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The emerging landscape of breast cancer susceptibility
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instance of
scholarly article
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title
The emerging landscape of breast cancer susceptibility
(English)
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main subject
breast cancer
1 reference
based on heuristic
inferred from title
author
Nazneen Rahman
object named as
Nazneen Rahman
series ordinal
2
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Michael Stratton
series ordinal
1
object named as
Michael R Stratton
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language of work or name
English
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publication date
January 2008
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published in
Nature Genetics
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volume
40
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page(s)
17-22
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issue
1
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exact match
https://scigraph.springernature.com/pub.10.1038/ng.2007.53
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cites work
Breast cancer and breastfeeding: collaborative reanalysis of individual data from 47 epidemiological studies in 30 countries, including 50302 women with breast cancer and 96973 women without the disease
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
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inferred from DOI database lookup
High constant incidence in twins and other relatives of women with breast cancer.
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stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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inferred from DOI database lookup
Linkage of early-onset familial breast cancer to chromosome 17q21
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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inferred from DOI database lookup
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.
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https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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Identification of the breast cancer susceptibility gene BRCA2
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https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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inferred from DOI database lookup
Cancer Incidence in BRCA1 mutation carriers
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
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inferred from DOI database lookup
Cancer risks in BRCA2 mutation carriers
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
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inferred from DOI database lookup
Prevalence and penetrance of BRCA1 and BRCA2 mutations in a population-based series of breast cancer cases. Anglian Breast Cancer Study Group
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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The roles of BRCA1 and BRCA2 and associated proteins in the maintenance of genomic stability
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https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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The genetic epidemiology of breast cancer genes
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
based on heuristic
inferred from DOI database lookup
Models of genetic susceptibility to breast cancer
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https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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inferred from DOI database lookup
20q11.1 amplification in giant-cell tumor of bone: Array CGH, FISH, and association with outcome.
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https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations
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reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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inferred from DOI database lookup
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles
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reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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inferred from DOI database lookup
A recurrent mutation in PALB2 in Finnish cancer families.
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reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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Genome-wide association study identifies novel breast cancer susceptibility loci
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
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reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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inferred from DOI database lookup
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer
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reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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The Chk2 protein kinase
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https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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The ATM-mediated DNA-damage response: taking shape.
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reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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inferred from DOI database lookup
BACH1 is a DNA repair protein supporting BRCA1 damage response
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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inferred from DOI database lookup
CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies
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stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
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inferred from DOI database lookup
A single ataxia telangiectasia gene with a product similar to PI-3 kinase
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
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inferred from DOI database lookup
Cancer risks and mortality in heterozygous ATM mutation carriers
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Biallelic inactivation of BRCA2 in Fanconi anemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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inferred from DOI database lookup
Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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inferred from DOI database lookup
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J
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reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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inferred from DOI database lookup
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
based on heuristic
inferred from DOI database lookup
Fanconi anemia is associated with a defect in the BRCA2 partner PALB2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygosity for aCHEK2*1100delC mutation identified in familial colorectal cancer does not lead to a severe clinical phenotype
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
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inferred from DOI database lookup
Commonly studied single-nucleotide polymorphisms and breast cancer: results from the Breast Cancer Association Consortium
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
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inferred from DOI database lookup
A common coding variant in CASP8 is associated with breast cancer risk
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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inferred from DOI database lookup
A common variant associated with prostate cancer in European and African populations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
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inferred from DOI database lookup
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
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inferred from DOI database lookup
Multiple regions within 8q24 independently affect risk for prostate cancer
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A common genetic risk factor for colorectal and prostate cancer
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Patterns of somatic mutation in human cancer genomes
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
based on heuristic
inferred from DOI database lookup
Histopathology of BRCA1- and BRCA2-associated breast cancer.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evaluation ofRAD50 in familial breast cancer predisposition
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Polygenic susceptibility to breast cancer and implications for prevention
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
based on heuristic
inferred from DOI database lookup
Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
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7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical management of BRCA1 and BRCA2 mutation carriers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG.2007.53
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG.2007.53
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PubMed ID
18163131
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