Genomic Factors Involved in Chromosome Rearrangements

Large Inverted Duplications in the Human Genome Form via a Fold-Back Mechanism

Karen E. Hermetz, S. Newman, K. Conneely, et al. (2014). PLoS Genetics. Cited 71 times. https://doi.org/10.1371/journal.pgen.1004139

Tandem Repeats and G-Rich Sequences Are Enriched at Human CNV Breakpoints

Promita Bose, Karen E. Hermetz, K. Conneely, et al. (2014). PLoS ONE. Cited 51 times. https://doi.org/10.1371/journal.pone.0101607

Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements.

Yue Luo, Karen E. Hermetz, J. M. Jackson, et al. (2011). Human molecular genetics. Cited 42 times. https://doi.org/10.1093/hmg/ddr293

Mouse model implicates GNB3 duplication in a childhood obesity syndrome

Ian Goldlust, Karen E. Hermetz, Lisa M. Catalano, et al. (2013). Proceedings of the National Academy of Sciences. Cited 34 times. https://doi.org/10.1073/pnas.1305999110

Density matters: comparison of array platforms for detection of copy-number variation and copy-neutral abnormalities

H. Mason-Suares, Wayne Kim, L. Grimmett, et al. (2013). Genetics in Medicine. Cited 32 times. https://doi.org/10.1038/gim.2013.36

A recurrent translocation is mediated by homologous recombination between HERV-H elements

Karen E. Hermetz, U. Surti, J. Cody, et al. (2012). Molecular Cytogenetics. Cited 23 times. https://doi.org/10.1186/1755-8166-5-6

Structural variation in subtelomeres.

M. K. Rudd. (2012). Methods in molecular biology. Cited 9 times. https://doi.org/10.1007/978-1-61779-507-7_6