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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:

Understanding the basis of auriculocondylar syndrome: Insights from human, mouse and zebrafish genetic studies
David E. Clouthier, Maria Rita Passos‐Bueno, André L. P. Tavares, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2013) Vol. 163, Iss. 4, pp. 306-317
Open Access | Times Cited: 55

Showing 26-50 of 55 citing articles:

Differing contributions of the first and second pharyngeal arches to tympanic membrane formation in the mouse and chick
Toshiko Furutera, Masaki Takechi, Taro Kitazawa, et al.
Development (2017) Vol. 144, Iss. 18, pp. 3315-3324
Open Access | Times Cited: 15
Genomic Analysis of Spontaneous Abortion in Holstein Heifers and Primiparous Cows
Kayleen F. Oliver, Alexandria Wahl, Mataya Dick, et al.
Genes (2019) Vol. 10, Iss. 12, pp. 954-954
Open Access | Times Cited: 14
Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndrome
Vanessa Luiza Romanelli Tavares, Roseli Maria Zechi‐Ceide, Débora Romeo Bertola, et al.
American Journal of Medical Genetics Part A (2017) Vol. 173, Iss. 4, pp. 938-945
Closed Access | Times Cited: 14
Modeling craniofacial development reveals spatiotemporal constraints on robust patterning of the mandibular arch
Lina Meinecke, Praveer Sharma, Huijing Du, et al.
PLoS Computational Biology (2018) Vol. 14, Iss. 11, pp. e1006569-e1006569
Open Access | Times Cited: 14
A Mouse Splice-Site Mutant and Individuals with Atypical Chromosome 22q11.2 Deletions Demonstrate the Crucial Role for Crkl in Craniofacial and Pharyngeal Development
Kerry A. Miller, Tiong Yang Tan, Megan F. Welfare, et al.
Molecular Syndromology (2014) Vol. 5, Iss. 6, pp. 276-286
Open Access | Times Cited: 11
Regulating Craniofacial Development at the 3′ End
André L. P. Tavares, Kristin Artinger, David E. Clouthier
Current topics in developmental biology/Current Topics in Developmental Biology (2015), pp. 335-375
Closed Access | Times Cited: 11
Loss‐of‐function of Endothelin receptor type A results in Oro‐Oto‐Cardiac syndrome
Amanda Barone Pritchard, Stanley M. Kanai, Bryan L. Krock, et al.
American Journal of Medical Genetics Part A (2020) Vol. 182, Iss. 5, pp. 1104-1116
Open Access | Times Cited: 11
Developmental mechanisms of the tympanic membrane in mammals and non‐mammalian amniotes
Masaki Takechi, Taro Kitazawa, Tatsuya Hirasawa, et al.
Congenital Anomalies (2015) Vol. 56, Iss. 1, pp. 12-17
Open Access | Times Cited: 9
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
Nkx2.5 regulates endothelin converting enzyme‐1 during pharyngeal arch patterning
Jennifer M. Iklé, André L. P. Tavares, M S King, et al.
genesis (2017) Vol. 55, Iss. 3
Open Access | Times Cited: 9
Mandibulofacial dysostosis with alopecia results from ETAR gain-of-function mutations via allosteric effects on ligand binding
Yukiko Kurihara, Toru Ekimoto, Christopher T. Gordon, et al.
Journal of Clinical Investigation (2023) Vol. 133, Iss. 4
Open Access | Times Cited: 3
The association of severe encephalopathy and question mark ear is highly suggestive of loss of MEF2C function
Christopher T. Gordon, Aude Tessier, Zeynep Demir, et al.
Clinical Genetics (2017) Vol. 93, Iss. 2, pp. 356-359
Closed Access | Times Cited: 7
A novel missense variant of the GNAI3 gene and recognisable morphological characteristics of the mandibula in ARCND1
Kumiko Yanagi, Noriko Morimoto, Manami Iso, et al.
Journal of Human Genetics (2021) Vol. 66, Iss. 10, pp. 1029-1034
Open Access | Times Cited: 7
Prenatal diagnosis of auriculocondylar syndrome with a novel missense variant of GNAI3: a case report
Xiaoliang Liu, Wei Sun, Jun Wang, et al.
BMC Pregnancy and Childbirth (2021) Vol. 21, Iss. 1
Open Access | Times Cited: 7
Viable Ednra Y129F mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation
Sibylle Sabrautzki, Michael A. Sandholzer, Bettina Lorenz‐Depiereux, et al.
Mammalian Genome (2016) Vol. 27, Iss. 11-12, pp. 587-598
Open Access | Times Cited: 6
Genetic factors in isolated and syndromic laryngeal cleft
Youjin Li, Xiaoqing Rui, Niu Li
Paediatric Respiratory Reviews (2019) Vol. 33, pp. 24-27
Closed Access | Times Cited: 6
Evolution of Zebrafish as a Novel Pharmacological Model in Endocrine Research
Umashanker Navik, Pushkar Singh Rawat, Prince Allawadhi, et al.
(2022), pp. 93-141
Closed Access | Times Cited: 4
Cyclophilin A as a Pro-Inflammatory Factor Exhibits Embryotoxic and Teratogenic Effects during Fetal Organogenesis
A. A. Kalinina, М. L. Semenova, Alexandra V. Bruter, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 14, pp. 11279-11279
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
New locus underlying auriculocondylar syndrome (ARCND): 430 kb duplication involvingTWIST1regulatory elements
Vanessa Luiza Romanelli Tavares, Sofia Ligia Guimarães-Ramos, Yan Zhou, et al.
Journal of Medical Genetics (2021) Vol. 59, Iss. 9, pp. 895-905
Open Access | Times Cited: 5
The crucial role of model systems in understanding the complexity of cell signaling in human neurocristopathies
Santiago Cerrizuela, Guillermo A. Vega‐López, Karla Méndez‐Maldonado, et al.
WIREs Mechanisms of Disease (2021) Vol. 14, Iss. 1
Closed Access | Times Cited: 5
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
Expression analysis of genes including Zfhx4 in mice and zebrafish reveals a temporospatial conserved molecular basis underlying craniofacial development
S. Liu, Lin Xu, Makoto Kashima, et al.
Developmental Dynamics (2024)
Open Access
A Novel Homozygous Frameshift Mutation in the PLCB4 Gene Associated with Auriculocondylar Syndrome 2 and Accompanied by Mild Intellectual Disability
Gülsüm KAYHAN, Hasan Hüseyin Kazan, Kübra OZTÜRK, et al.
Turkiye Klinikleri Journal of Case Reports (2022) Vol. 30, Iss. 4, pp. 258-262
Open Access | Times Cited: 1
Molecular Mechanism of Cranial Neural Crest Cell Development
Akiko Suzuki, Dhruvee R. Sangani, Junichi Iwata
(2014)
Closed Access

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