Seung-Yun Yoo

Affiliations: 
Gilead Sciences, San Dimas, CA, United States 
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"Seung-Yun Yoo"
Mean distance: 14.61 (cluster 11)
 
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Cross-listing: BCM Tree

Parents

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Huda Y. Zoghbi grad student 1997-2003 Baylor
Chris A. Walsh post-doc 2004-2007 Harvard Medical School

Collaborators

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Mark Pennesi collaborator 2001-2003 Baylor
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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
Yoon JS, Park HJ, Yoo SY, et al. (2008) Heterogeneity in the processing defect of SLC26A4 mutants. Journal of Medical Genetics. 45: 411-9
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
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