Difference between revisions of "Publications"

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* '''[https://www.nature.com/articles/s41588-019-0408-9 Genome-scale screens uncover JNK/JUN signaling as a key barrier from pluripotency to human endoderm differentiation.]''' Li QV, Dixon G, Verma N, Rosen BP, Gordillo M, Luo R, Xu C, Wang Q, Soh C-L, Yang D, Crespo M, Shukla A, Xiang Q, Dundar F, Zumbo P, Witkin M, Koche R, Betel D, Chen S, Massague J, Garippa R, Evans T, Beer MA, and Huangfu D. Nature Genetics 2019. 
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* '''[https://onlinelibrary.wiley.com/doi/full/10.1002/humu.23797 Integration of multiple epigenomic marks improves prediction of variant impact in saturation mutagenesis reporter assay.]''' Shigaki D, Adato O, Adhikar A, Dong S, Hawkins-Hooker A, Inoue F, Juven-Gershon T, Kenlay H, Martin B, Patra A, Penzar D, Schubach M, Xiong C, Yan Z, Boyle A, Kreimer A, Kulakovskiy IV, Reid J, Unger R, Yosef N, Shendure J, Ahituv N, Kircher M, and Beer MA.  Human Mutation 2019.
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* '''[https://stm.sciencemag.org/content/11/497/eaaw0790.abstract Epigenetic activation and memory at a novel TGFβ2 enhancer in systemic sclerosis fibroblasts.]''' Shin JY, Beckett JD, Shah A, McMahan Z, Paik J, Sampedro MM, MacFarlane EG, Beer MA, Warren D, Wigley FM, and Dietz HC.  Science Translational Medicine 2019.
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* '''[https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1006625 Local epigenomic state cannot discriminate interacting and non-interacting enhancer–promoter pairs with high accuracy.]''' Xi, W and Beer, MA.  PLOS Comp Biol 2018.
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* '''[https://www.sciencedirect.com/science/article/pii/S0002929718303707 Parkinson-Associated SNCA Enhancer Variants Revealed by Open Chromatin in Mouse Dopamine Neurons.]''' McClymont SA, Hook PW, Soto AI, Reed X, Law WD, Kerans SJ, Waite EL, Briceno NJ, Thole JF, Heckman MG, Diehl NN, Wszolek  ZK, Moore CD, Zhu H, Akiyama JA, Dickel DE, Visel A, Pennacchio LA, Ross OA, Beer MA, & McCallion AS. Am. Jour. Human Genetics 2018
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* '''[https://www.nature.com/articles/s41588-018-0156-2 Genetic determinants of co-accessible chromatin regions in activated T cells across humans.]''' Gate RE, Cheng CS, Aiden AP, Siba A, Tabaka M, Lituiev D, Machol I, Gordon MG, Subramaniam M, Shamim M, Hougen KL, Wortman I, Huang S-C, Durand NC, Feng T, De Jager PL, Chang HY, Lieberman Aiden E, Benoist C, Beer MA, Ye CJ & Regev A.  Nature Genetics 2018.
  
 
* '''[http://onlinelibrary.wiley.com/doi/10.1002/humu.23185/full Predicting enhancer activity and variant impact using gkm-SVM.]''' Beer, MA.  Human Mutation 2017.
 
* '''[http://onlinelibrary.wiley.com/doi/10.1002/humu.23185/full Predicting enhancer activity and variant impact using gkm-SVM.]''' Beer, MA.  Human Mutation 2017.
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* '''[http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0170403 Embryonic loss of human females with partial trisomy 19 identifies region critical for the single active X.]''' Migeon BR, Beer MA, and Bjornsson HT. Plos ONE 2017.
 
* '''[http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0170403 Embryonic loss of human females with partial trisomy 19 identifies region critical for the single active X.]''' Migeon BR, Beer MA, and Bjornsson HT. Plos ONE 2017.
  
* '''[http://bioinformatics.oxfordjournals.org/content/early/2016/05/05/bioinformatics.btw203 gkmSVM: an R package for gapped-kmer SVM.]''' [[Media:Bioinformatics-2016-Ghandi-bioinformatics-btw203.pdf|pdf]] [[Media:Tutorial.pdf|tutorial]] Ghandi, M, Mohammad-Noori M, Ghareghani N, Lee D, Garraway L, and Beer MA. Bioinformatics 2016.
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* '''[http://bioinformatics.oxfordjournals.org/content/early/2016/05/05/bioinformatics.btw203 gkmSVM: an R package for gapped-kmer SVM.]''' [[Media:Bioinformatics-2016-Ghandi-bioinformatics-btw203.pdf|pdf]] [[tutorial]] Ghandi, M, Mohammad-Noori M, Ghareghani N, Lee D, Garraway L, and Beer MA. Bioinformatics 2016.
  
 
* '''[http://elifesciences.org/content/5/e11613v1 Epigenomic landscapes of retinal rods and cones.]''' Mo, A, Luo, C, Davis, FP, Mukamel, EA, Henry, GL, Nery JR, Urich, MA, Picard, S, Lister, R, Eddy, SR, Beer, MA, Ecker, JR, and Nathans, J. eLife 2016.
 
* '''[http://elifesciences.org/content/5/e11613v1 Epigenomic landscapes of retinal rods and cones.]''' Mo, A, Luo, C, Davis, FP, Mukamel, EA, Henry, GL, Nery JR, Urich, MA, Picard, S, Lister, R, Eddy, SR, Beer, MA, Ecker, JR, and Nathans, J. eLife 2016.

Revision as of 19:07, 5 August 2019

  • A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies. Khanna H, Davis EE, Murga-Zamalloa CA, Estrada-Cuzcano A, Lopez I, den Hollander AI, Zonneveld MN, Othman MI, Waseem N, Chakarova CF, Maubaret C, Diaz-Font A, MacDonald I, Muzny DM, Wheeler DA, Morgan M, Lewis LR, Logan CV, Tan PL, Beer MA, Inglehearn CF, Lewis RA, Jacobson SG, Bergmann C, Beales PL, Attié-Bitach T, Johnson CA, Otto EA, Bhattacharya SS, Hildebrandt F, Gibbs RA, Koenekoop RK, Swaroop A, Katsanis N. 2009. Nat Genet. 41:739-45.



For a full list including my prior work in simulations of plasma turbulence, see my google scholar page.