selected publications
-
academic article
-
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer.
Nature Genetics.
50.
2018
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.
Nature Genetics.
50.
2018
Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants.
Nature Communications.
9.
2018
Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma.
Nature Communications.
9.
2018
Inherited variation in the xenobiotic transporter pathway and survival of multiple myeloma patients.
British Journal of Haematology.
183.
2018
Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study.
JAMA Oncology.
3.
2017
Association analysis identifies 65 new breast cancer risk loci.
Nature.
551.
2017
Body mass index and breast cancer survival: a Mendelian randomization analysis.
International Journal of Epidemiology.
46.
2017
Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility.
Nature Communications.
8.
2017
Identification of miRSNPs associated with the risk of multiple myeloma.
International Journal of Cancer.
140.
2017
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.
Nature Genetics.
49.
2017
A common variant within the HNF1B gene is associated with overall survival of multiple myeloma patients: Results from the IMMEnSE consortium and meta-analysis.
Oncotarget.
7.
2016
Breast Cancer Risk From Modifiable and Nonmodifiable Risk Factors Among White Women in the United States.
JAMA Oncology.
2.
2016
Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome.
Nature Communications.
7.
2016
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer.
Nature Communications.
7.
2016
Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for 13 Cancer Types.
Journal of the National Cancer Institute.
107.
2015
Association of CRP genetic variants with blood concentrations of C‐reactive protein and colorectal cancer risk.
International Journal of Cancer.
136.
2015
Association of breast cancer risk loci with breast cancer survival.
International Journal of Cancer.
137.
2015
Common germline polymorphisms associated with breast cancer-specific survival.
Breast Cancer Research.
17.
2015
Determinants of the t(14;18) translocation and their role in t(14;18)-positive follicular lymphoma.
Cancer Causes & Control.
26.
2015
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer.
Nature Genetics.
47.
2015
Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients.
Nature Communications.
6.
2015
Identification of Novel Genetic Markers of Breast Cancer Survival.
Journal of the National Cancer Institute.
107.
2015
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.
American Journal of Human Genetics.
97.
2015
Risk of multiple myeloma is associated with polymorphisms within telomerase genes and telomere length.
International Journal of Cancer.
136.
2015
Type 2 diabetes-related variants influence the risk of developing multiple myeloma: results from the IMMEnSE consortium.
Endocrine Related Cancer.
22.
2015
Variation at ABO histo‐blood group and FUT loci and diffuse and intestinal gastric cancer risk in a European population.
International Journal of Cancer.
136.
2015
A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer.
Nature Genetics.
46.
2014
Fine-Mapping the HOXB Region Detects Common Variants Tagging a Rare Coding Allele: Evidence for Synthetic Association in Prostate Cancer.
PLOS Genetics.
10.
2014
Genetic Variants and Multiple Myeloma Risk: IMMEnSE Validation of the Best Reported Associations—An Extensive Replication of the Associations from the Candidate Gene Era.
Cancer Epidemiology Biomarkers & Prevention.
23.
2014
Genetic association of gastric cancer with miRNA clusters including the cancer‐related genes MIR29, MIR25, MIR93 and MIR106: Results from the EPIC‐EURGAST study.
International Journal of Cancer.
135.
2014
Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33.
Human Molecular Genetics.
23.
2014
Prediagnostic telomere length and risk of B‐cell lymphoma—Results from the EPIC cohort study.
International Journal of Cancer.
135.
2014
Risk factors for cancers of unknown primary site: Results from the prospective EPIC cohort.
International Journal of Cancer.
135.
2014
The International Multiple Myeloma Research (IMMEnSE) Consortium: Genetics of Multiple Myeloma Risk and Prognosis.
Blood.
124.
2014
Type 2 Diabetes-Related Variants Influence on the Risk of Developing Multiple Myeloma: Results from the Immense Consortium.
Blood.
124.
2014
t(14;18) Translocation: A Predictive Blood Biomarker for Follicular Lymphoma.
Journal of Clinical Oncology.
32.
2014
-
dataset
-
Fine-Mapping the HOXB Region Detects Common Variants Tagging a Rare Coding Allele: Evidence for Synthetic Association in Prostate Cancer.
public-library-of-science.
2014
Haplotype analysis for rs117576373 and rs138213197 in the subset of 5500 PrCa cases and 4923 controls from the UK and Sweden for which both had been directly genotyped..
public-library-of-science.
2014
Haplotype analysis for rs145922598 and rs138213197 in the subset of 5500 PrCa cases and 4923 controls from the UK and Sweden genotyped for rs138213197..
public-library-of-science.
2014
PrCa association information for SNPs significant at P<10−6 in the iCOGS imputed data..
public-library-of-science.
2014
-
hide from search
-
An Absolute Risk Model to Identify Individuals at Elevated Risk for Pancreatic Cancer in the General Population.
public-library-of-science.
2013
Association between pancreatic cancer risk and smoking, personal history of diabetes, family history of pancreatic cancer, alcohol use, body mass index, and known genetic markers..
public-library-of-science.
2013
Genetic Variation in the HSD17B1 Gene and Risk of Prostate Cancer.
public-library-of-science.
2013
Participants' Characteristics, the PanScan Consortium..
public-library-of-science.
2013
Reclassification of lifetime risk of pancreatic cancer after adding genetic information to the risk model with both genetic and non-genetic covariates..
public-library-of-science.
2013
A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease.
Human Molecular Genetics.
2013
An Absolute Risk Model to Identify Individuals at Elevated Risk for Pancreatic Cancer in the General Population.
PLoS ONE.
2013
Genetic variation in the lactase gene, dairy product intake and risk for prostate cancer in the European prospective investigation into cancer and nutrition.
International Journal of Cancer.
2013
Hemochromatosis ( HFE ) gene mutations and risk of gastric cancer in the European Prospective Investigation into Cancer and Nutrition (EPIC) study.
Carcinogenesis.
2013
Menstrual and reproductive factors in women, genetic variation in CYP17A1, and pancreatic cancer risk in the European prospective investigation into cancer and nutrition (EPIC) cohort.
International Journal of Cancer.
2013
Vitamin C transporter gene (SLC23A1 and SLC23A2) polymorphisms, plasma vitamin C levels, and gastric cancer risk in the EPIC cohort.
Genes & Nutrition.
2013
Characteristics of the study populations..
public-library-of-science.
2011
Genetic Variability of the mTOR Pathway and Prostate Cancer Risk in the European Prospective Investigation on Cancer (EPIC).
public-library-of-science.
2011
SNPs genotyped in the first and second phase of the project..
public-library-of-science.
2011