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:
R106C TFG variant causes infantile neuroaxonal dystrophy “plus” syndrome
Alessia Catania, Roberta Battini, Tommaso Pippucci, et al.
Neurogenetics (2018) Vol. 19, Iss. 3, pp. 179-187
Closed Access | Times Cited: 17
Alessia Catania, Roberta Battini, Tommaso Pippucci, et al.
Neurogenetics (2018) Vol. 19, Iss. 3, pp. 179-187
Closed Access | Times Cited: 17
Showing 17 citing articles:
Toxoplasmosis accelerates the progression of hereditary spastic paraplegia
James R. Alvin, Carlos J. Ramírez‐Flores, Caitlin A. Mendina, et al.
mSphere (2025)
Open Access
James R. Alvin, Carlos J. Ramírez‐Flores, Caitlin A. Mendina, et al.
mSphere (2025)
Open Access
TFG binds LC3C to regulate ULK1 localization and autophagosome formation
Marianna Carinci, Beatrice Testa, Matteo Bordi, et al.
The EMBO Journal (2021) Vol. 40, Iss. 10
Open Access | Times Cited: 22
Marianna Carinci, Beatrice Testa, Matteo Bordi, et al.
The EMBO Journal (2021) Vol. 40, Iss. 10
Open Access | Times Cited: 22
TFG regulates secretory and endosomal sorting pathways in neurons to promote their activity and maintenance
Jennifer L. Peotter, Iryna Pustova, Molly M. Lettman, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 40
Open Access | Times Cited: 14
Jennifer L. Peotter, Iryna Pustova, Molly M. Lettman, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 40
Open Access | Times Cited: 14
The hereditary spastic paraplegias
John K. Fink
Handbook of clinical neurology (2023), pp. 59-88
Closed Access | Times Cited: 8
John K. Fink
Handbook of clinical neurology (2023), pp. 59-88
Closed Access | Times Cited: 8
Multiple roles for TFG ring complexes in neuronal cargo trafficking
Ziheng Zhang, Molly M. Lettman, Amber L. Schuh, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Ziheng Zhang, Molly M. Lettman, Amber L. Schuh, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
NovelTFGmutation causes autosomal-dominant spastic paraplegia and defects in autophagy
Ling Xu, Yaru Wang, Wenqing Wang, et al.
Journal of Medical Genetics (2023) Vol. 61, Iss. 4, pp. 325-331
Closed Access | Times Cited: 3
Ling Xu, Yaru Wang, Wenqing Wang, et al.
Journal of Medical Genetics (2023) Vol. 61, Iss. 4, pp. 325-331
Closed Access | Times Cited: 3
Continuum of phenotypes in hereditary motor and sensory neuropathy with proximal predominance and Charcot–Marie–Tooth patients with TFG mutation
Marzieh Khani, Hanieh Taheri, Hosein Shamshiri, et al.
American Journal of Medical Genetics Part A (2019) Vol. 179, Iss. 8, pp. 1507-1515
Closed Access | Times Cited: 8
Marzieh Khani, Hanieh Taheri, Hosein Shamshiri, et al.
American Journal of Medical Genetics Part A (2019) Vol. 179, Iss. 8, pp. 1507-1515
Closed Access | Times Cited: 8
Sural nerve pathology in TFG‐associated motor neuron disease with sensory neuropathy
Jia Li, Lingchao Meng, Rui Wu, et al.
Neuropathology (2019) Vol. 39, Iss. 3, pp. 194-199
Closed Access | Times Cited: 5
Jia Li, Lingchao Meng, Rui Wu, et al.
Neuropathology (2019) Vol. 39, Iss. 3, pp. 194-199
Closed Access | Times Cited: 5
Inherited motor-sensory neuropathy with upper limb predominance associated with the tropomyosin-receptor kinase fused gene
Gian Maria Fabrizi, Helle Høyer, Federica Taioli, et al.
Neuromuscular Disorders (2020) Vol. 30, Iss. 3, pp. 227-231
Closed Access | Times Cited: 5
Gian Maria Fabrizi, Helle Høyer, Federica Taioli, et al.
Neuromuscular Disorders (2020) Vol. 30, Iss. 3, pp. 227-231
Closed Access | Times Cited: 5
Homozygous TFG gene variants expanding the mutational and clinical spectrum of hereditary spastic paraplegia 57 and a review of literature
Mehdi Khorrami, Mohammad Amin Tabatabaiefar, Erfan Khorram, et al.
Journal of Human Genetics (2021) Vol. 66, Iss. 10, pp. 973-981
Closed Access | Times Cited: 5
Mehdi Khorrami, Mohammad Amin Tabatabaiefar, Erfan Khorram, et al.
Journal of Human Genetics (2021) Vol. 66, Iss. 10, pp. 973-981
Closed Access | Times Cited: 5
Toxoplasma gondii infection accelerates the progression of hereditary spastic paraplegia
James R. Alvin, Carlos J. Ramírez‐Flores, Caitlin A. Mendina, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
James R. Alvin, Carlos J. Ramírez‐Flores, Caitlin A. Mendina, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Cell type–specific gene therapy confers protection against motor neuron disease caused by a TFG variant
Molly M. Lettman, Caitlin A. Mendina, Emma Burkard, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 47
Closed Access
Molly M. Lettman, Caitlin A. Mendina, Emma Burkard, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 47
Closed Access
A novel TFG c.793C>G mutation in a Chinese pedigree with Charcot‐Marie‐Tooth disease 2
Dingwen Wu, Yanfang Li, Xinzhen Yin, et al.
Brain and Behavior (2020) Vol. 10, Iss. 9
Open Access | Times Cited: 3
Dingwen Wu, Yanfang Li, Xinzhen Yin, et al.
Brain and Behavior (2020) Vol. 10, Iss. 9
Open Access | Times Cited: 3
The hereditary spastic paraplegias
John K. Fink
Elsevier eBooks (2020), pp. 147-170
Closed Access | Times Cited: 1
John K. Fink
Elsevier eBooks (2020), pp. 147-170
Closed Access | Times Cited: 1
TFG: a novel regulator of ULK1-dependent autophagy
Francesco Cecconi, Francesca Nazio
Molecular & Cellular Oncology (2021) Vol. 8, Iss. 4
Open Access
Francesco Cecconi, Francesca Nazio
Molecular & Cellular Oncology (2021) Vol. 8, Iss. 4
Open Access
