(Q36787357)

16 August 2017

7 references

1 August 2019

28 September 2019

10 December 2019

11 December 2019

18 December 2019

19 December 2019

23 July 2020

Are the so-called low penetrance breast cancer genes, ATM, BRIP1, PALB2 and CHEK2, high risk for women with strong family histories? (English)

1 reference

RNA nucleotidyltransferases

16 August 2017

1 reference

1 August 2019

1 reference

28 September 2019

1 reference

10 December 2019

1 reference

11 December 2019

1 reference

18 December 2019

1 reference

19 December 2019

genetic predisposition to disease

1 reference

23 July 2020

Melissa C Southey

2

0 references

Graham Byrnes

object named as

Graham B Byrnes

series ordinal

1

0 references

John Hopper

series ordinal

3

object named as

John L Hopper

1 reference

16 August 2017

5 June 2008

8 references

16 August 2017

1 August 2019

28 September 2019

10 December 2019

11 December 2019

18 December 2019

19 December 2019

23 July 2020

Breast Cancer Research

9 references

16 August 2017

1 August 2019

28 September 2019

10 December 2019

11 December 2019

18 December 2019

19 December 2019

23 July 2020

10 September 2020

10

1 reference

16 August 2017

3

1 reference

16 August 2017

208

1 reference

https://scigraph.springernature.com/pub.10.1186/bcr2099

16 August 2017

0 references

cites work

Penetrance analysis of the PALB2 c.1592delT founder mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481495

Identification of a novel truncating PALB2 mutation and analysis of its contribution to early-onset breast cancer in French-Canadian women

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481495

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal 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=2481495

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=2481495

Analysis of PALB2/FANCN-associated breast cancer families

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481495

PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481495

Phenocopies in BRCA1 and BRCA2 families: evidence for modifier genes and implications for screening

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481495

ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481495

Population-based family studies in genetic epidemiology

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481495

CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 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=2481495

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=2481495

Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481495

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481495

Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58,209 women with breast cancer and 101,986 women without the disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481495

Family history and the risk of breast cancer: a systematic review and meta-analysis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481495

Modelling the Influence of Risk Factors on Familial Aggregation of Disease

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481495

Familial aggregation of a disease consequent upon correlation between relatives in a risk factor measured on a continuous scale

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481495

A recurrent mutation in PALB2 in Finnish cancer families.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481495

Population-based estimates of breast cancer risks associated with ATM gene variants c.7271T>G and c.1066-6T>G (IVS10-6T>G) from the Breast Cancer Family Registry

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2481495

Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles

5 September 2018

1 reference

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

21 January 2018

1 reference

Familial Risks, Early-Onset Breast Cancer, and BRCA1 and BRCA2 Germline Mutations

21 January 2018

1 reference

A protein-truncating mutation inCYP17A1 in three sisters with early-onset breast cancer

21 January 2018

1 reference

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

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18557994

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Polygenic susceptibility to breast cancer and implications for prevention

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18557994

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18557994

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/BCR2099

1 reference

PMC publication ID

2481495

Dimensions Publication ID

16 August 2017

0 references

1 reference

PMC publication ID

2481495

16 August 2017

PubMed publication ID

18557994

1 reference

PMC publication ID

2481495