Andrew Hughes - Publications

2014-2017 Washington University, Saint Louis, St. Louis, MO 

8 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
2020 Volkov LI, Kim-Han JS, Saunders LM, Poria D, Hughes AEO, Kefalov VJ, Parichy DM, Corbo JC. Thyroid hormone receptors mediate two distinct mechanisms of long-wavelength vision. Proceedings of the National Academy of Sciences of the United States of America. PMID 32541022 DOI: 10.1073/pnas.1920086117  0.76
2020 Perez-Cervantes C, Smith LA, Nadadur RD, Hughes AEO, Wang S, Corbo JC, Cepko C, Lonfat N, Moskowitz IP. Enhancer transcription identifies -regulatory elements for photoreceptor cell types. Development (Cambridge, England). PMID 31915147 DOI: 10.1242/dev.184432  0.76
2019 Murphy DP, Hughes AE, Lawrence KA, Myers CA, Corbo JC. -regulatory basis of sister cell type divergence in the vertebrate retina. Elife. 8. PMID 31633482 DOI: 10.7554/eLife.48216  0.76
2018 Hughes AEO, Myers CA, Corbo JC. A massively parallel reporter assay reveals context-dependent activity of homeodomain binding sites in vivo. Genome Research. PMID 30158147 DOI: 10.1101/gr.231886.117  0.76
2017 Hughes AE, Enright JM, Myers CA, Shen SQ, Corbo JC. Cell Type-Specific Epigenomic Analysis Reveals a Uniquely Closed Chromatin Architecture in Mouse Rod Photoreceptors. Scientific Reports. 7: 43184. PMID 28256534 DOI: 10.1038/srep43184  0.76
2015 Shen SQ, Myers CA, Hughes AE, Byrne LC, Flannery JG, Corbo JC. Massively parallel cis-regulatory analysis in the mammalian central nervous system. Genome Research. PMID 26576614 DOI: 10.1101/gr.193789.115  0.4
2014 Hughes AE, Magrini V, Demeter R, Miller CA, Fulton R, Fulton LL, Eades WC, Elliott K, Heath S, Westervelt P, Ding L, Conrad DF, White BS, Shao J, Link DC, et al. Clonal architecture of secondary acute myeloid leukemia defined by single-cell sequencing. Plos Genetics. 10: e1004462. PMID 25010716 DOI: 10.1371/journal.pgen.1004462  0.4
2012 Ramos E, Levinson BT, Chasnoff S, Hughes A, Young AL, Thornton K, Li A, Vallania FL, Province M, Druley TE. Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing. Bmc Genomics. 13: 683. PMID 23216810 DOI: 10.1186/1471-2164-13-683  0.4
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