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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:

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

Showing 1-25 of 516 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: 2583
Integrative Functional Genomic Analyses Implicate Specific Molecular Pathways and Circuits in Autism
Neelroop Parikshak, Rui Luo, Alice Zhang, et al.
Cell (2013) Vol. 155, Iss. 5, pp. 1008-1021
Open Access | Times Cited: 1020
Metabolic regulation of gene expression through histone acylations
Benjamin R. Sabari, Di Zhang, C. David Allis, et al.
Nature Reviews Molecular Cell Biology (2016) Vol. 18, Iss. 2, pp. 90-101
Open Access | Times Cited: 863
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: 767
REST and stress resistance in ageing and Alzheimer’s disease
Tao Lu, Liviu Aron, Joseph Zullo, et al.
Nature (2014) Vol. 507, Iss. 7493, pp. 448-454
Open Access | Times Cited: 720
The genetic architecture of the human cerebral cortex
Katrina L. Grasby, Neda Jahanshad, Jodie N. Painter, et al.
Science (2020) Vol. 367, Iss. 6484
Open Access | Times Cited: 713
Activity-Regulated Transcription: Bridging the Gap between Neural Activity and Behavior
Ee-Lynn Yap, Michael E. Greenberg
Neuron (2018) Vol. 100, Iss. 2, pp. 330-348
Open Access | Times Cited: 549
Evidence for 28 genetic disorders discovered by combining healthcare and research data
Joanna Kaplanis, Kaitlin E. Samocha, Laurens Wiel, et al.
Nature (2020) Vol. 586, Iss. 7831, pp. 757-762
Open Access | Times Cited: 496
Looping Back to Leap Forward: Transcription Enters a New Era
Michael Levine, Claudia Cattoglio, Robert Tjian
Cell (2014) Vol. 157, Iss. 1, pp. 13-25
Open Access | Times Cited: 480
Genetics and Genomics of Congenital Heart Disease
Samir Zaidi, Martina Brueckner
Circulation Research (2017) Vol. 120, Iss. 6, pp. 923-940
Open Access | Times Cited: 473
The Discovery of Ribosome Heterogeneity and Its Implications for Gene Regulation and Organismal Life
Naomi R. Genuth, Maria Barna
Molecular Cell (2018) Vol. 71, Iss. 3, pp. 364-374
Open Access | Times Cited: 433
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
Neurodevelopmental Disorders: From Genetics to Functional Pathways
Ilaria Parenti, Luis G. Rabaneda, Hanna Schoen, et al.
Trends in Neurosciences (2020) Vol. 43, Iss. 8, pp. 608-621
Open Access | Times Cited: 417
Topoisomerases facilitate transcription of long genes linked to autism
Ian King, Chandri Yandava, Angela M. Mabb, et al.
Nature (2013) Vol. 501, Iss. 7465, pp. 58-62
Open Access | Times Cited: 409
AP-1 Transcription Factors and the BAF Complex Mediate Signal-Dependent Enhancer Selection
Thomas Vierbuchen, Emi Ling, Christopher Cowley, et al.
Molecular Cell (2017) Vol. 68, Iss. 6, pp. 1067-1082.e12
Open Access | Times Cited: 387
Regulation of chromatin and gene expression by metabolic enzymes and metabolites
Xinjian Li, Gábor Egervári, Yugang Wang, et al.
Nature Reviews Molecular Cell Biology (2018) Vol. 19, Iss. 9, pp. 563-578
Open Access | Times Cited: 369
The epigenetics of aging and neurodegeneration
Roy Lardenoije, Artemis Iatrou, Günter Kenis, et al.
Progress in Neurobiology (2015) Vol. 131, pp. 21-64
Open Access | Times Cited: 360
De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability
Siobhan McCarthy, Jesse Gillis, Melissa Kramer, et al.
Molecular Psychiatry (2014) Vol. 19, Iss. 6, pp. 652-658
Open Access | Times Cited: 346
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: 345
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 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
Epigenetic Regulation in Neurodegenerative Diseases
Amit Berson, Raffaella Nativio, Shelley L. Berger, et al.
Trends in Neurosciences (2018) Vol. 41, Iss. 9, pp. 587-598
Open Access | Times Cited: 311
The Emerging Field of Neuroepigenetics
J. David Sweatt
Neuron (2013) Vol. 80, Iss. 3, pp. 624-632
Open Access | Times Cited: 303
Epigenetic Basis of Mental Illness
Eric J. Nestler, Catherine J. Peña, Marija Kundaković, et al.
The Neuroscientist (2015) Vol. 22, Iss. 5, pp. 447-463
Open Access | Times Cited: 297
Dynamics of BAF–Polycomb complex opposition on heterochromatin in normal and oncogenic states
Cigall Kadoch, Christina Williamson, Joseph P. Calarco, et al.
Nature Genetics (2016) Vol. 49, Iss. 2, pp. 213-222
Open Access | Times Cited: 270
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