Lista de obras - James G. Dowty - Dominio Público Uruguay

A PALB2 mutation associated with high risk of breast cancer

artículo científico publicado en 2010

Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers?

artículo científico publicado en 2013

Body mass index in early adulthood and colorectal cancer risk for carriers and non-carriers of germline mutations in DNA mismatch repair genes

artículo científico publicado en 2011

Body mass index in early adulthood and endometrial cancer risk for mismatch repair gene mutation carriers

artículo científico publicado en 2011

Breast Cancer Risk Prediction Using Clinical Models and 77 Independent Risk-Associated SNPs for Women Aged Under 50 Years: Australian Breast Cancer Family Registry

artículo científico publicado en 2015

Cancer Risks For Mismatch Repair Gene Mutation Carriers: A Population-Based Early Onset Case-Family Study

article

Cancer risk in 680,000 people exposed to computed tomography scans in childhood or adolescence: data linkage study of 11 million Australians

artículo científico publicado en 2013

Cancer risks for MLH1 and MSH2 mutation carriers

artículo científico publicado en 2013

Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer

artículo científico publicado en 2011

Cohort Profile: The Tasmanian Longitudinal Health STUDY (TAHS).

artículo científico publicado en 2016

Constitutional methylation of the BRCA1 promoter is specifically associated with BRCA1 mutation-associated pathology in early-onset breast cancer

artículo científico publicado en 2010

Criteria and prediction models for mismatch repair gene mutations: a review.

artículo científico

Dependence of colorectal cancer risk on the parent-of-origin of mutations in DNA mismatch repair genes

artículo científico publicado en 2011

Do the risks of Lynch syndrome-related cancers depend on the parent of origin of the mutation?

artículo científico publicado en 2020

Estimating risks for variants of unknown significance according to their predicted pathogenicity classes with application to BRCA1.

artículo científico publicado en 2014

Genome-Wide Measures of Peripheral Blood Dna Methylation and Prostate Cancer Risk in a Prospective Nested Case-Control Study

artículo científico publicado en 2017

Genome-wide DNA methylation assessment of ‘BRCA1-like’ early-onset breast cancer: Data from the Australian Breast Cancer Family Registry

article

Heritable DNA methylation marks associated with susceptibility to breast cancer

artículo científico publicado en 2018

Letter in response to “Identifying Lynch syndrome” by de la Chapelle et al

artículo científico publicado en 2010

Mammographic density defined by higher than conventional brightness thresholds better predicts breast cancer risk

artículo científico publicado en 2016

Melanoma risk for CDKN2A mutation carriers who are relatives of population-based case carriers in Australia and the UK

article

Molecular screening of all colorectal tumors diagnosed before age 50 years followed by genetic testing efficiently identifies Lynch syndrome cases

article

Morphological predictors of BRCA1 germline mutations in young women with breast cancer.

artículo científico publicado en 2011

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

artículo científico publicado en 2016

Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study

artículo científico publicado en 2007

Penetrance analysis of the PALB2 c.1592delT founder mutation

artículo científico publicado en 2008

Population-based estimate of prostate cancer risk for carriers of the HOXB13 missense mutation G84E.

artículo científico publicado en 2013

Predicting BRCA1 and BRCA2 gene mutation carriers: comparison of LAMBDA, BRCAPRO, Myriad II, and modified Couch models

artículo científico publicado en 2007

Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer

artículo científico publicado en 2016

Prevalence of PALB2 mutations in Australasian multiple-case breast cancer families

artículo científico publicado en 2013

Prospective validation of the breast cancer risk prediction model BOADICEA and a batch-mode version BOADICEACentre

artículo científico publicado en 2013

Publication policy or publication bias?

artículo científico publicado en 2005

Rare variants in the ATM gene and risk of breast cancer

artículo científico publicado en 2011

Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer

artículo científico publicado en 2014

Risks of Lynch syndrome cancers for MSH6 mutation carriers

artículo científico publicado en 2009

Role of tumour molecular and pathology features to estimate colorectal cancer risk for first-degree relatives

artículo científico publicado en 2014

Short-term risk of colorectal cancer in individuals with lynch syndrome: a meta-analysis.

artículo científico publicado en 2014

Testing for Gene-Environment Interactions Using a Prospective Family Cohort Design: Body Mass Index in Early and Later Adulthood and Risk of Breast Cancer.

artículo científico publicado en 2017

The Impact of a Comprehensive Risk Prediction Model for Colorectal Cancer on a Population Screening Program

artículo científico publicado en 2020

The RAD51D E233G variant and breast cancer risk: population-based and clinic-based family studies of Australian women

article

The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations

artículo científico publicado en 2008

The time-evolution of DCIS size distributions with applications to breast cancer growth and progression

artículo científico publicado en 2013

Towards more effective and equitable genetic testing for BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2008

Tumour morphology predicts PALB2 germline mutation status

artículo científico publicado en 2013

Using SNP genotypes to improve the discrimination of a simple breast cancer risk prediction model

artículo científico publicado en 2013

Using tumour pathology to identify people at high genetic risk of breast and colorectal cancers.

artículo científico publicado en 2012

Validation study of thelambdamodel for predicting theBRCA1orBRCA2mutation carrier status of North American Ashkenazi Jewish women

article

Lista de obras de James G. Dowty

A PALB2 mutation associated with high risk of breast cancer

Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers?

Body mass index in early adulthood and colorectal cancer risk for carriers and non-carriers of germline mutations in DNA mismatch repair genes

Body mass index in early adulthood and endometrial cancer risk for mismatch repair gene mutation carriers

Breast Cancer Risk Prediction Using Clinical Models and 77 Independent Risk-Associated SNPs for Women Aged Under 50 Years: Australian Breast Cancer Family Registry

Cancer Risks For Mismatch Repair Gene Mutation Carriers: A Population-Based Early Onset Case-Family Study

Cancer risk in 680,000 people exposed to computed tomography scans in childhood or adolescence: data linkage study of 11 million Australians

Cancer risks for MLH1 and MSH2 mutation carriers

Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer

Cohort Profile: The Tasmanian Longitudinal Health STUDY (TAHS).

Constitutional methylation of the BRCA1 promoter is specifically associated with BRCA1 mutation-associated pathology in early-onset breast cancer

Criteria and prediction models for mismatch repair gene mutations: a review.

Dependence of colorectal cancer risk on the parent-of-origin of mutations in DNA mismatch repair genes

Do the risks of Lynch syndrome-related cancers depend on the parent of origin of the mutation?

Estimating risks for variants of unknown significance according to their predicted pathogenicity classes with application to BRCA1.

Genome-Wide Measures of Peripheral Blood Dna Methylation and Prostate Cancer Risk in a Prospective Nested Case-Control Study

Genome-wide DNA methylation assessment of ‘BRCA1-like’ early-onset breast cancer: Data from the Australian Breast Cancer Family Registry

Heritable DNA methylation marks associated with susceptibility to breast cancer

Letter in response to “Identifying Lynch syndrome” by de la Chapelle et al

Mammographic density defined by higher than conventional brightness thresholds better predicts breast cancer risk

Melanoma risk for CDKN2A mutation carriers who are relatives of population-based case carriers in Australia and the UK

Molecular screening of all colorectal tumors diagnosed before age 50 years followed by genetic testing efficiently identifies Lynch syndrome cases

Morphological predictors of BRCA1 germline mutations in young women with breast cancer.

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study

Penetrance analysis of the PALB2 c.1592delT founder mutation

Population-based estimate of prostate cancer risk for carriers of the HOXB13 missense mutation G84E.

Predicting BRCA1 and BRCA2 gene mutation carriers: comparison of LAMBDA, BRCAPRO, Myriad II, and modified Couch models

Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer

Prevalence of PALB2 mutations in Australasian multiple-case breast cancer families

Prospective validation of the breast cancer risk prediction model BOADICEA and a batch-mode version BOADICEACentre

Publication policy or publication bias?

Rare variants in the ATM gene and risk of breast cancer

Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer

Risks of Lynch syndrome cancers for MSH6 mutation carriers

Role of tumour molecular and pathology features to estimate colorectal cancer risk for first-degree relatives

Short-term risk of colorectal cancer in individuals with lynch syndrome: a meta-analysis.

Testing for Gene-Environment Interactions Using a Prospective Family Cohort Design: Body Mass Index in Early and Later Adulthood and Risk of Breast Cancer.

The Impact of a Comprehensive Risk Prediction Model for Colorectal Cancer on a Population Screening Program

The RAD51D E233G variant and breast cancer risk: population-based and clinic-based family studies of Australian women

The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations

The time-evolution of DCIS size distributions with applications to breast cancer growth and progression

Towards more effective and equitable genetic testing for BRCA1 and BRCA2 mutation carriers

Tumour morphology predicts PALB2 germline mutation status

Using SNP genotypes to improve the discrimination of a simple breast cancer risk prediction model

Using tumour pathology to identify people at high genetic risk of breast and colorectal cancers.

Validation study of thelambdamodel for predicting theBRCA1orBRCA2mutation carrier status of North American Ashkenazi Jewish women