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Author Details
Full Name
Yi Yu
Affiliation
Tufts Medical Center
ORCID
Career Start Year
2005
Papers
31
H Index
21
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
28011711
Protective coding variants in CFH and PELI3 and a variant near CTRB1 are associated with age-related macular degenerationâ¿ .
Hum Mol Genet
2016
25788521
Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levels.
Hum Mol Genet
2015
26501415
Rare Variants in the Functional Domains of Complement Factor H Are Associated With Age-Related Macular Degeneration.
Invest Ophthalmol Vis Sci
2015
24498017
Three new genetic loci (R1210C in CFH, variants in COL8A1 and RAD51B) are independently related to progression to advanced macular degeneration.
PLoS One
2014
24847005
Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration.
Hum Mol Genet
2014
23455636
Seven new loci associated with age-related macular degeneration.
Nat Genet
2013
24036952
Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration.
Nat Genet
2013
23411794
Validation of a prediction algorithm for progression to advanced macular degeneration subtypes.
JAMA Ophthalmol
2013
22247473
Prospective assessment of genetic effects on progression to different stages of age-related macular degeneration using multistate Markov models.
Invest Ophthalmol Vis Sci
2012
23023008
Correction of phenotype misclassification based on high-discrimination genetic predictive risk models.
Epidemiology
2012
23038115
To Correct or Not to Correct-and How.
Epidemiology
2012
22705344
Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.
Ophthalmology
2012
22678500
Genetic factors for choroidal neovascularization associated with high myopia.
Invest Ophthalmol Vis Sci
2012
21122828
ARMS2/HTRA1 locus can confer differential susceptibility to the advanced subtypes of age-related macular degeneration.
Am J Ophthalmol
2011
22003108
Complement factor D in age-related macular degeneration.
Invest Ophthalmol Vis Sci
2011
22019782
A rare penetrant mutation in CFH confers high risk of age-related macular degeneration.
Nat Genet
2011
21959373
Risk models for progression to advanced age-related macular degeneration using demographic, environmental, genetic, and ocular factors.
Ophthalmology
2011
21665990
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.
Hum Mol Genet
2011
21488854
Glucuronic acid epimerase is associated with plasma triglyceride and high-density lipoprotein cholesterol levels in Turks.
Ann Hum Genet
2011
21447678
Association of variants in the LIPC and ABCA1 genes with intermediate and large drusen and advanced age-related macular degeneration.
Invest Ophthalmol Vis Sci
2011
20147890
Confirmation and generalization of an alcohol-dependence locus on chromosome 10q.
Neuropsychopharmacology
2010
20485328
Variation in nicotinic acetylcholine receptor genes is associated with multiple substance dependence phenotypes.
Neuropsychopharmacology
2010
19255376
Association of variants in MANEA with cocaine-related behaviors.
Arch Gen Psychiatry
2009
19265542
Performance of random forest when SNPs are in linkage disequilibrium.
BMC Bioinformatics
2009
18438686
Substance dependence low-density whole genome association study in two distinct American populations.
Hum Genet
2008
16740595
Intronic variants in the dopa decarboxylase (DDC) gene are associated with smoking behavior in European-Americans and African-Americans.
Hum Mol Genet
2006
17085484
Haplotype spanning TTC12 and ANKK1, flanked by the DRD2 and NCAM1 loci, is strongly associated to nicotine dependence in two distinct American populations.
Hum Mol Genet
2006
16061952
Multiple QTLs influencing triglyceride and HDL and total cholesterol levels identified in families with atherogenic dyslipidemia.
J Lipid Res
2005
16451606
Multifactor-dimensionality reduction versus family-based association tests in detecting susceptibility loci in discordant sib-pair studies.
BMC Genet
2005
16451610
Whole-genome variance components linkage analysis using single-nucleotide polymorphisms versus microsatellites on quantitative traits of derived phenotypes from factor analysis of electroencephalogram waves.
BMC Genet
2005
16451694
Genome-wide linkage analysis for alcohol dependence: a comparison between single-nucleotide polymorphism and microsatellite marker assays.
BMC Genet
2005
1 - 31 of 31
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