Kazumi Ida
Yokohama, Japan
Last Updated: 09/26/2026
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Found 13 publications
A polystyrene-film-based device for engineered cardiac tissues enables accurate analysis of drug responses on contractile properties.
Journal: Lab on a chip
Published: May 30, 2025
Integrative Transcriptomic-Histological Analysis in Dilated Cardiomyopathy Unveils FGFR1 Inhibition as Anti-Cardiac Fibrotic and Cardioprotective Therapy.
Journal: JACC. Basic to translational science
Published: December 12, 2024
Divergent variant patterns among 19 patients with Rubinstein-Taybi syndrome uncovered by comprehensive genetic analysis including whole genome sequencing.
Journal: Clinical genetics
Published: November 04, 2021
Mosaicism of a Truncating Variant of CASK Causes Congenital Heart Disease and Neurodevelopmental Disorder.
Journal: Molecular syndromology
Published: November 01, 2021
Familial total anomalous pulmonary venous return with 15q11.2 (BP1-BP2) microdeletion.
Journal: Journal of human genetics
Published: April 23, 2018
CNV analysis using whole exome sequencing identified biallelic CNVs of VPS13B in siblings with intellectual disability.
Journal: European journal of medical genetics
Published: March 12, 2018
Evaluation of a patient with classical Ehlers-Danlos syndrome due to a 9q34 duplication affecting COL5A1.
Journal: Congenital anomalies
Published: December 19, 2017
Haploinsufficiency of BCL11A associated with cerebellar abnormalities in 2p15p16.1 deletion syndrome.
Journal: Molecular genetics & genomic medicine
Published: November 16, 2016
Delineation of the KIAA2022 mutation phenotype: two patients with X-linked intellectual disability and distinctive features.
Journal: American journal of medical genetics. Part A
Published: August 13, 2014
Deletion of UBE3A in brothers with Angelman syndrome at the breakpoint with an inversion at 15q11.2.
Deletion of UBE3A in brothers with Angelman syndrome at the breakpoint with an inversion at 15q11.2.
Journal: American journal of medical genetics. Part A
Published: September 25, 2013
Refinement of the deletion in 8q22.2-q22.3: the minimum deletion size at 8q22.3 related to intellectual disability and epilepsy.
Journal: American journal of medical genetics. Part A
Published: September 25, 2013
De novo duplication of 17p13.1-p13.2 in a patient with intellectual disability and obesity.
Journal: American journal of medical genetics. Part A
Published: September 05, 2013
Last Updated: 09/26/2026