Shinya Yamamoto

Affiliations: 
Ph.D., M.D. AIST Tsukuba, Аист Снт, Moskovskaya oblast', Russia 
Area:
integrative neuroscience
Website:
http://staff.aist.go.jp/yamamoto-s/
Google:
"Shinya Yamamoto"
Mean distance: 14.54 (cluster 29)
 
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Publications

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Baldridge D, Wangler MF, Bowman AN, et al. (2021) Model organisms contribute to diagnosis and discovery in the undiagnosed diseases network: current state and a future vision. Orphanet Journal of Rare Diseases. 16: 206
Luo X, Schoch K, Jangam SV, et al. (2021) Rare deleterious de novo missense variants in RNF2/RING2 are associated with a neurodevelopmental disorder with unique clinical features. Human Molecular Genetics
Yamayoshi S, Yasuhara A, Ito M, et al. (2021) Antibody titers against SARS-CoV-2 decline, but do not disappear for several months. Eclinicalmedicine. 32: 100734
Kunimatsu J, Yamamoto S, Maeda K, et al. (2021) Environment-based object values learned by local network in the striatum tail. Proceedings of the National Academy of Sciences of the United States of America. 118
Gotoh M, Nagasaka K, Nakata M, et al. (2020) Brain Temperature Alters Contributions of Excitatory and Inhibitory Inputs to Evoked Field Potentials in the Rat Frontal Cortex. Frontiers in Cellular Neuroscience. 14: 593027
Barish S, Barakat TS, Michel BC, et al. (2020) BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms. American Journal of Human Genetics
Dutta D, Briere LC, Kanca O, et al. (2020) De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment. Human Molecular Genetics
Chung HL, Mao X, Wang H, et al. (2020) De Novo Variants in CDK19 Are Associated with a Syndrome Involving Intellectual Disability and Epileptic Encephalopathy. American Journal of Human Genetics
Chung HL, Wangler MF, Marcogliese PC, et al. (2020) Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms. Neuron
Graves HK, Jangam S, Tan KL, et al. (2019) A Genetic Screen for Genes That Impact Peroxisomes in Identifies Candidate Genes for Human Disease. G3 (Bethesda, Md.)
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