Tatsuhiko Tsunoda
0000-0002-5439-7918
6 papers found
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De novo ATP1A3 variants cause polymicrogyria
Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans
DeepInsight: A methodology to transform a non-image data to an image for convolution neural network architecture
Publisher Correction: IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis
Integrated analysis of human genetic association study and mouse transcriptome suggests LBH and SHF genes as novel susceptible genes for amyloid-β accumulation in Alzheimer’s disease
Discovery and characterization of coding and non-coding driver mutations in more than 2,500 whole cancer genomes
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