Assessment of rare BRCA1 and BRCA2 variants of unknown significance using hierarchical modeling (Q30426205)

17 October 2017

Assessment of rare BRCA1 and BRCA2 variants of unknown significance using hierarchical modeling (English)

1 reference

17 October 2017

1

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Patrick Concannon

2

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Leslie Bernstein

4

object named as

Leslie Bernstein

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17 October 2017

5

Kathleen E Malone

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17 October 2017

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Jonine L Bernstein

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17 October 2017

8

Sharon N Teraoka

1 reference

WECARE Study Collaborative Group

17 October 2017

12

object named as

WECARE Study Collaborative Group

1 reference

17 October 2017

Robert W Haile

3

1 reference

17 October 2017

Charles F Lynch

6

1 reference

17 October 2017

Xiaolin Liang

7

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17 October 2017

Anh T Diep

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17 October 2017

Duncan C Thomas

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17 October 2017

Colin B Begg

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17 October 2017

25 April 2011

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17 October 2017

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17 October 2017

35

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17 October 2017

5

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17 October 2017

389-397

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Hierarchical modeling for estimating relative risks of rare genetic variants: properties of the pseudo-likelihood method

17 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Population-based study of the risk of second primary contralateral breast cancer associated with carrying a mutation in BRCA1 or BRCA2.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Approaches for evaluating rare polymorphisms in genetic association studies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Evaluating cancer epidemiologic risk factors using multiple primary malignancies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Genetic variants on chromosome 5p12 are associated with risk of breast cancer in African American women: the Black Women's Health Study

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

An evaluation of statistical approaches to rare variant analysis in genetic association studies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Common vs. rare allele hypotheses for complex diseases

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Family history, genetic testing, and clinical risk prediction: pooled analysis of CHEK2 1100delC in 1,828 bilateral breast cancers and 7,030 controls

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Mouse embryonic stem cell-based functional assay to evaluate mutations in BRCA2

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

The use of hierarchical models for estimating relative risks of individual genetic variants: an application to a study of melanoma

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Variation of breast cancer risk among BRCA1/2 carriers

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Genome-wide association study identifies novel breast cancer susceptibility loci

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Comprehensive statistical study of 452 BRCA1 missense substitutions with classification of eight recurrent substitutions as neutral

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Study design: evaluating gene-environment interactions in the etiology of breast cancer - the WECARE study

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Hierarchical modeling of linkage disequilibrium: genetic structure and spatial relations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Hierarchical modeling of gene-environment interactions: estimating NAT2 genotype-specific dietary effects on adenomatous polyps

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

A note on the estimation of relative risks of rare genetic susceptibility markers.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Inherited predisposition of lung cancer: a hierarchical modeling approach to DNA repair and cell cycle control pathways.

20 June 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20587

Hierarchical Bayes prioritization of marker associations from a genome-wide association scan for further investigation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20587

Classification of rare missense substitutions, using risk surfaces, with genetic- and molecular-epidemiology applications.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20587

Many amino acid substitution variants identified in DNA repair genes during human population screenings are predicted to impact protein function

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20587

Using hierarchical modeling in genetic association studies with multiple markers: application to a case-control study of bladder cancer.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Average age-specific cumulative risk of breast cancer according to type and site of germline mutations in BRCA1 and BRCA2 estimated from multiple-case breast cancer families attending Australian family cancer clinics

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

Genetic polymorphisms in GSTM1, -P1, -T1, and CYP2E1 and the risk of adult brain tumors.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111904

A polymorphic stop codon in BRCA2

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21520273

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Searching for susceptibility alleles: emphasis on bilateral breast cancer

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21520273

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/GEPI.20587

1 reference

17 October 2017

1 reference

17 October 2017

1 reference