(Q36858843)

16 August 2017

Discriminatory accuracy from single-nucleotide polymorphisms in models to predict breast cancer risk (English)

1 reference

single-nucleotide polymorphism

16 August 2017

1 reference

1 reference

Mitchell H Gail

1

1 reference

PMCID

2528005

16 August 2017

language of work or name

English

0 references

publication date

8 July 2008

1 reference

Journal of the National Cancer Institute

16 August 2017

1 reference

16 August 2017

100

1 reference

16 August 2017

14

1 reference

16 August 2017

1037-1041

1 reference

Multiple loci identified in a genome-wide association study of prostate cancer

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2528005

Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2528005

Genome-wide association study identifies novel breast cancer susceptibility loci

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2528005

On criteria for evaluating models of absolute risk

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2528005

Limitations of the odds ratio in gauging the performance of a diagnostic, prognostic, or screening marker

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2528005

Average 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 studies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2528005

Validation of the Gail et al. model of breast cancer risk prediction and implications for chemoprevention

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2528005

Weighing the risks and benefits of tamoxifen treatment for preventing breast cancer

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2528005

Projecting absolute invasive breast cancer risk in white women with a model that includes mammographic density.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2528005

Estimates of the number of US women who could benefit from tamoxifen for breast cancer chemoprevention

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2528005

Validation studies for models projecting the risk of invasive and total breast cancer incidence.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2528005

A common coding variant in CASP8 is associated with breast cancer risk

4 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FJNCI%2FDJN180

Evidence for further breast cancer susceptibility genes in addition to BRCA1 and BRCA2 in a population-based study

21 January 2018

1 reference

12 December 2020

Polygenic susceptibility to breast cancer and implications for prevention

1 reference

12 December 2020

Polygenic inheritance of breast cancer: Implications for design of association studies

1 reference

12 December 2020

Projecting individualized probabilities of developing breast cancer for white females who are being examined annually

1 reference

12 December 2020

Health care in the age of genetic medicine

1 reference

12 December 2020

Cumulative association of five genetic variants with prostate cancer

1 reference

12 December 2020

Probability of detecting disease-associated single nucleotide polymorphisms in case-control genome-wide association studies.

1 reference

12 December 2020

Identifiers

DOI

10.1093/JNCI/DJN180

1 reference

16 August 2017

1 reference

16 August 2017

1 reference

PMCID

2528005