Li Liu

Mutation characteristics of the PAH gene in four nationality groups in Xinjiang of China

Yu-wei Jin, F. Song, Yan-ling Zhang, 2008, Journal of Genetics.

A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome.

K. Hayashi, M. Yamagishi, H. Higashida, 2013, Heart rhythm.

Social memory, amnesia, and autism: Brain oxytocin secretion is regulated by NAD+ metabolites and single nucleotide polymorphisms of CD38

Y. Minabe, H. Higashida, S. Yokoyama, 2012, Neurochemistry International.

Functional Characterization of Rare Variants Implicated in Susceptibility to Lone Atrial Fibrillation

K. Hayashi, M. Yamagishi, N. Makita, 2022 .

Long QT syndrome and associated gene mutation carriers in Japanese children: results from ECG screening examinations.

K. Hayashi, M. Yamagishi, H. Higashida, 2009, Clinical science.

A Study of Single Nucleotide Polymorphisms of the SLC19A1/RFC1 Gene in Subjects with Autism Spectrum Disorder

K. Hayashi, M. Yamagishi, H. Higashida, 2016, International journal of molecular sciences.

Functional Characterization of Rare Variants Implicated in Susceptibility to Lone Atrial Fibrillation

K. Hayashi, M. Yamagishi, N. Makita, 2015, Circulation. Arrhythmia and electrophysiology.