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Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|July 12, 2024
Pseudohypoparathyroidism type 1B with involuntary movements: a case report and literature reviewJunko Naganuma, Hiroshi Suzumura, Satomi Koyama, et al.Clinical Epigenetics|November 7, 2025
Investigation of methylation profiles in Silver-Russell syndrome to explore episignaturesKaori Hara-Isono, Takanobu Inoue, Akie Nakamura, et al.Clinical Epigenetics|May 27, 2021
ZNF445: a homozygous truncating variant in a patient with Temple syndrome and multilocus imprinting disturbanceMasayo Kagami, Kaori Hara-Isono, Keiko Matsubara, et al.The Journal of Obstetrics and Gynaecology Research|September 10, 2022
Quantitative assessment of coat-hanger ribs detected on three-dimensional ultrasound for prenatal diagnosis of Kagami-Ogata syndromeAkane Kuriki, Satoshi Hosoya, Katsusuke Ozawa, et al.BMC Medical Genomics|May 30, 2019
Transient multifocal genomic crisis creating chromothriptic and non-chromothriptic rearrangements in prezygotic testicular germ cellsAtsushi Hattori, Kohji Okamura, Yumiko Terada, et al.Clinical Epigenetics|February 9, 2019
Association of four imprinting disorders and ARTHiromitsu Hattori, Hitoshi Hiura, Akane Kitamura, et al.The Journal of Clinical Endocrinology and Metabolism|December 18, 2024
Temple Syndrome: Comprehensive Clinical Study in Genetically Confirmed 60 Japanese PatientsTomoe Ogawa, Hiromune Narusawa, Keisuke Nagasaki, et al.Clinical Epigenetics|March 2, 2019
Exploring the unique function of imprinting control centers in the PWS/AS-responsible region: finding from array-based methylation analysis in cases with variously sized microdeletionsKeiko Matsubara, Masatsune Itoh, Kenji Shimizu, et al.The Journal of Clinical Endocrinology and Metabolism|November 25, 2020
Role of Imprinting Disorders in Short Children Born SGA and Silver-Russell Syndrome SpectrumTomoko Fuke, Akie Nakamura, Takanobu Inoue, et al.The Journal of Clinical Endocrinology and Metabolism|May 18, 2022
Pathogenic Copy Number and Sequence Variants in Children Born SGA With Short Stature Without Imprinting DisordersKaori Hara-Isono, Akie Nakamura, Tomoko Fuke, et al.Pageof 11