Area of research
Genetics · Oncology
Research interest
Research interests include BRCA gene mutations in cancer, Genetic Associations and Epidemiology, PARP inhibition in cancer therapy, and DNA Repair Mechanisms.
The serotonin receptor 3E variant is a risk factor for female IBS-D
The alternative serotonin transporter promoter P2 impacts gene function in females with irritable bowel syndrome
Imputation of Missing Genotypes within LD-Blocks Relying on the Basic Coalescent and Beyond [Source Code]
Body mass index and breast cancer survival: a Mendelian randomization analysis
TP53-based interaction analysis identifies cis-eQTL variants for TP53BP2, FBXO28, and FAM53A that associate with survival and treatment outcome in breast cancer
Imputation of missing genotypes within LD-blocks relying on the basic coalescent and beyond: consideration of population growth and structure
Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent
No evidence that protein truncating variants in <i>BRIP1</i> are associated with breast cancer risk: implications for gene panel testing
Genetic predisposition to ductal carcinoma in situ of the breast
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21
Fine‐scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer
Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry
Genes associated with histopathologic features of triple negative breast tumors predict molecular subtypes
Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus
rs2735383, located at a microRNA binding site in the 3’UTR of NBS1, is not associated with breast cancer risk
Using next-generation DNA sequence data for genetic association tests based on allele counts with and without consideration of zero inflation
Association between the BsmI Polymorphism in the Vitamin D Receptor Gene and Breast Cancer Risk: Results from a Pakistani Case-Control Study
Fine-Scale Mapping of the 4q24 Locus Identifies Two Independent Loci Associated with Breast Cancer Risk
Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer
A polymorphism in the base excision repair gene PARP2 is associated with differential prognosis by chemotherapy among postmenopausal breast cancer patients
The SNP rs6500843 in 16p13.3 is associated with survival specifically among chemotherapy-treated breast cancer patients
Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium
Practical investigation of the performance of robust logistic regression to predict the genetic risk of hypertension
Tailored Selection of Study Individuals to be Sequenced in Order to Improve the Accuracy of Genotype Imputation
Exploring the association between genetic variation in the <scp>SUMO</scp> isopeptidase gene <scp><i>USPL1</i></scp> and breast cancer through integration of data from the population‐based <scp>GENICA</scp> study and external genetic databases