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 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

Showing 13 citing articles:

Therapeutic applicability of cannabidiol and other phytocannabinoids in epilepsy, multiple sclerosis and Parkinson's disease and in comorbidity with psychiatric disorders
Maria de Fátima dos Santos Sampaio, Yara Bezerra de Paiva, Tuane Bazanella Sampaio, et al.
Basic & Clinical Pharmacology & Toxicology (2024) Vol. 134, Iss. 5, pp. 574-601
Open Access | Times Cited: 12

Diagnostic utility of DNA methylation analysis in genetically unsolved pediatric epilepsies and CHD2 episignature refinement
Christy W. LaFlamme, Cassandra Rastin, Soham Sengupta, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 6

Molecular interactome of HNRNPU reveals regulatory networks in neuronal differentiation and DNA methylation
Marika Oksanen, Francesca Mastropasqua, Krystyna Mazan-Mamczarz, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access

Germline pathogenic variants in HNRNPU are associated with alterations in blood methylome
Sunwoo Lee, Eguzkine Ochoa, Magdalena Badura‐Stronka, et al.
European Journal of Human Genetics (2023) Vol. 31, Iss. 9, pp. 1040-1047
Open Access | Times Cited: 9

Identification of the DNA methylation signature of Mowat-Wilson syndrome
Stefano Giuseppe Caraffi, Liselot van der Laan, Kathleen Rooney, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 6, pp. 619-629
Open Access | Times Cited: 2

Genome-wide epistasis analysis reveals gene–gene interaction network on an intermediate endophenotype P-tau/Aβ42 ratio in ADNI cohort
Qiushi Zhang, Junfeng Liu, Hongwei Liu, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 2

Evaluating cell culture reliability in pediatric brain tumor primary cells through DNA methylation profiling
Lucia Pedace, Simone Pizzi, Luana Abballe, et al.
npj Precision Oncology (2024) Vol. 8, Iss. 1
Open Access | Times Cited: 2

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

Functional Insight into and Refinement of the Genomic Boundaries of the JARID2-Neurodevelopmental Disorder Episignature
Liselot van der Laan, Kathleen Rooney, Sadegheh Haghshenas, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 18, pp. 14240-14240
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

Genetic Testing for Epilepsy: A User Guide
Adelyn Beil, Mallory Wagner, Jill Nulle, et al.
Current Treatment Options in Neurology (2024) Vol. 26, Iss. 10, pp. 441-449
Closed Access

An expansion of the phenotype in individuals with SYNCRIP-Related Neurodevelopmental Disorder.
Tooba Shafiq, Jia Nuo Feng, Lindsay A. Phillips, et al.
Rare (2024), pp. 100052-100052
Open Access

Diagnostic Utility of Genome-wide DNA Methylation Analysis in Genetically Unsolved Developmental and Epileptic Encephalopathies and Refinement of a CHD2 Episignature
Christy W. LaFlamme, Cassandra Rastin, Soham Sengupta, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1

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