Rumiko Matsuoka - Concepedia

Author

Rumiko Matsuoka

Also Known As

Matsuoka, Rumiko, R Matsuoka, R. MATSUOKA, R. Matsuoka, RUMIKO MATSUOKA, Rumiko MATSUOKA, Rumiko Matsuoka, Yoshihito Atsumi

214

Publications

9.6K

Citations

H-Index

127

Concepts

All Affiliations

Tokyo Women's Medical University Keio University Toho University Jikei University School of Medicine Yokohama City University

About

Rumiko Matsuoka is an author at Tokyo Women's Medical University specializing in medicine, genetics, and cardiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	34	60	6.2K
2	Engineering	3	3	48
3	Natural Sciences	3	3	481
4	Health Sciences	2	2	142
5	Management	1	1	10

Rumiko Matsuoka

103

Publications

8.9K

Citations

H-Index

Page 1

	Year	Citations
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5 Vidu Garg, Irfan S. Kathiriya, R. Bowling Barnes, Nature Gata4 MutationsDevelopmental BiologyTranslational BiologyGenetic DisorderGenetics	2003	1.2K
Role of TBX1 in human del22q11.2 syndrome Hisato Yagi, Yoshiyuki Furutani, Hiromichi Hamada, The Lancet Genetic DisorderPathologyAutoimmunityHuman Del22q11.2 SyndromeMedicine	2003	877
Germline gain-of-function mutations in RAF1 cause Noonan syndrome Abdur Razzaque, Tsutomu Nishizawa, Yuta Komoike, Nature Genetics Genetic DisorderGeneticsPathologyMolecular GeneticsGermline Gain-of-function Mutations	2007	490
Myosin heavy chain messenger RNA and protein isoform transitions during cardiac hypertrophy. Interaction between hemodynamic and thyroid hormone-induced signals. Seigo Izumo, Anne‐Marie Lompré, Rumiko Matsuoka, Journal of Clinical Investigation Cardiac MuscleMolecular BiologyCellular PhysiologyAlpha-mhc MrnaCardiology	1987	447
VI. Genome Structure and Cognitive Map of Williams Syndrome Julie R. Korenberg, Xiaoning Chen, Hamao Hirota, Journal of Cognitive Neuroscience Developmental BiologyGenetic DisorderInterphase FluorescenceGeneticsGenome Structure	2000	287
<i>GATA6</i> mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling Kazuki Kodo, Tsutomu Nishizawa, Michiko Furutani, Proceedings of the National Academy of Sciences Cardiac MuscleSemaphorin-plexin SignalingGeneticsMolecular GeneticsCongenital Heart Anomaly	2009	237
A new nonsense mutation of <i>SMAD8</i> associated with pulmonary arterial hypertension M Shintani, Hisato Yagi, Takahiro Nakayama, Journal of Medical Genetics	2009	230
Phenotypes with <i>GATA4</i> or <i>NKX2.5</i> mutations in familial atrial septal defect Kayoko Hirayama‐Yamada, Mitsuhiro Kamisago, Kaoru Akimoto, American Journal of Medical Genetics Part A	2005	218
Novel Mechanism Associated With an Inherited Cardiac Arrhythmia Michiko Furutani, Matthew C. Trudeau, Nobuhisa Hagiwara, Circulation	1999	192
The impact of cardiac surgery in patients with trisomy 18 and trisomy 13 in Japan Jun Maeda, Hiroyuki Yamagishi, Yoshiyuki Furutani, American Journal of Medical Genetics Part A	2011	160

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