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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:

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: 36

Showing 1-25 of 36 citing articles:

Autism genes converge on asynchronous development of shared neuron classes
Bruna Paulsen, Silvia Velasco, Amanda J. Kedaigle, et al.
Nature (2022) Vol. 602, Iss. 7896, pp. 268-273
Open Access | Times Cited: 307
Single-cell brain organoid screening identifies developmental defects in autism
Chong Li, Jonas Simon Fleck, Catarina Martins‐Costa, et al.
Nature (2023) Vol. 621, Iss. 7978, pp. 373-380
Open Access | Times Cited: 126
Autism Spectrum Disorder: Brain Areas Involved, Neurobiological Mechanisms, Diagnoses and Therapies
Jacopo Lamanna, Jacopo Meldolesi
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 4, pp. 2423-2423
Open Access | Times Cited: 18
The Impact of Mmu17 Non-Hsa21 Orthologous Genes in the Ts65Dn Mouse Model of Down Syndrome: The Gold Standard Refuted
Fayçal Guedj, Elise Kane, Lauren A. Bishop, et al.
Biological Psychiatry (2023) Vol. 94, Iss. 1, pp. 84-97
Open Access | Times Cited: 18
Dendritic spine and synapse pathology in chromatin modifier-associated autism spectrum disorders and intellectual disability
Thomas James L. Ford, Byeong Tak Jeon, Hyunkyoung Lee, et al.
Frontiers in Molecular Neuroscience (2023) Vol. 15
Open Access | Times Cited: 16
Modeling Autism Spectrum Disorders with Induced Pluripotent Stem Cell-Derived Brain Organoids
John Lenon de Souza Santos, Cecília de Almeida Araújo, Clarissa Araújo Gurgel Rocha, et al.
Biomolecules (2023) Vol. 13, Iss. 2, pp. 260-260
Open Access | Times Cited: 13
Elucidating neuroepigenetic mechanisms to inform targeted therapeutics for brain disorders
Benjamin H. Weekley, Newaz I. Ahmed, Ian Maze
iScience (2025) Vol. 28, Iss. 3, pp. 112092-112092
Open Access
Chromatin remodeling and cancer: the critical influence of the SWI/SNF complex
Fengxiang Hao, Ying Zhang, Jiayi Hou, et al.
Epigenetics & Chromatin (2025) Vol. 18, Iss. 1
Open Access
Human Organoids as an Emerging Tool for Genome Screenings
Francesco Andreatta, Delilah Hendriks, Benedetta Artegiani
Annual Review of Biomedical Engineering (2025) Vol. 27, Iss. 1, pp. 157-183
Closed Access
Postnatal age-differential ASD-like transcriptomic, synaptic, and behavioral deficits in Myt1l-mutant mice
Seongbin Kim, Hyoseon Oh, Sang Han Choi, et al.
Cell Reports (2022) Vol. 40, Iss. 12, pp. 111398-111398
Open Access | Times Cited: 17
The Intellectual Disability Risk GeneKdm5bRegulates Long-Term Memory Consolidation in the Hippocampus
Leticia Pérez‐Sisqués, S. Bhatt, Rugilė Matulevičiūtė, et al.
Journal of Neuroscience (2024) Vol. 44, Iss. 19, pp. e1544232024-e1544232024
Open Access | Times Cited: 3
Early and Late Corrections in Mouse Models of Autism Spectrum Disorder
Changuk Chung, Wangyong Shin, Eunjoon Kim
Biological Psychiatry (2021) Vol. 91, Iss. 11, pp. 934-944
Closed Access | Times Cited: 22
Contribution of Age, Brain Region, Mood Disorder Pathology, and Interindividual Factors on the Methylome of Human Microglia
Lot D. de Witte, Zhaoyu Wang, Gijsje L.J.L. Snijders, et al.
Biological Psychiatry (2021) Vol. 91, Iss. 6, pp. 572-581
Open Access | Times Cited: 20
Single-cell brain organoid screening identifies developmental defects in autism
Chong Li, Jonas Simon Fleck, Catarina Martins‐Costa, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 14
Early postnatal serotonin modulation prevents adult-stage deficits in Arid1b-deficient mice through synaptic transcriptional reprogramming
Hyosang Kim, Doyoun Kim, Yisul Cho, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 13
Unraveling the genetic architecture of blood unfolded p-53 among non-demented elderlies: novel candidate genes for early Alzheimer's disease
Arash Yaghoobi, Seyed Amir Malekpour
BMC Genomics (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 2
Demultiplexing of Single-Cell RNA sequencing data using interindividual variation in gene expression
Isar Nassiri, Andrew Kwok, Aneesha Bhandari, et al.
Bioinformatics Advances (2024) Vol. 4, Iss. 1
Open Access | Times Cited: 2
Brain region and gene dosage-differential transcriptomic changes in Shank2-mutant mice
Ye-Eun Yoo, Taesun Yoo, Hyojin Kang, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 10
Pleiotropic effects of a high confidence Autism Spectrum Disorder gene, arid1b, on zebrafish sleep
Fusun Doldur-Balli, Amber Zimmerman, Brendan T Keenan, et al.
Neurobiology of Sleep and Circadian Rhythms (2023) Vol. 14, pp. 100096-100096
Open Access | Times Cited: 6
Behavioral as well as hippocampal transcriptomic and microglial responses differ across sexes in adult mouse offspring exposed to a dual genetic and environmental challenge
Micaël Carrier, Chin Wai Hui, Valérie Watters, et al.
Brain Behavior and Immunity (2023) Vol. 116, pp. 126-139
Closed Access | Times Cited: 6
Treatment of psychiatric comorbidities and interaction patterns in Coffin‐Siris syndrome: A case report of a 4‐year‐old girl
Ann‐Christin Jahnke‐Majorkovits, Christine Fauth, Manuela Gander, et al.
Clinical Case Reports (2024) Vol. 12, Iss. 2
Open Access | Times Cited: 1
Genetic background determines synaptic phenotypes in Arid1b-mutant mice
Hyosang Kim, Eunjoon Kim
Frontiers in Psychiatry (2024) Vol. 14
Open Access | Times Cited: 1
Mutational landscape of risk variants in comorbid depression and obesity: a next-generation sequencing approach
Ana M. Pérez-Gutiérrez, Rosario Carmona, Carlos Loucera, et al.
Molecular Psychiatry (2024) Vol. 29, Iss. 11, pp. 3553-3566
Closed Access | Times Cited: 1
Arid1b haploinsufficiency in pyramidal neurons causes cellular and circuit changes in neocortex but is not sufficient to produce behavioral or seizure phenotypes
Alec H. Marshall, Meretta A. Hanson, Danielle J. Boyle, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Early Chronic Memantine Treatment-Induced Transcriptomic Changes in Wild-Type and Shank2-Mutant Mice
Ye-Eun Yoo, Seungjoon Lee, Woohyun Kim, et al.
Frontiers in Molecular Neuroscience (2021) Vol. 14
Open Access | Times Cited: 9
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