Hiroko Morisaki
Tokyo, Japan
Last Updated: 09/26/2026
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Found 72 publications
Latent Vasculopathy of a Peripheral Pulmonary Artery in FBN1-Related Marfan Syndrome.
Journal: Pathology international
Published: May 08, 2026
Double Mutations in the FLNA and MYH11 Genes Causing Familial Thoracic Aortic Aneurysm and Dissection: A Report of Two Cases.
Journal: Internal medicine (Tokyo, Japan)
Published: February 23, 2026
Integrating ECG Into the Mayo Score Enhances Genotype Prediction in Hypertrophic Cardiomyopathy.
Journal: Journal of the American Heart Association
Published: February 12, 2026
Familial Sinus Node Dysfunction and Early-Onset Atrial Flutter Associated With a TBX5 Protein-Truncating Variant.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: December 07, 2025
The impact of FBN1 variant types on pregnancy-related aortic dissection in women with Marfan syndrome.
Journal: International journal of cardiology
Published: November 20, 2025
Maternal copy number variations detected by noninvasive prenatal testing in Japanese women.
Journal: Journal of human genetics
Published: September 09, 2025
Perinatal outcomes of fetal CNVs detected by genome-wide non-invasive prenatal testing in Japan.
Journal: Journal of human genetics
Published: July 25, 2025
Clinical Implications of Low Cell-Free DNA Fetal Fraction in Non-Invasive Prenatal Testing: A Retrospective Cohort Study of 40,716 Pregnancies.
Journal: Prenatal diagnosis
Published: April 07, 2025
Significance of noninvasive prenatal testing using massively parallel sequencing in women with twin or vanishing twin pregnancies.
Journal: Journal of human genetics
Published: October 29, 2024
JCS/JCC/JSPCCS 2024 Guideline on Genetic Testing and Counseling in Cardiovascular Disease.
Journal: Circulation journal : official journal of the Japanese Circulation Society
Published: September 29, 2024
A novel in-frame deletion flanking exon 54 of the FBN1 gene in a Japanese girl with Marfan syndrome.
A novel in-frame deletion flanking exon 54 of the FBN1 gene in a Japanese girl with Marfan syndrome.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: April 08, 2024
Hereditary Aortic Aneurysms and Dissections: Clinical Diagnosis and Genetic Testing.
Journal: Annals of vascular diseases
Published: February 04, 2024
Last Updated: 09/26/2026