Sailaja Peddada
Affiliations: | University of California, San Francisco, San Francisco, CA |
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| Engel SM, Joubert BR, Wu MC, et al. (2014) Neonatal genome-wide methylation patterns in relation to birth weight in the Norwegian Mother and Child Cohort. American Journal of Epidemiology. 179: 834-42 |
| Colaneri A, Wang T, Pagadala V, et al. (2013) A minimal set of tissue-specific hypomethylated CpGs constitute epigenetic signatures of developmental programming. Plos One. 8: e72670 |
| Colaneri A, Staffa N, Fargo DC, et al. (2011) Expanded methyl-sensitive cut counting reveals hypomethylation as an epigenetic state that highlights functional sequences of the genome. Proceedings of the National Academy of Sciences of the United States of America. 108: 9715-20 |
| Swanberg SE, Nagarajan RP, Peddada S, et al. (2009) Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism. Human Molecular Genetics. 18: 525-34 |
| Yasui DH, Peddada S, Bieda MC, et al. (2007) Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes. Proceedings of the National Academy of Sciences of the United States of America. 104: 19416-21 |
| Peddada S, Yasui DH, LaSalle JM. (2006) Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome. Human Molecular Genetics. 15: 2003-14 |
| Thatcher KN, Peddada S, Yasui DH, et al. (2005) Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples. Human Molecular Genetics. 14: 785-97 |