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Author

Yuta Inoue

Observed institution: Yokohama City University
ORCID: 0000-0002-7073-2843
Observed ORCID: 0000-0002-7073-2843
OpenAlex ID: A5014951929
Novel compound heterozygous ABCA2 variants cause IDPOGSA, a variable phenotypic syndrome with intellectual disability
2024 · Yuta Inoue, Naomi Tsuchida, et al. · Journal of Human Genetics · 10
Three KINSSHIP syndrome patients with mosaic and germline AFF3 variants
2022 · Yuta Inoue, Naomi Tsuchida, et al. · Clinical Genetics · 9
Genome sequencing provides high diagnostic yield and new etiological insights for intellectual disability and developmental delay
2025 · Kohei Hamanaka, Atsushi Fujita, et al. · npj Genomic Medicine · 7
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Completely resolved structural variants by optical genome mapping with adaptive sampling from CNV discovery
2026 · Li Fu, Chong Ae Kim, et al. · npj Genomic Medicine · 2
Blended Phenotypes in Individuals With Rare Diseases: A Brazilian Case Series
2025 · Caroline Brandão Piai, Gabriela Yumi Goto Salti, et al. · American Journal of Medical Genetics Part A · 1
A boy with drug-resistant epilepsy and aortopulmonary collateral arteries arising from a KCNT1 variant
2025 · Kentaro Okada, Takaaki Sawada, et al. · Brain and Development Case Reports · 1
Correction: Novel compound heterozygous ABCA2 variants cause IDPOGSA, a variable phenotypic syndrome with intellectual disability
2025 · Yuta Inoue, Naomi Tsuchida, et al. · Journal of Human Genetics
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A case of Baraitser–Winter cerebrofrontofacial syndrome diagnosed by whole-exome sequencing
2025 · Kenichi Suga, Hiroki Sato, et al. · Human Genome Variation
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Works count: 8
Citation count: 30
H-index: 3
I10-index: 1
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