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BOADICEA breast cancer risk prediction model: updates to cancer incidences, tumour pathology and web interface

British journal of cancer, 2014-01, Vol.110 (2), p.535-545

2014

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The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriers

Breast cancer research and treatment, 2012-04, Vol.132 (3), p.1119-1126

2012

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The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers

Cancer epidemiology, biomarkers & prevention, 2017-01, Vol.26 (1), p.126-135

2017

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Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers

JAMA : the journal of the American Medical Association, 2017-06, Vol.317 (23), p.2402

2017

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Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study

Molecular psychiatry, 2021-09, Vol.26 (9), p.5307-5319

2021

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Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

Nature communications, 2020-01, Vol.11 (1), p.163-12, Article 163

2020

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Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Nature genetics, 2017-12, Vol.49 (12), p.1767-1778

2017

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Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers

JNCI : Journal of the National Cancer Institute, 2017-07, Vol.109 (7)

2017

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Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

Nature genetics, 2013-04, Vol.45 (4), p.371-384

2013

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Identification of six new susceptibility loci for invasive epithelial ovarian cancer

Nature genetics, 2015-02, Vol.47 (2), p.164-171

2015

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Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170

Nature genetics, 2016-04, Vol.48 (4), p.374-386

2016

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Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

PLoS genetics, 2013, Vol.9 (3), p.e1003212-e1003212

2013

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Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference

Nature genetics, 2024-02, Vol.56 (2), p.222-233

2024

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The genomics of heart failure: design and rationale of the HERMES consortium

ESC Heart Failure, 2021-12, Vol.8 (6), p.5531-5541

2021

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Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk

PLoS genetics, 2013-03, Vol.9 (3), p.e1003173-e1003173

2013

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Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

Genome medicine, 2023-01, Vol.15 (1), p.7-18, Article 7

2023

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Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

Breast cancer research : BCR, 2012-02, Vol.14 (1), p.R33-R33

2012

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Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

Breast cancer research : BCR, 2016-06, Vol.18 (1), p.64, Article 64

2016

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Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers

PloS one, 2015-04, Vol.10 (4), p.e0120020

2015

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Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

Breast cancer research : BCR, 2014-12, Vol.16 (6), p.3416-3416, Article 3416

2014

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Publisher Correction: Shared heritability and functional enrichment across six solid cancers

Nature communications, 2019-09, Vol.10 (1), p.4386-8, Article 4386

2019

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DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers

PLoS genetics, 2014-04, Vol.10 (4), p.e1004256

2014

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Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

Cancer epidemiology, biomarkers & prevention, 2015-01, Vol.24 (1), p.308-316

2015

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BOADICEA breast cancer risk prediction model: updates to cancer incidences, tumour pathology and web interface

The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriers

The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers

Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations

Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers

The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study

Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study

Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170

Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference

The genomics of heart failure: design and rationale of the HERMES consortium

Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk

Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers

Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

Publisher Correction: Shared heritability and functional enrichment across six solid cancers

DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers

Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

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