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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:

DNA Methylation in the Diagnosis of Monogenic Diseases
Flavia Cerrato, Angela Sparago, Francesca Ariani, et al.
Genes (2020) Vol. 11, Iss. 4, pp. 355-355
Open Access | Times Cited: 34

Showing 1-25 of 34 citing articles:

Epigenetic Alterations in the Gastrointestinal Tract: Current and Emerging Use for Biomarkers of Cancer
William M. Grady, Ming Yu, Sanford D. Markowitz
Gastroenterology (2020) Vol. 160, Iss. 3, pp. 690-709
Open Access | Times Cited: 167
The emerging role of chromatin remodelers in neurodevelopmental disorders: a developmental perspective
Britt Mossink, Moritz Negwer, Dirk Schubert, et al.
Cellular and Molecular Life Sciences (2020) Vol. 78, Iss. 6, pp. 2517-2563
Open Access | Times Cited: 79
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance
Maria Vittoria Cubellis, Laura Pignata, Ankit Verma, et al.
Clinical Epigenetics (2020) Vol. 12, Iss. 1
Open Access | Times Cited: 50
Gene-specific somatic epigenetic mosaicism of FDFT1 underlies a non-hereditary localized form of porokeratosis
Sonoko Saito, Yuki Saito, Showbu Sato, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 5, pp. 896-912
Closed Access | Times Cited: 6
Temple syndrome and Kagami-Ogata syndrome: clinical presentations, genotypes, models and mechanisms
Rexxi D. Prasasya, Kristen V Grotheer, Linda D. Siracusa, et al.
Human Molecular Genetics (2020) Vol. 29, Iss. R1, pp. R107-R116
Open Access | Times Cited: 40
Epigenetic alterations in the gastrointestinal tract: Current and emerging use for biomarkers of cancer
William M. Grady
Advances in cancer research (2021), pp. 425-468
Closed Access | Times Cited: 37
DNA methylation episignature testing improves molecular diagnosis of Mendelian chromatinopathies
Jennifer Kerkhof, Gabriella Maria Squeo, Haley McConkey, et al.
Genetics in Medicine (2021) Vol. 24, Iss. 1, pp. 51-60
Open Access | Times Cited: 35
How to Translate DNA Methylation Biomarkers Into Clinical Practice
Wolfgang Wagner
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 26
Neonatal hyperinsulinemic hypoglycemia: case report of kabuki syndrome due to a novel KMT2D splicing-site mutation
Ettore Piro, Ingrid Anne Mandy Schierz, Vincenzo Antona, et al.
˜The œItalian Journal of Pediatrics/Italian journal of pediatrics (2020) Vol. 46, Iss. 1
Open Access | Times Cited: 39
Functional annotation of genomic variation: DNA methylation episignatures in neurodevelopmental Mendelian disorders
Bekim Sadiković, Michael A. Levy, Erfan Aref‐Eshghi
Human Molecular Genetics (2020) Vol. 29, Iss. R1, pp. R27-R32
Open Access | Times Cited: 33
Age-Related Alterations at Neuromuscular Junction: Role of Oxidative Stress and Epigenetic Modifications
Gabriella Dobrowolny, Alessandra Barbiera, Gigliola Sica, et al.
Cells (2021) Vol. 10, Iss. 6, pp. 1307-1307
Open Access | Times Cited: 30
Epigenetic Alterations in Inborn Errors of Immunity
Roberta Romano, Francesca Cillo, Cristina Moracas, et al.
Journal of Clinical Medicine (2022) Vol. 11, Iss. 5, pp. 1261-1261
Open Access | Times Cited: 19
Diagnostic utility of single-locus DNA methylation mark in Sotos syndrome developed by nanopore sequencing-based episignature
Takeshi Mizuguchi, Nobuhiko Okamoto, Taiki Hara, et al.
Clinical Epigenetics (2025) Vol. 17, Iss. 1
Open Access
Diagnostic Utility of Genome-Wide DNA Methylation Analysis in Mendelian Neurodevelopmental Disorders
Sadegheh Haghshenas, Pratibha Bhai, Erfan Aref‐Eshghi, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 23, pp. 9303-9303
Open Access | Times Cited: 32
Chromatin Structure and Dynamics: Focus on Neuronal Differentiation and Pathological Implication
Sophie Nothof, Frédérique Magdinier, Julien Van‐Gils
Genes (2022) Vol. 13, Iss. 4, pp. 639-639
Open Access | Times Cited: 17
Functional categorization of gene regulatory variants that cause Mendelian conditions
Yong-Han Hank Cheng, Stephanie C. Bohaczuk, Andrew B. Stergachis
Human Genetics (2024) Vol. 143, Iss. 4, pp. 559-605
Open Access | Times Cited: 3
Epigenetics of neuromuscular disorders
Fabio Coppedè
Epigenomics (2020) Vol. 12, Iss. 23, pp. 2125-2139
Closed Access | Times Cited: 18
Epigenetic reprogramming in gastrointestinal cancer: biology and translational perspectives
Yingjie Wang, Hongyu Liu, Mengsha Zhang, et al.
MedComm (2024) Vol. 5, Iss. 9
Open Access | Times Cited: 2
Distinguishing genetic alterations versus (epi)mutations in Silver-Russell syndrome and focus on the IGF1R gene
Alessandro Vimercati, Pierpaola Tannorella, Sara Guzzetti, et al.
The Journal of Clinical Endocrinology & Metabolism (2024)
Open Access | Times Cited: 2
The variability of SMCHD1 gene in FSHD patients: evidence of new mutations
Claudia Strafella, Valerio Caputo, Rosaria Maria Galota, et al.
Human Molecular Genetics (2019) Vol. 28, Iss. 23, pp. 3912-3920
Open Access | Times Cited: 15
Evidence of epigenetic landscape shifts in mucopolysaccharidosis IIIB and IVA
Viviana Vargas-López, Luisa F. Prada, Carlos Javier Alméciga-Díaz
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Advancing the Clinical and Molecular Understanding of Cornelia de Lange Syndrome: A Multidisciplinary Pediatric Case Series and Review of the Literature
Karolina Gruca-Stryjak, Emilia Doda-Nowak, Julia Dzierla, et al.
Journal of Clinical Medicine (2024) Vol. 13, Iss. 8, pp. 2423-2423
Open Access | Times Cited: 1
Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases
Pierpaola Tannorella, Daniele Minervino, Sara Guzzetti, et al.
Genes (2021) Vol. 12, Iss. 4, pp. 588-588
Open Access | Times Cited: 10
Age-related trajectories of DNA methylation network markers: a parenclitic network approach to a family-based cohort of patients with Down Syndrome
Mikhail Krivonosov, Tatiana Nazarenko, Maria Giulia Bacalini, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 6
Severe developmental expressive language disorder due to a frameshift mutation in exon 18 of SRCAP gene, far away from the mutational hotspot in exons 33 and 34 associated to the Floating-Harbor syndrome
Enrique Nogueira, Carmen Garma, Concepción Lobo, et al.
Neurological Sciences (2021) Vol. 42, Iss. 10, pp. 4349-4352
Closed Access | Times Cited: 5
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