phenotypes involving central vision loss. Investigative ophthalmology & visual science 2014 Sep 55 (9): 5510-21. Alapati Akhila, Goetz Kerry, Suk John, Navani Mili, Al-Tarouti Amani, Jayasundera Thiran, Tumminia Santa J, Lee Pauline, Ayyagari Rad |
[Molecular genetic diagnosis of Stargardt disease]. Vestnik oftalmologii 2017 133 (4): 4-11. Sheremet N L, Zhorzholadze N V, Ronzina I A, Grushke I G, Kurbatov S A, Chukhrova A L, Loginova A N, Shcherbakova P O, Tanas A S, Polyakov A V, Strel'nikov V |
Clinical and Genetic Characteristics Analysis of Korean Patients with Stargardt Disease Using Targeted Exome Sequencing. Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde 2018 Jul 1-11. Sung Youngje, Choi Seung Woo, Shim Sung Han, Song Won Kyu |
Prevalence and clinicoradiological features of spinocerebellar ataxia type 34 in a Japanese ataxia cohort. Parkinsonism & related disorders 2019 5 65 238-242. Ozaki Kokoro, Ansai Ayaka, Nobuhara Kouji, Araki Toshihiko, Kubodera Takayuki, Ishii Takashi, Higashi Miwa, Sato Nozomu, Soga Kazumasa, Mizusawa Hidehiro, Ishikawa Kinya, Yokota Takano |
Novel variants associated with Stargardt disease in Chinese patients. Gene 2020 6 754 144890. Hu Fangyuan, Gao Fengjuan, Li Jiankang, Xu Ping, Wang Dandan, Chen Fang, Zhang Shenghai, Wu Jiho |
Absence of Genotype/Phenotype Correlations Requires Molecular Diagnostic to Ascertain Stargardt and Stargardt-Like Swiss Patients. Genes 2021 6 12 (6): . Buhler Virginie M M, Berger Lieselotte, Schaller André, Zinkernagel Martin S, Wolf Sebastian, Escher Pasc |
Targeted next-generation sequencing identifies ABCA4 mutations in Chinese families with childhood-onset and adult-onset Stargardt disease. Bioscience reports 2021 5 41 (6): . Qu Ling-Hui, Jin Xin, Zeng Chao, Zhou Nian-Gou, Liu Yan-Hong, Lin |
Clinical and Genetic Spectrum of Stargardt Disease in Argentinean Patients. Frontiers in genetics 2021 4 12 646058. Mena Marcela D, Moresco Angélica A, Vidal Sofía H, Aguilar-Cortes Diana, Obregon María G, Fandiño Adriana C, Sendoya Juan M, Llera Andrea S, Podhajcer Osvaldo |
Genome-wide association study of brain arteriolosclerosis. Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 2022 Feb 271678X211066299. Shade Lincoln Mp, Katsumata Yuriko, Hohman Timothy J, Nho Kwangsik, Saykin Andrew J, Mukherjee Shubhabrata, Boehme Kevin L, Kauwe John Sk, Farrer Lindsay A, Schellenberg Gerard D, Haines Jonathan L, Mayeux Richard P, Schneider Julie A, Nelson Peter T, Fardo David |
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- Page last updated:Apr 22, 2024
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