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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 changes in lncRNA, splicing, and regional gene expression patterns in autism
Neelroop Parikshak, Vivek Swarup, T. Grant Belgard, et al.
Nature (2016) Vol. 540, Iss. 7633, pp. 423-427
Open Access | Times Cited: 660

Showing 26-50 of 660 citing articles:

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: 162
Neuronal defects in a human cellular model of 22q11.2 deletion syndrome
Themasap A. Khan, Omer Revah, Aaron Gordon, et al.
Nature Medicine (2020) Vol. 26, Iss. 12, pp. 1888-1898
Open Access | Times Cited: 160
Prenatal Origins of ASD: The When, What, and How of ASD Development
Eric Courchesne, Vahid Gazestani, Nathan E. Lewis
Trends in Neurosciences (2020) Vol. 43, Iss. 5, pp. 326-342
Open Access | Times Cited: 145
Genomics, convergent neuroscience and progress in understanding autism spectrum disorder
Helen Rankin Willsey, A. Jeremy Willsey, Belinda Wang, et al.
Nature reviews. Neuroscience (2022) Vol. 23, Iss. 6, pp. 323-341
Open Access | Times Cited: 141
Signalling pathways in autism spectrum disorder: mechanisms and therapeutic implications
Chen-Chen Jiang, Lishan Lin, Sen Long, et al.
Signal Transduction and Targeted Therapy (2022) Vol. 7, Iss. 1
Open Access | Times Cited: 133
Full-length transcript sequencing of human and mouse cerebral cortex identifies widespread isoform diversity and alternative splicing
Szi Kay Leung, Aaron R. Jeffries, Isabel Castanho, et al.
Cell Reports (2021) Vol. 37, Iss. 7, pp. 110022-110022
Open Access | Times Cited: 125
Innate immune dysfunction and neuroinflammation in autism spectrum disorder (ASD)
Heather K. Hughes, Rachel J. Moreno, Paul Ashwood
Brain Behavior and Immunity (2022) Vol. 108, pp. 245-254
Open Access | Times Cited: 122
Molecular signatures underlying neurofibrillary tangle susceptibility in Alzheimer’s disease
Marcos Otero-García, Sameehan Mahajani, Debia Wakhloo, et al.
Neuron (2022) Vol. 110, Iss. 18, pp. 2929-2948.e8
Open Access | Times Cited: 119
Reintroduction of the archaic variant of NOVA1 in cortical organoids alters neurodevelopment
Cleber A. Trujillo, Edward S. Rice, Nathan K. Schaefer, et al.
Science (2021) Vol. 371, Iss. 6530
Open Access | Times Cited: 113
mTOR-related synaptic pathology causes autism spectrum disorder-associated functional hyperconnectivity
Marco Pagani, Noemi Barsotti, Alice Bertero, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 113
Autism Spectrum Disorder: Neurodevelopmental Risk Factors, Biological Mechanism, and Precision Therapy
Xuan Wang, Binquan Wang, Chunyan Wu, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 3, pp. 1819-1819
Open Access | Times Cited: 108
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
Single-nuclei isoform RNA sequencing unlocks barcoded exon connectivity in frozen brain tissue
Simon A. Hardwick, Wen Hu, Anoushka Joglekar, et al.
Nature Biotechnology (2022) Vol. 40, Iss. 7, pp. 1082-1092
Open Access | Times Cited: 88
Comprehensive evaluation of deconvolution methods for human brain gene expression
Gavin J. Sutton, Daniel Poppe, Rebecca K. Simmons, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 85
Molecular and network-level mechanisms explaining individual differences in autism spectrum disorder
A. Buch, Petra E. Vértes, Jakob Seidlitz, et al.
Nature Neuroscience (2023) Vol. 26, Iss. 4, pp. 650-663
Open Access | Times Cited: 85
The Role of Gut Dysbiosis in the Pathophysiology of Neuropsychiatric Disorders
Nikhilesh Anand, Vasavi Rakesh Gorantla, Saravana Babu Chidambaram
Cells (2022) Vol. 12, Iss. 1, pp. 54-54
Open Access | Times Cited: 80
Modeling idiopathic autism in forebrain organoids reveals an imbalance of excitatory cortical neuron subtypes during early neurogenesis
Alexandre Jourdon, Feinan Wu, Jessica Mariani, et al.
Nature Neuroscience (2023) Vol. 26, Iss. 9, pp. 1505-1515
Open Access | Times Cited: 47
Single-cell genomics and regulatory networks for 388 human brains
Prashant S. Emani, Jason Liu, Declan Clarke, et al.
Science (2024) Vol. 384, Iss. 6698
Open Access | Times Cited: 45
Molecular cascades and cell type–specific signatures in ASD revealed by single-cell genomics
Brie Wamsley, Lucy Bicks, Yuyan Cheng, et al.
Science (2024) Vol. 384, Iss. 6698
Open Access | Times Cited: 36
Cortical gene expression architecture links healthy neurodevelopment to the imaging, transcriptomics and genetics of autism and schizophrenia
Richard Dear, Konrad Wagstyl, Jakob Seidlitz, et al.
Nature Neuroscience (2024) Vol. 27, Iss. 6, pp. 1075-1086
Open Access | Times Cited: 20
Autism spectrum disorder: pathogenesis, biomarker, and intervention therapy
Hongbin Zhuang, Zhiyuan Liang, Guanwei Ma, et al.
MedComm (2024) Vol. 5, Iss. 3
Open Access | Times Cited: 19
Comprehensive characterization of the transcriptional landscape in Alzheimer’s disease (AD) brains
Chengxuan Chen, Zhao Zhang, Yuan Liu, et al.
Science Advances (2025) Vol. 11, Iss. 1
Open Access | Times Cited: 2
Autism spectrum disorder: insights into convergent mechanisms from transcriptomics
Mathieu Quesnel-Vallières, Robert J. Weatheritt, Sabine P. Cordes, et al.
Nature Reviews Genetics (2018) Vol. 20, Iss. 1, pp. 51-63
Closed Access | Times Cited: 154
Autism-like phenotype and risk gene mRNA deadenylation by CPEB4 mis-splicing
Alberto Parras, Héctor Anta, María Santos‐Galindo, et al.
Nature (2018) Vol. 560, Iss. 7719, pp. 441-446
Open Access | Times Cited: 146
Dysregulation of Cortical Neuron DNA Methylation Profile in Autism Spectrum Disorder
Stefano Nardone, Dev Sharan Sams, Antonino Zito, et al.
Cerebral Cortex (2017) Vol. 27, Iss. 12, pp. 5739-5754
Open Access | Times Cited: 143

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