Breast cancer ▲ Public Health Genomics Knowledge Base (v1.2)

Public Health Genomics Knowledge Base (v1.2)






Last Updated: Sep 09, 2016

• The LSP1 rs3817198 T > C polymorphism contributes to increased breast cancer risk: a meta-analysis of twelve studies.
  Tang Jianzhou, et al. Oncotarget 2016 8
• A collaborative approach to cancer risk assessment services using genetic counselor extenders in a multi-system community hospital.
  Cohen Stephanie A et al. Breast cancer research and treatment 2016 Aug
• BRCA testing within the Department of Veterans Affairs: concordance with clinical practice guidelines.
  Chun Danielle S et al. Familial cancer 2016 Sep
• Contribution of extended family history in assessment of risk for breast and colon cancer.
  Solomon Benjamin L et al. BMC family practice 2016 17(1) 126
• Effect of decision aid for breast cancer prevention on decisional conflict in women with a BRCA1 or BRCA2 mutation: a multisite, randomized, controlled trial.
  Metcalfe Kelly A et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Sep
• Walking in the shoes of patients, not just in their genes: a patient-centered approach to genomic medicine.
  Arora Neeraj K et al. The patient 2015 Jun 8(3) 239-45
• Association between genetic risk score for telomere length and risk of breast cancer.
  Luu Hung N, et al. Cancer causes & control : CCC 2016 8
• Genetic Ancestry using Mitochondrial DNA in patients with Triple-negative breast cancer (GAMiT study).
  Rao Roshni, et al. Cancer 2016 9
• Ready to clone: CNV detection and breakpoint fine-mapping in breast and ovarian cancer susceptibility genes by high-resolution array CGH.
  Hackmann Karl, et al. Breast cancer research and treatment 2016 8
• Association between BHMT gene rs3733890 polymorphism and cancer risk: evidence from a meta-analysis.
  Xu Yue, et al. OncoTargets and therapy 2016 0 5225-33
• Analysis of DNA Repair Genes Polymorphisms in Breast Cancer.
  Romanowicz Hanna, et al. Pathology oncology research : POR 2016 8
• Association of PALB2 sequence variants with the risk of early-onset breast cancer in patients from Turkey.
  Cecener G, et al. Molecular biology reports 2016 8
• Association study confirms two susceptibility loci for breast cancer in Chinese Han women.
  Xu Minggui, et al. Breast cancer research and treatment 2016 8
• Circulating intestine-derived exosomal miR-328 in plasma, a possible biomarker for estimating BCRP function in the human intestines.
  Gotanda Keisuke, et al. Scientific reports 2016 0 32299
• Genetic variants in FGFR2 and TNRC9 genes are associated with breast cancer risk in Pakistani women.
  Mazhar Ayesha, et al. Molecular medicine reports 2016 8

• CDC Information (9)
• CDC-Authored Pub (12)

• Human (146)
• Pathogen (1)

• Human (5302)
• Pathogen (0)

• Human (471)
• Pathogen (0)

• Guidelines (23)
• Tier Table (19)
• Synthesis (53)

• Huamn (122)
• Pathogen (0)

Relevant Resources

• Cancer Genomics and Epidemiology Navigator (CGEN)
• Genetics and Genomics Competencies Center (G2C2)
• NIH Genetic Testing Registry
• NIH MedGen Database
• Online Mendelian Inheritance in Man (OMIM)
• PharmGKB