A. Hata

A. Hata, Y. Kohno, K. Fujii, 2008, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Angiotensinogen as a risk factor for essential hypertension in Japan.

J. Lalouel, A. Hata, K. Sato, 1994, The Journal of clinical investigation.

Association between childhood socioeconomic status and fruit and vegetable intake among older Japanese: The JAGES 2010 study.

A. Hata, K. Kondo, T. Fujiwara, 2018, Preventive medicine.

Cost-effectiveness of managing HBV reactivation in patients with resolved HBV infection treated with anti-CD20 antibody for B-cell non-Hodgkin lymphoma

A. Hata, M. Sugiyama, M. Mizokami, 2022, Scientific Reports.

Association of SLC6A9 gene variants with human essential hypertension.

T. Ogihara, T. Katsuya, T. Nakayama, 2009, Journal of atherosclerosis and thrombosis.

Association of SLC 6 A 9 Gene Variants with Human Essential Hypertension

T. Ogihara, T. Katsuya, T. Nakayama, 2007 .

Angiotensin II-induced cardiomyocyte hypertrophy and cardiac fibrosis in stroke-prone spontaneously hypertensive rats.

J. Obata, A. Hata, H. Takano, 2000, Journal of Laboratory and Clinical Medicine.

Validity assessment of self-reported medication use by comparing to pharmacy insurance claims

A. Hata, K. Nagashima, Yasunori Sato, 2015, BMJ Open.

Association of the GABRB3 Gene with Nonsyndromic Oral Clefts

A. Hata, Y. Matsubara, Y. Aoki, 2008, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

A1166C variant of angiotensin II type 1 receptor gene is associated with severe hypertension in pregnancy independently of T235 variant of angiotensinogen gene

A. Hata, H. Minakami, S. Fujimoto, 2004, Journal of Human Genetics.

Association Analysis of Genes Involved in the Maintenance of the Integrity of the Extracellular Matrix with Intracranial Aneurysms in a Japanese Cohort

C. Wijmenga, G. Rinkel, A. Hata, 2009, Cerebrovascular Diseases.

Lipoprotein lipase deficiency resulting from a nonsense mutation in exon 3 of the lipoprotein lipase gene.

M. Emi, R. Hegele, J. Lalouel, 1990, American journal of human genetics.

Compound heterozygote for lipoprotein lipase deficiency: Ser----Thr244 and transition in 3' splice site of intron 2 (AG----AA) in the lipoprotein lipase gene.

G. Luc, M. Emi, J. Lalouel, 1990, American Journal of Human Genetics.

Seroprevalence of hepatitis C virus infection and its genotype in Lanzhou, Western China

A. Hata, M. Mizokami, T. Ohno, 1995, Journal of medical virology.

Variations in ORAI1 Gene Associated with Kawasaki Disease

Toshihiro Tanaka, K. Ozaki, T. Hara, 2016, PloS one.

The confidence of school's nutrition project: urinary analysis

A. Hata, S. Sato, M. Yoshioka, 2015, Proceedings of the Nutrition Society.

Magnesium intake decreases Type 2 diabetes risk through the improvement of insulin resistance and inflammation: the Hisayama Study

T. Ninomiya, J. Hata, Y. Kiyohara, 2013, Diabetic medicine : a journal of the British Diabetic Association.

CD14 -550 C/T, which is related to the serum level of soluble CD14, is associated with the development of respiratory syncytial virus bronchiolitis in the Japanese population.

A. Hata, Y. Kohno, N. Shimojo, 2007, The Journal of infectious diseases.

Cyclosporin A Treatment for Kawasaki Disease Refractory to Initial and Additional Intravenous Immunoglobulin

A. Hata, N. Yoshikawa, Yoichi Suzuki, 2011, The Pediatric infectious disease journal.

Functional polymorphisms of the FPR1 gene and aggressive periodontitis in Japanese.

Y. Izumi, A. Hata, I. Ishikawa, 2007, Biochemical and biophysical research communications.

Diabetes Mellitus is Associated With Low Secretion Rates of Immunoglobulin A in Saliva

M. Ando, A. Tamakoshi, A. Hata, 2015, Journal of epidemiology.

Five familial hypercholesterolemic kindreds in Japan with novel mutations of the LDL receptor gene

M. Emi, A. Hata, M. Tsuji, 1998, Journal of Human Genetics.

Efficacy of primary treatment with immunoglobulin plus ciclosporin for prevention of coronary artery abnormalities in patients with Kawasaki disease predicted to be at increased risk of non-response to intravenous immunoglobulin (KAICA): a randomised controlled, open-label, blinded-endpoints, phase

Yasuhisa Fujii, A. Hata, T. Ariga, 2019, The Lancet.

Association of an IGHV3-66 gene variant with Kawasaki disease

Todd A. Johnson, Toshihiro Tanaka, T. Tsunoda, 2020, Journal of Human Genetics.

No association of polymorphisms in the 5' region of the CD14 gene and food allergy in a Japanese population.

A. Hata, Y. Kohno, N. Shimojo, 2007, Allergology international : official journal of the Japanese Society of Allergology.

Increase in eosinophil-derived neurotoxin level in school children with allergic disease

Y. Okamoto, A. Hata, T. Nakano, 2022, Asia Pacific allergy.

Association between Passive Smoking from the Mother and Pediatric Crohn’s Disease: A Japanese Multicenter Study

T. Sairenchi, A. Hata, Y. Haruyama, 2020, International journal of environmental research and public health.

Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans

N. Greene, A. Copp, C. Relton, 2011, Human molecular genetics.

Haplotype analysis of the human collectin placenta 1 (hCL-P1) gene

A. Hata, Y. Makita, Yasuhiko Suzuki, 2003, Journal of Human Genetics.

Spine and Rib Abnormalities and Stature in Spondylocostal Dysostosis

A. Hata, Y. Makita, S. Ikegawa, 2006, Spine.

The Factor V Leiden Mutation Is Not a Common Cause of Pregnancy-Induced Hypertension in Japan

A. Hata, R. Kishi, S. Fujimoto, 1999, Seminars in thrombosis and hemostasis.

Ethnic Difference in Contribution of Sp1 Site Variation of COLIA1 Gene in Genetic Predisposition to Osteoporosis

T. Nakajima, M. Emi, A. Hata, 1999, Calcified Tissue International.

Missense mutation (Gly----Glu188) of human lipoprotein lipase imparting functional deficiency.

M. Emi, R. Hegele, J. Lalouel, 1990, The Journal of biological chemistry.

Angiotensinogen gene polymorphism in Japanese patients with hypertrophic cardiomyopathy.

A. Hata, A. Kitabatake, H. Okamoto, 1997, American heart journal.

Relationship between RANTES polymorphisms and respiratory syncytial virus bronchiolitis in a Japanese infant population.

Y. Okamoto, A. Hata, Y. Kohno, 2011, Japanese journal of infectious diseases.

Angiotensin Converting Enzyme as a Genetic Risk Factor for Coronary Artery Spasm

A. Hata, Y. Ogata, Y. Numata, 2013 .

Angiotensin II type 1 receptor gene polymorphisms in patients with cardiac hypertrophy.

A. Hata, A. Kitabatake, S. Chiba, 1998, Japanese heart journal.

Association between a variant of the glutathione S-transferase P1 gene (GSTP1) and hypertension in pregnancy in Japanese: interaction with parity, age, and genetic factors.

A. Hata, H. Minakami, S. Fujimoto, 2003, Seminars in thrombosis and hemostasis.

Insertion/Deletion Polymorphism of the Angiotensin-Converting Enzyme Gene and Preeclampsia in Japanese Patients

A. Hata, H. Minakami, S. Fujimoto, 2005, Seminars in thrombosis and hemostasis.

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

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

Prevalence of hepatitis C virus infection in Nanjing, Southern China

A. Hata, M. Mizokami, J. Lau, 1997, European Journal of Epidemiology.

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

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

Responsible Genetic Factors for Vasculitis in Kawasaki Disease

A. Hata, Y. Onouchi, 2011 .

Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion

J. Inazawa, A. Hata, R. Kosaki, 2012, Journal of Human Genetics.

Association between Serum Biotin Levels and Cedar Pollinosis in Japanese Schoolchildren.

Y. Okamoto, A. Hata, Y. Kohno, 2021, Journal of nutritional science and vitaminology.

Novel mutations of the LDL Receptor Gene in Familial Hypercholesterolemia Pedigrees in Hokkaido

M. Emi, A. Hata, M. Tsuji, 2000 .

Evaluation of clinical usefulness of second‐generation HCV core antigen assay: comparison with COBAS AMPLICOR HCV MONITOR assay version 2.0

O. Yokosuka, A. Hata, F. Imazeki, 2005, Liver international : official journal of the International Association for the Study of the Liver.

Fas Polymorphisms Influence Susceptibility to Autoimmune Hepatitis

O. Yokosuka, A. Hata, F. Imazeki, 2005, The American Journal of Gastroenterology.

The CASK gene harbored in a deletion detected by array‐CGH as a potential candidate for a gene causative of X‐linked dominant mental retardation

O. Migita, J. Inazawa, A. Hata, 2008, American journal of medical genetics. Part A.

Identification of a Gly862 to Ser substitution in the type I collagen gene from a single spermatozoon.

A. Hata, Y. Yagami, K. Suzumori, 1996, Molecular human reproduction.

Breastfeeding promotes egg white sensitization in early infancy

A. Hata, Y. Kohno, M. Taniguchi, 2020, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Association of a variant of the angiotensinogen gene with pure type of hypertension in pregnancy in the Japanese: implication of a racial difference and significance of an age factor.

A. Hata, R. Kishi, S. Fujimoto, 1999, American journal of medical genetics.

Induction of the Matrix Metalloproteinase 13 Gene in Bronchial Epithelial Cells by Interferon and Identification of its Novel Functional Polymorphism

Y. Okamoto, Hiroko Watanabe, A. Hata, 2015, Inflammation.

Implementation of a self-sampling HPV test for non-responders to cervical cancer screening in Japan: secondary analysis of the ACCESS trial

A. Hata, K. Nagashima, H. Hanaoka, 2022, Scientific Reports.

Chronological changes in the epidemiological characteristics of upper urinary tract urolithiasis in Japan

H. Nishimatsu, T. Matsuda, A. Hata, 2018, International journal of urology : official journal of the Japanese Urological Association.

Chronological changes in epidemiological characteristics of lower urinary tract urolithiasis in Japan

H. Nishimatsu, A. Hata, K. Akakura, 2018, International journal of urology : official journal of the Japanese Urological Association.

Replication of genetic association studies in asthma and related phenotypes

Y. Okamoto, A. Hata, Y. Kohno, 2010, Journal of Human Genetics.

Association study of the C3 gene with adult and childhood asthma

Y. Okamoto, A. Hata, Y. Kohno, 2008, Journal of Human Genetics.

Mutation of the Follicle-Stimulating Hormone Receptor Gene 5′-Untranslated Region Associated With Female Hypertension

T. Ogihara, T. Katsuya, T. Nakayama, 2006, Hypertension.

The critical monosomic segment involved in 4p- syndrome: A high-resolution banding study on five inherited cases

A. Hata, K. Narahara, Y. Yokoyama, 1984, Japanese Journal of Human Genetics.

The galanin signaling cascade is a candidate pathway regulating oncogenesis in human squamous cell carcinoma

Hideaki Shimada, Takashi Sugimoto, Yoshitaka Okamoto, 2009, Genes, chromosomes & cancer.

Lower Frequency of Daily Teeth Brushing Is Related to High Prevalence of Cardiovascular Risk Factors

A. Hata, K. Ueno, M. Fujita, 2009, Experimental biology and medicine.

Hepatitis B virus reactivation in patients with rheumatoid arthritis: Analysis of the National Database of Japan

A. Hata, M. Sugiyama, M. Mizokami, 2018, Journal of viral hepatitis.

Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene.

M. Emi, J. Lalouel, M. Robertson, 1990, Nucleic acids research.

Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn's disease in Japanese patients

Yusuke Nakamura, M. Kubo, A. Hata, 2007, Journal of Human Genetics.

CD40 ligand gene and Kawasaki disease

Yusuke Nakamura, Yoshikazu Nakamura, Kazunobu Ouchi, 2004, European Journal of Human Genetics.

Development of a nomogram to predict probability of positive initial prostate biopsy among Japanese patients.

Tomohiko Ichikawa, A. Hata, T. Ichikawa, 2006, Urology.

Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies

Y. Fukushima, J. Inazawa, S. Saitoh, 2011, Journal of Human Genetics.

A conserved imprinting control region at the HYMAI/ZAC domain is implicated in transient neonatal diabetes mellitus.

R. A. Drewell, M. Oshimura, M. Surani, 2001, Human molecular 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.

Study protocol of the ACCESS trial: a randomised trial to evaluate the effectiveness of human papillomavirus testing by self-sampling in cervical cancer screening uptake and precancer detection

A. Hata, K. Nagashima, H. Hanaoka, 2022, BMJ Open.

Inflammatory cytokine profiles during Cyclosporin treatment for immunoglobulin-resistant Kawasaki disease.

Jun Abe, Norishige Yoshikawa, A. Hata, 2012, Cytokine.

Integrated analysis of expression and genome alteration reveals putative amplified target genes in esophageal cancer.

N. Seki, A. Hata, H. Shimada, 2007, Oncology reports.

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

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

Association of CCR2-CCR5 Haplotypes and CCL3L1 Copy Number with Kawasaki Disease, Coronary Artery Lesions, and IVIG Responses in Japanese Children

Teiji Akagi, Susumu Furukawa, Jane C. Burns, 2010, PloS one.

Effect of Obesity on Incidence of Type 2 Diabetes Declines with Age Among Japanese Women

A. Hata, K. Ueno, M. Fujita, 2009, Experimental biology and medicine.

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.

Association between blood manganese level during pregnancy and birth size: The Japan environment and children's study (JECS).

A. Hata, H. Nitta, S. Nakayama, 2019, Environmental research.

High-Resolution Mapping for Essential Hypertension Using Microsatellite Markers

Jerzy K. Kulski, T. Ogihara, K. Nakao, 2007, Hypertension.

A genome-wide association study identifies three new risk loci for Kawasaki disease

Yusuke Nakamura, Tatsuhiko Tsunoda, Kouichi Ozaki, 2012, Nature Genetics.

Common variants in CASP3 confer susceptibility to Kawasaki disease.

Yusuke Nakamura, Tatsuhiko Tsunoda, Kouichi Ozaki, 2010, Human molecular genetics.

A genomewide linkage analysis of Kawasaki disease: evidence for linkage to chromosome 12

Yusuke Nakamura, Tatsuhiko Tsunoda, Yoshikazu Nakamura, 2006, Journal of Human Genetics.

Positive association of genetic variants in the upstream region of NKX2-3 with Crohn’s disease in Japanese patients

M. Kubo, Y. Nakamura, A. Takahashi, 2008, Gut.

Susceptibility genes for Kawasaki disease: toward implementation of personalized medicine

A. Hata, Y. Onouchi, 2009, Journal of Human Genetics.

Common Variants in the ATP2B1 Gene Are Associated With Susceptibility to Hypertension: The Japanese Millennium Genome Project

P. Munroe, M. Caulfield, T. Ogihara, 2010, Hypertension.

Association of TNFRSF4 gene polymorphisms with essential hypertension

T. Ogihara, T. Ohkubo, Y. Imai, 2008, Journal of hypertension.

FokI Variant of Vitamin D Receptor Gene and Factors Related to Atherosclerosis Associated With Ossification of the Posterior Longitudinal Ligament of the Spine: A Multi-Hospital Case-Control Study

A. Hata, S. Sasaki, T. Yokoyama, 2008, Spine.

Phenotypic expression of heterozygous lipoprotein lipase deficiency in the extended pedigree of a proband homozygous for a missense mutation.

M. Emi, J. Lalouel, A. Hata, 1990, The Journal of clinical investigation.

Chiba study of Mother and Children's Health (C-MACH): cohort study with omics analyses

A. Hata, K. Sakurai, H. Fukuoka, 2016, BMJ Open.

High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project.

T. Ogihara, Yusuke Nakamura, A. Sekine, 2007, Human molecular genetics.

Haplotypes of angiotensinogen in essential hypertension.

J. Lalouel, X. Jeunemaître, J. Tichet, 1997, American journal of human genetics.

A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro.

John Quackenbush, T. Nakajima, J. Lalouel, 1997, The Journal of clinical investigation.

TRIC-A channels in vascular smooth muscle contribute to blood pressure maintenance.

T. Ogihara, S. Umemura, Shinichiro Yamamoto, 2011, Cell metabolism.

A. Hata, K. Nagashima, Yasunori Sato, 2016, PloS one.

A. Hata, K. Nagashima, Yasunori Sato, 2017, International journal of environmental research and public health.

An association between maternal smoking and preeclampsia in Japanese women.

A. Hata, S. Fujimoto, G. Kobashi, 2002, Seminars in thrombosis and hemostasis.

Mutations in exon 3 of the lipoprotein lipase gene segregating in a family with hypertriglyceridemia, pancreatitis, and non-insulin-dependent diabetes.

J. Lalouel, A. Hata, L. Kwong, 1993, The Journal of clinical investigation.

Impact of coronavirus disease 2019 pandemic on breast cancer surgery using the National Database of Japan

A. Hata, T. Fujisawa, Y. Onouchi, 2023, Scientific Reports.

Changes in the number of cancer diagnosis practices due to the COVID-19 pandemic: interrupted time-series analysis using the National Database of Japan

A. Hata, T. Fujisawa, Y. Onouchi, 2023, Journal of Cancer Research and Clinical Oncology.

Evaluation of contrast visual acuity in patients with retinitis pigmentosa

A. Hagiwara, A. Hata, T. Sugawara, 2009, Clinical ophthalmology.

BMI mediates the association between low educational level and higher blood pressure during pregnancy in Japan

A. Hata, Y. Ohya, T. Fujiwara, 2013, BMC Public Health.

Additional outreach effort of providing an opportunity to obtain a kit for fecal immunochemical test during the general health check-up to improve colorectal cancer screening rate in Japan: A longitudinal study

A. Hata, T. Fujisawa, M. Fujita, 2020, PloS one.

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.

Ring 18 mosaicism in identical twins

A. Hata, Y. Kuroki, Yasuyuki Suzuki, 2004, Human Genetics.

Association of gamma-glutamyltransferase with incidence of type 2 diabetes in Japan

A. Hata, K. Ueno, M. Fujita, 2010, Experimental biology and medicine.

Novel intragenic duplications and mutations of CASK in patients with mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH)

J. Inazawa, A. Hata, I. Imoto, 2011, Human Genetics.

Research Article Sex and age differences in the effect of obesity on incidence of hypertension in the Japanese population: A large historical cohort study

A. Hata, M. Fujita, 2014 .

Adverse childhood experiences and fruit and vegetable intake among older adults in Japan.

A. Hata, K. Kondo, T. Fujiwara, 2020, Eating behaviors.

Association of the MMP9 gene with childhood cedar pollen sensitization and pollinosis

Y. Okamoto, A. Hata, Y. Kohno, 2012, Journal of Human Genetics.

Investigation of novel variations of ORAI1 gene and their association with Kawasaki disease

Toshihiro Tanaka, T. Hara, A. Hata, 2019, Journal of Human Genetics.

Participant mothers’ attitudes toward genetic analysis in a birth cohort study

A. Hata, K. Sakurai, C. Mori, 2021, Journal of Human Genetics.

Survey of motivation to participate in a birth cohort

A. Hata, C. Mori, M. Fujita, 2016, Journal of Human Genetics.

Absence of association between a common mutation in the methylenetetrahydrofolate reductase gene and preeclampsia in Japanese women.

A. Hata, R. Kishi, T. Asano, 2000, American journal of medical genetics.

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.

Multivariate analysis of genetic and acquired factors; T235 variant of the angiotensinogen gene is a potent independent risk factor for preeclampsia.

M. Kanamori, A. Hata, S. Fujimoto, 2001, Seminars in thrombosis and hemostasis.

Methylenetetrahydrofolate reductase genotype, vitamin B12, and folate influence plasma homocysteine in hemodialysis patients.

A. Hata, Y. Makita, H. Takano, 2002, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[Susceptibility genes for Kawasaki disease].

A. Hata, Y. Onouchi, 2014, Nihon rinsho. Japanese journal of clinical medicine.

Acceptability of self-sampling human papillomavirus test for cervical cancer screening in Japan: A questionnaire survey in the ACCESS trial

A. Hata, H. Hanaoka, T. Kasai, 2023, PloS one.

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.

Changes in colorectal cancer treatment during the COVID-19 pandemic in Japan: Interrupted time-series analysis using the National Database of Japan

A. Hata, T. Fujisawa, Y. Onouchi, 2023, Cancer epidemiology.

Urinary Sodium and Potassium excretion among Year 4 pupils in Choshi city, Japan

A. Hata, S. Sato, M. Yoshioka, 2015, Proceedings of the Nutrition Society.

Association Study of Matrix Metalloproteinase-12 Gene Polymorphisms and Asthma in a Japanese Population

Y. Okamoto, Hiroko Watanabe, A. Hata, 2012, International Archives of Allergy and Immunology.

Further analysis of microsatellite marker in the BDNF gene

K. Hashimoto, M. Iyo, E. Shimizu, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Recurrence of osteogenesis imperfecta because of paternal mosaicism: Gly862→Ser substitution in a type I collagen gene (COL1A1)

Y. Fukushima, A. Hata, M. Sasaki, 1995, Human Genetics.

ITPKC and CASP3 polymorphisms and risks for IVIG unresponsiveness and coronary artery lesion formation in Kawasaki disease

T Tanaka, Toshihiro Tanaka, K. Ozaki, 2011, The Pharmacogenomics Journal.

A Commentary on For what am I participating? The need for communication after receiving consent from biobanking project participants: experience in Japan

A. Hata, Midori Yamamoto, 2011, Journal of Human Genetics.

[Multifactorial disease].

A. Hata, 2010, Nihon rinsho. Japanese journal of clinical medicine.

The M235T variant of the angiotensinogen gene and the body mass index are useful markers for prevention of hypertension in pregnancy: a tree-based analysis of gene-environment interaction.

A. Hata, S. Fujimoto, G. Kobashi, 2002, Seminars in Thrombosis and Hemostasis.

Handheld flow meter improves COPD detectability regardless of using a conventional questionnaire: A split‐sample validation study

A. Hata, K. Nagashima, T. Fujisawa, 2020, Respirology.