Yoshihiro Asano

Recurrent de novo pathogenic variant of WASF1 in a Japanese patient with neurodevelopmental disorder with absent language and variable seizures

Toshiyuki Yamamoto, Yusaku Miyamoto, Tomoe Yanagishita, 2021, Human Genome Variation.

A novel nonsense variant in ARID1B causing simultaneous RNA decay and exon skipping is associated with Coffin-Siris syndrome

M. Masuno, T. Otomo, T. Moriwaki, 2022, Human Genome Variation.

Novel BCL11B truncation variant in a patient with developmental delay, distinctive features, and early craniosynostosis

Toshiyuki Yamamoto, Y. Aihara, Kentaro Chiba, 2022, Human Genome Variation.

Genetic basis of cardiomyopathy and the genotypes involved in prognosis and left ventricular reverse remodeling

H. Aburatani, N. Hagiwara, I. Komuro, 2018, Scientific Reports.

Association Between Genetic Diagnosis and Clinical Outcomes in Patients With Heritable Thoracic Aortic Disease

K. Nishimura, T. Noguchi, S. Ogata, 2023, Journal of the American Heart Association.

Craniofacial and dental characteristics of three Japanese individuals with genetically diagnosed SATB2‐associated syndrome

T. Inubushi, Toshiyuki Yamamoto, K. Fujioka, 2023, American journal of medical genetics. Part A.

Novel BCL11B truncation variant in a patient with developmental delay, distinctive features, and early craniosynostosis

Toshiyuki Yamamoto, Y. Aihara, Kentaro Chiba, 2022, Human Genome Variation.

RNF213 p.R4810K Variant Increases the Risk of Vasospastic Angina

K. Nishimura, M. Ihara, T. Noguchi, 2023, JACC: Asia.

A family with brachydactyly mental retardation syndrome with a missense variant in HDAC4

K. Ozono, Kenichi Yamamoto, T. Kubota, 2023, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Estimation of crossbridge-state during cardiomyocyte beating using second harmonic generation

Tomonobu M. Watanabe, Y. Sakata, S. Miyagawa, 2022, Life Science Alliance.

Clinical Outcomes and Genetic Analyses of Restrictive Cardiomyopathy in Children

S. Kogaki, K. Ozono, H. Ishida, 2023, Circulation. Genomic and precision medicine.

Novel TRPS1 frameshift variant in tricho-rhino-phalangeal syndrome type I accompanied by zinc deficiency.

Hiromune Narusawa, Daisuke Watanabe, Ayumi Yonei, 2023, European journal of medical genetics.

Cardiac Magnetic Resonance Imaging Findings in Filamin C Variant-Associated Arrhythmogenic Left Ventricular Cardiomyopathy.

T. Hirai, S. Oda, S. Takashio, 2023, Circulation journal : official journal of the Japanese Circulation Society.

MYH9-related disorder with sole presentation of end-stage kidney disease and long-term, recurrence-free living after living donor renal transplantation: a case report.

H. Kishikawa, K. Yamanaka, Yohei Miyashita, 2024, CEN case reports.