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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:

Autosomal recessive Treacher Collins syndrome due to POLR1C mutations: Report of a new family and review of the literature
Leïla Ghesh, Marie Vincent, Anne‐Sophie Delemazure, et al.
American Journal of Medical Genetics Part A (2019) Vol. 179, Iss. 7, pp. 1390-1394
Closed Access | Times Cited: 19

Showing 19 citing articles:

Clinical spectrum of POLR3-related leukodystrophy caused by biallelic POLR1C pathogenic variants
Laurence Gauquelin, Ferdy Kurniawan Cayami, László Sztriha, et al.
Neurology Genetics (2019) Vol. 5, Iss. 6
Open Access | Times Cited: 45
A systematic review on Treacher Collins syndrome: Correlation between molecular genetic findings and clinical severity
Zulvikar Syambani Ulhaq, Dian Kesumapramudya Nurputra, Gita Vita Soraya, et al.
Clinical Genetics (2022) Vol. 103, Iss. 2, pp. 146-155
Closed Access | Times Cited: 24
Diabetes, Oxidative Stress, and DNA Damage Modulate Cranial Neural Crest Cell Development and the Phenotype Variability of Craniofacial Disorders
Sharien Fitriasari, Paul A. Trainor
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 22
A novel intronic TCOF1 pathogenic variant in a Chinese family with Treacher Collins syndrome
Haojie Sun, Xinda Xu, Binjun Chen, et al.
BMC Medical Genomics (2024) Vol. 17, Iss. 1
Open Access | Times Cited: 2
Systematic Review of Current Audiological Treatment Options for Patients with Treacher Collins Syndrome (TCS) and Surgical and Audiological Experiences of an Otorhinolaryngologist with TCS
Ivana Marinac, Robert Trotić, Andro Košec
Journal of Personalized Medicine (2024) Vol. 14, Iss. 1, pp. 81-81
Open Access | Times Cited: 1
p53 inhibitor or antioxidants reduce the severity of ethmoid plate deformities in zebrafish Type 3 Treacher Collins syndrome model
Zulvikar Syambani Ulhaq, May‐Su You, Yun‐Jin Jiang, et al.
International Journal of Biological Macromolecules (2024) Vol. 266, pp. 131216-131216
Closed Access | Times Cited: 1
Pan-cancer integrated bioinformatic analysis of RNA polymerase subunits reveal RNA Pol I member CD3EAP regulates cell growth by modulating autophagy
Nikita Bhandari, Disha Acharya, Annesha Chatterjee, et al.
Cell Cycle (2023) Vol. 22, Iss. 18, pp. 1986-2002
Closed Access | Times Cited: 3
Genetics and Epigenetics in the Genesis and Development of Microtia
Xin Chen, Jing Ma, Tianyu Zhang
Journal of Craniofacial Surgery (2024)
Open Access
Nubp2 is required for cranial neural crest survival in the mouse
Andrew DiStasio, David Paulding, Praneet Chaturvedi, et al.
Developmental Biology (2019) Vol. 458, Iss. 2, pp. 189-199
Open Access | Times Cited: 3
Description of Total Population Hospital Admissions for Treacher Collins Syndrome in Australia
Mohammed Junaid, Linda Slack‐Smith, Kingsley Wong, et al.
The Cleft Palate-Craniofacial Journal (2021) Vol. 59, Iss. 9, pp. 1167-1175
Closed Access | Times Cited: 3
Prevention methods for Treacher Collins syndrome: A systematic review
Peipei Guo, Bo Pan, Haiyue Jiang, et al.
International Journal of Pediatric Otorhinolaryngology (2020) Vol. 134, pp. 110062-110062
Closed Access | Times Cited: 2
16p12.1 deletion orthologs are expressed in motile neural crest cells and are important for regulating craniofacial development inXenopus laevis
Micaela Lasser, Jessica Bolduc, Luke Murphy, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 2
circPOLR1C Promotes the Development of Esophageal Cancer by Adsorbing miR-361-3p and Regulating Cancer Cell Apoptosis and Metastasis
Yong Fang, Jun Yin, Yaxing Shen, et al.
Journal of Oncology (2022) Vol. 2022, pp. 1-20
Open Access | Times Cited: 1
A novelde novohemizygousARHGEF9mutation associated with severe intellectual disability and epilepsy: a case report
Tong Qiu, Qian Dai, Qiu Wang
Journal of International Medical Research (2021) Vol. 49, Iss. 11
Open Access | Times Cited: 1
Distinct Interaction Modes for the Eukaryotic RNA Polymerase Alpha-like Subunits
Alana E. Belkevich, Haleigh G. Pascual, Aula M. Fakhouri, et al.
Molecular and Cellular Biology (2023) Vol. 43, Iss. 6, pp. 269-282
Open Access
Nubp2is required for cranial neural crest survival in the mouse
Andrew DiStasio, David Paulding, Praneet Chatuverdi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2019)
Open Access
A Novel Missense Variant in the TCOF1 Gene in one Chinese Case With Treacher Collins Syndrome
Bin Yin, Yu-Ya Pang, Jiayu Shi, et al.
The Cleft Palate-Craniofacial Journal (2022) Vol. 61, Iss. 2, pp. 192-199
Closed Access
[Three-dimensional measurement analysis of midface morphology in Treacher Collins syndromes].
Yanxian Lin, Xiaoyang Ma, Yuanliang Huang, et al.
PubMed (2021) Vol. 35, Iss. 1, pp. 86-94
Closed Access
Early Clinical Investigations and Management of Syndromes Affecting Craniofacial and Dental Structures
Theodosia Bartzela
Springer eBooks (2021), pp. 271-297
Closed Access
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