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Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis

American Journal of Respiratory and Critical Care Medicine(2024)10.1164/rccm.202308-1370ocSource: DataRank Database

Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis is a research paper published in American Journal of Respiratory and Critical Care Medicine (2024). On theSindex it has a DataRank of 0.775. It has been cited 15 times, with 15 citing works in its 1-hop citation network.

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0.775DataRank · unranked

Scored on demand from live citation data

Open Access15 citations · 15 citing works in its network

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Linked data & code

Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis · University of Muenster, Institutional Repository MIAMI

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (11 grants)OA: hybridTopics (46)Linked Datasets (1)DataCite Reuse (1)IDs (PubMed)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (2/2)

Has DOI
Indexed in repositories

Accessible (1/2)

Open Access

Interoperable (2/2)

DataCite relations
Linked datasets

Reusable (0/3)

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DataRank Breakdown

Base Score 54%Citation Network 46%

Base Score Contribution

0.416

From this paper's citation signal

Citation Network Contribution

0.359

From 11 citing papers with measurable signal

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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 15 citers.

Severe bronchiectasis and chronic rhinosinusitis due to homozygous WFDC2 Variants: The first three cases reported from Japan
Respiratory Medicine Case Reports20252 citations16 referencesContributes 0.069
The founder missense mutation of WFDC2 in Koreans leads to severe respiratory distress accompanied by bronchiectasis and rhinosinusitis
medRxiv20242 citations19 referencesContributes 0.058
Severe Bronchiectasis and Chronic Rhinosinusitis Due to Homozygous WFDC2 Variants: The First Three Cases Reported from Japan
Research Square20251 citations13 referencesContributes 0.053
Diagnostic utility of standardized assessment of ciliary ultrastructure by transmission electron microscopy in primary ciliary dyskinesia: a Japanese perspective
Respiratory Investigation20252 citations26 referencesContributes 0.042
Human epididymis protein 4-annexin II binding promotes aberrant epithelial-fibroblast crosstalk in pulmonary fibrosis
Communications Biology20256 citations47 referencesContributes 0.041

Authors (41)

Lawrence E. Ostrowski ORCID,Tabea Nöthe-Menchen ORCID,Johanna Raidt ORCID,Andre Schramm,Heike Olbrich ORCID

Live enrichment

PubMed:19022398

French National Research Agency (ANR)

Grant: ANR-21-ESRE-0052

French National Research Agency (ANR)

Grant: ANR-19-P3IA-0002

National Institutes of Health

Grant: 5UM1HG006504-07

Yale Center for Mendelian Genomics

National Institutes of Health

Grant: 5U54HL096458-14

Genetic Disorder of Mucocilary Clearance

National Institutes of Health

Grant: 3P30DK065988-10S1

Correction Core

French National Research Agency (ANR)

Grant: ANR-19-CE14-0027

Single-cell Analysis of Human Airway Regeneration and Remodeling in Asthma

National Institutes of Health

Grant: 5U2CTR002818-03

Data Management and Coordinating Center: Rare Diseases Clinical Research Network

National Institutes of Health

Grant: 5R01HL071798-04

Pathogenesis of PCD Lung Disease

National Institutes of Health

Grant: 1R01HL117836-01

Functional Studies of Novel Genes Mutated in Primary Ciliary Dyskinesia

Wellcome Trust

Grant: 210585

Impact of missense mutations in recessive Mendelian disease: insight from ciliopathies

European Commission

Grant: 305404

Better Experimental Screening and Treatment for Primary Ciliary Dyskinesia

hybridLicense: cc-by

publisherhttps://doi.org/10.1164/rccm.202308-1370oc

publisherhttps://www.atsjournals.org/doi/pdf/10.1164/rccm.202308-1370OC

repositoryhttps://research.vumc.nl/en/publications/e8bb126c-2a3d-45e4-8f1e-7cfc221e3b08

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC11197063/pdf/rccm.202308-1370OC.pdf

repositoryhttps://repositorium.uni-muenster.de/transfer/miami/71cc78db-826b-46fc-a58f-b798061b5f3a

Fields of Study

03 medical and health sciences0303 health sciences

Keywords

AdultMalePulmonary and Respiratory MedicineTherapeutic Advances in Cystic Fibrosis ResearchSanger sequencingAdolescentClinical Management of Tracheal and Airway Disorders610 Medicine and healthImmunology610chronic lung diseaseGeneCystic fibrosis576Young AdultNasal PolypsWAP Four-Disulfide Core Domain Protein 2Primary ciliary dyskinesiaPseudomonasPseudomonas; infertility; chronic lung diseaseHealth SciencesPathologyGeneticsHumansMucociliary clearanceChildNeonatal Lung Development and Respiratory MorbiditySalivaLungBiologyInternal medicineinfo:eu-repo/classification/ddc/610Bronchopulmonary Dysplasiaddc:610FOS: Clinical medicineOriginal ArticlesMiddle AgedBronchiectasisFOS: Biological sciencesMedicine and healthMutationMedicineFemaleinfertility

Sustainable Development Goals

SDG 3: 3. Good health

Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis

10.17879/66928491944University of Muenster, Institutional Repository MIAMI

Related Papers (1)

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N/A

1.4DataRank · unranked

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co-cited

10.1016/j.exer.2020.108206