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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:

Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries
Michael E. Talkowski, Jill A. Rosenfeld, Ian Blumenthal, et al.
Cell (2012) Vol. 149, Iss. 3, pp. 525-537
Open Access | Times Cited: 572

Showing 1-25 of 572 citing articles:

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: 1385
Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders
Brian J. O’Roak, Laura Vives, Wenqing Fu, et al.
Science (2012) Vol. 338, Iss. 6114, pp. 1619-1622
Open Access | Times Cited: 1222
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: 1156
Multi-platform discovery of haplotype-resolved structural variation in human genomes
Mark Chaisson, Ashley D. Sanders, Xuefang Zhao, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 831
A structural variation reference for medical and population genetics
Ryan L. Collins, Harrison Brand, Konrad J. Karczewski, et al.
Nature (2020) Vol. 581, Iss. 7809, pp. 444-451
Open Access | Times Cited: 825
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: 816
Maternal immune activation and abnormal brain development across CNS disorders
Irène Knuesel, Laurie Chicha, Markus Britschgi, et al.
Nature Reviews Neurology (2014) Vol. 10, Iss. 11, pp. 643-660
Closed Access | Times Cited: 778
Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development
Raphael Bernier, Christelle Golzio, Bo Xiong, et al.
Cell (2014) Vol. 158, Iss. 2, pp. 263-276
Open Access | Times Cited: 711
Structural variation in the 3D genome
Malte Spielmann, Darío G. Lupiáñez, Stefan Mundlos
Nature Reviews Genetics (2018) Vol. 19, Iss. 7, pp. 453-467
Closed Access | Times Cited: 632
Phenotypic impact of genomic structural variation: insights from and for human disease
Joachim Weischenfeldt, Orsolya Symmons, François Spitz, et al.
Nature Reviews Genetics (2013) Vol. 14, Iss. 2, pp. 125-138
Closed Access | Times Cited: 608
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: 582
From neural development to cognition: unexpected roles for chromatin
Jehnna L. Ronan, Wei Wu, Robert H. Crabtree
Nature Reviews Genetics (2013) Vol. 14, Iss. 5, pp. 347-359
Open Access | Times Cited: 516
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: 483
Low Incidence of Off-Target Mutations in Individual CRISPR-Cas9 and TALEN Targeted Human Stem Cell Clones Detected by Whole-Genome Sequencing
Adrian Veres, Bridget S. Gosis, Qiurong Ding, et al.
Cell stem cell (2014) Vol. 15, Iss. 1, pp. 27-30
Open Access | Times Cited: 465
Systems biology and gene networks in neurodevelopmental and neurodegenerative disorders
Neelroop Parikshak, Michael J. Gandal, Daniel H. Geschwind
Nature Reviews Genetics (2015) Vol. 16, Iss. 8, pp. 441-458
Open Access | Times Cited: 431
A de novo convergence of autism genetics and molecular neuroscience
Niklas Krumm, Brian J. O’Roak, Jay Shendure, et al.
Trends in Neurosciences (2014) Vol. 37, Iss. 2, pp. 95-105
Open Access | Times Cited: 428
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: 419
Genetics and genomics of psychiatric disease
Daniel H. Geschwind, Jonathan Flint
Science (2015) Vol. 349, Iss. 6255, pp. 1489-1494
Open Access | Times Cited: 405
Molecular genetic testing and the future of clinical genomics
Sara Huston, Nicholas Katsanis
Nature Reviews Genetics (2013) Vol. 14, Iss. 6, pp. 415-426
Open Access | Times Cited: 403
Serotonin in the Modulation of Neural Plasticity and Networks: Implications for Neurodevelopmental Disorders
Klaus‐Peter Lesch, Jonas Waider
Neuron (2012) Vol. 76, Iss. 1, pp. 175-191
Open Access | Times Cited: 387
The role of de novo mutations in the genetics of autism spectrum disorders
Michael Ronemus, Ivan Iossifov, Dan Levy, et al.
Nature Reviews Genetics (2014) Vol. 15, Iss. 2, pp. 133-141
Closed Access | Times Cited: 374
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
CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors
Aarathi Sugathan, Marta Biagioli, Christelle Golzio, et al.
Proceedings of the National Academy of Sciences (2014) Vol. 111, Iss. 42
Open Access | Times Cited: 319
A mitochondrial bioenergetic etiology of disease
Douglas C. Wallace
Journal of Clinical Investigation (2013) Vol. 123, Iss. 4, pp. 1405-1412
Open Access | Times Cited: 313
A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP
Céline Helsmoortel, Anneke T. Vulto-van Silfhout, Bradley P. Coe, et al.
Nature Genetics (2014) Vol. 46, Iss. 4, pp. 380-384
Open Access | Times Cited: 313
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