(Q34181407)

31 July 2017

1 reference

title

Genetics of keratoconus: where do we stand? (English)

1 reference

31 July 2017

3

Altaf A Kondkar

1 reference

31 July 2017

Khaled K Abu-Amero

1

1 reference

31 July 2017

Abdulrahman M Al-Muammar

series ordinal

2

1 reference

31 July 2017

publication date

28 August 2014

1 reference

31 July 2017

published in

Journal of Ophthalmology

1 reference

31 July 2017

volume

2014

1 reference

31 July 2017

page(s)

641708

1 reference

Creative Commons Attribution 3.0 Unported

31 July 2017

copyright license

start time

1 January 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

cites work

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5 July 2018

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Replication and meta-analysis of candidate loci identified variation at RAB3GAP1 associated with keratoconus

5 July 2018

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Interleukin 1 beta promoter polymorphism is associated with keratoconus in a Japanese population

5 July 2018

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Genetic association of COL5A1 variants in keratoconus patients suggests a complex connection between corneal thinning and keratoconus

5 July 2018

1 reference

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Investigation of VSX1 sequence variants in South Indian patients with sporadic cases of keratoconus

5 July 2018

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An association between the calpastatin (CAST) gene and keratoconus

5 July 2018

1 reference

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Insights into keratoconus from a genetic perspective

5 July 2018

1 reference

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Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Model animals for the study of oxidative stress from complex II.

5 July 2018

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Variation in the lysyl oxidase (LOX) gene is associated with keratoconus in family-based and case-control studies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

A new mutation in EDA gene in X-linked hypohidrotic ectodermal dysplasia associated with keratoconus

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Mutation analysis of VSX1 and SOD1 in Iranian patients with keratoconus

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

A single-base substitution in the seed region of miR-184 causes EDICT syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Novel mutation and three other sequence variants segregating with phenotype at keratoconus 13q32 susceptibility locus.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Mutation altering the miR-184 seed region causes familial keratoconus with cataract

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Mutational screening of VSX1, SPARC, SOD1, LOX, and TIMP3 in keratoconus.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Mitochondrial complex 1 gene analysis in keratoconus.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Comparative transcriptome and network biology analyses demonstrate antiproliferative and hyperapoptotic phenotypes in human keratoconus corneas

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

High-resolution analysis of DNA copy number alterations in patients with isolated sporadic keratoconus.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Sequence variants in COL4A1 and COL4A2 genes in Ecuadorian families with keratoconus

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Analysis of the VSX1 gene in keratoconus patients from Saudi Arabia.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Familial segregation of a VSX1 mutation adds a new dimension to its role in the causation of keratoconus.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Variable ocular phenotypes of posterior polymorphous corneal dystrophy caused by mutations in the ZEB1 gene

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Unusual presentation of presumed posterior polymorphous dystrophy associated with iris heterochromia, band keratopathy, and keratoconus

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Polymorphisms in COL4A3 and COL4A4 genes associated with keratoconus

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Absence of pathogenic mutations in VSX1 and SOD1 genes in patients with keratoconus.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Evaluation of differentially expressed genes identified in keratoconus

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Collagen cross-linkage: a comprehensive review and directions for future research

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

CRB1 gene mutations are associated with keratoconus in patients with leber congenital amaurosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Marked reduction of alcohol dehydrogenase in keratoconus corneal fibroblasts

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Association of -31T>C and -511 C>T polymorphisms in the interleukin 1 beta (IL1B) promoter in Korean keratoconus patients

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Genetic mapping in human disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Deleterious mutations in the Zinc-Finger 469 gene cause brittle cornea syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Comparative expression analysis of aquaporin-5 (AQP5) in keratoconic and healthy corneas

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Keratoconus is not associated with mutations in COL8A1 and COL8A2.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Longitudinal study of keratoconus progression

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

The Dundee University Scottish Keratoconus study: demographics, corneal signs, associated diseases, and eye rubbing

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Expression of VSX1 in human corneal keratocytes during differentiation into myofibroblasts in response to wound healing.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Two-stage genome-wide linkage scan in keratoconus sib pair families

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

SOD1: a candidate gene for keratoconus

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Incidence and severity of keratoconus in Asir province, Saudi Arabia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Gene expression profile studies of human keratoconus cornea for NEIBank: a novel cornea-expressed gene and the absence of transcripts for aquaporin 5.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

VSX1 mutational analysis in a series of Italian patients affected by keratoconus: detection of a novel mutation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Microarray analysis identified differentially expressed genes in keratocytes from keratoconus patients

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

MicroRNAs: genomics, biogenesis, mechanism, and function

5 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

5 July 2018

https://api.crossref.org/works/10.1155%2F2014%2F641708

VSX1: a gene for posterior polymorphous dystrophy and keratoconus

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Genomewide scans of complex human diseases: true linkage is hard to find

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Does ethnic origin influence the incidence or severity of keratoconus?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Genetic epidemiological study of keratoconus: evidence for major gene determination

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Atopy and keratoconus: a multivariate analysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Baseline findings in the Collaborative Longitudinal Evaluation of Keratoconus (CLEK) Study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Keratoconus and Turner's syndrome.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Epithelial injury induces keratocyte apoptosis: hypothesized role for the interleukin-1 system in the modulation of corneal tissue organization and wound healing

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Leber congenital amaurosis and its association with keratoconus and keratoglobus.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Keratoconus and related noninflammatory corneal thinning disorders

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

A 48-year clinical and epidemiologic study of keratoconus

5 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

5 July 2018

https://api.crossref.org/works/10.1155%2F2014%2F641708

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Corneal ectasias: study cohorts and epidemiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Influence of ethnic origin on the incidence of keratoconus and associated atopic disease in Asians and white patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Epidemiology of keratoconus in an Iranian population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Prevalence and associations of keratoconus in rural maharashtra in central India: the central India eye and medical study

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Keratoconus clinical findings according to different age and gender groups.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Longitudinal study of the normal eyes in unilateral keratoconus patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Familial keratoconus with cataract: linkage to the long arm of chromosome 15 and exclusion of candidate genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Linkage analysis in keratoconus: replication of locus 5q21.2 and identification of other suggestive Loci.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Keratoconus in 18 pairs of twins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Computerized corneal tomography and associated features in a large New Zealand keratoconic population

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Documenting the corneal phenotype associated with the MIR184 c.57C>T mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Mutational analysis of MIR184 in sporadic keratoconus and myopia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Molecular Screening of Keratoconus Susceptibility Sequence Variants in VSX1, TGFBI, DOCK9, STK24, and IPO5 Genes in Polish Patients and Novel TGFBI Variant Identification.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Identity-by-descent approach to gene localisation in eight individuals affected by keratoconus from north-west Tasmania, Australia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Identification of a new locus for isolated familial keratoconus at 2p24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

A locus for autosomal dominant keratoconus maps to human chromosome 3p14-q13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Common single nucleotide polymorphisms and keratoconus in the Han Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Mutational screening of VSX1 in keratoconus patients from the European population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

VSX1 gene variants are associated with keratoconus in unrelated Korean patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Three VSX1 gene mutations, L159M, R166W, and H244R, are not associated with keratoconus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

The point mutation and polymorphism in keratoconus candidate gene TGFBI in Chinese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Accumulation of mitochondrial DNA damage in keratoconus corneas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Increased stress-induced generation of reactive oxygen species and apoptosis in human keratoconus fibroblasts.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Hypersensitive response to oxidative stress in keratoconus corneal fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Keratoplasty in patients with intellectual disability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Identification of differentially expressed genes in keratoconus epithelium analyzed on microarrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

A Prospective Study of Filaggrin Null Mutations in Keratoconus Patients with or without Atopic Disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2014%2F641708

Association of Lysyl oxidase (LOX) Polymorphisms with the Risk of Keratoconus in an Iranian Population.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Genetics and clinical characteristics of keratoconus

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

BIGH3 mutation spectrum in corneal dystrophies

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Keratoconus associated with chromosome 13 ring abnormality

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4164130

Mitochondrial sequence changes in keratoconus patients

28 October 2018

1 reference

12 December 2020

Brittle cornea syndrome and its delineation from the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VI): report on 23 patients and review of the literature

1 reference

12 December 2020

Keratoconus associated with other corneal dystrophies

1 reference

12 December 2020

Keratoconus in Costello syndrome

1 reference

12 December 2020

Congenital contractural arachnodactyly, keratoconus, and probable Marfan syndrome in the same pedigree

1 reference

12 December 2020

A locus for autosomal dominant keratoconus: linkage to 16q22.3-q23.1 in Finnish families

1 reference

12 December 2020

Genomewide linkage scan in a multigeneration Caucasian pedigree identifies a novel locus for keratoconus on chromosome 5q14.3-q21.1.

1 reference

12 December 2020

Keratoconus associated with a chromosome 7,11 translocation

1 reference

12 December 2020

Computerized corneal topography in a paediatric population with Down syndrome

1 reference

12 December 2020

A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13

1 reference

12 December 2020

Prevalence and associated factors of keratoconus in Jerusalem: a cross-sectional study

1 reference

12 December 2020

Segregation analysis suggests that keratoconus is a complex non-mendelian disease

1 reference

12 December 2020

Topographic indications of emerging keratoconus in teenage New Zealanders

1 reference

12 December 2020

The genetics of keratoconus

1 reference

12 December 2020

Keratoconus and Fuchs' corneal endothelial dystrophy in a patient and her family

1 reference

12 December 2020

Is consanguinity a risk factor for keratoconus?

1 reference

12 December 2020

Fine mapping of the keratoconus with cataract locus on chromosome 15q and candidate gene analysis

1 reference

12 December 2020

Analysis of the SOD1 Gene in Keratoconus Patients from Saudi Arabia

1 reference

12 December 2020

A new case of keratoconus associated with Williams-Beuren syndrome

1 reference

12 December 2020

Evaluating the Association Between Keratoconus and the Corneal Thickness Genes in an Independent Australian Population

1 reference

12 December 2020

Ultrastructure of the cornea epithelium in keratoconus

1 reference

12 December 2020

Changes in lysyl oxidase (LOX) distribution and its decreased activity in keratoconus corneas

1 reference

12 December 2020

Identifiers

DOI

10.1155/2014/641708

1 reference

31 July 2017

1 reference

31 July 2017

1 reference