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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:

ITPR1 Mutation Contributes to Hemifacial Microsomia Spectrum
Zhixu Liu, Hao Sun, Jiewen Dai, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 11

Showing 11 citing articles:

The etiology, clinical features, and treatment options of hemifacial microsomia
Songyuan Luo, Hao Sun, Qian Bian, et al.
Oral Diseases (2023) Vol. 29, Iss. 6, pp. 2449-2462
Closed Access | Times Cited: 20
Splicing Defects and Cell Death Cause SF3B2 -Linked Craniofacial Microsomia
Shuyun Rao, Kristin E.N. Watt, Lorena Maili, et al.
Journal of Dental Research (2025)
Closed Access
Functional and Genetic Analyses Unveil the Implication of CDC27 in Hemifacial Microsomia
Wenjie Song, Xin Xia, Yue Fan, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 9, pp. 4707-4707
Open Access | Times Cited: 3
Detailed Analysis of ITPR1 Missense Variants Guides Diagnostics and Therapeutic Design
Jussi‐Pekka Tolonen, Ricardo Parolin Schnekenberg, Simon J. McGowan, et al.
Movement Disorders (2023) Vol. 39, Iss. 1, pp. 141-151
Open Access | Times Cited: 7
Extending the PAX1 spectrum: a dominantly inherited variant causes oculo-auriculo-vertebral syndrome
Shannon Carter, Bridget J. Fellows, Kate Gibson, et al.
European Journal of Human Genetics (2022) Vol. 30, Iss. 10, pp. 1178-1181
Open Access | Times Cited: 7
Hemifacial microsomia is linked to a rare homozygous variant V162I in FRK and validated in zebrafish
Jianjun Xiong, Xi Wang, Chunxin Fan, et al.
Oral Diseases (2022) Vol. 29, Iss. 8, pp. 3472-3480
Closed Access | Times Cited: 5
Exploration of Novel Genetic Evidence and Clinical Significance Into Hemifacial Microsomia Pathogenesis
Xuetong Wang, Yuanhao Chai, Yan Zhang, et al.
Journal of Craniofacial Surgery (2023) Vol. 34, Iss. 2, pp. 834-838
Closed Access | Times Cited: 2
Gene–environment interactions in the pathogenesis of common craniofacial anomalies
Sharien Fitriasari, Paul A. Trainor
Current topics in developmental biology/Current Topics in Developmental Biology (2022), pp. 139-168
Closed Access | Times Cited: 3
ITPR1-Associated Spinocerebellar Ataxia with Craniofacial Features - Additional Evidence for Germline Mosaicism
Robert Kleyner, Nathaniel Ung, Mohammad Arif, et al.
Molecular Case Studies (2023), pp. mcs.a006303-mcs.a006303
Open Access | Times Cited: 1
ITPR1 variant-induced autosomal dominant hereditary spastic paraplegia in a Chinese family
Rui Li, Xuan Liu, Chenming Ke, et al.
Frontiers in Neurology (2024) Vol. 15
Open Access
Extreme-Phenotype Genome-Wide Association Analysis for Growth Traits in Spotted Sea Bass (Lateolabrax maculatus) Using Whole-Genome Resequencing
Zhengkui Zhou, Guangming Shao, Yibo Shen, et al.
Animals (2024) Vol. 14, Iss. 20, pp. 2995-2995
Open Access
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