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Sailaja Peddada - Publications

Affiliations: 
University of California, San Francisco, San Francisco, CA 
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7 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
2014 Engel SM, Joubert BR, Wu MC, Olshan AF, Håberg SE, Ueland PM, Nystad W, Nilsen RM, Vollset SE, Peddada SD, London SJ. Neonatal genome-wide methylation patterns in relation to birth weight in the Norwegian Mother and Child Cohort. American Journal of Epidemiology. 179: 834-42. PMID 24561991 DOI: 10.1093/Aje/Kwt433  0.311
2013 Colaneri A, Wang T, Pagadala V, Kittur J, Staffa NG, Peddada SD, Isganaitis E, Patti ME, Birnbaumer L. A minimal set of tissue-specific hypomethylated CpGs constitute epigenetic signatures of developmental programming. Plos One. 8: e72670. PMID 24069155 DOI: 10.1371/Journal.Pone.0072670  0.391
2011 Colaneri A, Staffa N, Fargo DC, Gao Y, Wang T, Peddada SD, Birnbaumer L. 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. PMID 21602498 DOI: 10.1073/pnas.1105713108  0.366
2009 Swanberg SE, Nagarajan RP, Peddada S, Yasui DH, LaSalle JM. Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism. Human Molecular Genetics. 18: 525-34. PMID 19000991 DOI: 10.1093/Hmg/Ddn380  0.723
2007 Yasui DH, Peddada S, Bieda MC, Vallero RO, Hogart A, Nagarajan RP, Thatcher KN, Farnham PJ, Lasalle JM. 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. PMID 18042715 DOI: 10.1073/Pnas.0707442104  0.439
2006 Peddada S, Yasui DH, LaSalle JM. 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. PMID 16682435 DOI: 10.1093/Hmg/Ddl124  0.687
2005 Thatcher KN, Peddada S, Yasui DH, Lasalle JM. 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. PMID 15689352 DOI: 10.1093/Hmg/Ddi073  0.642
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