Shinichi Morishita

Chiba University — Japan

Biochemistry, Genetics and Molecular Biology · Life Sciences

51h-index11.0kcitations324works2.62yr avg
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Research Topics

Genomics and Phylogenetic Studies(34), Chromosomal and Genetic Variations(29), Data Mining Algorithms and Applications(28), RNA and protein synthesis mechanisms(25), Epigenetics and DNA Methylation(21)

Publications324 total

Sequential omics analysis reveals molecular signatures of malignant transformation in recurrent meningiomas
Acta Neuropathologica Communications·2025· 1 citedOpen Access
Centromere methylation and genome divergence during vertebrate speciation
2025Open Access
CGC1, a new reference genome for <i>Caenorhabditis elegans</i>
Genome Research·2025· 4 citedOpen Access
Approximating edit distances between complex tandem repeats efficiently
Bioinformatics·2025Open Access
In-frame deletion variant of ABCD1 in a sporadic case of adrenoleukodystrophy
Human Genome Variation·2025Open Access
Immunopeptidomics Combined with Full-Length Transcriptomics Uncovers Diverse Cryptic Neoantigens
SSRN Electronic Journal·2025Open Access
CGC1, a new reference genome for <i>Caenorhabditis elegans</i>
2024· 3 citedOpen Access
Frequency of FGF14 intronic GAA repeat expansion in patients with multiple system atrophy and undiagnosed ataxia in the Japanese population
European Journal of Human Genetics·2024· 6 citedOpen Access
110 - Validation of the area under the Watts factor curve during the voiding cycle as a novel parameter for diagnosing detrusor underactivity in females
Continence·2024Open Access
A novel de novo disease‐causing variant in <i>ATL1</i> in a pediatric patient with spastic paraplegia
Neurology and Clinical Neuroscience·2024Open Access
A Novel &lt;i&gt;De Novo&lt;/i&gt; Variant in &lt;i&gt;KCNH5&lt;/i&gt; in a Patient with Refractory Epileptic Encephalopathy
Internal Medicine·2024Open Access
A polygenic score method boosted by non-additive models
Nature Communications·2024· 15 citedOpen Access
Genome-wide association analysis identifies PLA2G4C as a susceptibility locus for Multiple System Atrophy
Research Square (Research Square)·2024Open Access
<scp><i>SPTLC2</i></scp> variants are associated with early‐onset <scp>ALS</scp> and <scp>FTD</scp> due to aberrant sphingolipid synthesis
Annals of Clinical and Translational Neurology·2024· 10 citedOpen Access
A whole-genome shotgun approach to human reference genome sequencing
Nature Reviews Genetics·2024
Meningiomas in patients with neurofibromatosis type 2 predominantly comprise ‘immunogenic subtype’ tumours characterised by macrophage infiltration
Acta Neuropathologica Communications·2023· 10 citedOpen Access
A landscape of complex tandem repeats within individual human genomes
Nature Communications·2023· 13 citedOpen Access
High-fat diet in early life triggers both reversible and persistent epigenetic changes in the medaka fish (Oryzias latipes)
BMC Genomics·2023· 13 citedOpen Access
Phase-separated nuclear bodies of nucleoporin fusions promote condensation of MLL1/CRM1 and rearrangement of 3D genome structure
Cell Reports·2023· 34 citedOpen Access
A Japanese family with idiopathic basal ganglia calcification carrying a novel XPR1 variant
Journal of the Neurological Sciences·2023· 9 cited
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Frequent Co-authors

Jun Yoshimura(14), Koichiro Doi(12), Shoji Tsuji(11), Hiroyuki Ishiura(10), Jun Mitsui(10), Sumio Sugano(8), Jun Sese(8), Yoichiro Nakatani(6), Hiroyuki Takeda(6), Takeshi Fukuda(6), Takeshi Tokuyama(6), Wei Qü(5), Atsushi Toyoda(5), Yuji Takahashi(5), Yutaka Suzuki(5), Yoshiyuki Sakaki(5), Atsuko Shimada(4), Asao Fujiyama(4), Kouji Matsushima(4), Yaeko Ichikawa(4)