Y. Sakata

Sequence Analysis of Fibroblast Growth Factor Receptor 2 (FGFR2) in Japanese Patients with Craniosynostosis

K. Tokunaga, T. Takato, Y. Yamazaki, 2001, The Journal of craniofacial surgery.

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.

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

Toshiyuki Yamamoto, Y. Asano, Yusaku Miyamoto, 2021, Human genome variation.

Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases

M. Kanai, Y. Kamatani, Y. Okada, 2020, Nature Genetics.

Significant association of HLA-B and HLA-DRB1 alleles with cleft lip with or without cleft palate.

K. Tokunaga, N. Tsuchiya, T. Takato, 1999, Tissue antigens.

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

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