Julie A. Douglas, Ph.D.
Affiliations: | 2001 | University of Michigan, Ann Arbor, Ann Arbor, MI |
Area:
Biostatistics Biology, GeneticsGoogle:
"Julie Douglas"Parents
Sign in to add mentor| Michael L. Boehnke | grad student | 2001 | University of Michigan | |
| (Methods for resolving genotype and haplotype ambiguity in human genetic data.) | ||||
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Publications
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| Chen H, Douglas J, Gordon W, et al. (2018) Abstract 224: Evidence for a shared genetic basis between breast cancer and mammographic density phenotypes Epidemiology |
| Lindström S, Thompson DJ, Paterson AD, et al. (2015) Corrigendum: Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk. Nature Communications. 6: 8358 |
| Stone J, Thompson DJ, Dos Santos Silva I, et al. (2015) Novel Associations between Common Breast Cancer Susceptibility Variants and Risk-Predicting Mammographic Density Measures. Cancer Research. 75: 2457-67 |
| Lindström S, Thompson DJ, Paterson AD, et al. (2014) Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk. Nature Communications. 5: 5303 |
| Johnson AM, Zuhlke KA, Plotts C, et al. (2014) Mutational landscape of candidate genes in familial prostate cancer. The Prostate. 74: 1371-8 |
| Shah KP, Douglas JA. (2013) A method to prioritize quantitative traits and individuals for sequencing in family-based studies. Plos One. 8: e62545 |
| Montasser ME, Douglas JA, Roy-Gagnon MH, et al. (2011) Determinants of blood pressure response to low-salt intake in a healthy adult population. Journal of Clinical Hypertension (Greenwich, Conn.). 13: 795-800 |
| Iniesta MD, Gorin MA, Chien LC, et al. (2010) Absence of CHEK2*1100delC mutation in families with hereditary breast cancer in North America. Cancer Genetics and Cytogenetics. 202: 136-40 |
| Van Hout CV, Levin AM, Rampersaud E, et al. (2010) Extent and distribution of linkage disequilibrium in the Old Order Amish. Genetic Epidemiology. 34: 146-50 |
| Gorin MA, Iniesta MD, Douglas JA, et al. (2009) Absence of the CHEK2*1100delC mutation in non-BRCA1/2 families with multiple cancer types in a high-risk clinic population of Caucasian ancestry. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 27: 11040 |