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Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization

JNCI : Journal of the National Cancer Institute, 2015-11, Vol.107 (11), p.djv219

2015

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Nonsense mutation p.Q548X in BLM, the gene mutated in Bloom’s syndrome, is associated with breast cancer in Slavic populations

Breast cancer research and treatment, 2013-01, Vol.137 (2), p.533-539

2013

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Analysis of a RECQL splicing mutation, c.1667_1667+3delAGTA, in breast cancer patients and controls from Central Europe

Familial cancer, 2017-04, Vol.16 (2), p.181-186

2017

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Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK21100delC Carriers

Journal of clinical oncology, 2016-08, Vol.34 (23), p.2750-2760

2016

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Cell-type-specific enrichment of risk-associated regulatory elements at ovarian cancer susceptibility loci

Human molecular genetics, 2015-07, Vol.24 (13), p.3595-3607

2015

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Spectrum and Frequency of Germline IFANCM/I Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases

Cancers, 2023-06, Vol.15 (13)

2023

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Assessment of an APOBEC3B truncating mutation, c.783delG, in patients with breast cancer

Breast cancer research and treatment, 2017-02, Vol.162 (1), p.31-37

2017

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Prevalence of PALB2 mutation c.509_510delGA in unselected breast cancer patients from Central and Eastern Europe

Familial cancer, 2014-06, Vol.13 (2), p.137-142

2014

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Mutation analysis of the SLX4/FANCP gene in hereditary breast cancer

Breast cancer research and treatment, 2011-12, Vol.130 (3), p.1021-1028

2011

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Risk of Estrogen Receptor–Positive and –Negative Breast Cancer and Single–Nucleotide Polymorphism 2q35-rs13387042

JNCI : Journal of the National Cancer Institute, 2009-07, Vol.101 (14), p.1012-1018

2009

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Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases

Cancers, 2023, Vol.15 (13), p.3313

2023

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Mutation Analysis of the ERCC4/FANCQ Gene in Hereditary Breast Cancer: e85334

PloS one, 2014-01, Vol.9 (1)

2014

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Genome-wide association study for ovarian cancer susceptibility using pooled DNA

Twin research and human genetics, 2012-10, Vol.15 (5), p.615-623

2012

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Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci

JNCI : Journal of the National Cancer Institute, 2022-11, Vol.114 (11), p.1533-1544

2022

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nonsense mutation (E1978X) in the ATM gene is associated with breast cancer

Breast cancer research and treatment, 2009-11, Vol.118 (1), p.207-211

2009

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A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium

Human molecular genetics, 2014-04, Vol.23 (7), p.1934-1946

2014

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Missense Variants in ATM in 26,101 Breast Cancer Cases and 29,842 Controls

Cancer epidemiology, biomarkers & prevention, 2010-09, Vol.19 (9), p.2143-2151

2010

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A nonsense mutation (E1978X) in the ATM gene is associated with breast cancer

Breast cancer research and treatment, 2009, Vol.118 (1), p.207-211

2009

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A nonsense mutation (E1978X) in the gene is associated with breast cancer

Breast cancer research and treatment, 2008-09, Vol.118 (1), p.207-211

2008

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Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization

Nonsense mutation p.Q548X in BLM, the gene mutated in Bloom’s syndrome, is associated with breast cancer in Slavic populations

Analysis of a RECQL splicing mutation, c.1667_1667+3delAGTA, in breast cancer patients and controls from Central Europe

Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK21100delC Carriers

Cell-type-specific enrichment of risk-associated regulatory elements at ovarian cancer susceptibility loci

Spectrum and Frequency of Germline IFANCM/I Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases

Assessment of an APOBEC3B truncating mutation, c.783delG, in patients with breast cancer

Prevalence of PALB2 mutation c.509_510delGA in unselected breast cancer patients from Central and Eastern Europe

Mutation analysis of the SLX4/FANCP gene in hereditary breast cancer

Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe

Risk of Estrogen Receptor–Positive and –Negative Breast Cancer and Single–Nucleotide Polymorphism 2q35-rs13387042

Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases

Mutation Analysis of the ERCC4/FANCQ Gene in Hereditary Breast Cancer: e85334

Genome-wide association study for ovarian cancer susceptibility using pooled DNA

Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci

nonsense mutation (E1978X) in the ATM gene is associated with breast cancer

A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium

Missense Variants in ATM in 26,101 Breast Cancer Cases and 29,842 Controls

A nonsense mutation (E1978X) in the ATM gene is associated with breast cancer

A nonsense mutation (E1978X) in the gene is associated with breast cancer

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