N. Carolyn Schanen - Publications

Neuroscience, Human Genetics University of California, Los Angeles, Los Angeles, CA 

6 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
2015 Pitcher MR, Herrera JA, Buffington SA, Kochukov MY, Merritt JK, Fisher AR, Schanen NC, Costa-Mattioli M, Neul JL. Rett syndrome like phenotypes in the R255X Mecp2 mutant mouse are rescued by MECP2 transgene. Human Molecular Genetics. 24: 2662-72. PMID 25634563 DOI: 10.1093/Hmg/Ddv030  0.344
2012 Wegiel J, Schanen NC, Cook EH, Sigman M, Brown WT, Kuchna I, Nowicki K, Wegiel J, Imaki H, Ma SY, Marchi E, Wierzba-Bobrowicz T, Chauhan A, Chauhan V, Cohen IL, et al. Differences between the pattern of developmental abnormalities in autism associated with duplications 15q11.2-q13 and idiopathic autism. Journal of Neuropathology and Experimental Neurology. 71: 382-97. PMID 22487857 DOI: 10.1097/Nen.0B013E318251F537  0.304
2009 Hogart A, Leung KN, Wang NJ, Wu DJ, Driscoll J, Vallero RO, Schanen NC, LaSalle JM. Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number. Journal of Medical Genetics. 46: 86-93. PMID 18835857 DOI: 10.1136/Jmg.2008.061580  0.381
2008 Kumar A, Kamboj S, Malone BM, Kudo S, Twiss JL, Czymmek KJ, LaSalle JM, Schanen NC. Analysis of protein domains and Rett syndrome mutations indicate that multiple regions influence chromatin-binding dynamics of the chromatin-associated protein MECP2 in vivo. Journal of Cell Science. 121: 1128-37. PMID 18334558 DOI: 10.1242/Jcs.016865  0.318
2007 Nishimura Y, Martin CL, Vazquez-Lopez A, Spence SJ, Alvarez-Retuerto AI, Sigman M, Steindler C, Pellegrini S, Schanen NC, Warren ST, Geschwind DH. Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways. Human Molecular Genetics. 16: 1682-98. PMID 17519220 DOI: 10.1093/Hmg/Ddm116  0.332
2005 Ham AL, Kumar A, Deeter R, Schanen NC. Does genotype predict phenotype in Rett syndrome? Journal of Child Neurology. 20: 768-78. PMID 16225834 DOI: 10.1177/08830738050200091301  0.309
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