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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:

Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue
Chloe C. Y. Wong, Rebecca G. Smith, Eilís Hannon, et al.
Human Molecular Genetics (2019) Vol. 28, Iss. 13, pp. 2201-2211
Open Access | Times Cited: 83

Showing 1-25 of 83 citing articles:

Maternal immune activation and neuroinflammation in human neurodevelopmental disorders
Velda X. Han, Shrujna Patel, Hannah Jones, et al.
Nature Reviews Neurology (2021) Vol. 17, Iss. 9, pp. 564-579
Closed Access | Times Cited: 422
An Overview of the Main Genetic, Epigenetic and Environmental Factors Involved in Autism Spectrum Disorder Focusing on Synaptic Activity
Elena Masini, Eleonora Loi, Ana Florencia Vega-Benedetti, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 21, pp. 8290-8290
Open Access | Times Cited: 186
Broad transcriptomic dysregulation occurs across the cerebral cortex in ASD
Michael J. Gandal, Jillian R. Haney, Brie Wamsley, et al.
Nature (2022) Vol. 611, Iss. 7936, pp. 532-539
Open Access | Times Cited: 161
The neuropathology of autism: A systematic review of post-mortem studies of autism and related disorders
Rana Fetit, Robert F. Hillary, David J. Price, et al.
Neuroscience & Biobehavioral Reviews (2021) Vol. 129, pp. 35-62
Open Access | Times Cited: 106
Recalibrating the epigenetic clock: implications for assessing biological age in the human cortex
Gemma Shireby, Jonathan Davies, Paul T. Francis, et al.
Brain (2020) Vol. 143, Iss. 12, pp. 3763-3775
Open Access | Times Cited: 138
Integrative genomics identifies a convergent molecular subtype that links epigenomic with transcriptomic differences in autism
Gokul Ramaswami, Hyejung Won, Michael J. Gandal, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 85
Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes
Charles E. Mordaunt, Julia M. Jianu, Benjamin I. Laufer, et al.
Genome Medicine (2020) Vol. 12, Iss. 1
Open Access | Times Cited: 73
Developments in diagnostic applications of saliva in human organ diseases
Yangyang Cui, Mengying Yang, Jia Zhu, et al.
Medicine in Novel Technology and Devices (2022) Vol. 13, pp. 100115-100115
Open Access | Times Cited: 66
Genetic contributions to autism spectrum disorder
Alexandra Havdahl, Maria Niarchou, Anna Starnawska, et al.
Psychological Medicine (2021) Vol. 51, Iss. 13, pp. 2260-2273
Open Access | Times Cited: 61
Can epigenetics shine a light on the biological pathways underlying major mental disorders?
Luis Alameda, Giulia Trotta, Harriet Quigley, et al.
Psychological Medicine (2022) Vol. 52, Iss. 9, pp. 1645-1665
Open Access | Times Cited: 45
Epigenomic signatures reveal mechanistic clues and predictive markers for autism spectrum disorder
Janine M. LaSalle
Molecular Psychiatry (2023) Vol. 28, Iss. 5, pp. 1890-1901
Open Access | Times Cited: 36
Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants
M. Siu, Darci T. Butcher, Andrei L. Turinsky, et al.
Clinical Epigenetics (2019) Vol. 11, Iss. 1
Open Access | Times Cited: 61
DNA Methylation Biomarkers for Young Children with Idiopathic Autism Spectrum Disorder: A Systematic Review
Andrea Stoccoro, Eugenia Conti, Elena Scaffei, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 11, pp. 9138-9138
Open Access | Times Cited: 17
Brain cell-type shifts in Alzheimer’s disease, autism, and schizophrenia interrogated using methylomics and genetics
Chloe X. Yap, Daniel Vo, Matthew G. Heffel, et al.
Science Advances (2024) Vol. 10, Iss. 21
Open Access | Times Cited: 8
Neuroimmune mechanisms in autism etiology - untangling a complex problem using human cellular models
Janay M. Vacharasin, Joseph Ward, Mikayla McCord, et al.
Oxford Open Neuroscience (2024) Vol. 3
Open Access | Times Cited: 7
Circuits for social learning: A unified model and application to Autism Spectrum Disorder
Marilena M. DeMayo, Larry J. Young, Ian B. Hickie, et al.
Neuroscience & Biobehavioral Reviews (2019) Vol. 107, pp. 388-398
Open Access | Times Cited: 52
Epigenetic Delay in the Neurodevelopmental Trajectory of DNA Methylation States in Autism Spectrum Disorders
Michael J. Corley, Naurú Idalia Vargas-Maya, Alina P.S. Pang, et al.
Frontiers in Genetics (2019) Vol. 10
Open Access | Times Cited: 47
Epigenetics of Autism Spectrum Disorder: Histone Deacetylases
Chieh-En Jane Tseng, Christopher J. McDougle, Jacob M. Hooker, et al.
Biological Psychiatry (2021) Vol. 91, Iss. 11, pp. 922-933
Closed Access | Times Cited: 39
Microbiota-gut-brain axis in autism spectrum disorder
You Yu, Fangqing Zhao
Journal of genetics and genomics/Journal of Genetics and Genomics (2021) Vol. 48, Iss. 9, pp. 755-762
Closed Access | Times Cited: 38
DNA methylation signature as a biomarker of major neuropsychiatric disorders
Zeinab Shirvani-Farsani, Zahra Maloum, Zahra Bagheri‐Hosseinabadi, et al.
Journal of Psychiatric Research (2021) Vol. 141, pp. 34-49
Open Access | Times Cited: 36
Paving the Way toward Personalized Medicine: Current Advances and Challenges in Multi-OMICS Approach in Autism Spectrum Disorder for Biomarkers Discovery and Patient Stratification
Areej G. Mesleh, Sara Abdulla, Omar M. A. El‐Agnaf
Journal of Personalized Medicine (2021) Vol. 11, Iss. 1, pp. 41-41
Open Access | Times Cited: 34
Epigenetic Alterations of Brain Non-Neuronal Cells in Major Mental Diseases
Hamid M. Abdolmaleky, Marian Martin, Jin‐Rong Zhou, et al.
Genes (2023) Vol. 14, Iss. 4, pp. 896-896
Open Access | Times Cited: 16
Quantifying the proportion of different cell types in the human cortex using DNA methylation profiles
Eilís Hannon, Emma Dempster, Jonathan Davies, et al.
BMC Biology (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 6
Resolving the Synaptic versus Developmental Dichotomy of Autism Risk Genes
Whitney E. Heavner, Stephen Smith
Trends in Neurosciences (2020) Vol. 43, Iss. 4, pp. 227-241
Open Access | Times Cited: 37
Profiling allele-specific gene expression in brains from individuals with autism spectrum disorder reveals preferential minor allele usage
Chang‐Hoon Lee, Eun Yong Kang, Michael J. Gandal, et al.
Nature Neuroscience (2019) Vol. 22, Iss. 9, pp. 1521-1532
Open Access | Times Cited: 36
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