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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:

Haploinsufficiency of MeCP2-interacting transcriptional co-repressor SIN3A causes mild intellectual disability by affecting the development of cortical integrity
J.S. Witteveen, Marjolein H. Willemsen, Thaís Caroline Dallabona Dombroski, et al.
Nature Genetics (2016) Vol. 48, Iss. 8, pp. 877-887
Closed Access | Times Cited: 88

Showing 1-25 of 88 citing articles:

Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
Holly A.F. Stessman, Bo Xiong, Bradley P. Coe, et al.
Nature Genetics (2017) Vol. 49, Iss. 4, pp. 515-526
Open Access | Times Cited: 512
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: 424
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
Development of prefrontal cortex
Sharon M. Kolk, Pasko Rakić
Neuropsychopharmacology (2021) Vol. 47, Iss. 1, pp. 41-57
Open Access | Times Cited: 209
Multivariate GWAS of psychiatric disorders and their cardinal symptoms reveal two dimensions of cross-cutting genetic liabilities
Travis T. Mallard, Richard Karlsson Linnér, Andrew D. Grotzinger, et al.
Cell Genomics (2022) Vol. 2, Iss. 6, pp. 100140-100140
Open Access | Times Cited: 76
Impact of life adversity and gene expression on psychiatric symptoms in children and adolescents: findings from the Brazilian high risk cohort study
Vanessa Kiyomi Ota, Adrielle Martins Oliveira, Amanda Bugiga, et al.
Frontiers in Psychiatry (2025) Vol. 16
Open Access | Times Cited: 1
Disruption of MeCP2–TCF20 complex underlies distinct neurodevelopmental disorders
Jian Zhou, Hamdan Hamdan, Hari Krishna Yalamanchili, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 4
Open Access | Times Cited: 32
In vivo epigenetic editing of Sema6a promoter reverses transcallosal dysconnectivity caused by C11orf46/Arl14ep risk gene
Cyril Peter, Atsushi Saito, Yuto Hasegawa, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 45
SCAPER localizes to primary cilia and its mutation affects cilia length, causing Bardet-Biedl syndrome
Ohad Wormser, Libe Gradstein, Yuval Yogev, et al.
European Journal of Human Genetics (2019) Vol. 27, Iss. 6, pp. 928-940
Open Access | Times Cited: 44
Virtual ChIP-seq: predicting transcription factor binding by learning from the transcriptome
Mehran Karimzadeh, Michael M. Hoffman
Genome biology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 28
Mitotic block and epigenetic repression underlie neurodevelopmental defects and neurobehavioral deficits in congenital heart disease
George C. Gabriel, Hisato Yagi, Tuantuan Tan, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Witteveen–Kolk Syndrome With Cleft Palate: A Case Report and Review of the Literature
Etkin Boynuyoğun, Yusuf Irmak, Murat Kara, et al.
The Cleft Palate-Craniofacial Journal (2025)
Closed Access
Regulatory non-coding somatic mutations as drivers of neuroblastoma
Annalaura Montella, Matilde Tirelli, Vito Alessandro Lasorsa, et al.
British Journal of Cancer (2025)
Open Access
TBC1D24 regulates axonal outgrowth and membrane trafficking at the growth cone in rodent and human neurons
Davide Aprile, Floriana Fruscione, Sımona Baldassari, et al.
Cell Death and Differentiation (2019) Vol. 26, Iss. 11, pp. 2464-2478
Open Access | Times Cited: 33
Haploinsufficiency of RREB1 causes a Noonan-like RASopathy via epigenetic reprogramming of RAS-MAPK pathway genes
Oliver A. Kent, Manipa Saha, Étienne Coyaud, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 32
Comprehensive study of 28 individuals with SIN3A-related disorder underscoring the associated mild cognitive and distinctive facial phenotype
Meena Balasubramanian, Alexander J.M. Dingemans, Shadi Albaba, et al.
European Journal of Human Genetics (2021) Vol. 29, Iss. 4, pp. 625-636
Open Access | Times Cited: 26
A KDM5–Prospero transcriptional axis functions during early neurodevelopment to regulate mushroom body formation
Hayden A. M. Hatch, Helen M. Belálcazar, Owen J. Marshall, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 26
Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder
Xénia Latypova, Marie Vincent, Alice Mollé, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 5, pp. 929-941
Open Access | Times Cited: 26
Structure of a SIN3–HDAC complex from budding yeast
Zhouyan Guo, Chu Chen, Yichen Lu, et al.
Nature Structural & Molecular Biology (2023) Vol. 30, Iss. 6, pp. 753-760
Closed Access | Times Cited: 10
Rescuing lung development through embryonic inhibition of histone acetylation
Giangela Stokes, Zhuowei Li, Nicole Talaba, et al.
Science Translational Medicine (2024) Vol. 16, Iss. 732
Open Access | Times Cited: 3
Report on Witteveen-Kolk syndrome caused by large fragment deletion in the 15q24.1 - q24.2 region in infants with early onset and literature review
Haohui Tang, Jin-Long Xu, Ling Ge, et al.
˜The œItalian Journal of Pediatrics/Italian journal of pediatrics (2025) Vol. 51, Iss. 1
Open Access
Virtual ChIP-seq: predicting transcription factor binding by learning from the transcriptome
Mehran Karimzadeh, Michael M. Hoffman
bioRxiv (Cold Spring Harbor Laboratory) (2018)
Open Access | Times Cited: 30
Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder
Suzanna G.M. Frints, Ayşegül Ozantürk, Germán Rodríguez Criado, et al.
Molecular Psychiatry (2018) Vol. 24, Iss. 11, pp. 1748-1768
Open Access | Times Cited: 29
Multivariate GWAS of psychiatric disorders and their cardinal symptoms reveal two dimensions of cross-cutting genetic liabilities
Travis T. Mallard, Richard Karlsson Linnér, Andrew D. Grotzinger, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2019)
Open Access | Times Cited: 27
Transcriptional corepressor SIN3A regulates hippocampal synaptic plasticity via Homer1/mGluR5 signaling
Morgan S. Bridi, Hannah Schoch, Cédrick Florian, et al.
JCI Insight (2020) Vol. 5, Iss. 5
Open Access | Times Cited: 25
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