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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:

Systems Analysis of the 22q11.2 Microdeletion Syndrome Converges on a Mitochondrial Interactome Necessary for Synapse Function and Behavior
Avanti Gokhale, Cortnie Hartwig, A. Freeman, et al.
Journal of Neuroscience (2019), pp. 1983-18
Open Access | Times Cited: 48

Showing 1-25 of 48 citing articles:

Neuronal defects in a human cellular model of 22q11.2 deletion syndrome
Themasap A. Khan, Omer Revah, Aaron Gordon, et al.
Nature Medicine (2020) Vol. 26, Iss. 12, pp. 1888-1898
Open Access | Times Cited: 159
Energy matters: presynaptic metabolism and the maintenance of synaptic transmission
Sunan Li, Zu‐Hang Sheng
Nature reviews. Neuroscience (2021) Vol. 23, Iss. 1, pp. 4-22
Closed Access | Times Cited: 138
Mitochondrial deficits in human iPSC-derived neurons from patients with 22q11.2 deletion syndrome and schizophrenia
Jianping Li, Sean K. Ryan, Erik DeBoer, et al.
Translational Psychiatry (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 84
Emerging evidence for astrocyte dysfunction in schizophrenia
Eva Cristina de Oliveira Figueiredo, Corrado Calì, Francesco Petrelli, et al.
Glia (2022) Vol. 70, Iss. 9, pp. 1585-1604
Open Access | Times Cited: 52
The multifaceted role of mitochondria in autism spectrum disorder
Igor Khaliulin, Wajeha Hamoudi, Haitham Amal
Molecular Psychiatry (2024)
Open Access | Times Cited: 8
Rare Genetic Diseases: Nature's Experiments on Human Development
Chelsea E. Lee, Kaela S. Singleton, Melissa Wallin, et al.
iScience (2020) Vol. 23, Iss. 5, pp. 101123-101123
Open Access | Times Cited: 69
The Role of Alpha-Synuclein and Other Parkinson’s Genes in Neurodevelopmental and Neurodegenerative Disorders
C. Alejandra Morato Torres, Zinah Wassouf, Faria Zafar, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 16, pp. 5724-5724
Open Access | Times Cited: 50
The mitochondrial citrate carrier SLC25A1 regulates metabolic reprogramming and morphogenesis in the developing heart
Chiemela Ohanele, Jessica N. Peoples, Anja Karlstaedt, et al.
Communications Biology (2024) Vol. 7, Iss. 1
Open Access | Times Cited: 6
Mitochondrial Dysfunction in Schizophrenia
Peiyan Ni, Sangmi Chung
BioEssays (2020) Vol. 42, Iss. 6
Closed Access | Times Cited: 45
An interaction-based model for neuropsychiatric features of copy-number variants
Matthew Jensen, Santhosh Girirajan
PLoS Genetics (2019) Vol. 15, Iss. 1, pp. e1007879-e1007879
Open Access | Times Cited: 44
Abnormalities of synaptic mitochondria in autism spectrum disorder and related neurodevelopmental disorders
Liliana Rojas-Charry, Leonardo Nardi, Axel Methner, et al.
Journal of Molecular Medicine (2020) Vol. 99, Iss. 2, pp. 161-178
Open Access | Times Cited: 40
Association of Mitochondrial Biogenesis With Variable Penetrance of Schizophrenia
Jianping Li, Oanh Tran, T. Blaine Crowley, et al.
JAMA Psychiatry (2021) Vol. 78, Iss. 8, pp. 911-911
Open Access | Times Cited: 40
Mitochondrial Dysfunction: A Common Denominator in Neurodevelopmental Disorders?
Xilma R. Ortiz‐González
Developmental Neuroscience (2021) Vol. 43, Iss. 3-4, pp. 222-229
Open Access | Times Cited: 39
APOE expression and secretion are modulated by mitochondrial dysfunction
Meghan E. Wynne, Oluwaseun Ogunbona, Alicia R. Lane, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 16
Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes
Mikhail Vysotskiy, Xue Zhong, Tyne W. Miller‐Fleming, et al.
Genome Medicine (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 28
Disrupted transcriptional networks regulated by CHD1L during neurodevelopment underlie the mirrored neuroanatomical and growth phenotypes of the 1q21.1 copy number variant
Marianne Victoria Lemée, Maria Nicla Loviglio, Ye Tao, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Molecular Systems Biology of Neurodevelopmental Disorders, Rett Syndrome as an Archetype
Victor Faúndez, Meghan E. Wynne, Amanda Crocker, et al.
Frontiers in Integrative Neuroscience (2019) Vol. 13
Open Access | Times Cited: 34
Transcriptomic networks implicate neuronal energetic abnormalities in three mouse models harboring autism and schizophrenia-associated mutations
Aaron Gordon, Annika Forsingdal, Ib Vestergaard Klewe, et al.
Molecular Psychiatry (2019) Vol. 26, Iss. 5, pp. 1520-1534
Open Access | Times Cited: 34
Anatomical and molecular characterization of parvalbumin-cholecystokinin co-expressing inhibitory interneurons: implications for neuropsychiatric conditions
Steven F. Grieco, Kevin G. Johnston, Pan Gao, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 12, pp. 5293-5308
Open Access | Times Cited: 9
Behavioral Phenotypes and Comorbidity in 3q29 Deletion Syndrome: Results from the 3q29 Registry
Rebecca M. Pollak, Michael Mortillo, Melissa M. Murphy, et al.
Journal of Autism and Developmental Disorders (2024)
Open Access | Times Cited: 3
Mitochondrial Proteostasis Requires Genes Encoded in a Neurodevelopmental Syndrome Locus
Avanti Gokhale, Chelsea E. Lee, Stephanie A. Zlatic, et al.
Journal of Neuroscience (2021) Vol. 41, Iss. 31, pp. 6596-6616
Open Access | Times Cited: 22
Heterogeneous Expression of Nuclear Encoded Mitochondrial Genes Distinguishes Inhibitory and Excitatory Neurons
Meghan E. Wynne, Alicia R. Lane, Kaela S. Singleton, et al.
eNeuro (2021) Vol. 8, Iss. 4, pp. ENEURO.0232-21.2021
Open Access | Times Cited: 22
Review: Genes Involved in Mitochondrial Physiology Within 22q11.2 Deleted Region and Their Relevance to Schizophrenia
David Kolář, Branislav Krajčovič, Lenka Kletečková, et al.
Schizophrenia Bulletin (2023) Vol. 49, Iss. 6, pp. 1637-1653
Closed Access | Times Cited: 8
Modeling and Predicting Developmental Trajectories of Neuropsychiatric Dimensions Associated With Copy Number Variations
Noboru Hiroi, Takahira Yamauchi
The International Journal of Neuropsychopharmacology (2019) Vol. 22, Iss. 8, pp. 488-500
Open Access | Times Cited: 23
Increased expression of SLC25A1/CIC causes an autistic-like phenotype with altered neuron morphology
Michael J. Rigby, Nicola Salvatore Orefice, Alexis J. Lawton, et al.
Brain (2021) Vol. 145, Iss. 2, pp. 500-516
Open Access | Times Cited: 18
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