EDITORIAL
Published on 13 Feb 2023
Editorial: Genetics and epigenetics of chronic kidney disease
doi 10.3389/fmed.2023.1078300
- 1,066 views
- 1 citation
- Frontiers in Medicine
- Nephrology
- Research Topics
- Genetics And Epigenetics of Chronic Kidney Disease
Genetics And Epigenetics of Chronic Kidney Disease
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Articles
ORIGINAL RESEARCH
Published on 20 Oct 2022
Renal X-inactivation in female individuals with X-linked Alport syndrome primarily determined by age
doi 10.3389/fmed.2022.953643
- 1,626 views
- 3 citations
ORIGINAL RESEARCH
Published on 28 Sep 2022
SMOC2 gene interacts with APOL1 in the development of end-stage kidney disease: A genome-wide association study
doi 10.3389/fmed.2022.971297
- 1,870 views
- 2 citations
ORIGINAL RESEARCH
Published on 07 Jul 2022
Spatially Resolved Transcriptomes of Mammalian Kidneys Illustrate the Molecular Complexity and Interactions of Functional Nephron Segments
doi 10.3389/fmed.2022.873923
- 4,790 views
- 17 citations
REVIEW
Published on 05 Jul 2022
Chromatin Methylation Abnormalities in Autosomal Dominant Polycystic Kidney Disease
doi 10.3389/fmed.2022.921631
- 3,251 views
- 5 citations
ORIGINAL RESEARCH
Published on 20 Jun 2022
N6-Methyladenosine Methylomic Landscape of Ureteral Deficiency in Reflux Uropathy and Obstructive Uropathy
doi 10.3389/fmed.2022.924579
- 1,856 views
- 1 citation
ORIGINAL RESEARCH
Published on 17 Jun 2022
Combined Preimplantation Genetic Testing for Genetic Kidney Disease: Genetic Risk Identification, Assisted Reproductive Cycle, and Pregnancy Outcome Analysis
doi 10.3389/fmed.2022.936578
- 3,210 views
- 4 citations
ORIGINAL RESEARCH
Published on 09 Jun 2022
The Clinical and Genetic Features in Chinese Children With Steroid-Resistant or Early-Onset Nephrotic Syndrome: A Multicenter Cohort Study
doi 10.3389/fmed.2022.885178
- 3,066 views
- 5 citations
STUDY PROTOCOL
Published on 26 May 2022
The HIDDEN Protocol: An Australian Prospective Cohort Study to Determine the Utility of Whole Genome Sequencing in Kidney Failure of Unknown Aetiology
doi 10.3389/fmed.2022.891223
- 1,348 views
- 4 citations
REVIEW
Published on 06 May 2022
An Updated Review and Meta Analysis of Lipoprotein Glomerulopathy
doi 10.3389/fmed.2022.905007
- 4,299 views
- 9 citations
CASE REPORT
Published on 07 Apr 2022
Late-Onset Bartter Syndrome Type II Due to a Novel Compound Heterozygous Mutation in KCNJ1 Gene: A Case Report and Literature Review
doi 10.3389/fmed.2022.862514
- 2,234 views
- 6 citations
CASE REPORT
Published on 31 Jan 2022
Case Report: A Pathogenic Missense Variant of WT1 Cosegregates With Proteinuria in a Six-Generation Chinese Family With IgA Nephropathy
doi 10.3389/fmed.2021.810940
- 1,802 views
- 2 citations
Published in
Frontiers in Medicine
- Nephrology
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- 54kTopic views
- 35kArticle views
- 17kArticle downloads