Kenji Kurosawa
Kanagawa Children's Medical Center(JP)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, Genetic Syndromes and Imprinting, Genomics and Rare Diseases, Prenatal Screening and Diagnostics
Most-Cited Works
- → Germline mutations in HRAS proto-oncogene cause Costello syndrome(2005)668 cited
- → Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome(2006)598 cited
- → Gain-of-Function Mutations in RIT1 Cause Noonan Syndrome, a RAS/MAPK Pathway Syndrome(2013)329 cited
- → Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes(2008)288 cited
- → Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain(1997)205 cited
- → Spectrum of MLL2 (ALR) mutations in 110 cases of Kabuki syndrome(2011)194 cited
- → <title>Methods for identification of images acquired with digital cameras</title>