about
Association studies of 22 candidate SNPs with late-onset Alzheimer's diseaseRarity of the Alzheimer disease-protective APP A673T variant in the United StatesRefinement of the physical location and the genomic characterization of the CRSP2 (EXLM1) gene on Xp11.4Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAXCommon variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.Genome-wide association analysis of age-at-onset in Alzheimer's diseaseGenome-wide association study of Alzheimer's diseaseConnecting the dots: potential of data integration to identify regulatory SNPs in late-onset Alzheimer's disease GWAS findings.Genetic Determinants of Survival in Patientswith Alzheimer’s Disease.Genetic determinants of disease progression in Alzheimer's diseaseAssociation of CLU and PICALM variants with Alzheimer's disease.Replication study of genome-wide associated SNPs with late-onset Alzheimer's diseaseA novel compound heterozygous mutation in the cellular retinaldehyde-binding protein gene (RLBP1) in a patient with retinitis punctata albescens.A novel RPGR exon ORF15 mutation in a family with X-linked retinitis pigmentosa and Coats'-like exudative vasculopathy.Specificity of the STAT4 genetic association for severe disease manifestations of systemic lupus erythematosusInvestigation of an amyloid precursor protein protective mutation (A673T) in a North American case-control sample of late-onset Alzheimer's disease.PPARG and ADIPOQ gene polymorphisms increase type 2 diabetes mellitus risk in Asian Indian Sikhs: Pro12Ala still remains as the strongest predictor.Association of APOE polymorphisms and stressful life events with dementia in a Pakistani population.Functional and genetic characterization of the promoter region of apolipoprotein H (beta2-glycoprotein I)A rare duplication on chromosome 16p11.2 is identified in patients with psychosis in Alzheimer's diseaseComprehensive evaluation of the association of APOE genetic variation with plasma lipoprotein traits in U.S. whites and African blacks.Impact of genetic variants in human scavenger receptor class B type I (SCARB1) on plasma lipid traits.A multiethnic replication study of plasma lipoprotein levels-associated SNPs identified in recent GWAS.Genetic variation in imprinted genes is associated with risk of late-onset Alzheimer's diseaseAPOE gene polymorphism and risk of coronary stenosis in Pakistani population.More evidence for association of a rare TREM2 mutation (R47H) with Alzheimer's disease risk.Genome-wide copy-number variation study of psychosis in Alzheimer's disease.Genetic contribution of SCARB1 variants to lipid traits in African Blacks: a candidate gene association study.Resequencing of LPL in African Blacks and associations with lipoprotein-lipid levelsNovel late-onset Alzheimer disease loci variants associate with brain gene expression.Resequencing of the CETP gene in American whites and African blacks: Association of rare and common variants with HDL-cholesterol levelsIdentification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European AncestryFunctional significance of lipoprotein lipase HindIII polymorphism associated with the risk of coronary artery diseaseApolipoprotein H promoter polymorphisms in relation to lupus and lupus-related phenotypes.X-linked cone-rod dystrophy (locus COD1): identification of mutations in RPGR exon ORF15Lipoprotein lipase gene sequencing and plasma lipid profile.Multiple signals at the extended 8p23 locus are associated with susceptibility to systemic lupus erythematosus.Genetic link of type 1 diabetes susceptibility loci with rheumatoid arthritis in Pakistani patients.A replication study of 49 Type 2 diabetes risk variants in a Punjabi Pakistani population.Association of 32 type 1 diabetes risk loci in Pakistani patients.
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F. Yesim Demirci
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F. Yesim Demirci
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F. Yesim Demirci
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F. Yesim Demirci
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F. Yesim Demirci
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F. Yesim Demirci
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P106
P1153
56753143900
P21
P31
P496
0000-0001-6907-9843