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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:

Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect
Vanessa Luiza Romanelli Tavares, Christopher T. Gordon, Roseli Maria Zechi‐Ceide, et al.
European Journal of Human Genetics (2014) Vol. 23, Iss. 4, pp. 481-485
Open Access | Times Cited: 31

Showing 1-25 of 31 citing articles:

Neurocristopathies: New insights 150 years after the neural crest discovery
Guillermo A. Vega‐López, Santiago Cerrizuela, Celeste Tríbulo, et al.
Developmental Biology (2018) Vol. 444, pp. S110-S143
Open Access | Times Cited: 180
Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology
John R. Shaffer, Ekaterina Orlova, Myoung Keun Lee, et al.
PLoS Genetics (2016) Vol. 12, Iss. 8, pp. e1006149-e1006149
Open Access | Times Cited: 159
Mutations in the Endothelin Receptor Type A Cause Mandibulofacial Dysostosis with Alopecia
Christopher T. Gordon, K. Nicole Weaver, Roseli Maria Zechi‐Ceide, et al.
The American Journal of Human Genetics (2015) Vol. 96, Iss. 4, pp. 519-531
Open Access | Times Cited: 44
Dominant-negative Gα subunits are a mechanism of dysregulated heterotrimeric G protein signaling in human disease
Arthur Marivin, Anthony Leyme, Kshitij Parag‐Sharma, et al.
Science Signaling (2016) Vol. 9, Iss. 423
Open Access | Times Cited: 35
GNAI3 mediated by Lin28A regulates lipopolysaccharide-induced inflammation and osteogenic differentiation in periodontal stem cells by mediating the NF-κB/NLRP3 inflammasome pathway
Ling Guo, Hua Sun, Jiao Pu
Archives of Oral Biology (2024) Vol. 163, pp. 105974-105974
Closed Access | Times Cited: 3
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
Role of GATA binding protein 4 (GATA4) in the regulation of tooth development via GNAI3
Shuyu Guo, Yuxin Zhang, Tingting Zhou, et al.
Scientific Reports (2017) Vol. 7, Iss. 1
Open Access | Times Cited: 25
Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases
Nancy Végas, Zeynep Demir, Christopher T. Gordon, et al.
Human Mutation (2022) Vol. 43, Iss. 5, pp. 582-594
Open Access | Times Cited: 13
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
Respiratory and gastrointestinal dysfunctions associated with auriculo‐condylar syndrome and a homozygous PLCB4 loss‐of‐function mutation
Chiara Leoni, Christopher T. Gordon, Giacomo Della Marca, et al.
American Journal of Medical Genetics Part A (2016) Vol. 170, Iss. 6, pp. 1471-1478
Closed Access | Times Cited: 19
Wdr68 Mediates Dorsal and Ventral Patterning Events for Craniofacial Development
Estibaliz Alvarado, Mina Yousefelahiyeh, Greg Alvarado, et al.
PLoS ONE (2016) Vol. 11, Iss. 11, pp. e0166984-e0166984
Open Access | Times Cited: 19
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
Endothelin signaling in development
Stanley M. Kanai, David E. Clouthier
Development (2023) Vol. 150, Iss. 24
Open Access | Times Cited: 5
DCAF7/WDR68 is required for normal levels of DYRK1A and DYRK1B
Mina Yousefelahiyeh, Jingyi Xu, Estibaliz Alvarado, et al.
PLoS ONE (2018) Vol. 13, Iss. 11, pp. e0207779-e0207779
Open Access | Times Cited: 15
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
Deciphering the function of the fifth class of Gα proteins: regulation of ionic homeostasis as unifying hypothesis
Asmaa A. Abu Obaid, Ivan Ivandić, Sigrun I. Korsching
Cellular and Molecular Life Sciences (2024) Vol. 81, Iss. 1
Open Access | Times Cited: 1
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
Autoregulatory circuit regulating basolateral cargo export from the TGN: role of the orphan receptor GPRC5A in PKD signaling and cell polarity
Rosaria Di Martino, Anita Capalbo, Lucia Sticco, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 9
Genetic analysis of 55 cases with fetal skeletal dysplasia
Ying Bai, Yue Sun, Ning Liu, et al.
Orphanet Journal of Rare Diseases (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 6
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
Guanine and nucleotide binding protein 3 promotes odonto/osteogenic differentiation of apical papilla stem cells via JNK and ERK signaling pathways
Yang Zhang, Lichan Yuan, Meng Li, et al.
International Journal of Molecular Medicine (2018)
Open Access | Times Cited: 6
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 Genetics of Facial Morphology
Joanne B. Cole, Richard A. Spritz
Encyclopedia of Life Sciences (2017), pp. 1-9
Closed Access | Times Cited: 3
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
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