# Hitoshi Suzuki

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/hitoshi-suzuki/

## Facts

| Field | Value |
| --- | --- |
| Citations | 12,300 |
| Field | Renal Diseases and Glomerulopathies |
| h-index | 58 |
| i10-index | 177 |
| Last Known Institution | Juntendo University Urayasu Hospital |
| OpenAlex ID | https://openalex.org/A5018314623 |
| ORCID iD | 0000-0002-1901-2111 |
| Works | 502 |

## Researcher papers

- [The Pathophysiology of IgA Nephropathy](https://scholariq.org/papers/the-pathophysiology-of-iga-nephropathy/)
- [Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens](https://scholariq.org/papers/discovery-of-new-risk-loci-for-iga-nephropathy-implicates-genes-involved-in/)
- [Aberrantly glycosylated IgA1 in IgA nephropathy patients is recognized by IgG antibodies with restricted heterogeneity](https://scholariq.org/papers/aberrantly-glycosylated-iga1-in-iga-nephropathy-patients-is-recognized-by-igg/)
- [Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis](https://scholariq.org/papers/geographic-differences-in-genetic-susceptibility-to-iga-nephropathy-gwas/)
- [New Inuyama classification; new criteria for histological assessment of chronic hepatitis](https://scholariq.org/papers/new-inuyama-classification-new-criteria-for-histological-assessment-of-chronic/)
- [IgA1-secreting cell lines from patients with IgA nephropathy produce aberrantly glycosylated IgA1](https://scholariq.org/papers/iga1-secreting-cell-lines-from-patients-with-iga-nephropathy-produce-aberrantly/)
- [Autoantibodies Targeting Galactose-Deficient IgA1 Associate with Progression of IgA Nephropathy](https://scholariq.org/papers/autoantibodies-targeting-galactose-deficient-iga1-associate-with-progression-of/)
- [Aberrant glycosylation of IgA1 is inherited in both pediatric IgA nephropathy and Henoch–Schönlein purpura nephritis](https://scholariq.org/papers/aberrant-glycosylation-of-iga1-is-inherited-in-both-pediatric-iga-nephropathy/)
- [IgA nephropathy and IgA vasculitis with nephritis have a shared feature involving galactose-deficient IgA1-oriented pathogenesis](https://scholariq.org/papers/iga-nephropathy-and-iga-vasculitis-with-nephritis-have-a-shared-feature/)
- [The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis](https://scholariq.org/papers/the-genetic-architecture-of-membranous-nephropathy-and-its-potential-to-improve/)
- [A digest from evidence-based clinical practice guideline for IgA nephropathy 2020](https://scholariq.org/papers/a-digest-from-evidence-based-clinical-practice-guideline-for-iga-nephropathy/)

## Researcher topics

- [Renal Diseases and Glomerulopathies](https://scholariq.org/topics/renal-diseases-and-glomerulopathies/)
- [Chronic Kidney Disease and Diabetes](https://scholariq.org/topics/chronic-kidney-disease-and-diabetes/)
- [Systemic Lupus Erythematosus Research](https://scholariq.org/topics/systemic-lupus-erythematosus-research/)
- [Vasculitis and related conditions](https://scholariq.org/topics/vasculitis-and-related-conditions/)
- [Platelet Disorders and Treatments](https://scholariq.org/topics/platelet-disorders-and-treatments/)

## Researcher university

- [Juntendo University Urayasu Hospital](https://scholariq.org/institutions/juntendo-university-urayasu-hospital/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.