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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