I. Inoue

K. Takakura, T. Hori, I. Inoue, 1999, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

The destruction box of human Geminin is critical for proliferation and tumor growth in human colon cancer cells

Anindya Dutta, Kenichi Yoshida, I. Inoue, 2004, Oncogene.

AMBRA1 controls antigen-driven activation and proliferation of naïve T cells.

M. Kimura, M. Ohtsuka, I. Inoue, 2020, International immunology.

AMBRA1 is involved in T cell receptor-mediated metabolic reprogramming through an ATG7-independent pathway.

M. Kimura, M. Ohtsuka, I. Inoue, 2017, Biochemical and biophysical research communications.

Identification of FAZF as a novel BMP2‐induced transcription factor during osteoblastic differentiation

Kenichi Yoshida, I. Inoue, R. Ikeda, 2007, Journal of cellular biochemistry.

The small heat shock protein alphaB-crystallin inhibits differentiation-induced caspase 3 activation and myogenic differentiation.

Kenichi Yoshida, T. Furukawa, S. Akiyama, 2006, Biological & pharmaceutical bulletin.

Detection of Ancient Viruses and Long-Term Viral Evolution

I. Inoue, Naoko T Fujito, Ryota Sugimoto, 2022, Viruses.

Survey of Attitudes of Japanese Women Toward Genetic/Genomic Research

I. Inoue, N. Ishii, M. Motojima, 2014, Journal of empirical research on human research ethics : JERHRE.

Retinoic acid-inducible gene-I (RIG-I) is induced by IFN-γ in human mesangial cells in culture: possible involvement of RIG-I in the inflammation in lupus nephritis

E. Ito, I. Inoue, A. Tajima, 2010, Lupus.

Novel MXD4–NUTM1 fusion transcript identified in primary ovarian undifferentiated small round cell sarcoma

Shujiro Okuda, K. Yoshihara, T. Enomoto, 2018, Genes, chromosomes & cancer.

The landscape of genetic alterations of UVB‐induced skin tumors in DNA repair‐deficient mice

T. Fukumoto, I. Inoue, C. Nishigori, 2022, Experimental dermatology.

Estrogen promotes Leydig cell engulfment by macrophages in male infertility.

G. Gao, K. Korach, Daishu Han, 2014, The Journal of clinical investigation.

Zebrafish Numb homologue: Phylogenetic evolution and involvement in regulation of left–right asymmetry

K. Arai, Sumiko Watanabe, I. Inoue, 2006, Mechanisms of Development.

Possible Association between Dysfunction of Vitamin D Binding Protein (GC Globulin) and Migraine Attacks

E. Nagata, A. Hata, I. Inoue, 2014, PloS one.

Gene Expression Profiling Reveals Distinct Molecular Signatures Associated With the Rupture of Intracranial Aneurysm Clinical

I. Inoue, H. Kasuya, H. Nakaoka, 2014 .

Differential Effects of Chromosome 9p21 Variation on Subphenotypes of Intracranial Aneurysm: Site Distribution

A. Hata, I. Inoue, A. Tajima, 2010, Stroke.

Gene Expression Changes During the Chondrogenic Differentiation of Human Mesenchymal Stem Cells

Kenichi Yoshida, I. Inoue, R. Ikeda, 2007 .

Significance of Mitochondrial DNA Haplogroup on Epidermal Growth Factor Receptor Mutation in Japanese Patients With Lung Adenocarcinoma

T. Furukawa, I. Inoue, C. Koriyama, 2021, AntiCancer Research.

Sortilin is upregulated during osteoblastic differentiation of mesenchymal stem cells and promotes extracellular matrix mineralization

S. Maeda, I. Inoue, K. Yone, 2002, Journal of cellular physiology.

Genome-wide linkage and exome analyses identify variants of HMCN1 for splenic epidermoid cyst

I. Inoue, A. Narita, Y. Hayashi, 2014, BMC Medical Genetics.

APOBEC mediated mutagenesis drives genomic heterogeneity in endometriosis

K. Yoshihara, T. Enomoto, I. Inoue, 2022, Journal of Human Genetics.

Molecular cloning and functional analysis of a factor that binds to the proximal promoter of human angiotensinogen

T. Nakajima, J. Lalouel, I. Inoue, 2002, Journal of Human Genetics.

Novel therapeutic strategy for cervical cancer harboring FGFR3-TACC3 fusions

Shujiro Okuda, R. Verhaak, K. Yoshihara, 2018, Oncogenesis.

Genome-wide association study revealed novel loci which aggravate asymptomatic hyperuricaemia into gout

Y. Kamatani, Y. Okada, T. Merriman, 2019, Annals of the rheumatic diseases.

A Bead-based Normalization for Uniform Sequencing depth (BeNUS) protocol for multi-samples sequencing exemplified by HLA-B

Hideki Nagasaki, I. Inoue, K. Hosomichi, 2014, BMC Genomics.

Particular human leukocyte antigen alleles are associated with biochemical traits in the Japanese population.

H. Inoko, I. Inoue, A. Narita, 2011, Human immunology.

Evaluating the performance of Affymetrix SNP Array 6.0 platform with 400 Japanese individuals

Katsushi Tokunaga, Asako Koike, Nao Nishida, 2008, BMC Genomics.

APOBEC: A molecular driver in cervical cancer pathogenesis

I. Inoue, H. Nakaoka, A. K. Munirajan, 2020, Cancer Letters.

External apical root resorption and the interleukin-1B gene polymorphism in the Japanese population

I. Inoue, A. Tajima, K. Maki, 2009 .

Clonal Expansion and Diversification of Cancer-Associated Mutations in Endometriosis and Normal Endometrium.

K. Yoshihara, T. Enomoto, Kenichi Tanaka, 2018, Cell reports.

Comprehensive genetic exploration of selective tooth agenesis of mandibular incisors by exome sequencing

Y. Kikkawa, N. Nonaka, I. Inoue, 2017, Human Genome Variation.

Association of the growth hormone receptor gene polymorphisms with mandibular height in a Korean population.

T. Nakajima, I. Inoue, A. Tajima, 2009, Archives of oral biology.

Regulation of the hepatitis C virus genome replication by miR-199a.

Yoshiki Murakami, Ituro Inoue, Hussein H. Aly, 2009, Journal of hepatology.

Thymidine phosphorylase inhibits apoptosis induced by cisplatin.

H. Okumura, T. Furukawa, S. Akiyama, 2003, Biochemical and biophysical research communications.

Germline mutations of multiple breast cancer-related genes are differentially associated with triple-negative breast cancers and prognostic factors

Dahai Liu, Dong Wang, I. Inoue, 2020, Journal of Human Genetics.

A Systems Genetics Approach Provides a Bridge from Discovered Genetic Variants to Biological Pathways in Rheumatoid Arthritis

Shinji Sato, Ituro Inoue, Hidetoshi Inoko, 2011, PloS one.

Lineage-Specific Homogenization of the Polyubiquitin Gene Among Human and Great Apes

N. Saitou, T. Nakajima, T. Ishida, 2003, Journal of Molecular Evolution.

Genetics of Hearing Loss

I. Inoue, N. Mahdieh, B. Rabbani, 2012 .

Long non-coding RNA p10247, high expressed in breast cancer (lncRNA-BCHE), is correlated with metastasis

Qiang Li, I. Inoue, Hua You, 2018, Clinical & Experimental Metastasis.

Long non-coding RNA p10247, high expressed in breast cancer (lncRNA-BCHE), is correlated with metastasis

Qiang Li, I. Inoue, Hua You, 2018, Clinical & Experimental Metastasis.

Systematic identification and characterization of regulatory elements derived from human endogenous retroviruses

Ituro Inoue, Hirofumi Nakaoka, Shiro Yamada, 2017, PLoS genetics.

Sensitization of Gastric Cancer Cells to Irinotecan by p53 Activation

Shun Zhang, I. Inoue, O. Hino, 2019, BPB Reports.

Nucleotide diversity and haplotype structure of the human angiotensinogen gene in two populations.

L. Jorde, T. Nakajima, M. Emi, 2002, American journal of human genetics.

Spatiotemporal dynamics of clonal selection and diversification in normal endometrial epithelium

R. Verhaak, Kazuki Tainaka, K. Yoshihara, 2022, Nature Communications.

Spatiotemporal dynamics of clonal selection and diversification in normal endometrial epithelium

R. Verhaak, Kazuki Tainaka, K. Yoshihara, 2022, Nature communications.

Population genetics: past, present, and future

J. Ott, I. Inoue, S. Yamazaki, 2020, Human Genetics.

The impact of next-generation sequencing technologies on HLA research

Ituro Inoue, Takashi Shiina, T. Shiina, 2015, Journal of Human Genetics.

Phase-defined complete sequencing of the HLA genes by next-generation sequencing

Ituro Inoue, Hirofumi Nakaoka, I. Inoue, 2013, BMC Genomics.

A genome-wide association study of third molar agenesis in Japanese and Korean populations

I. Inoue, R. Kimura, K. Maki, 2013, Journal of Human Genetics.

Genetic and phenotypic landscape of the major histocompatibilty complex region in the Japanese population

M. Kanai, Y. Kamatani, Y. Okada, 2019, Nature Genetics.

Multiple common and rare variants of ABCG2 cause gout

T. Merriman, K. Wakai, N. Shinomiya, 2017, RMD Open.

The Admixed Origin of Japanese Population from HLA Alleles

H. Inoko, I. Inoue, H. Nakaoka, 2014 .

Detection of Ancestry Informative HLA Alleles Confirms the Admixed Origins of Japanese Population

H. Inoko, A. Shinagawa, I. Inoue, 2013, PloS one.

Amino-acid substitutions in the IKAP gene product significantly increase risk for bronchial asthma in children

Yusuke Nakamura, M. Unoki, I. Inoue, 2001, Journal of Human Genetics.

Molecular Characterization of an Intact p53 Pathway Subtype in High-Grade Serous Ovarian Cancer

H. Tsuda, K. Yoshihara, T. Enomoto, 2014, PloS one.

Association of positional and functional candidate genes FGF1, FBN2, and LOX on 5q31 with intracranial aneurysm

T. Nakajima, T. Hori, I. Inoue, 2003, Journal of Human Genetics.

Genome-wide association database developed in the Japanese Integrated Database Project

Katsushi Tokunaga, Asako Koike, Nao Nishida, 2009, Journal of Human Genetics.

A genome-wide linkage and a haplotype association studies mapped intracranial aneurysm to elastin locus on chromosome 7

I. Inoue, H. Kasuya, H. Onda, 2003 .

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

Cue Hyunkyu Lee, M. Fornage, A. Hofman, 2018, Journal of the American Heart Association.

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

Cue Hyunkyu Lee, Gao T. Wang, Benjamin J. Wright, 2016, Journal of the American Heart Association : Cardiovascular and Cerebrovascular Disease.

No novel, high penetrant gene might remain to be found in Japanese patients with unknown MODY

S. Sugano, Yutaka Suzuki, J. Takeda, 2018, Journal of Human Genetics.

A frameshift variant of CYP2C8 was identified in a patient who suffered from rhabdomyolysis after administration of cerivastatin

Ituro Inoue, Hiroshi Ozaki, Saburo Kanai, 2004, Journal of Human Genetics.

Systematic screening of lysyl oxidase-like (LOXL) family genes demonstrates that LOXL2 is a susceptibility gene to intracranial aneurysms

T. Hori, A. Hata, I. Inoue, 2007, Human Genetics.

Conditional expression of MCM7 increases tumor growth without altering DNA replication activity

Kenichi Yoshida, I. Inoue, 2003, FEBS letters.

Identification of SNP markers for common CNV regions and association analysis of risk of subarachnoid aneurysmal hemorrhage in Japanese population.

H. Shin, H. Cheong, Sangsoo Kim, 2008, Biochemical and biophysical research communications.

Proposing a molecular classification associated with hypercoagulation in ovarian clear cell carcinoma.

Shujiro Okuda, K. Yoshihara, T. Enomoto, 2021, Gynecologic oncology.

Germline and somatic mutations of homologous recombination-associated genes in Japanese ovarian cancer patients

K. Yoshihara, T. Enomoto, T. Motoyama, 2019, Scientific Reports.

Germline copy number variations in BRCA1‐associated ovarian cancer patients

Ituro Inoue, Masayuki Sekine, Kosuke Yoshihara, 2011, Genes, chromosomes & cancer.

Genomewide linkage analysis of familial prostate cancer in the Japanese population

I. Inoue, H. Yamanaka, Kazuhiro Suzuki, 2004, Journal of Human Genetics.

Linkage and association analyses of the osteoprotegerin gene locus with human osteoporosis

T. Nakajima, K. Ikari, A. Hata, 2002, Journal of Human Genetics.

Movements of Ancient Human Endogenous Retroviruses Detected in SOX2-Expressing Cells

K. Tomizawa, I. Inoue, T. Era, 2020, bioRxiv.

Identification of novel exonic mobile element insertions in epithelial ovarian cancers

K. Yoshihara, T. Enomoto, Kenichi Tanaka, 2015, Human Genome Variation.

Concurrent isolated retroperitoneal HGSC and STIC defined by somatic mutation analysis: a case report

K. Yoshihara, T. Enomoto, T. Motoyama, 2019, Diagnostic Pathology.

Peptide binding to Geminin and inhibitory for DNA replication.

Kenichi Yoshida, I. Inoue, 2004, Biochemical and biophysical research communications.

Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk

Yusuke Nakamura, Ituro Inoue, Georg Auburger, 2011, Proceedings of the National Academy of Sciences.

Genome-wide association analysis with selective genotyping identifies candidate loci for adult height at 8q21.13 and 15q22.33-q23 in Mongolians

H. Inoko, I. Inoue, A. Oka, 2008, Human Genetics.

Genetics of Diabetes: Are They Thrifty Genotype?

I. Inoue, H. Nakaoka, 2017 .

Meta-analysis of genetic association studies: methodologies, between-study heterogeneity and winner's curse

Ituro Inoue, Hirofumi Nakaoka, I. Inoue, 2009, Journal of Human Genetics.

Natural selection and population history in the human angiotensinogen gene (AGT): 736 complete AGT sequences in chromosomes from around the world.

N. Saitou, L. Jorde, T. Nakajima, 2004, American journal of human genetics.

Comprehensive discovery of CRISPR-targeted terminally redundant sequences in the human gut metagenome: Viruses, plasmids, and more

Hiroshi Mori, Ituro Inoue, Ken Kurokawa, 2021, PLoS Comput. Biol..

Aggregation of rare/low-frequency variants of the mitochondria respiratory chain-related proteins in rheumatoid arthritis patients

H. Inoko, T. Shiina, I. Inoue, 2015, Journal of Human Genetics.

Genetic and phenotypic landscape of the major histocompatibilty complex region in the Japanese population

M. Kanai, Y. Kamatani, Y. Okada, 2019, Nature Genetics.

Decoding the diversity of killer immunoglobulin-like receptors by deep sequencing and a high-resolution imputation method

Y. Kamatani, Y. Okada, K. Matsuda, 2022, Cell genomics.

HLA-DPB1*04:01 allele is associated with non-obstructive azoospermia in Japanese patients

I. Inoue, T. Jinam, H. Nakaoka, 2013, Human Genetics.

Associations between six classical HLA loci and rheumatoid arthritis: a comprehensive analysis.

H. Inoko, I. Inoue, A. Narita, 2012, Tissue antigens.

Allelic and haplotypic HLA diversity in indigenous Malaysian populations explored using Next Generation Sequencing.

N. Saitou, M. Phipps, I. Inoue, 2021, Human Immunology.

Analysis of HLA gene polymorphisms in East Africans reveals evidence of gene flow in two Semitic populations from Sudan

M. Jaeger, M. Netea, I. Inoue, 2021, European Journal of Human Genetics.

Distribution of HLA haplotypes across Japanese Archipelago: similarity, difference and admixture

I. Inoue, H. Nakaoka, 2015, Journal of Human Genetics.

Identification of a novel variant of the RET proto-oncogene in a novel family with Hirschsprung’s disease

S. Ieiri, I. Inoue, K. Hosomichi, 2017, Pediatric Surgery International.

Silver Nanoscale Hexagonal Column Chips for Detecting Cell-free DNA and Circulating Nucleosomes in Cancer Patients

M. Onimaru, I. Inoue, M. Ohba, 2015, Scientific Reports.

TRIM39 and RNF39 are associated with Behçet's disease independently of HLA-B∗51 and -A∗26.

H. Inoko, T. Shiina, I. Inoue, 2010, Biochemical and Biophysical Research Communications - BBRC.

A partial nuclear genome of the Jomons who lived 3000 years ago in Fukushima, Japan

N. Saitou, I. Inoue, A. Tajima, 2016, Journal of Human Genetics.

High-Risk Ovarian Cancer Based on 126-Gene Expression Signature Is Uniquely Characterized by Downregulation of Antigen Presentation Pathway

Tatsuhiko Tsunoda, Hiroyuki Seki, Daichi Shigemizu, 2012, Clinical Cancer Research.

Gene Expression Profile for Predicting Survival in Advanced-Stage Serous Ovarian Cancer Across Two Independent Datasets

Ituro Inoue, Yoshiki Kudo, Kosuke Yoshihara, 2010, PloS one.

Unique characteristics of the Ainu population in Northern Japan

N. Saitou, K. Tokunaga, I. Inoue, 2015, Journal of Human Genetics.

Integration of hepatitis B virus DNA into the myeloid/lymphoid or mixed‐lineage leukemia (MLL4) gene and rearrangements of MLL4 in human hepatocellular carcinoma

Takehide Asano, Yoshiki Murakami, Ituro Inoue, 2008, Human mutation.

Comprehensive genetic testing approach for major inherited kidney diseases, using next-generation sequencing with a custom panel

Ituro Inoue, Shinichi Uchida, Sei Sasaki, 2017, Clinical and Experimental Nephrology.

ARID1A protein expression is retained in ovarian endometriosis with ARID1A loss-of-function mutations: implication for the two-hit hypothesis

K. Yoshihara, T. Enomoto, T. Motoyama, 2020, Scientific Reports.

Different mutation profiles between epithelium and stroma in endometriosis and normal endometrium.

K. Yoshihara, T. Enomoto, T. Motoyama, 2019, Human reproduction.

Genetic Susceptibility to OPLL

I. Inoue, 2006 .

COL6A1, the Candidate Gene for Ossification of the Posterior Longitudinal Ligament, Is Associated With Diffuse Idiopathic Skeletal Hyperostosis in Japanese

Toshihiro Tanaka, K. Pavelka, I. Inoue, 2005, Spine.

Simple cloning strategy using GFPuv gene as positive/negative indicator.

H. Inoko, M. Ohtsuka, I. Inoue, 2011, Analytical biochemistry.

ANRIL is implicated in the regulation of nucleus and potential transcriptional target of E2F1.

Kenichi Yoshida, I. Inoue, A. Tajima, 2010, Oncology reports.

Collagen Type I &agr;2 (COL1A2) Is the Susceptible Gene for Intracranial Aneurysms

Ituro Inoue, Tomokatsu Hori, Hiroyuki Akagawa, 2004, Stroke.

Identification of ancient viruses from metagenomic data of the Jomon people

J. Inoue, I. Inoue, H. Nakaoka, 2020, Journal of Human Genetics.

Comprehensive microbiome analysis of tonsillar crypts in IgA nephropathy

Takuji Yamada, K. Kurokawa, Yusuke Suzuki, 2016, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Germline Variants of Prostate Cancer in Japanese Families

I. Inoue, H. Nakaoka, K. Hosomichi, 2016, PloS one.

Association of the Jun dimerization protein 2 gene with intracranial aneurysms in Japanese and Korean cohorts as compared to a Dutch cohort

I. Inoue, Y. Ruigrok, A. Tajima, 2010, Neuroscience.

Network-based gene expression analysis of intracranial aneurysm tissue reveals role of antigen presenting cells

K. Takakura, M. Bonin, I. Inoue, 2008, Neuroscience.

HLA-DPB1*04:01 allele is associated with non-obstructive azoospermia in Japanese patients

Kenichi Tanaka, I. Inoue, T. Jinam, 2013, Human Genetics.

Gene expression profiling of advanced‐stage serous ovarian cancers distinguishes novel subclasses and implicates ZEB2 in tumor progression and prognosis

Ituro Inoue, Yoshiki Kudo, Kosuke Yoshihara, 2009, Cancer science.

Gene‐expression profiles in human nasal polyp tissues and identification of genetic susceptibility in aspirin‐intolerant asthma

H. Inoue, I. Inoue, Y. Kurono, 2009, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Polymorphisms in the prostaglandin E2 receptor subtype 2 gene confer susceptibility to aspirin-intolerant asthma: a candidate gene approach.

T. Nakajima, Kenichi Yoshida, S. Goto, 2004, Human molecular genetics.

The Alanine/Threonine Polymorphism of the Alpha-1-Antichymotrypsin (SERPINA3) Gene and Ruptured Intracranial Aneurysms in the Japanese Population

Ituro Inoue, Tomokatsu Hori, Hiroyuki Akagawa, 2006, Cerebrovascular Diseases.

Role of p 38 Mitogen-Activated Protein Kinase on Cerebral Vasospasm After Subarachnoid Hemorrhage

T. Hori, S. Goto, I. Inoue, 2004 .

Expression of MCM10 and TopBP1 is regulated by cell proliferation and UV irradiation via the E2F transcription factor

Ituro Inoue, Kenichi Yoshida, Kenichi Yoshida, 2004, Oncogene.

The Relationship between TP53 Gene Status and Carboxylesterase 2 Expression in Human Colorectal Cancer

I. Inoue, H. Orita, T. Yokomizo, 2018, Disease markers.

The Relationship between TP 53 Gene Status and Carboxylesterase 2 Expression in Human Colorectal Cancer

I. Inoue, H. Orita, T. Yokomizo, 2018 .

Molecular modeling of the dimeric structure of human lipoprotein lipase and functional studies of the carboxyl-terminal domain.

T. Nakajima, I. Inoue, Yoko Kobayashi, 2002, European journal of biochemistry.

Expression of retinoic acid-inducible gene-I in vascular smooth muscle cells stimulated with interferon-gamma.

S. Yagihashi, T. Fujita, I. Inoue, 2004, Life sciences.

Further evidence for an association between mandibular height and the growth hormone receptor gene in a Japanese population.

Ituro Inoue, Koutaro Maki, Tetsutaro Yamaguchi, 2009, American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics.

Exome resequencing combined with linkage analysis identifies novel PTH1R variants in primary failure of tooth eruption in Japanese

Ituro Inoue, Tatsuo Shirota, Koutaro Maki, 2011, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Endoglin Is Not a Major Susceptibility Gene for Intracranial Aneurysm Among Japanese

T. Nakajima, T. Hori, I. Inoue, 2003, Stroke.

The genetics of intracranial aneurysms

Ituro Inoue, I. Inoue, B. Krischek, 2006, Journal of Human Genetics.

Meta-analysis of genome-wide association scans for genetic susceptibility to endometriosis in Japanese population

K. Yoshihara, K. Tokunaga, R. Kuwano, 2010, Journal of Human Genetics.

A nonsynonymous variant of IL1A is associated with endometriosis in Japanese population

K. Yoshihara, K. Haino, Kenichi Tanaka, 2013, Journal of Human Genetics.

Exome sequences of toque macaques (Macaca sinica) of Sri Lanka reveal many amino acid changes

N. Saitou, N. Osada, I. Inoue, 2019, bioRxiv.

Spatial genomic diversity associated with APOBEC mutagenesis in squamous cell carcinoma arising from ovarian teratoma

K. Yoshihara, T. Motoyama, I. Inoue, 2023, Cancer science.

Rapid and cost-effective high-throughput sequencing for identification of germline mutations of BRCA1 and BRCA2

A. Hata, K. Matsushita, F. Nomura, 2017, Journal of Human Genetics.

Subtype-specific gout susceptibility loci and enrichment of selection pressure on ABCG2 and ALDH2 identified by subtype genome-wide meta-analyses of clinically defined gout patients

Y. Kamatani, Y. Okada, T. Merriman, 2020, Annals of the Rheumatic Diseases.

Exome and copy number variation analyses of Mayer–Rokitansky–Küster– Hauser syndrome

T. Shiina, Shingo Suzuki, I. Inoue, 2018, Human Genome Variation.

Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms

Katsuhito Yasuno, A. Hata, I. Inoue, 2010, Journal of Human Genetics.

Influence of endothelial nitric oxide synthase T-786C single nucleotide polymorphism on aneurysm size.

Ituro Inoue, Tomokatsu Hori, Hiroyuki Akagawa, 2005, Journal of neurosurgery.

Improved loop-mediated isothermal amplification for HLA-DRB1 genotyping using RecA and a restriction enzyme for enhanced amplification specificity

H. Inoko, M. Kimura, I. Inoue, 2013, Immunogenetics.

SNP-based heritability estimates of gout and its subtypes determined by genome-wide association studies of clinically defined gout

Y. Okada, K. Matsuo, K. Wakai, 2022, Rheumatology.

Dysfunctional missense variant of OAT10/SLC22A13 decreases gout risk and serum uric acid levels

N. Osada, N. Shinomiya, T. Tamura, 2019, Annals of the rheumatic diseases.

Is there any evidence for linkage on chromosome 17cen in affected Japanese sib-pairs with an intracranial aneurysm?

T. Hori, I. Inoue, A. Tajima, 2006, Journal of Human Genetics.

Haplotypes ofAngiotensinogen inEssential Hypertension

X. Jeunemaître, A. Hata, I. Inoue, 1997 .

A haplotype spanning two genes, ELN and LIMK1, decreases their transcripts and confers susceptibility to intracranial aneurysms.

T. Hori, Jong-Young Lee, A. Hata, 2006, Human molecular genetics.

Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhage

Ituro Inoue, Joon Seol Bae, H. Shin, 2010, Journal of Human Genetics.

A Bead-based Normalization for Uniform Sequencing depth (BeNUS) protocol for multi-samples sequencing exemplified by HLA-B

Hideki Nagasaki, I. Inoue, K. Hosomichi, 2014, BMC Genomics.

Systematic identification and characterization of regulatory elements derived from human endogenous retroviruses

I. Inoue, Jumpei Ito, H. Nakaoka, 2017, PLoS Genetics.

No novel, high penetrant gene might remain to be found in Japanese patients with unknown MODY

S. Sugano, Yutaka Suzuki, S. Tsuji, 2018, Journal of Human Genetics.

Genetics of Diabetes: Are They Thrifty Genotype?

I. Inoue, H. Nakaoka, 2017 .

Distinct haplogroups with star-like diversification in the APOBEC3 regulatory region indicate ancient viral pandemics before and during the Out-of-Africa migration of modern humans

I. Inoue, Y. Satta, Naoko T Fujito, 2023, bioRxiv.

Increased expression of ephrin A1 in brain arteriovenous malformation: DNA microarray analysis

T. Hori, I. Inoue, H. Ujiié, 2007, Neurosurgical Review.

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

Cue Hyunkyu Lee, M. Fornage, L. Kiemeney, 2016, Journal of the American Heart Association.

Genome-wide association study of intracranial aneurysm identifies three new risk loci

Alejandro F Frangi, L. Peltonen, C. Wijmenga, 2010, Nature Genetics.

Clonal Expansion and Diversification of Cancer-Associated Mutations in Endometriosis and Normal Endometrium.

K. Yoshihara, T. Enomoto, Kenichi Tanaka, 2018, Cell reports.

Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes

A. Takahashi, N. Hamajima, N. Shinomiya, 2015, Annals of the rheumatic diseases.

Genome-wide association study of degenerative bony changes of the temporomandibular joint.

I. Inoue, R. Kimura, K. Maki, 2014, Oral diseases.

I. Inoue, H. Nakaoka, 2017 .

AMBRA1 p.Gln30Arg Mutation, Identified in a Cowden Syndrome Family, Exhibits Hyperproliferative Potential in hTERT-RPE1 Cells

I. Inoue, Toyoaki Natsume, Naoko T Fujito, 2022, International journal of molecular sciences.

Sensitization of Gastric Cancer Cells to Irinotecan by p53 Activation

Shun Zhang, I. Inoue, O. Hino, 2019 .

Expressed sequence tags from cynomolgus monkey (Macaca fascicularis) liver: A systematic identification of drug‐metabolizing enzymes

S. Sugano, H. Wakaguri, K. Hashimoto, 2008, FEBS letters.

HLA-B*39:01:01 is a novel risk factor for antithyroid drug-induced agranulocytosis in Japanese population

I. Inoue, A. Oka, H. Nakaoka, 2020, The Pharmacogenomics Journal.