Miho Ishida
William Harvey Research Institute(GB)University College London(GB)
Publications by Year
Research Areas
Genetic Syndromes and Imprinting, Prenatal Screening and Diagnostics, Epigenetics and DNA Methylation, Renal and related cancers, Kruppel-like factors research
Most-Cited Works
- → Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS(2013)343 cited
- → The role of imprinted genes in humans(2012)182 cited
- → The role and interaction of imprinted genes in human fetal growth(2015)150 cited
- → Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome(2013)107 cited
- → Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate(2016)103 cited
- → Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome(2014)100 cited
- → Chondroitin 4-O-Sulfotransferase-1 Regulates E Disaccharide Expression of Chondroitin Sulfate Required for Herpes Simplex Virus Infectivity(2006)96 cited
- → Chondroitin 4-O-Sulfotransferase-1 Modulates Wnt-3a Signaling through Control of E Disaccharide Expression of Chondroitin Sulfate(2008)93 cited
- → Genetic Analyses in Small-for-Gestational-Age Newborns(2018)61 cited
- → Paternally Expressed, Imprinted Insulin-Like Growth Factor-2 in Chorionic Villi Correlates Significantly with Birth Weight(2014)43 cited