Benjamin Ponder, Ph.D.
Affiliations: | 2007 | Communication Studies | Northwestern University, Evanston, IL |
Area:
Rhetoric and Composition Language, American Studies, United States History, American LiteratureGoogle:
"Benjamin Ponder"Parents
Sign in to add mentorDavid Zarefsky | grad student | 2007 | Northwestern | |
(Independence unfurled: "Common Sense" and the constitution of the American public.) |
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Publications
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Campbell TM, Castro MA, de Santiago I, et al. (2016) FGFR2 risk SNPs confer breast cancer risk by augmenting estrogen responsiveness. Carcinogenesis |
Castro MA, de Santiago I, Campbell TM, et al. (2015) Regulators of genetic risk of breast cancer identified by integrative network analysis. Nature Genetics |
Jones JO, Chin SF, Wong-Taylor LA, et al. (2013) TOX3 mutations in breast cancer. Plos One. 8: e74102 |
Fletcher MN, Castro MA, Wang X, et al. (2013) Master regulators of FGFR2 signalling and breast cancer risk. Nature Communications. 4: 2464 |
Maia AT, Antoniou AC, O'Reilly M, et al. (2012) Effects of BRCA2 cis-regulation in normal breast and cancer risk amongst BRCA2 mutation carriers. Breast Cancer Research : Bcr. 14: R63 |
Cho HS, Toyokawa G, Daigo Y, et al. (2012) The JmjC domain-containing histone demethylase KDM3A is a positive regulator of the G1/S transition in cancer cells via transcriptional regulation of the HOXA1 gene. International Journal of Cancer. Journal International Du Cancer. 131: E179-89 |
Meyer KB, Maia AT, O'Reilly M, et al. (2011) A functional variant at a prostate cancer predisposition locus at 8q24 is associated with PVT1 expression Plos Genetics. 7 |
Yoshimatsu M, Toyokawa G, Hayami S, et al. (2011) Dysregulation of PRMT1 and PRMT6, Type I arginine methyltransferases, is involved in various types of human cancers. International Journal of Cancer. Journal International Du Cancer. 128: 562-73 |
Pooley KA, Tyrer J, Shah M, et al. (2010) No association between TERT-CLPTM1L single nucleotide polymorphism rs401681 and mean telomere length or cancer risk Cancer Epidemiology Biomarkers and Prevention. 19: 1862-1865 |
Wang X, Pankratz VS, Fredericksen Z, et al. (2010) Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers. Human Molecular Genetics. 19: 2886-97 |