Ippei Okada
Yokohama City University(JP)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Ocular Disorders and Treatments, Advanced biosensing and bioanalysis techniques, Cellular transport and secretion, Bone and Dental Protein Studies
Most-Cited Works
- → De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy(2008)541 cited
- → Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome(2012)519 cited
- → STXBP1 mutations in early infantile epileptic encephalopathy with suppression‐burst pattern(2010)155 cited
- → Dominant-Negative Mutations in α-II Spectrin Cause West Syndrome with Severe Cerebral Hypomyelination, Spastic Quadriplegia, and Developmental Delay(2010)152 cited
- → SMOC1 Is Essential for Ocular and Limb Development in Humans and Mice(2010)116 cited
- → Paternal mosaicism of an STXBP1 mutation in OS(2010)47 cited
- → De novo 5q14.3 translocation 121.5‐kb upstream of MEF2C in a patient with severe intellectual disability and early‐onset epileptic encephalopathy(2011)27 cited
- → Whole‐exome sequencing identified a homozygous FNBP4 mutation in a family with a condition similar to microphthalmia with limb anomalies(2013)21 cited
- → Spatial and temporal expression analysis of BMP signal modifiers, Smoc1 and Smoc2, from postnatal to adult developmental stages in the mouse testis(2024)1 cited
- → Countermeasures for Pantograph Heads Damageby Detecting Frost on Overhead Contact Linewith the Pantograph Monitoring System(2023)