Author

Kazuyuki Komatsu

Observed name: 小松, 和幸

Institutions: Hamamatsu University, Hamamatsu University School of Medicine

Observed institutions: Hamamatsu University, Hamamatsu University School of Medicine

ORCID: 0000-0001-9861-8412

Observed ORCID: 0000-0001-9861-8412

OpenAlex ID: A5032045445

RNA sequencing and target long-read sequencing reveal an intronic transposon insertion causing aberrant splicing

2023 · Ryota Kawakami, Takuya Hiraide, et al. · Journal of Human Genetics · 14

A new case of concurrent existence of PRRT2-associated paroxysmal movement disorders with c.649dup variant and 16p11.2 microdeletion syndrome

2022 · Kazuyuki Komatsu, Shinobu Fukumura, et al. · Brain and Development · 10

Identification of 5’ untranslated region variants in genes involved in neurodevelopmental disorders

2026 · Taiju Hayashi, Sachiko Miyamoto, et al. · Journal of Human Genetics · 6

Identifying pathogenic variants in rare pediatric neurological diseases using exome sequencing

2024 · Kazuyuki Komatsu, Mitsuhiro Kato, et al. · Scientific Reports · 3

Genomic Profiling of Pediatric Solid Tumors With a Dual DNA / RNA Panel: JCCG‐TOP2 Study

2025 · Kayoko Tao, Takako Yoshioka, et al. · Cancer Science · 2

Characterization of KMT2A::MATR3 fusion in a patient with acute lymphoblastic leukemia and monitoring of minimal residual disease by nanoplate digital PCR

2022 · Kazuyuki Komatsu, Kimiyoshi Sakaguchi, et al. · Pediatric Blood & Cancer · 2

Hemizygous loss-of-function variants of EIF1AX are associated with a syndromic neurodevelopmental disorder

2026 · Kazuyuki Komatsu, Atsushi Sugie, et al. · European Journal of Human Genetics · 1

Myocardial testosterone glucuronide and disease phenotypes in hypertrophic cardiomyopathy

2026 · Takenori Ikoma, Keitaro Akita, et al. · ESC Heart Failure · 1

Successful Cytotoxic Chemotherapy‐Free Bridging to Hematopoietic Stem Cell Transplantation With Dasatinib and Prednisolone/Blinatumomab for Relapsed Pediatric Philadelphia Chromosome–Positive Acute Lymphoblastic Leukemia

2026 · Shota Hagino, Kazuyuki Komatsu, et al. · Pediatric Blood & Cancer

Correction: Hemizygous loss-of-function variants of EIF1AX are associated with a syndromic neurodevelopmental disorder

2026 · Kazuyuki Komatsu, Atsushi Sugie, et al. · European Journal of Human Genetics

Pontocerebellar hypoplasia type 9 with a novel combination of compound heterozygous variants in AMPD2

2026 · Shuhei Dohi, Junko Hotta, et al. · Human Genome Variation

Molecular analysis of testicular germ cell tumor in a male patient with 45,X/46,XY mosaicism: case report with review of literature

2026 · Shinichiro Sano, Kazuyuki Komatsu, et al. · Endocrine Journal

PPP1R12A-related urogenital and/or brain malformation syndrome in a 46,XX individual with Müllerian duct anomalies: expanding the phenotypic spectrum

2026 · Yuki Murai, Jun Horie, et al. · Clinical Pediatric Endocrinology

病期iホジキンリンパ腫に対する放射線療法を省略したvamp療法の有用性

2020 · 坂口, 公祥, 川上, 領太, et al. · Institutional Repositories DataBase (IRDB)

Works count: 14

Citation count: 39

H-index: 3

I10-index: 2