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Clear Evidence of LAMA5 Gene Biallelic Truncating Variants Causing Infantile Nephrotic Syndrome

Kidney360(2021)10.34067/kid.0004952021Source: DataRank Database

Clear Evidence of LAMA5 Gene Biallelic Truncating Variants Causing Infantile Nephrotic Syndrome is a research paper published in Kidney360 (2021). On theSindex it has a DataRank of 0. It has been cited 16 times.

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Open Access16 citations

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (6 grants)Impact (FWCI 0.81)OA: goldTopics (43)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 (19)

China Nagano ORCID,Kiyotoshi Sekiguchi ORCID,Atsushi Tashiro ORCID,Noriko Sugawara ORCID,Haruhide Sakaguchi ORCID

Live enrichment

PubMed:35419533 PMC:PMC8986055 OpenAlex:https://openalex.org/W3207668578

Grants-in-Aid for Scientific Research (KAKENHI) from the Ministry of Education, Culture, Sports, Science and Technology of Japan

Grant: 18K15713

Collaborative Research Program of Institute for Protein Research, Osaka University

Grant: CR-21-06

National Institutes of Health

Grant: R01DK078314

National Institutes of Health

Grant: R01DK058366

National Institutes of Health

Grant: 5R01DK078314-04

LAMININ BETA2 AND GLOMERULAR FILTRATION

National Institutes of Health

Grant: 2R01DK058366-16

STRUCTURE AND FUNCTION OF CD2AP IN THE KIDNEY

FWCI

0.81

Citation Percentile

0.7%

Citation Trend

2021

2022

2023

2024

2025

2026

gold

journalhttps://doi.org/10.34067/kid.0004952021

publisherhttps://doi.org/10.34067/kid.0004952021

publisherhttps://www.ovid.com/10.34067/KID.0004952021

repositoryhttps://pubmed.ncbi.nlm.nih.gov/35419533

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/8986055

Fields of Study

Renal and related cancersRenal Diseases and Glomerulopathies0301 basic medicine0303 health sciences03 medical and health sciencesChildFemaleGlomerular Basement MembraneHumansLamininMaleMutationNephrotic SyndromeProteinuriaNephrosis, congenital

MeSH Terms

ChildFemaleHumansLamininMaleMutationNephrotic SyndromeProteinuriaGlomerular Basement Membrane

Keywords

Nephrotic syndromeGeneticsGeneMedicineBiologyPediatricsInternal medicinePathologyClinical NephrologySrnsLama5MaleProteinuriaGlomerular Basement MembraneMutationHumansFemaleLamininChild

Sustainable Development Goals

SDG 0: Good health and well-being

Clear Evidence of LAMA5 Gene Biallelic Truncating Variants Causing Infantile Nephrotic Syndrome

FAIR Checklist

Authors (19)

Funding (6 grants)

Impact

Open Access

Topics

Annotations (Europe PMC)