T. Fuke

发表

Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients

K. Yamazawa, T. Ogata, Takanobu Inoue, 2020, Clinical Epigenetics.

Molecular and clinical analyses of two patients with UPD(16)mat detected by screening 94 patients with Silver-Russell syndrome phenotype of unknown aetiology

K. Yamazawa, T. Ogata, Takanobu Inoue, 2018, Journal of Medical Genetics.

A novel de novo point mutation of the OCT‐binding site in the IGF2/H19‐imprinting control region in a Beckwith–Wiedemann syndrome patient

T. Ogata, H. Soejima, H. Koseki, 2014, Clinical genetics.

Role of Imprinting Disorders in Short Children Born SGA and Silver-Russell Syndrome Spectrum

K. Yamazawa, T. Ogata, Takanobu Inoue, 2020, The Journal of clinical endocrinology and metabolism.

Frequency and clinical characteristics of distinct etiologies in patients with Silver-Russell syndrome diagnosed based on the Netchine-Harbison clinical scoring system

K. Yamazawa, T. Ogata, A. Nakamura, 2022, Journal of Human Genetics.

IMAGe syndrome: clinical and genetic implications based on investigations in three Japanese patients

T. Ogata, G. Nishimura, T. Hasegawa, 2014, Clinical endocrinology.

Molecular and Clinical Studies in 138 Japanese Patients with Silver-Russell Syndrome

K. Yamazawa, T. Ogata, K. Hata, 2013, PloS one.

Paternal uniparental disomy 14 and related disorders

T. Ogata, K. Matsuoka, K. Kurosawa, 2012, Epigenetics.

Genetic heterogeneity of patients with suspected Silver-Russell syndrome: genome-wide copy number analysis in 82 patients without imprinting defects

K. Yamazawa, T. Ogata, A. Oka, 2017, Clinical Epigenetics.

Epimutations of the IG-DMR and the MEG3-DMR at the 14q32.2 imprinted region in two patients with Silver–Russell Syndrome-compatible phenotype

T. Ogata, S. Mizuno, K. Nakabayashi, 2014, European Journal of Human Genetics.

Genome-wide methylation analysis in Silver–Russell syndrome, Temple syndrome, and Prader–Willi syndrome

K. Yamazawa, T. Ogata, S. Saitoh, 2020, Clinical epigenetics.

Polyhydramnios associated with Prader–Willi syndrome

K. Yakubo, T. Fukuiya, T. Ikeda, 2015, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

Genetic heterogeneity of patients with suspected Silver-Russell syndrome: genome-wide copy number analysis in 82 patients without imprinting defects

K. Yamazawa, T. Ogata, Takanobu Inoue, 2017, Clinical Epigenetics.

Isolated central nervous system (CNS) relapse in a case of childhood systemic anaplastic large cell lymphoma without initial CNS involvement.

N. Kiyokawa, J. Fujimoto, K. Sugita, 2003, Journal of pediatric hematology/oncology.

Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients

K. Yamazawa, T. Ogata, Takanobu Inoue, 2020, Clinical Epigenetics.

Risk assessment of assisted reproductive technology and parental age at childbirth for the development of uniparental disomy-mediated imprinting disorders caused by aneuploid gametes

K. Yamazawa, T. Ogata, A. Nakamura, 2023, Clinical Epigenetics.

Pathogenic copy number and sequence variants in children born SGA with short stature without imprinting disorders.

K. Yamazawa, T. Ogata, A. Nakamura, 2022, The Journal of clinical endocrinology and metabolism.