論文
1. Kurotaki N, Imaizumi K, Harada N, Masuno M, Kondoh T, Nagai T, Ohashi H, Naritomi K, Tsukahara M, Makita Y, Sugimoto T, Sonoda T, Hasegawa T, Chinen Y, Tomita H, Kinoshita A, Mizuguchi T, Yoshiura Ki K, Ohta T, Kishino T, Fukushima Y, Niikawa N, Matsumoto N.
Haploinsufficiency of NSD1 causes Sotos syndrome. Nature Genetics, 30 (4): 365-366, 2002

2. Yoneda Y, Saitsu H, Touyama M, Makita Y, Miyamoto A, Hamada K, Kurotaki N, Tomita H, Nishiyama K, Tsurusaki Y, Doi H, Miyake N, Ogata K, Naritomi K, Matsumoto N.
Missense mutations in the DNA-binding/dimerization domain of NFIX cause Sotos-like features. Journal of Human Genetics, 57(3):207-211. 2012

3. Ono C, Yu Z, Kasahara Y, Kikuchi Y, Ishii N, Tomita H.
Fluorescently activated cell sorting followed by microarray profiling of helper T cell subtypes from human peripheral blood. Plos One,9(11): e111405. 2014