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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 chromatin basis of neurodevelopmental disorders: Rethinking dysfunction along the molecular and temporal axes
Michele Gabriele, Alejandro Tobon, Giuseppe D’Agostino, et al.
Progress in Neuro-Psychopharmacology and Biological Psychiatry (2018) Vol. 84, pp. 306-327
Open Access | Times Cited: 90

Showing 1-25 of 90 citing articles:

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
Enhancers in disease: molecular basis and emerging treatment strategies
Annique Claringbould, Judith B. Zaugg
Trends in Molecular Medicine (2021) Vol. 27, Iss. 11, pp. 1060-1073
Open Access | Times Cited: 139
The Why of YY1: Mechanisms of Transcriptional Regulation by Yin Yang 1
Thijs C. J. Verheul, Levi van Hijfte, Elena Perenthaler, et al.
Frontiers in Cell and Developmental Biology (2020) Vol. 8
Open Access | Times Cited: 130
Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling
Monica Frega, Katrin Linda, Jason M. Keller, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 121
Regulation of Adult Neurogenesis in Mammalian Brain
Maria Victoria Niklison-Chirou, Massimiliano Agostini, Ivano Amelio, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 14, pp. 4869-4869
Open Access | Times Cited: 107
Chromatin Regulation of Neuronal Maturation and Plasticity
David A. Gallegos, Urann Chan, Liangfu Chen, et al.
Trends in Neurosciences (2018) Vol. 41, Iss. 5, pp. 311-324
Open Access | Times Cited: 90
Dosage analysis of the 7q11.23 Williams region identifies BAZ1B as a major human gene patterning the modern human face and underlying self-domestication
Matteo Zanella, Alessandro Vitriolo, Alejandro Andirkó, et al.
Science Advances (2019) Vol. 5, Iss. 12
Open Access | Times Cited: 83
The emerging role of chromatin remodelers in neurodevelopmental disorders: a developmental perspective
Britt Mossink, Moritz Negwer, Dirk Schubert, et al.
Cellular and Molecular Life Sciences (2020) Vol. 78, Iss. 6, pp. 2517-2563
Open Access | Times Cited: 79
CHD8 haploinsufficiency links autism to transient alterations in excitatory and inhibitory trajectories
Carlo Emanuele Villa, Cristina Cheroni, Christoph Dotter, et al.
Cell Reports (2022) Vol. 39, Iss. 1, pp. 110615-110615
Open Access | Times Cited: 62
The Epigenome in Neurodevelopmental Disorders
Julia Reichard, Geraldine Zimmer‐Bensch
Frontiers in Neuroscience (2021) Vol. 15
Open Access | Times Cited: 58
How can same-gene mutations promote both cancer and developmental disorders?
Ruth Nussinov, Chung‐Jung Tsai, Hyunbum Jang
Science Advances (2022) Vol. 8, Iss. 2
Open Access | Times Cited: 46
Landscape of mSWI/SNF chromatin remodeling complex perturbations in neurodevelopmental disorders
Alfredo M. Valencia, Akshay Sankar, Pleuntje J. van der Sluijs, et al.
Nature Genetics (2023) Vol. 55, Iss. 8, pp. 1400-1412
Open Access | Times Cited: 39
Microglia-mediated synaptic pruning as a key deficit in neurodevelopmental disorders: Hype or hope?
Annika Mordelt, Lot D. de Witte
Current Opinion in Neurobiology (2023) Vol. 79, pp. 102674-102674
Open Access | Times Cited: 37
Neurodevelopmental disorders, like cancer, are connected to impaired chromatin remodelers, PI3K/mTOR, and PAK1-regulated MAPK
Ruth Nussinov, Bengi Ruken Yavuz, M. Kaan Arici, et al.
Biophysical Reviews (2023) Vol. 15, Iss. 2, pp. 163-181
Open Access | Times Cited: 35
miRNA biogenesis and inherited disorders: clinico-molecular insights
Dylan Pelletier, Bárbara Rivera, Marc R. Fabian, et al.
Trends in Genetics (2023) Vol. 39, Iss. 5, pp. 401-414
Closed Access | Times Cited: 31
Chromatin remodeler Activity-Dependent Neuroprotective Protein (ADNP) contributes to syndromic autism
Claudio Peter D’Incal, Kirsten Esther Van Rossem, Kevin De Man, et al.
Clinical Epigenetics (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 23
Pathogenic variants in chromatin‐related genes: Linking immune dysregulation to neuroregression and acute neuropsychiatric disorders
Russell C. Dale, Shekeeb S. Mohammad, Velda X. Han, et al.
Developmental Medicine & Child Neurology (2025)
Open Access | Times Cited: 1
Tracking and interpreting long-range chromatin interactions with super-resolution live-cell imaging
Hugo B. Brandão, Michele Gabriele, Anders S. Hansen
Current Opinion in Cell Biology (2020) Vol. 70, pp. 18-26
Open Access | Times Cited: 68
Allostery, and how to define and measure signal transduction
Ruth Nussinov, Chung‐Jung Tsai, Hyunbum Jang
Biophysical Chemistry (2022) Vol. 283, pp. 106766-106766
Open Access | Times Cited: 36
Epigenetic Effects of Polybrominated Diphenyl Ethers on Human Health
Robert G. Poston, Ramendra N. Saha
International Journal of Environmental Research and Public Health (2019) Vol. 16, Iss. 15, pp. 2703-2703
Open Access | Times Cited: 50
Distinct Pathogenic Genes Causing Intellectual Disability and Autism Exhibit a Common Neuronal Network Hyperactivity Phenotype
Monica Frega, Martijn Selten, Britt Mossink, et al.
Cell Reports (2020) Vol. 30, Iss. 1, pp. 173-186.e6
Open Access | Times Cited: 49
Neurobiology of ARID1B haploinsufficiency related to neurodevelopmental and psychiatric disorders
Jeffrey J. Moffat, Amanda L. Smith, Eui‐Man Jung, et al.
Molecular Psychiatry (2021) Vol. 27, Iss. 1, pp. 476-489
Open Access | Times Cited: 34
Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype
Paolo Zanoni, Katharina Steindl, Deepanwita Sengupta, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 8, pp. 1474-1483
Open Access | Times Cited: 33
Neurodevelopmental disorders, immunity, and cancer are connected
Ruth Nussinov, Chung‐Jung Tsai, Hyunbum Jang
iScience (2022) Vol. 25, Iss. 6, pp. 104492-104492
Open Access | Times Cited: 24
The omics era: a nexus of untapped potential for Mendelian chromatinopathies
Aileen A. Nava, Valerie A. Arboleda
Human Genetics (2023) Vol. 143, Iss. 4, pp. 475-495
Open Access | Times Cited: 14
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