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:

Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711
Jiyong Wang, Aidin Foroutan, Ellen Richardson, et al.
European Journal of Human Genetics (2022) Vol. 30, Iss. 4, pp. 420-427
Open Access | Times Cited: 14

Showing 14 citing articles:

Electroencephalographic and Epilepsy Findings in ZNF711 Variants: A Case Series of Two Siblings
Michele Minerva, Lorenzo Perilli, Samanta Carbone, et al.
Neurology International (2025) Vol. 17, Iss. 1, pp. 14-14
Open Access

Cardiac differentiation roadmap for analysis of plasticity and balanced lineage commitment
Rebecca R. Snabel, Carla Cofiño‐Fabrés, Marijke P. Baltissen, et al.
Stem Cell Reports (2025), pp. 102422-102422
Open Access

Formerly degenerate seventh zinc finger domain from transcription factor ZNF711 rehabilitated by experimental NMR structure
Antonio J. Rua, Andrei T. Alexandrescu
Protein Science (2024) Vol. 33, Iss. 9
Closed Access | Times Cited: 2

Regulatory Start-Stop Elements in 5’ Untranslated Regions Pervasively Modulate Translation
Justin Rendleman, Solomon A. Haizel, Shaohuan Wu, et al.
(2023)
Open Access | Times Cited: 3

Genome-wide CNV analysis uncovers novel pathogenic regions in cohort of five multiplex families with neurodevelopmental disorders
Behjat Ul Mudassir, Mashael Alhumaidi Alotaibi, Nadeem Kizilbash, et al.
Heliyon (2023) Vol. 9, Iss. 9, pp. e19718-e19718
Open Access | Times Cited: 2

Clinical findings in individuals with duplication of genes associated with X‐linked intellectual disability
Nikhil Sahajpal, Catherine A. Ziats, Alka Chaubey, et al.
Clinical Genetics (2023) Vol. 105, Iss. 2, pp. 173-184
Closed Access | Times Cited: 2

No April fools in clinical genomics
Alisdair McNeill
European Journal of Human Genetics (2022) Vol. 30, Iss. 4, pp. 389-390
Open Access | Times Cited: 3

Regulatory start-stop elements in 5’ untranslated regions pervasively modulate translation
Justin Rendleman, Solomon A. Haizel, Shaohuan Wu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 4

Single-cell roadmap of cardiac differentiation identifies roles for ZNF711 and retinoic acid in balanced epicardial and cardiomyocyte lineage commitment
Rebecca R. Snabel, Carla Cofiño‐Fabrés, Marijke P. Baltissen, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access

Contiguous Gene Syndromes and Hearing Loss: A Clinical Report of Xq21 Deletion and Comprehensive Literature Review
Maria Teresa Bonati, Agnese Feresin, Paolo Prontera, et al.
Genes (2024) Vol. 15, Iss. 6, pp. 677-677
Open Access

Elucidation of the Gene Regulatory Network Related to Spinal Muscular Atrophy
Kerui Huang, Yazhou Huang, Xingxin Fang, et al.
Cytology and Genetics (2024) Vol. 58, Iss. 6, pp. 615-626
Closed Access

ZNF711 puts a spell on DNA
R. Frank Kooy
European Journal of Human Genetics (2022) Vol. 30, Iss. 4, pp. 396-397
Open Access | Times Cited: 2

Identification of DCAF1 by Clinical Exome Sequencing and Methylation Analysis as a Candidate Gene for Autism and Intellectual Disability: A Case Report
Jeffery L. Clothier, Amy Grooms, Patricia Porter‐Gill, et al.
Journal of Personalized Medicine (2022) Vol. 12, Iss. 6, pp. 886-886
Open Access | Times Cited: 1

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