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Response to Dominguez-Valentin M et al. 2019: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Genetics in medicine, 2020-04, Vol.22 (4), p.811-812

2020

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Efficacy of tamoxifen based on cytochrome P450 2D6, CYP2C19 and SULT1A1 genotype in the Italian Tamoxifen Prevention Trial

The pharmacogenomics journal, 2011-04, Vol.11 (2), p.100-107

2011

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Large-scale genotyping identifies 41 new loci associated with breast cancer risk

Nature genetics, 2013-04, Vol.45 (4), p.353-361

2013

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Genome-wide association analysis identifies three new breast cancer susceptibility loci

Nature genetics, 2012-03, Vol.44 (3), p.312-318

2012

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Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

Genetics in medicine, 2021-04, Vol.23 (4), p.705-712

2021

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FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women

European journal of human genetics : EJHG, 2023-05, Vol.31 (5), p.578-587

2023

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The BRCA2 c.68‐7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity

Human mutation, 2018-05, Vol.39 (5), p.729-741

2018

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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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Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk

Human molecular genetics, 2015-01, Vol.24 (1), p.285-298

2015

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Genetic predisposition to in situ and invasive lobular carcinoma of the breast

PLoS genetics, 2014-04, Vol.10 (4), p.e1004285

2014

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Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers

Human genetics, 2011-11, Vol.130 (5), p.685-699

2011

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Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

Nature genetics, 2020-06, Vol.52 (6), p.572-581

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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Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

Human mutation, 2018-05, Vol.39 (5), p.593-620

2018

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Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

Nature genetics, 2017-05, Vol.49 (5), p.680-691

2017

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Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

Genetics in medicine, 2020-10, Vol.22 (10), p.1653-1666

2020

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Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

Nature genetics, 2020-01, Vol.52 (1), p.56-73

2020

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

Journal of medical genetics, 2016-12, Vol.53 (12), p.800-811

2016

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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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Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

Human mutation, 2019-09, Vol.40 (9), p.1557-1578

2019

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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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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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The role of genetic breast cancer susceptibility variants as prognostic factors

Human molecular genetics, 2012-09, Vol.21 (17), p.3926-3939

2012

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Polygenic risk modeling for prediction of epithelial ovarian cancer risk

European journal of human genetics : EJHG, 2022-03, Vol.30 (3), p.349-362

2022

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Functional Variants at the 11q13 Risk Locus for Breast Cancer Regulate Cyclin D1 Expression through Long-Range Enhancers

American journal of human genetics, 2013-04, Vol.92 (4), p.489-503

2013

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Response to Dominguez-Valentin M et al. 2019: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Efficacy of tamoxifen based on cytochrome P450 2D6, CYP2C19 and SULT1A1 genotype in the Italian Tamoxifen Prevention Trial

Large-scale genotyping identifies 41 new loci associated with breast cancer risk

Genome-wide association analysis identifies three new breast cancer susceptibility loci

Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women

The BRCA2 c.68‐7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity

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

Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk

Genetic predisposition to in situ and invasive lobular carcinoma of the breast

Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers

Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

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

Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

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

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

Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

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

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

The role of genetic breast cancer susceptibility variants as prognostic factors

Polygenic risk modeling for prediction of epithelial ovarian cancer risk

Functional Variants at the 11q13 Risk Locus for Breast Cancer Regulate Cyclin D1 Expression through Long-Range Enhancers

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