Noriko Aoi

Nihon University — Japan

Medicine · Health Sciences

19h-index789citations40works0.02yr avg
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Research Topics

Hormonal Regulation and Hypertension(14), Eicosanoids and Hypertension Pharmacology(7), Pharmacogenetics and Drug Metabolism(6), Renin-Angiotensin System Studies(6), Heart Failure Treatment and Management(5)

Publications40 total

Subtype prediction in primary aldosteronism: measurement of circadian variation of adrenocortical hormones and 24‐h urinary aldosterone
Clinical Endocrinology·2015· 17 cited
A Haplotype of the <i>GOSR2</i> Gene Is Associated with Myocardial Infarction in Japanese Men
Genetic Testing and Molecular Biomarkers·2013· 14 citedOpen Access
A haplotype of the GOSR2 gene is associated with essential hypertension in Japanese men
Clinical Biochemistry·2013· 7 cited
Association of the smoothelin (<i>SMTN</i>) gene with cerebral infarction in men: A haplotype-based case–control study
Vascular Medicine·2012· 4 cited
Haplotype of smoothelin gene associated with essential hypertension
Hereditas·2012· 8 citedOpen Access
The insulin-like growth factor-1 gene is associated with cerebral infarction in Japanese subjects
Hereditas·2012· 2 citedOpen Access
A Haplotype of the <i>SMTN</i> Gene Associated with Myocardial Infarction in Japanese Women
Genetic Testing and Molecular Biomarkers·2012· 5 cited
Association between SIRT2 gene polymorphism and height in healthy, elderly Japanese subjects
Translational research·2012· 10 cited
Haplotype-based case-control study of CYP4A11 gene and myocardial infarction
Hereditas·2012· 22 citedOpen Access
Association study: SLC6A18 gene and myocardial infarction
Clinical Biochemistry·2011· 4 cited
Association of the insulin-like growth factor1 gene with myocardial infarction in Japanese subjects
Hereditas·2010· 13 citedOpen Access
Association of HSD3B1 and HSD3B2 gene polymorphisms with essential hypertension, aldosterone level, and left ventricular structure
European Journal of Endocrinology·2010· 41 citedOpen Access
[Establishment of genetic testing for Gitelman's syndrome].
PubMed·2010
Purinergic receptor P2Y, G-protein coupled, 2 (P2RY2) gene is associated with cerebral infarction in Japanese subjects
Hypertension Research·2009· 15 citedOpen Access
Haplotype-based case–control study between human apurinic/apyrimidinic endonuclease 1/redox effector factor-1 gene and cerebral infarction
Clinical Biochemistry·2009· 13 cited
日本人男性におけるプリン作動性受容体P2Y,G蛋白質共役,2 (P2RY2)遺伝子と心筋梗塞との関係
Circulation·2009· 9 cited
Association of the Purinergic Receptor P2Y, G-Protein Coupled, 2 (P2RY2) Gene With Myocardial Infarction in Japanese Men
Circulation Journal·2009· 19 citedOpen Access
Association of extracellular superoxide dismutase gene with cerebral infarction in women: a haplotype-based case-control study
Hereditas·2008· 18 citedOpen Access
A haplotype of the CYP4F2 gene associated with myocardial infarction in Japanese men
Molecular Genetics and Metabolism·2008· 29 cited
Human uncoupling protein 2 and 3 genes are associated with obesity in Japanese
Endocrine·2008· 25 cited
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Frequent Co-authors

Masayoshi Soma(38), Tomohiro Nakayama(33), Naoyuki Sato(24), Mikano Sato(23), Yoichi Izumi(20), Kotoko Kosuge(18), Koichí Matsumoto(16), Yukio Ozawa(13), Akira Haketa(11), Shigeaki Hinohara(11), Yuji Kasamaki(10), Masakatsu Ohta(10), Nobutaka Doba(9), Yitong Ma(8), Katsuo Kanmatsuse(8), Shinichiro Kokubun(8), Zhen-Yan Fu(7), Atsushi Shindo(5), Dolkun Rahmutula(5), Masanori Shimodaira(5)