Paper · 37077496

Identification of a novel mutation in the FGF10 gene in a Chinese family with obvious congenital lacrimal duct dysplasia in lacrimo-auriculo-dento-digital syndrome.

Zhang HY and 10 others. Int J Ophthalmol, 2023. Cited by 3 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Identification of a novel mutation in the FGF10 gene in a Chinese family with obvious congenital lacrimal duct dysplasia in lacrimo-auriculo-dento-digital syndrome. Papers, record 37077496. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/37077496

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title: Identification of a novel mutation in the FGF10 gene in a Chinese family with obvious congenital lacrimal duct dysplasia in lacrimo-auriculo-dento-digital syndrome.; PubMed
Journal: Int J Ophthalmol; PubMed
Year: 2023; PubMed
Publication types: Journal Article; PubMed
PubMed: https://pubmed.ncbi.nlm.nih.gov/37077496/; PubMed
DOI: https://doi.org/10.18240/ijo.2023.04.02; PubMed
PMC: https://pmc.ncbi.nlm.nih.gov/articles/PMC10089906/; PubMed
The journal: https://conductscience.org/library/journal-index/101553860; PubMed
Citations, by iCite: 3; iCite
Relative citation ratio, by iCite: 0.65; iCite
Revised in PubMed: 2023-04-21; PubMed

Authors11

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

Order	Author	Forename
1	Zhang HY	Hong-Yang
2	Zhang CY	Chun-Yan
3	Wang F	Fei
4	Tao H	Hai
5	Tian YP	Ya-Ping
6	Zhou XB	Xi-Bin
7	Bai F	Fang
8	Wang P	Peng
9	Cui JY	Jia-Yi
10	Zhang MJ	Min-Jie

1 to 10 of 11Source PubMed

See all 11 authors

Topics0

NLM's MeSH indexing of the paper, its major topics first.

None in this release.

Grants0

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

None in this release.

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References25

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

Order	PMID	Title	Journal	Year	In Papers	Source
1	32,360,081	[Congenital nasolacrymal duct obstruction: pulled monocanalicular intubation (Monoka) versus pushed monocanalicular intubation (Masterka)].	J Fr Ophtalmol	2020	https://conductscience.org/library/papers/32360081	PubMed
2	31,102,704	Punctal agenesis: Embryology, presentation, management modalities and outcomes.	Ann Anat	2019	https://conductscience.org/library/papers/31102704	PubMed
3	29,138,288	Fibroblast growth factors: key players in regeneration and tissue repair.	Development	2017	https://conductscience.org/library/papers/29138288	PubMed
4	34,743,465	[Chinese expert consensus on diagnosis and treatment of congenital nasolacrimal duct obstruction (2021)].	Zhonghua Yan Ke Za Zhi	2021	https://conductscience.org/library/papers/34743465	PubMed
5	32,715,658	Lacrimo-auriculo-dento-digital syndrome: A novel mutation in a Korean family and review of literature.	Mol Genet Genomic Med	2020	https://conductscience.org/library/papers/32715658	PubMed
6	20,164,922	Variability in gene expression underlies incomplete penetrance.	Nature	2010	https://conductscience.org/library/papers/20164922	PubMed
7	31,445,546	Newborn With a Swelling Cherry Eye.	Ann Emerg Med	2019	https://conductscience.org/library/papers/31445546	PubMed
8	16,501,574	Mutations in different components of FGF signaling in LADD syndrome.	Nat Genet	2006	https://conductscience.org/library/papers/16501574	PubMed
9	19,755,711	Differential interactions of FGFs with heparan sulfate control gradient formation and branching morphogenesis.	Sci Signal	2009	https://conductscience.org/library/papers/19755711	PubMed
10	33,449,148	Cell signaling regulation in salivary gland development.	Cell Mol Life Sci	2021	https://conductscience.org/library/papers/33449148	PubMed

1 to 10 of 25

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Cited by2

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 3 citations.

PMID	Title	Journal	Year	In Papers	Source
40,103,946	Bibliometric and visualized analysis of research hotpots and future prospects in lacrimal duct obstruction disease (1900 to 2024).	Int J Ophthalmol	2025	https://conductscience.org/library/papers/40103946	PubMed
38,909,058	Deciphering the etiology of undiagnosed ocular anomalies along with systemic alterations in pediatric patients through whole exome sequencing.	Sci Rep	2024	https://conductscience.org/library/papers/38909058	PubMed

Genes1

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

Gene	NCBI Gene ID	Linked by	In Genes
FGF10	2,255	PubTator's text mining	https://conductscience.org/library/genes/2255

Source NCBI Gene

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed: 2026-11-06; PubMed
iCite: 2026-11-05; iCite
PMC's ID file: 2026-11-05; PMC's ID file
NIH RePORTER's grant and paper links: 2026-11-01; NIH RePORTER's grant and paper links
Trials: 2026-11-12
Gene search: 2026-11-11
Pipelines: 2026-09-18

Sources 11

ChEMBL, through Open TargetsCC BY-SA 3.0
ClinicalTrials.govNo license stated
HGNCCC0
iCiteCC BY 4.0
NCBI GenePublic domain (US government)
NIH RePORTER's grant and paper linksPublic domain
Open TargetsCC0 1.0
PMC's ID filePublic domain (US government)
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0

Each source's terms

ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
ClinicalTrials.govnone stated
HGNCCC0: https://www.genenames.org/about/license/
iCiteCC BY 4.0
NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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