about
Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thicknessAssessing the genetic architecture of epithelial ovarian cancer histological subtypes.Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA.ABCA transporter gene expression and poor outcome in epithelial ovarian cancer.Functional polymorphisms in the TERT promoter are associated with risk of serous epithelial ovarian and breast cancers.Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process.Most common 'sporadic' cancers have a significant germline genetic component.Associations between depression and anxiety symptoms and retinal vessel caliber in adolescents and young adultsGenome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortiumThe role of KRAS rs61764370 in invasive epithelial ovarian cancer: implications for clinical testingPlatinum sensitivity-related germline polymorphism discovered via a cell-based approach and analysis of its association with outcome in ovarian cancer patientsRetinal microvessels reflect familial vulnerability to psychotic symptoms: A comparison of twins discordant for psychotic symptoms and controls.Shared genetics underlying epidemiological association between endometriosis and ovarian cancer.Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium.Pooled genome wide association detects association upstream of FCRL3 with Graves' disease.Genome-wide Analysis Identifies Novel Loci Associated with Ovarian Cancer Outcomes: Findings from the Ovarian Cancer Association Consortium.Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error.Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer.Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancerAssessing the Genetic Predisposition of Education on Myopia: A Mendelian Randomization Study.Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.Genome-wide association study for ovarian cancer susceptibility using pooled DNA.ABCB1 (MDR1) polymorphisms and ovarian cancer progression and survival: a comprehensive analysis from the Ovarian Cancer Association Consortium and The Cancer Genome Atlas.GWAS study using DNA pooling strategy identifies association of variant rs4910623 in OR52B4 gene with anti-VEGF treatment response in age-related macular degeneration.A genome-wide association study of essential hypertension in an Australian population using a DNA pooling approach.Association of vitamin D levels and risk of ovarian cancer: a Mendelian randomization studyWhen do myopia genes have their effect? Comparison of genetic risks between children and adults.Association of Polymorphisms in MACRO Domain Containing 2 With Thyroid-Associated Orbitopathy.Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology.Genetic risk scores and family history as predictors of schizophrenia in Nordic registers.Genome-wide association study of paclitaxel and carboplatin disposition in women with epithelial ovarian cancer.Sex-specific manifestation of genetic risk for attention deficit hyperactivity disorder in the general population.A genome-wide association study of IgM antibody against phosphorylcholine: shared genetics and phenotypic relationship to chronic lymphocytic leukemia.Genome-wide analysis of adolescent psychotic-like experiences shows genetic overlap with psychiatric disorders.
P50
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P50
description
statistical geneticist
@en
name
Yi Lu
@ast
Yi Lu
@en
Yi Lu
@es
Yi Lu
@nl
type
label
Yi Lu
@ast
Yi Lu
@en
Yi Lu
@es
Yi Lu
@nl
prefLabel
Yi Lu
@ast
Yi Lu
@en
Yi Lu
@es
Yi Lu
@nl
P1053
G-9292-2018
P106
P31
P496
0000-0001-9933-3654