selected publications
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academic article
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Inherited variation in the xenobiotic transporter pathway and survival of multiple myeloma patients.
British Journal of Haematology.
183.
2018
Body mass index and breast cancer survival: a Mendelian randomization analysis.
International Journal of Epidemiology.
46.
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
Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation.
Nature Communications.
7.
2016
A Genome-wide Pleiotropy Scan for Prostate Cancer Risk.
European Urology.
67.
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
Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients.
Nature Communications.
6.
2015
Risk of multiple myeloma is associated with polymorphisms within telomerase genes and telomere length.
International Journal of Cancer.
136.
2015
Coffee and tea consumption, genotype‐based CYP1A2 and NAT2 activity and colorectal cancer risk—Results from the EPIC cohort study.
International Journal of Cancer.
135.
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 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
Prostate Cancer (PCa) Risk Variants and Risk of Fatal PCa in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium.
European Urology.
65.
2014
Type 2 Diabetes-Related Variants Influence on the Risk of Developing Multiple Myeloma: Results from the Immense Consortium.
Blood.
124.
2014
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dataset
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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
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hide from search
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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