Michiko Furutani

Germline gain-of-function mutations in RAF1 cause Noonan syndrome

Abdur Razzaque, Tsutomu Nishizawa, Yuta Komoike et al. · Nature Genetics · 2007 · 490 citations

Genetic Disorder, Genetics, Pathology +3

<i>GATA6</i> mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling

Kazuki Kodo, Tsutomu Nishizawa, Michiko Furutani et al. · Proceedings of the National Academy of Sciences · 2009 · 237 citations · Full text

Cardiac Muscle, Semaphorin-plexin Signaling, Genetics +19

Phenotypes with <i>GATA4</i> or <i>NKX2.5</i> mutations in familial atrial septal defect

Kayoko Hirayama‐Yamada, Mitsuhiro Kamisago, Kaoru Akimoto et al. · American Journal of Medical Genetics Part A · 2005 · 218 citations

Novel Mechanism Associated With an Inherited Cardiac Arrhythmia

Michiko Furutani, Matthew C. Trudeau, Nobuhisa Hagiwara et al. · Circulation · 1999 · 192 citations

Implications of Mutations of Activin Receptor-Like Kinase 1 Gene (&lt;i&gt;ALK1&lt;/i&gt;) in Addition to Bone Morphogenetic Protein Receptor II Gene (&lt;i&gt;BMPR2&lt;/i&gt;) in Children With Pulmonary Arterial Hypertension

Maya Fujiwara, Hisato Yagi, Rumiko Matsuoka et al. · Circulation Journal · 2007 · 108 citations · Full text