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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:

Identification of mutations in AP4S1/SPG52 through next generation sequencing in three families
Alessandra Tessa, Roberta Battini, Anna Rubegni, et al.
European Journal of Neurology (2016) Vol. 23, Iss. 10, pp. 1580-1587
Closed Access | Times Cited: 32

Showing 1-25 of 32 citing articles:

Hereditary ataxias and paraparesias: clinical and genetic update
Livia Parodi, Giulia Coarelli, Giovanni Stévanin, et al.
Current Opinion in Neurology (2018) Vol. 31, Iss. 4, pp. 462-471
Closed Access | Times Cited: 90
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study
Angelica D’Amore, Alessandra Tessa, Carlo Casali, et al.
Frontiers in Neurology (2018) Vol. 9
Open Access | Times Cited: 74
Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia
Darius Ebrahimi‐Fakhari, Julian Teinert, Robert Behne, et al.
Brain (2019)
Open Access | Times Cited: 62
Clinical and genetic characterization of AP4B1‐associated SPG47
Darius Ebrahimi‐Fakhari, Chi Vicky Cheng, Kira A. Dies, et al.
American Journal of Medical Genetics Part A (2017) Vol. 176, Iss. 2, pp. 311-318
Closed Access | Times Cited: 58
Impaired flickering of the permeability transition pore causes SPG7 spastic paraplegia
Irene Sambri, Filomena Massa, Francesca Gullo, et al.
EBioMedicine (2020) Vol. 61, pp. 103050-103050
Open Access | Times Cited: 40
Role of glial cells in motor neuron degeneration in hereditary spastic paraplegias
Manaswini Vijayaraghavan, S. R. Murali, Gitika Thakur, et al.
Frontiers in Cellular Neuroscience (2025) Vol. 19
Open Access
The genetic etiology in cerebral palsy mimics: The results from a Greek tertiary care center
Vasiliki Zouvelou, Dèlia Yubero, Loukia Apostolakopoulou, et al.
European Journal of Paediatric Neurology (2019) Vol. 23, Iss. 3, pp. 427-437
Closed Access | Times Cited: 34
Current Knowledge of Endolysosomal and Autophagy Defects in Hereditary Spastic Paraplegia
Liriopé Toupenet Marchesi, Marion Leblanc, Giovanni Stévanin
Cells (2021) Vol. 10, Iss. 7, pp. 1678-1678
Open Access | Times Cited: 26
Clinical and neuroimaging features of autosomal recessive spastic paraplegia 35 (SPG35): case reports, new mutations, and brief literature review
Francesco Mari, Beatrice Berti, Alessandro Romano, et al.
Neurogenetics (2018) Vol. 19, Iss. 2, pp. 123-130
Closed Access | Times Cited: 24
Loss of ap4s1 in zebrafish leads to neurodevelopmental defects resembling spastic paraplegia 52
Angelica D’Amore, Alessandra Tessa, Valentina Naef, et al.
Annals of Clinical and Translational Neurology (2020) Vol. 7, Iss. 4, pp. 584-589
Open Access | Times Cited: 22
Clinical Characteristics Suggestive of a Genetic Cause in Cerebral Palsy: A Systematic Review
Anna M. Janzing, Erik A. Eklund, Tom J. de Koning, et al.
Pediatric Neurology (2024) Vol. 153, pp. 144-151
Open Access | Times Cited: 2
An Ultra-Rare Mixed Phenotype with Combined AP-4 and ERF Mutations: The First Report in a Pediatric Patient and a Literature Review
Alessandro Orsini, Andrea Santangelo, Alessandra Carmignani, et al.
Genes (2024) Vol. 15, Iss. 4, pp. 436-436
Open Access | Times Cited: 2
Leigh-like neuroimaging features associated with new biallelic mutations in OPA1
Anna Rubegni, Tiziana Pisano, Giacomo Maria Bacci, et al.
European Journal of Paediatric Neurology (2017) Vol. 21, Iss. 4, pp. 671-677
Closed Access | Times Cited: 22
Hereditary spastic paraplegias proteome: common pathways and pathogenetic mechanisms
Chiara Martinello, Emanuele Panza, Antonio Orlacchio
Expert Review of Proteomics (2023) Vol. 20, Iss. 7-9, pp. 171-188
Closed Access | Times Cited: 6
SPG2 mimicking multiple sclerosis in a family identified using next generation sequencing
Anna Rubegni, Carla Battisti, Alessandra Tessa, et al.
Journal of the Neurological Sciences (2017) Vol. 375, pp. 198-202
Closed Access | Times Cited: 20
Ap4b1-knockout mouse model of hereditary spastic paraplegia type 47 displays motor dysfunction, aberrant brain morphology and ATG9A mislocalization
Joseph M. Scarrott, João Alves-Cruzeiro, Paolo Marchi, et al.
Brain Communications (2022) Vol. 5, Iss. 1
Open Access | Times Cited: 9
Clinical and molecular studies in two new cases of ARSACS
Ivana Ricca, Federica Morani, Giacomo Maria Bacci, et al.
Neurogenetics (2019) Vol. 20, Iss. 1, pp. 45-49
Closed Access | Times Cited: 15
The role of AP-4 in cargo export from the trans-Golgi network and hereditary spastic paraplegia
Rafael Mattera, Raffaella De Pace, Juan S. Bonifacino
Biochemical Society Transactions (2020) Vol. 48, Iss. 5, pp. 1877-1888
Closed Access | Times Cited: 11
Tepsin binds LC3B to promote ATG9A export and delivery at the cell periphery
Natalie Wallace, John E. Gadbery, Cameron I. Cohen, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
Utilizing RNA and outlier analysis to identify an intronic splice‐altering variant inAP4S1in a sibling pair with progressive spastic paraplegia
Carmel G. McCullough, Szabolcs Szelinger, Newell Belnap, et al.
Human Mutation (2019) Vol. 41, Iss. 2, pp. 412-419
Open Access | Times Cited: 8
AP4S1 splice-site mutation in a case of spastic paraplegia type 52 with polymicrogyria
Susana Carmona, Clara Marecos, Marta Amorim, et al.
Neurology Genetics (2018) Vol. 4, Iss. 5
Open Access | Times Cited: 6
Neuroimaging patterns in paediatric onset hereditary spastic paraplegias
Claudia Dosi, Rosa Pasquariello, Chiara Ticci, et al.
Journal of the Neurological Sciences (2021) Vol. 425, pp. 117441-117441
Closed Access | Times Cited: 5
Congenital cerebral palsy: genetic cause and nosological integrity
P. I. Sokolov, N. V. Chebanenko, В П Зыков, et al.
Russian Journal of Child Neurology (2021) Vol. 15, Iss. 3-4, pp. 65-77
Open Access | Times Cited: 4
AP-4 loss in CRISPR-edited zebrafish affects early embryo development
Olivia G. Pembridge, Natalie Wallace, Thomas P. Clements, et al.
Advances in Biological Regulation (2022) Vol. 87, pp. 100945-100945
Open Access | Times Cited: 3
Combined generalized and focal epilepsy with reflex features in Adaptor protein complex 4-associated hereditary spastic paraplegias: a cohort observational study
Emanuele Bartolini, Anna Rita Ferrari, Filippo M. Santorelli, et al.
Seizure (2024) Vol. 121, pp. 186-193
Closed Access
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