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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:

Urinary Concentration Defects and Mechanisms Underlying Nephronophthisis
Rajesh Krishnan, Lorraine Eley, John A. Sayer
Kidney & Blood Pressure Research (2008) Vol. 31, Iss. 3, pp. 152-162
Open Access | Times Cited: 28

Showing 1-25 of 28 citing articles:

Impaired Wnt–β-catenin signaling disrupts adult renal homeostasis and leads to cystic kidney ciliopathy
Madeline A. Lancaster, Carrie M Louie, Jennifer L. Silhavy, et al.
Nature Medicine (2009) Vol. 15, Iss. 9, pp. 1046-1054
Open Access | Times Cited: 165
Many Genes—One Disease? Genetics of Nephronophthisis (NPHP) and NPHP-Associated Disorders
Shalabh Srivastava, Elisa Molinari, Shreya Raman, et al.
Frontiers in Pediatrics (2018) Vol. 5
Open Access | Times Cited: 114
Missing-in-metastasis MIM/MTSS1 promotes actin assembly at intercellular junctions and is required for integrity of kidney epithelia
Juha Saarikangas, Pieta K. Mattila, Markku Varjosalo, et al.
Journal of Cell Science (2011) Vol. 124, Iss. 8, pp. 1245-1255
Closed Access | Times Cited: 79
NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development
Jungyeon Won, Caralina Marín de Evsikova, Richard S. Smith, et al.
Human Molecular Genetics (2010) Vol. 20, Iss. 3, pp. 482-496
Open Access | Times Cited: 75
The Ciliary Protein Nephrocystin-4 Translocates the Canonical Wnt Regulator Jade-1 to the Nucleus to Negatively Regulate β-Catenin Signaling
Lori Borgal, Sandra Habbig, Julia Hatzold, et al.
Journal of Biological Chemistry (2012) Vol. 287, Iss. 30, pp. 25370-25380
Open Access | Times Cited: 52
Nephronophthisis: A Genetically Diverse Ciliopathy
Roslyn Simms, Ann Marie Hynes, Lorraine Eley, et al.
International Journal of Nephrology (2011) Vol. 2011, pp. 1-10
Open Access | Times Cited: 51
Nephronophthisis
Roslyn Simms, Lorraine Eley, John A. Sayer
European Journal of Human Genetics (2008) Vol. 17, Iss. 4, pp. 406-416
Open Access | Times Cited: 57
Vasopressin-2 Receptor Signaling and Autosomal Dominant Polycystic Kidney Disease
Markus M. Rinschen, Bernhard Schermer, Thomas Benzing
Journal of the American Society of Nephrology (2014) Vol. 25, Iss. 6, pp. 1140-1147
Open Access | Times Cited: 41
Renal Ciliopathies: Sorting Out Therapeutic Approaches for Nephronophthisis
Marijn Stokman, Sophie Saunier, Alexandre Benmerah
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 26
The ubiquitin ligase NEDD4-2/NEDD4L regulates both sodium homeostasis and fibrotic signaling to prevent end-stage renal disease
Jantina Manning, Sonia S. Shah, Andrej Nikolic, et al.
Cell Death and Disease (2021) Vol. 12, Iss. 4
Open Access | Times Cited: 21
Impaired water reabsorption in mice deficient in the type VI adenylyl cyclase (AC6)
Chen‐Li Chien, Yu‐Shuo Wu, Hsing‐Lin Lai, et al.
FEBS Letters (2010) Vol. 584, Iss. 13, pp. 2883-2890
Closed Access | Times Cited: 35
Renal phenotype in Bardet-Biedl syndrome: a combined defect of urinary concentration and dilution is associated with defective urinary AQP2 and UMOD excretion
Miriam Zacchia, Enza Zacchia, Enrica Zona, et al.
AJP Renal Physiology (2016) Vol. 311, Iss. 4, pp. F686-F694
Open Access | Times Cited: 20
The Kidney in Bardet-Biedl Syndrome: Possible Pathogenesis of Urine Concentrating Defect
Miriam Zacchia, Valentina Di Iorio, Francesco Trepiccione, et al.
Kidney Diseases (2017) Vol. 3, Iss. 2, pp. 57-65
Open Access | Times Cited: 19
Functional modelling of a novel mutation in BBS5
Mohamed H. Al‐Hamed, Charles van Lennep, Ann Marie Hynes, et al.
Cilia (2014) Vol. 3, Iss. 1
Open Access | Times Cited: 16
Identification of an NPHP1 deletion causing adult form of nephronophthisis
Alireza Haghighi, S Savaj, Hamidreza Haghighi-Kakhki, et al.
Irish Journal of Medical Science (1971 -) (2015) Vol. 185, Iss. 3, pp. 589-595
Closed Access | Times Cited: 14
Nephrocystin-1 interacts directly with Ack1 and is expressed in human collecting duct
Lorraine Eley, Shabbir H. Moochhala, Roslyn Simms, et al.
Biochemical and Biophysical Research Communications (2008) Vol. 371, Iss. 4, pp. 877-882
Closed Access | Times Cited: 12
Knockdown of the BBS10 Gene Product Affects Apical Targeting of AQP2 in Renal Cells: A Possible Explanation for the Polyuria Associated with Bardet-Biedl Syndrome
Miriam Zacchia
Journal of Genetic Syndromes & Gene Therapy (2014) Vol. 05, Iss. 03
Closed Access | Times Cited: 8
A bell‐shaped pattern of urinary aquaporin‐2‐bearing extracellular vesicle release in an experimental model of nephronophthisis
Nobuyuki Mikoda, Hiroko Sonoda, Sayaka Oshikawa, et al.
Physiological Reports (2019) Vol. 7, Iss. 9, pp. e14092-e14092
Open Access | Times Cited: 7
Atypical histological abnormalities in an adult patient with nephronophthisis harboring NPHP1 deletion: a case report
Maiko Akira, Hitoshi Suzuki, Arisa Ikeda, et al.
BMC Nephrology (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 7
NPHP3 splice acceptor site variant is associated with infantile nephronophthisis and asphyxiating thoracic dystrophy; A rare combination
Ambreen Ijaz, Fatima Alfadhli, Azizah Alharbi, et al.
European Journal of Medical Genetics (2022) Vol. 65, Iss. 10, pp. 104578-104578
Closed Access | Times Cited: 4
Juvenile Nephropathy in a Boxer Dog Resembling the Human Nephronophthisis-Medullary Cystic Kidney Disease Complex
Angelo Basile, Andrea Onetti Muda, Konstantinos Giannakakis, et al.
Journal of Veterinary Medical Science (2011) Vol. 73, Iss. 12, pp. 1669-1675
Open Access | Times Cited: 3
A case report of NPHP1 deletion in Chinese twins with nephronophthisis
Feng Chen, Limeng Dai, Jun Zhang, et al.
BMC Medical Genetics (2020) Vol. 21, Iss. 1
Open Access | Times Cited: 3
Renal Cystic Diseases
Carrie L. Phillips, Maha Al-Khawaja
Elsevier eBooks (2013), pp. 15-46
Closed Access | Times Cited: 2
Juvenile nephronophthisis and dysthyroidism: a rare association
Fateme Shamekhi Amiri, Ariana Kariminejad
CEN Case Reports (2017) Vol. 6, Iss. 1, pp. 98-104
Open Access | Times Cited: 2
Nephronophthisis
John A. Sayer, Judith Goodship
(2013), pp. 60-75
Closed Access
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