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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:

Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2
Erik Boot, Nancy J. Butcher, Sean Udow, et al.
Neurology (2018) Vol. 90, Iss. 23
Open Access | Times Cited: 41

Showing 1-25 of 41 citing articles:

Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome
Erik Boot, Sólveig Óskarsdóttir, Joanne C. Y. Loo, et al.
Genetics in Medicine (2023) Vol. 25, Iss. 3, pp. 100344-100344
Open Access | Times Cited: 53
Molecular genetics of 22q11.2 deletion syndrome
Bernice E. Morrow, Donna M. McDonald‐McGinn, Beverly S. Emanuel, et al.
American Journal of Medical Genetics Part A (2018) Vol. 176, Iss. 10, pp. 2070-2081
Open Access | Times Cited: 125
Neurobiological perspective of 22q11.2 deletion syndrome
Janneke Zinkstok, Erik Boot, Anne S. Bassett, et al.
The Lancet Psychiatry (2019) Vol. 6, Iss. 11, pp. 951-960
Open Access | Times Cited: 97
Juvenile parkinsonism: Differential diagnosis, genetics, and treatment
Nicki Niemann, Joseph Jankovic
Parkinsonism & Related Disorders (2019) Vol. 67, pp. 74-89
Closed Access | Times Cited: 95
Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from theENIGMAworking groups onCNVs
Ida E. Sønderby, Christopher R. K. Ching, Sophia I. Thomopoulos, et al.
Human Brain Mapping (2021) Vol. 43, Iss. 1, pp. 300-328
Open Access | Times Cited: 56
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
Deep Brain Stimulation in Patients With Mutations in Parkinson's Disease–Related Genes: A Systematic Review
L.M. de Oliveira, Egberto Reis Barbosa, Camila C. Aquino, et al.
Movement Disorders Clinical Practice (2019) Vol. 6, Iss. 5, pp. 359-368
Open Access | Times Cited: 43
A mouse model of 22q11.2 deletions: Molecular and behavioral signatures of Parkinson’s disease and schizophrenia
Akiko Sumitomo, Kouta Horike, Kazuko Hirai, et al.
Science Advances (2018) Vol. 4, Iss. 8
Open Access | Times Cited: 45
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
Prevalence of Parkinson's Disease in 22q11.2 Deletion Syndrome: A Multicenter Study
Emma N. M. M. von Scheibler, Ann Swillen, Gabriela M. Repetto, et al.
Movement Disorders Clinical Practice (2025)
Open Access
Clinical and neuroimaging phenotypes of genetic parkinsonism from infancy to adolescence
Hugo Morales‐Briceño, Shekeeb S. Mohammad, Bart Post, et al.
Brain (2019) Vol. 143, Iss. 3, pp. 751-770
Open Access | Times Cited: 31
Psychosis in Parkinson’s disease and parkinsonism in antipsychotic-naive schizophrenia spectrum psychosis: clinical, nosological and pathobiological challenges
John L. Waddington
Acta Pharmacologica Sinica (2020) Vol. 41, Iss. 4, pp. 464-470
Open Access | Times Cited: 31
Cognition- and circuit-based dysfunction in a mouse model of 22q11.2 microdeletion syndrome: effects of stress
Anushree Tripathi, Michael Spedding, Esther Schenker, et al.
Translational Psychiatry (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 28
Identification of a DNA Methylation Episignature in the 22q11.2 Deletion Syndrome
Kathleen Rooney, Michael A. Levy, Sadegheh Haghshenas, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 16, pp. 8611-8611
Open Access | Times Cited: 24
22q11.2 Deletion Syndrome–Associated Parkinson's Disease
Erik Boot, Anne S. Bassett, Connie Marras
Movement Disorders Clinical Practice (2018) Vol. 6, Iss. 1, pp. 11-16
Open Access | Times Cited: 31
Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review
Emma N. M. M. von Scheibler, Agnies M. van Eeghen, Tom J. de Koning, et al.
Movement Disorders Clinical Practice (2022) Vol. 10, Iss. 1, pp. 17-31
Open Access | Times Cited: 15
Pediatric-Onset Epilepsy and Developmental Epileptic Encephalopathies Followed by Early-Onset Parkinsonism
Carlotta Spagnoli, Carlo Fusco, Francesco Pisani
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 4, pp. 3796-3796
Open Access | Times Cited: 8
The contribution of CNVs to the most common aging-related neurodegenerative diseases
Giulia Gentile, Valentina La Cognata, Sebastiano Cavallaro
Aging Clinical and Experimental Research (2020) Vol. 33, Iss. 5, pp. 1187-1195
Closed Access | Times Cited: 23
Adverse effects of antipsychotic medication in patients with 22q11.2 deletion syndrome: A systematic review
Janna N. de Boer, Erik Boot, Lissa van Gils, et al.
American Journal of Medical Genetics Part A (2019) Vol. 179, Iss. 11, pp. 2292-2306
Open Access | Times Cited: 14
Tremor and Parkinsonism in Chromosomopathies — A Systematic Review
Vanessa Carvalho, Joaquim J. Ferreira, Leonor Correia Guedes
Movement Disorders (2021) Vol. 36, Iss. 9, pp. 2017-2025
Closed Access | Times Cited: 12
Salivary α‐Synuclein as a Candidate Biomarker of Parkinsonism in 22q11.2 Deletion Syndrome
Martina Fanella, Emanuele Cerulli Irelli, Tommaso Accinni, et al.
Movement Disorders Clinical Practice (2024) Vol. 11, Iss. 7, pp. 808-813
Closed Access | Times Cited: 1
Drug-induced parkinsonism in a patient with DiGeorge syndrome: a case report
Clancy Cerejo, Nicolas De Cleene, Gerald Walser, et al.
Frontiers in Neuroscience (2024) Vol. 18
Open Access | Times Cited: 1
Untargeted metabolic analysis in dried blood spots reveals metabolic signature in 22q11.2 deletion syndrome
Dorinde Korteling, Marco P. Boks, Ania Fiksinski, et al.
Translational Psychiatry (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 7
Analysis of REM sleep without atonia in 22q11.2 deletion syndrome determined by domiciliary polysomnography: a cross sectional study
Jorge Mauro, Mario Díaz, T. Córdova, et al.
SLEEP (2021) Vol. 45, Iss. 2
Open Access | Times Cited: 8
How to approach a patient with parkinsonism – red flags for atypical parkinsonism
Eoin Mulroy, María Stamelou, Kailash P. Bhatia
International review of neurobiology (2019), pp. 1-34
Closed Access | Times Cited: 7
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