Benjamin Ponder, Ph.D.

Affiliations: 
2007 Communication Studies Northwestern University, Evanston, IL 
Area:
Rhetoric and Composition Language, American Studies, United States History, American Literature
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"Benjamin Ponder"

Parents

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David 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
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