Last Updated: May 19, 2016
- Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kConFab.
Li Hongyan et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 May - Mutation Spectra of BRCA Genes in Iranian Women with Early Onset Breast Cancer - 15 Years Experience.
Yassaee Vahid Reza, et al. Asian Pacific journal of cancer prevention : APJCP 2016 0 149-53 - Triple negative status and BRCA mutations in contralateral breast cancer: a population-based study.
Pellegrino Benedetta, et al. Acta bio-medica : Atenei Parmensis 2016 0 (1) 54-63 - Interaction between Hormonal Receptor Status, Age and Survival in Patients with BRCA1/2 Germline Mutations: A Systematic Review and Meta-Regression.
Templeton Arnoud J, et al. PloS one 2016 0 (5) e0154789 - Differences of Variable Number Tandem Repeats in XRCC5 Promoter Are Associated with Increased or Decreased Risk of Breast Cancer in BRCA Gene Mutation Carriers.
Cui Jian, et al. Frontiers in oncology 2016 0 92 - Assessing biases of information contained in pedigrees for the classification of BRCA-genetic variants: a study arising from the ENIGMA analytical working group.
Kerkhofs C H H, et al. Hereditary cancer in clinical practice 2016 0 10 - Clinical and pathological features of BRCA1/2 tumors in a sample of high-risk Moroccan breast cancer patients.
Jouhadi Hassan, et al. BMC research notes 2016 0 (1) 248 - Which BRCA genetic testing programs are ready for implementation in health care? A systematic review of economic evaluations
D? Andrea E, et al. Genetics in Medicine (2016) April 14 - Identification of Novel BRCA Founder Mutations in Middle Eastern Breast Cancer Patients Using Capture and Sanger Sequencing Analysis.
Bu Rong, et al. International journal of cancer 2016 4 - Frequency and Significance of Abnormal Pancreatic Imaging in Patients with BRCA1 and BRCA2 Genetic Mutations.
Chahla Elie, et al. Scientifica 2016 0 5619358 - Olaparib maintenance therapy in patients with platinum-sensitive, relapsed serous ovarian cancer and a BRCA mutation: Overall survival adjusted for postprogression poly(adenosine diphosphate ribose) polymerase inhibitor therapy.
Matulonis Ursula A, et al. Cancer 2016 4 - Mutation detection rates associated with specific selection criteria for BRCA1/2 testing in 1854 high-risk families: A monocentric Italian study.
Azzollini Jacopo, et al. European journal of internal medicine 2016 4 - Decreased Expression of BRCA2 Accelerates Sporadic Breast Cancer Progression.
Saha Soumi, et al. Indian journal of surgical oncology 2015 12 (4) 378-83 - Impact of Clinical Genetics Attendance at a Gynecologic Oncology Tumor Board on Referrals for Genetic Counseling and BRCA Mutation Testing.
Cohen Paul A et al. International journal of gynecological cancer : official journal of the International Gynecological Cancer Society 2016 Apr - BRCA1 Gene Mutations and Influence of Chemotherapy on Autophagy and Apoptotic Mechanisms in Egyptian Breast Cancer Patients.
Abdel-Mohsen Mohamed Ahmed, et al. Asian Pacific journal of cancer prevention : APJCP 2016 0 (3) 1285-92 - Highly favorable outcome in BRCA-mutated metastatic breast cancer patients receiving high-dose chemotherapy and autologous hematopoietic stem cell transplantation.
Boudin L, et al. Bone marrow transplantation 2016 4 - Family history predictors of BRCA1/BRCA2 mutation status among Tunisian breast/ovarian cancer families.
Riahi Aouatef et al. Breast cancer (Tokyo, Japan) 2016 Mar - UK BRCA mutation testing in patients with ovarian cancer.
George Angela et al. British journal of cancer 2015 Dec 113 Suppl 1S17-21 - BRCA testing, treatment patterns and survival in platinum-sensitive recurrent ovarian cancer - an observational cohort study.
Unni Sudhir K et al. Journal of ovarian research 2016 9(1) 18 - Molecular insights into the OGG1 gene, a cancer risk modifier in BRCA1 and BRCA2 mutations carriers.
Benitez-Buelga Carlos, et al. Oncotarget 2016 3 - Beyond BRCA: Lynch Syndrome
My gene counsel, March 22, 2016 - Beyond BRCA: Lynch Syndrome
My gene counsel, March 22, 2016 - Bad Luck Or Bad Genes? Dealing With BRCA And 'A Cancer In The Family',
NPR, March 14, 2016 - Eligibility Criteria and Genetic Testing Results from a High-Risk Cohort for Hereditary Breast and Ovarian Cancer Syndrome in Southeastern Ontario.
Vidal Ricardo Dos Santos et al. The Journal of molecular diagnostics : JMD 2016 Feb - FORCE family letter for BRCA1 and BRCA2 carriers[PDF 64.08 KB]
Disease: Breast Cancer|Ovarian Cancer; Type: Tools; State: Multiple States - Breast cancer in high-risk Afrikaner families: Is BRCA founder mutation testing sufficient?
Seymour Heather Jessica et al. South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 2016 106(3) 264-7 - A cost analysis of a cancer genetic service model in the UK.
Slade Ingrid et al. Journal of community genetics 2016 Feb - Contribution of mammography to MRI screening in BRCA mutation carriers by BRCA status and age: individual patient data meta-analysis.
Phi Xuan-Anh, et al. British journal of cancer 2016 2 - Prioritizing Variants in Complete Hereditary Breast and Ovarian Cancer (HBOC) Genes in Patients Lacking known BRCA Mutations.
Caminsky Natasha G, et al. Human mutation 2016 2 - Low prevalence of HER2 positivity amongst BRCA1 and BRCA2 mutation carriers and in primary BRCA screens.
Evans D G, et al. Breast cancer research and treatment 2016 2 (3) 597-601
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