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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:

Beyond the Exome: The Non-coding Genome and Enhancers in Neurodevelopmental Disorders and Malformations of Cortical Development
Elena Perenthaler, Soheil Yousefi, Eva Niggl, et al.
Frontiers in Cellular Neuroscience (2019) Vol. 13
Open Access | Times Cited: 67

Showing 1-25 of 67 citing articles:

The Spectrum of PAX6 Mutations and Genotype-Phenotype Correlations in the Eye
Dulce Lima Cunha, Gavin Arno, Marta Cortón, et al.
Genes (2019) Vol. 10, Iss. 12, pp. 1050-1050
Open Access | Times Cited: 160
Recommendations for clinical interpretation of variants found in non-coding regions of the genome
Jamie M. Ellingford, Joo Wook Ahn, Richard D. Bagnall, et al.
Genome Medicine (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 138
International consensus recommendations on the diagnostic work-up for malformations of cortical development
Renske Oegema, Tahsin Stefan Barakat, Martina Wilke, et al.
Nature Reviews Neurology (2020) Vol. 16, Iss. 11, pp. 618-635
Open Access | Times Cited: 98
Mapping the molecular and cellular complexity of cortical malformations
Esther Klingler, Fiona Francis, Denis Jabaudon, et al.
Science (2021) Vol. 371, Iss. 6527
Open Access | Times Cited: 94
Impact of predictive, preventive and precision medicine strategies in epilepsy
Rima Nabbout, Mathieu Kuchenbuch
Nature Reviews Neurology (2020) Vol. 16, Iss. 12, pp. 674-688
Closed Access | Times Cited: 77
Learning interpretable cellular and gene signature embeddings from single-cell transcriptomic data
Yifan Zhao, Huiyu Cai, Zuobai Zhang, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 69
The landscape of GWAS validation; systematic review identifying 309 validated non-coding variants across 130 human diseases
Ammar J. Alsheikh, Sabrina Wollenhaupt, Emily A. King, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 54
Recent advances in epilepsy genomics and genetic testing
Malavika Hebbar, Heather C. Mefford
F1000Research (2020) Vol. 9, pp. 185-185
Open Access | Times Cited: 69
Interpreting the impact of noncoding structural variation in neurodevelopmental disorders
Eva D’haene, Sarah Vergult
Genetics in Medicine (2020) Vol. 23, Iss. 1, pp. 34-46
Open Access | Times Cited: 53
Re‐analysis of whole genome sequencing ends a diagnostic odyssey: Case report of an RNU4‐2 related neurodevelopmental disorder
Rachel Schot, Federico Ferraro, Geert Geeven, et al.
Clinical Genetics (2024) Vol. 106, Iss. 4, pp. 512-517
Open Access | Times Cited: 7
Tetrahedral DNA nanostructures enhance transcription isothermal amplification for multiplex detection of non-coding RNAs
Eun Sung Lee, Ji-Su Woo, Jiye Shin, et al.
Biosensors and Bioelectronics (2024) Vol. 250, pp. 116055-116055
Closed Access | Times Cited: 6
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases
Elena Perenthaler, Anita Nikoncuk, Soheil Yousefi, et al.
Acta Neuropathologica (2019) Vol. 139, Iss. 3, pp. 415-442
Open Access | Times Cited: 54
BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms
Scott Barish, Tahsin Stefan Barakat, Brittany C. Michel, et al.
The American Journal of Human Genetics (2020) Vol. 107, Iss. 6, pp. 1096-1112
Open Access | Times Cited: 42
An epigenome atlas of neural progenitors within the embryonic mouse forebrain
Christopher T. Rhodes, Joyce J. Thompson, Apratim Mitra, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 26
Advances in Genomics for Drug Development
Roberto Spreafico, Leah Soriaga, Jirka Grosse, et al.
Genes (2020) Vol. 11, Iss. 8, pp. 942-942
Open Access | Times Cited: 39
Parallel functional testing identifies enhancers active in early postnatal mouse brain
Jason T. Lambert, Linda Su-Feher, Karol Cichewicz, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 32
The Emerging Role of Mitochondrial Dysfunction in the Pathogenesis of Idiopathic Inflammatory Myopathies
Jorge A. González-Chapa, Marina Barguil Macêdo, Christian Lood
Rambam Maimonides Medical Journal (2023) Vol. 14, Iss. 2, pp. e0006-e0006
Open Access | Times Cited: 12
Pseudogenes in Cancer: State of the Art
Arturo Kenzuke Nakamura-García, Jesús Espinal‐Enríquez
Cancers (2023) Vol. 15, Iss. 16, pp. 4024-4024
Open Access | Times Cited: 11
Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneity
Elena Cellini, Annalisa Vetro, Valerio Conti, et al.
European Journal of Human Genetics (2019) Vol. 27, Iss. 6, pp. 909-918
Open Access | Times Cited: 30
Differential analysis of chromatin accessibility and gene expression profiles identifies cis-regulatory elements in rat adipose and muscle
Venugopalan D. Nair, Mital Vasoya, Vishnu Nair, et al.
Genomics (2021) Vol. 113, Iss. 6, pp. 3827-3841
Open Access | Times Cited: 24
The non-coding genome in Autism Spectrum Disorders
S. Dominguez-Alonso, Ángel Carracedo, Cristina Rodriguez‐Fontenla
European Journal of Medical Genetics (2023) Vol. 66, Iss. 6, pp. 104752-104752
Open Access | Times Cited: 10
Artificial intelligence-based approaches for the detection and prioritization of genomic mutations in congenital surgical diseases
Qiongfen Lin, Paul Kwong‐Hang Tam, Clara Sze-Man Tang
Frontiers in Pediatrics (2023) Vol. 11
Open Access | Times Cited: 9
DeepRegFinder: deep learning-based regulatory elements finder
Aarthi Ramakrishnan, George Wangensteen, Sarah Kim, et al.
Bioinformatics Advances (2024) Vol. 4, Iss. 1
Open Access | Times Cited: 3
Deciphering congenital anomalies for the next generation
Monica H. Wojcik, Pankaj B. Agrawal
Molecular Case Studies (2020) Vol. 6, Iss. 5, pp. a005504-a005504
Open Access | Times Cited: 22
Profiling of Chromatin Accessibility in Pigs across Multiple Tissues and Developmental Stages
Jingyi Bai, Yu Lin, Jiaman Zhang, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 13, pp. 11076-11076
Open Access | Times Cited: 7
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