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BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors

Genetics in medicine, 2019-08, Vol.21 (8), p.1708-1718

2019

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CanRisk Tool-A Web Interface for the Prediction of Breast and Ovarian Cancer Risk and the Likelihood of Carrying Genetic Pathogenic Variants

Cancer epidemiology, biomarkers & prevention, 2021-03, Vol.30 (3), p.469-473

2021

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Using human genetics to understand the disease impacts of testosterone in men and women

Nature medicine, 2020-02, Vol.26 (2), p.252-258

2020

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Germline BRCA mutation and outcome in young-onset breast cancer (POSH): a prospective cohort study

The lancet oncology, 2018-02, Vol.19 (2), p.169-180

2018

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Comprehensive functional annotation of 77 prostate cancer risk loci

PLoS genetics, 2014-01, Vol.10 (1), p.e1004102

2014

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Genome-wide association studies in common cancers—what have we learnt?

Current opinion in genetics & development, 2010-06, Vol.20 (3), p.201-209

2010

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The contribution of rare variation to prostate cancer heritability

Nature genetics, 2016-01, Vol.48 (1), p.30-35

2016

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A Systematic Genetic Assessment of 1,433 Sequence Variants of Unknown Clinical Significance in the BRCA1 and BRCA2 Breast Cancer–Predisposition Genes

American journal of human genetics, 2007-11, Vol.81 (5), p.873-883

2007

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Combined quantitative measures of ER, PR, HER2, and KI67 provide more prognostic information than categorical combinations in luminal breast cancer

Modern pathology, 2019-09, Vol.32 (9), p.1244-1256

2019

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Evaluating clinician acceptability of the prototype CanRisk tool for predicting risk of breast and ovarian cancer: A multi-methods study

PloS one, 2020-03, Vol.15 (3), p.e0229999

2020

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

Nature genetics, 2007-02, Vol.39 (2), p.165-167

2007

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The contributions of breast density and common genetic variation to breast cancer risk

JNCI : Journal of the National Cancer Institute, 2015-05, Vol.107 (5), p.1

2015

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

Nature genetics, 2006-11, Vol.38 (11), p.1239-1241

2006

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Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14

Nature genetics, 2013-06, Vol.45 (6), p.686-689

2013

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Evidence of a Causal Association Between Insulinemia and Endometrial Cancer: A Mendelian Randomization Analysis

JNCI : Journal of the National Cancer Institute, 2015-09, Vol.107 (9), p.1

2015

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A genome-wide association study of testicular germ cell tumor

Nature genetics, 2009-07, Vol.41 (7), p.807-810

2009

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Potential of polygenic risk scores for improving population estimates of women's breast cancer genetic risks

Genetics in medicine, 2021-11, Vol.23 (11), p.2114-2121

2021

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Inhibition of mTOR induces autophagy and reduces toxicity of polyglutamine expansions in fly and mouse models of Huntington disease

Nature genetics, 2004-06, Vol.36 (6), p.585-595

2004

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Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk

Nature communications, 2020-10, Vol.11 (1), p.5116-11, Article 5116

2020

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Cancer Risks and Mortality in Heterozygous ATM Mutation Carriers

JNCI : Journal of the National Cancer Institute, 2005-06, Vol.97 (11), p.813-822

2005

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Most common 'sporadic' cancers have a significant germline genetic component

Human molecular genetics, 2014-11, Vol.23 (22), p.6112-6118

2014

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Genomic risk prediction of coronary artery disease in women with breast cancer: a prospective cohort study

Breast cancer research : BCR, 2021-09, Vol.23 (1), p.94-11, Article 94

2021

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Letter to the editor: a response to Ming's study on machine learning techniques for personalized breast cancer risk prediction

Breast cancer research : BCR, 2020-02, Vol.22 (1), p.17-17, Article 17

2020

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Polygenic risk scores in cancer screening: a glass half full or half empty?

The lancet oncology, 2023-06, Vol.24 (6), p.579-581

2023

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Risk Factors for the Incidence of Breast Cancer: Do They Affect Survival From the Disease?

Journal of clinical oncology, 2008-07, Vol.26 (20), p.3310-3316

2008

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BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors

CanRisk Tool-A Web Interface for the Prediction of Breast and Ovarian Cancer Risk and the Likelihood of Carrying Genetic Pathogenic Variants

Using human genetics to understand the disease impacts of testosterone in men and women

Germline BRCA mutation and outcome in young-onset breast cancer (POSH): a prospective cohort study

Comprehensive functional annotation of 77 prostate cancer risk loci

Genome-wide association studies in common cancers—what have we learnt?

The contribution of rare variation to prostate cancer heritability

A Systematic Genetic Assessment of 1,433 Sequence Variants of Unknown Clinical Significance in the BRCA1 and BRCA2 Breast Cancer–Predisposition Genes

Combined quantitative measures of ER, PR, HER2, and KI67 provide more prognostic information than categorical combinations in luminal breast cancer

Evaluating clinician acceptability of the prototype CanRisk tool for predicting risk of breast and ovarian cancer: A multi-methods study

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

The contributions of breast density and common genetic variation to breast cancer risk

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

Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14

Evidence of a Causal Association Between Insulinemia and Endometrial Cancer: A Mendelian Randomization Analysis

A genome-wide association study of testicular germ cell tumor

Potential of polygenic risk scores for improving population estimates of women's breast cancer genetic risks

Inhibition of mTOR induces autophagy and reduces toxicity of polyglutamine expansions in fly and mouse models of Huntington disease

Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk

Cancer Risks and Mortality in Heterozygous ATM Mutation Carriers

Most common 'sporadic' cancers have a significant germline genetic component

Genomic risk prediction of coronary artery disease in women with breast cancer: a prospective cohort study

Letter to the editor: a response to Ming's study on machine learning techniques for personalized breast cancer risk prediction

Polygenic risk scores in cancer screening: a glass half full or half empty?

Risk Factors for the Incidence of Breast Cancer: Do They Affect Survival From the Disease?

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