Kayoko Hirayama-Yamada

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

Jonathan C. Cohen, D. Srivastava, R. Matsuoka, 2003, Nature.

Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect

M. Furutani, R. Matsuoka, S. Imamura, 2005, American journal of medical genetics. Part A.

Missense Mutations in the PTPN11 as a Cause of Cardiac Defects Associated with Noonan Syndrome

R. Matsuoka, S. Imamura, Kayoko Hirayama-Yamada, 2007 .

A Novel Titin Truncation Variant Linked to Familial Dilated Cardiomyopathy Found in a Japanese Family and Its Functional Analysis in Genome-Edited Model Cells.

A. Kimura, Kayoko Hirayama-Yamada, Natsuko F. Inagaki, 2021, International heart journal.

Genetic background of Japanese patients with pediatric hypertrophic and restrictive cardiomyopathy

A. Kimura, K. Tanimoto, Kayoko Hirayama-Yamada, 2018, Journal of Human Genetics.

Genetic background of Japanese patients with pediatric hypertrophic and restrictive cardiomyopathy

A. Kimura, K. Tanimoto, Kayoko Hirayama-Yamada, 2018, Journal of Human Genetics.