Masayo Nomura

A SNP in the ABCC11 gene is the determinant of human earwax type

Koh-ichiro Yoshiura, Akira Kinoshita, Takafumi Ishida et al. · Nature Genetics · 2006 · 292 citations · Full text

Allelic Variant, Genetic Disorder, Natural Sciences +10

Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair

Yuka Nakazawa, Kensaku Sasaki, Norisato Mitsutake et al. · Nature Genetics · 2012 · 210 citations · Full text

Genome Instability, Genetic Disorder, Medicine +6

BAC array CGH reveals genomic aberrations in idiopathic mental retardation

Noriko Miyake, Osamu Shimokawa, Naoki Harada et al. · American Journal of Medical Genetics Part A · 2006 · 64 citations

Paroxysmal kinesigenic choreoathetosis (PKC): confirmation of linkage to 16p11-q21, but unsuccessful detection of mutations among 157 genes at the PKC-critical region in seven PKC families

Taeko Kikuchi, Masayo Nomura, Hiroaki Tomita et al. · Journal of Human Genetics · 2007 · 44 citations · Full text

Direct intra-cardiomuscular transfer of β2-adrenergic receptor gene augments cardiac output in cardiomyopathic hamsters

Ki-ichiro Tomiyasu, Yoshihisa Oda, Masayo Nomura et al. · Gene Therapy · 2000 · 31 citations

Molecular Pharmacology, Cardiomyopathy, Cardiac Muscle +8