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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:

RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects
Marc Jeanpierre, G. Macé, Mélanie Parisot, et al.
Journal of Medical Genetics (2011) Vol. 48, Iss. 7, pp. 497-504
Open Access | Times Cited: 63

Showing 1-25 of 63 citing articles:

RET revisited: expanding the oncogenic portfolio
Lois M. Mulligan
Nature reviews. Cancer (2014) Vol. 14, Iss. 3, pp. 173-186
Closed Access | Times Cited: 477
Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans
Asaf Vivante, Stefan Kohl, Daw‐Yang Hwang, et al.
Pediatric Nephrology (2014) Vol. 29, Iss. 4, pp. 695-704
Open Access | Times Cited: 207
Receptor tyrosine kinase inhibitors in cancer
Nasim Ebrahimi, Elmira Fardi, Hajarossadat Ghaderi, et al.
Cellular and Molecular Life Sciences (2023) Vol. 80, Iss. 4
Open Access | Times Cited: 61
RET gene mutations (genotype and phenotype) of multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma
Geoffrey W. Krampitz, Jeffrey A. Norton
Cancer (2014) Vol. 120, Iss. 13, pp. 1920-1931
Open Access | Times Cited: 124
Genetics of Congenital Anomalies of the Kidney and Urinary Tract: The Current State of Play
Valentina Capone, William Morello, Francesca Taroni, et al.
International Journal of Molecular Sciences (2017) Vol. 18, Iss. 4, pp. 796-796
Open Access | Times Cited: 123
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
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
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 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
Novel perspectives for investigating congenital anomalies of the kidney and urinary tract (CAKUT)
Kirsten Y. Renkema, Paul Winyard, Ilya Skovorodkin, et al.
Nephrology Dialysis Transplantation (2011) Vol. 26, Iss. 12, pp. 3843-3851
Open Access | Times Cited: 105
Severe Prenatal Renal Anomalies Associated with Mutations in HNF1B or PAX2 Genes
Leire Madariaga, Vincent Morinière, Marc Jeanpierre, et al.
Clinical Journal of the American Society of Nephrology (2013) Vol. 8, Iss. 7, pp. 1179-1187
Open Access | Times Cited: 100
Traditional and targeted exome sequencing reveals common, rare and novel functional deleterious variants in RET-signaling complex in a cohort of living US patients with urinary tract malformations
Rajshekhar Chatterjee, Enrique Ramos, Mary Hoffman, et al.
Human Genetics (2012) Vol. 131, Iss. 11, pp. 1725-1738
Open Access | Times Cited: 85
To bud or not to bud: the RET perspective in CAKUT
T. Keefe Davis, Masato Hoshi, Sanjay Jain
Pediatric Nephrology (2013) Vol. 29, Iss. 4, pp. 597-608
Open Access | Times Cited: 77
Multiple Endocrine Neoplasia
Jeffrey A. Norton, Geoffrey W. Krampitz, Robert T. Jensen
Surgical Oncology Clinics of North America (2015) Vol. 24, Iss. 4, pp. 795-832
Open Access | Times Cited: 76
RET receptor signaling: Function in development, metabolic disease, and cancer
Masahide Takahashi
Proceedings of the Japan Academy Series B (2022) Vol. 98, Iss. 3, pp. 112-125
Open Access | Times Cited: 35
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
Targeted gene sequencing and whole‐exome sequencing in autopsied fetuses with prenatally diagnosed kidney anomalies
Maria Rasmussen, Lone Sunde, Marlene Louise Nielsen, et al.
Clinical Genetics (2017) Vol. 93, Iss. 4, pp. 860-869
Open Access | Times Cited: 55
Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT)
Anne Kosfeld, Martin Kreuzer, Christoph Daniel, et al.
Human Genetics (2015) Vol. 135, Iss. 1, pp. 69-87
Closed Access | Times Cited: 29
Reciprocal Spatiotemporally Controlled Apoptosis Regulates Wolffian Duct Cloaca Fusion
Masato Hoshi, Antoine Reginensi, Matthew S. Joens, et al.
Journal of the American Society of Nephrology (2018) Vol. 29, Iss. 3, pp. 775-783
Open Access | Times Cited: 24
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
Development of the urogenital system is regulated via the 3′UTR of GDNF
Hao Li, Madis Jakobson, Roxana Ola, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 23
Renal agenesis-related genes are associated with Herlyn-Werner-Wunderlich syndrome
Lin Li, Chunfang Chu, Shenghui Li, et al.
Fertility and Sterility (2021) Vol. 116, Iss. 5, pp. 1360-1369
Closed Access | Times Cited: 19
Deciphering the mutation spectrum in south Indian children with congenital anomalies of the kidney and urinary tract
Ambili Narikot, Varsha Chhotusing Pardeshi, A. M. Shubha, et al.
BMC Nephrology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 11
The genetic etiologies of bilateral renal agenesis
Gregory W. Kirschen, Karin J. Blakemore, Huda B. Al‐Kouatly, et al.
Prenatal Diagnosis (2024) Vol. 44, Iss. 2, pp. 205-221
Closed Access | Times Cited: 2
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