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Systems Analysis Implicates WAVE2 Complex in the Pathogenesis of Developmental Left-Sided Obstructive Heart Defects

JACC Basic to Translational Science(2020)10.1016/j.jacbts.2020.01.012Source: DataRank Database

Systems Analysis Implicates WAVE2 Complex in the Pathogenesis of Developmental Left-Sided Obstructive Heart Defects is a research paper published in JACC Basic to Translational Science (2020). On theSindex it has a DataRank of 1.1. It has been cited 28 times, with 26 citing works in its 1-hop citation network.

N/A

1.1DataRank · unranked

Scored on demand from live citation data

Open Access28 citations · 26 citing works in its network

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Linked data & code

dbgap

DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?

›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (35 grants)Impact (FWCI 0.89)OA: goldTopics (69)IDs (PubMed, PMC, OpenAlex)Annotations (1)SDGs (2)

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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DataRank Breakdown

Base Score 47%Citation Network 53%

Base Score Contribution

0.505

From this paper's citation signal

Citation Network Contribution

0.576

From 19 citing papers with measurable signal

Learn more about DataRank methodology →

Top 5 citers driving the network score

Ranked by each citer's contribution to N(p) — log1p(C_q) divided by its reference count — out of 26 citers.

Discovering biomarkers associated and predicting cardiovascular disease with high accuracy using a novel nexus of machine learning techniques for precision medicine
Scientific Reports2024834 citations63 referencesContributes 0.107
A de novo heterozygous POU3F3 genotype for the p.(Q214*) variant in a fetus with transient isolated bilateral mild ventriculomegaly: a case report and review of the literature
Frontiers in Pediatrics20235 citations20 referencesContributes 0.090
Complex congenital cardiovascular anomaly in a patient with AGO1‐associated disorder
American Journal of Medical Genetics Part A20225 citations25 referencesContributes 0.072
The cellular architecture and molecular determinants of the zebrafish fusogenic synapse
Developmental Cell202232 citations65 referencesContributes 0.054
A novel homozygous splice donor variant in the LRPPRC gene causing Leigh syndrome with epilepsy, a French-Canadian disorder in a Saudi family: case report
Frontiers in Pediatrics20234 citations31 referencesContributes 0.052

Authors (26)

Andrew D. Rouillard ORCID,Nicolas Fernandez ORCID,Zichen Wang ORCID,Alexander Lachmann ORCID,Sunita S. Shankaran

Live enrichment

PubMed:32368696 PMC:PMC7188873 OpenAlex:https://openalex.org/W3015764232

National Institutes of Health

Grant: 5T32HL007915

National Institutes of Health

Grant: 5U54HG006504

National Institutes of Health

Grant: U01-HL098147

National Institutes of Health

Grant: U01-HL098160

National Institutes of Health

Grant: U01-HL098188

National Institutes of Health

Grant: U01-HL098123

National Institutes of Health

Grant: U01-HL098162

National Institutes of Health

Grant: U01-HL098163

National Center for Advancing Translational Sciences

Grant: U01 HL098153

NIH HHS

Grant: S10 OD018521

NHLBI NIH HHS

Grant: U01 HL098147

NHLBI NIH HHS

Grant: U01 HL098160

NCI NIH HHS

Grant: U24 CA224260

NHLBI NIH HHS

Grant: U01 HL098163

NHLBI NIH HHS

Grant: T32 HL007915

NHLBI NIH HHS

Grant: U01 HL098188

NHLBI NIH HHS

Grant: UM1 HL098123

NHLBI NIH HHS

Grant: UM1 HL098160

NHGRI NIH HHS

Grant: U54 HG006504

NHLBI NIH HHS

Grant: U54 HL127624

NHLBI NIH HHS

Grant: U01 HL098162

NCATS NIH HHS

Grant: UL1 TR001863

NHLBI NIH HHS

Grant: U01 HL098123

National Institutes of Health

Grant: 5U01HL098153-02

The Genetic Basis of Conotruncal Defects

National Institutes of Health

Grant: 2T32HL007915-11

Training in Molecular Therapeutics for Pediatric Cardiology

National Institutes of Health

Grant: 1U54HG006504-01

Yale Center for Mendelian Disorders

National Institutes of Health

Grant: 5U01HL098162-05

Genetic determinants of human heterotaxy and aortic arch malformation

National Institutes of Health

Grant: 5U01HL098163-06

Molecular approaches to gene identification in congenital heart disease

National Institutes of Health

Grant: 5U01HL098188-03

NHLBI Pediatric Translational Consortium Administrative Coordinating Center

National Institutes of Health

Grant: 5U01HL098123-02

Genomic studies of secundum atrial septal defects

National Institutes of Health

Grant: 5U01HL098160-06

Genome-wide Analysis of Cardiac Development in Zebrafish

National Institutes of Health

Grant: 1U01HL098147-01

Copy Number Variants for Discovery of Congenital Heart Genes

National Institutes of Health

Simons Foundation

Howard Hughes Medical Institute

FWCI

0.89

Citation Percentile

0.7%

Citation Trend

2020

2021

2022

2023

2024

2025

2026

goldLicense: cc-by-nc-nd

journalhttps://ars.els-cdn.com/content/image/1-s2.0-S2452302X20300590-fx1_lrg.jpg

publisherhttps://ars.els-cdn.com/content/image/1-s2.0-S2452302X20300590-fx1_lrg.jpg

publisherhttps://api.elsevier.com/content/article/PII:S2452302X20300590?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S2452302X20300590?httpAccept=text/plain

journalhttps://doi.org/10.1016/j.jacbts.2020.01.012

Fields of Study

Congenital heart defects researchCongenital Heart Disease StudiesCardiomyopathy and Myosin Studies0301 basic medicine03 medical and health sciences0303 health sciences

Keywords

ZebrafishPathogenesisBiologyProbandSmall GTPaseCRISPRGeneticsGeneSignal transductionDiseaseBioinformaticsCell biologyMedicinePathologyMutationImmunologyCongenital heart diseasesystems biologyTranslational GenomicsHlhs, Hypoplastic Left Heart SyndromeChd, Congenital Heart DiseasePpi, Protein-protein InteractionCrispr, Clustered Regularly Interspaced Short Palindromic RepeatsLvoto, Left Ventricular Outflow Tract ObstructionCorum, Comprehensive Resource Of Mammalian Protein ComplexesGobp, Gene Ontology Biological ProcessesHhe, High Heart ExpressionHtx, HeterotaxyMgi, Mouse Genome InformaticsPcgc, Pediatric Cardiac Genomics ConsortiumCtd, Conotruncal DefectPPIClinical SciencesHTX610Cardiorespiratory Medicine and HaematologyCardiovascularGOBPMouse Genome Informaticsprotein-protein interactionPRECLINICAL RESEARCHLVOTOCardiovascular Medicine and HaematologyCORUMleft ventricular outflow tract obstruction2.1 Biological and endogenous factorsAetiologyMGIBiomedical and Clinical Scienceshypoplastic left heart syndromeHLHSheterotaxyCTDPCGCPediatric Cardiac Genomics ConsortiumHeart DiseaseCHDHHEComprehensive Resource of Mammalian Protein Complexesconotruncal defecthigh heart expressionGene Ontology biological processesclustered regularly interspaced short palindromic repeats

Sustainable Development Goals

SDG 3: 3. Good healthSDG 0: Good health and well-being

Related Papers (2)

GATA6 mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm

N/A

1.4DataRank · unranked

eLife(2020)

co-cited

10.7554/elife.53278

Transcriptome variation in human tissues revealed by long-read sequencing

N/A

6.6DataRank · unranked

Nature(2022)

co-cited

10.1038/s41586-022-05035-y

Systems Analysis Implicates WAVE2 Complex in the Pathogenesis of Developmental Left-Sided Obstructive Heart Defects

FAIR Checklist

DataRank Breakdown

Top 5 citers driving the network score

Authors (26)

Funding (35 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)

Related Papers (2)