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学位論文・関西医大誌
学術雑誌掲載論文
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学会発表
（最終更新日：2026-05-11 16:27:00）
ヒガサ コウイチロウ
HIGASA KOUICHIROU
日笠 幸一郎
所属
附属生命医学研究所ゲノム解析部門
職種
研究所教授
■
学術雑誌掲載論文
1.
原著(症例報告除く)
Thiazoline-related innate fear stimuli orchestratehypothermia and anti-hypoxia via sensory TRPA1activation 2021/04
2.
原著(症例報告除く)
Predicting mild familial exudative vitreoretinopathy with autosomal dominant inheritance using deep learning. 2026/04
3.
原著(症例報告除く)
Whole-genome sequencing of 3135 individuals representing the genetic diversity of the Japanese population. 2026/04
4.
原著(症例報告除く)
Anamorelin in Cancer Cachexia: Gut Microbiota Effects and CONUT Score as a Predictor of Response. 2025/11
5.
原著(症例報告除く)
HMGA2 links morphological evolution and microenvironment dynamics to systemic therapy response in clear cell renal cell carcinoma. 2025/11
6.
症例報告
Elderly-onset iatrogenic cerebral amyloid angiopathy presenting with lobar and deep haemorrhages. 2025/10
7.
原著(症例報告除く)
Whole-genome sequencing reveals rare and structural variants contributing to psoriasis and identifies CERCAM as a risk gene. 2025/10
8.
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The Arf pathway is required for resolving endoplasmic reticulum stress during T-cell activation 2025/09
9.
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Fecal Bifidobacterium Serves as a Predictor of Postoperative Recurrence After Neoadjuvant Chemotherapy in Pancreatic Cancer. 2025/08
10.
原著(症例報告除く)
Molecular Insights into the Superiority of Platelet Lysate over FBS for hASC Expansion and Wound Healing 2025/07
11.
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Blood DNA virome associates with autoimmune diseases and COVID-19 2025/01
12.
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Nerve Enlargement in Patients with INF2 Variants Causing Peripheral Neuropathy and Focal Segmental Glomerulosclerosis 2025/01
13.
原著(症例報告除く)
Raman signatures of type A and B influenza viruses: molecular origin of the " catch and kill" inactivation mechanism mediated by micrometric silicon nitride powder 2025/01
14.
その他
川崎病の罹患感受性因子としての腸内細菌叢の乱れ 2025
15.
症例報告
VANGL2とGRHL2のヘテロミスセンス変異を認めた脊髄脂肪腫の1例 2024/04
16.
症例報告
二分脊椎症における遺伝子変異と形態異常 2024/04
17.
原著(症例報告除く)
Familial Exudative Vitreoretinopathy With and Without Pathogenic Variants of Norrin/β-Catenin Signaling Genes 2024/03
18.
原著(症例報告除く)
OLIG2 translocates to chromosomes during mitosis via a temperature downshift: a novel neural cold response of mitotic bookmarking 2024/01
19.
原著(症例報告除く)
Raman Fingerprints of SARS-CoV-2 Omicron Subvariants: Molecular Roots of Virological Characteristics and Evolutionary Directions 2023/11
20.
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Dysbiosis of the gut microbiota as a susceptibility factor for Kawasaki disease 2023/10
21.
原著(症例報告除く)
Raman Multi-Omic Snapshot and Statistical Validation of Structural Differences between Herpes Simplex Type I and Epstein-Barr Viruses 2023/10
22.
原著(症例報告除く)
Relationship between circulating mitochondrial DNA and microRNA in patients with major depression 2023/10
23.
症例報告
Adenoid ameloblastoma with BRAF p.V600E mutation revealing ameloblastomatous origin: a first case report 2023/09
24.
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Changes in Multiple microRNA Levels with Antidepressant Treatment Are Associated with Remission and Interact with Key Pathways: A Comprehensive microRNA Analysis 2023/07
25.
原著(症例報告除く)
Characterization of cytoskeletal and structural effects of INF2 variants causing glomerulopathy and neuropathy 2023/07
26.
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Rap1 organizes lymphocyte front-back polarity via RhoA signaling and talin1 2023/07
27.
原著(症例報告除く)
OLIG2 is an in vivo bookmarking transcription factor in the developing neural tube in mouse 2023/05
28.
症例報告
ゲノム解析にて特定したtubulin遺伝子の変異を有する難治性脳形成障害 2023/05
29.
原著(症例報告除く)
Ago2 and a miRNA reduce Topoisomerase 1 for enhancing DNA cleavage in antibody diversification by activation-induced cytidine deaminase 2023/04
30.
症例報告
全ゲノム解析を用いた難治性脳形成障害の遺伝子異常検索 2023/04
31.
原著(症例報告除く)
Areas of Crush Nuclear Streaming Should Be Included as Tumor Content in the Era of Molecular Diagnostics 2023/03
32.
症例報告
新規subtypeとみなされるBRAF mutationが検出されたadenoid ameloblastomaの一例 2023/03
33.
原著(症例報告除く)
Deep learning-based predictions of clear and eosinophilic phenotypes in clear cell renal cell carcinoma 2023/01
34.
その他
Activation-induced cytidine deaminase(AID)による免疫記憶形成に必要なAgo2-miRNA依存的なtopoisomerase1(Top1)の調節機構 2023
35.
その他
Ago2とmiRNAはAID依存性の抗体遺伝子組換えにおけるDNA切断を促進するためにDNAトポイソメラーゼ1を減少させる 2023
36.
その他
本邦のうつ病患者における疾患発症,薬物治療反応性に関するゲノムワイド関連解析(GWAS) 2023
37.
原著(症例報告除く)
Accelerated Angiogenesis of Human Umbilical Vein Endothelial Cells Under Negative Pressure Was Associated With the Regulation of Gene Expression Involved in the Proliferation and Migration 2022/12
38.
原著(症例報告除く)
Multidimensional analyses of the pathomechanism caused by the non-catalytic GNE variant, c.620A>T, in patients with GNE myopathy 2022/12
39.
症例報告
Successful pregnancy and delivery in a young-onset hypertrophic cardiomyopathy patient with a novel doublet-base substitution in the MYH7 gene 2022/10
40.
原著(症例報告除く)
Development and validation of a vascularity-based architectural classification for clear cell renal cell carcinoma: correlation with conventional pathological prognostic factors, gene expression patterns, and clinical outcomes 2022/06
41.
その他
Correction to: Development and validation of a vascularity-based architectural classification for clear cell renal cell carcinoma: correlation with conventional pathological prognostic factors, gene expression patterns, and clinical outcomes 2022/05
42.
原著(症例報告除く)
Multiple Pre-Treatment miRNAs Levels in Untreated Major Depressive Disorder Patients Predict Early Response to Antidepressants and Interact with Key Pathways 2022/03
43.
原著(症例報告除く)
PBRM1 Immunohistochemical Expression Profile Correlates with Histomorphological Features and Endothelial Expression of Tumor Vasculature for Clear Cell Renal Cell Carcinoma 2022/02
44.
原著(症例報告除く)
Histologic-Based Tumor-Associated Immune Cells Status in Clear Cell Renal Cell Carcinoma Correlates with Gene Signatures Related to Cancer Immunity and Clinical Outcomes 2022/01
45.
その他
【ゲノム医療におけるデータベース-使い方とコツ】一般集団・多因子疾患関連バリアントのデータベース Human Genetic Variation Database(HGVD) 2022/01
46.
原著(症例報告除く)
Eosinophilic features in clear cell renal cell carcinoma correlate with outcomes of immune checkpoint and angiogenesis blockade 2021/09
47.
原著(症例報告除く)
Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data 2021/06
48.
原著(症例報告除く)
Population dynamics in the Japanese Archipelago since the Pleistocene revealed by the complete mitochondrial genome sequences 2021/06
49.
原著(症例報告除く)
Positive renal familial history in IgA nephropathy is associated with worse renal outcomes: a single-center longitudinal study 2021/06
50.
症例報告
Combined Single Nucleotide Variants of ORAI1 and BLK in a Child with Refractory Kawasaki Disease 2021/05
51.
原著(症例報告除く)
Genotype-Phenotype Correlations in RP1-Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN 2021/05
52.
原著(症例報告除く)
Digenic mutations in ALDH2 and ADH5 impair formaldehyde clearance and cause a multisystem disorder, AMeD syndrome. 2020/12
53.
原著(症例報告除く)
EYS is a major gene involved in retinitis pigmentosa in Japan: genetic landscapes revealed by stepwise genetic screening 2020/11
54.
原著(症例報告除く)
Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease. 2020/11
55.
原著(症例報告除く)
Association of ALPL variants with serum alkaline phosphatase and bone traits in the general Japanese population: The Nagahama Study. 2020/03
56.
原著(症例報告除く)
Legacy Data Confounds Genomics Studies 2020/01
57.
原著(症例報告除く)
IgG4-related disease in the Japanese population: a genome-wide association study. 2019/09
58.
原著(症例報告除く)
Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population. 2019/04
59.
原著(症例報告除く)
National platform for Rare Diseases Data Registry of Japan 2019/01
60.
原著(症例報告除く)
Accurate diagnosis of mismatch repair deficiency in colorectal cancer using high-quality DNA samples from cultured stem cells. 2018/12
61.
原著(症例報告除く)
A mutation in transcription factor MAFB causes Focal Segmental Glomerulosclerosis with Duane Retraction Syndrome 2018/08
62.
原著(症例報告除く)
Regional genetic differences among Japanese populations and performance of genotype imputation using whole-genome reference panel of the Tohoku Medical Megabank Project. 2018/07
63.
原著(症例報告除く)
Risk allele of FZD4 gene for familial exudative vitreoretinopathy 2018/06
64.
原著(症例報告除く)
Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy. 2018/04
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全件表示(64件)
