Keratoconus
What's New
Last Posted: May 07, 2024
- Targeted next-generation sequencing analysis in Italian patients with keratoconus.
Marco Lombardo, et al. Eye (London, England) 2024 0 - Genetic variants in the FOXO1 and ZNF469 genes are associated with keratoconus in Sweden: a case-control study.
Wolf Wonneberger, et al. BMC ophthalmology 2024 0 (1) 36 - Association between Polymorphism rs61876744 in PNPLA2 Gene and Keratoconus in a Saudi Cohort.
Altaf A Kondkar, et al. Genes 2023 0 (12) - Impact of a 50bp insertion/deletion polymorphism of the superoxide dismutase-1 on oxidative stress status and risk of keratoconus.
Mohammad-Reza Sedaghat, et al. Experimental eye research 2023 0 109742 - Identification of genetic variants in two families with Keratoconus.
Qinghong Lin, et al. BMC medical genomics 2023 0 (1) 299 - Mitochondrial DNA heteroplasmy analysis in keratoconus patients from China.
Liyan Xu, et al. Frontiers in genetics 2023 0 1251951 - Much higher prevalence of keratoconus than announced results of the Gutenberg Health Study (GHS).
Susanne Marx-Gross, et al. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 2023 0 1-7 - Natural history and predictors for progression in pediatric keratoconus.
Antunes-Foschini Rosalia, et al. Scientific reports 2023 0 (1) 4940 - Association of 2 Lysyl Oxidase Gene Single Nucleotide Polymorphisms with Keratoconus: A Nationwide Registration Study.
Niazi Sana, et al. Ophthalmology science 2023 0 (2) 100247 - TSC1 Mutations in Keratoconus Patients With or Without Tuberous Sclerosis.
Bykhovskaya Yelena, et al. Investigative ophthalmology & visual science 2017 0 (14) 6462-6469 - Analysis of VSX1 Variations in Brazilian Subjects with Keratoconus.
da Silva Dulceria Costa, et al. Journal of ophthalmic & vision research 2018 0 (3) 266-273 - [A novel VSX1 gene mutation identified in a sporadic keratoconus patient from China].
Guan T, et al. [Zhonghua yan ke za zhi] Chinese journal of ophthalmology 2018 0 (3) 212-217 - Role of extracellular matrix remodelling gene SNPs in keratoconus.
Abdullah O A, et al. British journal of biomedical science 2019 0 (1) 13-18 - Corneal elevation changes after forced eyelid closure in healthy participants and in patients with keratoconus.
Atalay Eray, et al. Clinical & experimental optometry 2019 0 (6) 590-595 - Corneal Perforation After Corneal Cross-Linking in Keratoconus Associated With Potentially Pathogenic ZNF469 Mutations.
Zhang Wenlin, et al. Cornea 2019 0 (8) 1033-1039 - Anterior segment parameters in Behçet's patients with ocular involvement.
Ozbek-Uzman Selma, et al. International ophthalmology 2020 0 (6) 1387-1395 - Absence of significant genetic alterations in the VSX1, SOD1, TIMP3, and LOX genes in Brazilian patients with Keratoconus.
Lopes Alessandro Garcia, et al. Ophthalmic genetics 2021 0 (1) 73-79 - Understanding the role of corneal biomechanics-associated genetic variants by bioinformatic analyses.
Sun Xiao, et al. International ophthalmology 2021 0 (3) 981-988 - IL1A and IL1B gene polymorphisms and keratoconus susceptibility: evidence from an updated meta-analysis.
Harati-Sadegh Mahdiyeh, et al. Ophthalmic genetics 2021 0 (5) 503-513 - USH2A gene variants cause Keratoconus and Usher syndrome phenotypes in Pakistani families.
Ahmed Asif Naveed, et al. BMC ophthalmology 2021 0 (1) 191 - Whole mitochondrial genome analysis in Chinese patients with keratoconus.
Xu Liyan, et al. Molecular vision 2021 0 270-282 - Resequencing of candidate genes for Keratoconus reveals a role for Ehlers-Danlos Syndrome genes.
Fransen Erik, et al. European journal of human genetics : EJHG 2021 0 (12) 1745-1755 - OP-3?Personalised model to predict keratoconus progression from demographic, topographic and genetic data.
Li Olivia, et al. BMJ open ophthalmology 2022 0 (Suppl 1) A1-A2 - Protective and pathogenic role of collagen subtypes genes COL4A3 and COL4A4 polymorphisms in the onset of keratoconus in South-Asian Pakistani cohort.
Khashim Alswailmi Farhan, et al. Saudi journal of biological sciences 2022 0 (1) 103503 - A comprehensive molecular genetic analysis of keratoconus patients from assam, a northeastern state of India.
Chakravarty Mrigyanka, et al. European journal of ophthalmology 2022 0 (3) 1361-1369 - Evaluating the association between MPDZ-NF1B rs1324183 and keratoconus in an independent northwestern Chinese population.
Yuan Shiqin, et al. BMC ophthalmology 2022 0 (1) 129 - Non-genetic risk factors for keratoconus.
Song Minji, et al. Clinical & experimental optometry 2022 0 1-11 - Personalized Model to Predict Keratoconus Progression From Demographic, Topographic, and Genetic Data.
Maile Howard P, et al. American journal of ophthalmology 2022 0 321-329 - A novel variant in TGFBI causes keratoconus in a two-generation Chinese family.
Lin Qinghong, et al. Ophthalmic genetics 2021 0 (2) 159-163 - Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis of rare ZNF469 variants in familial keratoconus.
Davidson Alice E, et al. Investigative ophthalmology & visual science 2015 0 (1) 578-86
More
About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Page last updated:May 18, 2024
- Content source: