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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:

Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks
Elizabeth K. Ruzzo, Laura Pérez‐Cano, Jae-Yoon Jung, et al.
Cell (2019) Vol. 178, Iss. 4, pp. 850-866.e26
Open Access | Times Cited: 395

Showing 1-25 of 395 citing articles:

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Kyle Satterstrom, Jack A. Kosmicki, Jiebiao Wang, et al.
Cell (2020) Vol. 180, Iss. 3, pp. 568-584.e23
Open Access | Times Cited: 1873
Autism spectrum disorder: definition, epidemiology, causes, and clinical evaluation
Holly Hodges, Casey Fealko, Neelkamal Soares
Translational Pediatrics (2020) Vol. 9, Iss. S1, pp. S55-S65
Open Access | Times Cited: 680
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Jack Fu, F. Kyle Satterstrom, Minshi Peng, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1320-1331
Open Access | Times Cited: 358
Autism genes converge on asynchronous development of shared neuron classes
Bruna Paulsen, Silvia Velasco, Amanda J. Kedaigle, et al.
Nature (2022) Vol. 602, Iss. 7896, pp. 268-273
Open Access | Times Cited: 303
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes
Xueya Zhou, Pamela Feliciano, Chang Shu, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1305-1319
Open Access | Times Cited: 256
Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms
Rebecca L. Walker, Gokul Ramaswami, Christopher Hartl, et al.
Cell (2019) Vol. 179, Iss. 3, pp. 750-771.e22
Open Access | Times Cited: 240
Autism spectrum disorder at the crossroad between genes and environment: contributions, convergences, and interactions in ASD developmental pathophysiology
Cristina Cheroni, Nicolò Caporale, Giuseppe Testa
Molecular Autism (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 194
Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development
Ashley L. Lennox, Mariah L. Hoye, Ruiji Jiang, et al.
Neuron (2020) Vol. 106, Iss. 3, pp. 404-420.e8
Open Access | Times Cited: 174
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders
Tianyun Wang, Kendra Hoekzema, Davide Vecchio, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 165
Spatial and cell type transcriptional landscape of human cerebellar development
Kimberly A. Aldinger, Zachary Thomson, Ian G. Phelps, et al.
Nature Neuroscience (2021) Vol. 24, Iss. 8, pp. 1163-1175
Open Access | Times Cited: 155
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: 140
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: 126
Recent ultra-rare inherited variants implicate new autism candidate risk genes
Amy B. Wilfert, Tychele N. Turner, Shwetha C. Murali, et al.
Nature Genetics (2021) Vol. 53, Iss. 8, pp. 1125-1134
Open Access | Times Cited: 107
The contributions of rare inherited and polygenic risk to ASD in multiplex families
Matilde Cirnigliaro, Timothy S. Chang, Stephanie A. Arteaga, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 31
Open Access | Times Cited: 50
Single nucleus multiomics identifies ZEB1 and MAFB as candidate regulators of Alzheimer’s disease-specific cis-regulatory elements
Ashlyn G. Anderson, Brianne B. Rogers, Jacob M. Loupe, et al.
Cell Genomics (2023) Vol. 3, Iss. 3, pp. 100263-100263
Open Access | Times Cited: 49
Identification of astrocyte regulators by nucleic acid cytometry
Iain C. Clark, Michael A. Wheeler, Hong‐Gyun Lee, et al.
Nature (2023) Vol. 614, Iss. 7947, pp. 326-333
Open Access | Times Cited: 48
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: 45
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: 38
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: 30
Leveraging single-cell ATAC-seq and RNA-seq to identify disease-critical fetal and adult brain cell types
Samuel S. Kim, Buu Truong, Karthik A. Jagadeesh, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 18
A subpopulation of cortical neurons altered by mutations in the autism risk gene DDX3X
Michael Flores, Marta García-Forn, Alexa von Mueffling, et al.
Biology Open (2025) Vol. 14, Iss. 1
Open Access | Times Cited: 2
From Cohorts to Molecules: Adverse Impacts of Endocrine Disrupting Mixtures
Nicolò Caporale, Michelle Leemans, Lina Birgersson, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2017)
Open Access | Times Cited: 139
The role of glutathione redox imbalance in autism spectrum disorder: A review
Geir Bjørklund, Alexey A. Tinkov, Božena Hosnedlová, et al.
Free Radical Biology and Medicine (2020) Vol. 160, pp. 149-162
Open Access | Times Cited: 127
Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus
Sheng Chih Jin, Weilai Dong, Adam J. Kundishora, et al.
Nature Medicine (2020) Vol. 26, Iss. 11, pp. 1754-1765
Open Access | Times Cited: 125
Genetic Advances in Autism
Anita Thapar, Michael Rutter
Journal of Autism and Developmental Disorders (2020) Vol. 51, Iss. 12, pp. 4321-4332
Open Access | Times Cited: 119
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