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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:

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: 19

Showing 19 citing articles:

Succinic acid modified chitosan hydrogel mediates in-situ bioenergetic remodeling of neural cells for neuronal differentiation and spinal cord injury repair
Tingting Xu, Jingwen Zhao, Muke Zhou, et al.
Chemical Engineering Journal (2024) Vol. 487, pp. 150466-150466
Closed Access | Times Cited: 5
HMGA1 promotes the progression of esophageal squamous cell carcinoma by elevating TKT-mediated upregulation of pentose phosphate pathway
Mengjie Liu, Yuan Zhao, Qiu‐Tong Li, et al.
Cell Death and Disease (2024) Vol. 15, Iss. 7
Open Access | Times Cited: 5
Identification of deep intronic variants in junctional epidermolysis bullosa using genome sequencing and splicing assays
Fuying Chen, Ruoqu Wei, Yumeng Wang, et al.
npj Genomic Medicine (2025) Vol. 10, Iss. 1
Open Access
Screening of mitochondrial-related biomarkers connected with immune infiltration for acute respiratory distress syndrome through WGCNA and machine learning
Wei Sun, Su Tu
Medicine (2025) Vol. 104, Iss. 10, pp. e41497-e41497
Open Access
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
Superior COL7A1 and TGM1 gene expression in difficult-to-transfect skin cell mediated by highly branched poly(β-amino esters) through stepwise fractionation
Chaolan Pan, Chenfei Wang, Yitong Zhao, et al.
Journal of Controlled Release (2024) Vol. 370, pp. 82-94
Closed Access | Times Cited: 2
Proprotein convertases regulate trafficking and maturation of key proteins within the secretory pathway
Laura Cendron, Sylvia Rothenberger, Leonardo Cassari, et al.
Advances in protein chemistry and structural biology (2022), pp. 1-54
Closed Access | Times Cited: 8
Clinical and molecular characterization of a patient with MBTPS1 related spondyloepiphyseal dysplasia: Evidence of pathogenicity for a synonymous variant
Yeqing Yuan, Qiaoli Zhou, Chunli Wang, et al.
Frontiers in Pediatrics (2023) Vol. 10
Open Access | Times Cited: 4
Exome Sequencing Reveals Biallelic Mutations in MBTPS1 Gene in a Girl with a Very Rare Skeletal Dysplasia
Víctor Raggio, Soledad Rodríguez, Sandra Feder, et al.
Diagnostics (2024) Vol. 14, Iss. 3, pp. 313-313
Open Access | Times Cited: 1
Mitochondrial fumarate promotes ischemia/reperfusion‐induced tubular injury
Zuo‐Lin Li, Ming‐Min Huang, Meng‐Yao Yu, et al.
Acta Physiologica (2024) Vol. 240, Iss. 4
Closed Access | Times Cited: 1
Association of autoimmune and allergic diseases with senile cataract: a bidirectional two-sample Mendelian randomization study
Weichen Yuan, Xiangrui Li, Guan Wang, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access | Times Cited: 1
A gain-of-function variant in SREBF1 causes generalized skin hyperpigmentation with congenital cataracts
Huijun Wang, Yuan Wu, Jennifer A. Bassetti, et al.
British Journal of Dermatology (2024) Vol. 191, Iss. 5, pp. 805-815
Closed Access | Times Cited: 1
Site-1 protease inhibits mitochondrial respiration by controlling the TGF-β target gene Mss51
Muhammad Mousa, Lahari Vuppaladhadiam, Meredith O. Kelly, et al.
Cell Reports (2023) Vol. 42, Iss. 4, pp. 112336-112336
Open Access | Times Cited: 3
OSBPL2 compound heterozygous variants cause dyschromatosis, ichthyosis, deafness and atopic disease syndrome
Yumeng Wang, Anqi Zhao, Naihui Zhou, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2024) Vol. 1870, Iss. 5, pp. 167207-167207
Open Access
ADAM17 variant causes hair loss via ubiquitin ligase TRIM47 mediated degradation
Xiaoxiao Wang, Chaolan Pan, Luyao Zheng, et al.
JCI Insight (2024) Vol. 9, Iss. 13
Open Access
Endoplasmic Reticulum-Targeting Highly Branched Poly(β-amino ester)s for Skin Gene Delivery
Chenfei Wang, Wei He, Rui Guo, et al.
ACS Materials Letters (2024) Vol. 6, Iss. 11, pp. 5048-5057
Closed Access
The Role of Sphingolipids and Sphingosine-1-phosphate—Sphingosine-1-phosphate-receptor Signaling in Psoriasis
Kana Masuda‐Kuroki, Shahrzad Alimohammadi, Anna Di Nardo
Cells (2023) Vol. 12, Iss. 19, pp. 2352-2352
Open Access | Times Cited: 1
A case of MBTPS1‐related disorder due to compound heterozygous variants in MBTPS1 gene: Genotype–phenotype expansion and the emergence of a novel syndrome
Khurram Liaqat, Kayla Treat, Lili Mantcheva, et al.
American Journal of Medical Genetics Part A (2023) Vol. 194, Iss. 5
Open Access | Times Cited: 1
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