Mitsuru Murata - Concepedia

Author

Mitsuru Murata

Also Known As

Keisuke Kouyama, Kenji Yokoyama, M Murata, M. MURATA, M. Murata, M. Murata A, M. Murata C, M. Ogawa, M., Murata, MITSURU MURATA

325

Publications

8.1K

Citations

H-Index

186

Concepts

All Affiliations

Keio University Keio University Hospital Waseda University Nara Medical University The University of Osaka

About

Mitsuru Murata is an author at Keio University specializing in medicine, thrombosis, and hematology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	31	70	3K
2	Health Sciences	12	13	513
3	Public Health	12	13	972
4	Engineering	5	5	288
5	Natural Sciences	4	4	276

Mitsuru Murata

129

Publications

Citations

H-Index

Page 1

	Year	Citations
The role of von Willebrand factor and fibrinogen in platelet aggregation under varying shear stress. Y. Ikeda, Makoto Handa, K Kawano, Journal of Clinical Investigation	1991	614
Correlation between Serum Resistin Level and Adiposity in Obese Individuals Koichiro Azuma, Fuminori Katsukawa, Shuji Oguchi, Obesity Research	2003	369
Low-Dose Aspirin for Primary Prevention of Cardiovascular Events in Japanese Patients 60 Years or Older With Atherosclerotic Risk Factors Yasuo Ikeda, Kazuyuki Shimada, Tamio Teramoto, JAMA	2014	296
The Frequent 5,10-Methylenetetrahydrofolate Reductase C677T Polymorphism Is Associated with a Common Haplotype in Whites, Japanese, and Africans Nurit Rosenberg, Mitsuru Murata, Yasuo Ikeda, The American Journal of Human Genetics Common HaplotypeHaplotype DeterminationHuman VariationMedicineGenetics	2002	242
A <sup>192</sup> Arg Variant of the Human Paraoxonase <i>(HUMPONA)</i> Gene Polymorphism Is Associated With an Increased Risk for Coronary Artery Disease in the Japanese Takeru Zama, Mitsuru Murata, Yumiko Matsubara, Arteriosclerosis Thrombosis and Vascular Biology GeneticsGenetic EpidemiologyHuman PolymorphismPathologyMolecular Genetics	1997	156
Gene sensor using ferrocenyl oligonucleotide Toshihiro Ihara, Masamichi Nakayama, Mitsuru Murata, Chemical Communications EngineeringBioelectrochemistryDna AnalysisMolecular BiologyDna Nanotechnology	1997	154
Pregnancy‐induced thrombocytopenia and TTP, and the risk of fetal death, in Upshaw–Schulman syndrome: a series of 15 pregnancies in 9 genotyped patients Yoshihiro Fujimura, Masanori Matsumoto, Koichi Kokame, British Journal of Haematology Reproductive HealthGenetic EpidemiologyPathologyGynecologyUpshaw–schulman Syndrome	2008	139
Identification of Three Tyrosine Residues of Glycoprotein Ibα with Distinct Roles in von Willebrand Factor and α-Thrombin Binding Patrizia Marchese, Mitsuru Murata, M. Mazzucato, Journal of Biological Chemistry	1995	121
Prevalence of genetic mutations in protein S, protein C and antithrombin genes in Japanese patients with deep vein thrombosis Toshiyuki Miyata, Yukiko Sato, Junko Ishikawa, Thrombosis Research ThrombosisEpidemiologyGenetic MutationsVenous DiseaseVenous Thrombosis	2008	116
Detection of von Willebrand factor-cleaving protease (ADAMTS-13) in human platelets Misako Suzuki, Mitsuru Murata, Yumiko Matsubara, Biochemical and Biophysical Research Communications ThrombosisHuman PlateletsBlood PlateletMedicineHematology	2003	111

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