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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 10 (of 10 Records)

Query Trace: Disease and ELOVL4[original query]
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
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
[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
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