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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:

A familial PLCB4 mutation causing auriculocondylar syndrome 2 with variable severity
Amira Nabil, Sahar El Shafei, Nihal M. El Shakankiri, et al.
European Journal of Medical Genetics (2020) Vol. 63, Iss. 6, pp. 103917-103917
Closed Access | Times Cited: 22

Showing 22 citing articles:

Clinical Profiles and Genetic Spectra of 814 Chinese Children With Short Stature
Xin Li, Ruen Yao, Guoying Chang, et al.
The Journal of Clinical Endocrinology & Metabolism (2021) Vol. 107, Iss. 4, pp. 972-985
Open Access | Times Cited: 28
Genomics in Egypt: Current Status and Future Aspects
Eman El-Attar, Rasha Mohamed Helmy Elkaffas, Sarah Ahmed Aglan, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 21
Phospholipase C β4 promotes RANKL-dependent osteoclastogenesis by interacting with MKK3 and p38 MAPK
Dong-Kyo Lee, Xian Jin, Poo-Reum Choi, et al.
Experimental & Molecular Medicine (2025)
Open Access
Auriculocondylar syndrome 2 caused by a novel PLCB4 variant in a male Chinese neonate: A case report and review of the literature
Y L Zhang, Yuwei Zhao, Liying Dai, et al.
Molecular Genetics & Genomic Medicine (2024) Vol. 12, Iss. 4
Open Access | Times Cited: 3
Auriculocondylar syndrome: Pathogenesis, clinical manifestations and surgical therapies
Qingqing Li, Zhiyuan Jiang, Liyuan Zhang, et al.
Journal of the Formosan Medical Association (2023) Vol. 122, Iss. 9, pp. 822-842
Open Access | Times Cited: 7
Auriculocondylar syndrome 2 results from the dominant-negative action of PLCB4 variants
Stanley M. Kanai, Caleb Heffner, Timothy C. Cox, et al.
Disease Models & Mechanisms (2022) Vol. 15, Iss. 4
Open Access | Times Cited: 11
Mir24-2-5p suppresses the osteogenic differentiation with Gnai3 inhibition presenting a direct target via inactivating JNK-p38 MAPK signaling axis
Li Meng, Lichan Yuan, Jieli Ni, et al.
International Journal of Biological Sciences (2021) Vol. 17, Iss. 15, pp. 4238-4253
Open Access | Times Cited: 13
Further phenotypic delineation of the auriculocondylar syndrome type 2 with literature review
Ewelina Bukowska‐Olech, Anna Sowińska‐Seidler, Filip Łojek, et al.
Journal of Applied Genetics (2020) Vol. 62, Iss. 1, pp. 107-113
Open Access | Times Cited: 13
Novel GNAI3 mutation in a Chinese family with auriculocondylar syndrome and treatment of severe dentofacial deformities: a 5-year follow-up case report
Yulin Shi, Rong Liang, Siying Liu, et al.
BMC Oral Health (2024) Vol. 24, Iss. 1
Open Access | Times Cited: 1
The Polymorphism at PLCB4 Promoter (rs6086746) Changes the Binding Affinity of RUNX2 and Affects Osteoporosis Susceptibility: An Analysis of Bioinformatics-Based Case-Control Study and Functional Validation
Dung-Jang Tsai, Wen-Hui Fang, Li-Wei Wu, et al.
Frontiers in Endocrinology (2021) Vol. 12
Open Access | Times Cited: 9
Heterogeneity in biomarkers, mitogenome and genetic disorders of Arab population with special emphasis on large-scale whole-exome sequencing
J. Francis Borgio
Archives of Medical Science (2021)
Open Access | Times Cited: 8
Bilateral choanal stenosis in auriculocondylar syndrome caused by a PLCB4 variant
Lé Shon Peart, Joanna Gonzalez, Stephanie Bivona, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 4, pp. 1307-1310
Closed Access | Times Cited: 6
AllelePred: A Simple Allele Frequencies Ensemble Predictor for Different Single Nucleotide Variants
Turki M. Sobahy, Olaa Motwalli, Meshari Alazmi
IEEE/ACM Transactions on Computational Biology and Bioinformatics (2023) Vol. 20, Iss. 1, pp. 796-801
Open Access | Times Cited: 2
A homozygous missense variant in the PLCB4 gene causes severe phenotype of auriculocondylar syndrome type 2
Khawla El Fizazi, Abdelhamid Bouramtane, Meriame Abbassi, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 11, pp. 2673-2678
Open Access | Times Cited: 2
Two Chinese Patients of Auriculocondylar Syndrome 2: A Novel PLCB4 Splicing Variant and 5-Year Follow-up
Yunting Lin, Ye Zhang, Jian Ma, et al.
The Cleft Palate-Craniofacial Journal (2024)
Closed Access
Phospholipase C β4 promotes RANKL-dependent osteoclastogenesis by interacting with MKK3 and p38 MAPK
Dong-Kyo Lee, Xian Jin, Poo-Reum Choi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Novel GNAI3 mutation in a Chinese auriculocondylar syndrome family and treatment of severe dentofacial deformities: A 5-years follow-up case report
Yulin Shi, Rong Liang, Siying Liu, et al.
Research Square (Research Square) (2024)
Open Access
Pathogenic Germline Variants in Uveal Melanoma Driver and BAP1‐Associated Genes in Finnish Patients with Uveal Melanoma
Pauliina Repo, Eveliina Jakkula, Juho Hiltunen, et al.
Pigment Cell & Melanoma Research (2024)
Open Access
Signaling, Physiology, and Targeting of GPCR ‐Regulated Phospholipase C Enzymes
Naincy R. Chandan, Alan V. Smrcka, H. T. Phan
(2022), pp. 458-520
Closed Access | Times Cited: 1
Investigação funcional do novo locus candidato, HDAC9, causativo da síndrome aurículo-condilar
Sofia Lígia Guimarães Ramos
(2021)
Open Access
AllelePred: A Simple Allele Frequencies Ensemble Predictor for Different Single Nucleotide Variants
Turki M. Sobahy, Meshari Alazmi
(2021)
Open Access
AllelePred: A Simple Allele Frequencies Ensemble Predictor for Different Single Nucleotide Variants
Turki M. Sobahy, Meshari Alazmi
(2021)
Open Access
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