Risk prediction of complex diseases from family history and known susceptibility loci, with applications for cancer screening

scientific article

Risk prediction of complex diseases from family history and known susceptibility loci, with applications for cancer screening is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/J.AJHG.2011.04.001
P8608Fatcat IDrelease_idax4okiczaotecxcpv2xdjr5q
P932PMC publication ID3146722
P698PubMed publication ID21529750
P5875ResearchGate publication ID51086075

P50authorStacey S. ChernyQ30505187
Hon-Cheong SoQ56884917
P2093author name stringPak C Sham
Johnny S H Kwan
P2860cites workPotential etiologic and functional implications of genome-wide association loci for human diseases and traitsQ22066284
Estimation of significance thresholds for genomewide association scansQ24289532
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 studiesQ24531993
Screening for breast cancer: an update for the U.S. Preventive Services Task ForceQ24615837
Screening for breast cancer: U.S. Preventive Services Task Force recommendation statementQ28265041
American Cancer Society guideline for the early detection of prostate cancer: update 2010Q28274848
Tamoxifen for prevention of breast cancer: report of the National Surgical Adjuvant Breast and Bowel Project P-1 StudyQ28283241
A HapMap harvest of insights into the genetics of common diseaseQ29614875
Screening and prostate-cancer mortality in a randomized European studyQ29617485
Number needed to screen: development of a statistic for disease screening.Q30454244
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 diseaseQ30665466
???Q26995732
Overcoming the winner's curse: estimating penetrance parameters from case-control dataQ31105516
Benefits and harms of prostate-specific antigen screening for prostate cancer: an evidence update for the U.S. Preventive Services Task ForceQ33357480
Weighing the risks and benefits of tamoxifen treatment for preventing breast cancerQ33765709
A unifying framework for evaluating the predictive power of genetic variants based on the level of heritability explainedQ33769562
Breast cancer susceptibility: current knowledge and implications for genetic counsellingQ34161642
Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2Q34384153
On criteria for evaluating models of absolute riskQ36072628
The BOADICEA model of genetic susceptibility to breast and ovarian cancerQ36695832
Hereditary breast cancer: from bench to bedside.Q37289132
Estimating risks of common complex diseases across genetic and environmental factors: the example of Crohn disease.Q37363244
Systematic review: comparative effectiveness of medications to reduce risk for primary breast cancerQ37634207
NCCN clinical practice guidelines in oncology: breast cancer screening and diagnosisQ37636597
Assessing women at high risk of breast cancer: a review of risk assessment modelsQ37739036
Family-based genetic risk prediction of multifactorial diseaseQ39325731
Use and misuse of the receiver operating characteristic curve in risk predictionQ40241086
Genetic susceptibility to breast cancerQ41130542
Recurrence risks for multifactorial inheritanceQ41551199
Gauging the performance of SNPs, biomarkers, and clinical factors for predicting risk of breast cancerQ42791172
Effect of age, breast density, and family history on the sensitivity of first screening mammographyQ45149178
Upward bias in odds ratio estimates from genome-wide association studiesQ46129490
Effect size measures in genetic association studies and age-conditional risk predictionQ47414840
Genetic analysis of durations: correlated frailty model applied to survival of Danish twins.Q50559114
A breast cancer prediction model incorporating familial and personal risk factors.Q52000310
Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseasesQ57233959
The emerging landscape of breast cancer susceptibilityQ57272203
Projecting individualized probabilities of developing breast cancer for white females who are being examined annuallyQ69396132
The multifactorial model for the inheritance of liability to disease and its implications for relatives at riskQ69407093
Multifactorial qualitative traits: genetic analysis and prediction of recurrence risksQ69737347
The inheritance of liability to diseases with variable age of onset, with particular reference to diabetes mellitusQ72304054
Autosomal dominant inheritance of early-onset breast cancer. Implications for risk predictionQ72752023
Risk estimation for healthy women from breast cancer families: new insights and new strategiesQ75337203
Polygenes, risk prediction, and targeted prevention of breast cancerQ81523323
Screening for prostate cancer: U.S. Preventive Services Task Force recommendation statementQ81740105
P433issue5
P407language of work or nameEnglishQ1860
P921main subjectsusceptibility locusQ62091149
P304page(s)548-565
P577publication date2011-04-28
P1433published inAmerican Journal of Human GeneticsQ4744249
P1476titleRisk prediction of complex diseases from family history and known susceptibility loci, with applications for cancer screening
P478volume88

Reverse relations

cites work (P2860)
Q37589578A scoring strategy combining statistics and functional genomics supports a possible role for common polygenic variation in autism
Q36055011Analysis of case-control association studies with known risk variants
Q21144905Comparison of family history and SNPs for predicting risk of complex disease
Q31064480Constructing Hypothetical Risk Data from the Area under the ROC Curve: Modelling Distributions of Polygenic Risk
Q90575699Cumulative evidence for relationships between multiple variants of HNF1B and the risk of prostate and endometrial cancers
Q37409157Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42,103 individuals
Q30251440Developing and evaluating polygenic risk prediction models for stratified disease prevention
Q28084601Do Health Professionals Need Additional Competencies for Stratified Cancer Prevention Based on Genetic Risk Profiling?
Q96576411Efficient polygenic risk scores for biobank scale data by exploiting phenotypes from inferred relatives
Q90929499Estimation of complex effect-size distributions using summary-level statistics from genome-wide association studies across 32 complex traits
Q36524374Explicit Modeling of Ancestry Improves Polygenic Risk Scores and BLUP Prediction
Q39033094Exploring the predictive power of polygenic scores derived from genome-wide association studies: a study of 10 complex traits
Q34943534Genetic and environmental components of family history in type 2 diabetes
Q27027720Genetic risk prediction in complex disease
Q47994728Improving Disease Prediction by Incorporating Family Disease History in Risk Prediction Models with Large-Scale Genetic Data
Q42145797Improving polygenic risk prediction from summary statistics by an empirical Bayes approach
Q37614763Incorporating genomics into breast and prostate cancer screening: assessing the implications
Q92095785Liability threshold modeling of case-control status and family history of disease increases association power
Q35899657Machine learning derived risk prediction of anorexia nervosa
Q48232613Multifactorial disease risk calculator: Risk prediction for multifactorial disease pedigrees
Q33896815Pitfalls of predicting complex traits from SNPs
Q30734382Polygenic risk and the development and course of asthma: an analysis of data from a four-decade longitudinal study
Q38798713Polygenic scores via penalized regression on summary statistics
Q39782065Predicting quantitative traits from genome and phenome with near perfect accuracy
Q36583004Prediction of breast cancer risk based on profiling with common genetic variants
Q41584352Prediction of individual genetic risk to prostate cancer using a polygenic score
Q37059182Projecting the performance of risk prediction based on polygenic analyses of genome-wide association studies
Q34434004Research review: Polygenic methods and their application to psychiatric traits
Q90175282The Maudsley environmental risk score for psychosis
Q37578078The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers
Q35547325The contribution of genetic variants to disease depends on the ruler
Q36339854Two-Variance-Component Model Improves Genetic Prediction in Family Datasets.
Q36255311Using Breast Cancer Risk Associated Polymorphisms to Identify Women for Breast Cancer Chemoprevention

Search more.