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A breast cancer prediction model incorporating familial and personal risk factors

Statistics in medicine, 2004-04, Vol.23 (7), p.1111-1130

2004

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The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the population

Human molecular genetics, 2014-09, Vol.23 (17), p.4703-4709

2014

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Folate Intake and Ovarian Cancer Risk among Women with Endometriosis: A Case-Control Study from the Ovarian Cancer Association Consortium

Cancer epidemiology, biomarkers & prevention, 2023-08, Vol.32 (8), p.1087-1096

2023

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Tunnelling with Full-Face Shielded Machines: A 3D Numerical Analysis of an Earth Pressure Balance (EPB) Excavation Sequence Using the Finite Element Method (FEM)

Geosciences (Basel), 2023-08, Vol.13 (8), p.244

2023

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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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Telomere length in prospective and retrospective cancer case-control studies

Cancer research (Chicago, Ill.), 2010-04, Vol.70 (8), p.3170-3176

2010

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The admixture maximum likelihood test to test for association between rare variants and disease phenotypes

BMC bioinformatics, 2013-06, Vol.14 (1), p.177-177, Article 177

2013

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Evidence of a genetic link between endometriosis and ovarian cancer

Fertility and sterility, 2016-01, Vol.105 (1), p.35-43.e10

2016

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Estimating the effect of treatment in a proportional hazards model in the presence of non-compliance and contamination

Journal of the Royal Statistical Society. Series B, Statistical methodology, 2007-09, Vol.69 (4), p.565-588

2007

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Evaluating the power to discriminate between highly correlated SNPs in genetic association studies

Genetic epidemiology, 2010-07, Vol.34 (5), p.463-468

2010

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Association between common variation in 120 candidate genes and breast cancer risk

PLoS genetics, 2007-03, Vol.3 (3), p.e42-e42

2007

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Common Polymorphisms in the Prostaglandin Pathway Genes and Their Association with Breast Cancer Susceptibility and Survival

Clinical cancer research, 2009-03, Vol.15 (6), p.2181-2191

2009

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ABO blood group and risk of epithelial ovarian cancer within the Ovarian Cancer Association Consortium

Cancer causes & control, 2012-11, Vol.23 (11), p.1805-1810

2012

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Association of single-nucleotide polymorphisms in the cell cycle genes with breast cancer in the British population

Carcinogenesis (New York), 2008-02, Vol.29 (2), p.333-341

2008

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Association between common germline genetic variation in 94 candidate genes or regions and risks of invasive epithelial ovarian cancer

PloS one, 2009-06, Vol.4 (6), p.e5983-e5983

2009

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Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

Nature genetics, 2018-07, Vol.50 (7), p.928-936

2018

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Common Single-Nucleotide Polymorphisms in DNA Double-Strand Break Repair Genes and Breast Cancer Risk

Cancer epidemiology, biomarkers & prevention, 2008-12, Vol.17 (12), p.3482-3489

2008

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Prediction of breast cancer risk based on profiling with common genetic variants

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

2015

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A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer

Nature genetics, 2014-10, Vol.46 (10), p.1103-1109

2014

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Detecting rare copy number variants from Illumina genotyping arrays with the CamCNV pipeline: Segmentation of z‐scores improves detection and reliability

Genetic epidemiology, 2021-04, Vol.45 (3), p.237-248

2021

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Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer

JNCI : Journal of the National Cancer Institute, 2015-11, Vol.107 (11), p.1

2015

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Tunnelling with Full-Face Shielded Machines: A 3D Numerical Analysis of an Earth Pressure Balance

Geosciences (Basel), 2023-08, Vol.13 (8)

2023

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Comprehensive epithelial tubo-ovarian cancer risk prediction model incorporating genetic and epidemiological risk factors

Journal of medical genetics, 2022-07, Vol.59 (7), p.632

2022

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A breast cancer prediction model incorporating familial and personal risk factors

The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the population

Folate Intake and Ovarian Cancer Risk among Women with Endometriosis: A Case-Control Study from the Ovarian Cancer Association Consortium

Tunnelling with Full-Face Shielded Machines: A 3D Numerical Analysis of an Earth Pressure Balance (EPB) Excavation Sequence Using the Finite Element Method (FEM)

A genome-wide association scan (GWAS) for mean telomere length within the COGS project: identified loci show little association with hormone-related cancer risk

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

Telomere length in prospective and retrospective cancer case-control studies

The admixture maximum likelihood test to test for association between rare variants and disease phenotypes

Evidence of a genetic link between endometriosis and ovarian cancer

Robust Tests for Additive Gene-Environment Interaction in Case-Control Studies Using Gene-Environment Independence

Estimating the effect of treatment in a proportional hazards model in the presence of non-compliance and contamination

Evaluating the power to discriminate between highly correlated SNPs in genetic association studies

Association between common variation in 120 candidate genes and breast cancer risk

Common Polymorphisms in the Prostaglandin Pathway Genes and Their Association with Breast Cancer Susceptibility and Survival

ABO blood group and risk of epithelial ovarian cancer within the Ovarian Cancer Association Consortium

Association of single-nucleotide polymorphisms in the cell cycle genes with breast cancer in the British population

Association between common germline genetic variation in 94 candidate genes or regions and risks of invasive epithelial ovarian cancer

Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

Common Single-Nucleotide Polymorphisms in DNA Double-Strand Break Repair Genes and Breast Cancer Risk

Prediction of breast cancer risk based on profiling with common genetic variants

A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer

Detecting rare copy number variants from Illumina genotyping arrays with the CamCNV pipeline: Segmentation of z‐scores improves detection and reliability

Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer

Tunnelling with Full-Face Shielded Machines: A 3D Numerical Analysis of an Earth Pressure Balance

Comprehensive epithelial tubo-ovarian cancer risk prediction model incorporating genetic and epidemiological risk factors

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