Seung-Yun Yoo
Affiliations: | Gilead Sciences, San Dimas, CA, United States |
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"Seung-Yun Yoo"Cross-listing: Neurotree
Parents
Sign in to add mentor| Huda Y. Zoghbi | grad student | 1997-2003 | Baylor College of Medicine |
| Chris A. Walsh | post-doc | 2004-2007 | Harvard Medical School (Neurotree) |
Collaborators
Sign in to add collaborator| Mark Pennesi | collaborator | 2001-2003 | Baylor College of Medicine |
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Publications
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| Ouyang Q, Nakayama T, Baytas O, et al. (2016) Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features. Proceedings of the National Academy of Sciences of the United States of America |
| Ching MS, Shen Y, Tan WH, et al. (2010) Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 937-47 |
| Morrow EM, Yoo SY, Flavell SW, et al. (2008) Identifying autism loci and genes by tracing recent shared ancestry. Science (New York, N.Y.). 321: 218-23 |
| Rajab A, Yoo SY, Abdulgalil A, et al. (2006) An autosomal recessive form of spastic cerebral palsy (CP) with microcephaly and mental retardation. American Journal of Medical Genetics. Part A. 140: 1504-10 |
| Deuel TA, Liu JS, Corbo JC, et al. (2006) Genetic interactions between doublecortin and doublecortin-like kinase in neuronal migration and axon outgrowth. Neuron. 49: 41-53 |
| Bowman AB, Yoo SY, Dantuma NP, et al. (2005) Neuronal dysfunction in a polyglutamine disease model occurs in the absence of ubiquitin-proteasome system impairment and inversely correlates with the degree of nuclear inclusion formation. Human Molecular Genetics. 14: 679-91 |
| Yoo SY, Pennesi ME, Weeber EJ, et al. (2003) SCA7 knockin mice model human SCA7 and reveal gradual accumulation of mutant ataxin-7 in neurons and abnormalities in short-term plasticity. Neuron. 37: 383-401 |