Frazer KA - Search Results

1

Insights into the Mutational Burden of Human Induced Pluripotent Stem Cells from an Integrative Multi-Omics Approach.

D'Antonio M, Benaglio P, Jakubosky D, Greenwald WW, Matsui H, Donovan MKR, Li H, Smith EN, D'Antonio-Chronowska A, Frazer KA. D'Antonio M, et al. Among authors: frazer ka. Cell Rep. 2018 Jul 24;24(4):883-894. doi: 10.1016/j.celrep.2018.06.091. Cell Rep. 2018. PMID: 30044985 Free PMC article.

2

Identification of high-confidence somatic mutations in whole genome sequence of formalin-fixed breast cancer specimens.

Yost SE, Smith EN, Schwab RB, Bao L, Jung H, Wang X, Voest E, Pierce JP, Messer K, Parker BA, Harismendy O, Frazer KA. Yost SE, et al. Among authors: frazer ka. Nucleic Acids Res. 2012 Aug;40(14):e107. doi: 10.1093/nar/gks299. Epub 2012 Apr 6. Nucleic Acids Res. 2012. PMID: 22492626 Free PMC article.

3

High-resolution mutational profiling suggests the genetic validity of glioblastoma patient-derived pre-clinical models.

Yost SE, Pastorino S, Rozenzhak S, Smith EN, Chao YS, Jiang P, Kesari S, Frazer KA, Harismendy O. Yost SE, et al. Among authors: frazer ka. PLoS One. 2013;8(2):e56185. doi: 10.1371/journal.pone.0056185. Epub 2013 Feb 18. PLoS One. 2013. PMID: 23441165 Free PMC article.

4

Mutascope: sensitive detection of somatic mutations from deep amplicon sequencing.

Yost SE, Alakus H, Matsui H, Schwab RB, Jepsen K, Frazer KA, Harismendy O. Yost SE, et al. Among authors: frazer ka. Bioinformatics. 2013 Aug 1;29(15):1908-9. doi: 10.1093/bioinformatics/btt305. Epub 2013 May 27. Bioinformatics. 2013. PMID: 23712659 Free PMC article.

5

Whole transcriptome sequencing enables discovery and analysis of viruses in archived primary central nervous system lymphomas.

DeBoever C, Reid EG, Smith EN, Wang X, Dumaop W, Harismendy O, Carson D, Richman D, Masliah E, Frazer KA. DeBoever C, et al. Among authors: frazer ka. PLoS One. 2013 Sep 4;8(9):e73956. doi: 10.1371/journal.pone.0073956. eCollection 2013. PLoS One. 2013. PMID: 24023918 Free PMC article.

6

miR-150 influences B-cell receptor signaling in chronic lymphocytic leukemia by regulating expression of GAB1 and FOXP1.

Mraz M, Chen L, Rassenti LZ, Ghia EM, Li H, Jepsen K, Smith EN, Messer K, Frazer KA, Kipps TJ. Mraz M, et al. Among authors: frazer ka. Blood. 2014 Jul 3;124(1):84-95. doi: 10.1182/blood-2013-09-527234. Epub 2014 May 1. Blood. 2014. PMID: 24787006 Free PMC article.

7

Effective filtering strategies to improve data quality from population-based whole exome sequencing studies.

Carson AR, Smith EN, Matsui H, Brækkan SK, Jepsen K, Hansen JB, Frazer KA. Carson AR, et al. Among authors: frazer ka. BMC Bioinformatics. 2014 May 2;15:125. doi: 10.1186/1471-2105-15-125. BMC Bioinformatics. 2014. PMID: 24884706 Free PMC article.

8

Biased estimates of clonal evolution and subclonal heterogeneity can arise from PCR duplicates in deep sequencing experiments.

Smith EN, Jepsen K, Khosroheidari M, Rassenti LZ, D'Antonio M, Ghia EM, Carson DA, Jamieson CH, Kipps TJ, Frazer KA. Smith EN, et al. Among authors: frazer ka. Genome Biol. 2014 Aug 7;15(8):420. doi: 10.1186/s13059-014-0420-4. Genome Biol. 2014. PMID: 25103687 Free PMC article.

9

Consanguinity and rare mutations outside of MCCC genes underlie nonspecific phenotypes of MCCD.

Shepard PJ, Barshop BA, Baumgartner MR, Hansen JB, Jepsen K, Smith EN, Frazer KA. Shepard PJ, et al. Among authors: frazer ka. Genet Med. 2015 Aug;17(8):660-7. doi: 10.1038/gim.2014.157. Epub 2014 Nov 6. Genet Med. 2015. PMID: 25356967 Free PMC article.

10

Associations Between Common and Rare Exonic Genetic Variants and Serum Levels of 20 Cardiovascular-Related Proteins: The Tromsø Study.

Solomon T, Smith EN, Matsui H, Braekkan SK; INVENT Consortium; Wilsgaard T, Njølstad I, Mathiesen EB, Hansen JB, Frazer KA. Solomon T, et al. Among authors: frazer ka. Circ Cardiovasc Genet. 2016 Aug;9(4):375-83. doi: 10.1161/CIRCGENETICS.115.001327. Epub 2016 Jun 21. Circ Cardiovasc Genet. 2016. PMID: 27329291 Free PMC article.

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