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Maturation Delay of Human GABAergic Neurogenesis in Fragile X Syndrome Pluripotent Stem Cells

Stem Cells Translational Medicine(2022)10.1093/stcltm/szac022Source: DataRank Database

Maturation Delay of Human GABAergic Neurogenesis in Fragile X Syndrome Pluripotent Stem Cells is a research paper published in Stem Cells Translational Medicine (2022). On theSindex it has a DataRank of 0. It has been cited 22 times.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access22 citations

Cite:

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (10 grants)Impact (FWCI 3.04)OA: goldTopics (66)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 (12)

I. V. Sokolova ORCID,Alain Domissy ORCID,Joshua Davis ORCID,Lee Rao,Kagistia Hana Utami ORCID

Live enrichment

PubMed:35556144 PMC:PMC9216490 OpenAlex:https://openalex.org/W4226317345

National Institutes of Health

Grant: R33MH087925

California Institute for Regenerative Medicine

Grant: TR3-05603

California Institute for Regenerative Medicine

Grant: RT3-07655 DISC2-09073

California Institute for Regenerative Medicine

Grant: DISC2P-11595

California Institute for Regenerative Medicine

Grant: TR1-01250

California Institute for Regenerative Medicine

Grant: RT1-01108

California Institute for Regenerative Medicine

Grant: GC1R-06673-A

NIDA NIH HHS

Grant: R01 DA053801

National Institutes of Health

Grant: 5R33MH087925-04

Autism iPSCs for Studying Function and Dysfunction in Human Neural Development

Scripps Research Skaggs Graduate School of Chemical and Biological Sciences

FWCI

3.04

Citation Percentile

0.9%

Citation Trend

2022

2023

2024

2025

2026

goldLicense: cc-by-nc

journalhttps://academic.oup.com/stcltm/article-pdf/11/6/613/44170494/szac022.pdf

publisherhttps://academic.oup.com/stcltm/article-pdf/11/6/613/44170494/szac022.pdf

journalhttps://doi.org/10.1093/stcltm/szac022

repositoryhttps://pubmed.ncbi.nlm.nih.gov/35556144

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/9216490

Fields of Study

Genetics and Neurodevelopmental DisordersCongenital heart defects researchAutism Spectrum Disorder Research03 medical and health sciences0303 health sciencesAutism Spectrum DisorderEpigenesis, GeneticFragile X Messenger Ribonucleoprotein 1Fragile X SyndromeHumansNeurogenesisPluripotent Stem Cells

MeSH Terms

Autism Spectrum DisorderFragile X SyndromeHumansPluripotent Stem CellsEpigenesis, GeneticFragile X Mental Retardation ProteinFragile X Messenger Ribonucleoprotein 1Neurogenesis

Keywords

NeurogenesisFragile X syndromeNeuroscienceFMR1BiologyInduced pluripotent stem cellGABAergicInhibitory postsynaptic potentialGene silencingEmbryonic stem cellGeneticsFragile xGeneAutismHescsGabaergic NeuronsHuman IpscsPluripotent Stem CellsAutism Spectrum DisorderIntellectual and Developmental Disabilities (IDD)Medical BiotechnologyClinical SciencesRegenerative MedicineEpigenesis, GeneticFragile X Mental Retardation ProteinRare DiseasesGeneticStem Cell Research - Nonembryonic - Human6162.1 Biological and endogenous factorsHumansStem Cell Research - Embryonic - HumanAetiologyPediatricFragile X Messenger Ribonucleoprotein 1Stem Cell Research - Induced Pluripotent Stem CellStem Cell Research - Induced Pluripotent Stem Cell - HumanNeurosciences600Stem Cell ResearchBrain DisordersMental HealthNeurologicalStem Cell Research - Nonembryonic - Non-HumanBiochemistry and Cell BiologyEpigenesis

Sustainable Development Goals

SDG 0: Good health and well-being