Kaori Hojo
Okayama Prefecture(JP)
Publications by Year
Research Areas
Epigenetics and DNA Methylation, Genetic Neurodegenerative Diseases, Genetics and Neurodevelopmental Disorders, Cancer-related gene regulation, Hereditary Neurological Disorders
Most-Cited Works
- → Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss(2011)393 cited
- → Defects of mutant DNMT1 are linked to a spectrum of neurological disorders(2015)118 cited
- → Aberrant signature methylome by DNMT1 hot spot mutation in hereditary sensory and autonomic neuropathy 1E(2014)63 cited
- → Hereditary sensory neuropathy with deafness and dementia: a clinical and neuroimaging study(1999)18 cited
- → Expanded genetic insight and clinical experience of DNMT1-complex disorder(2020)13 cited
- → Inflammatory glial activation in the brain of a patient with hereditary sensory neuropathy type 1 with deafness and dementia(2004)9 cited
- → Congenital Myotonic Dystrophy: Molecular Diagnosis and Clinical Study(1995)7 cited
- → Successful pregnancy and delivery in a patient with neurogenic orthostatic hypotension and achalasia: A case report.(1990)1 cited
- [Two cases of myotonic dystrophy diagnosed by DNA analysis].(1995)
- → In hereditary sensoriy and automic neuropathy 1e (hsan1e), dnmt1 hotspot mutation Y495C cause premature degradation of mutant proteins and aberrant signature methyrome(2017)