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Eunju Seong, Ph.D. - Publications

Affiliations: 
University of Michigan, Ann Arbor, Ann Arbor, MI 
Area:
genetics, behavioral, psychiatric, neurological
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10 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Seong E, Insolera R, Dulovic M, Kamsteeg EJ, Trinh J, Brüggemann N, Sandford E, Li S, Ozel AB, Li JZ, Jewett T, Kievit AJA, Münchau A, Shakkottai V, Klein C, et al. Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects. Annals of Neurology. PMID 29604224 DOI: 10.1002/Ana.25220  0.475
2007 Newell-Litwa K, Seong E, Burmeister M, Faundez V. Neuronal and non-neuronal functions of the AP-3 sorting machinery. Journal of Cell Science. 120: 531-41. PMID 17287392 DOI: 10.1242/Jcs.03365  0.501
2005 Seong E, Wainer BH, Hughes ED, Saunders TL, Burmeister M, Faundez V. Genetic analysis of the neuronal and ubiquitous AP-3 adaptor complexes reveals divergent functions in brain. Molecular Biology of the Cell. 16: 128-40. PMID 15537701 DOI: 10.1091/Mbc.E04-10-0892  0.499
2005 Bomar JM, Benke PJ, Slattery EL, Puttagunta R, Taylor LP, Seong E, Nystuen A, Chen W, Albin RL, Patel PD, Kittles RA, Sheffield VC, Burmeister M. Erratum: Corrigendum: Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse Nature Genetics. 37: 555-555. DOI: 10.1038/Ng0505-555B  0.471
2004 Seong E, Saunders TL, Stewart CL, Burmeister M. To knockout in 129 or in C57BL/6: that is the question. Trends in Genetics : Tig. 20: 59-62. PMID 14746984 DOI: 10.1016/J.Tig.2003.12.006  0.455
2003 Bomar JM, Benke PJ, Slattery EL, Puttagunta R, Taylor LP, Seong E, Nystuen A, Chen W, Albin RL, Patel PD, Kittles RA, Sheffield VC, Burmeister M. Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse. Nature Genetics. 35: 264-9. PMID 14556008 DOI: 10.1038/Ng1255  0.532
2003 Qiao X, Pennesi M, Seong E, Gao H, Burmeister M, Wu SM. Photoreceptor degeneration and rd1 mutation in the grizzled/mocha mouse strain. Vision Research. 43: 859-65. PMID 12668055 DOI: 10.1016/S0042-6989(02)00393-0  0.519
2003 Kantheti P, Diaz ME, Peden AE, Seong EE, Dolan DF, Robinson MS, Noebels JL, Burmeister ML. Genetic and phenotypic analysis of the mouse mutant mh2J, an Ap3d allele caused by IAP element insertion. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 14: 157-67. PMID 12647238 DOI: 10.1007/s00335-002-2238-8  0.525
2002 Seong E, Seasholtz AF, Burmeister M. Mouse models for psychiatric disorders. Trends in Genetics : Tig. 18: 643-50. PMID 12446150 DOI: 10.1016/S0168-9525(02)02807-X  0.508
1999 Karolyi IJ, Burrows HL, Ramesh TM, Nakajima M, Lesh JS, Seong E, Camper SA, Seasholtz AF. Altered anxiety and weight gain in corticotropin-releasing hormone-binding protein-deficient mice. Proceedings of the National Academy of Sciences of the United States of America. 96: 11595-600. PMID 10500222 DOI: 10.1073/Pnas.96.20.11595  0.303
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