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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 1-25 of 52 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
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: 116
Delineation of a Human Mendelian Disorder of the DNA Demethylation Machinery: TET3 Deficiency
David B. Beck, Ana Petracovici, Chongsheng He, et al.
The American Journal of Human Genetics (2020) Vol. 106, Iss. 2, pp. 234-245
Open Access | Times Cited: 94
Gene domain-specific DNA methylation episignatures highlight distinct molecular entities of ADNP syndrome
Eric G. Bend, Erfan Aref‐Eshghi, David B. Everman, et al.
Clinical Epigenetics (2019) Vol. 11, Iss. 1
Open Access | Times Cited: 89
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
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
The Genetics of Intellectual Disability
Sandra Jansen, Lisenka E.L.M. Vissers, Bert B.A. de Vries
Brain Sciences (2023) Vol. 13, Iss. 2, pp. 231-231
Open Access | Times Cited: 35
Redefining cerebral palsies as a diverse group of neurodevelopmental disorders with genetic aetiology
Clare L. van Eyk, Michael Fahey, Jozef Gécz
Nature Reviews Neurology (2023) Vol. 19, Iss. 9, pp. 542-555
Closed Access | Times Cited: 28
Applying genomic and transcriptomic advances to mitochondrial medicine
William L. Macken, Jana Vandrovcová, Michael G. Hanna, et al.
Nature Reviews Neurology (2021) Vol. 17, Iss. 4, pp. 215-230
Open Access | Times Cited: 44
Rare diseases of epigenetic origin: Challenges and opportunities
Maggie P. Fu, Sarah M. Merrill, Mehul Sharma, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 20
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
DNA methylation episignature and comparative epigenomic profiling of HNRNPU-related neurodevelopmental disorder
Kathleen Rooney, Liselot van der Laan, Slavica Trajkova, et al.
Genetics in Medicine (2023) Vol. 25, Iss. 8, pp. 100871-100871
Closed Access | Times Cited: 13
Detection of Constitutional Structural Variants by Optical Genome Mapping
Ulrich Broeckel, M. Anwar Iqbal, Brynn Levy, et al.
Journal of Molecular Diagnostics (2024) Vol. 26, Iss. 3, pp. 213-226
Open Access | Times Cited: 5
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
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
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
DNA methylation biomarkers of intellectual/developmental disability across the lifespan
Janine M. LaSalle
Journal of Neurodevelopmental Disorders (2025) Vol. 17, Iss. 1
Open Access
Current and future diagnostics of congenital heart disease (CHD)
Marc‐Phillip Hitz, Gregor Dombrowsky, Н А Мельник, et al.
Medizinische Genetik (2025) Vol. 37, Iss. 2, pp. 95-102
Closed 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
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
Genome‐wide DNA methylation profiling confirms a case of low‐level mosaic Kabuki syndrome 1
Carolina Montaño, Jacquelyn Britton, Jacqueline Harris, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 7, pp. 2217-2225
Open Access | Times Cited: 15
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
X‐Linked intellectual disability update 2022
Charles E. Schwartz, Raymond J. Louie, Annick Toutain, et al.
American Journal of Medical Genetics Part A (2022) Vol. 191, Iss. 1, pp. 144-159
Closed Access | Times Cited: 14
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