Associated Papers
Using the Reactome Graph Database to generate pathway fingerprints for cancer-related genes, and using the fingerprints to gain insights into cancer, comorbidity, and cancer gene networks.
Iengar P et al.
Computational Biology and Chemistry, 2026
Integrating epidemiology and genomics data to estimate the prevalence of acquired cysteine drug targets in the U.S. cancer patient population.
Arun AS et al.
The Pharmacogenomics Journal, 2025
40044654 (PubMed )
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Spinocerebellar ataxia type 23 (SCA23): a review.
Wu F et al.
Journal of Neurology, 2021
Intrafamilial phenotypic variation in spinocerebellar ataxia type 23.
Satoh S et al.
Cerebellum & Ataxias, 2020
The first Japanese familial case of spinocerebellar ataxia 23 with a novel mutation in the PDYN gene.
Saigoh K et al.
Parkinsonism & Related Disorders, 2015
The frequency of spinocerebellar ataxia type 23 in a UK population.
Fawcett K et al.
Journal of Neurology, 2013
Spinocerebellar ataxia type 23 is an uncommon SCA subtype in the Chinese Han population.
Liu YT et al.
Neuroscience Letters, 2012
Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23.
Bakalkin G et al.
American Journal of Human Genetics, 2010
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