Publication updates

README.md

@@ -281,7 +281,9 @@ Ewels P, Magnusson M, Lundin S, Käller M. MultiQC: summarize analysis results f
 
 The following publications utilize **CpG_Me**:
 
-Laufer BI, Gomez JA, Jianu JM, LaSalle, JM.  Stable DNMT3L Overexpression in SH-SY5Y Neurons Recreates a Facet of the Genome-Wide Down Syndrome DNA Methylation Signature. *bioRxiv* preprint, 2020. **doi**:[10.1101/2020.11.09.374793](https://doi.org/10.1101/2020.11.09.374793)
+Laufer BI*, Gomez JA*, Jianu JM, LaSalle, JM.  Stable DNMT3L Overexpression in SH-SY5Y Neurons Recreates a Facet of the Genome-Wide Down Syndrome DNA Methylation Signature. *Epigenetics & Chromatin*, 2021. **doi**:[10.1186/s13072-021-00387-7](https://doi.org/10.1186/s13072-021-00387-7)
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+Maggio, AG., Shu, HT., Laufer, BI., Hwang, H., Bi, C., Lai, Y., LaSalle, JM., Hu, VW. Impact of exposures to persistent endocrine disrupting compounds on the sperm methylome in regions associated with neurodevelopmental disorders. *medRxiv* preprint, 2021. **doi**:[10.1101/2021.02.21.21252162](https://doi.org/10.1101/2021.02.21.21252162)
 
 Mordaunt CE, Jianu JM, Laufer BI, Zhu Y, Dunaway KW, Bakulski KM, Feinberg JI, Volk HE, Lyall K, Croen LA, Newschaffer CJ, Ozonoff S, Hertz-Picciotto I, Fallin DM, Schmidt RJ, LaSalle JM. Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes. *Genome Medicine*, 2020. **doi**: [10.1186/s13073-020-00785-8](https://doi.org/10.1186/s13073-020-00785-8)