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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:

Site-1 protease deficiency causes human skeletal dysplasia due to defective inter-organelle protein trafficking
Yuji Kondo, Jianxin Fu, Hua Wang, et al.
JCI Insight (2018) Vol. 3, Iss. 14
Open Access | Times Cited: 50

Showing 1-25 of 50 citing articles:

The Multifaceted Biology of PCSK9
Nabil G. Seidah, Annik Prat
Endocrine Reviews (2021) Vol. 43, Iss. 3, pp. 558-582
Open Access | Times Cited: 148
The role of the Golgi apparatus in disease (Review)
Jianyang Liu, Yan Huang, Ting Li, et al.
International Journal of Molecular Medicine (2021) Vol. 47, Iss. 4
Open Access | Times Cited: 122
Osteogenesis Imperfecta: Mechanisms and Signaling Pathways Connecting Classical and Rare OI Types
Milena Jovanovic, Gali Guterman‐Ram, Joan C. Marini
Endocrine Reviews (2021) Vol. 43, Iss. 1, pp. 61-90
Open Access | Times Cited: 116
TRMT6/61A-dependent base methylation of tRNA-derived fragments regulates gene-silencing activity and the unfolded protein response in bladder cancer
Zhangli Su, Ida Monshaugen, Briana Wilson, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 83
Lysosomal enzyme trafficking: from molecular mechanisms to human diseases
Thomas Braulke, Jan E. Carette, Wilhelm Palm
Trends in Cell Biology (2023) Vol. 34, Iss. 3, pp. 198-210
Closed Access | Times Cited: 28
Genetic Disorders of the Extracellular Matrix
Shireen R. Lamandé, John F. Bateman
The Anatomical Record (2019) Vol. 303, Iss. 6, pp. 1527-1542
Open Access | Times Cited: 71
Update on the Genetics of Osteogenesis Imperfecta
Milena Jovanovic, Joan C. Marini
Calcified Tissue International (2024) Vol. 115, Iss. 6, pp. 891-914
Open Access | Times Cited: 7
Bone biology: insights from osteogenesis imperfecta and related rare fragility syndromes
Roberta Besio, Chi‐Wing Chow, Francesca Tonelli, et al.
FEBS Journal (2019) Vol. 286, Iss. 15, pp. 3033-3056
Open Access | Times Cited: 53
Hepatic SREBP signaling requires SPRING to govern systemic lipid metabolism in mice and humans
Sebastian Hendrix, Jenina Kingma, Roelof Ottenhoff, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 15
How Do Enveloped Viruses Exploit the Secretory Proprotein Convertases to Regulate Infectivity and Spread?
Nabil G. Seidah, Antonella Pasquato, Ursula Andréo
Viruses (2021) Vol. 13, Iss. 7, pp. 1229-1229
Open Access | Times Cited: 30
Site-1 protease controls osteoclastogenesis by mediating LC3 transcription
Zeyu Zheng, Xuyang Zhang, Bao Huang, et al.
Cell Death and Differentiation (2021) Vol. 28, Iss. 6, pp. 2001-2018
Open Access | Times Cited: 29
S1P defects cause a new entity of cataract, alopecia, oral mucosal disorder, and psoriasis‐like syndrome
Fuying Chen, Cheng Ni, Xiaoxiao Wang, et al.
EMBO Molecular Medicine (2022) Vol. 14, Iss. 5
Open Access | Times Cited: 21
Regulatory mechanisms of the cAMP-responsive element binding protein 3 (CREB3) family in cancers
Yu-Xiong Wang, Faping Li, Bin Liu, et al.
Biomedicine & Pharmacotherapy (2023) Vol. 166, pp. 115335-115335
Open Access | Times Cited: 12
Case Report: Recombinant human growth hormone therapy in a patient with spondyloepiphyseal dysplasia, Kondo-Fu type
Congli Chen, Jin Wu, Ying Liu
Frontiers in Pediatrics (2023) Vol. 11
Open Access | Times Cited: 11
SPRING is a Dedicated Licensing Factor for SREBP-Specific Activation by S1P
Sebastian Hendrix, Josephine M.E. Tan, Klevis Ndoj, et al.
Molecular and Cellular Biology (2024) Vol. 44, Iss. 4, pp. 123-137
Open Access | Times Cited: 4
Proteolytic processing of secretory pathway kinase Fam20C by site-1 protease promotes biomineralization
Xinxin Chen, Jianchao Zhang, Pulan Liu, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 32
Open Access | Times Cited: 26
Supply chain logistics – the role of the Golgi complex in extracellular matrix production and maintenance
John Hellicar, Nicola L. Stevenson, David Stephens, et al.
Journal of Cell Science (2022) Vol. 135, Iss. 1
Open Access | Times Cited: 17
Structural basis for substrate selectivity by site-one protease revealed by studies with a small-molecule inhibitor
Ashley V. Bullington, Ilaria Micallo, B.S. Bajaj, et al.
Proceedings of the National Academy of Sciences (2025) Vol. 122, Iss. 18
Open Access
Mechanistic insights into skeletal development gained from genetic disorders
Raymond K. H. Yip, Danny Chan, Kathryn S.E. Cheah
Current topics in developmental biology/Current Topics in Developmental Biology (2019), pp. 343-385
Closed Access | Times Cited: 26
New developments in chondrocyte ER-stress and related diseases
Michael D. Briggs, Ella P. Dennis, Helen F. Dietmar, et al.
F1000Research (2020) Vol. 9, pp. 290-290
Open Access | Times Cited: 25
Site-1 and site-2 proteases: A team of two in regulated proteolysis
Tatyana Danyukova, Kenneth Schöneck, Sandra Pohl
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research (2021) Vol. 1869, Iss. 1, pp. 119138-119138
Open Access | Times Cited: 22
One test for all: whole exome sequencing significantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver–Russell syndrome
Robert Meyer, Matthias Begemann, Christian Thomas Hübner, et al.
Orphanet Journal of Rare Diseases (2021) Vol. 16, Iss. 1
Open Access | Times Cited: 19
SPRING licenses S1P-mediated cleavage of SREBP2 by displacing an inhibitory pro-domain
Sebastian Hendrix, Vincent Dartigue, Hailee Hall, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 2
Spondyloepimetaphyseal dysplasia with elevated plasma lysosomal enzymes caused by homozygous variant in MBTPS1
Daniel R. Carvalho, Carlos E. Speck‐Martins, Jaime Moritz Brum, et al.
American Journal of Medical Genetics Part A (2020) Vol. 182, Iss. 7, pp. 1796-1800
Open Access | Times Cited: 16
Identification of a New Variant of the MBTPS1 Gene of the Kondo-Fu Type of Spondyloepiphyseal Dysplasia (SEDKF) in a Saudi Patient
Maha Alotaibi, Ali Mohammed Aldossari, Anish Khan, et al.
Case Reports in Pediatrics (2022) Vol. 2022, pp. 1-5
Open Access | Times Cited: 10
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