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Genetic Diversity in the Suppressyn Gene Sequence: From Polymorphisms to Loss-of-Function Mutations

Biomolecules(2025)10.3390/biom15071051Source: DataRank Database

Genetic Diversity in the Suppressyn Gene Sequence: From Polymorphisms to Loss-of-Function Mutations is a research paper published in Biomolecules (2025). On theSindex it has a DataRank of 0. It has been cited 2 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access2 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (6 grants)Impact (FWCI 2.19)OA: goldTopics (40)IDs (PubMed, PMC, OpenAlex)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (5)

Danny J. Schust ORCID,Takeshi Nagamatsu ORCID,Yoshihiro Jinno,Yoshiki Kudo ORCID,Jun Sugimoto

Live enrichment

PubMed:40723922 PMC:PMC12293451 OpenAlex:https://openalex.org/W4412512631

JSPS KAKENHI

Grant: JP25462567

JSPS KAKENHI

Grant: JP20K09644

JSPS KAKENHI

Grant: JP17K11238

JSPS KAKENHI

Grant: 1R01HD094937

JSPS KAKENHI

Grant: 1R21A1145071

National Institutes of Health

Grant: 5R01HD094937-02

Modeling normal and abnormal trophoblasts

FWCI

2.19

Citation Percentile

0.9%

Citation Trend

2025

2026

goldLicense: cc-by

journalhttps://www.mdpi.com/2218-273X/15/7/1051/pdf?version=1753064231

publisherhttps://www.mdpi.com/2218-273X/15/7/1051/pdf?version=1753064231

publisherhttps://www.mdpi.com/2218-273X/15/7/1051/pdf

journalhttps://doi.org/10.3390/biom15071051

repositoryhttps://pubmed.ncbi.nlm.nih.gov/40723922

Fields of Study

Neonatal Respiratory Health ResearchPregnancy and preeclampsia studiesCongenital Diaphragmatic Hernia Studies0303 health sciences03 medical and health sciences

MeSH Terms

Loss of Function MutationFemaleHumansPlacentaPolymorphism, GeneticPregnancyTrophoblastsGenetic Variation

Keywords

BiologyLoss functionGeneticsGeneCoding regionMutationTrophoblastPathogenesisPlacentaPhenotypeFetusImmunologyPregnancyCell fusionSNPLoss-of-functionEndogenous Retroviruses (Erv)SuppressynPolymorphism, GeneticGenetic VariationMicrobiologyQR1-502ArticleTrophoblastsLoss of Function MutationHumansFemale

Sustainable Development Goals

SDG 0: Good health and well-being