Akira Nishimura‐Tadaki

Renal complications in 6p duplication syndrome: Microarray‐based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS)

Y. Fukushima, N. Matsumoto, K. Koike, 2015, American journal of medical genetics. Part A.

De novo 19q13.42 duplications involving NLRP gene cluster in a patient with systemic-onset juvenile idiopathic arthritis

N. Matsumoto, N. Miyake, Y. Tsurusaki, 2011, Journal of Human Genetics.

Homozygous c.14576G>A variant of RNF213 predicts early-onset and severe form of moyamoya disease

Y. Kuroiwa, N. Matsumoto, S. Morita, 2012, Neurology.

Neurodevelopmental features in 2q23.1 microdeletion syndrome: Report of a new patient with intractable seizures and review of literature

Y. Fukushima, N. Matsumoto, K. Koike, 2012, American journal of medical genetics. Part A.