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A case–control evaluation of 143 single nucleotide polymorphisms for breast cancer risk stratification with classical factors and mammographic density

International journal of cancer, 2020-04, Vol.146 (8), p.2122-2129

2020

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The importance of ethnicity: Are breast cancer polygenic risk scores ready for women who are not of White European origin?

International journal of cancer, 2022-01, Vol.150 (1), p.73-79

2022

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A Dominantly Inherited 5′ UTR Variant Causing Methylation-Associated Silencing of BRCA1 as a Cause of Breast and Ovarian Cancer

American journal of human genetics, 2018-08, Vol.103 (2), p.213-220

2018

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Breast cancer incidence and early diagnosis in a family history risk and prevention clinic: 33-year experience in 14,311 women

Breast cancer research and treatment, 2021-10, Vol.189 (3), p.677-687

2021

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Use of Single-Nucleotide Polymorphisms and Mammographic Density Plus Classic Risk Factors for Breast Cancer Risk Prediction

JAMA oncology, 2018-04, Vol.4 (4), p.476

2018

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Dominant‐negative pathogenic variant BRIP1 c.1045G>C is a high‐risk allele for non‐mucinous epithelial ovarian cancer: A case‐control study

Clinical genetics, 2022-01, Vol.101 (1), p.48-54

2022

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Clinical utility of testing for PALB2 and CHEK2 c.1100delC in breast and ovarian cancer

Genetics in medicine, 2021-10, Vol.23 (10), p.1969-1976

2021

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Extended gene panel testing in lobular breast cancer

Familial cancer, 2022-04, Vol.21 (2), p.129-136

2022

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Barrett associated MHC and FOXF1 variants also increase esophageal carcinoma risk

International journal of cancer, 2013-10, Vol.133 (7), p.1751-1755

2013

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Gene Panel Testing for Breast Cancer Reveals Differential Effect of Prior BRCA1/2 Probability

Cancers, 2021-08, Vol.13 (16), p.4154

2021

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A Novel Automated Approach to Mutation-Cancer Relation Extraction by Incorporating Heterogeneous Knowledge

IEEE journal of biomedical and health informatics, 2023-02, Vol.27 (2), p.1096-1105

2023

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Polymorphisms in alcohol-metabolizing enzymes and esophageal carcinoma susceptibility: a Dutch Caucasian case-control study

Journal of human genetics, 2013-11, Vol.58 (11), p.742-748

2013

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Breast cancer pathology and stage are better predicted by risk stratification models that include mammographic density and common genetic variants

Breast cancer research and treatment, 2019-07, Vol.176 (1), p.141-148

2019

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Breast cancer risk stratification in women of screening age: Incremental effects of adding mammographic density, polygenic risk, and a gene panel

Genetics in medicine, 2022-07, Vol.24 (7), p.1485-1494

2022

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Constitutional de novo deletion CNV encompassing REST predisposes to diffuse hyperplastic perilobar nephroblastomatosis (HPLN)

Journal of medical genetics, 2021-09, Vol.58 (9), p.581

2021

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Sensitivity of BRCA1/2 testing in high-risk breast/ovarian/male breast cancer families: little contribution of comprehensive RNA/NGS panel testing

European journal of human genetics : EJHG, 2016-11, Vol.24 (11), p.1591-1597

2016

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EPICURE: Ensemble Pretrained Models for Extracting Cancer Mutations from Literature

2021 IEEE 34th International Symposium on Computer-Based Medical Systems (CBMS), 2021, p.461-467

2021

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IEEE_Xplore

Transmission of molecularly undetectable circulating parasite clones leads to high infection complexity in mosquitoes post feeding

International journal for parasitology, 2018-07, Vol.48 (8), p.671-677

2018

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Heritability of mammographic breast density

Quantitative imaging in medicine and surgery, 2020-12, Vol.10 (12), p.2387-2391

2020

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Sa1980 Barrett Associated MHC and FOXF1 Genotypes Also Increase Esophageal Carcinoma Risk in Caucasians: A Dutch Case-Control Study

Gastroenterology (New York, N.Y. 1943), 2013-05, Vol.144 (5), p.S-350-S-350

2013

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Prospective evaluation of a breast-cancer risk model integrating classical risk factors and polygenic risk in 15 cohorts from six countries

International journal of epidemiology, 2022-01, Vol.50 (6), p.1897-1911

2022

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Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk

JNCI : Journal of the National Cancer Institute, 2021-03, Vol.113 (3), p.329-337

2021

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Dominant‐negative pathogenic variant BRIP1 c. 1045G >C is a high‐risk allele for non‐mucinous epithelial ovarian cancer: A case‐control study

Clinical genetics, 2022-01, Vol.101 (1), p.48-54

2022

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Prospective evaluation of a breast-cancer risk model integrating classical risk factors and polygenic risk in 15 cohorts from six countries

International journal of epidemiology, 2022-01, Vol.50 (6), p.1897-1911

2022

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Two truncating variants in FANCC and breast cancer risk

Scientific reports, 2019-08, Vol.9 (1), p.12524-14, Article 12524

2019

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A case–control evaluation of 143 single nucleotide polymorphisms for breast cancer risk stratification with classical factors and mammographic density

The importance of ethnicity: Are breast cancer polygenic risk scores ready for women who are not of White European origin?

A Dominantly Inherited 5′ UTR Variant Causing Methylation-Associated Silencing of BRCA1 as a Cause of Breast and Ovarian Cancer

Breast cancer incidence and early diagnosis in a family history risk and prevention clinic: 33-year experience in 14,311 women

Use of Single-Nucleotide Polymorphisms and Mammographic Density Plus Classic Risk Factors for Breast Cancer Risk Prediction

Dominant‐negative pathogenic variant BRIP1 c.1045G>C is a high‐risk allele for non‐mucinous epithelial ovarian cancer: A case‐control study

Clinical utility of testing for PALB2 and CHEK2 c.1100delC in breast and ovarian cancer

Extended gene panel testing in lobular breast cancer

Barrett associated MHC and FOXF1 variants also increase esophageal carcinoma risk

Gene Panel Testing for Breast Cancer Reveals Differential Effect of Prior BRCA1/2 Probability

A Novel Automated Approach to Mutation-Cancer Relation Extraction by Incorporating Heterogeneous Knowledge

Polymorphisms in alcohol-metabolizing enzymes and esophageal carcinoma susceptibility: a Dutch Caucasian case-control study

Breast cancer pathology and stage are better predicted by risk stratification models that include mammographic density and common genetic variants

Breast cancer risk stratification in women of screening age: Incremental effects of adding mammographic density, polygenic risk, and a gene panel

Constitutional de novo deletion CNV encompassing REST predisposes to diffuse hyperplastic perilobar nephroblastomatosis (HPLN)

Sensitivity of BRCA1/2 testing in high-risk breast/ovarian/male breast cancer families: little contribution of comprehensive RNA/NGS panel testing

EPICURE: Ensemble Pretrained Models for Extracting Cancer Mutations from Literature

Transmission of molecularly undetectable circulating parasite clones leads to high infection complexity in mosquitoes post feeding

Heritability of mammographic breast density

Sa1980 Barrett Associated MHC and FOXF1 Genotypes Also Increase Esophageal Carcinoma Risk in Caucasians: A Dutch Case-Control Study

Prospective evaluation of a breast-cancer risk model integrating classical risk factors and polygenic risk in 15 cohorts from six countries

Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk

Dominant‐negative pathogenic variant BRIP1 c. 1045G >C is a high‐risk allele for non‐mucinous epithelial ovarian cancer: A case‐control study

Prospective evaluation of a breast-cancer risk model integrating classical risk factors and polygenic risk in 15 cohorts from six countries

Two truncating variants in FANCC and breast cancer risk

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