about
Imputation and subset based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33Analysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer typesIdentification of a CpG island methylator phenotype that defines a distinct subgroup of gliomaGenome-wide association studies identify four ER negative-specific breast cancer risk lociEpigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancerPolymorphisms in genes involved in estrogen and progesterone metabolism and mammographic density changes in women randomized to postmenopausal hormone therapy: results from a pilot studyFemale chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosomeCombined effects of MDM2 SNP309 and TP53 R72P polymorphisms, and soy isoflavones on breast cancer risk among Chinese women in SingaporePALB2, CHEK2 and ATM rare variants and cancer risk: data from COGSGenome-wide association study identifies multiple loci associated with bladder cancer riskGenome-wide interaction study of smoking and bladder cancer riskA multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility lociLarge-scale genotyping identifies 41 new loci associated with breast cancer risk.Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.Methodological Considerations in Estimation of Phenotype Heritability Using Genome-Wide SNP Data, Illustrated by an Analysis of the Heritability of Height in a Large Sample of African Ancestry Adults.Exome-wide association study of endometrial cancer in a multiethnic populationComprehensive analyses of DNA repair pathways, smoking and bladder cancer risk in Los Angeles and Shanghai.Polymorphisms in the FGF2 gene and risk of serous ovarian cancer: results from the ovarian cancer association consortium.Elevated 4-aminobiphenyl and 2,6-dimethylaniline hemoglobin adducts and increased risk of bladder cancer among lifelong nonsmokers--The Shanghai Bladder Cancer StudyVariation in NF-κB signaling pathways and survival in invasive epithelial ovarian cancerHaplotypes of DNMT1 and DNMT3B are associated with mutagen sensitivity induced by benzo[a]pyrene diol epoxide among smokersGenetic variation in the progesterone receptor gene and risk of endometrial cancer: a haplotype-based approach.Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A.Hormone metabolism genes and mammographic density in Singapore Chinese women.The 19q12 bladder cancer GWAS signal: association with cyclin E function and aggressive diseaseCommon non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association ConsortiumSun exposure, vitamin D receptor gene polymorphisms, and risk of advanced prostate cancer.Genetic variation in TYMS in the one-carbon transfer pathway is associated with ovarian carcinoma types in the Ovarian Cancer Association ConsortiumGenetic polymorphisms of epidermal growth factor in relation to risk of hepatocellular carcinoma: two case-control studies.Genome-wide testing of putative functional exonic variants in relationship with breast and prostate cancer risk in a multiethnic population.Antiretroviral therapy modifies the genetic effect of known type 2 diabetes-associated risk variants in HIV-infected women.Effect of reproductive factors and oral contraceptives on breast cancer risk in BRCA1/2 mutation carriers and noncarriers: results from a population-based study.Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1.Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21.Hormone metabolism pathway genes and mammographic density change after quitting estrogen and progestin combined hormone therapy in the California Teachers StudyAssociation of the calcyon neuron-specific vesicular protein gene (CALY) with adolescent smoking initiation in China and CaliforniaEvidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer riskFine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.The association of polymorphisms in hormone metabolism pathway genes, menopausal hormone therapy, and breast cancer risk: a nested case-control study in the California Teachers Study cohort.
P50
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P50
description
researcher ORCID ID = 0000-0002-5404-5218
@en
wetenschapper
@nl
name
David Van Den Berg
@ast
David Van Den Berg
@en
David Van Den Berg
@es
David Van Den Berg
@nl
type
label
David Van Den Berg
@ast
David Van Den Berg
@en
David Van Den Berg
@es
David Van Den Berg
@nl
altLabel
David J Van Den Berg
@en
prefLabel
David Van Den Berg
@ast
David Van Den Berg
@en
David Van Den Berg
@es
David Van Den Berg
@nl
P1053
G-8598-2017
P106
P21
P31
P496
0000-0002-5404-5218