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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Developmental Genetics and Congenital Anomalies of the Kidney and Urinary Tract
Natalie Uy, Kimberly J. Reidy
Journal of Pediatric Genetics (2015) Vol. 05, Iss. 01, pp. 051-060
Open Access | Times Cited: 44

Showing 1-25 of 44 citing articles:

Chronic kidney disease
Paola Romagnani, Giuseppe Remuzzi, Richard J. Glassock, et al.
Nature Reviews Disease Primers (2017) Vol. 3, Iss. 1
Open Access | Times Cited: 765
Chronic kidney disease
Paola Romagnani, Rajiv Agarwal, Juliana C.N. Chan, et al.
Nature Reviews Disease Primers (2025) Vol. 11, Iss. 1
Closed Access | Times Cited: 8
Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice
Lara De Tomasi, Pierre David, Camille Humbert, et al.
The American Journal of Human Genetics (2017) Vol. 101, Iss. 5, pp. 803-814
Open Access | Times Cited: 96
Renal development in the fetus and premature infant
Stacy D. Rosenblum, Abhijeet Pal, Kimberly J. Reidy
Seminars in Fetal and Neonatal Medicine (2017) Vol. 22, Iss. 2, pp. 58-66
Open Access | Times Cited: 94
The role of chromatin-related epigenetic modulations in CAKUT
Lars König, Miriam Schmidts
Current topics in developmental biology/Current Topics in Developmental Biology (2025)
Closed Access | Times Cited: 1
Whole-exome sequencing for prenatal diagnosis of fetuses with congenital anomalies of the kidney and urinary tract
Tingying Lei, Fang Fu, Ru Li, et al.
Nephrology Dialysis Transplantation (2017) Vol. 32, Iss. 10, pp. 1665-1675
Open Access | Times Cited: 64
Prenatal genetic considerations of congenital anomalies of the kidney and urinary tract (CAKUT)
Asha N. Talati, Carolyn Webster, Neeta L. Vora
Prenatal Diagnosis (2019) Vol. 39, Iss. 9, pp. 679-692
Open Access | Times Cited: 64
Loss-of-function mutations inKIF14cause severe microcephaly and kidney development defects in humans and zebrafish
Madeline Louise Reilly, Marijn Stokman, Virginie Magry, et al.
Human Molecular Genetics (2018) Vol. 28, Iss. 5, pp. 778-795
Open Access | Times Cited: 39
The Kidney
Christina Nguyen, Caitlin G. Peterson
Elsevier eBooks (2025), pp. 297-310.e2
Closed Access
Complex Management of Bilateral Congenital Hydronephrosis in a Pediatric Patient: A Multidisciplinary Approach
Nadica Motofelea, Ionela Florica Tamasan, Sonia Tănăsescu, et al.
Healthcare (2025) Vol. 13, Iss. 9, pp. 998-998
Open Access
Analysis of Kallikrein 6, Acetyl-α-Tubulin, and Aquaporin 1 and 2 Expression Patterns During Normal Human Nephrogenesis and in Congenital Anomalies of the Kidney and Urinary Tract (CAKUT)
Nela Kelam, Marin Ogorevc, Ivona Gotovac, et al.
Genes (2025) Vol. 16, Iss. 5, pp. 499-499
Open Access
Whole‐exome sequencing in the evaluation of fetal congenital anomalies of the kidney and urinary tract detected by ultrasonography
Tingying Lei, Fang Fu, Ru Li, et al.
Prenatal Diagnosis (2020) Vol. 40, Iss. 10, pp. 1290-1299
Closed Access | Times Cited: 29
Spectrum of congenital anomalies of the kidney and urinary tract (CAKUT) including renal parenchymal malformations during fetal life and the implementation of prenatal exome sequencing (WES)
Josefine Theresia Koenigbauer, Laura Fangmann, Charlotte Reinhardt, et al.
Archives of Gynecology and Obstetrics (2023) Vol. 309, Iss. 6, pp. 2613-2622
Open Access | Times Cited: 10
Deep learning prediction of renal anomalies for prenatal ultrasound diagnosis
Olivier Miguel, Emily Kaczmarek, I.K. Lee, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 3
Morphogenesis of the kidney and lung requires branch-tip directed activity of the Adamts18 metalloprotease
Elisabeth A. Rutledge, Riana K. Parvez, Kieran M. Short, et al.
Developmental Biology (2019) Vol. 454, Iss. 2, pp. 156-169
Open Access | Times Cited: 29
Impact of next generation sequencing on our understanding of CAKUT
Anukrati Nigam, Nine V.A.M. Knoers, Kirsten Y. Renkema
Seminars in Cell and Developmental Biology (2018) Vol. 91, pp. 104-110
Closed Access | Times Cited: 24
Practical Approach to Congenital Anomalies of the Kidneys: Focus on Anomalies With Insufficient or Abnormal Nephron Development: Renal Dysplasia, Renal Hypoplasia, and Renal Tubular Dysgenesis
Alexia Gazeu, Sophie Collardeau‐Frachon
Pediatric and Developmental Pathology (2024)
Closed Access | Times Cited: 2
The First Thousand Days: Kidney Health and Beyond
Chien‐Ning Hsu, You‐Lin Tain
Healthcare (2021) Vol. 9, Iss. 10, pp. 1332-1332
Open Access | Times Cited: 15
Intrauterine low-protein diet disturbs metanephric gene expression and induces urinary tract developmental abnormalities in mice
Minghui Yu, Lihong Tan, Jing Chen, et al.
Biochemical and Biophysical Research Communications (2019) Vol. 513, Iss. 3, pp. 732-739
Closed Access | Times Cited: 16
Mouse Models of Congenital Kidney Anomalies
Satu Kuure, Hannu Sariola
Advances in experimental medicine and biology (2020), pp. 109-136
Open Access | Times Cited: 15
Microarray analysis in pregnancies with isolated unilateral kidney agenesis
Lena Sagi‐Dain, Idit Maya, Amir Peleg, et al.
Pediatric Research (2018) Vol. 83, Iss. 4, pp. 825-828
Open Access | Times Cited: 13
Prenatal findings and molecular cytogenetic analyses of a de novo interstitial deletion of 1q23.3 encompassing PBX1 gene
Manna Sun, Jiwu Lou, Qiaoyi Li, et al.
Taiwanese Journal of Obstetrics and Gynecology (2019) Vol. 58, Iss. 2, pp. 292-295
Open Access | Times Cited: 10
Improving renal phenotype and evolving extra-renal features of 17q12 deletion encompassing the HNF1B gene
Roxana Cleper, Adi Reches, Dana Shapira, et al.
Translational Pediatrics (2021) Vol. 10, Iss. 12, pp. 3130-3139
Open Access | Times Cited: 9
Chronic Kidney Disease Management in Developing Countries
Danielle A. Badro
Springer eBooks (2023), pp. 1-146
Closed Access | Times Cited: 3
Comprehensive analysis of the relationship between xanthine oxidoreductase activity and chronic kidney disease
Yiyuan Zhang, Xiaobao Ding, Lihao Guo, et al.
iScience (2023) Vol. 26, Iss. 11, pp. 107332-107332
Open Access | Times Cited: 3
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