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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 1-25 of 55 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
News from the endothelin-3/EDNRB signaling pathway: Role during enteric nervous system development and involvement in neural crest-associated disorders
Nadège Bondurand, Sylvie Dufour, Véronique Pingault
Developmental Biology (2018) Vol. 444, pp. S156-S169
Open Access | Times Cited: 71
Zebrafish Models of Human Skeletal Disorders: Embryo and Adult Swimming Together
Marta Carnovali, Giuseppe Banfi, Massimo Mariotti
BioMed Research International (2019) Vol. 2019, pp. 1-13
Open Access | Times Cited: 68
Neural crest contributions to the ear: Implications for congenital hearing disorders
Kristina Ritter, Donna M. Martin
Hearing Research (2018) Vol. 376, pp. 22-32
Open Access | Times Cited: 51
Negative regulation of Endothelin signaling by SIX1 is required for proper maxillary development
André L. P. Tavares, Timothy C. Cox, Robert Maxson, et al.
Development (2017)
Open Access | Times Cited: 49
The ontogeny of Robin sequence
Robrecht J. H. Logjes, Corstiaan C. Breugem, Gijs van Haaften, et al.
American Journal of Medical Genetics Part A (2018) Vol. 176, Iss. 6, pp. 1349-1368
Open Access | Times Cited: 49
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
Systems biology of facial development: contributions of ectoderm and mesenchyme
Joan E. Hooper, Weiguo Feng, Hong Li, et al.
Developmental Biology (2017) Vol. 426, Iss. 1, pp. 97-114
Open Access | Times Cited: 43
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
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
Hand1 phosphoregulation within the distal arch neural crest is essential for craniofacial morphogenesis
Beth A. Firulli, Robyn K. Fuchs, Joshua W. Vincentz, et al.
Development (2014) Vol. 141, Iss. 15, pp. 3050-3061
Open Access | Times Cited: 31
MicroRNA Profiling during Craniofacial Development: Potential Roles for Mir23b and Mir133b
Hai‐Lei Ding, Joan E. Hooper, Peter Batzel, et al.
Frontiers in Physiology (2016) Vol. 7
Open Access | Times Cited: 31
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
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
Meta-analysis of genome-wide association studies for litter size in sheep
Mohsen Gholizadeh, Seyed Mehdi Esmaeili-Fard
Theriogenology (2021) Vol. 180, pp. 103-112
Open Access | Times Cited: 20
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
Recapitulation of Neural Crest Specification and EMT via Induction from Neural Plate Border-like Cells
Gerson Shigeru Kobayashi, Camila Manso Musso, Danielle de Paula Moreira, et al.
Stem Cell Reports (2020) Vol. 15, Iss. 3, pp. 776-788
Open Access | Times Cited: 20
Whole-genome resequencing reveals selection signatures for caviar yield in Russian sturgeon (Acipenser gueldenstaedtii)
Hailiang Song, Boyu Zhu, Dong Tian, et al.
Aquaculture (2023) Vol. 568, pp. 739312-739312
Closed Access | Times Cited: 7
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
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
vwa1 Knockout in Zebrafish Causes Abnormal Craniofacial Chondrogenesis by Regulating FGF Pathway
Xiaomin Niu, Fuyu Zhang, Lu Ping, et al.
Genes (2023) Vol. 14, Iss. 4, pp. 838-838
Open Access | Times Cited: 6
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
Endothelin signaling in development
Stanley M. Kanai, David E. Clouthier
Development (2023) Vol. 150, Iss. 24
Open Access | Times Cited: 5
Cre recombinase-regulated Endothelin1 transgenic mouse lines: Novel tools for analysis of embryonic and adult disorders
André L. P. Tavares, David E. Clouthier
Developmental Biology (2015) Vol. 400, Iss. 2, pp. 191-201
Open Access | Times Cited: 15
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