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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:

Ataxia and hypogonadism caused by the loss of ubiquitin ligase activity of the U box protein CHIP
Chang-he Shi, Jonathan C. Schisler, Carrie E. Rubel, et al.
Human Molecular Genetics (2013) Vol. 23, Iss. 4, pp. 1013-1024
Open Access | Times Cited: 139

Showing 1-25 of 139 citing articles:

Developmental alterations in Huntington's disease neural cells and pharmacological rescue in cells and mice
Ryan G. Lim, Lisa Salazar, Daniel K. Wilton, et al.
Nature Neuroscience (2017) Vol. 20, Iss. 5, pp. 648-660
Open Access | Times Cited: 207
Diagnostic Utility of Genome-wide DNA Methylation Testing in Genetically Unsolved Individuals with Suspected Hereditary Conditions
Erfan Aref‐Eshghi, Eric G. Bend, Samantha Colaiacovo, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 4, pp. 685-700
Open Access | Times Cited: 160
Genetics of congenital hypogonadotropic hypogonadism: peculiarities and phenotype of an oligogenic disease
Biagio Cangiano, Du Soon Swee, Richard Quinton, et al.
Human Genetics (2020) Vol. 140, Iss. 1, pp. 77-111
Closed Access | Times Cited: 149
The chaperone-assisted selective autophagy complex dynamics and dysfunctions
B. Tedesco, Leen Vendredy, Vincent Timmerman, et al.
Autophagy (2023) Vol. 19, Iss. 6, pp. 1619-1641
Open Access | Times Cited: 53
Overcoming the divide between ataxias and spastic paraplegias: Shared phenotypes, genes, and pathways
Matthis Synofzik, Rebecca Schüle
Movement Disorders (2017) Vol. 32, Iss. 3, pp. 332-345
Open Access | Times Cited: 160
A Comprehensive Atlas of E3 Ubiquitin Ligase Mutations in Neurological Disorders
Arlene J. George, Yarely C. Hoffiz, Antoinette J. Charles, et al.
Frontiers in Genetics (2018) Vol. 9
Open Access | Times Cited: 151
The Classification of Autosomal Recessive Cerebellar Ataxias: a Consensus Statement from the Society for Research on the Cerebellum and Ataxias Task Force
Marie Beaudin, Antoni Matilla‐Dueñas, Bing-Weng Soong, et al.
The Cerebellum (2019) Vol. 18, Iss. 6, pp. 1098-1125
Open Access | Times Cited: 107
Heterozygous STUB1 mutation causes familial ataxia with cognitive affective syndrome (SCA48)
David Genı́s, Sara Ortega‐Cubero, Héctor San Nicolás, et al.
Neurology (2018) Vol. 91, Iss. 21
Closed Access | Times Cited: 96
Loss-of-Function Mutations inPNPLA6Encoding Neuropathy Target Esterase Underlie Pubertal Failure and Neurological Deficits in Gordon Holmes Syndrome
A. Kemal Topaloğlu, Alejandro Lomniczi, Doris Kretzschmar, et al.
The Journal of Clinical Endocrinology & Metabolism (2014) Vol. 99, Iss. 10, pp. E2067-E2075
Open Access | Times Cited: 94
Discovering Genes Essential to the Hypothalamic Regulation of Human Reproduction Using a Human Disease Model: Adjusting to Life in the “-Omics” Era
Maria Stamou, Kimberly H. Cox, William F. Crowley
Endocrine Reviews (2015) Vol. 36, Iss. 6, pp. 603-621
Open Access | Times Cited: 82
STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
Ketil Heimdal, Mònica Sánchez-Guixé, Ingvild Aukrust, et al.
Orphanet Journal of Rare Diseases (2014) Vol. 9, Iss. 1
Open Access | Times Cited: 69
CHCHD2 gene mutations in familial and sporadic Parkinson's disease
Changhe Shi, Chengyuan Mao, Shuyu Zhang, et al.
Neurobiology of Aging (2015) Vol. 38, pp. 217.e9-217.e13
Closed Access | Times Cited: 68
A Decade of Boon or Burden: What Has the CHIP Ever Done for Cellular Protein Quality Control Mechanism Implicated in Neurodegeneration and Aging?
Vibhuti Joshi, Ayeman Amanullah, Arun Upadhyay, et al.
Frontiers in Molecular Neuroscience (2016) Vol. 9
Open Access | Times Cited: 67
Ubiquitin signaling in neurodegenerative diseases: an autophagy and proteasome perspective
François Le Guerroué, Richard J. Youle
Cell Death and Differentiation (2020) Vol. 28, Iss. 2, pp. 439-454
Open Access | Times Cited: 64
NOTCH2NLC Intermediate‐Length Repeat Expansions Are Associated with Parkinson Disease
Changhe Shi, Yu Fan, Jing Yang, et al.
Annals of Neurology (2020) Vol. 89, Iss. 1, pp. 182-187
Closed Access | Times Cited: 59
CHIP as a therapeutic target for neurological diseases
Shuo Zhang, Zhengwei Hu, Chengyuan Mao, et al.
Cell Death and Disease (2020) Vol. 11, Iss. 9
Open Access | Times Cited: 53
STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutations
Stefanie N. Hayer, Tine Deconinck, Benjamin Bender, et al.
Orphanet Journal of Rare Diseases (2017) Vol. 12, Iss. 1
Open Access | Times Cited: 60
Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts
Matthis Synofzik, Rebecca Schüle, Martin Schulze, et al.
Orphanet Journal of Rare Diseases (2014) Vol. 9, Iss. 1, pp. 57-57
Open Access | Times Cited: 59
The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian families
Maria Lieto, Vittorio Riso, Daniele Galatolo, et al.
European Journal of Neurology (2019) Vol. 27, Iss. 3, pp. 498-505
Closed Access | Times Cited: 54
CHIP Regulates Aquaporin-2 Quality Control and Body Water Homeostasis
Qi Wu, Hanne B. Moeller, Donté A. Stevens, et al.
Journal of the American Society of Nephrology (2017) Vol. 29, Iss. 3, pp. 936-948
Open Access | Times Cited: 52
Spinocerebellar ataxia 48 presenting with ataxia associated with cognitive, psychiatric, and extrapyramidal features: A report of two Italian families
Giovanna De Michele, Maria Lieto, Daniele Galatolo, et al.
Parkinsonism & Related Disorders (2019) Vol. 65, pp. 91-96
Closed Access | Times Cited: 51
Genetic Regulation of Puberty Timing in Humans
Felix R. Day, John R. B. Perry, Ken K. Ong
Neuroendocrinology (2015) Vol. 102, Iss. 4, pp. 247-255
Open Access | Times Cited: 50
Autosomal recessive cerebellar ataxia of adult onset due to STUB1 Mutations
Chantal Depondt, Simona Donatello, Nicolas Simonis, et al.
Neurology (2014) Vol. 82, Iss. 19, pp. 1749-1750
Closed Access | Times Cited: 45
Counterregulation of cAMP-directed kinase activities controls ciliogenesis
Monia Porpora, Simona Sauchella, Laura Rinaldi, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 45
A novelRAB39Bgene mutation in X-linked juvenile parkinsonism with basal ganglia calcification
Changhe Shi, Shuyu Zhang, Zhi-hua Yang, et al.
Movement Disorders (2016) Vol. 31, Iss. 12, pp. 1905-1909
Closed Access | Times Cited: 42
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