about
Large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes: the GENOMOS study.Seq4SNPs: new software for retrieval of multiple, accurately annotated DNA sequences, ready formatted for SNP assay design.GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition lociGenome-wide association analysis of pain severity in dysmenorrhea identifies association at chromosome 1p13.2, near the nerve growth factor locus.Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture.Genes contributing to pain sensitivity in the normal population: an exome sequencing study.The association between common vitamin D receptor gene variations and osteoporosis: a participant-level meta-analysis.TGF-β signaling pathway and breast cancer susceptibility.Large-scale analysis of association between LRP5 and LRP6 variants and osteoporosisCommon variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer risk.Genetic and Environmental Risk for Chronic Pain and the Contribution of Risk Variants for Major Depressive Disorder: A Family-Based Mixed-Model AnalysisAssociation of ESR1 gene tagging SNPs with breast cancer riskDifferential methylation of the TRPA1 promoter in pain sensitivityLarge-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: the GENOMOS study.Phytoestrogen exposure correlation with plasma estradiol in postmenopausal women in European Prospective Investigation of Cancer and Nutrition-Norfolk may involve diet-gene interactions.Correction: Large-Scale Evidence for the Effect of the COLIA1 Sp1 Polymorphism on Osteoporosis Outcomes: The GENOMOS Study.Association of gene variants in the transforming growth factor beta signalling pathways with invasive breast cancer risk.Association of gene variants in the TGF-beta signalling pathways with invasive breast cancer risk.From association to cause: fine mapping of the TNRC9 gene region, a novel susceptibility locus identified in the first genome-wide association study for breast cancer.Modest protective effects of isoflavones from a red clover-derived dietary supplement on cardiovascular disease risk factors in perimenopausal women, and evidence of an interaction with ApoE genotype in 49-65 year-old women.A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus.Registered access: authorizing data accessPhytoestrogen Exposure, Polymorphisms in COMT, CYP19, ESR1, and SHBG Genes, and Their Associations With Prostate Cancer RiskA common coding variant in CASP8 is associated with breast cancer riskDifferential Genetic Effects of ESR1 Gene Polymorphisms on Osteoporosis OutcomesElucidating the molecular genetic basis of cluster headache: delineation of the genetic architecture by exome sequencingGene-nutrient interactions: dietary behaviour associated with high coronary heart disease risk particularly affects serum LDL cholesterol in apolipoprotein E epsilon4-carrying free-living individualsAuthor Correction: Leveraging European infrastructures to access 1 million human genomes by 2022Functional confirmation that the R1488* variant in SCN9A results in complete loss-of-function of Nav1.7.Federated discovery and sharing of genomic data using BeaconsPublisher Correction: Federated discovery and sharing of genomic data using BeaconsLeveraging European infrastructures to access 1 million human genomes by 2022
P50
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P50
description
hulumtuese
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researcher
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wetenschapper
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հետազոտող
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name
Serena Scollen
@ast
Serena Scollen
@en
Serena Scollen
@es
Serena Scollen
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Serena Scollen
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type
label
Serena Scollen
@ast
Serena Scollen
@en
Serena Scollen
@es
Serena Scollen
@nl
Serena Scollen
@sl
prefLabel
Serena Scollen
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Serena Scollen
@en
Serena Scollen
@es
Serena Scollen
@nl
Serena Scollen
@sl
P106
P21
P31
P496
0000-0002-9311-1337