Clinical application of breast cancer risk assessment models

scientific article published on March 2010

Clinical application of breast cancer risk assessment models is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

External links are
P356DOI10.2217/FON.10.5
P698PubMed publication ID20222793

P2093author name stringBanu K Arun
Jennifer K Litton
Kaylene Ready
P2860cites workAverage risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studiesQ24531993
Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2Q28212276
Tamoxifen for prevention of breast cancer: report of the National Surgical Adjuvant Breast and Bowel Project P-1 StudyQ28283241
American Cancer Society guidelines for breast screening with MRI as an adjunct to mammographyQ28295438
Characterization of BRCA1 and BRCA2 mutations in a large United States sampleQ28383993
Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage ConsortiumQ29619206
Predicting the likelihood of carrying a BRCA1 or BRCA2 mutation: validation of BOADICEA, BRCAPRO, IBIS, Myriad and the Manchester scoring system using data from UK genetics clinicsQ31152672
A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genesQ34115258
Risk-reducing salpingo-oophorectomy in women with a BRCA1 or BRCA2 mutationQ34129784
Prophylactic oophorectomy in carriers of BRCA1 or BRCA2 mutationsQ34129787
Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2Q34384153
BRCA1 and BRCA2 mutation predictions using the BOADICEA and BRCAPRO models and penetrance estimation in high-risk French-Canadian familiesQ34480647
Cancer risks in BRCA2 mutation carriersQ34504452
Cancer Incidence in BRCA1 mutation carriersQ34527264
Evaluation of breast cancer risk assessment packages in the family history evaluation and screening programmeQ35441054
A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPROQ35445946
Does this patient have a family history of cancer? An evidence-based analysis of the accuracy of family cancer historyQ35895179
Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselorsQ35986971
Risk prediction models for familial breast cancerQ36430753
Prediction of BRCA Mutations Using the BRCAPRO Model in Clinic-Based African American, Hispanic, and Other Minority Families in the United StatesQ37155632
Value of adding single-nucleotide polymorphism genotypes to a breast cancer risk modelQ37246495
Performance of prediction models for BRCA mutation carriage in three racial/ethnic groups: findings from the Northern California Breast Cancer Family RegistryQ37252756
Accuracy of the BRCAPRO model among women with bilateral breast cancerQ37363896
Projecting individualized absolute invasive breast cancer risk in African American womenQ40149673
Evaluation of widely used models for predicting BRCA1 and BRCA2 mutationsQ43073772
The pathology of familial breast cancer: predictive value of immunohistochemical markers estrogen receptor, progesterone receptor, HER-2, and p53 in patients with mutations in BRCA1 and BRCA2.Q43974233
Cancer risk prediction models: a workshop on development, evaluation, and applicationQ44065523
Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individualsQ46796026
Validation of the Gail et al. model for predicting individual breast cancer risk.Q50603613
A breast cancer prediction model incorporating familial and personal risk factors.Q52000310
Assessing BRCA carrier probabilities in extended families.Q52997805
Clinico-pathological characteristics of BRCA1- and BRCA2-related breast cancer.Q53409967
Risk of breast cancer recurrence and contralateral breast cancer in relation to BRCA1 and BRCA2 mutation status following breast-conserving surgery and radiotherapy.Q54645721
BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genesQ57309394
P433issue3
P407language of work or nameEnglishQ1860
P921main subjectrisk assessment modelQ117383677
P304page(s)355-365
P577publication date2010-03-01
P1433published inFuture OncologyQ2781597
P1476titleClinical application of breast cancer risk assessment models
P478volume6

Reverse relations

cites work (P2860)
Q36963403Breast cancer in the young: role of the geneticist
Q36393157Breast cancer risk assessment with five independent genetic variants and two risk factors in Chinese women
Q37670809Implications of single nucleotide polymorphisms in CD44 exon 2 for risk of breast cancer
Q44820973Prevalence and differentiation of hereditary breast and ovarian cancers in Japan