
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:
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
Dalila Pinto, Elsa Delaby, Daniele Merico, et al.
The American Journal of Human Genetics (2014) Vol. 94, Iss. 5, pp. 677-694
Open Access | Times Cited: 945
Dalila Pinto, Elsa Delaby, Daniele Merico, et al.
The American Journal of Human Genetics (2014) Vol. 94, Iss. 5, pp. 677-694
Open Access | Times Cited: 945
Showing 1-25 of 945 citing articles:
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis, Xin He, Arthur P. Goldberg, et al.
Nature (2014) Vol. 515, Iss. 7526, pp. 209-215
Open Access | Times Cited: 2588
Silvia De Rubeis, Xin He, Arthur P. Goldberg, et al.
Nature (2014) Vol. 515, Iss. 7526, pp. 209-215
Open Access | Times Cited: 2588
Pathway enrichment analysis and visualization of omics data using g:Profiler, GSEA, Cytoscape and EnrichmentMap
Jüri Reimand, Ruth Isserlin, Véronique Voisin, et al.
Nature Protocols (2019) Vol. 14, Iss. 2, pp. 482-517
Open Access | Times Cited: 1545
Jüri Reimand, Ruth Isserlin, Véronique Voisin, et al.
Nature Protocols (2019) Vol. 14, Iss. 2, pp. 482-517
Open Access | Times Cited: 1545
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
Stephan Sanders, Xin He, A. Jeremy Willsey, et al.
Neuron (2015) Vol. 87, Iss. 6, pp. 1215-1233
Open Access | Times Cited: 1391
Stephan Sanders, Xin He, A. Jeremy Willsey, et al.
Neuron (2015) Vol. 87, Iss. 6, pp. 1215-1233
Open Access | Times Cited: 1391
Most genetic risk for autism resides with common variation
Trent Gaugler, Lambertus Klei, Stephan Sanders, et al.
Nature Genetics (2014) Vol. 46, Iss. 8, pp. 881-885
Open Access | Times Cited: 1159
Trent Gaugler, Lambertus Klei, Stephan Sanders, et al.
Nature Genetics (2014) Vol. 46, Iss. 8, pp. 881-885
Open Access | Times Cited: 1159
Autism spectrum disorder
Catherine Lord, Traolach Brugha, Tony Charman, et al.
Nature Reviews Disease Primers (2020) Vol. 6, Iss. 1
Open Access | Times Cited: 1146
Catherine Lord, Traolach Brugha, Tony Charman, et al.
Nature Reviews Disease Primers (2020) Vol. 6, Iss. 1
Open Access | Times Cited: 1146
Sex/Gender Differences and Autism: Setting the Scene for Future Research
Meng‐Chuan Lai, Michael Lombardo, Bonnie Auyeung, et al.
Journal of the American Academy of Child & Adolescent Psychiatry (2014) Vol. 54, Iss. 1, pp. 11-24
Open Access | Times Cited: 914
Meng‐Chuan Lai, Michael Lombardo, Bonnie Auyeung, et al.
Journal of the American Academy of Child & Adolescent Psychiatry (2014) Vol. 54, Iss. 1, pp. 11-24
Open Access | Times Cited: 914
From the genetic architecture to synaptic plasticity in autism spectrum disorder
Thomas Bourgeron
Nature reviews. Neuroscience (2015) Vol. 16, Iss. 9, pp. 551-563
Closed Access | Times Cited: 885
Thomas Bourgeron
Nature reviews. Neuroscience (2015) Vol. 16, Iss. 9, pp. 551-563
Closed Access | Times Cited: 885
NMR Spectroscopy for Metabolomics Research
Abdul‐Hamid Emwas, Raja Roy, Ryan T. McKay, et al.
Metabolites (2019) Vol. 9, Iss. 7, pp. 123-123
Open Access | Times Cited: 880
Abdul‐Hamid Emwas, Raja Roy, Ryan T. McKay, et al.
Metabolites (2019) Vol. 9, Iss. 7, pp. 123-123
Open Access | Times Cited: 880
A copy number variation map of the human genome
Mehdi Zarrei, Jeffrey R. MacDonald, Daniele Merico, et al.
Nature Reviews Genetics (2015) Vol. 16, Iss. 3, pp. 172-183
Closed Access | Times Cited: 842
Mehdi Zarrei, Jeffrey R. MacDonald, Daniele Merico, et al.
Nature Reviews Genetics (2015) Vol. 16, Iss. 3, pp. 172-183
Closed Access | Times Cited: 842
The Changing Epidemiology of Autism Spectrum Disorders
Kristen Lyall, Lisa Croen, Julie L. Daniels, et al.
Annual Review of Public Health (2017) Vol. 38, Iss. 1, pp. 81-102
Open Access | Times Cited: 837
Kristen Lyall, Lisa Croen, Julie L. Daniels, et al.
Annual Review of Public Health (2017) Vol. 38, Iss. 1, pp. 81-102
Open Access | Times Cited: 837
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
Ryan K. C. Yuen, Daniele Merico, Matt Bookman, et al.
Nature Neuroscience (2017) Vol. 20, Iss. 4, pp. 602-611
Open Access | Times Cited: 821
Ryan K. C. Yuen, Daniele Merico, Matt Bookman, et al.
Nature Neuroscience (2017) Vol. 20, Iss. 4, pp. 602-611
Open Access | Times Cited: 821
An Overview of Autism Spectrum Disorder, Heterogeneity and Treatment Options
Anne Masi, Marilena M. DeMayo, Nick Glozier, et al.
Neuroscience Bulletin (2017) Vol. 33, Iss. 2, pp. 183-193
Open Access | Times Cited: 784
Anne Masi, Marilena M. DeMayo, Nick Glozier, et al.
Neuroscience Bulletin (2017) Vol. 33, Iss. 2, pp. 183-193
Open Access | Times Cited: 784
Advancing the understanding of autism disease mechanisms through genetics
Luis de la Torre-Ubieta, Hyejung Won, Jason L. Stein, et al.
Nature Medicine (2016) Vol. 22, Iss. 4, pp. 345-361
Open Access | Times Cited: 775
Luis de la Torre-Ubieta, Hyejung Won, Jason L. Stein, et al.
Nature Medicine (2016) Vol. 22, Iss. 4, pp. 345-361
Open Access | Times Cited: 775
The Human Phenotype Ontology in 2017
Sebastian Köhler, Nicole Vasilevsky, Mark Engelstad, et al.
Nucleic Acids Research (2016) Vol. 45, Iss. D1, pp. D865-D876
Open Access | Times Cited: 755
Sebastian Köhler, Nicole Vasilevsky, Mark Engelstad, et al.
Nucleic Acids Research (2016) Vol. 45, Iss. D1, pp. D865-D876
Open Access | Times Cited: 755
A Highly Conserved Program of Neuronal Microexons Is Misregulated in Autistic Brains
Manuel Irimia, Robert J. Weatheritt, Jonathan D. Ellis, et al.
Cell (2014) Vol. 159, Iss. 7, pp. 1511-1523
Open Access | Times Cited: 646
Manuel Irimia, Robert J. Weatheritt, Jonathan D. Ellis, et al.
Cell (2014) Vol. 159, Iss. 7, pp. 1511-1523
Open Access | Times Cited: 646
Excess of rare, inherited truncating mutations in autism
Niklas Krumm, Tychele N. Turner, Carl Baker, et al.
Nature Genetics (2015) Vol. 47, Iss. 6, pp. 582-588
Open Access | Times Cited: 596
Niklas Krumm, Tychele N. Turner, Carl Baker, et al.
Nature Genetics (2015) Vol. 47, Iss. 6, pp. 582-588
Open Access | Times Cited: 596
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia
The Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium
Molecular Autism (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 587
The Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium
Molecular Autism (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 587
Whole-genome sequencing of quartet families with autism spectrum disorder
Ryan K. C. Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, et al.
Nature Medicine (2015) Vol. 21, Iss. 2, pp. 185-191
Closed Access | Times Cited: 512
Ryan K. C. Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, et al.
Nature Medicine (2015) Vol. 21, Iss. 2, pp. 185-191
Closed Access | Times Cited: 512
Transcriptome analysis reveals dysregulation of innate immune response genes and neuronal activity-dependent genes in autism
Simone Gupta, Shannon Ellis, Foram N. Ashar, et al.
Nature Communications (2014) Vol. 5, Iss. 1
Open Access | Times Cited: 484
Simone Gupta, Shannon Ellis, Foram N. Ashar, et al.
Nature Communications (2014) Vol. 5, Iss. 1
Open Access | Times Cited: 484
Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia
Giulio Genovese, Menachem Fromer, Eli A. Stahl, et al.
Nature Neuroscience (2016) Vol. 19, Iss. 11, pp. 1433-1441
Open Access | Times Cited: 472
Giulio Genovese, Menachem Fromer, Eli A. Stahl, et al.
Nature Neuroscience (2016) Vol. 19, Iss. 11, pp. 1433-1441
Open Access | Times Cited: 472
Genetic Causes and Modifiers of Autism Spectrum Disorder
Lauren Rylaarsdam, Alicia Guemez‐Gamboa
Frontiers in Cellular Neuroscience (2019) Vol. 13
Open Access | Times Cited: 456
Lauren Rylaarsdam, Alicia Guemez‐Gamboa
Frontiers in Cellular Neuroscience (2019) Vol. 13
Open Access | Times Cited: 456
Structure, Function, and Pharmacology of Glutamate Receptor Ion Channels
Kasper B. Hansen, Lonnie P. Wollmuth, Derek Bowie, et al.
Pharmacological Reviews (2021) Vol. 73, Iss. 4, pp. 1469-1658
Open Access | Times Cited: 450
Kasper B. Hansen, Lonnie P. Wollmuth, Derek Bowie, et al.
Pharmacological Reviews (2021) Vol. 73, Iss. 4, pp. 1469-1658
Open Access | Times Cited: 450
Microglia and Beyond: Innate Immune Cells As Regulators of Brain Development and Behavioral Function
Kathryn M. Lenz, Lars H. Nelson
Frontiers in Immunology (2018) Vol. 9
Open Access | Times Cited: 440
Kathryn M. Lenz, Lars H. Nelson
Frontiers in Immunology (2018) Vol. 9
Open Access | Times Cited: 440
Genome-wide prediction and functional characterization of the genetic basis of autism spectrum disorder
Arjun Krishnan, Ran Zhang, Vicky Yao, et al.
Nature Neuroscience (2016) Vol. 19, Iss. 11, pp. 1454-1462
Open Access | Times Cited: 425
Arjun Krishnan, Ran Zhang, Vicky Yao, et al.
Nature Neuroscience (2016) Vol. 19, Iss. 11, pp. 1454-1462
Open Access | Times Cited: 425
Autism spectrum disorder: neuropathology and animal models
Merina Varghese, Neha U. Keshav, Sarah Jacot-Descombes, et al.
Acta Neuropathologica (2017) Vol. 134, Iss. 4, pp. 537-566
Open Access | Times Cited: 422
Merina Varghese, Neha U. Keshav, Sarah Jacot-Descombes, et al.
Acta Neuropathologica (2017) Vol. 134, Iss. 4, pp. 537-566
Open Access | Times Cited: 422