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Journal of Human Genetics|March 21, 2009
Physicians' opinion for 'new' genetic testing in JapanTakako Ohata, Atsushi Tsuchiya, Maiko Watanabe, et al.Rinsho Shinkeigaku = Clinical Neurology|May 31, 2013
[Survey on the attitude toward genetic testing of neurologists certified by the Japanese Society of Neurology]Kunihiro Yoshida, Takako Ohata, Kaori Muto, et al.Maternal and Child Health Journal|November 9, 2022
Risk Factors of Preterm Birth in Okinawa Prefecture, the Southernmost Island Prefecture of JapanYoshino Kinjyo, Tadatsugu Kinjo, Keiko Mekaru, et al.Journal of Human Genetics|March 18, 2006
Complete hydatidiform mole and normal live birth following intracytoplasmic sperm injectionHaruka Hamanoue, Nobuko Umezu, Mika Okuda, et al.American Journal of Medical Genetics. Part A|March 9, 2007
FBN2, FBN1, TGFBR1, and TGFBR2 analyses in congenital contractural arachnodactylyAkira Nishimura, Haruya Sakai, Shiro Ikegawa, et al.Journal of Human Genetics|April 15, 2006
A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in NaganoTakako Ohata, Kunihiro Yoshida, Haruya Sakai, et al.Cerebellum (London, England)|October 16, 2008
Severity and progression rate of cerebellar ataxia in 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA) in the endemic Nagano Area of JapanKunihiro Yoshida, Yusaku Shimizu, Hiroshi Morita, et al.Human Mutation|January 7, 2010
Molecular and clinical analysis of RAF1 in Noonan syndrome and related disorders: dephosphorylation of serine 259 as the essential mechanism for mutant activationTomoko Kobayashi, Yoko Aoki, Tetsuya Niihori, et al.Nature Medicine|March 17, 2023
Genetic association analysis of 77,539 genomes reveals rare disease etiologiesDaniel Greene, , Daniela Pirri, et al.Pageof 1