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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:

Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data
Kin Y. Mok, Una Sheerin, Javier Simón‐Sánchez, et al.
The Lancet Neurology (2016) Vol. 15, Iss. 6, pp. 585-596
Open Access | Times Cited: 89

Showing 1-25 of 89 citing articles:

Shared mechanisms across the major psychiatric and neurodegenerative diseases
Thomas S. Wingo, Yue Liu, Ekaterina S. Gerasimov, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 116
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
New Genes Causing Hereditary Parkinson’s Disease or Parkinsonism
Andreas Puschmann
Current Neurology and Neuroscience Reports (2017) Vol. 17, Iss. 9
Open Access | Times Cited: 99
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
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
Next-generation sequencing and bioinformatics in rare movement disorders
Michael Zech, J C Winkelmann
Nature Reviews Neurology (2024) Vol. 20, Iss. 2, pp. 114-126
Closed Access | Times Cited: 10
The role of genetics and genomics in clinical psychiatry
Margret R. Hoehe, Deborah J. Morris‐Rosendahl
Dialogues in Clinical Neuroscience (2018) Vol. 20, Iss. 3, pp. 169-177
Open Access | Times Cited: 65
The genetic architecture of schizophrenia: review of large-scale genetic studies
Hidekazu Kato, Hiroki Kimura, Itaru Kushima, et al.
Journal of Human Genetics (2022) Vol. 68, Iss. 3, pp. 175-182
Closed Access | Times Cited: 36
Epigenome-wide association study of human frontal cortex identifies differential methylation in Lewy body pathology
Lasse Pihlstrøm, Gemma Shireby, Hanneke Geut, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 34
Copy number variability in Parkinson’s disease: assembling the puzzle through a systems biology approach
Valentina La Cognata, Giovanna Morello, Velia D’Agata, et al.
Human Genetics (2016) Vol. 136, Iss. 1, pp. 13-37
Open Access | Times Cited: 58
Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome
Adam C. Cunningham, Sue Delport, Wendy Cumines, et al.
The British Journal of Psychiatry (2018) Vol. 212, Iss. 1, pp. 27-33
Open Access | Times Cited: 48
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
Comprehensive analysis of a novel mouse model of the 22q11.2 deletion syndrome: a model with the most common 3.0-Mb deletion at the human 22q11.2 locus
Ryo� Saito, Michinori Koebis, Taku Nagai, et al.
Translational Psychiatry (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 44
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
Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson’s disease
Nancy J. Butcher, Connie Marras, Margarita Pondal, et al.
Brain (2017) Vol. 140, Iss. 5, pp. 1371-1383
Open Access | Times Cited: 47
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
Local and global chromatin interactions are altered by large genomic deletions associated with human brain development
Xianglong Zhang, Ying Zhang, Xiaowei Zhu, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 45
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
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
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
High-depth whole-genome sequencing identifies structure variants, copy number variants and short tandem repeats associated with Parkinson’s disease
Chaodong Wang, Hankui Liu, Xuying Li, et al.
npj Parkinson s Disease (2024) Vol. 10, Iss. 1
Open Access | Times Cited: 4
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
Progress in the genetic analysis of Parkinson’s disease
Andrew Singleton, John Hardy
Human Molecular Genetics (2019) Vol. 28, Iss. R2, pp. R215-R218
Open Access | Times Cited: 34
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
Gene4PD: A Comprehensive Genetic Database of Parkinson’s Disease
Bin Li, Guihu Zhao, Qiao Zhou, et al.
Frontiers in Neuroscience (2021) Vol. 15
Open Access | Times Cited: 24
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