Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbanceTatsuki Urakawa, Masayo Kagami, Hidenobu Soejima et al.|Clinical Epigenetics|2024Cited by 13
Comprehensive Study on Central Precocious Puberty: Molecular and Clinical Analyses in 90 PatientsHiromune Narusawa, Masayo Kagami, Satoshi Narumi et al.|The Journal of Clinical Endocrinology & Metabolism|2024Cited by 8
(Epi)genetic and clinical characteristics in 84 patients with pseudohypoparathyroidism type 1BTatsuki Urakawa, Masayo Kagami, Shinichiro Sano et al.|European Journal of Endocrinology|2023Cited by 4
A comprehensive long-read sequencing system to assess DNA methylation at differentially methylated regions and imprinting-disorder-related genesTatsuki Urakawa, Masayo Kagami, Atsushi Hattori et al.|Genome Medicine|2025Cited by 3
Beckwith-Wiedemann syndrome with long QT caused by a deletion involving KCNQ1 but not KCNQ1OT1:TSS-DMRTatsuki Urakawa, Masayo Kagami, Junichi Ozawa et al.|European Journal of Medical Genetics|2022Cited by 2