S. Inoue

发表

Biological Monitoring of Human Exposure to Neonicotinoids Using Urine Samples, and Neonicotinoid Excretion Kinetics

H. Okuda, A. Koizumi, Tamon Niisoe, 2016, PloS one.

RNF213 Rare Variants in Slovakian and Czech Moyamoya Disease Patients

M. Brozman, A. Koizumi, Kouji H. Harada, 2016, PloS one.

Deletion of 2 amino acids in IHH in a Japanese family with brachydactyly type A1

H. Okuda, A. Koizumi, Kouji H. Harada, 2021, BMC Medical Genomics.

Autosomal dominant moyamoya disease maps to chromosome 17q25.3

K. Nozaki, K. Houkin, N. Hashimoto, 2008, Neurology.

Identification of MMP1 as a novel risk factor for intracranial aneurysms in ADPKD using iPSC models

K. Nakao, T. Ichisaka, S. Yamanaka, 2016, Scientific Reports.

Search on Chromosome 17 Centromere Reveals TNFRSF13B as a Susceptibility Gene for Intracranial Aneurysm: A Preliminary Study

K. Nozaki, F. Matsuda, N. Hashimoto, 2006, Circulation.

Mutation analysis in PKD1 of Japanese autosomal dominant polycystic kidney disease patients

Yuichiro Yamada, A. Koizumi, Kayoko Inoue, 2002, Human mutation.

Characterization of two novel mutations of the antithrombin gene observed in Japanese thrombophilic patients.

N. Hamasaki, Kumiko Watanabe, Miyuki Ono, 2005, Thrombosis research.

Protein S and protein C gene mutations in Japanese deep vein thrombosis patients.

N. Hamasaki, D. Kang, Kumiko Watanabe, 2005, Clinical biochemistry.

Characterization of two mutations of the protein S gene observed in Japanese thrombophilic patients.

N. Hamasaki, D. Kang, Miyuki Ono, 2005 .

Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan

T. Shioya, T. Shindo, M. Manabe, 2002, Human mutation.

Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder

W. Gahl, T. Eggermann, E. Babu, 2004, Nature Genetics.

Evaluation of a mass screening program for lysinuric protein intolerance in the northern part of Japan.

A. Koizumi, Kayoko Inoue, S. Inoue, 2003, Genetic Testing.

Model-Based Linkage Analyses Confirm Chromosome 19q13.3 as a Susceptibility Locus for Intracranial Aneurysm

K. Nozaki, N. Hashimoto, A. Koizumi, 2007, Stroke.

Paradoxical increases in serum levels of highly chlorinated PCBs in aged women in clear contrast to robust decreases in dietary intakes from 1980 to 2003 in Japan

T. Takeshita, K. Murata, M. Ikeda, 2009, Environmental health and preventive medicine.

Combination of Linkage and Association Studies for Brain Arteriovenous Malformation

A. Koizumi, J. Jafar, H. Yamakawa, 2007, Stroke.

Assessment of human exposure to polychlorinated biphenyls and polybrominated diphenyl ethers in Japan using archived samples from the early 1980s and mid-1990s.

S. Fujii, T. Takeshita, K. Murata, 2005, Environmental research.

Genome-Wide Scan for Japanese Familial Intracranial Aneurysms: Linkage to Several Chromosomal Regions

K. Nozaki, N. Hashimoto, A. Koizumi, 2004, Circulation.

Association analyses confirming a susceptibility locus for intracranial aneurysm at chromosome 14q23

K. Nozaki, N. Hashimoto, A. Koizumi, 2008, Journal of Human Genetics.

Identification of simultaneous mutation of fibrinogen α chain and protein C genes in a Japanese kindred

N. Hamasaki, Kumiko Watanabe, A. Shibuya, 2003, British journal of haematology.

Association Analysis of Common Variants of ELN, NOS2A, APOE and ACE2 to Intracranial Aneurysm

K. Nozaki, N. Hashimoto, A. Koizumi, 2006, Stroke.

Single nucleotide polymorphisms and haplotypes of protein C and protein S genes in the Thai population

N. Hamasaki, S. Fucharoen, P. Angchaisuksiri, 2006, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Dimorphic gene expression patterns of anorexigenic and orexigenic peptides in hypothalamus account male and female hyperphagia in Akita type 1 diabetic mice.

M. Fujimiya, A. Asakawa, A. Koizumi, 2007, Biochemical and biophysical research communications.

A nonsense polymorphism (Y319X) of the solute carrier family 6 member 18 (SLC6A18) gene is not associated with hypertension and blood pressure in Japanese.

A. Koizumi, Kouji H. Harada, Kayoko Inoue, 2006, The Tohoku journal of experimental medicine.

Secular Trends and Geographical Variations in the Dietary Intake of Polybrominated Diphenyl Ethers (PBDEs) Using Archived Samples from the Early 1980s and Mid 1990s in Japan

S. Fujii, T. Takeshita, K. Murata, 2005, Journal of occupational health.

Familial episodic limb pain in kindreds with novel Nav1.9 mutations

Takeshi Yoshida, H. Okuda, Y. Kato, 2018, PloS one.

Autosomal dominant moyamoya disease maps to chromosome 17q25.3

K. Nozaki, K. Houkin, N. Hashimoto, 2008, Neurology.