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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:

Update on the 22q11.2 deletion syndrome and its relevance to schizophrenia
Lily Van, Erik Boot, Anne S. Bassett
Current Opinion in Psychiatry (2017) Vol. 30, Iss. 3, pp. 191-196
Closed Access | Times Cited: 93

Showing 1-25 of 93 citing articles:

Epigenetic Modifications in Schizophrenia and Related Disorders: Molecular Scars of Environmental Exposures and Source of Phenotypic Variability
Juliet Richetto, Urs Meyer
Biological Psychiatry (2020) Vol. 89, Iss. 3, pp. 215-226
Open Access | Times Cited: 143
Association between schizophrenia and autism spectrum disorder: A systematic review and meta‐analysis
Zhen Zheng, Peng Zheng, Xiaobing Zou
Autism Research (2018) Vol. 11, Iss. 8, pp. 1110-1119
Closed Access | Times Cited: 122
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
Isabelle Cleynen, Worrawat Engchuan, Matthew S. Hestand, et al.
Molecular Psychiatry (2020) Vol. 26, Iss. 8, pp. 4496-4510
Open Access | Times Cited: 115
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
Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology
Sébastien Jacquemont, Guillaume Huguet, Marieke Klein, et al.
American Journal of Psychiatry (2022) Vol. 179, Iss. 3, pp. 189-203
Open Access | Times Cited: 47
Aberrantly High Levels of Somatic LINE-1 Expression and Retrotransposition in Human Neurological Disorders
Diane Terry, Scott E. Devine
Frontiers in Genetics (2020) Vol. 10
Open Access | Times Cited: 66
Non-Coding RNA as Novel Players in the Pathophysiology of Schizophrenia
Andrew S. Gibbons, Madhara Udawela, Brian Dean
Non-Coding RNA (2018) Vol. 4, Iss. 2, pp. 11-11
Open Access | Times Cited: 61
Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome
Ania Fiksinski, Maude Schneider, Clodagh M. Murphy, et al.
American Journal of Medical Genetics Part A (2018) Vol. 176, Iss. 10, pp. 2182-2191
Open Access | Times Cited: 60
A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome
Ania Fiksinski, Gil D. Hoftman, Jacob Vorstman, et al.
Molecular Psychiatry (2022) Vol. 28, Iss. 1, pp. 341-353
Open Access | Times Cited: 35
Epigenetic Targets in Schizophrenia Development and Therapy
Agnieszka Wawrzczak‐Bargieła, Wiktor Bilecki, Marzena Maćkowiak
Brain Sciences (2023) Vol. 13, Iss. 3, pp. 426-426
Open Access | Times Cited: 17
Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Clinical Approach
Aleksandra Szczawińska-Popłonyk, Eyal Schwartzmann, Zuzanna Chmara, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 9, pp. 8317-8317
Open Access | Times Cited: 17
Advances in the understanding of the pathophysiology of schizophrenia and bipolar disorder through induced pluripotent stem cell models
Andrea Perrottelli, Francesco Flavio Marzocchi, Edoardo Caporusso, et al.
Journal of Psychiatry and Neuroscience (2024) Vol. 49, Iss. 2, pp. E109-E125
Open Access | Times Cited: 6
Synaptic and Gene Regulatory Mechanisms in Schizophrenia, Autism, and 22q11.2 Copy Number Variant–Mediated Risk for Neuropsychiatric Disorders
Jennifer K. Forsyth, Daniel Nachun, Michael J. Gandal, et al.
Biological Psychiatry (2019) Vol. 87, Iss. 2, pp. 150-163
Open Access | Times Cited: 52
Shorter telomere length in schizophrenia: Evidence from a real-world population and meta-analysis of most recent literature
Patrizia Russo, Giulia Prinzi, Stefania Proietti, et al.
Schizophrenia Research (2018) Vol. 202, pp. 37-45
Closed Access | Times Cited: 48
Prenatal adverse environment is associated with epigenetic age deceleration at birth and hypomethylation at the hypoxia-responsive EP300 gene
Helena Palma‐Gudiel, E. Eixarch, F. Crispi, et al.
Clinical Epigenetics (2019) Vol. 11, Iss. 1
Open Access | Times Cited: 43
Untargeted metabolomic, and proteomic analysis identifies metabolic biomarkers and pathway alterations in individuals with 22q11.2 deletion syndrome
Marwa Zafarullah, Kathleen Angkustsiri, Austin Quach, et al.
Metabolomics (2024) Vol. 20, Iss. 2
Open Access | Times Cited: 5
Association between increased BMI and cognitive function in first-episode drug-naïve male schizophrenia
Xing Deng, Shuiping Lu, Yan Li, et al.
Frontiers in Psychiatry (2024) Vol. 15
Open Access | Times Cited: 5
Genomic Disorders in Psychiatry—What Does the Clinician Need to Know?
Chelsea Lowther, Gregory Costain, Danielle Baribeau, et al.
Current Psychiatry Reports (2017) Vol. 19, Iss. 11
Closed Access | Times Cited: 42
Cognitive functions associated with developing prefrontal cortex during adolescence and developmental neuropsychiatric disorders
Takeshi Sakurai, Nao J. Gamo
Neurobiology of Disease (2018) Vol. 131, pp. 104322-104322
Closed Access | Times Cited: 42
Can Animal Models of Copy Number Variants That Predispose to Schizophrenia Elucidate Underlying Biology?
Annika Forsingdal, Trine N. Jørgensen, Line Olsen, et al.
Biological Psychiatry (2018) Vol. 85, Iss. 1, pp. 13-24
Closed Access | Times Cited: 40
Retinal vascular tortuosity in schizophrenia and bipolar disorder
Abhishek Appaji, Bhargavi Nagendra, Dona Maria Chako, et al.
Schizophrenia Research (2019) Vol. 212, pp. 26-32
Open Access | Times Cited: 40
Obesity and cardiometabolic disease: Insights from genetic studies
Satya Dash
Canadian Journal of Cardiology (2025)
Closed Access
Subthreshold Autism and ADHD: A Brief Narrative Review for Frontline Clinicians
Michael Ogundele, Michael Morton
Pediatric Reports (2025) Vol. 17, Iss. 2, pp. 42-42
Open Access
Psychosis: A Link Between Autism and Schizophrenia Spectrum Disorders
James R. Bell, Autumn L. Parson, Sydney Daneman, et al.
Current Behavioral Neuroscience Reports (2025) Vol. 12, Iss. 1
Closed Access
Intellectual disability: dendritic anomalies and emerging genetic perspectives
Tam Quach, Harrison J. Stratton, Rajesh Khanna, et al.
Acta Neuropathologica (2020) Vol. 141, Iss. 2, pp. 139-158
Open Access | Times Cited: 32
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