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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:

Frameshift mutations at the C-terminus of HIST1H1E result in a specific DNA hypomethylation signature
Andrea Ciolfi, Erfan Aref‐Eshghi, Simone Pizzi, et al.
Clinical Epigenetics (2020) Vol. 12, Iss. 1
Open Access | Times Cited: 45

Showing 1-25 of 45 citing articles:

Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders
Erfan Aref‐Eshghi, Jennifer Kerkhof, Victor P. Pedro, et al.
The American Journal of Human Genetics (2020) Vol. 106, Iss. 3, pp. 356-370
Open Access | Times Cited: 246
The interplay between DNA and histone methylation: molecular mechanisms and disease implications
Yinglu Li, Xiao Chen, Chao Lü
EMBO Reports (2021) Vol. 22, Iss. 5
Open Access | Times Cited: 149
Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders
Bekim Sadiković, Michael A. Levy, Jennifer Kerkhof, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 6, pp. 1065-1074
Open Access | Times Cited: 147
Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders
Michael A. Levy, Haley McConkey, Jennifer Kerkhof, et al.
Human Genetics and Genomics Advances (2021) Vol. 3, Iss. 1, pp. 100075-100075
Open Access | Times Cited: 117
Host methylation predicts SARS-CoV-2 infection and clinical outcome
Iain R. Konigsberg, Bret Barnes, Monica Campbell, et al.
Communications Medicine (2021) Vol. 1, Iss. 1
Open Access | Times Cited: 59
Functional correlation of genome‐wide DNA methylation profiles in genetic neurodevelopmental disorders
Michael A. Levy, Raissa Relator, Haley McConkey, et al.
Human Mutation (2022) Vol. 43, Iss. 11, pp. 1609-1628
Open Access | Times Cited: 49
Anatomy of DNA methylation signatures: Emerging insights and applications
Eric Chater‐Diehl, Sarah J. Goodman, Cheryl Cytrynbaum, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 8, pp. 1359-1366
Open Access | Times Cited: 45
Premature aging disorders: A clinical and genetic compendium
Franziska Schnabel, Uwe Kornak, Bernd Wollnik
Clinical Genetics (2020) Vol. 99, Iss. 1, pp. 3-28
Open Access | Times Cited: 44
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
Integrative omics approaches to advance rare disease diagnostics
Dmitrii Smirnov, Nikita Konstantinovskiy, Holger Prokisch
Journal of Inherited Metabolic Disease (2023) Vol. 46, Iss. 5, pp. 824-838
Open Access | Times Cited: 11
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
Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile
Andrea Ciolfi, Aidin Foroutan, Alessandro Capuano, et al.
Clinical Epigenetics (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 25
Identification of a DNA Methylation Episignature in the 22q11.2 Deletion Syndrome
Kathleen Rooney, Michael A. Levy, Sadegheh Haghshenas, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 16, pp. 8611-8611
Open Access | Times Cited: 24
DNA methylation profiling in Kabuki syndrome: reclassification of germline KMT2D VUS and sensitivity in validating postzygotic mosaicism
Marcello Niceta, Andrea Ciolfi, Marco Ferilli, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 7, pp. 819-826
Closed Access | Times Cited: 3
DNA Methylation Profiling for Diagnosing Undifferentiated Sarcoma with Capicua Transcriptional Receptor (CIC) Alterations
Evelina Miele, Rita De Vito, Andrea Ciolfi, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 5, pp. 1818-1818
Open Access | Times Cited: 25
Histone H1 regulates non-coding RNA turnover on chromatin in a m6A-dependent manner
José Miguel Fernández-Justel, Cristina Santa-María, Sara Martín-Vírgala, et al.
Cell Reports (2022) Vol. 40, Iss. 11, pp. 111329-111329
Open Access | Times Cited: 14
Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood
Michael A. Levy, David B. Beck, Kay Metcalfe, et al.
npj Genomic Medicine (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 19
Chiari 1 malformation and exome sequencing in 51 trios: the emerging role of rare missense variants in chromatin-remodeling genes
Aldesia Provenzano, Andrea La Barbera, Mirko Scagnet, et al.
Human Genetics (2020) Vol. 140, Iss. 4, pp. 625-647
Open Access | Times Cited: 16
Reprogramming of the epigenome in neurodevelopmental disorders
Khadija Wilson, Elizabeth G. Porter, Benjamin A. García
Critical Reviews in Biochemistry and Molecular Biology (2021) Vol. 57, Iss. 1, pp. 73-112
Open Access | Times Cited: 15
Clinical Utility of a Unique Genome-Wide DNA Methylation Signature for KMT2A-Related Syndrome
Aidin Foroutan, Sadegheh Haghshenas, Pratibha Bhai, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 3, pp. 1815-1815
Open Access | Times Cited: 9
Adult-onset KMT2B-related dystonia
Edoardo Monfrini, Andrea Ciolfi, Francesco Cavallieri, et al.
Brain Communications (2022) Vol. 4, Iss. 6
Open Access | Times Cited: 9
Post-Translation Modifications and Mutations of Human Linker Histone Subtypes: Their Manifestation in Disease
Ashok Kumar, Preeti Maurya, Jeffrey J. Hayes
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 2, pp. 1463-1463
Open Access | Times Cited: 5
Detection of a DNA Methylation Signature for the Intellectual Developmental Disorder, X-Linked, Syndromic, Armfield Type
Sadegheh Haghshenas, Michael A. Levy, Jennifer Kerkhof, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 3, pp. 1111-1111
Open Access | Times Cited: 12
Genome-Wide DNA Methylation Profiling Solves Uncertainty in Classifying NSD1 Variants
Marco Ferilli, Andrea Ciolfi, Lucia Pedace, et al.
Genes (2022) Vol. 13, Iss. 11, pp. 2163-2163
Open Access | Times Cited: 8
Pan-Cancer Analysis of the Tumorigenic Effect and Prognostic Diagnostic Value of FAM111B in Human Carcinomas
Hengmiao Wu, Chao Liang
International Journal of General Medicine (2023) Vol. Volume 16, pp. 1845-1865
Open Access | Times Cited: 4
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