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Atsuko Okazaki

Machine learning approaches to explore digenic inheritance
2022 · Atsuko Okazaki, Jurg Ott · Trends in Genetics · 46
Population genetics: past, present, and future
2020 · Atsuko Okazaki, Satoru Yamazaki, et al. · Human Genetics · 28
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A heterozygous LAMA5 variant may contribute to slowly progressive, vinculin-enhanced familial FSGS and pulmonary defects
2022 · Jun-Ya Kaimori, Yamato Kikkawa, et al. · JCI Insight · 8
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Genotype Pattern Mining for Pairs of Interacting Variants Underlying Digenic Traits
2021 · Atsuko Okazaki, Sukanya Horpaopan, et al. · Genes · 8
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Cyclosporine A Treatment of Proteinuria in a New Case of MAFB-Associated Glomerulopathy without Extrarenal Involvement: A Case Report
2021 · Jun-Ya Kaimori, Tatsuhiko Mori, et al. · The Nephron journals/Nephron journals · 7
Severe spinal cord hypoplasia due to a novel ATAD3A compound heterozygous deletion
2022 · Tomohiro Ebihara, Taro Nagatomo, et al. · Molecular Genetics and Metabolism Reports · 6
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Venous thromboembolism is caused by prothrombin p.Arg541Trp mutation in Japanese individuals
2021 · Jumpei Yamamoto, Masaya Yamamoto, et al. · Human Genome Variation · 6
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Microstripe pattern substrate consisting of alternating planar and nanoprotrusive regions improved hiPSC-derived cardiomyocytes’ unidirectional alignment and functional properties
2024 · Hideo Saotome, Yukiko Yatsuka, et al. · Biomedical Materials · 4
Case Report of Left Ventricular Noncompaction Cardiomyopathy Characterized by Undulating Phenotypes in Adult Patients
2021 · Wataru Miyake, Mayu Minemoto, et al. · International Heart Journal · 3
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Utility and Limitations of Genetic Testing in the Routine Care of Cardiovascular Disease Patients in a General Hospital
2025 · Daiki Tomidokoro, Kotaro Mori, et al. · International Heart Journal · 2
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Genetic Landscape of Masticatory Muscle Tendon–Aponeurosis Hyperplasia
2023 · Rina Tajima, Atsuko Okazaki, et al. · Genes · 2
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Non-invasive urinary heteroplasmy screening outperforms blood testing for certain mitochondrial DNA variants in mitochondrial disease patients
2026 · Atsuko Okazaki, Yukiko Yatsuka, et al. · Molecular Genetics and Metabolism
Nanopore-based haplotype-resolved X chromosome inactivation for severity assessment in X-linked disorders: An AIFM1 study with a mosaic PDHA1 carrier
2026 · Kohta Nakamura, Atsuko Okazaki, et al. · Human Genetics and Genomics Advances
Genetic Landscape and Prognostic Factors in Pediatric Mitochondrial Cardiomyopathy: A 20-Year Comprehensive Study
2026 · Atsuko Okazaki, Yukiko Yatsuka, et al. · Journal of Molecular and Cellular Cardiology Plus
Simultaneous Assessment of Genetic and Epigenetic Contributions to the Plasma Lipid Levels with Respect to Cardiovascular Risk
2026 · Fumihiko Takeuchi, Masaya Yamamoto, et al. · Journal of Atherosclerosis and Thrombosis
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P013: Advances in multi-omics diagnostics studies of mitochondrial diseases in Japan
2025 · Yasushi Okazaki, Kei Murayama, et al. · Genetics in Medicine Open
P204: Impact of measuring mitochondrial DNA heteroplasmy rates using different tissues in 103 patients with mitochondrial disease
2025 · Atsuko Okazaki, Yukiko Yatsuka, et al. · Genetics in Medicine Open
Association test for rare variants using the hamming distance
2018 · Suhyun Hwangbo, Jin Young Jang, et al. · International Journal of Data Mining and Bioinformatics
Works count: 18
Citation count: 120
H-index: 6
I10-index: 2
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