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:

Integrated genome-wide Alu methylation and transcriptome profiling analyses reveal novel epigenetic regulatory networks associated with autism spectrum disorder
Thanit Saeliw, Chayanin Tangsuwansri, Surangrat Thongkorn, et al.
Molecular Autism (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 55

Showing 26-50 of 55 citing articles:

Untangle the Multi-Facet Functions of Auts2 as an Entry Point to Understand Neurodevelopmental Disorders
Wenbin Pang, Xi‐Nan Yi, Ling Li, et al.
Frontiers in Psychiatry (2021) Vol. 12
Open Access | Times Cited: 15

Altered DNA Methylation of the Alu Y Subfamily in Schizophrenia and Bipolar Disorder
Shufen Li, Lu Zong, Yu Hou, et al.
Epigenomics (2019) Vol. 11, Iss. 6, pp. 581-586
Closed Access | Times Cited: 15

Integrated microRNA–mRNA Expression Profiling Identifies Novel Targets and Networks Associated with Autism
Pritmohinder S. Gill, Harsh Dweep, Shannon Rose, et al.
Journal of Personalized Medicine (2022) Vol. 12, Iss. 6, pp. 920-920
Open Access | Times Cited: 7

Network-Based Integrative Analysis of Genomics, Epigenomics and Transcriptomics in Autism Spectrum Disorders
Noemi Di Nanni, Matteo Bersanelli, Francesca Anna Cupaioli, et al.
International Journal of Molecular Sciences (2019) Vol. 20, Iss. 13, pp. 3363-3363
Open Access | Times Cited: 9

Differential DNA Methylation from Autistic Children Enriches Evidence for Genes Associated with ASD and New Candidate Genes
Mirna Edith Morales-Marín, Xochitl Helga Castro Martínez, Federico Centeno-Cruz, et al.
Brain Sciences (2023) Vol. 13, Iss. 10, pp. 1420-1420
Open Access | Times Cited: 3

CpG methylation changes in Alu repetitive sequences in normal aging due to diastolic hypertension in human dermal fibroblasts from the facial area
Suvinai Jiraboonsri, Panicha Hemvipat, Supitcha Kamolratanakul, et al.
Biomedical Reports (2023) Vol. 20, Iss. 1
Open Access | Times Cited: 3

An Alu insertion map of the Indian population: identification and analysis in 1021 genomes of the IndiGen project
P. Prakrithi, Khushboo Singhal, Disha Sharma, et al.
NAR Genomics and Bioinformatics (2022) Vol. 4, Iss. 1
Open Access | Times Cited: 3

Retrotransposon SINEs in Age-Related Diseases: Mechanisms and Therapeutic Implications
Suleman Shah, Siyi Yu, Chen Zhang, et al.
Ageing Research Reviews (2024) Vol. 101, pp. 102539-102539
Closed Access

Histone and DNA Methylome in Neurodegenerative, Neuropsychiatric and Neurodevelopmental Disorders
Harsha Rani, Vijayalakshmi Mahadevan
RNA technologies (2019), pp. 63-102
Closed Access | Times Cited: 3

Genetic etiology of autism spectrum disorder in the African population: a scoping review
Olivier Hakizimana, Janvier Hitayezu, Jeanne P. Uyisenga, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access

Primate-specific retrotransposons and the evolution of circadian networks in the human brain
Manci Li, Peter A. Larsen
Neuroscience & Biobehavioral Reviews (2021) Vol. 131, pp. 988-1004
Closed Access | Times Cited: 3

Ambient air pollution and human epigenetic modifications
Rongbin Xu, Shuai Li, Michael J. Abramson, et al.
Elsevier eBooks (2021), pp. 299-343
Closed Access | Times Cited: 2

Methods in epigenetics-based systems biology and their applications
Sascha Jung, Muhammad Ali, Antonio del Sol
Elsevier eBooks (2020), pp. 615-646
Closed Access | Times Cited: 1

Faculty Opinions recommendation of The heterogeneity problem: approaches to identify psychiatric subtypes.
Vikram Patel
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature (2019)
Open Access

Sparse principal component analysis based on genome network for correcting cell type heterogeneity in epigenome-wide association studies
Rui Miao, Qi Dang, Jie Cai, et al.
Medical & Biological Engineering & Computing (2022) Vol. 60, Iss. 9, pp. 2601-2618
Closed Access

ASPECTOS GENÉTICOS DO TRANSTORNO DO ESPECTRO AUTISTA (TEA)
Maria Denise Fernandes Carvalho de Andrade, Ellaine Dóris Fernandes Carvalho, Krishnamurti de Moraes Carvalho
Amplla Editora eBooks (2022), pp. 148-163
Open Access

ANÁLISE QUALITATIVA E QUANTITATIVA SOBRE A SAÚDE E A EDUCAÇÃO DE CRIANÇA COM TRANSTORNO DO ESPECTRO DO AUTISMO
José Marciel Araújo Porcino, Giuliana Cavalcanti Vasconcelos
Amplla Editora eBooks (2022), pp. 78-90
Open Access

CONSIDERAÇÕES NEUROPSICOLÓGICAS NO TRATAMENTO DO TRANSTORNO DO ESPECTRO DO AUTISMO E SUA INTERFACE COM A IMITAÇÃO
José Marciel Araújo Porcino, Natália Macedo Pinheiro, Telma Maria da Silva Ferreira Souza, et al.
Amplla Editora eBooks (2022), pp. 328-340
Open Access

TEA LEVE: ANTIGA SINDROME DE ASPERGER
Bruno Mileno Magalhães de Carvalho, Lara Emannuely Alves Ferreira, Sahda Elouf Simão, et al.
Amplla Editora eBooks (2022), pp. 122-131
Open Access

TRANSTORNO DO ESPECTRO AUTISTA E DIAGNÓSTICO POR IMAGEM
Yuri Borges Morais, Levy da Costa Felix, Sayd Douglas Rolim Carneiro Oliveira
Amplla Editora eBooks (2022), pp. 281-293
Open Access

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