Publications
- 1. Frenkel S, Bernstein CN, Jin Y, Sargent M, Kuang Q, Jiang W, et al. Genome-wide copy number variant data for inflammatory bowel disease in a Caucasian population. Data Br. Elsevier; 2019; 104203. doi:10.1016/J.DIB.2019.104203 (abstract)
- Frenkel S, Bernstein CN, Sargent M, Kuang Q, Jiang W, Wei J, et al. (2019) Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease. PLoS ONE 14(6): e0217846. https://doi.org/10.1371/journal.pone.0217846 (abstract)
- Frenkel S, Bernstein CN, Sargent M, Jiang W, Kuang Q, Xu W, et al. Copy number variation-based gene set analysis reveals cytokine signalling pathways associated with psychiatric comorbidity in patients with inflammatory bowel disease. Genomics. 2019; doi:10.1016/j.ygeno.2019.05.001 (abstract)
- Paz A, Frenkel S, Snir S, Kirzhner V, Korol A. 2014. Functional implications of structural heterogeneity of the human genome: functionally related genes tend to reside in organizationally similar genome regions. BMC Genomics 15:252. doi: 10.1186/1471-2164-15-252 (abstract)
- Frenkel S, Kirzhner V, Korol A. 2012. Organizational Heterogeneity of Vertebrate Genomes. PLoS ONE 7(2): e32076. doi:10.1371/journal.pone.0032076 (abstract)
- Kirzhner V., Frenkel S., Korol A. 2011. Minimal-Dot Plot: “Old Tale in New Skin” about Sequence Comparison. Information Sciences 181:1454–1462. (abstract)