Yoko Sugie

Clinical Efficacy of Fluvoxamine and Functional Polymorphism in a Serotonin Transporter Gene on Childhood Autism

Yoko Sugie, Hideo Sugie, Tokiko Fukuda et al. · Journal of Autism and Developmental Disorders · 2005 · 82 citations

Psychiatry, Syndromic Autism, Psychiatric Genetics +14

De novo variants in SETD1B are associated with intellectual disability, epilepsy and autism

Takuya Hiraide, Mitsuko Nakashima, Kaori Yamoto et al. · Human Genetics · 2018 · 75 citations

Neurodevelopmental Disorders, Syndromic Autism, Genetic Disorder +8

Effects of skyrin, a receptor-selective glucagon antagonist, in rat and human hepatocytes.

Jeremy C. Parker, R. Kirk McPherson, Kim Andrews et al. · Diabetes · 2000 · 63 citations · Full text

Cellular Pharmacology, Pharmacotherapy, Experimental Pharmacology +17

Genetic analysis of Japanese patients with myophosphorylase deficiency (McArdle's disease): single-codon deletion in exon 17 is the predominant mutation

Hideo Sugie, Yoko Sugie, Masataka Ito et al. · Clinica Chimica Acta · 1995 · 36 citations

Genetic Analysis, Mendelian Disorder, Genetic Disorder +11

Recurrent Myoglobinuria in a Child With Mental Retardation: Phosphoglycerate Kinase Deficiency

Hideo Sugie, Yoko Sugie, Mitsuhiro Nishida et al. · Journal of Child Neurology · 1989 · 34 citations

Energy Metabolism, Biochemistry, Medicine +15