Germline BRCA1 mutations increase prostate cancer risk (Q35949522)

11 August 2017

Germline BRCA1 mutations increase prostate cancer risk (English)

1 reference

11 August 2017

1 reference

E Saunders

4

0 references

Tokhir Dadaev

T Dadaev

5

0 references

Daniel Leongamornlert

D Leongamornlert

1

0 references

Elena Castro

E Castro

6

0 references

Rosalind Eeles

R Eeles

17

0 references

Douglas F. Easton

14

D Easton

1 reference

11 August 2017

18

Z Kote-Jarai

1 reference

11 August 2017

11

E Sawyer

1 reference

11 August 2017

N Mahmud

2

1 reference

11 August 2017

M Tymrakiewicz

3

1 reference

11 August 2017

C Goh

7

1 reference

11 August 2017

K Govindasami

8

1 reference

11 August 2017

M Guy

9

1 reference

11 August 2017

L O'Brien

10

1 reference

11 August 2017

A Hall

12

1 reference

11 August 2017

R Wilkinson

13

1 reference

11 August 2017

UKGPCS Collaborators

15

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11 August 2017

D Goldgar

16

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11 August 2017

language of work or name

English

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publication date

1 May 2012

1 reference

British Journal of Cancer

11 August 2017

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11 August 2017

106

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11 August 2017

10

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11 August 2017

1697-1701

1 reference

https://scigraph.springernature.com/pub.10.1038/bjc.2012.146

11 August 2017

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cites work

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BRCA2 is a moderate penetrance gene contributing to young-onset prostate cancer: implications for genetic testing in prostate cancer patients

2 October 2017

1 reference

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A risk prediction algorithm based on family history and common genetic variants: application to prostate cancer with potential clinical impact

2 October 2017

1 reference

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2 October 2017

1 reference

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BRCA1 mutations do not increase prostate cancer risk: results from a meta-analysis including new data

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

MutationTaster evaluates disease-causing potential of sequence alterations

2 October 2017

1 reference

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ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

2 October 2017

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A method and server for predicting damaging missense mutations

2 October 2017

1 reference

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Detection of nonneutral substitution rates on mammalian phylogenies

2 October 2017

1 reference

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Identification of deleterious mutations within three human genomes

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Age-dependent penetrance of different germline mutations in the BRCA1 gene

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Multiple newly identified loci associated with prostate cancer susceptibility

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Breast cancer risk associated with BRCA1 and BRCA2 in diverse populations

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Improving sequence variant descriptions in mutation databases and literature using the Mutalyzer sequence variation nomenclature checker.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Estimates of the cancer incidence and mortality in Europe in 2006.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Assessing prostate cancer risk: results from the Prostate Cancer Prevention Trial

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Computational approaches for predicting the biological effect of p53 missense mutations: a comparison of three sequence analysis based methods

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Cancer Incidence in BRCA1 mutation carriers

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Contribution of BRCA1 and BRCA2 mutations to breast and ovarian cancer in Pakistan

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Variation in cancer risks, by mutation position, in BRCA2 mutation carriers

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

dbSNP: the NCBI database of genetic variation

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

The breast cancer information core: database design, structure, and scope

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Primer3 on the WWW for general users and for biologist programmers

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Cancer risks in BRCA2 mutation carriers

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

CpG methylation within the 5' regulatory region of the BRCA1 gene is tumor specific and includes a putative CREB binding site

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Familial prostate cancer: the evidence and the Cancer Research Campaign/British Prostate Group (CRC/BPG) UK Familial Prostate Cancer Study

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Founding BRCA1 mutations in hereditary breast and ovarian cancer in southern Sweden

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

dbNSFP: a lightweight database of human nonsynonymous SNPs and their functional predictions

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Heredity and prostate cancer: a study of World War II veteran twins

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

No germline mutations in the dimerization domain of MXI1 in prostate cancer clusters. The CRC/BPG UK Familial Prostate Cancer Study Collaborators. Cancer Research Campaign/British Prostate Group

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Genetic variants associated with predisposition to prostate cancer and potential clinical implications

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

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

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

BRCA1 and BRCA2 mutations in Danish families with hereditary breast and/or ovarian cancer.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

BRCA1 mutations and prostate cancer in Poland

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Prevalence of BRCA1 mutation carriers among U.S. non-Hispanic Whites.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

BRCA mutations and risk of prostate cancer in Ashkenazi Jews

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

A CREB site in the BRCA1 proximal promoter acts as a constitutive transcriptional element

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3349179

Heterogeneous prevalence of recurrent BRCA1 and BRCA2 mutations in Spain according to the geographical area: implications for genetic testing

24 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FBJC.2012.146

Functional analysis of CpG methylation in the BRCA1 promoter region

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22516946

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Studies of genetic factors in prostate cancer in a twin population

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22516946

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/BJC.2012.146

1 reference

11 August 2017

1 reference

11 August 2017

1 reference