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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:

AUTS2 Gene: Keys to Understanding the Pathogenesis of Neurodevelopmental Disorders
Kei Hori, Kazumi Shimaoka, Mikio Hoshino
Cells (2021) Vol. 11, Iss. 1, pp. 11-11
Open Access | Times Cited: 47

Showing 1-25 of 47 citing articles:

Machine learning approaches to identify systemic lupus erythematosus in anti-nuclear antibody-positive patients using genomic data and electronic health records
Chih-Wei Chung, Seng‐Cho T. Chou, Tzu‐Hung Hsiao, et al.
BioData Mining (2024) Vol. 17, Iss. 1
Open Access | Times Cited: 5
High-resolution whole-genome DNA methylation revealed unique signatures of painful diabetic neuropathy
Katarzyna Malgorzata Kwiatkowska, Paolo Garagnani, Massimiliano Bonafè, et al.
Diabetes (2025)
Open Access
The microcephaly-associated transcriptional regulator AUTS2 cooperates with Polycomb complex PRC2 to produce upper-layer neurons in mice
Kazumi Shimaoka, Kei Hori, Satoshi Miyashita, et al.
The EMBO Journal (2025)
Open Access
Single-Cell Resolution of Individual Variation in Hypothalamic Neurons Allows Targeted Manipulation Affecting Social Motivation
Simona Sarafinovska, Sarah K. Koester, Li Fang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Genetic variants associated with the development of stress disorders: A systematic review of GWAS
Yana Zorkina, Elizaveta Golubeva, О. И. Гурина, et al.
S S Korsakov Journal of Neurology and Psychiatry (2025) Vol. 125, Iss. 3, pp. 12-12
Closed Access
Thrombosis-related circulating miR-16-5p is associated with disease severity in patients hospitalised for COVID-19
Ceren Eyileten, Zofia Wicik, Sérgio Nery Simões, et al.
RNA Biology (2022) Vol. 19, Iss. 1, pp. 963-979
Open Access | Times Cited: 19
Networks of placental DNA methylation correlate with maternal serum PCB concentrations and child neurodevelopment
Julia S. Mouat, Xueshu Li, Kari Neier, et al.
Environmental Research (2023) Vol. 220, pp. 115227-115227
Open Access | Times Cited: 11
Genome-wide detection of positive and balancing signatures of selection shared by four domesticated rainbow trout populations (Oncorhynchus mykiss)
Katy Paul, Gwendal Restoux, Florence Phocas
Genetics Selection Evolution (2024) Vol. 56, Iss. 1
Open Access | Times Cited: 4
Investigating the impact of severe maternal SARS-CoV-2 infection on infant DNA methylation and neurodevelopment
Rachel Hill, Andrew S. Gibbons, Wittaya Suwakulsiri, et al.
Molecular Psychiatry (2024)
Closed Access | Times Cited: 4
CRS: a circadian rhythm score model for predicting prognosis and treatment response in cancer patients
Yuwei Liu, Shuang Guo, Yue Sun, et al.
Journal of Translational Medicine (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 10
Atrophin‐1 Function and Dysfunction in Dentatorubral–Pallidoluysian Atrophy
Bartosz Nowak, Emilia Kozłowska, Weronika Pawlik, et al.
Movement Disorders (2023) Vol. 38, Iss. 4, pp. 526-536
Open Access | Times Cited: 8
DNA methylation in people with anorexia nervosa: Epigenome-wide patterns in actively ill, long-term remitted, and healthy-eater women
Howard Steiger, Linda Booij, Lea Thaler, et al.
The World Journal of Biological Psychiatry (2022) Vol. 24, Iss. 3, pp. 254-259
Open Access | Times Cited: 12
Clinical profiling of MRD48 and functional characterization of two novel pathogenic RAC1 variants
Manuela Priolo, Erika Zara, Francesca Clementina Radio, et al.
European Journal of Human Genetics (2023) Vol. 31, Iss. 7, pp. 805-814
Closed Access | Times Cited: 6
The altered expression of cytoskeletal and synaptic remodeling proteins during epilepsy
Yanbao Xin, Guojiao Lin, Tianbao Hua, et al.
Open Life Sciences (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 5
Characterization of genomic regions escaping epigenetic reprogramming in sheep
Camila Urbano Braz, Matilde Maria Passamonti, Hasan Khatib
Current Zoology (2023) Vol. 10, Iss. 1
Open Access | Times Cited: 5
H2A monoubiquitination: insights from human genetics and animal models
Charles W. Ryan, Emily Peirent, Samantha L. Regan, et al.
Human Genetics (2023) Vol. 143, Iss. 4, pp. 511-527
Closed Access | Times Cited: 4
Single-cell RNA sequencing analysis of vestibular schwannoma reveals functionally distinct macrophage subsets
Paramita Baruah, Christopher B. Mahony, Jennifer L. Marshall, et al.
British Journal of Cancer (2024) Vol. 130, Iss. 10, pp. 1659-1669
Open Access | Times Cited: 1
AUTS2 disruption causes neuronal differentiation defects in human cerebral organoids through hyperactivation of the WNT/β-catenin pathway
Zhuangzhuang Geng, Yen Teng Tai, Qiang Wang, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
FGF8-mediated gene regulation affects regional identity in human cerebral organoids
Michele Bertacchi, Gwendoline Maharaux, Agnès Loubat, et al.
eLife (2024) Vol. 13
Open Access | Times Cited: 1
Circulating cell-free DNA methylation mirrors alterations in cerebral patterns in epilepsy
Ricardo Martins-Ferreira, Bárbara Leal, João Chaves, et al.
Clinical Epigenetics (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 6
Disruption of the gene regulatory programme in neurodevelopmental disorders
Aoife Griffin, Arun Mahesh, Vijay Tiwari
Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms (2022) Vol. 1865, Iss. 7, pp. 194860-194860
Open Access | Times Cited: 5
auts2 Features and Expression Are Highly Conserved during Evolution Despite Different Evolutionary Fates Following Whole Genome Duplication
Constance Merdrignac, Antoine Clément, Jérôme Montfort, et al.
Cells (2022) Vol. 11, Iss. 17, pp. 2694-2694
Open Access | Times Cited: 4
Deciphering the role of germline complex de novo structural variations in rare disorders
Hyunchul Jung, Tsun-Po Yang, Susan Walker, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
A novel AUTS2 variant in a patient with global developmental delay and intellectual disability
Mohammad Shboul, Reem Darweesh, Mohammad El-Khateeb, et al.
Jordan Journal of Biological Sciences (2024) Vol. 17, Iss. 02, pp. 217-222
Open Access
Complex de novo structural variants are an underestimated cause of rare disorders
Raheleh Rahbari, Hyunchul Jung, Tsun-Po Yang, et al.
Research Square (Research Square) (2024)
Open Access
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