Tatsuhiko Tsunoda

Tatsuhiko Tsunoda's AcademicInfluence.com Rankings

Tatsuhiko Tsunoda

Biology

#13698

World Rank

#17254

Historical Rank

Bioinformatics

#175

World Rank

#177

Historical Rank

Genetics

#1538

World Rank

#1641

Historical Rank

biology Degrees

Download Badge

Biology

Tatsuhiko Tsunoda's Degrees

PhD Genetics University of Tokyo
Masters Bioinformatics Kyoto University
Bachelors Biology University of Tokyo

Similar Degrees You Can Earn

Best Online Bachelor's in Biology 2026

Why Is Tatsuhiko Tsunoda Influential?

(Suggest an Edit or Addition)

(See a Problem?)

Tatsuhiko Tsunoda's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

A second generation human haplotype map of over 3.1 million SNPs (2007) (4567)
International network of cancer genome projects (2010) (1839)
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease (2009) (1235)
Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis (2003) (1076)
Integrated molecular analysis of clear-cell renal cell carcinoma (2013) (909)
Whole-genome sequencing of liver cancers identifies etiological influences on mutation patterns and recurrent mutations in chromatin regulators (2012) (777)
Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarction (2002) (730)
SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations (2008) (717)
An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis (2003) (618)
Toward information extraction: identifying protein names from biological papers. (1998) (612)
Genome-wide analysis of gene expression in human hepatocellular carcinomas using cDNA microarray: identification of genes involved in viral carcinogenesis and tumor progression. (2001) (556)
Meta-analysis identifies six new susceptibility loci for atrial fibrillation (2012) (535)
Whole-genome mutational landscape and characterization of noncoding and structural mutations in liver cancer (2016) (528)
A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians (2009) (487)
Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. (2005) (463)
Overexpression of LSD1 contributes to human carcinogenesis through chromatin regulation in various cancers (2011) (420)
ITPKC functional polymorphism associated with Kawasaki disease susceptibility and formation of coronary artery aneurysms (2008) (415)
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
Meta-analysis identifies common variants associated with body mass index in East Asians (2012) (372)
A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities (2005) (364)
Identification by cDNA microarray of genes involved in ovarian carcinogenesis. (2000) (349)
Multiancestry association study identifies new asthma risk loci that colocalize with immune cell enhancer marks (2017) (337)
Genome-wide association study identifies three new susceptibility loci for adult asthma in the Japanese population (2011) (319)
Expression profiles of non-small cell lung cancers on cDNA microarrays: Identification of genes for prediction of lymph-node metastasis and sensitivity to anti-cancer drugs (2003) (309)
Estimating transcription factor bindability on DNA (1999) (308)
Alterations of gene expression during colorectal carcinogenesis revealed by cDNA microarrays after laser-capture microdissection of tumor tissues and normal epithelia. (2001) (304)
Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population (2012) (298)
Association of a novel long non‐coding RNA in 8q24 with prostate cancer susceptibility (2011) (295)
Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population (2010) (293)
Dysregulation of PRMT1 and PRMT6, Type I arginine methyltransferases, is involved in various types of human cancers (2011) (285)
A genome-wide association study identifies three new risk loci for Kawasaki disease (2012) (268)
Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk. (2009) (265)
Meta-analysis identifies multiple loci associated with kidney function–related traits in east Asian populations (2012) (264)
A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B (2010) (261)
A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility (2010) (254)
A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population (2009) (251)
Identification of membrane-type matrix metalloproteinase-1 as a target of the β-catenin/Tcf4 complex in human colorectal cancers (2002) (251)
Molecular Features of the Transition from Prostatic Intraepithelial Neoplasia (PIN) to Prostate Cancer (2004) (242)
An integrated database of chemosensitivity to 55 anticancer drugs and gene expression profiles of 39 human cancer cell lines. (2002) (241)
A functional SNP in CILP, encoding cartilage intermediate layer protein, is associated with susceptibility to lumbar disc disease (2005) (239)
Significant effect of polymorphisms in CYP2D6 and ABCC2 on clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients. (2010) (231)
Genome-wide cDNA microarray analysis of gene expression profiles in pancreatic cancers using populations of tumor cells and normal ductal epithelial cells selected for purity by laser microdissection (2004) (228)
Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations (2012) (226)
Analyses of non-coding somatic drivers in 2,658 cancer whole genomes (2020) (220)
Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis (2013) (218)
A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis (2011) (218)
A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population. (2011) (206)
Genetic variations in the gene encoding ELMO1 are associated with susceptibility to diabetic nephropathy. (2005) (206)
Overexpression of the JmjC histone demethylase KDM5B in human carcinogenesis: involvement in the proliferation of cancer cells through the E2F/RB pathway (2010) (203)
Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarction (2003) (202)
Molecular diagnosis of colorectal tumors by expression profiles of 50 genes expressed differentially in adenomas and carcinomas (2002) (202)
Prediction of sensitivity of esophageal tumors to adjuvant chemotherapy by cDNA microarray analysis of gene-expression profiles. (2001) (200)
Thymic stromal lymphopoietin gene promoter polymorphisms are associated with susceptibility to bronchial asthma. (2011) (194)
Prepublication data sharing (2009) (190)
Integrating Genetic, Transcriptional, and Functional Analyses to Identify 5 Novel Genes for Atrial Fibrillation (2014) (177)
Prediction of sensitivity of advanced non-small cell lung cancers to gefitinib (Iressa, ZD1839). (2004) (177)
Diverse transcriptional initiation revealed by fine, large‐scale mapping of mRNA start sites (2001) (174)
Whole-genome mutational landscape of liver cancers displaying biliary phenotype reveals hepatitis impact and molecular diversity (2015) (172)
Genome-wide analysis of gene expression in intestinal-type gastric cancers using a complementary DNA microarray representing 23,040 genes. (2002) (170)
Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations (2010) (168)
ITPA polymorphism affects ribavirin-induced anemia and outcomes of therapy--a genome-wide study of Japanese HCV virus patients. (2010) (165)
Genome-wide cDNA microarray screening to correlate gene expression profiles with sensitivity of 85 human cancer xenografts to anticancer drugs. (2002) (164)
Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index. (2014) (163)
Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers (2011) (163)
Genome-wide analysis of gene expression in synovial sarcomas using a cDNA microarray. (2002) (163)
A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population (2010) (161)
Functional haplotypes of PADI 4 , encoding citrullinating enzyme peptidylarginine deiminase 4 , are associated with rheumatoid arthritis (2003) (161)
Association of the gene encoding wingless-type mammary tumor virus integration-site family member 5B (WNT5B) with type 2 diabetes. (2004) (159)
Novel Calmodulin Mutations Associated With Congenital Arrhythmia Susceptibility (2014) (159)
Predicting response to methotrexate, vinblastine, doxorubicin, and cisplatin neoadjuvant chemotherapy for bladder cancers through genome-wide gene expression profiling. (2006) (157)
DeepInsight: A methodology to transform a non-image data to an image for convolution neural network architecture (2019) (155)
Common variants in DVWA on chromosome 3p24.3 are associated with susceptibility to knee osteoarthritis (2008) (155)
Molecular features of hormone-refractory prostate cancer cells by genome-wide gene expression profiles. (2007) (154)
High-Risk Ovarian Cancer Based on 126-Gene Expression Signature Is Uniquely Characterized by Downregulation of Antigen Presentation Pathway (2012) (154)
Common variant in 6q26-q27 is associated with distal colon cancer in an Asian population (2011) (154)
Gene expression profiles of small-cell lung cancers: molecular signatures of lung cancer. (2006) (153)
Classification of sensitivity or resistance of cervical cancers to ionizing radiation according to expression profiles of 62 genes selected by cDNA microarray analysis. (2002) (149)
Genome-wide association study identifies three novel loci for type 2 diabetes. (2014) (149)
Histone lysine methyltransferase SETD8 promotes carcinogenesis by deregulating PCNA expression. (2012) (147)
Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese. (2014) (137)
Genome-wide cDNA microarray analysis of gene-expression profiles involved in ovarian endometriosis. (2003) (134)
Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues. (2003) (132)
Genes associated with liver metastasis of colon cancer, identified by genome-wide cDNA microarray. (2004) (129)
Common variants in CASP3 confer susceptibility to Kawasaki disease. (2010) (128)
Genome‐wide analysis of gene expression in human intrahepatic cholangiocarcinoma (2005) (126)
A functional single nucleotide polymorphism in the core promoter region of CALM1 is associated with hip osteoarthritis in Japanese. (2005) (125)
A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population. (2013) (124)
Comparison of gene-expression profiles between diffuse- and intestinal-type gastric cancers using a genome-wide cDNA microarray (2004) (123)
Multiple Loci Are Associated with White Blood Cell Phenotypes (2011) (123)
Prevalence of Allergic Rhinitis and Sensitization to Common Aeroallergens in a Japanese Population (2009) (122)
Photosynthesis nuclear genes generally lack TATA-boxes: a tobacco photosystem I gene responds to light through an initiator. (2002) (122)
Up-regulation of the ectodermal-neural cortex 1 (ENC1) gene, a downstream target of the beta-catenin/T-cell factor complex, in colorectal carcinomas. (2001) (119)
Association analyses of East Asian individuals and trans‐ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels (2017) (119)
Comparison of gene expression profiles between Opisthorchis viverrini and non‐Opisthorchis viverrini associated human intrahepatic cholangiocarcinoma (2006) (118)
Whole-genome sequencing and comprehensive variant analysis of a Japanese individual using massively parallel sequencing (2010) (114)
Functional SNPs in CD244 increase the risk of rheumatoid arthritis in a Japanese population (2008) (114)
Enhanced expression of EHMT2 is involved in the proliferation of cancer cells through negative regulation of SIAH1. (2011) (114)
New Sequence Variants in HLA Class II/III Region Associated with Susceptibility to Knee Osteoarthritis Identified by Genome-Wide Association Study (2010) (114)
A Genome-Wide Association Study Identified AFF1 as a Susceptibility Locus for Systemic Lupus Eyrthematosus in Japanese (2012) (112)
Polygenic burdens on cell-specific pathways underlie the risk of rheumatoid arthritis (2017) (112)
Genome-wide analysis of organ-preferential metastasis of human small cell lung cancer in mice. (2003) (104)
A single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations. (2012) (103)
Association of solute carrier family 12 (sodium/chloride) member 3 with diabetic nephropathy, identified by genome-wide analyses of single nucleotide polymorphisms. (2003) (102)
Genome-wide screening of genes showing altered expression in liver metastases of human colorectal cancers by cDNA microarray. (2001) (102)
Genome-wide gene-expression profiles of breast-cancer cells purified with laser microbeam microdissection: identification of genes associated with progression and metastasis. (2004) (101)
Genome-wide profiling of gene expression in 29 normal human tissues with a cDNA microarray. (2002) (100)
Lumbar disc degeneration is linked to a carbohydrate sulfotransferase 3 variant. (2013) (99)
SNPs in BRAP associated with risk of myocardial infarction in Asian populations (2009) (98)
Prediction of response to neoadjuvant chemotherapy for osteosarcoma by gene-expression profiles. (2004) (97)
Integrative pathway enrichment analysis of multivariate omics data (2018) (96)
Predicting Response to Methotrexate, Vinblastine, Doxorubicin, and Cisplatin Neoadjuvant Chemotherapy for Bladder Cancers through Genome-Wide Gene Expression Profiling (2005) (96)
A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population (2006) (96)
An improved discriminative filter bank selection approach for motor imagery EEG signal classification using mutual information (2017) (95)
Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci. (2015) (95)
Isolation of a novel human gene, MARKL1, homologous to MARK3 and its involvement in hepatocellular carcinogenesis. (2001) (92)
The JmjC domain‐containing histone demethylase KDM3A is a positive regulator of the G1/S transition in cancer cells via transcriptional regulation of the HOXA1 gene (2012) (91)
A Deep Learning Approach for Motor Imagery EEG Signal Classification (2016) (91)
Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus. (2011) (90)
A Single Nucleotide Polymorphism within the Acetyl-Coenzyme A Carboxylase Beta Gene Is Associated with Proteinuria in Patients with Type 2 Diabetes (2010) (90)
Growth and gene expression profile analyses of endometrial cancer cells expressing exogenous PTEN. (2001) (88)
Association between a single-nucleotide polymorphism in the promoter of the human interleukin-3 gene and rheumatoid arthritis in Japanese patients, and maximum-likelihood estimation of combinatorial effect that two genetic loci have on susceptibility to the disease. (2001) (87)
Prediction of chemosensitivity for patients with acute myeloid leukemia, according to expression levels of 28 genes selected by genome-wide complementary DNA microarray analysis. (2002) (84)
A replication study confirmed the EDAR gene to be a major contributor to population differentiation regarding head hair thickness in Asia (2008) (84)
Predictive value of the IL28B polymorphism on the effect of interferon therapy in chronic hepatitis C patients with genotypes 2a and 2b. (2011) (83)
Histone lysine methyltransferase Wolf-Hirschhorn syndrome candidate 1 is involved in human carcinogenesis through regulation of the Wnt pathway. (2011) (83)
Single nucleotide polymorphisms in the gene encoding Krüppel-like factor 7 are associated with type 2 diabetes (2005) (83)
Identification of Nine Novel Loci Associated with White Blood Cell Subtypes in a Japanese Population (2011) (80)
Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis (2020) (80)
Prediction of outcome of advanced cervical cancer to thermoradiotherapy according to expression profiles of 35 genes selected by cDNA microarray analysis. (2004) (79)
Analysis of single-nucleotide polymorphisms in Japanese rheumatoid arthritis patients shows additional susceptibility markers besides the classic shared epitope susceptibility sequences. (2004) (78)
Combined Genetic and Genealogic Studies Uncover a Large BAP1 Cancer Syndrome Kindred Tracing Back Nine Generations to a Common Ancestor from the 1700s (2015) (77)
Radioimmunotherapy of human synovial sarcoma using a monoclonal antibody against FZD10 (2008) (77)
Association between single-nucleotide polymorphisms in selectin genes and immunoglobulin A nephropathy. (2002) (77)
Predict Gram-Positive and Gram-Negative Subcellular Localization via Incorporating Evolutionary Information and Physicochemical Features Into Chou's General PseAAC (2015) (76)
Identification of a Human Clonogenic Progenitor with Strict Monocyte Differentiation Potential: A Counterpart of Mouse cMoPs (2017) (75)
A genomewide linkage analysis of Kawasaki disease: evidence for linkage to chromosome 12 (2006) (75)
Whole genome sequencing discriminates hepatocellular carcinoma with intrahepatic metastasis from multi-centric tumors. (2017) (74)
Genome-wide gene expression profile analysis of esophageal squamous cell carcinomas. (2006) (73)
Performance comparison of four commercial human whole-exome capture platforms (2015) (73)
A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups (2014) (73)
CYP2D6 genotyping for functional-gene dosage analysis by allele copy number detection. (2009) (73)
Genetic variations in the gene encoding TFAP2B are associated with type 2 diabetes mellitus (2005) (72)
WHSC1 Promotes Oncogenesis through Regulation of NIMA-Related Kinase-7 in Squamous Cell Carcinoma of the Head and Neck (2014) (72)
Integrated Analysis of Whole Genome and Transcriptome Sequencing Reveals Diverse Transcriptomic Aberrations Driven by Somatic Genomic Changes in Liver Cancers (2014) (70)
Validation study of the prediction system for clinical response of M‐VAC neoadjuvant chemotherapy (2007) (70)
Comprehensive gene expression profiling of anaplastic thyroid cancers with cDNA microarray of 25 344 genes. (2004) (69)
Circulating Tumor DNA Analysis for Liver Cancers and Its Usefulness as a Liquid Biopsy (2015) (69)
The Histone Demethylase JMJD2B Plays an Essential Role in Human Carcinogenesis through Positive Regulation of Cyclin-Dependent Kinase 6 (2011) (67)
A genome-wide association study identifies locus at 10q22 associated with clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients in Japanese. (2012) (67)
Association study of COL9A2 with lumbar disc disease in the Japanese population (2006) (67)
Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patients (2003) (66)
Deregulation of the histone demethylase JMJD2A is involved in human carcinogenesis through regulation of the G(1)/S transition. (2013) (66)
Polymorphisms in the 3′ UTR in the neurocalcin δ gene affect mRNA stability, and confer susceptibility to diabetic nephropathy (2007) (63)
Variation of gene-based SNPs and linkage disequilibrium patterns in the human genome. (2004) (62)
Brain wave classification using long short-term memory network based OPTICAL predictor (2019) (62)
Expression profiles of metastatic brain tumor from lung adenocarcinomas on cDNA microarray. (2006) (62)
A Genome-Wide Association Study of Nephrolithiasis in the Japanese Population Identifies Novel Susceptible Loci at 5q35.3, 7p14.3, and 13q14.1 (2012) (61)
Genome-wide gene expression profiles of clear cell renal cell carcinoma: identification of molecular targets for treatment of renal cell carcinoma. (2006) (58)
Genome-wide analysis of gene-expression profiles in chronic myeloid leukemia cells using a cDNA microarray. (2003) (58)
Identification of a Susceptibility Locus for Severe Adolescent Idiopathic Scoliosis on Chromosome 17q24.3 (2013) (58)
Prediction of Sensitivity to STI571 among Chronic Myeloid Leukemia Patients by Genome‐wide cDNA Microarray Analysis (2002) (58)
Morphological and microarray analyses of human hepatocytes from xenogeneic host livers (2013) (56)
The histone methyltransferase Wolf–Hirschhorn syndrome candidate 1‐like 1 (WHSC1L1) is involved in human carcinogenesis (2013) (56)
PSSM-Suc: Accurately predicting succinylation using position specific scoring matrix into bigram for feature extraction. (2017) (56)
IL-28B predicts response to chronic hepatitis C therapy--fine-mapping and replication study in Asian populations. (2011) (56)
Analysis of gene-expression profiles after gamma irradiation of normal human fibroblasts. (2006) (55)
SucStruct: Prediction of succinylated lysine residues by using structural properties of amino acids. (2017) (53)
Functional Variants in NFKBIE and RTKN2 Involved in Activation of the NF-κB Pathway Are Associated with Rheumatoid Arthritis in Japanese (2012) (53)
A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese (2014) (52)
Single nucleotide polymorphisms in TNFSF 15 confer susceptibility to Crohn ’ s disease (2005) (52)
KIF1A mutation in a patient with progressive neurodegeneration (2014) (51)
Calbindin 1, fibroblast growth factor 20, and α-synuclein in sporadic Parkinson’s disease (2008) (51)
PhoglyStruct: Prediction of phosphoglycerylated lysine residues using structural properties of amino acids (2018) (51)
A functional SNP in EDG2 increases susceptibility to knee osteoarthritis in Japanese. (2008) (51)
A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in Japanese. (2011) (51)
Identification of histological markers for malignant glioma by genome-wide expression analysis: dynein, α-PIX and sorcin (2005) (50)
Association of single-nucleotide polymorphisms in MTMR9 gene with obesity. (2007) (50)
Coding SNP in tenascin-C Fn-III-D domain associates with adult asthma. (2005) (50)
Identification of AXUD1, a novel human gene induced by AXIN1 and its reduced expression in human carcinomas of the lung, liver, colon and kidney (2001) (49)
Analysis of gene-expression profiles in testicular seminomas using a genome-wide cDNA microarray. (2003) (49)
Improving succinylation prediction accuracy by incorporating the secondary structure via helix, strand and coil, and evolutionary information from profile bigrams (2018) (48)
Microarray Analysis of Gene‐expression Profiles in Diffuse Large B‐cell Lymphoma: Identification of Genes Related to Disease Progression (2002) (47)
OPAL: prediction of MoRF regions in intrinsically disordered protein sequences (2018) (47)
Success: evolutionary and structural properties of amino acids prove effective for succinylation site prediction (2018) (47)
Discovery and characterization of coding and non-coding driver mutations in more than 2,500 whole cancer genomes (2017) (46)
A practical method to detect SNVs and indels from whole genome and exome sequencing data (2013) (46)
Combinational effect of genes for the renin–angiotensin system in conferring susceptibility to diabetic nephropathy (2006) (45)
Identification of AF17 as a downstream gene of the beta-catenin/T-cell factor pathway and its involvement in colorectal carcinogenesis. (2001) (45)
Chromothripsis-like chromosomal rearrangements induced by ionizing radiation using proton microbeam irradiation system (2016) (45)
FGFR2 is associated with hair thickness in Asian populations (2009) (44)
Expression profiling to predict postoperative prognosis for estrogen receptor‐negative breast cancers by analysis of 25,344 genes on a cDNA microarray (2004) (44)
Defects in autophagosome-lysosome fusion underlie Vici syndrome, a neurodevelopmental disorder with multisystem involvement (2017) (43)
Pathway analysis of genome-wide data improves warfarin dose prediction (2013) (43)
Population-genetic nature of copy number variations in the human genome (2009) (42)
Lessons for pharmacogenomics studies: association study between CYP2D6 genotype and tamoxifen response. (2010) (41)
MoRFPred-plus: Computational Identification of MoRFs in Protein Sequences using Physicochemical Properties and HMM profiles. (2018) (41)
The subcellular localization and activity of cortactin is regulated by acetylation and interaction with Keap1 (2015) (41)
Functional single-nucleotide polymorphisms in the secretogranin III (SCG3) gene that form secretory granules with appetite-related neuropeptides are associated with obesity. (2007) (39)
Expression profiles of two types of human knee-joint cartilage (2003) (38)
Genetic Variation in the SLC8A1 Calcium Signaling Pathway Is Associated With Susceptibility to Kawasaki Disease and Coronary Artery Abnormalities (2016) (38)
Growth hormone-dependent pathogenesis of human hepatic steatosis in a novel mouse model bearing a human hepatocyte-repopulated liver. (2011) (38)
The oncogenic polycomb histone methyltransferase EZH2 methylates lysine 120 on histone H2B and competes ubiquitination. (2013) (38)
Enhanced Expression of EHMT 2 Is Involved in the Proliferation of Cancer Cells through Negative Regulation of SIAH 11 , 2 (2014) (38)
Activation of an Estrogen/ Estrogen Receptor Signaling by BIG3 Through Its Inhibitory Effect on Nuclear Transport of PHB2/REA in Breast Cancer (2009) (38)
Expression profile analysis of colon cancer cells in response to sulindac or aspirin. (2002) (37)
HLA-DQB1*03 Confers Susceptibility to Chronic Hepatitis C in Japanese: A Genome-Wide Association Study (2013) (37)
IRX4 at 5p15 suppresses prostate cancer growth through the interaction with vitamin D receptor, conferring prostate cancer susceptibility. (2012) (35)
Isolation of HELAD1, a novel human helicase gene up-regulated in colorectal carcinomas (2002) (34)
Assessing the clinical utility of a genetic risk score constructed using 49 susceptibility alleles for type 2 diabetes in a Japanese population. (2013) (33)
SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population (2011) (33)
Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population (2015) (33)
Transcriptome analysis of distinct mouse strains reveals kinesin light chain-1 splicing as an amyloid-β accumulation modifier (2014) (33)
Protein fold recognition using HMM-HMM alignment and dynamic programming. (2016) (32)
Risk prediction models for dementia constructed by supervised principal component analysis using miRNA expression data (2019) (32)
Novel splicing mutation in the ASXL3 gene causing Bainbridge–Ropers syndrome (2016) (32)
Targeted next‐generation sequencing in the diagnosis of neurodevelopmental disorders (2015) (32)
Single-nucleotide polymorphisms in the class II region of the major histocompatibility complex in Japanese patients with immunoglobulin A nephropathy (2002) (32)
Decimation filter with Common Spatial Pattern and Fishers Discriminant Analysis for motor imagery classification (2016) (31)
Combined burden and functional impact tests for cancer driver discovery using DriverPower (2020) (31)
Reproducibility, Performance, and Clinical Utility of a Genetic Risk Prediction Model for Prostate Cancer in Japanese (2012) (31)
OPAL+: Length‐Specific MoRF Prediction in Intrinsically Disordered Protein Sequences (2018) (31)
Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans (2020) (31)
A genome-wide association analysis identifies NMNAT2 and HCP5 as susceptibility loci for Kawasaki disease (2017) (30)
Lag Analysis of Genetic Networks in the Cell Cycle of Budding Yeast (2001) (30)
Hierarchical Maximum Likelihood Clustering Approach (2017) (30)
The Construction of Risk Prediction Models Using GWAS Data and Its Application to a Type 2 Diabetes Prospective Cohort (2014) (30)
An integrative machine learning approach for prediction of toxicity-related drug safety (2018) (30)
Association of a single-nucleotide polymorphism in the immunoglobulin μ-binding protein 2 gene with immunoglobulin A nephropathy (2005) (29)
Activation of an estrogen/estrogen receptor signaling by BIG3 through its inhibitory effect on nuclear transport of PHB2/REA in breast cancer (2009) (29)
Divisive hierarchical maximum likelihood clustering (2017) (29)
CUL1, a component of E3 ubiquitin ligase, alters lymphocyte signal transduction with possible effect on rheumatoid arthritis (2005) (28)
Sample Size for Successful Genome-Wide Association Study of Major Depressive Disorder (2018) (27)
Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility (2011) (27)
Identification of independent risk loci for Graves’ disease within the MHC in the Japanese population (2011) (27)
Genome-wide association study of warfarin maintenance dose in a Brazilian sample. (2015) (27)
Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes (2015) (27)
Predicting response of bladder cancers to gemcitabine and carboplatin neoadjuvant chemotherapy through genome-wide gene expression profiling. (2011) (26)
Predicting MoRFs in protein sequences using HMM profiles (2016) (25)
An algorithm for inferring complex haplotypes in a region of copy-number variation. (2008) (24)
Inferring genetic networks from DNA microarray data by multiple regression analysis. (2000) (24)
TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis (2015) (23)
Novel MCA/ID syndrome with ASH1L mutation (2017) (23)
A comparison of machine learning classifiers for dementia with Lewy bodies using miRNA expression data (2019) (23)
Gene expression patterns as marker for 5-year postoperative prognosis of primary breast cancers (2004) (22)
IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis (2018) (22)
Discovery of a Cynomolgus Monkey Family With Retinitis Pigmentosa. (2018) (22)
Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes (2016) (22)
Prognosis prediction model for conversion from mild cognitive impairment to Alzheimer’s disease created by integrative analysis of multi-omics data (2020) (20)
Profiling the inhibitory receptors LAG-3, TIM-3, and TIGIT in renal cell carcinoma reveals malignancy (2020) (20)
Deep Learning Approach for Automated Detection of Myopic Maculopathy and Pathologic Myopia in Fundus Images. (2021) (19)
Truncating mutation in NFIA causes brain malformation and urinary tract defects (2015) (18)
Structural Basis and Genotype–Phenotype Correlations of INSR Mutations Causing Severe Insulin Resistance (2017) (18)
A novel missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria and cleft palate (2017) (18)
Systematic analysis of mutation distribution in three dimensional protein structures identifies cancer driver genes (2016) (17)
DeepFeature: feature selection in nonimage data using convolutional neural network (2021) (17)
Phenotypic Variability of ANK2 Mutations in Patients With Inherited Primary Arrhythmia Syndromes. (2016) (17)
Predicting response to docetaxel neoadjuvant chemotherapy for advanced breast cancers through genome-wide gene expression profiling. (2009) (17)
MOCSphaser: a haplotype inference tool from a mixture of copy number variation and single nucleotide polymorphism data (2008) (17)
Identification of biomarkers associated with migraine with aura (2009) (16)
Association of an IGHV3-66 gene variant with Kawasaki disease (2020) (16)
Structure-activity relationship of clovamide and its related compounds for the inhibition of amyloid β aggregation. (2018) (15)
A combination of genetic and biochemical analyses for the diagnosis of PI3K-AKT-mTOR pathway-associated megalencephaly (2017) (15)
A combination of targeted enrichment methodologies for whole-exome sequencing reveals novel pathogenic mutations (2015) (15)
Hepatitis C Virus Infection Suppresses the Interferon Response in the Liver of the Human Hepatocyte Chimeric Mouse (2011) (15)
ALDH18A1-related cutis laxa syndrome with cyclic vomiting (2016) (14)
Unveiling synapse pathology in spinal bulbar muscular atrophy by genome-wide transcriptome analysis of purified motor neurons derived from disease specific iPSCs (2020) (14)
Linkage disequilibrium of evolutionarily conserved regions in the human genome (2006) (14)
Integrated analysis of human genetic association study and mouse transcriptome suggests LBH and SHF genes as novel susceptible genes for amyloid-β accumulation in Alzheimer’s disease (2018) (14)
Time and Memory Efficient Algorithm for Extracting Palindromic and Repetitive Subsequences in Nucleic Acid Sequences (1998) (14)
Navigating the disease landscape: knowledge representations for contextualizing molecular signatures (2018) (13)
A case report of reversible generalized seizures in a patient with Waardenburg syndrome associated with a novel nonsense mutation in the penultimate exon of SOX10 (2018) (13)
Prediction of response to peginterferon‐alfa‐2b plus ribavirin therapy in Japanese patients infected with hepatitis C virus genotype 1b (2011) (13)
Stepwise iterative maximum likelihood clustering approach (2016) (13)
Role of a heterotrimeric G‐protein, Gi2, in the corticogenesis: possible involvement in periventricular nodular heterotopia and intellectual disability (2017) (13)
Whole genome sequencing and mutation rate analysis of trios with paternal dioxin exposure (2018) (12)
MYCN de novo gain-of-function mutation in a patient with a novel megalencephaly syndrome (2018) (12)
Discovering MoRFs by trisecting intrinsically disordered protein sequence into terminals and middle regions (2019) (12)
Bigram-PGK: phosphoglycerylation prediction using the technique of bigram probabilities of position specific scoring matrix (2019) (12)
Forecasting the spread of COVID-19 using LSTM network (2021) (11)
Multiplexed single-cell pathology reveals the association of CD8 T-cell heterogeneity with prognostic outcomes in renal cell carcinoma (2021) (11)
SumSec: Accurate Prediction of Sumoylation Sites Using Predicted Secondary Structure (2018) (11)
Predicting protein-peptide binding sites with a Deep Convolutional Neural Network. (2020) (11)
HseSUMO: Sumoylation site prediction using half-sphere exposures of amino acids residues (2019) (11)
Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL 6 locus (2011) (10)
WHSC 1 Promotes Oncogenesis through Regulation of NIMA-Related Kinase-7 in Squamous Cell Carcinoma of the Head and Neck (2015) (10)
Attenuation of Progressive Hearing Loss in DBA/2J Mice by Reagents that Affect Epigenetic Modifications Is Associated with Up-Regulation of the Zinc Importer Zip4 (2015) (10)
Empirical Bayes Estimation of Semi-parametric Hierarchical Mixture Models for Unbiased Characterization of Polygenic Disease Architectures (2016) (10)
Arete – candidate gene prioritization using biological network topology with additional evidence types (2017) (10)
The prediction models for postoperative overall survival and disease‐free survival in patients with breast cancer (2017) (9)
Integrative immunogenomic analysis of gastric cancer dictates novel immunological classification and the functional status of tumor‐infiltrating cells (2020) (9)
Genetic differences in the two main groups of the Japanese population based on autosomal SNPs and haplotypes (2012) (9)
Novel compound heterozygous variants in PLK4 identified in a patient with autosomal recessive microcephaly and chorioretinopathy (2016) (9)
Single-nucleotide polymorphisms in GALNT8 are associated with the response to interferon therapy for chronic hepatitis C. (2013) (9)
Recombination rates of genes expressed in human tissues. (2008) (9)
A novel homozygous missense mutation in the SH3-binding motif of STAMBP causing microcephaly-capillary malformation syndrome (2018) (9)
2D–EM clustering approach for high-dimensional data through folding feature vectors (2017) (8)
Sudden death in a case of megalencephaly capillary malformation associated with a de novo mutation in AKT3 (2014) (8)
Gene masking - a technique to improve accuracy for cancer classification with high dimensionality in microarray data (2016) (8)
Landscape of prognostic signatures and immunogenomics of the AXL/GAS6 axis in renal cell carcinoma (2021) (8)
Subject-Specific-Frequency-Band for Motor Imagery EEG Signal Recognition Based on Common Spatial Spectral Pattern (2019) (8)
Single-stranded and double-stranded DNA-binding protein prediction using HMM profiles. (2020) (8)
Siblings with optic neuropathy and RTN4IP1 mutation (2017) (8)
Genome-wide association study suggests four variants influencing outcomes with ranibizumab therapy in exudative age-related macular degeneration (2018) (7)
A deletion mutation in myosin heavy chain 11 causing familial thoracic aortic dissection in two Japanese pedigrees. (2015) (7)
Unique characteristics of tertiary lymphoid structures in kidney clear cell carcinoma: prognostic outcome and comparison with bladder cancer (2022) (7)
De novo ATP1A3 variants cause polymicrogyria (2021) (7)
Genome-Wide Association Study Identifies Pharmacogenomic Loci Linked with Specific Antihypertensive Drug Treatment and New-Onset Diabetes (2016) (7)
Erratum: Whole-genome mutational landscape and characterization of noncoding and structural mutations in liver cancer (2016) (7)
A functional SNP in FLT1 increases risk of coronary artery disease in a Japanese population (2016) (7)
Identification of a set of genes associated with response to interleukin-2 and interferon-α combination therapy for renal cell carcinoma through genome-wide gene expression profiling. (2010) (6)
Effects of clovamide and its related compounds on the aggregations of amyloid polypeptides (2021) (6)
Gene expression dataset for whole cochlea of Macaca fascicularis (2018) (5)
Inferring Haplotypes of Copy Number Variations From High-Throughput Data With Uncertainty (2011) (5)
Primary microcephaly with anterior predominant pachygyria caused by novel compound heterozygous mutations in ASPM. (2015) (5)
A novel genetic syndrome with STARD9 mutation and abnormal spindle morphology (2017) (5)
Clustering of Small-Sample Single-Cell RNA-Seq Data via Feature Clustering and Selection (2019) (4)
Splicing QTL analysis focusing on coding sequences reveals mechanisms for disease susceptibility loci (2022) (4)
ELF3 Overexpression as Prognostic Biomarker for Recurrence of Stage II Colorectal Cancer (2021) (4)
MotifCombinator: a web-based tool to search for combinations of cis-regulatory motifs (2007) (4)
Single-nucleotide polymorphisms in GALNT 8 are associated with the response to interferon therapy for chronic hepatitis C (2012) (3)
Computational Prediction of Lysine Pupylation Sites in Prokaryotic Proteins Using Position Specific Scoring Matrix into Bigram for Feature Extraction (2019) (3)
Structural basis of ethnic-specific variants of PAX4 associated with type 2 diabetes (2020) (3)
Four pedigrees with aminoacyl-tRNA synthetase abnormalities (2021) (3)
Association between high immune activity and worse prognosis in uveal melanoma and low-grade glioma in TCGA transcriptomic data (2021) (3)
A hypomorphic variant in EYS detected by genome-wide association study contributes toward retinitis pigmentosa (2021) (3)
Genome-wide Analysis of Gene Expression in Human Hepatocellular Carcinomas Using cDNA Microarray : Identification of Genes Involved in Viral Carcinogenesis and Tumor Progression 1 (2001) (3)
Environmental factor dependent maximum likelihood method for association study targeted to personalized medicine. (2000) (3)
Phase I/II study of novel HLA-A24 restricted DEPDC1 and MPHOSPH1 peptide vaccine for bladder cancer. (2010) (3)
Whole Genome Sequencing of a Vietnamese Family from a Dioxin Contamination Hotspot Reveals Novel Variants in the Son with Undiagnosed Intellectual Disability (2018) (3)
Abstract 13371: CALM2 Mutations Associated With Atypical Juvenile Long QT Syndrome (2013) (3)
Application of cepstrum analysis and linear predictive coding for motor imaginary task classification (2015) (2)
Homozygous ADCY5 mutation causes early-onset movement disorder with severe intellectual disability (2021) (2)
Automatic extraction of position specific cooccurrence of transcription factor bindings on promoters. (1998) (2)
The subcellular localization and activity of cortactin is regulated by acetylation and interaction with Keap 1 (2015) (2)
980: Predicting Response to M-VAC Neoadjuvant Chemotherapy for Bladder Cancers through Genomewide Gene Expression Profiling (2006) (2)
Immune subtypes and neoantigen-related immune evasion in advanced colorectal cancer (2022) (2)
SPECTRA: a tool for enhanced brain wave signal recognition (2021) (2)
Publisher Correction: IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis (2018) (2)
Quantification of multicellular colonization in tumor metastasis using exome‐sequencing data (2020) (2)
Integrated analysis of human genetic association study and mouse transcriptome suggests LBH and SHF genes as novel susceptible genes for amyloid-β accumulation in Alzheimer’s disease (2018) (2)
Novel Calmodulin (CALM2) Mutations Associated with Congenital Arrhythmia Susceptibility (2)
Clinical usefulness of multigene screening with phenotype-driven bioinformatics analysis for the diagnosis of patients with monogenic diabetes or severe insulin resistance. (2020) (2)
Exploring predictive biomarkers from clinical genome-wide association studies via multidimensional hierarchical mixture models (2018) (2)
hzAnalyzer: detection, quantification, and visualization of contiguous homozygosity in high-density genotyping datasets (2011) (2)
Making a haplotype catalog with estimated frequencies based on SNP homozygotes (2010) (2)
144 GENOME-WIDE ASSOCIATION STUDY IDENTIFIES MULTIPLE NEW SUSCEPTIBILITY LOCI FOR PROSTATE CANCER IN JAPANESE POPULATION (2011) (1)
Abstract 5177: Genome-wide profiling of somatic mutations in liver cancers revealed significantly mutated genes and non-coding regions in liver cancers (2014) (1)
Gene expression profiling of DBA/2J mice cochleae treated with l-methionine and valproic acid (2015) (1)
Hemorrhagic shock and encephalopathy syndrome in a patient with a de novo heterozygous variant in KIF1A (2021) (1)
Importance of dimensionality reduction in protein fold recognition (2015) (1)
Erratum: A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities (2005) (1)
Abstract 1179: Combined genetic and genealogic studies uncover a large BAP1 cancer syndrome kindred, tracing back nine generations to a common ancestor from the 1700s (2016) (1)
DeepInsight-FS: Selecting features for non-image data using convolutional neural network (2020) (1)
A novel homozygous missense mutation in the SH3-binding motif of STAMBP causing microcephaly-capillary malformation syndrome (2018) (1)
A comparison of machine learning classifiers for dementia with Lewy bodies using miRNA expression data (2019) (1)
CNN-Pred: Prediction of single-stranded and double-stranded DNA-binding protein using convolutional neural networks. (2022) (1)
Quantification of multicellular colonization in tumor metastasis using exome sequencing data (2019) (1)
SYNFRIZZ: A first-in-human (FIH) study of a radiolabeled monoclonal antibody (Mab) targeting frizzled homolog 10 (FZD10) in patients (pts) with advanced synovial sarcomas (SyS). (2017) (1)
1325-P: Effectiveness of Comprehensive Gene Panel-Based Next-Generation Sequencing with Phenotype-Driven Bioinformatics Analysis for Diagnosis of Atypical Diabetes (2019) (1)
Predicting Response toMethotrexate , Vinblastine , Doxorubicin , and Cisplatin Neoadjuvant Chemotherapy for Bladder Cancers through Genome-Wide Gene Expression Profiling (2005) (1)
MotifCombinator : A Web Tool to Search for Combinations of Cis-Regulatory Motifs (2006) (0)
Divisive hierarchical maximum likelihood clustering (2017) (0)
The Future of and Beyond GWAS (2019) (0)
Efficient generation and developmental analysis of basal forebrain cholinergic neurons from mouse embryonic stem cells (2011) (0)
OE-009 Identification of a Locus on Chromosome 5p that Confers Risk of Coronary Artery Disease by Genome Wide Association Study(OE02,ACS/AMI (Basic) (IHD),Oral Presentation (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Society) (2009) (0)
Abstract 2970: Whole genome sequencing analysis of multiple liver cancer nodules for determination of causal events for multi-occurrence (2015) (0)
Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate (2019) (0)
Systematic detection of Mendelian and non-Mendelian variants associated with retinitis pigmentosa by genome-wide association study (2019) (0)
Gene expression dataset for whole cochlea of Macaca fascicularis (2018) (0)
Utility of tissue-specific gene expression scores for gene prioritization in Mendelian diseases (2022) (0)
Pathway analysis of genome-wide data improves warfarin dose prediction (2013) (0)
Xenografts to Anticancer Drugs Expression Profiles with Sensitivity of 85 Human Cancer Genome-wide cDNA Microarray Screening to Correlate Gene Updated (2002) (0)
2D–EM clustering approach for high-dimensional data through folding feature vectors (2017) (0)
Stepwise iterative maximum likelihood clustering approach (2016) (0)
TRANSCRIPTOME ANALYSIS OF DISTINCT MOUSE STRAINS REVEALS KLC1 SPLICE VARIANT E AS AN ABETA ACCUMULATION MODIFIER (2014) (0)
Refractory epilepsy and regression in a patient with a de novo heterozygous POGZ mutation (2019) (0)
Abstract 5200: Genome-wide integrative analysis for the determination of the consequence of AT-rich interacting domain 2 (ARID2) depletion in hepatocellular carcinoma. (2013) (0)
Revisiting the definition of glioma recurrence based on a phylogenetic investigation of primary and re-emerging tumor samples: a case report (2022) (0)
Discovering MoRFs by trisecting intrinsically disordered protein sequence into terminals and middle regions (2019) (0)
Prognosis prediction model for conversion from mild cognitive impairment to Alzheimer’s disease created by integrative analysis of multi-omics data (2020) (0)
Expression Quantitative Trait Loci Analysis of Stable Warfarin Dose Identifies Novel Associations : Finding Signal within the Noise (2013) (0)
Development of gene and protein expression screening-based toxicogenomics system using human primary normal neuronal cells (Proceedings of the 32nd Annual Meeting) (2005) (0)
HseSUMO: Sumoylation site prediction using half-sphere exposures of amino acids residues (2019) (0)
Genotyping and Statistical Analysis (2019) (0)
Abstract 12257: Calmodulin Interacting Genes as a Novel Candidate for Pathogenesis of Long-QT Syndrome (2015) (0)
Structural basis of ethnic-specific variants of PAX4 associated with type 2 diabetes (2021) (0)
Discrimination of Drug Sensitivity of Cancer Using cDNA Microarray and Multivariate Statistical Analysis (1999) (0)
Diagnosis System of Drug Sensitivity of Cancer Using cDNA Microarray and Multivariate Statistical Analysis (2000) (0)
Abstract 4796: A founder mutation in the BAP1 gene among four caucasian families with high incidences of malignant peritoneal mesothelioma and uveal melanoma: a molecular and genealogical study in a 10-generation BAP1 cancer syndrome kindred (2015) (0)
Palindrome Analysis: Distribution of Complete-Matched Inverted Repeats with a Moderate Length Spacer (1998) (0)
Molecular and Cellular Pathobiology Histone Lysine Methyltransferase SETD 8 Promotes Carcinogenesis by Deregulating PCNA Expression (2012) (0)
Genotype–Phenotype Correlations and Structural Basis of INSR and IGF1R Mutations Causing Severe Insulin/IGF-1 Resistance (2018) (0)
DeepInsight-3D for precision oncology: an improved anti-cancer drug response prediction from high-dimensional multi-omics data with convolutional neural networks (2022) (0)
Success: evolutionary and structural properties of amino acids prove effective for succinylation site prediction (2018) (0)
Unveiling synapse pathology in spinal bulbar muscular atrophy by genome-wide transcriptome analysis of purified motor neurons derived from disease specific iPSCs (2020) (0)
DeepInsight: Methodology to Handle Non-image Data, such as Genomics Data, with Deep Learning (2020) (0)
SYSTEMATIC ANALYSIS OF PLANT TATALESS PROMOTERS (2001) (0)
Genome-wide association study suggests four variants influencing outcomes with ranibizumab therapy in exudative age-related macular degeneration (2018) (0)
Decoding Activation of ILC2 using Time-Dependent Cell-State Selection (2021) (0)
Genome-Wide Analysis of Gene Expression in Intestinal-Type Gastric Cancers Using a Complementary DNA Microarray Representing 23 , 040 Genes 1 (2002) (0)
Predicting MoRFs in protein sequences using HMM profiles (2016) (0)
Computational Pipelines and Workflows in Bioinformatics (2019) (0)
Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate (2019) (0)
Targeted deep sequencing analyses of long QT syndrome in a Japanese population (2022) (0)
Evaluation of human iPS cells by neural differentiation and tumorigenicity (2011) (0)
Identification of a functional variant in CHST3 associated with the susceptibility for lumbar disc degeneration (2012) (0)
Epithelia Laser-Capture Microdissection of Tumor Tissues and Normal Carcinogenesis Revealed by cDNA Microarrays after Alterations of Gene Expression during Colorectal Updated (2001) (0)
Genotype-Structure-Phenotype Correlations of Disease-Associated IGF1R Variants and Similarities to Those of INSR Variants (2021) (0)
Core promoter architecture characteristic of photosynthesis nuclear genes (2001) (0)
Splicing QTL analysis focusing on coding sequences reveals pathogenicity of disease susceptibility loci (2022) (0)
Title: WHSC1 Promotes Oncogenesis through Regulation of NIMA-related-kinase-7 in Squamous Cell Carcinoma of the Head and Neck (2014) (0)
Exploring predictive biomarkers from clinical genome-wide association studies via multidimensional hierarchical mixture models (2018) (0)
MP08-08 GENOMIC LANDSCAPE AND MOLECULAR CHARACTERIZATION OF RENAL CELL CARCINOMA IN DIALYSIS PATIENTS (2020) (0)
Defects in autophagosome-lysosome fusion underlie Vici syndrome, a neurodevelopmental disorder with multisystem involvement (2017) (0)
Association between high immune activity and worse prognosis in uveal melanoma and low-grade glioma in TCGA transcriptomic data (2022) (0)
28. Synthesis of 1α, 25 (OH)_2D_3 and 24,25 (OH)_2 D_3 in Human Fetal Membranes and Placenta (1986) (0)
Genome-wide association study to identify genes related to myocardial infarction (2002) (0)

This paper list is powered by the following services:

What Schools Are Affiliated With Tatsuhiko Tsunoda?

Tatsuhiko Tsunoda is affiliated with the following schools:

Tatsuhiko Tsunoda's Academic­Influence.com Rankings

Tatsuhiko Tsunoda's Degrees

Similar Degrees You Can Earn

Why Is Tatsuhiko Tsunoda Influential?

Tatsuhiko Tsunoda's Published Works

Published Works

What Schools Are Affiliated With Tatsuhiko Tsunoda?

Tatsuhiko Tsunoda's AcademicInfluence.com Rankings