(Q33870714)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

24 March 2020

0 references

1 reference

title

Genetic associations for keratoconus: a systematic review and meta-analysis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

24 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

24 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

24 March 2020

Sarah Tsz Ue Ma

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

24 March 2020

Xin Ting Yu

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

24 March 2020

Li Ma

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

24 March 2020

Wai Kit Chu

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

24 March 2020

Yu Meng Wang

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

24 March 2020

Alvin L Young

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

24 March 2020

Chi Pui Pang

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

24 March 2020

Vishal Jhanji

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

24 March 2020

Li Jia Chen

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

24 March 2020

language of work or name

English

0 references

publication date

4 July 2017

1 reference

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24 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

24 March 2020

volume

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

24 March 2020

issue

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

24 March 2020

page(s)

4620

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution 4.0 International

24 March 2020

start time

4 July 2017

1 reference

April 2022 Public Data File from Crossref

copyrighted

0 references

cites work

Changing Indications in Penetrating Keratoplasty: A Systematic Review of 34 Years of Global Reporting

1 reference

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Genetic Associations of Primary Angle-Closure Disease: A Systematic Review and Meta-analysis.

5 July 2018

1 reference

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LOX Mutations Predispose to Thoracic Aortic Aneurysms and Dissections.

5 July 2018

1 reference

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Association of Common Variants in LOX with Keratoconus: A Meta-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=5496893

Lack of association between polymorphisms of the DNA base excision repair genes MUTYH and hOGG1 and keratoconus in a Polish subpopulation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

Screening of the Seed Region of MIR184 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=5496893

Genetic Evidence for Differential Regulation of Corneal Epithelial and Stromal Thickness

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

Redox regulation of FoxO transcription factors

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

Contemporary Treatment Paradigms 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=5496893

The genetic and environmental factors 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=5496893

WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

Validation of rs2956540:G>C and rs3735520:G>A association with keratoconus in a population of European descent

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

Central corneal thickness correlates with oxygen levels in the human anterior chamber angle

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

Does cigarette smoking alter the risk of pterygium? A systematic review and meta-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=5496893

Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

Closing the quality gap: revisiting the state of the science (vol. 3: quality improvement interventions to address health disparities).

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

Association of the hepatocyte growth factor gene with keratoconus in an Australian population

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

Replication and meta-analysis of candidate loci identified variation at RAB3GAP1 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=5496893

ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

Genetic association of COL5A1 variants in keratoconus patients suggests a complex connection between corneal thinning 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=5496893

Investigation of VSX1 sequence variants in South Indian patients with sporadic cases 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=5496893

SirT1 regulation of antioxidant genes is dependent on the formation of a FoxO3a/PGC-1α complex

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

Mutation spectrum in RAB3GAP1, RAB3GAP2, and RAB18 and genotype-phenotype correlations in warburg micro syndrome and Martsolf 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=5496893

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=5496893

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=5496893

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=5496893

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=5496893

Mpdz null allele in an avian model of retinal degeneration and mutations in human leber congenital amaurosis and retinitis pigmentosa

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette 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=5496893

Fad104, a positive regulator of adipogenesis, negatively regulates osteoblast differentiation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

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=5496893

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=5496893

Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

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=5496893

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=5496893

COL5A1 signal peptide mutations interfere with protein secretion and cause classic Ehlers-Danlos 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=5496893

Evaluation of corneal topography with Orbscan II in first-degree relatives of 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=5496893

A mutation in the inner mitochondrial membrane peptidase 2-like gene (Immp2l) affects mitochondrial function and impairs fertility in mice

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

Estimation of the incidence and factors predictive of corneal scarring 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=5496893

MONGOLISM (DOWN'S SYNDROME) 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=5496893

The forkhead transcription factor Foxo1 regulates adipocyte differentiation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

Forkhead transcription factor FOXO3a protects quiescent cells from oxidative stress

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

Quantifying heterogeneity in a meta-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=5496893

Publication and related bias in meta-analysis: power of statistical tests and prevalence in the literature

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

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=5496893

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=5496893

Keratoconus in two pairs of identical twins

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

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=5496893

Meta-analysis in clinical trials

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

5 July 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

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/10.1038%2FS41598-017-04393-2

Topographic evaluation of relatives of patients with keratoconus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

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/10.1038%2FS41598-017-04393-2

Disease severity and family history in keratoconus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

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/10.1038%2FS41598-017-04393-2

Polymorphism of the APEX nuclease 1 gene in keratoconus and Fuchs endothelial corneal dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

Polymorphism Analysis of VSX1 and SOD1 Genes in Greek Patients with Keratoconus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

Mitochondrial DNA copy number, but not haplogroup is associated with keratoconus in Han Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

Evaluation of possible relationship between COL4A4 gene polymorphisms and risk of keratoconus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

Polymorphism analysis of COL4A3 and COL4A4 genes in Greek patients with keratoconus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

Common single nucleotide polymorphisms and keratoconus in the Han Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

VSX1 gene variants are associated with keratoconus in unrelated Korean patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

Evaluating the Association between Keratoconus and Reported Genetic Loci in a Han Chinese Population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

Genetic analysis of RXR alpha developmental function: convergence of RXR and RAR signaling pathways in heart and eye morphogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

Association of hepatocyte growth factor promoter polymorphism with severity of interstitial lung disease in Japanese patients with systemic sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

Genetics and clinical characteristics of keratoconus

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5496893

Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases

29 October 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

7 January 2021

Mutational Analysis of Pre-miR-184 and hsa-mir-568 in Greek Patients With Sporadic Keratoconus

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

7 January 2021

Analysis of the SOD1 Gene in Keratoconus Patients from Saudi Arabia

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

7 January 2021

Relationship between IL1β-511C>T and ILRN VNTR polymorphisms and keratoconus

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FS41598-017-04393-2

7 January 2021

Polymorphism of the LIG3 gene in keratoconus and Fuchs endothelial corneal dystrophy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28676647

12 December 2020

inferred from PubMed ID database lookup

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28676647

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1038/S41598-017-04393-2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

24 March 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json

24 March 2020

PubMed publication ID

28676647

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28676647%20AND%20SRC:MED&resulttype=core&format=json