N. Ogawa

Evaluating Japanese patients with the Marfan syndrome using high-throughput microarray-based mutational analysis of fibrillin-1 gene.

S. Tsuji, S. Takamoto, R. Nagai, 2011, The American journal of cardiology.

Circulating transforming growth factor β-1 level in Japanese patients with Marfan syndrome.

S. Takamoto, R. Nagai, T. Morota, 2013, International heart journal.

Missense mutations in FBN1 exons 41 and 42 cause Weill–Marchesani syndrome with thoracic aortic disease and Marfan syndrome

D. Milewicz, R. Lewis, D. Guo, 2013, American journal of medical genetics. Part A.

Genome-Wide Association Study of Coronary Artery Disease

R. Nagai, H. Morita, Y. Imai, 2010, International journal of hypertension.

Evaluating Japanese patients with the Marfan syndrome using high-throughput microarray-based mutational analysis of fibrillin-1 gene.

S. Tsuji, S. Takamoto, R. Nagai, 2011, The American journal of cardiology.