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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:

Integrin Alpha 8 Recessive Mutations Are Responsible for Bilateral Renal Agenesis in Humans
Camille Humbert, Flora Silbermann, Bharti Morar, et al.
The American Journal of Human Genetics (2014) Vol. 94, Iss. 2, pp. 288-294
Open Access | Times Cited: 97

Showing 1-25 of 97 citing articles:

The extracellular matrix in development
David A. Cruz Walma, Kenneth M. Yamada
Development (2020) Vol. 147, Iss. 10
Open Access | Times Cited: 323
Exploring the genetic basis of early-onset chronic kidney disease
Asaf Vivante, Friedhelm Hildebrandt
Nature Reviews Nephrology (2016) Vol. 12, Iss. 3, pp. 133-146
Open Access | Times Cited: 315
Genetic, environmental, and epigenetic factors involved in CAKUT
Nayia Nicolaou, Kirsten Y. Renkema, Ernie M.H.F. Bongers, et al.
Nature Reviews Nephrology (2015) Vol. 11, Iss. 12, pp. 720-731
Closed Access | Times Cited: 293
Basement Membranes in Development and Disease
Rei Sekiguchi, Kenneth M. Yamada
Current topics in developmental biology/Current Topics in Developmental Biology (2018), pp. 143-191
Open Access | Times Cited: 196
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract
Amelie T. van der Ven, Dervla M. Connaughton, Hadas Ityel, et al.
Journal of the American Society of Nephrology (2018) Vol. 29, Iss. 9, pp. 2348-2361
Open Access | Times Cited: 171
Congenital Anomalies of the Kidney and the Urinary Tract (CAKUT)
Maria M. Rodríguez
Fetal and Pediatric Pathology (2014) Vol. 33, Iss. 5-6, pp. 293-320
Open Access | Times Cited: 156
Novel Insights into the Pathogenesis of Monogenic Congenital Anomalies of the Kidney and Urinary Tract
Amelie T. van der Ven, Asaf Vivante, Friedhelm Hildebrandt
Journal of the American Society of Nephrology (2017) Vol. 29, Iss. 1, pp. 36-50
Open Access | Times Cited: 131
Differential regulation of mouse and human nephron progenitors by the Six family of transcriptional regulators
Lori L. O’Brien, Qiuyu Guo, Youngjin Lee, et al.
Development (2016) Vol. 143, Iss. 4, pp. 595-608
Open Access | Times Cited: 126
Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract
Laurence Heidet, Vincent Morinière, C. Henry, et al.
Journal of the American Society of Nephrology (2017) Vol. 28, Iss. 10, pp. 2901-2914
Open Access | Times Cited: 100
Next-generation sequencing for research and diagnostics in kidney disease
Kirsten Y. Renkema, Marijn Stokman, Rachel H. Giles, et al.
Nature Reviews Nephrology (2014) Vol. 10, Iss. 8, pp. 433-444
Closed Access | Times Cited: 98
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
Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract
Asaf Vivante, Daw‐Yang Hwang, Stefan Kohl, et al.
Journal of the American Society of Nephrology (2016) Vol. 28, Iss. 1, pp. 69-75
Open Access | Times Cited: 90
The genetic basis of congenital anomalies of the kidney and urinary tract
Maayan Kagan, Oren Pleniceanu, Asaf Vivante
Pediatric Nephrology (2022) Vol. 37, Iss. 10, pp. 2231-2243
Closed Access | Times Cited: 44
The genetics and pathogenesis of CAKUT
Caroline M. Kolvenbach, Shirlee Shril, Friedhelm Hildebrandt
Nature Reviews Nephrology (2023) Vol. 19, Iss. 11, pp. 709-720
Closed Access | Times Cited: 39
A Gene Implicated in Activation of Retinoic Acid Receptor Targets Is a Novel Renal Agenesis Gene in Humans
Patrick D. Brophy, Maria Rasmussen, Mrutyunjaya Parida, et al.
Genetics (2017) Vol. 207, Iss. 1, pp. 215-228
Open Access | Times Cited: 77
The expanding phenotypic spectra of kidney diseases: insights from genetic studies
Marijn Stokman, Kirsten Y. Renkema, Rachel H. Giles, et al.
Nature Reviews Nephrology (2016) Vol. 12, Iss. 8, pp. 472-483
Closed Access | Times Cited: 74
The contribution of branching morphogenesis to kidney development and disease
Kieran M. Short, Ian Smyth
Nature Reviews Nephrology (2016) Vol. 12, Iss. 12, pp. 754-767
Closed Access | Times Cited: 74
Cell–Cell Interactions Driving Kidney Morphogenesis
Alexander N. Combes, Jamie A. Davies, Melissa H. Little
Current topics in developmental biology/Current Topics in Developmental Biology (2015), pp. 467-508
Closed Access | Times Cited: 72
INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES
Publisher Chandrasekhara Rao Baru
ADVANCED SCIENCES INDEX (2014)
Closed Access | Times Cited: 70
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
Molecular causes of congenital anomalies of the kidney and urinary tract (CAKUT)
Stefan Kohl, Sandra Habbig, Lutz T. Weber, et al.
Molecular and Cellular Pediatrics (2021) Vol. 8, Iss. 1
Open Access | Times Cited: 44
Mutations of the SLIT2–ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract
Daw‐Yang Hwang, Stefan Kohl, Xueping Fan, et al.
Human Genetics (2015) Vol. 134, Iss. 8, pp. 905-916
Open Access | Times Cited: 64
Expression Profiles of ITGA8 and VANGL2 Are Altered in Congenital Anomalies of the Kidney and Urinary Tract (CAKUT)
Nikola Pavlović, Nela Kelam, Anita Racetin, et al.
Molecules (2024) Vol. 29, Iss. 14, pp. 3294-3294
Open Access | Times Cited: 5
Pax genes in renal development, disease and regeneration
Richa Sharma, Oraly Sanchez-Ferras, Maxime Bouchard
Seminars in Cell and Developmental Biology (2015) Vol. 44, pp. 97-106
Closed Access | Times Cited: 49
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
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