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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:

FAM20C Overview: Classic and Novel Targets, Pathogenic Variants and Raine Syndrome Phenotypes
Ícela Palma-Lara, Monserrat Pérez-Ramírez, Patricia García Alonso-Themann, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 15, pp. 8039-8039
Open Access | Times Cited: 21

Showing 21 citing articles:

Passing the post: roles of posttranslational modifications in the form and function of extracellular matrix
Josephine C. Adams
AJP Cell Physiology (2023) Vol. 324, Iss. 5, pp. C1179-C1197
Open Access | Times Cited: 12
Mutant Fam20c knock-in mice recapitulate both lethal and non-lethal human Raine Syndrome
Mengnan Chen, Dongmei Sun, Siu-Pok Yee, et al.
BMC Molecular and Cell Biology (2025) Vol. 26, Iss. 1
Open Access
Gingival proteomics reveals the role of TGF beta and YAP/TAZ signaling in Raine syndrome fibrosis
Cláudio Rodrigues Rezende Costa, Rym Chalgoumi, Amina Baker, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 3
Fam20C in Human Diseases: Emerging Biological Functions and Therapeutic Implications
Xu Rong-sheng, Huidan Tan, Jiahui Zhang, et al.
Frontiers in Molecular Biosciences (2021) Vol. 8
Open Access | Times Cited: 19
Osteocytes and the pathogenesis of hypophosphatemic rickets
Miwa Yamazaki, Toshimi Michigami
Frontiers in Endocrinology (2022) Vol. 13
Open Access | Times Cited: 12
The Intricacies of Renal Phosphate Reabsorption—An Overview
Valerie Walker
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 9, pp. 4684-4684
Open Access | Times Cited: 2
Epigenetic and transcriptional activation of the secretory kinase FAM20C as an oncogene in glioma
Bo Gong, Yi Chu Liang, Qian Zhang, et al.
Journal of genetics and genomics/Journal of Genetics and Genomics (2023) Vol. 50, Iss. 6, pp. 422-433
Open Access | Times Cited: 6
The odontoblastic differentiation of dental mesenchymal stem cells: molecular regulation mechanism and related genetic syndromes
Houwen Pan, Yiling Yang, Hongyuan Xu, et al.
Frontiers in Cell and Developmental Biology (2023) Vol. 11
Open Access | Times Cited: 6
Comparative N-Glycoproteomic Investigation of Eggshell Cuticle and Mineralized Layer Proteins
Lingsen Zeng, Xuefeng Shi, Xuan Lin, et al.
Journal of Agricultural and Food Chemistry (2023) Vol. 71, Iss. 27, pp. 10448-10458
Closed Access | Times Cited: 5
Fam20c regulates the calpain proteolysis system through phosphorylating Calpasatatin to maintain cell homeostasis
Xinpeng Liu, Lili Jiang, Wenxuan Zhang, et al.
Journal of Translational Medicine (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 4
FAM20A: a potential diagnostic biomarker for lung squamous cell carcinoma
Yalin Zhang, Qin Sun, Youcai Liang, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access | Times Cited: 1
Mutations of family with sequence similarity 20‐member C gene causing lethal and nonlethal Raine syndrome causes hypophosphatemia rickets
Peihong Liu, Jiaxuan Li, Linghao Tang, et al.
Journal of Cellular Physiology (2023) Vol. 238, Iss. 11, pp. 2556-2569
Closed Access | Times Cited: 2
Intracranial calcification in Fam20c-deficient mice recapitulates human Raine syndrome
Hua Zhang, Yongbo Lu, Phillip R. Kramer, et al.
Neuroscience Letters (2023) Vol. 802, pp. 137176-137176
Open Access | Times Cited: 1
Potential Role of Protein Kinase FAM20C on the Brain in Raine Syndrome, an In Silico Analysis
Ícela Palma-Lara, Patricia García Alonso-Themann, Javier Pérez‐Durán, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 10, pp. 8904-8904
Open Access | Times Cited: 1
Knocking out FAM20C in pre-osteoblasts leads to up-regulation of osteoclast differentiation to affect long bone development
Lili Jiang, Xinpeng Liu, Lixue Liu, et al.
Gene (2024) Vol. 915, pp. 148396-148396
Open Access
Genetic causes of hypophosphatemia
Nuria Puente, Pablo Solís-Sánchez, José A. Riancho
Minerva Medica (2024) Vol. 115, Iss. 3
Closed Access
Bone marrow transplantation reduces FGF-23 levels and restores bone formation in myelodysplastic neoplasms
Heike Weidner, Ulrike Baschant, María G. Ledesma-Colunga, et al.
Leukemia (2024) Vol. 38, Iss. 8, pp. 1853-1857
Open Access
Identification of a circadian-based prognostic signature predicting cancer-associated fibroblasts infiltration and immunotherapy response in bladder cancer
Li Zhou, Jiaming He, Zhiming Hu, et al.
Aging (2024)
Open Access
Mutant Fam20c knock-in mice recapitulate both lethal and non-lethal human Raine Syndrome
Mengnan Chen, Dongmei Sun, Sui-Pok Yee, et al.
Research Square (Research Square) (2024)
Closed Access
Compound heterozygous FAM20C gene variants in a patient with severe Raine syndrome: a case report
Camelia Chirteș, Alina Bogliș, Andrea Tóth, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access
FAM20C: A key protein kinase in multiple diseases
Rui Zhang, Yanming Ren, Ju Yan, et al.
Genes & Diseases (2023) Vol. 12, Iss. 2, pp. 101179-101179
Open Access
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