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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 Signatures in Mendelian Developmental Disorders as a Diagnostic Bridge Between Genotype and Phenotype
Bekim Sadiković, Erfan Aref‐Eshghi, Michael A. Levy, et al.
Epigenomics (2019) Vol. 11, Iss. 5, pp. 563-575
Closed Access | Times Cited: 52

Showing 26-50 of 52 citing articles:

Histone demethylase KDM5C is a SAHA-sensitive central hub at the crossroads of transcriptional axes involved in multiple neurodevelopmental disorders
Loredana Poeta, Agnese Padula, Benedetta Attianese, et al.
Human Molecular Genetics (2019) Vol. 28, Iss. 24, pp. 4089-4102
Open Access | Times Cited: 24
Danon Disease: Entire LAMP2 Gene Deletion with Unusual Clinical Presentation—Case Report and Review of the Literature
Adel Shalata, Marina Bar‐Shai, Yarin Hadid, et al.
Genes (2023) Vol. 14, Iss. 8, pp. 1539-1539
Open Access | Times Cited: 7
Molecular signatures in Mendelian neurodevelopment: a focus on ubiquitination driven DNA methylation aberrations
Liselot van der Laan, Nicky ten Voorde, Marcel M.A.M. Mannens, et al.
Frontiers in Molecular Neuroscience (2024) Vol. 17
Open Access | Times Cited: 2
DNA Methylation Signature for JARID2-Neurodevelopmental Syndrome
Eline A. Verberne, Liselot van der Laan, Sadegheh Haghshenas, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 14, pp. 8001-8001
Open Access | Times Cited: 11
Novel PUF60 variant suggesting an interaction between Verheij and Cornelia de Lange syndrome: phenotype description and review of the literature
Amarens Hoogenboom, Farah A. Falix, Liselot van der Laan, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 4, pp. 435-439
Open Access | Times Cited: 2
DNA methylation episignature and comparative epigenomic profiling for Pitt-Hopkins syndrome caused by TCF4 variants
Liselot van der Laan, Peter Lauffer, Kathleen Rooney, et al.
Human Genetics and Genomics Advances (2024) Vol. 5, Iss. 3, pp. 100289-100289
Open Access | Times Cited: 2
Customised next-generation sequencing multigene panel to screen a large cohort of individuals with chromatin-related disorder
Gabriella Maria Squeo, Bartolomeo Augello, Valentina Massa, et al.
Journal of Medical Genetics (2020) Vol. 57, Iss. 11, pp. 760-768
Closed Access | Times Cited: 17
Dna Methylation Episignatures are Sensitive and Specific Biomarkers for Detection of Patients with Kat6A / Kat6B Variants
Niels Vos, Jack Reilly, Mariet W. Elting, et al.
Epigenomics (2023) Vol. 15, Iss. 6, pp. 351-367
Closed Access | Times Cited: 6
Episignature Mapping of TRIP12 Provides Functional Insight into Clark–Baraitser Syndrome
Liselot van der Laan, Kathleen Rooney, Mariëlle Alders, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 22, pp. 13664-13664
Open Access | Times Cited: 8
Epigenetic studies and pediatric research
Joseph A. Bellanti
Pediatric Research (2019) Vol. 87, Iss. 2, pp. 378-384
Open Access | Times Cited: 12
Blepharophimosis with intellectual disability and Helsmoortel‐Van Der Aa Syndrome share episignature and phenotype
Camilla Sarli, Liselot van der Laan, Jack Reilly, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2024)
Open Access | Times Cited: 1
Survey of the Landscape of Society Practice Guidelines for Genetic Testing of Neurodevelopmental Disorders
Siddharth Srivastava, Jordan J. Cole, Julie S. Cohen, et al.
Annals of Neurology (2024) Vol. 96, Iss. 5, pp. 900-913
Open Access | Times Cited: 1
Genome-wide DNA methylation profiling and exome sequencing resolved a long-time misdiagnosed case
Annalisa Paparella, Gabriella Maria Squeo, Eleonora Di Venere, et al.
Journal of Human Genetics (2022) Vol. 67, Iss. 9, pp. 547-551
Closed Access | Times Cited: 7
Altered DNA methylation at age-associated CpG sites in children with growth disorders: impact on age estimation?
F. Mayer, Julia C. Becker, Christina Reinauer, et al.
International Journal of Legal Medicine (2022) Vol. 136, Iss. 4, pp. 987-996
Open Access | Times Cited: 7
Identification of a DNA methylation signature for Renpenning syndrome (RENS1), a spliceopathy
Sadegheh Haghshenas, Aidin Foroutan, Pratibha Bhai, et al.
European Journal of Human Genetics (2023) Vol. 31, Iss. 8, pp. 879-886
Open Access | Times Cited: 3
DNA methylation episignature, extension of the clinical features, and comparative epigenomic profiling of Hao-Fountain syndrome caused by variants in USP7
Liselot van der Laan, Karim Karimi, Kathleen Rooney, et al.
Genetics in Medicine (2023) Vol. 26, Iss. 3, pp. 101050-101050
Open Access | Times Cited: 3
The discovery of the DNA methylation episignature for Duchenne muscular dystrophy
Leighton Schreyer, Jack Reilly, Haley McConkey, et al.
Neuromuscular Disorders (2022) Vol. 33, Iss. 1, pp. 5-14
Closed Access | Times Cited: 5
Methylome Profiling in Fabry Disease in Clinical Practice: A Proof of Concept
Teodolinda Di Risi, Mariella Cuomo, Roberta Vinciguerra, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 20, pp. 12110-12110
Open Access | Times Cited: 3
The Illumina Infinium methylation assay for genome-wide methylation analyses
Kazuhiko Nakabayashi
Elsevier eBooks (2020), pp. 117-140
Closed Access | Times Cited: 4
DNA methylation analysis in patients with neurodevelopmental disorders improves variant interpretation and reveals complexity
Slavica Trajkova, Jennifer Kerkhof, Matteo Rossi Sebastiano, et al.
Human Genetics and Genomics Advances (2024) Vol. 5, Iss. 3, pp. 100309-100309
Open Access
CUL3-Related Neurodevelopmental Disorder: Clinical Phenotype of 20 New Individuals and Identification of a Potential Phenotype-Associated Episignature
Liselot van der Laan, Ananília Silva, Lotte Kleinendorst, et al.
Human Genetics and Genomics Advances (2024) Vol. 6, Iss. 1, pp. 100380-100380
Open Access
Methylation assay in KMT2B-related dystonia: a novel diagnostic validation tool
Gleyson Francisco da Silva Carvalho, Claudio Melo de Gusmão, Beatriz Martins Wolff, et al.
Clinical Epigenetics (2024) Vol. 16, Iss. 1
Open Access
Survey of the Landscape of Society Practice Guidelines for Genetic Testing of Neurodevelopmental Disorders
Siddharth Srivastava, Jordan J. Cole, Julie S. Cohen, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access
EpiSigns
Jack Reilly, Jennifer Kerkhof, Bekim Sadiković
Advances in Molecular Pathology (2020) Vol. 3, pp. 29-39
Closed Access | Times Cited: 3
Host methylation predicts SARS-CoV-2 infection and clinical outcome
Iain R. Konigsberg, Bret Barnes, Monica Campbell, et al.
Research Square (Research Square) (2021)
Open Access | Times Cited: 2

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