Sailaja Peddada, PhD

Title(s)Specialist, Biochemistry and Biophysics
SchoolSchool of Medicine
Address499 Illinois, #349
San Francisco CA 94158
Phone415-514-0448
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Variants in tubule epithelial regulatory elements mediate most heritable differences in human kidney function. Nat Genet. 2024 Sep 10. Loeb GB, Kathail P, Shuai RW, Chung R, Grona RJ, Peddada S, Sevim V, Federman S, Mader K, Chu AY, Davitte J, Du J, Gupta AR, Ye CJ, Shafer S, Przybyla L, Rapiteanu R, Ioannidis NM, Reiter JF. PMID: 39256582.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    2. Variants in tubule epithelial regulatory elements mediate most heritable differences in human kidney function. bioRxiv. 2024 Jun 22. Loeb GB, Kathail P, Shuai R, Chung R, Grona RJ, Peddada S, Sevim V, Federman S, Mader K, Chu A, Davitte J, Du J, Gupta AR, Ye CJ, Shafer S, Przybyla L, Rapiteanu R, Ioannidis N, Reiter JF. PMID: 38948875; PMCID: PMC11212968.
      View in: PubMed   Mentions:
    3. Functional genomics in stem cell models: considerations and applications. Front Cell Dev Biol. 2023; 11:1236553. Shevade K, Peddada S, Mader K, Przybyla L. PMID: 37554308; PMCID: PMC10404852.
      View in: PubMed   Mentions:
    4. SOX2 O-GlcNAcylation alters its protein-protein interactions and genomic occupancy to modulate gene expression in pluripotent cells. Elife. 2016 Mar 07; 5:e10647. Myers SA, Peddada S, Chatterjee N, Friedrich T, Tomoda K, Krings G, Thomas S, Maynard J, Broeker M, Thomson M, Pollard K, Yamanaka S, Burlingame AL, Panning B. PMID: 26949256; PMCID: PMC4841768.
      View in: PubMed   Mentions: 36     Fields:    Translation:AnimalsCells
    5. Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism. Hum Mol Genet. 2009 Feb 01; 18(3):525-34. Swanberg SE, Nagarajan RP, Peddada S, Yasui DH, LaSalle JM. PMID: 19000991; PMCID: PMC2638799.
      View in: PubMed   Mentions: 36     Fields:    Translation:HumansAnimalsCells
    6. Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes. Proc Natl Acad Sci U S A. 2007 Dec 04; 104(49):19416-21. Yasui DH, Peddada S, Bieda MC, Vallero RO, Hogart A, Nagarajan RP, Thatcher KN, Farnham PJ, Lasalle JM. PMID: 18042715; PMCID: PMC2148304.
      View in: PubMed   Mentions: 189     Fields:    Translation:HumansCells
    7. Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome. Hum Mol Genet. 2006 Jun 15; 15(12):2003-14. Peddada S, Yasui DH, LaSalle JM. PMID: 16682435; PMCID: PMC1931415.
      View in: PubMed   Mentions: 56     Fields:    Translation:HumansAnimalsCells
    8. Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples. Hum Mol Genet. 2005 Mar 15; 14(6):785-97. Thatcher KN, Peddada S, Yasui DH, Lasalle JM. PMID: 15689352.
      View in: PubMed   Mentions: 49     Fields:    Translation:HumansCells
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