Yoko Kuroki
Yokohama, Japan
Last Updated: 09/26/2026
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Found 43 publications
Early Pubertal Progression and Increased 11-Oxygenated Androgens in a Girl with Wiedemann-Steiner Syndrome and a KMT2A Variant: A Case Report.
Journal: Molecular syndromology
Published: January 29, 2026
Correction to: Opioid use in patients aged 90 years or older with terminal cancer in a palliative care unit: a single-center retrospective observational study.
Journal: Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer
Published: December 03, 2025
Opioid use in patients aged 90 years or older with terminal cancer in a palliative care unit: a single-center retrospective observational study.
Journal: Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer
Published: July 22, 2025
A comprehensive long-read sequencing system to assess DNA methylation at differentially methylated regions and imprinting-disorder-related genes.
Journal: Genome medicine
Published: May 02, 2025
ACAN Repeat Number Polymorphism in Patients with Idiopathic Short Stature.
Journal: Cytogenetic and genome research
Published: February 20, 2025
De Novo Splice Site Variant of TCF12 in a Boy With Isolated Kallmann Syndrome.
Journal: Case reports in endocrinology
Published: February 10, 2025
De novo retrotransposon insertion into the FGFR1 gene in a boy with congenital hypogonadotropic hypogonadism: a case report.
Journal: Frontiers in endocrinology
Published: January 23, 2025
CTCF Is Essential for the Development and Maintenance of CALM-AF10-Induced Leukemia.
Journal: Cancer science
Published: December 27, 2024
DNA methylation changes in the genome of patients with hypogonadotropic hypogonadism.
Journal: Heliyon
Published: May 29, 2024
Isodicentric Y Chromosome with Multiple Breakpoints in the Pseudoautosomal Region 1.
Journal: Cytogenetic and genome research
Published: February 29, 2024
Long-read next-generation sequencing for molecular diagnosis of pediatric endocrine disorders.
Journal: Annals of pediatric endocrinology & metabolism
Published: February 09, 2024
Loss of NOL10 leads to impaired disease progression of NUP98::DDX10 leukemia.
Journal: Leukemia
Published: January 25, 2024
Last Updated: 09/26/2026