S. Ono

Apolipoprotein H variant modifies plasma triglyceride phenotype in familial hypercholesterolemia: a molecular study in an eight-generation hyperlipidemic family.

M. Emi, S. Hunt, P. Hopkins, 2003, Journal of atherosclerosis and thrombosis.

Growth hormone receptor variant (L526I) modifies plasma HDL cholesterol phenotype in familial hypercholesterolemia: Intra‐familial association study in an eight‐generation hyperlipidemic kindred

M. Emi, S. Hunt, P. Hopkins, 2003, American journal of medical genetics. Part A.

Serum lipid metabolism abnormalities and change in lipoprotein contents in patients with advanced-stage renal disease.

T. Kinouchi, T. Komoda, M. Tsumura, 2001, Clinica chimica acta; international journal of clinical chemistry.

Hypertriglyceridemia associated with amino acid variation Asn985Tyr of theRP1 gene

M. Emi, Y. Ezura, H. Bujo, 2003, Journal of Human Genetics.

A promoter SNP (−1323T>C) in G-substrate gene (GSBS) correlates with hypercholesterolemia

M. Emi, S. Umemura, Y. Ezura, 2003, Journal of Human Genetics.