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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:

Neurological manifestation of 22q11.2 deletion syndrome
Michael Bayat, Allan Bayat
Neurological Sciences (2022) Vol. 43, Iss. 3, pp. 1695-1700
Closed Access | Times Cited: 22

Showing 22 citing articles:

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
Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors
Francesca Cillo, Emma Coppola, Federico Habetswallner, et al.
Genes (2024) Vol. 15, Iss. 3, pp. 321-321
Open Access | Times Cited: 7
Modeling the enigma of complex disease etiology
Lynn M. Schriml, Richard Lichenstein, Katharine Bisordi, et al.
Journal of Translational Medicine (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 12
Behavioral and Psychiatric Disorders in Syndromic Autism
Ann Genovese, Merlin G. Butler
Brain Sciences (2024) Vol. 14, Iss. 4, pp. 343-343
Open Access | Times Cited: 4
Clozapine Use Among Individuals With Schizophrenia Occurring on the Background of Intellectual Disability and Rare Genetic Variation
Mark Ainsley Colijn
Journal of Clinical Psychopharmacology (2025)
Closed Access
Drug Treatment of Psychiatric Symptoms Occurring in the Context of Other Conditions

(2025), pp. 803-864
Closed Access
The citrate transporters SLC13A5 and SLC25A1 elicit different metabolic responses and phenotypes in the mouse
Gonzalo Fernandez-Fuente, Katherine A. Overmyer, Alexis J. Lawton, et al.
Communications Biology (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 9
Intracellular Citrate/acetyl-CoA flux and endoplasmic reticulum acetylation: Connectivity is the answer
Gonzalo Fernandez-Fuente, Michael J. Rigby, Luigi Puglielli
Molecular Metabolism (2022) Vol. 67, pp. 101653-101653
Open Access | Times Cited: 14
The effectiveness and tolerability of pharmacotherapy for psychosis in 22q11.2 Deletion Syndrome: A systematic review
Maya Tanham, Renee Chen, Nicola Warren, et al.
Australian & New Zealand Journal of Psychiatry (2024) Vol. 58, Iss. 5, pp. 393-403
Closed Access | Times Cited: 2
Neuroanatomical Correlates of Cognitive Dysfunction in 22q11.2 Deletion Syndrome
Simon Smerconish, J. Eric Schmitt
Genes (2024) Vol. 15, Iss. 4, pp. 440-440
Open Access | Times Cited: 2
WONOEP appraisal: Genetic insights into early onset epilepsies
Anne Quatraccioni, Silvia Cases‐Cunillera, Ganna Balagura, et al.
Epilepsia (2024) Vol. 65, Iss. 11, pp. 3138-3154
Open Access | Times Cited: 1
Cytogenomic epileptology
Ivan Y. Iourov, Alexandr Gerasimov, Maria A. Zelenova, et al.
Molecular Cytogenetics (2023) Vol. 16, Iss. 1
Open Access | Times Cited: 3
Clinical management of psychosis in 22q11.2 deletion syndrome
Anton Iftimovici, Marie‐Odile Krebs, Boris Chaumette
Journal of Psychiatry and Neuroscience (2022) Vol. 47, Iss. 6, pp. E391-E392
Open Access | Times Cited: 4
Acute Onset, Relapsing–Remitting Choreiform Movement Disorder in A Girl with 22q11.2 Deletion Syndrome
Silvia Saottini, Sara Brunetti, Anna Molinaro, et al.
Journal of Pediatric Neurology (2024)
Closed Access
DiGeorge Syndrome
Dena Oaklander, Khalid I. Afzal, Karam Radwan
(2024), pp. 141-155
Closed Access
Neuroinflammation and Oxidative Stress in Individuals Affected by DiGeorge Syndrome
Michela Menghi, Ginevra Micangeli, Francesca Tarani, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 4, pp. 4242-4242
Open Access | Times Cited: 1
Severe Pediatric Dystonia Responding to Deep Brain Stimulation in 22q11.2 Microduplication Syndrome: Rare Clinical Presentation
Hanin Algethami, Sara Breitbart, Nebras M. Warsi, et al.
Movement Disorders Clinical Practice (2023) Vol. 11, Iss. 3, pp. 309-311
Closed Access | Times Cited: 1
Structural Cerebellar Abnormalities and Parkinsonism in Patients with 22q11.2 Deletion Syndrome
Claudia Piervincenzi, Martina Fanella, Nikolaos Petsas, et al.
Brain Sciences (2022) Vol. 12, Iss. 11, pp. 1533-1533
Open Access | Times Cited: 1
Juvenile Parkinson’s disease and 22q11.2 microdeletion syndrome
Carla Palleis, Annika Eißner, Stefanie Förderreuther, et al.
Der Nervenarzt (2023) Vol. 94, Iss. 6, pp. 546-550
Open Access
The Subtlety of 22q11.2 Deletion Syndrome in a Preterm Neonate
Laura Cline, P. Aranda, Amy J. Jnah
Neonatal Network The Journal of Neonatal Nursing (2023) Vol. 42, Iss. 3, pp. 137-144
Closed Access
Structural aging of human neurons is opposite of the changes in schizophrenia
Ryuta Mizutani, Rino Saiga, Yoshiro Yamamoto, et al.
PLoS ONE (2023) Vol. 18, Iss. 6, pp. e0287646-e0287646
Open Access
Acetyl-CoA and acetylation in biology and disease
Luigi Puglielli, Michael J. Rigby, Gonzalo Fernandez-Fuente
Elsevier eBooks (2023), pp. 483-506
Closed Access
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