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:
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
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
Showing 15 citing articles:
Synaptic dysfunction and extracellular matrix dysregulation in dopaminergic neurons from sporadic and E326K-GBA1 Parkinson’s disease patients
Idan Rosh, Utkarsh Tripathi, Yara Hussein, et al.
npj Parkinson s Disease (2024) Vol. 10, Iss. 1
Open Access | Times Cited: 10
Idan Rosh, Utkarsh Tripathi, Yara Hussein, et al.
npj Parkinson s Disease (2024) Vol. 10, Iss. 1
Open Access | Times Cited: 10
Dopamine synthesis and transport: current and novel therapeutics for parkinsonisms
Mary Dayne Sia Tai, Gloria Gamiz-Arco, Aurora Martı́nez
Biochemical Society Transactions (2024) Vol. 52, Iss. 3, pp. 1275-1291
Open Access | Times Cited: 5
Mary Dayne Sia Tai, Gloria Gamiz-Arco, Aurora Martı́nez
Biochemical Society Transactions (2024) Vol. 52, Iss. 3, pp. 1275-1291
Open Access | Times Cited: 5
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
Emma N. M. M. von Scheibler, Ann Swillen, Gabriela M. Repetto, et al.
Movement Disorders Clinical Practice (2025)
Open Access
Bewegungsstörungen und Neurotransmittererkrankungen bei Kindern und Jugendlichen
Birgit Assmann
Springer Reference Medizin (2025), pp. 1-18
Closed Access
Birgit Assmann
Springer Reference Medizin (2025), pp. 1-18
Closed Access
Dementia in Rare Genetic Neurodevelopmental Disorders
Hadassa Kwetsie, Malu van Schaijk, Sven J. van der Lee, et al.
Neurology (2024) Vol. 102, Iss. 11
Open Access | Times Cited: 2
Hadassa Kwetsie, Malu van Schaijk, Sven J. van der Lee, et al.
Neurology (2024) Vol. 102, Iss. 11
Open Access | Times Cited: 2
Dystonia Linked to EIF4A2 Haploinsufficiency: A Disorder of Protein Translation Dysfunction
Philip Harrer, Matěj Škorvánek, Volker Kittke, et al.
Movement Disorders (2023) Vol. 38, Iss. 10, pp. 1914-1924
Open Access | Times Cited: 6
Philip Harrer, Matěj Škorvánek, Volker Kittke, et al.
Movement Disorders (2023) Vol. 38, Iss. 10, pp. 1914-1924
Open Access | Times Cited: 6
Natural history of adults with KBG syndrome: A physician-reported experience
Allan Bayat, Hannah Grimes, Elke de Boer, et al.
Genetics in Medicine (2024) Vol. 26, Iss. 8, pp. 101170-101170
Closed Access | Times Cited: 2
Allan Bayat, Hannah Grimes, Elke de Boer, et al.
Genetics in Medicine (2024) Vol. 26, Iss. 8, pp. 101170-101170
Closed Access | Times Cited: 2
Insights into the Pathobiology of GM1 Gangliosidosis from Single-Nucleus Transcriptomic Analysis of CNS Cells in a Mouse Model
Sichi Liu, Ting Xie, Yonglan Huang
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 17, pp. 9712-9712
Open Access | Times Cited: 1
Sichi Liu, Ting Xie, Yonglan Huang
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 17, pp. 9712-9712
Open Access | Times Cited: 1
A case of early-onset Parkinson’s disease in a patient with KBG syndrome
Luca Magistrelli, Elena Contaldi, Fjorilda Caushi, et al.
Neurological Sciences (2023) Vol. 44, Iss. 12, pp. 4537-4539
Closed Access | Times Cited: 3
Luca Magistrelli, Elena Contaldi, Fjorilda Caushi, et al.
Neurological Sciences (2023) Vol. 44, Iss. 12, pp. 4537-4539
Closed Access | Times Cited: 3
Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome
Emma Nicolette Maximiliane Maria Boersma- von Scheibler
(2023)
Open Access | Times Cited: 2
Emma Nicolette Maximiliane Maria Boersma- von Scheibler
(2023)
Open Access | Times Cited: 2
PPP2R5D heterozygous pathogenic variant causes early-onset parkinsonism and treatment implications: A case report
Wai Yan Yau, Srimathy Vijayan, Gianina Ravenscroft
Parkinsonism & Related Disorders (2024) Vol. 124, pp. 106976-106976
Closed Access
Wai Yan Yau, Srimathy Vijayan, Gianina Ravenscroft
Parkinsonism & Related Disorders (2024) Vol. 124, pp. 106976-106976
Closed Access
Parkinsonism in people with intellectual disability
Erik Boot, Agnies M. van Eeghen, Bas R. Bloem, et al.
Parkinsonism & Related Disorders (2024) Vol. 128, pp. 107079-107079
Closed Access
Erik Boot, Agnies M. van Eeghen, Bas R. Bloem, et al.
Parkinsonism & Related Disorders (2024) Vol. 128, pp. 107079-107079
Closed Access
Do we care? Reporting of genetic diagnoses in multidisciplinary intellectual disability care: a retrospective chart review
Annelieke R. Müller, Erik Boot, Stijn B Notermans, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access
Annelieke R. Müller, Erik Boot, Stijn B Notermans, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access
Bewegungsstörungen und Neurotransmittererkrankungen bei Kindern und Jugendlichen
Birgit Assmann, Christine Klein
Springer Reference Medizin (2024), pp. 1-18
Closed Access
Birgit Assmann, Christine Klein
Springer Reference Medizin (2024), pp. 1-18
Closed Access
Juvenile Parkinsonism Associated With Dihydropyrimidinase Deficiency
Jiaqing Li, Sanqing Xu
PEDIATRICS (2024)
Closed Access
Jiaqing Li, Sanqing Xu
PEDIATRICS (2024)
Closed Access
