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

Public Health Genomics Knowledge Base (v1.2)




Last Updated: Nov 16, 2016

• Genomic Disparities in Breast Cancer Among Latinas.
  Lynce Filipa et al. Cancer control : journal of the Moffitt Cancer Center 2016 Oct 23(4) 359-372
• Why Is Cancer Genetic Counseling Underutilized by Women Identified as at Risk for Hereditary Breast Cancer? Patient Perceptions of Barriers Following a Referral Letter.
  Kne Alyssa et al. Journal of genetic counseling 2016 Nov
• Association of Polymorphisms in FCGR2A and FCGR3A With Degree of Trastuzumab Benefit in the Adjuvant Treatment of ERBB2/HER2–Positive Breast Cancer
  PG Gavin et al, JAMA Oncology, November 3, 2016
• Predictive Value of FcR Polymorphisms A Further Step on the Long and Winding Road to Application
  R Dolcetti, JAMA Oncology, November 3, 2016
• Validation of an Efficient Screening Tool to Identify Low-Income Women at High Risk for Hereditary Breast Cancer.
  Stewart Susan L et al. Public health genomics 2016 Oct
• Evaluation of human epidermal growth factor receptor 2 (HER2) single nucleotide polymorphisms (SNPs) in normal and breast tumor tissues and their link with breast cancer prognostic factors.
  Furrer Daniela, et al. Breast (Edinburgh, Scotland) 2016 10 191-196
• GSTP1, GSTM1, and GSTT1 polymorphisms as predictors of response to chemotherapy in patients with breast cancer: a meta-analysis.
  Kong Xiangzhen, et al. Cancer chemotherapy and pharmacology 2016 10
• Note of the methodological flaws in the paper entitled "GSTT1 and GSTM1 polymorphisms predict treatment outcome for breast cancer: a systematic review and meta-analysis".
  Qiu Mali, et al. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2016 9 (9) 12897-12899
• Whole-exome sequencing of Finnish hereditary breast cancer families.
  Määttä Kirsi, et al. European journal of human genetics : EJHG 2016 10
• http://www.mdedge.com/jcso/article/110048/gynecologic-cancer/hereditary-breast-and-ovarian-cancer-risk-assessment-minority
  Disease: Breast Cancer|Ovarian Cancer; Type: Data|Program; State: Georgia
• Implementing a screening tool for identifying patients at risk for hereditary breast and ovarian cancer: a statewide initiative.
  Disease: Ovarian Cancer|Breast Cancer; Type: Data|Program; State: Georgia
• Inherited chromosomally-integrated human herpesvirus 6 and breast cancer.
  Gravel Annie, et al. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2016 10
• Altered mitochondrial DNA copy number contributes to human cancer risk: evidence from an updated meta-analysis.
  Hu Liwen, et al. Scientific reports 2016 10 35859
• The impact of ERBB-family germline single nucleotide polymorphisms on survival response to adjuvant trastuzumab treatment in HER2-positive breast cancer.
  Toomey Sinead, et al. Oncotarget 2016 10
• Triple negative breast cancer in North of Morocco: clinicopathologic and prognostic features.
  Derkaoui Touria, et al. BMC women's health 2016 10 (1) 68

• CDC Information (12)
• CDC-Authored Pub (13)

• Human (167)
• Pathogen (1)

• Human (5393)
• Pathogen (0)

• Human (500)
• Pathogen (0)

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

• Huamn (117)
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Relevant Resources

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