(Q37155632)

English

Prediction of BRCA Mutations Using the BRCAPRO Model in Clinic-Based African American, Hispanic, and Other Minority Families in the United States

scientific article published on 02 February 2009

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scholarly article

1 reference

Europe PubMed Central

18 August 2017

Prediction of BRCA Mutations Using the BRCAPRO Model in Clinic-Based African American, Hispanic, and Other Minority Families in the United States (English)

1 reference

Europe PubMed Central

18 August 2017

United States of America

1 reference

based on heuristic

inferred from title

Olufunmilayo Olopade

8

object named as

Olufunmilayo I Olopade

1 reference

Europe PubMed Central

18 August 2017

Saundra S. Buys

4

object named as

Saundra S Buys

1 reference

Europe PubMed Central

18 August 2017

3

object named as

Mary Daly

1 reference

Europe PubMed Central

18 August 2017

author name string

Dezheng Huo

1

1 reference

Europe PubMed Central

18 August 2017

Ruby T Senie

2

1 reference

Europe PubMed Central

18 August 2017

Shelly Cummings

5

1 reference

Europe PubMed Central

18 August 2017

Jacqueline Ogutha

6

1 reference

Europe PubMed Central

18 August 2017

Kisha Hope

7

1 reference

Europe PubMed Central

18 August 2017

language of work or name

0 references

publication date

2 February 2009

1 reference

Europe PubMed Central

18 August 2017

Journal of Clinical Oncology

1 reference

Europe PubMed Central

18 August 2017

27

1 reference

Europe PubMed Central

18 August 2017

1184-1190

1 reference

Europe PubMed Central

18 August 2017

8

1 reference

Europe PubMed Central

18 August 2017

Validity of models for predicting BRCA1 and BRCA2 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

6 September 2017

Clinical practice. Management of an inherited predisposition to breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

6 September 2017

Limited family structure and BRCA gene mutation status in single cases of breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

6 September 2017

Meta-analysis of BRCA1 and BRCA2 penetrance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

6 September 2017

Incorporating medical interventions into carrier probability estimation for genetic counseling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

6 September 2017

Evaluation of models to predict BRCA germline mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

6 September 2017

Application of BRCA1 and BRCA2 mutation carrier prediction models in breast and/or ovarian cancer families of French Canadian descent

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

6 September 2017

BayesMendel: an R environment for Mendelian risk prediction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

6 September 2017

Optimal selection of individuals for BRCA mutation testing: a comparison of available methods

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

6 September 2017

BRCA1 and BRCA2 mutation predictions using the BOADICEA and BRCAPRO models and penetrance estimation in high-risk French-Canadian families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

6 September 2017

The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

6 September 2017

A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

6 September 2017

Log odds of carrying an Ancestral Mutation in BRCA1 or BRCA2 for a Defined personal and family history in an Ashkenazi Jewish woman (LAMBDA)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

6 September 2017

A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

6 September 2017

Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

6 September 2017

Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

6 September 2017

Comparing the areas under two or more correlated receiver operating characteristic curves: a nonparametric approach

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

6 September 2017

Probabilistic prediction in patient management and clinical trials

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

27 June 2018

Prevalence of pathogenic BRCA1 mutation carriers in 5 US racial/ethnic groups

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

3 September 2018

Assessing BRCA carrier probabilities in extended families.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

3 September 2018

Evaluation of widely used models for predicting BRCA1 and BRCA2 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

3 September 2018

Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

3 September 2018

BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

20 October 2018

Validation study of thelambdamodel for predicting theBRCA1orBRCA2mutation carrier status of North American Ashkenazi Jewish women

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2667822

4 December 2018

Genetic testing in diverse populations: are researchers doing enough to get out the correct message?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19188678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Models for predicting BRCA1 and BRCA2 mutations in Han Chinese familial breast and/or ovarian cancer patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19188678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pretest prediction of BRCA1 or BRCA2 mutation by risk counselors and the computer model BRCAPRO

1 reference

https://pubmed.ncbi.nlm.nih.gov/19188678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Confronting genetic testing disparities: knowledge is power

1 reference

https://pubmed.ncbi.nlm.nih.gov/19188678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/19188678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA1 and BRCA2 genetic testing in Hispanic patients: mutation prevalence and evaluation of the BRCAPRO risk assessment model

1 reference

https://pubmed.ncbi.nlm.nih.gov/19188678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic testing in an ethnically diverse cohort of high-risk women: a comparative analysis of BRCA1 and BRCA2 mutations in American families of European and African ancestry

1 reference

https://pubmed.ncbi.nlm.nih.gov/19188678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Racial differences in the use of BRCA1/2 testing among women with a family history of breast or ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/19188678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1200/JCO.2008.17.5869

1 reference

Europe PubMed Central

18 August 2017

1 reference

Europe PubMed Central

18 August 2017

1 reference

Europe PubMed Central

18 August 2017

ResearchGate publication ID

0 references

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