Ikuko Kondo
Hokkaido University of Science(JP)Meiji University(JP)Hokkaido University(JP)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Genomic variations and chromosomal abnormalities, Parkinson's Disease Mechanisms and Treatments
Most-Cited Works
- → Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p(1994)722 cited
- → Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans(2002)704 cited
- → The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein(1999)411 cited
- Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2).(1991)
- → Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome(2015)208 cited
- → DNA polymorphism at the locus for human cholesteryl ester transfer protein (CETP) is associated with high density lipoprotein cholesterol and apolipoprotein levels(1989)179 cited