ReviewF1000Research2020
Duplex kidney formation: developmental mechanisms and genetic predisposition.
Review in F1000Research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
16 citing papers in PubMed, 39 citations in OpenAlex.
- Superselective renal artery embolization for complex duplex kidney with multiple prior surgeries: a case report.Frontiers in surgery · 2026Article
- Ureter development and associated congenital anomalies.Nature reviews. Nephrology · 2025Review
- Endoscopic management of ureteric stenosis and calculi in bilateral incomplete renal duplication: A case study.BioMedicine · 2025Article
- Complete Duplex Right Kidney With Upper Moiety Hydronephrosis due to Ureteral Stone: A Rare Case.Case reports in medicine · 2025Article
- First use and evaluation of a novel 6.3 Fr disposable flexible ureteroscope for stone management in duplex kidney: a case report.Translational andrology and urology · 2024Article
- Pathophysiology of Congenital Anomalies of the Kidney and Urinary Tract: A Comprehensive Review.Cells · 2024Review
- Congenital anomalies of the kidney and urinary tract.Frontiers in medicine · 2024Review
- Diagnostic Yield and Benefits of Whole Exome Sequencing in CAKUT Patients Diagnosed in the First Thousand Days of Life.Kidney international reports · 2023Article
- Transcriptional regulation by the NSL complex enables diversification of IFT functions in ciliated versus nonciliated cells.Science advances · 2023Article
- The evolution of the discrete multirenculate kidney in mammals from ecological and molecular perspectives.Genome biology and evolution · 2023Article
- Duplex kidney complicated with preoperative inferior nephroblastoma rupture in children: a case report and literature review.BMC pediatrics · 2021Review
- Urinary Incontinence in Adulthood in a Course of Ectopic Ureter-Description of Two Clinical Cases with Review of Literature.International journal of environmental research and public health · 2021Review
- Cecr2 mutant mice as a model for human cat eye syndrome.Scientific reports · 2021Article
- Article
- A Unique Case of Incomplete Bifid Ureter and Associated Arterial Variations.Case reports in urology · 2021Article
- Overexpression of Long Non-coding RNA 4933425B07Frontiers in cell and developmental biology · 2021Article
Corrections and comments
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Congenital abnormalities of the kidney and urinary tract (CAKUT) are a highly diverse group of diseases that together belong to the most common abnormalities detected in the new-born child. Consistent with this diversity, CAKUT are caused by mutations in a large number of genes and present a wide spectrum of phenotypes. In this review, we will focus on duplex kidneys, a relatively frequent form of CAKUT that is often asymptomatic but predisposes to vesicoureteral reflux and hydronephrosis. We will summarise the molecular programs responsible for ureter induction, review the genes that have been identified as risk factors in duplex kidney formation and discuss molecular and cellular mechanisms that may lead to this malformation.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.