# Gil Chernin

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/gil-chernin/

## Facts

| Field | Value |
| --- | --- |
| Citations | 3,108 |
| Field | Renal Diseases and Glomerulopathies |
| h-index | 26 |
| i10-index | 42 |
| Last Known Institution | FIND |
| OpenAlex ID | https://openalex.org/A5033668078 |
| ORCID iD | 0000-0001-7514-156X |
| Works | 90 |

## Researcher papers

- [COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness](https://scholariq.org/papers/coq6-mutations-in-human-patients-produce-nephrotic-syndrome-with-sensorineural/)
- [ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling](https://scholariq.org/papers/arhgdia-mutations-cause-nephrotic-syndrome-via-defective-rho-gtpase-signaling/)
- [Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome](https://scholariq.org/papers/whole-exome-sequencing-of-patients-with-steroid-resistant-nephrotic-syndrome/)
- [Finerenone in Patients With Chronic Kidney Disease and Type 2 Diabetes by Sodium–Glucose Cotransporter 2 Inhibitor Treatment: The FIDELITY Analysis](https://scholariq.org/papers/finerenone-in-patients-with-chronic-kidney-disease-and-type-2-diabetes-by-sodium/)
- [A Novel TRPC6 Mutation That Causes Childhood FSGS](https://scholariq.org/papers/a-novel-trpc6-mutation-that-causes-childhood-fsgs/)
- [A Systematic Approach to Mapping Recessive Disease Genes in Individuals from Outbred Populations](https://scholariq.org/papers/a-systematic-approach-to-mapping-recessive-disease-genes-in-individuals-from/)
- [Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations](https://scholariq.org/papers/genotype-phenotype-correlation-in-nephrotic-syndrome-caused-by-wt1-mutations/)
- [Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy](https://scholariq.org/papers/individuals-with-mutations-in-xpnpep3-which-encodes-a-mitochondrial-protein/)
- [Exome Sequencing Reveals Cubilin Mutation as a Single-Gene Cause of Proteinuria](https://scholariq.org/papers/exome-sequencing-reveals-cubilin-mutation-as-a-single-gene-cause-of-proteinuria/)
- [Anemia and iron deficiency in COPD patients: prevalence and the effects of correction of the anemia with erythropoiesis stimulating agents and intravenous iron](https://scholariq.org/papers/anemia-and-iron-deficiency-in-copd-patients-prevalence-and-the-effects-of/)
- [Effect of semaglutide on COVID-19 and other infections: an analysis from the FLOW randomized clinical trial](https://scholariq.org/papers/effect-of-semaglutide-on-covid-19-and-other-infections-an-analysis-from-the-flow/)
- [Kidney and Survival Benefits of Semaglutide in Diabetes With Chronic Kidney Disease](https://scholariq.org/papers/kidney-and-survival-benefits-of-semaglutide-in-diabetes-with-chronic-kidney/)

## Researcher topics

- [Renal Diseases and Glomerulopathies](https://scholariq.org/topics/renal-diseases-and-glomerulopathies/)
- [Dialysis and Renal Disease Management](https://scholariq.org/topics/dialysis-and-renal-disease-management/)
- [Blood Pressure and Hypertension Studies](https://scholariq.org/topics/blood-pressure-and-hypertension-studies/)
- [Chronic Kidney Disease and Diabetes](https://scholariq.org/topics/chronic-kidney-disease-and-diabetes/)
- [Diabetes Treatment and Management](https://scholariq.org/topics/diabetes-treatment-and-management/)

## Researcher university

- [FIND](https://scholariq.org/institutions/find/)

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