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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:

The contribution of de novo coding mutations to autism spectrum disorder
Ivan Iossifov, Brian J. O’Roak, Stephan Sanders, et al.
Nature (2014) Vol. 515, Iss. 7526, pp. 216-221
Open Access | Times Cited: 2499

Showing 51-75 of 2499 citing articles:

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: 396
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population
Elise Robinson, Beaté St Pourcain, Verneri Anttila, et al.
Nature Genetics (2016) Vol. 48, Iss. 5, pp. 552-555
Open Access | Times Cited: 361
Regional missense constraint improves variant deleteriousness prediction
Kaitlin E. Samocha, Jack A. Kosmicki, Konrad J. Karczewski, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2017)
Open Access | Times Cited: 359
Exogenous and evoked oxytocin restores social behavior in the Cntnap2 mouse model of autism
Olga Peñagarikano, María T. Lázaro, Xiao‐Hong Lu, et al.
Science Translational Medicine (2015) Vol. 7, Iss. 271
Open Access | Times Cited: 356
Targeted capture in evolutionary and ecological genomics
Matthew R. Jones, Jeffrey M. Good
Molecular Ecology (2015) Vol. 25, Iss. 1, pp. 185-202
Open Access | Times Cited: 356
DNA methylation in human diseases
Zelin Jin, Yun Liu
Genes & Diseases (2018) Vol. 5, Iss. 1, pp. 1-8
Open Access | Times Cited: 352
The Dynamic Landscape of Open Chromatin during Human Cortical Neurogenesis
Luis de la Torre-Ubieta, Jason L. Stein, Hyejung Won, et al.
Cell (2018) Vol. 172, Iss. 1-2, pp. 289-304.e18
Open Access | Times Cited: 348
Genomic Patterns of De Novo Mutation in Simplex Autism
Tychele N. Turner, Bradley P. Coe, Diane E. Dickel, et al.
Cell (2017) Vol. 171, Iss. 3, pp. 710-722.e12
Open Access | Times Cited: 344
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment
Justin Cotney, Rebecca Muhle, Stephan Sanders, et al.
Nature Communications (2015) Vol. 6, Iss. 1
Open Access | Times Cited: 342
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples
Jack A. Kosmicki, Kaitlin E. Samocha, Daniel P. Howrigan, et al.
Nature Genetics (2017) Vol. 49, Iss. 4, pp. 504-510
Open Access | Times Cited: 342
De novo genic mutations among a Chinese autism spectrum disorder cohort
Tianyun Wang, Hui Guo, Bo Xiong, et al.
Nature Communications (2016) Vol. 7, Iss. 1
Open Access | Times Cited: 332
Chromatin and gene-regulatory dynamics of the developing human cerebral cortex at single-cell resolution
Alexandro E. Trevino, Fabian Müller, Jimena Andersen, et al.
Cell (2021) Vol. 184, Iss. 19, pp. 5053-5069.e23
Open Access | Times Cited: 330
Neurodevelopmental disorders—the history and future of a diagnostic concept
Deborah J. Morris‐Rosendahl, Marc-Antoine Crocq
Dialogues in Clinical Neuroscience (2020) Vol. 22, Iss. 1, pp. 65-72
Open Access | Times Cited: 326
Recurrent de novo mutations implicate novel genes underlying simplex autism risk
Brian J. O’Roak, Holly A.F. Stessman, Evan A. Boyle, et al.
Nature Communications (2014) Vol. 5, Iss. 1
Open Access | Times Cited: 316
Cell-Type-Specific Alternative Splicing Governs Cell Fate in the Developing Cerebral Cortex
Xiaochang Zhang, Ming Hui Chen, Xuebing Wu, et al.
Cell (2016) Vol. 166, Iss. 5, pp. 1147-1162.e15
Open Access | Times Cited: 316
Mutations in Human Accelerated Regions Disrupt Cognition and Social Behavior
Ryan N. Doan, Byoung-Il Bae, Beatriz Cubelos, et al.
Cell (2016) Vol. 167, Iss. 2, pp. 341-354.e12
Open Access | Times Cited: 314
Systematic reanalysis of clinical exome data yields additional diagnoses: implications for providers
Aaron M. Wenger, Harendra Guturu, Jonathan A. Bernstein, et al.
Genetics in Medicine (2016) Vol. 19, Iss. 2, pp. 209-214
Open Access | Times Cited: 300
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
Claire Redin, Harrison Brand, Ryan L. Collins, et al.
Nature Genetics (2016) Vol. 49, Iss. 1, pp. 36-45
Open Access | Times Cited: 294
Drug development for neurodevelopmental disorders: lessons learned from fragile X syndrome
Elizabeth Berry‐Kravis, Lothar Lindemann, Aia Elise Jønch, et al.
Nature Reviews Drug Discovery (2017) Vol. 17, Iss. 4, pp. 280-299
Open Access | Times Cited: 290
Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity
Bradley P. Coe, Holly A.F. Stessman, Arvis Sulovari, et al.
Nature Genetics (2018) Vol. 51, Iss. 1, pp. 106-116
Open Access | Times Cited: 287
The ASD Living Biology: from cell proliferation to clinical phenotype
Eric Courchesne, Tiziano Pramparo, Vahid Gazestani, et al.
Molecular Psychiatry (2018) Vol. 24, Iss. 1, pp. 88-107
Open Access | Times Cited: 283
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
Donna M. Werling, Harrison Brand, Joon‐Yong An, et al.
Nature Genetics (2018) Vol. 50, Iss. 5, pp. 727-736
Open Access | Times Cited: 280
A complete reference genome improves analysis of human genetic variation
Sergey Aganezov, Stephanie M. Yan, Daniela C. Soto, et al.
Science (2022) Vol. 376, Iss. 6588
Open Access | Times Cited: 278
Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA
Tychele N. Turner, Fereydoun Hormozdiari, Michael H. Duyzend, et al.
The American Journal of Human Genetics (2015) Vol. 98, Iss. 1, pp. 58-74
Open Access | Times Cited: 277
Whole-genome deep-learning analysis identifies contribution of noncoding mutations to autism risk
Jian Zhou, Christopher Y. Park, Chandra L. Theesfeld, et al.
Nature Genetics (2019) Vol. 51, Iss. 6, pp. 973-980
Open Access | Times Cited: 273

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