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:
A novel combination of biallelic IFT122 variants associated with cranioectodermal dysplasia: A case report
Qi Yang, Qiang Zhang, Fei Chen, et al.
Experimental and Therapeutic Medicine (2021) Vol. 21, Iss. 4
Open Access | Times Cited: 7
Qi Yang, Qiang Zhang, Fei Chen, et al.
Experimental and Therapeutic Medicine (2021) Vol. 21, Iss. 4
Open Access | Times Cited: 7
Showing 7 citing articles:
Mechanism of IFT-A polymerization into trains for ciliary transport
Shimi Meleppattu, Haixia Zhou, Jin Dai, et al.
Cell (2022) Vol. 185, Iss. 26, pp. 4986-4998.e12
Open Access | Times Cited: 36
Shimi Meleppattu, Haixia Zhou, Jin Dai, et al.
Cell (2022) Vol. 185, Iss. 26, pp. 4986-4998.e12
Open Access | Times Cited: 36
Cilia kinases in skeletal development and homeostasis
Sara P. Abraham, Alexandru Niţă, Pavel Krejčı́, et al.
Developmental Dynamics (2021) Vol. 251, Iss. 4, pp. 577-608
Open Access | Times Cited: 4
Sara P. Abraham, Alexandru Niţă, Pavel Krejčı́, et al.
Developmental Dynamics (2021) Vol. 251, Iss. 4, pp. 577-608
Open Access | Times Cited: 4
Case Report: Sequential Liver After Kidney Transplantation in a Patient With Sensenbrenner Syndrome (Cranioectodermal Dysplasia)
J Ryzko, Joanna Walczak‐Sztulpa, Piotr Czubkowski, et al.
Frontiers in Pediatrics (2022) Vol. 10
Open Access | Times Cited: 3
J Ryzko, Joanna Walczak‐Sztulpa, Piotr Czubkowski, et al.
Frontiers in Pediatrics (2022) Vol. 10
Open Access | Times Cited: 3
WDR35 variants in a cranioectodermal dysplasia patient with early onset end‐stage renal disease and retinal dystrophy
Joanna Walczak‐Sztulpa, Anna Wawrocka, Weronika Sikora, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 10, pp. 3071-3077
Closed Access | Times Cited: 3
Joanna Walczak‐Sztulpa, Anna Wawrocka, Weronika Sikora, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 10, pp. 3071-3077
Closed Access | Times Cited: 3
A novel variant in IFT122 associated with a severe phenotype of cranioectodermal dysplasia
Shiho Nagayama, Hironori Takahashi, Fuyuki Hasegawa, et al.
Congenital Anomalies (2024) Vol. 64, Iss. 4, pp. 177-181
Closed Access
Shiho Nagayama, Hironori Takahashi, Fuyuki Hasegawa, et al.
Congenital Anomalies (2024) Vol. 64, Iss. 4, pp. 177-181
Closed Access
The Skeletal Ciliopathies
Isabella Collins, A.K. Wann
Biology of extracellular matrix (2024), pp. 321-342
Closed Access
Isabella Collins, A.K. Wann
Biology of extracellular matrix (2024), pp. 321-342
Closed Access
Resolved Severe Primary Hypothyroidism in Sensenbrenner Syndrome Post Hepatorenal Transplantation: A Case Report
Khalid Al Noaim, Majid Alfadhel, Aurore Carré, et al.
Hormone Research in Paediatrics (2022) Vol. 96, Iss. 4, pp. 426-431
Closed Access
Khalid Al Noaim, Majid Alfadhel, Aurore Carré, et al.
Hormone Research in Paediatrics (2022) Vol. 96, Iss. 4, pp. 426-431
Closed Access
