Design and analysis issues in a population-based, case-control-family study of the genetic epidemiology of breast cancer and the Co-operative Family Registry for Breast Cancer Studies (CFRBCS).
about
Genomewide scans of complex human diseases: true linkage is hard to findAfter BRCA1 and BRCA2-what next? Multifactorial segregation analyses of three-generation, population-based Australian families affected by female breast cancer.The androgen receptor CAG repeat polymorphism and modification of breast cancer risk in BRCA1 and BRCA2 mutation carriersNo evidence for association of ataxia-telangiectasia mutated gene T2119C and C3161G amino acid substitution variants with risk of breast cancerLog odds of carrying an Ancestral Mutation in BRCA1 or BRCA2 for a Defined personal and family history in an Ashkenazi Jewish woman (LAMBDA)The intronic G13964C variant in p53 is not a high-risk mutation in familial breast cancer in AustraliaThe AIB1 glutamine repeat polymorphism is not associated with risk of breast cancer before age 40 years in Australian womenSpouses and unrelated friends of probands as controls for stroke genetics studiesAlcohol, tobacco and breast cancer--collaborative reanalysis of individual data from 53 epidemiological studies, including 58,515 women with breast cancer and 95,067 women without the diseasePopulation-based, case-control-family design to investigate genetic and environmental influences on melanoma risk: Australian Melanoma Family StudyUsing SNP genotypes to improve the discrimination of a simple breast cancer risk prediction modelCHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies.Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource.A PALB2 mutation associated with high risk of breast cancer.Novel Associations between Common Breast Cancer Susceptibility Variants and Risk-Predicting Mammographic Density MeasuresAdvances in breast cancer: pathways to personalized medicineClinical and pathological features of BRCA1/2 tumors in a sample of high-risk Moroccan breast cancer patients.Unconditional analyses can increase efficiency in assessing gene-environment interaction of the case-combined-control design.BRCA1 promoter deletions in young women with breast cancer and a strong family history: a population-based studyRisk factors for breast cancer in young women by oestrogen receptor and progesterone receptor status.Cytomegalovirus, Epstein-Barr virus and risk of breast cancer before age 40 years: a case-control study.Tumour morphology of early-onset breast cancers predicts breast cancer risk for first-degree relatives: the Australian Breast Cancer Family Registry.Prospective validation of the breast cancer risk prediction model BOADICEA and a batch-mode version BOADICEACentre.A genome wide linkage search for breast cancer susceptibility genes.Family history and risk of breast cancer: an analysis accounting for family structureGenetic, functional, and histopathological evaluation of two C-terminal BRCA1 missense variants.
P2860
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P2860
Design and analysis issues in a population-based, case-control-family study of the genetic epidemiology of breast cancer and the Co-operative Family Registry for Breast Cancer Studies (CFRBCS).
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh
1999年學術文章
@zh-hant
name
Design and analysis issues in ...... reast Cancer Studies (CFRBCS).
@en
type
label
Design and analysis issues in ...... reast Cancer Studies (CFRBCS).
@en
prefLabel
Design and analysis issues in ...... reast Cancer Studies (CFRBCS).
@en
P2093
P50
P1476
Design and analysis issues in ...... Breast Cancer Studies (CFRBCS)
@en
P2093
D J Jolley
D J Venter
M A Jenkins
M R McCredie
P304
P356
10.1093/OXFORDJOURNALS.JNCIMONOGRAPHS.A024232
P577
1999-01-01T00:00:00Z