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Scopus著者プロファイル
宮 冬樹
医学部臨床遺伝学センター
ウェブサイト
https://k-ris.keio.ac.jp/html/100015902_ja.html
h-index
2344
被引用数
23
h 指数
Pureの文献数とScopusの被引用数に基づいて算出されます
2000
2025
年別の研究成果
概要
フィンガープリント
ネットワーク
研究成果
(112)
類似のプロファイル
(6)
フィンガープリント
Fuyuki Miyaが活動している研究トピックを掘り下げます。このトピックラベルは、この研究者の研究成果に基づきます。これらがまとまってユニークなフィンガープリントを構成します。
並べ替え順
重み付け
アルファベット順
Biochemistry, Genetics and Molecular Biology
Intellectual Disability
100%
Exome Sequencing
88%
Genetics
80%
Autosomal Recessive Inheritance
62%
Exon
52%
Mouse
50%
Gene Expression
45%
Pedigree
39%
Microarrays
39%
Missense Mutation
39%
Exome
33%
Candidate Gene
32%
Gene Mutation
31%
NEDD4L
31%
Whole Genome Sequencing
31%
Indel
31%
PI3K/AKT/mTOR Pathway
31%
Human Genetics
31%
Genotyping
31%
Cisplatin
31%
Missense
29%
Messenger RNA
29%
Genome-Wide Association Study
29%
Methylation
26%
Allele
25%
Genotype Phenotype Correlation
25%
Gene Expression Profiling
23%
Autophagy
21%
Carcinogenesis
21%
Zebra Fish
19%
Embryogenesis
19%
Dysplasia
19%
Germ Cell
18%
Germline
18%
Genetic Disorder
17%
Retinitis pigmentosa
15%
Fibronectin Type III Domain
15%
Hox Gene
15%
TIGIT
15%
Aminoacyl tRNA Synthetase
15%
Disease Modeling
15%
Nuclear Factor I A
15%
2,5-Dimethoxy-4-iodoamphetamine
15%
Macaca
15%
Carcinogenic Activity
15%
Hedgehog Signaling Pathway
15%
Ornithine
15%
AKT3
15%
Transfection
15%
IDH1
15%
Medicine and Dentistry
Neoplasm
38%
Hepatocyte
31%
Periventricular Heterotopia
31%
Retinitis pigmentosa
31%
Recurrent Disease
31%
Cleft Palate
31%
Brain Calcification
31%
Biological Marker
23%
Brain Malformation
19%
Metastatic Carcinoma
19%
Diagnosis
19%
Microgyria
19%
In Vitro
18%
Tonic-Clonic Seizure
17%
Colorectal Cancer
17%
Exome Sequencing
17%
Collapsin Response Mediator Protein 2
15%
Growth Hormone
15%
Genome Wide Association Study
15%
Phylogeny
15%
Interferon
15%
Waardenburg Syndrome
15%
Alexander Disease
15%
Bladder Cancer
15%
Retina Degeneration
15%
Fatty Liver
15%
Neoadjuvant Chemotherapy
15%
Hepatitis C
15%
Antisense Oligonucleotide
15%
Muscle Disease
15%
Induced Pluripotent Stem Cell
15%
Monocyte
15%
Neurodegeneration
15%
Autosomal Recessive Inheritance
15%
Clear Cell Renal Cell Carcinoma
15%
Skeletal Muscle
15%
Nonsense Mutation
15%
Craniofacial Malformation
15%
Gemcitabine
15%
Human Genetics
15%
Histone Methyltransferase
15%
Hox Gene
15%
Cancer
15%
Carboplatin
15%
Exon
15%
Urinary Tract
15%
Prognostic Signature
15%
Missense Mutation
15%
Fetus Echography
15%
Tomography
15%
Keyphrases
Periventricular Nodular Heterotopia
31%
Polymicrogyria
19%
Genome-wide Association Study
19%
Rheumatoid Arthritis
18%
Overexpression
18%
DPYSL2
15%
Late-onset Epileptic Spasms
15%
Epileptic Spasms
15%
Gene Prioritization
15%
Gene Expression Score
15%
Type 2 Diabetes Mellitus (T2DM)
15%
Human Liver chimeric Mice
15%
NEDD4
15%
Splicing QTL
15%
Prognostic Biomarker
15%
EPG5
15%
Vici Syndrome
15%
Multisystem Involvement
15%
Synapse Dysfunction
15%
ELF3
15%
AKT3
15%
Indel Detection
15%
Capillary Malformation
15%
Retinal Ciliopathy
15%
Stage II Colorectal Cancer
15%
AP3D1
15%
Ethnic-specific
15%
Bladder Cancer
15%
HECT Domain
15%
Neoadjuvant Chemotherapy
15%
DOT1L
15%
Hypomorphic mutation
15%
Response Predictors
15%
Gemcitabine
15%
Missense mutation
15%
Atorvastatin
15%
FBXO28
15%
Plasma Parameters
15%
Statins
15%
Xenopus Laevis
15%
Human Genetics
15%
TUBA1A
15%
Hydranencephaly
15%
Nanopore Long-read Sequencing
15%
Glioma Recurrence
15%
Immunological Classification
15%
Comb-like
15%
Split Read
15%
Deletion Detection
15%
Gene Expression Data
15%
