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:
Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation
Monika Hartig, Arcangela Iuso, Tobias B. Haack, et al.
The American Journal of Human Genetics (2011) Vol. 89, Iss. 4, pp. 543-550
Open Access | Times Cited: 250
Monika Hartig, Arcangela Iuso, Tobias B. Haack, et al.
The American Journal of Human Genetics (2011) Vol. 89, Iss. 4, pp. 543-550
Open Access | Times Cited: 250
Showing 1-25 of 250 citing articles:
Iron metabolism in the CNS: implications for neurodegenerative diseases
Tracey A. Rouault
Nature reviews. Neuroscience (2013) Vol. 14, Iss. 8, pp. 551-564
Open Access | Times Cited: 430
Tracey A. Rouault
Nature reviews. Neuroscience (2013) Vol. 14, Iss. 8, pp. 551-564
Open Access | Times Cited: 430
Hereditary spastic paraplegia: Clinical-genetic characteristics and evolving molecular mechanisms
Temistocle Lo Giudice, Federica Lombardi, Filippo M. Santorelli, et al.
Experimental Neurology (2014) Vol. 261, pp. 518-539
Open Access | Times Cited: 310
Temistocle Lo Giudice, Federica Lombardi, Filippo M. Santorelli, et al.
Experimental Neurology (2014) Vol. 261, pp. 518-539
Open Access | Times Cited: 310
Neurodegeneration with brain iron accumulation
Susan J. Hayflick, Manju A. Kurian, Penelope Hogarth
Handbook of clinical neurology (2018), pp. 293-305
Open Access | Times Cited: 282
Susan J. Hayflick, Manju A. Kurian, Penelope Hogarth
Handbook of clinical neurology (2018), pp. 293-305
Open Access | Times Cited: 282
Neuropathology of genetic synucleinopathies with parkinsonism: Review of the literature
Susanne A. Schneider, Roy N. Alcalay
Movement Disorders (2017) Vol. 32, Iss. 11, pp. 1504-1523
Open Access | Times Cited: 274
Susanne A. Schneider, Roy N. Alcalay
Movement Disorders (2017) Vol. 32, Iss. 11, pp. 1504-1523
Open Access | Times Cited: 274
Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance
Josef Finsterer, Wolfgang N. Löscher, Stefan Quasthoff, et al.
Journal of the Neurological Sciences (2012) Vol. 318, Iss. 1-2, pp. 1-18
Open Access | Times Cited: 264
Josef Finsterer, Wolfgang N. Löscher, Stefan Quasthoff, et al.
Journal of the Neurological Sciences (2012) Vol. 318, Iss. 1-2, pp. 1-18
Open Access | Times Cited: 264
Connie Marras, Anthony E. Lang, Bart P.C. van de Warrenburg, et al.
Movement Disorders (2016) Vol. 31, Iss. 4, pp. 436-457
Closed Access | Times Cited: 260
Neurodegeneration with Brain Iron Accumulation: Diagnosis and Management
Penelope Hogarth
Journal of Movement Disorders (2015) Vol. 8, Iss. 1, pp. 1-13
Open Access | Times Cited: 200
Penelope Hogarth
Journal of Movement Disorders (2015) Vol. 8, Iss. 1, pp. 1-13
Open Access | Times Cited: 200
Cerebral Iron Deposition in Neurodegeneration
Petr Dušek, Tim Hofer, Jan Alexander, et al.
Biomolecules (2022) Vol. 12, Iss. 5, pp. 714-714
Open Access | Times Cited: 90
Petr Dušek, Tim Hofer, Jan Alexander, et al.
Biomolecules (2022) Vol. 12, Iss. 5, pp. 714-714
Open Access | Times Cited: 90
Iron imbalance in neurodegeneration
Sonia Levi, Maddalena Ripamonti, Andrea Stefano Moro, et al.
Molecular Psychiatry (2024) Vol. 29, Iss. 4, pp. 1139-1152
Open Access | Times Cited: 50
Sonia Levi, Maddalena Ripamonti, Andrea Stefano Moro, et al.
Molecular Psychiatry (2024) Vol. 29, Iss. 4, pp. 1139-1152
Open Access | Times Cited: 50
Brain Iron Homeostasis: From Molecular Mechanisms To Clinical Significance and Therapeutic Opportunities
Neena Singh, Swati Haldar, Ajai K. Tripathi, et al.
Antioxidants and Redox Signaling (2013) Vol. 20, Iss. 8, pp. 1324-1363
Open Access | Times Cited: 190
Neena Singh, Swati Haldar, Ajai K. Tripathi, et al.
Antioxidants and Redox Signaling (2013) Vol. 20, Iss. 8, pp. 1324-1363
Open Access | Times Cited: 190
Exome Sequence Reveals Mutations in CoA Synthase as a Cause of Neurodegeneration with Brain Iron Accumulation
Sabrina Dusi, Lorella Valletta, Tobias B. Haack, et al.
The American Journal of Human Genetics (2013) Vol. 94, Iss. 1, pp. 11-22
Open Access | Times Cited: 188
Sabrina Dusi, Lorella Valletta, Tobias B. Haack, et al.
The American Journal of Human Genetics (2013) Vol. 94, Iss. 1, pp. 11-22
Open Access | Times Cited: 188
New NBIA subtype
Penelope Hogarth, Allison Gregory, Michael C. Kruer, et al.
Neurology (2012) Vol. 80, Iss. 3, pp. 268-275
Open Access | Times Cited: 167
Penelope Hogarth, Allison Gregory, Michael C. Kruer, et al.
Neurology (2012) Vol. 80, Iss. 3, pp. 268-275
Open Access | Times Cited: 167
Iron dysregulation in movement disorders
Petr Dušek, Joseph Jankovic, Weidong Le
Neurobiology of Disease (2012) Vol. 46, Iss. 1, pp. 1-18
Closed Access | Times Cited: 163
Petr Dušek, Joseph Jankovic, Weidong Le
Neurobiology of Disease (2012) Vol. 46, Iss. 1, pp. 1-18
Closed Access | Times Cited: 163
Iron and Copper in Mitochondrial Diseases
Wenjing Xu, Tomasa Barrientos, Nancy C. Andrews
Cell Metabolism (2013) Vol. 17, Iss. 3, pp. 319-328
Open Access | Times Cited: 160
Wenjing Xu, Tomasa Barrientos, Nancy C. Andrews
Cell Metabolism (2013) Vol. 17, Iss. 3, pp. 319-328
Open Access | Times Cited: 160
Neurodegeneration with brain iron accumulation: update on pathogenic mechanisms
Sonia Levi, Dario Finazzi
Frontiers in Pharmacology (2014) Vol. 5
Open Access | Times Cited: 154
Sonia Levi, Dario Finazzi
Frontiers in Pharmacology (2014) Vol. 5
Open Access | Times Cited: 154
Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosology
Christelle Tesson, Jeanette Koht, Giovanni Stévanin
Human Genetics (2015) Vol. 134, Iss. 6, pp. 511-538
Open Access | Times Cited: 132
Christelle Tesson, Jeanette Koht, Giovanni Stévanin
Human Genetics (2015) Vol. 134, Iss. 6, pp. 511-538
Open Access | Times Cited: 132
Review: Insights into molecular mechanisms of disease in neurodegeneration with brain iron accumulation: unifying theories
Charles Arber, A. Li, Henry Houlden, et al.
Neuropathology and Applied Neurobiology (2015) Vol. 42, Iss. 3, pp. 220-241
Open Access | Times Cited: 124
Charles Arber, A. Li, Henry Houlden, et al.
Neuropathology and Applied Neurobiology (2015) Vol. 42, Iss. 3, pp. 220-241
Open Access | Times Cited: 124
Genetics and Pathophysiology of Neurodegeneration with Brain Iron Accumulation (NBIA)
Susanne A. Schneider, Petr Dušek, John Hardy, et al.
Current Neuropharmacology (2013) Vol. 11, Iss. 1, pp. 59-79
Open Access | Times Cited: 121
Susanne A. Schneider, Petr Dušek, John Hardy, et al.
Current Neuropharmacology (2013) Vol. 11, Iss. 1, pp. 59-79
Open Access | Times Cited: 121
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
Nicki Niemann, Joseph Jankovic
Parkinsonism & Related Disorders (2019) Vol. 67, pp. 74-89
Closed Access | Times Cited: 95
Neurodegeneration with Brain Iron Accumulation: Genetic Diversity and Pathophysiological Mechanisms
Esther Meyer, Manju A. Kurian, Susan J. Hayflick
Annual Review of Genomics and Human Genetics (2015) Vol. 16, Iss. 1, pp. 257-279
Closed Access | Times Cited: 93
Esther Meyer, Manju A. Kurian, Susan J. Hayflick
Annual Review of Genomics and Human Genetics (2015) Vol. 16, Iss. 1, pp. 257-279
Closed Access | Times Cited: 93
Parkinson’s disease-associated iPLA2-VIA/ PLA2G6 regulates neuronal functions and α-synuclein stability through membrane remodeling
Akio Mori, Taku Hatano, Tsuyoshi Inoshita, et al.
Proceedings of the National Academy of Sciences (2019) Vol. 116, Iss. 41, pp. 20689-20699
Open Access | Times Cited: 80
Akio Mori, Taku Hatano, Tsuyoshi Inoshita, et al.
Proceedings of the National Academy of Sciences (2019) Vol. 116, Iss. 41, pp. 20689-20699
Open Access | Times Cited: 80
Neurodegeneration with Brain Iron Accumulation Disorders: Valuable Models Aimed at Understanding the Pathogenesis of Iron Deposition
Sonia Levi, Valeria Tiranti
Pharmaceuticals (2019) Vol. 12, Iss. 1, pp. 27-27
Open Access | Times Cited: 79
Sonia Levi, Valeria Tiranti
Pharmaceuticals (2019) Vol. 12, Iss. 1, pp. 27-27
Open Access | Times Cited: 79
Hereditary Spastic Paraplegia
Harvey S. Singer, Jonathan W. Mink, Donald L. Gilbert, et al.
Elsevier eBooks (2022), pp. 415-440
Closed Access | Times Cited: 65
Harvey S. Singer, Jonathan W. Mink, Donald L. Gilbert, et al.
Elsevier eBooks (2022), pp. 415-440
Closed Access | Times Cited: 65
A human adipose tissue cell-type transcriptome atlas
Marthe Norreen-Thorsen, Eike C. Struck, Sofia Öling, et al.
Cell Reports (2022) Vol. 40, Iss. 2, pp. 111046-111046
Open Access | Times Cited: 52
Marthe Norreen-Thorsen, Eike C. Struck, Sofia Öling, et al.
Cell Reports (2022) Vol. 40, Iss. 2, pp. 111046-111046
Open Access | Times Cited: 52
Interactions of dopamine, iron, and alpha-synuclein linked to dopaminergic neuron vulnerability in Parkinson's disease and Neurodegeneration with Brain Iron Accumulation disorders
Rachel M. Wise, Annika Wagener, Urban M. Fietzek, et al.
Neurobiology of Disease (2022) Vol. 175, pp. 105920-105920
Open Access | Times Cited: 47
Rachel M. Wise, Annika Wagener, Urban M. Fietzek, et al.
Neurobiology of Disease (2022) Vol. 175, pp. 105920-105920
Open Access | Times Cited: 47
