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:
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
Christopher T. Gordon, Aude Tessier, Zeynep Demir, et al.
Clinical Genetics (2017) Vol. 93, Iss. 2, pp. 356-359
Closed Access | Times Cited: 7
Showing 7 citing articles:
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
Y L Zhang, Yuwei Zhao, Liying Dai, et al.
Molecular Genetics & Genomic Medicine (2024) Vol. 12, Iss. 4
Open Access | Times Cited: 3
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
Nancy Végas, Zeynep Demir, Christopher T. Gordon, et al.
Human Mutation (2022) Vol. 43, Iss. 5, pp. 582-594
Open Access | Times Cited: 13
Comprehensive investigation of the phenotype of MEF2C‐related disorders in human patients: A systematic review
Jessica A. Cooley Coleman, Sara M. Sarasua, Luigi Boccuto, et al.
American Journal of Medical Genetics Part A (2021) Vol. 185, Iss. 12, pp. 3884-3894
Closed Access | Times Cited: 17
Jessica A. Cooley Coleman, Sara M. Sarasua, Luigi Boccuto, et al.
American Journal of Medical Genetics Part A (2021) Vol. 185, Iss. 12, pp. 3884-3894
Closed Access | Times Cited: 17
Variable paralog expression underlies phenotype variation
Raisa Bailon‐Zambrano, Juliana Sucharov, Abigail Mumme-Monheit, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 11
Raisa Bailon‐Zambrano, Juliana Sucharov, Abigail Mumme-Monheit, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 11
Selective breeding modifies mef2ca mutant incomplete penetrance by tuning the opposing Notch pathway
Juliana Sucharov, Kuval Ray, Elliott P. Brooks, et al.
PLoS Genetics (2019) Vol. 15, Iss. 12, pp. e1008507-e1008507
Open Access | Times Cited: 13
Juliana Sucharov, Kuval Ray, Elliott P. Brooks, et al.
PLoS Genetics (2019) Vol. 15, Iss. 12, pp. e1008507-e1008507
Open Access | Times Cited: 13
A Technique of Autologous Costal Cartilage Graft Combined With Auricular Cartilage Folding to Correct Question Mark Ear in a Single Procedure
Bei He, Bingqing Wang, Qingguo Zhang
Ear Nose & Throat Journal (2024)
Open Access
Bei He, Bingqing Wang, Qingguo Zhang
Ear Nose & Throat Journal (2024)
Open Access
Variable paralog expression underlies phenotype variation
Raisa Bailon‐Zambrano, Juliana Sucharov, Abigail Mumme-Monheit, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
Raisa Bailon‐Zambrano, Juliana Sucharov, Abigail Mumme-Monheit, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
