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Genetic Testing|November 4, 2008
One third of Japanese patients with multiple osteochondromas may have mutations in genes other than EXT1 or EXT2Hirofumi Kojima, Takahito Wada, Hiroshi Seki, et al.Brain & Development|December 6, 2011
Sporadic hemiplegic migraine presenting as acute encephalopathyKayo Ohmura, Yasuhiro Suzuki, Yoshiaki Saito, et al.Journal of Human Genetics|September 18, 2020
The short-term mortality and morbidity of very low birth weight infants with trisomy 18 or trisomy 13 in JapanHidenori Kawasaki, Takahiro Yamada, Yoshimitsu Takahashi, et al.No to Hattatsu = Brain and Development|March 26, 2015
[A family with creatine transporter deficiency diagnosed with urinary creatine/creatinine ratio and the family history: the third Japanese familial case]Fumihito Nozaki, Tomohiro Kumada, Minoru Shibata, et al.The Journal of Pediatrics|July 8, 2020
Epidemiology of Birth Defects in Very Low Birth Weight Infants in JapanHidenori Kawasaki, Takahiro Yamada, Yoshimitsu Takahashi, et al.Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|July 18, 2012
Visualization of the spatial positioning of the SNRPN, UBE3A, and GABRB3 genes in the normal human nucleus by three-color 3D fluorescence in situ hybridizationRie Kawamura, Hideyuki Tanabe, Takahito Wada, et al.Pediatric Neurology|January 30, 2002
Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxiaTakahito Wada, Norio Kobayashi, Yoshio Takahashi, et al.Journal of Human Genetics|July 5, 2022
Mortality and morbidity of infants with trisomy 21, weighing 1500 grams or less, in JapanHidenori Kawasaki, Takahiro Yamada, Yoshimitsu Takahashi, et al.Journal of Genetic Counseling|April 30, 2025
Qualitative analysis of the needs of parents of children with rare genetic diseases, following their diagnosis obtained by whole-exome sequencingMii Takatsuka, Akira Inaba, Akiko Yoshida, et al.Journal of Human Genetics|July 6, 2007
Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in JapanKunihiro Yoshida, Takahito Wada, Akihiro Sakurai, et al.Pageof 8