Christi J. van Asperen · researcher, ORCID id # 0000-0002-1436-7650 · YYNN

Christi J. van Asperen

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researcher, ORCID id # 0000-0002-1436-7650

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Works
8

Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-BRCA1/2 breast cancer families

scientific article published on 11 June 2019

Clustering of known low and moderate risk alleles rather than a novel recessive high-risk gene in non-BRCA1/2 sib trios affected with breast cancer

scientific article published on 07 May 2020

Homozygosity for aCHEK2*1100delC mutation identified in familial colorectal cancer does not lead to a severe clinical phenotype

scientific article published on 01 June 2005

Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics

scientific article

Intronic variants in BRCA1 and BRCA2 that affect RNA splicing can be reliably selected by splice-site prediction programs

scientific article published on 01 January 2009

The CHEK2*1100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families

scientific article published on 01 December 2003

Breast Cancer Susceptibility—Towards Individualised Risk Prediction

scholarly article

The functional impact of variants of uncertain significance in BRCA2

scientific article published on 10 July 2018

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university teacher

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