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Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertension

JCI Insight(2024)10.1172/jci.insight.172152Source: DataRank Database

Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertension is a research paper published in JCI Insight (2024). On theSindex it has a DataRank of 0. It has been cited 4 times.

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Open Access4 citations

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Enrichment:Funding (10 grants)Impact (FWCI 1.02)OA: goldTopics (36)IDs (PubMed, PMC, OpenAlex)Annotations (1)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 (24)

Edmond Wonkam‐Tingang ORCID,Monesha Gupta‐Malhotra ORCID,S. Shahrukh Hashmi ORCID,Yixing Han ORCID,Aarti Jajoo

Live enrichment

PubMed:38716726 PMC:PMC11141928 OpenAlex:https://openalex.org/W4396688595

Baylor College of Medicine

Grant: Precision Medicine/Population Health Initiative

National Heart Lung and Blood Institute

Grant: K23HL089391

National Human Genome Research Institute and National Heart Lung and Blood Institute

Grant: UM1 HG006542

National Institutes of Health

Grant: P30 CA125123

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Grant: P50HD103555

National Human Genome Research Institute

Grant: K08 HG008986

National Institute of General Medical Sciences

Grant: T32GM008307-25

National Human Genome Research Institute

Grant: ZIAHG200412

NHGRI NIH HHS

Grant: U01 HG011758

NIGMS NIH HHS

Grant: T32 GM008307

FWCI

1.02

Citation Percentile

0.8%

Citation Trend

2025

goldLicense: cc-by

journalhttps://doi.org/10.1172/jci.insight.172152

publisherhttps://doi.org/10.1172/jci.insight.172152

publisherhttps://insight.jci.org/articles/view/172152/files/pdf

repositoryhttps://pubmed.ncbi.nlm.nih.gov/38716726

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/11141928

Fields of Study

Hormonal Regulation and HypertensionIon Transport and Channel RegulationRenin-Angiotensin System Studies

MeSH Terms

Exome SequencingEssential HypertensionAdolescentChildChild, PreschoolCytoskeletal ProteinsFemaleHumansInfantInfant, NewbornMaleNerve Tissue ProteinsNuclear ProteinsPedigreeUnited StatesAge of OnsetGenetic Predisposition to DiseaseMutation, MissenserhoA GTP-Binding ProteinYoung AdultExome

Keywords

Exome sequencingMendelian inheritanceExomeGeneticsMedicineMutationBiologyBioinformaticsGenePopulation geneticsHypertensionGenetic variation

Sustainable Development Goals

SDG 0: Zero hunger

Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertension

FAIR Checklist

Authors (24)

Funding (10 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)