S. Morishita

Taro L. Saito, T. Matsukawa, S. Tsuji, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Ataxic phenotype with altered CaV3.1 channel property in a mouse model for spinocerebellar ataxia 42

S. Tsuji, Yukihiro Nakamura, N. Matsumoto, 2019, Neurobiology of Disease.

Comprehensive investigation of RNF213 nonsynonymous variants associated with intracranial artery stenosis

S. Tsuji, S. Morishita, N. Saito, 2020, Scientific Reports.

Proceedings - 2011 IEEE International Conference on Bioinformatics and Biomedicine, BIBM 2011: Preface

Yi Pan, Xiaohua Hu, Stephen T. C. Wong, 2011, IEEE International Conference on Bioinformatics and Biomedicine.

Proceedings of the 4th ACM SIGKDD Workshop on Data Mining in Bioinformatics (BIOKDD 2004), August 22th, 2004, Seattle, Washington, USA

Mohammed J. Zaki, Isidore Rigoutsos, Shinichi Morishita, 2004, BIOKDD.

Long-read metagenomic exploration of extrachromosomal mobile genetic elements in the human gut

M. Hattori, S. Morishita, Suguru Nishijima, 2019, Microbiome.

ANovel Mutation in ELOVL 4 Leading to Spinocerebellar Ataxia ( SCA ) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia A Broadened Spectrum of SCA 34

S. Tsuji, N. Matsumoto, S. Morishita, 2015 .

A Novel Mutation in ELOVL4 Leading to Spinocerebellar Ataxia (SCA) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia: A Broadened Spectrum of SCA34.

S. Tsuji, N. Matsumoto, S. Morishita, 2015, JAMA neurology.

Targeted deep sequencing of DNA from multiple tissue types improves the diagnostic rate and reveals a highly diverse phenotype of mosaic neurofibromatosis type 2

S. Tsuji, S. Morishita, N. Saito, 2020, Journal of Medical Genetics.

Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-α2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?

J. Sese, T. Tsukahara, I. Nishino, 2006 .

Expression profile analysis in cells overexpressing DRPLA cDNA to explore the roles of DRPLAp as a transcriptional coregulator

T. Matsukawa, S. Morishita, H. Ishiura, 2022, Neurology and Clinical Neuroscience.

Reconstruction of the vertebrate ancestral genome reveals dynamic genome reorganization in early vertebrates.

Y. Kohara, S. Morishita, H. Takeda, 2007, Genome research.

Whole Genome Shotgun Sequencing

Shinichi Morishita, Masahiro Kasahara, S. Morishita, 2006 .

Investigating the mitochondrial genomic landscape of Arabidopsis thaliana by long-read sequencing

Shinichi Morishita, Bansho Masutani, Shin-ichi Arimura, 2021, PLoS Comput. Biol..

Approximate String Search

Shinichi Morishita, Masahiro Kasahara, S. Morishita, 2006 .

Context-dependent DNA polymerization effects can masquerade as DNA modification signals

A. Fire, S. Morishita, M. Shoura, 2021, BMC Genomics.

Exome analysis reveals a Japanese family with spinocerebellar ataxia, autosomal recessive 1

I. Kanazawa, S. Tsuji, S. Morishita, 2013, Journal of the Neurological Sciences.

ATF6α/β-mediated adjustment of ER chaperone levels is essential for development of the notochord in medaka fish

Taro L. Saito, Y. Sakaki, A. Toyoda, 2013, Molecular biology of the cell.

A gain-of-function screen identifies wdb and lkb1 as lifespan-extending genes in Drosophila.

S. Morishita, T. Aigaki, M. Tsuda, 2011, Biochemical and biophysical research communications.

ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19.

Robert H. Brown, A. Fujiyama, A. Toyoda, 2013, American journal of human genetics.

Comprehensive and quantitative analysis of yeast deletion mutants defective in apical and isotropic bud growth

Y. Ohya, S. Morishita, S. Nogami, 2009, Current Genetics.

Involvement of Rho-type GTPase in control of cell size in Saccharomyces cerevisiae.

Y. Ohya, S. Morishita, Y. Kikuchi, 2007, FEMS yeast research.

The genome sequence of silkworm, Bombyx mori.

Yoshiaki Nagamura, Nobukazu Namiki, Shinichi Morishita, 2004, DNA research : an international journal for rapid publication of reports on genes and genomes.

Dynactin is involved in a checkpoint to monitor cell wall synthesis in Saccharomyces cerevisiae

Y. Ohya, S. Morishita, M. Yukawa, 2004, Nature Cell Biology.

Title: Context-dependent DNA Polymerization Effects Can Masquerade as DNA 1 Modification Signals 2

A. Fire, S. Morishita, M. Shoura, 2021 .

A recurrent de novo FAM111A mutation causes kenny–caffey syndrome type 2

S. Tsuji, S. Morishita, S. Kitanaka, 2014, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Exome sequencing shows a novel de novo mutation in ATL1

S. Tsuji, S. Morishita, H. Ishiura, 2014 .

Splice-site mutations in KIF5A in the Japanese case series of amyotrophic lateral sclerosis

T. Matsukawa, S. Tsuji, S. Morishita, 2020, neurogenetics.

Clinical and mutational spectrum of Charcot–Marie–Tooth disease type 2Z caused by MORC2 variants in Japan

S. Tsuji, S. Morishita, H. Ishiura, 2017, European journal of neurology.

Clinical and genetic diversities of Charcot‐Marie‐Tooth disease with MFN2 mutations in a large case study

S. Tsuji, S. Morishita, M. Nakagawa, 2017, Journal of the peripheral nervous system : JPNS.

Simple String Search

Shinichi Morishita, Masahiro Kasahara, S. Morishita, 2006 .

Space-Efficient String Search

Shinichi Morishita, Masahiro Kasahara, S. Morishita, 2006 .

Towards Mining Gene Expression Database

Teruyoshi Hishiki, Shinichi Morishita, Kousaku Okubo, 1999, 1999 ACM SIGMOD Workshop on Research Issues in Data Mining and Knowledge Discovery.

Segmental duplications in the silkworm genome

S. Morishita, Zhenglin Zhu, M. Kasahara, 2013, BMC Genomics.

A Simple but Powerful Heuristic Method for Accelerating $k$ -Means Clustering of Large-Scale Data in Life Science

Kazuki Ichikawa, Shinichi Morishita, S. Morishita, 2014, IEEE/ACM Transactions on Computational Biology and Bioinformatics.

Chromatin-Associated Periodicity in Genetic Variation Downstream of Transcriptional Start Sites

Sumio Sugano, Shinichi Morishita, Yuji Kohara, 2009, Science.

Development of Image Processing Program for Yeast Cell Morphology

Shinichi Morishita, Yoshikazu Ohya, Ayaka Saka, 2004, J. Bioinform. Comput. Biol..

Complete fusion of a transposon and herpesvirus created the Teratorn mobile element in medaka fish

S. Morishita, H. Takeda, M. Kumagai, 2017, Nature Communications.

SCMD: Saccharomyces cerevisiae Morphological Database

Shinichi Morishita, Yoshikazu Ohya, Daisuke Watanabe, 2004, Nucleic Acids Res..

Comparative analysis of chimpanzee and human Y chromosomes unveils complex evolutionary pathway

M. Hattori, Y. Sakaki, N. Saitou, 2006, Nature Genetics.

Identification of candidate genes involved in the etiology of sporadic Tourette syndrome by exome sequencing

K. Kasai, S. Tsuji, Y. Kawakubo, 2017, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing

Yuji Takahashi, Jun Goto, Shinichi Morishita, 2013, Bioinform..

siDirect 2.0: updated software for designing functional siRNA with reduced seed-dependent off-target effect

Shinichi Morishita, Jun Yoshimura, Yuki Naito, 2009, BMC Bioinformatics.

5′SAGE: 5′-end Serial Analysis of Gene Expression database

Tomoyuki Yamada, Sumio Sugano, Shinichi Morishita, 2004, Nucleic Acids Res..

Comparing the Human and Fish Genomes

S. Morishita, Yoichiro Nakatani, W. Qu, 2013 .

Large hypomethylated domains serve as strong repressive machinery for key developmental genes in vertebrates

Taro L. Saito, S. Sugano, Yutaka Suzuki, 2014, Development.

Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease

Shinichi Morishita, Yasuo Terao, Yuko Saito, 2019, Nature Genetics.

Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

T. Naoe, S. Tsuzuki, M. Taniwaki, 2016, Nature Genetics.

Hypomethylated domain-enriched DNA motifs prepattern the accessible nucleosome organization in teleosts

S. Morishita, H. Takeda, Ryohei Nakamura, 2017, Epigenetics & Chromatin.

Landscape of CpG methylation of individual repetitive elements

Kazuki Ichikawa, Yuji Takahashi, Yuta Suzuki, 2015 .

A linear time algorithm for detecting long genomic regions enriched with a specific combination of epigenetic states

Kazuki Ichikawa, Shinichi Morishita, S. Morishita, 2015, BMC Genomics.

Coordinated Changes in DNA Methylation in Antigen-Specific Memory CD4 T Cells

M. Hattori, S. Sugano, Yutaka Suzuki, 2013, The Journal of Immunology.

Integrative analysis of genomic alterations in triple-negative breast cancer in association with homologous recombination deficiency

Shinichi Morishita, Hiromi Nakamura, Yasushi Totoki, 2017, PLoS genetics.

Antigen-Specific Memory CD 4 T Cells Coordinated Changes in DNA Methylation in

Suzuki, Abe, M. Hattori, 2013 .

Genome-wide pro fi ling of DNA methylation in human cancer cells

M. Hattori, S. Sugano, K. Matsushima, 2011 .

Extremely slow rate of evolution in the HOX cluster revealed by comparison between Tanzanian and Indonesian coelacanths.

Taro L. Saito, S. Sugano, Yutaka Suzuki, 2012, Gene.

Overexpression of Larp4B downregulates dMyc and reduces cell and organ sizes in Drosophila.

S. Morishita, T. Aigaki, M. Tsuda, 2018, Biochemical and biophysical research communications.

The time is ripe to investigate human centromeres by long-read sequencing

S. Morishita, Yutaka Suzuki, 2021, DNA research : an international journal for rapid publication of reports on genes and genomes.

Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy

S. Tsuji, S. Morishita, M. Yamaguchi, 2018, Brain : a journal of neurology.

Hamster PIWI proteins bind to piRNAs with stage-specific size variations during oocyte maturation

Y. Sakakibara, T. Itoh, A. Toyoda, 2020, bioRxiv.

BodyMap incorporated PCR-based expression profiling data and a gene ranking system

Shinichi Morishita, Jun Sese, Kousaku Okubo, 2001, Nucleic Acids Res..

BodyMap: a human and mouse gene expression database

Teruyoshi Hishiki, Shinichi Morishita, Kousaku Okubo, 2000, Nucleic Acids Res..

High-Resolution Analysis of the 5′-End Transcriptome Using a Next Generation DNA Sequencer

Sumio Sugano, Shinichi Morishita, Budrul Ahsan, 2009, PloS one.

Accelerated off-target search algorithm for siRNA

Tomoyuki Yamada, Shinichi Morishita, S. Morishita, 2005, Bioinform..

siDirect: highly effective, target-specific siRNA design software for mammalian RNA interference

Tomoyuki Yamada, Shinichi Morishita, Yuki Naito, 2004, Nucleic Acids Res..

dsCheck: highly sensitive off-target search software for double-stranded RNA-mediated RNA interference

Tomoyuki Yamada, Shinichi Morishita, Yuki Naito, 2005, Nucleic Acids Res..

KDD Cup 2001 report

David Page, Jie Cheng, Shinichi Morishita, 2002, SKDD.

UTGB/medaka: genomic resource database for medaka biology

Nobuyoshi Shimizu, Jun Yang, Atsushi Shimizu, 2007, Nucleic Acids Res..

Clinical and molecular genetic characterization of two female patients harboring the Xq27.3q28 deletion with different ratios of X chromosome inactivation

S. Morishita, J. Mitsui, J. Yoshimura, 2020, Human mutation.

PrimerStation: a highly specific multiplex genomic PCR primer design server for the human genome

Tomoyuki Yamada, Shinichi Morishita, Haruhiko Soma, 2006, Nucleic Acids Res..

CTCF looping is established during gastrulation in medaka embryos

Neva C. Durand, S. Morishita, H. Takeda, 2018, bioRxiv.

Centromere evolution and CpG methylation during vertebrate speciation

S. Morishita, H. Takeda, Ryohei Nakamura, 2017, Nature Communications.

Long-read metagenomic exploration of extrachromosomal mobile genetic elements in the human gut

M. Hattori, S. Morishita, Suguru Nishijima, 2019, Microbiome.

Novel De Novo KCND3 Mutation in a Japanese Patient with Intellectual Disability, Cerebellar Ataxia, Myoclonus, and Dystonia

T. Matsukawa, S. Tsuji, Toshihiro Hayashi, 2018, The Cerebellum.

Ataxic form of autosomal recessive PEX10-related peroxisome biogenesis disorders with a novel compound heterozygous gene mutation and characteristic clinical phenotype

T. Matsukawa, S. Tsuji, S. Morishita, 2017, Journal of the Neurological Sciences.

Associations between nucleosome phasing, sequence asymmetry, and tissue-specific expression in a set of inbred Medaka species

S. Sugano, Yutaka Suzuki, A. Fire, 2015, BMC Genomics.

A framework and an algorithm to detect low-abundance DNA by a handy sequencer and a palm-sized computer

Shinichi Morishita, Bansho Masutani, S. Morishita, 2018, Bioinform..

A framework and an algorithm to detect low‐abundance DNA by a handy sequencer and a palm‐sized computer

Shinichi Morishita, Bansho Masutani, S. Morishita, 2018, Bioinformatics.

Comparative Analysis of Genome and Epigenome in Closely Related Medaka Species Identifies Conserved Sequence Preferences for DNA Hypomethylated Domains

S. Sugano, Yutaka Suzuki, S. Morishita, 2016, Zoological Science.

The Gene Resource Locator: gene locus maps for transcriptome analysis

Tomoyuki Yamada, Shinichi Morishita, Jun Ogasawara, 2002, Nucleic Acids Res..

Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease

T. Matsukawa, S. Tsuji, Jun Shinmi, 2019, Nature Genetics.

Gene expression profile in human leukocytes.

Shinichi Morishita, Jun Sese, Shin-ichi Hashimoto, 2003, Blood.

Variant between CPT1B and CHKB associated with susceptibility to narcolepsy

Emmanuel Mignot, Katsushi Tokunaga, Shinichi Morishita, 2008, Nature Genetics.

Somatic GJA4 gain-of-function mutation in orbital cavernous venous malformations

S. Ishikawa, D. Komura, T. Matsukawa, 2022, Angiogenesis.

On Classification and Regression

Shinichi Morishita, S. Morishita, 1998, Discovery Science.

Comparative DNA sequence analysis of mouse and human CC chemokine gene clusters.

S. Kuhara, K. Hashimoto, S. Morishita, 2003, Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research.

Assessing Cell-to-Cell DNA Methylation Variability on Individual Long Reads

S. Tsuji, S. Morishita, H. Takeda, 2016, Scientific Reports.

MachiBase: a Drosophila melanogaster 5′-end mRNA transcription database

Atsushi Sasaki, Shinichi Morishita, Taro L. Saito, 2008, Nucleic Acids Res..

Atypical parkinsonism caused by Pro105Leu mutation of prion protein

T. Matsukawa, S. Tsuji, G. Oyama, 2016, Neurology: Genetics.

Amnionless-mediated glycosylation is crucial for cell surface targeting of cubilin in renal and intestinal cells

H. Ueda, S. Tsuji, S. Morishita, 2018, Scientific Reports.

Early prediction of functional prognosis in neurofibromatosis type 2 patients based on genotype–phenotype correlation with targeted deep sequencing

S. Morishita, N. Saito, T. Ota, 2022, Scientific Reports.

TBCD may be a causal gene in progressive neurodegenerative encephalopathy with atypical infantile spinal muscular atrophy

N. Kenmochi, S. Tsuji, T. Uechi, 2016, Journal of Human Genetics.

Recurrent DUX4 fusions in B cell acute lymphoblastic leukemia of adolescents and young adults

Shinichi Morishita, Koichiro Doi, Shigeki Ohtake, 2016, Nature Genetics.

HiC-Hiker: a probabilistic model to determine contig orientation in chromosome-length scaffolds with Hi-C

Ryo Nakabayashi, Shinichi Morishita, S. Morishita, 2020, Bioinform..

Altered expression of Crb2 in podocytes expands a variation of CRB2 mutations in steroid-resistant nephrotic syndrome

S. Tsuji, S. Morishita, A. Shimizu, 2017, Pediatric Nephrology.

Mutations in MME cause an autosomal‐recessive Charcot–Marie–Tooth disease type 2

S. Tsuji, J. Kira, S. Morishita, 2016, Annals of neurology.

CNV analysis using whole exome sequencing identified biallelic CNVs of VPS13B in siblings with intellectual disability.

S. Tsuji, S. Morishita, Y. Tsurusaki, 2018, European journal of medical genetics.

Neuroimaging, genetic, and enzymatic study in a Japanese family with a GBA gross deletion.

S. Tsuji, H. Onishi, S. Morishita, 2019, Parkinsonism & related disorders.

Modeling neurological diseases with induced pluripotent cells reprogrammed from immortalized lymphoblastoid cell lines

H. Okano, S. Tsuji, R. Hashimoto, 2016, Molecular Brain.

Diversity of Ca2+-Induced Morphology Revealed by Morphological Phenotyping of Ca2+-Sensitive Mutants of Saccharomyces cerevisiae

Y. Ohya, S. Morishita, D. Hirata, 2007, Eukaryotic Cell.

G1/S cyclin-dependent kinase regulates small GTPase Rho1p through phosphorylation of RhoGEF Tus1p in Saccharomyces cerevisiae.

Shinichi Morishita, Yoshikazu Ohya, Mitsuhiro Abe, 2008, Molecular biology of the cell.

Corrigendum: Recurrent DUX4 fusions in B cell acute lymphoblastic leukemia of adolescents and young adults.

T. Naoe, S. Tsuzuki, M. Taniwaki, 2016, Nature genetics.

Cloning and expression of a brain-specific putative UDP-GalNAc: polypeptide N-acetylgalactosaminyltransferase gene.

S. Morishita, M. Konishi, N. Itoh, 2005, Biological & pharmaceutical bulletin.

Clinicopathological features of the first Asian family having vocal cord and pharyngeal weakness with distal myopathy due to a MATR3 mutation

S. Tsuji, S. Morishita, Y. Ando, 2015, Neuropathology and applied neurobiology.

Poster: Robust estimation of DNA methylation with local regression

Atsushi Sasaki, Shinichi Morishita, S. Morishita, 2011, 2011 IEEE 1st International Conference on Computational Advances in Bio and Medical Sciences (ICCABS).

Complete fusion of a transposon and herpesvirus created the Teratorn mobile element in medaka fish

S. Morishita, H. Takeda, M. Kumagai, 2017, Nature Communications.

Burden of rare variants in causative genes for amyotrophic lateral sclerosis (ALS) accelerates age at onset of ALS

T. Matsukawa, S. Tsuji, S. Morishita, 2018, Journal of Neurology, Neurosurgery, and Psychiatry.

Complex hereditary peripheral neuropathies caused by novel variants in mitochondrial-related nuclear genes

I. Nishino, S. Morishita, M. Yamaguchi, 2022, Journal of Neurology.

Transversing itemset lattices with statistical metric pruning

Shinichi Morishita, Jun Sese, J. Sese, 2000, PODS '00.

Novel GBE1 mutation in a Japanese family with adult polyglucosan body disease

T. Matsukawa, S. Tsuji, S. Morishita, 2017, Neurology: Genetics.

Molecular epidemiological study of familial amyotrophic lateral sclerosis in Japanese population by whole-exome sequencing and identification of novel HNRNPA1 mutation

T. Matsukawa, S. Tsuji, M. Sonoo, 2018, Neurobiology of Aging.

Genome-wide association study identifies a new susceptibility locus in PLA2G4C for Multiple System Atrophy.

Sonja W. Scholz, A. Singleton, Y. Kusakabe, 2023, medRxiv.

Slowly progressive d-bifunctional protein deficiency with survival to adulthood diagnosed by whole-exome sequencing

T. Matsukawa, S. Tsuji, S. Morishita, 2017, Journal of the Neurological Sciences.

Computing Highly Specific and Noise-tolerant Oligomers Efficiently

TOMOYUKI YAMADA, SHINICHI MORISHITA, S. Morishita, 2004, J. Bioinform. Comput. Biol..

Answering the Most Correlated N Association Rules Efficiently

Shinichi Morishita, Jun Sese, J. Sese, 2002, PKDD.

28. UTGB Toolkit for Personalized Genome Browsers

Atsushi Sasaki, Shinichi Morishita, Taro L. Saito, 2012 .

Genome analysis

Atsushi Sasaki, Shinichi Morishita, Taro L. Saito, 2008 .

Constrained clusters of gene expression profiles with pathological features

Shinichi Morishita, Jun Sese, Morito Monden, 2004, Bioinform..

JTK: targeted diploid genome assembler

S. Morishita, Bansho Masutani, Yoshihiko Suzuki, 2023, Bioinformatics.

High-fat diet in early life triggers both reversible and persistent epigenetic changes in the medaka fish (Oryzias latipes)

S. Morishita, H. Takeda, Yoshimi Kunishima, 2023, bioRxiv.

HNF1B‐driven three‐dimensional chromatin structure for molecular classification in pancreatic cancers

A. Toyoda, S. Morishita, M. Otsuka, 2022, Cancer science.

A Japanese family with idiopathic basal ganglia calcification carrying a novel XPR1 variant

S. Morishita, Y. Uesaka, H. Ishiura, 2023, Journal of the Neurological Sciences.

Finding long tandem repeats in long noisy reads

Gene Myers, Shinichi Morishita, Kazuki Ichikawa, 2020, Bioinform..

AgIn: measuring the landscape of CpG methylation of individual repetitive elements

S. Turner, J. Korlach, S. Tsuji, 2016, Bioinform..

The Myocardial Accumulation of Aggregated Desmin Protein in a Case of Desminopathy with a de novo DES p.R406W Mutation.

M. Ono, S. Morishita, Yukako Shintani-Domoto, 2023, Internal medicine.

Phase-separated nuclear bodies of nucleoporin fusions promote condensation of MLL1/CRM1 and rearrangement of 3D genome structure.

Y. Ohkawa, S. Morishita, T. Tomonaga, 2023, Cell reports.

Novel COL6A2 mutation in a case of limb girdle muscular dystrophy phenotype with autosomal recessive inheritance

S. Tsuji, S. Morishita, H. Ishiura, 2016 .

Modeling neurological diseases with induced pluripotent cells reprogrammed from immortalized lymphoblastoid cell lines

H. Okano, S. Tsuji, R. Hashimoto, 2016, Molecular Brain.

Decomposing mosaic tandem repeats accurately from long reads

S. Morishita, Bansho Masutani, Riki Kawahara, 2023, Bioinform..

BodyMap: a collection of 3' ESTs for analysis of human gene expression information.

K Shimizu, K. Murakawa, J. Sese, 2000, Genome research.

Corrigendum: Comparative analysis of chimpanzee and human Y chromosomes unveils complex evolutionary pathway

M. Hattori, Y. Sakaki, N. Saitou, 2006, Nature Genetics.

Hypomethylated domain-enriched DNA motifs prepattern the accessible nucleosome organization in teleosts

S. Morishita, H. Takeda, Ryohei Nakamura, 2017, Epigenetics & Chromatin.

A Simple but Powerful Heuristic Method for Accelerating $k$ -Means Clustering of Large-Scale Data in Life Science

S. Morishita, Kazuki Ichikawa, 2014, IEEE/ACM Transactions on Computational Biology and Bioinformatics.

Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy

S. Sugano, Yutaka Suzuki, A. Fujiyama, 2018, Nature Genetics.

Sporadic progressive myoclonic epilepsy with early‐onset dementia caused by a de novo mutation in PSEN1

S. Tsuji, S. Morishita, H. Ishiura, 2019, Neurology and Clinical Neuroscience.

Accelerating Path-free XML Queries in RDBMS

Hongyan Wu, Shinichi Morishita, Taro L. Saito, 2010 .

Chromatin-Associated Periodicity in Genetic Variation Downstream of Transcriptional Start Sites

Taro L. Saito, A. Fire, S. Sugano, 2009, Science.

Weighted Majority Decision among Several Region Rules for Scientific Discovery

Shinichi Morishita, Akihiro Nakaya, Hideharu Furukawa, 1999, Discovery Science.

Data mining tools for the Saccharomyces cerevisiae morphological database

Shinichi Morishita, Jun Sese, Yoshikazu Ohya, 2005, Nucleic Acids Res..