☰

Dan Levy, Ph.D. - Publications

Affiliations: 
2005 University of California, Berkeley, Berkeley, CA, United States 
Tree Info Similar researchers PubMed Report error

11 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 Vasudevan A, Baruah PS, Smith JC, Wang Z, Sayles NM, Andrews P, Kendall J, Leu J, Chunduri NK, Levy D, Wigler M, Storchová Z, Sheltzer JM. Single-Chromosomal Gains Can Function as Metastasis Suppressors and Promoters in Colon Cancer. Developmental Cell. 52: 413-428.e6. PMID 32097652 DOI: 10.1016/J.Devcel.2020.01.034  0.362
2016 Wang Z, Andrews P, Kendall J, Ma B, Hakker I, Rodgers L, Ronemus M, Wigler M, Levy D. SMASH, a fragmentation and sequencing method for genomic copy number analysis. Genome Research. PMID 27197213 DOI: 10.1101/Gr.201491.115  0.323
2014 Warburton D, Ronemus M, Kline J, Jobanputra V, Williams I, Anyane-Yeboa K, Chung W, Yu L, Wong N, Awad D, Yu CY, Leotta A, Kendall J, Yamrom B, Lee YH, ... ... Levy D, et al. The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease. Human Genetics. 133: 11-27. PMID 23979609 DOI: 10.1007/S00439-013-1353-9  0.315
2012 Heald R, Levy D, Wilbur J, Loughlin R, Kieserman E. Mechanisms of Nuclear, Spindle and Mitotic Chromosome Scaling Biophysical Journal. 102: 233a. DOI: 10.1016/J.Bpj.2011.11.1281  0.335
2011 Levy D, Ronemus M, Yamrom B, Lee YH, Leotta A, Kendall J, Marks S, Lakshmi B, Pai D, Ye K, Buja A, Krieger A, Yoon S, Troge J, Rodgers L, et al. Rare de novo and transmitted copy-number variation in autistic spectrum disorders. Neuron. 70: 886-97. PMID 21658582 DOI: 10.1016/J.Neuron.2011.05.015  0.309
2011 Navin N, Kendall J, Troge J, Andrews P, Rodgers L, McIndoo J, Cook K, Stepansky A, Levy D, Esposito D, Muthuswamy L, Krasnitz A, McCombie WR, Hicks J, Wigler M. Tumour evolution inferred by single-cell sequencing. Nature. 472: 90-4. PMID 21399628 DOI: 10.1038/Nature09807  0.31
2009 Varadan V, Kamalakaran S, Russnes HG, Levy D, Kendall J, Janevski A, Riggs M, Banerjee N, Synnestvedt M, Schlichting E, Kåresen R, Lucito R, Wigler M, Dimitrova N, Naume B, et al. Genome-Wide DNA Methylation Profiles of Breast Tumors Reveal Loci Associated with Relapse Risk. Cancer Research. 69: 4046-4046. DOI: 10.1158/0008-5472.Sabcs-09-4046  0.308
2007 Levy D, Reeder C, Loucas B, Hlatky L, Chen A, Cornforth M, Sachs R. Interpreting chromosome aberration spectra. Journal of Computational Biology : a Journal of Computational Molecular Cell Biology. 14: 144-55. PMID 17456013 DOI: 10.1089/Cmb.2006.0127  0.573
2004 Levy D, Vazquez M, Cornforth M, Loucas B, Sachs RK, Arsuaga J. Comparing DNA damage-processing pathways by computer analysis of chromosome painting data Journal of Computational Biology. 11: 626-641. PMID 15579235 DOI: 10.1089/Cmb.2004.11.626  0.563
2004 Sachs RK, Levy D, Hahnfeldt P, Hlatky L. Quantitative analysis of radiation-induced chromosome aberrations Cytogenetic and Genome Research. 104: 142-148. PMID 15162028 DOI: 10.1159/000077479  0.55
2000 Sachs RK, Levy D, Chen AM, Simpson PJ, Cornforth MN, Ingerman EA, Hahnfeldt P, Hlatky LR. Random breakage and reunion chromosome aberration formation model; an interaction-distance version based on chromatin geometry. International Journal of Radiation Biology. 76: 1579-88. PMID 11133039 DOI: 10.1080/09553000050201064  0.623
Show low-probability matches.