林 菀俞
職稱 副教授
姓名 林 菀俞
聯絡電話 (02)33668106
電子郵件 linwy@ntu.edu.tw
研究專長 統計遺傳學、遺傳流行病學、生物統計學
臺大學術庫 http://ah.ntu.edu.tw/web/Teacher!one.action?tid=581
年度 論文名稱
2015 Yan Q, Tiwari HK, Yi N, Gao G, Zhang K, Lin W-Y, Lou X-Y, Cui X, Liu N, A Sequence Kernel Association Test for Dichotomous Traits in Family Samples under a Generalized Linear Mixed Model, Human Heredity, 2, pp60-68
2014 Xu HM, Sun XW, Qi T, Lin W-Y, Liu N, Lou XY*, Multivariate Dimensionality Reduction Approaches to Identify Gene-Gene and Gene-Environment Interactions Underlying Multiple Complex Traits, PLoS ONE, 9, ppe108103-0
2014 Yan Q, Tiwari HK, Yi N, Lin W-Y, Gao G, Lou X-Y, Cui X, Liu N*, Kernel-Machine Testing Coupled with a Rank-Truncation Method for Genetic Pathway Analysis, Genetic Epidemiology, 5, pp447-456
2014 Li P, Tiwari HK, Lin W-Y, Allison DB, Chung WK, Leibel RL, Yi N*, Liu N*, Genetic Association Analysis of 30 Genes Related to Obesity in European American Population, International Journal of Obesity, 5, pp724-729
2014 Lin W-Y*, Association Testing of Clustered Rare Causal Variants in Case-Control Studies, PLoS ONE, 4, ppe94337-0
2014 Chen Y-M, Lin W-Y, Chan C-C*, The impact of petrochemical industrialisation on life expectancy and per capita income in Taiwan: an 11-year longitudinal study, BMC Public Health, pp247-0
2014 Lin W-Y*, Lou XY, Gao G, Liu N*, Rare Variant Association Testing by Adaptive Combination of P-values, PLoS ONE, 1, ppe85728-7
2014 Lin W-Y*, Adaptive Combination of P-Values for Family-Based Association Testing with Sequence Data, PLoS ONE, 12, ppe115971-0
2013 Lin W-Y, Dubuisson O, Rubicz R, Liu N, Allison DB, Curran JE, Comuzzie AG, Blangero J, Leach CT, Goring H, Dhurandhar NV*, Response to Comment on: Lin et al. Long-Term Changes in Adiposity and Glycemic Control Are Associated With Past Adenovirus Infection. Diabetes Care 2013;36:701–707, Diabetes Care, 9, ppe162-0
2013 Lin W-Y*, Yi N, Lou XY, Zhi D, Zhang K, Gao G, Tiwari HK, Liu N*, Haplotype Kernel Association Test as a Powerful Method to Identify Chromosomal Regions Harboring Uncommon Causal Variants, Genetic Epidemiology, 6, pp560-570
2013 Lin W-Y, Dubuisson O, Rubicz R, Liu N, Allison DB, Curran JE, Comuzzie AG, Blangero J, Leach CT, Goring H, Dhurandhar NV*, Long-term changes in adiposity and glycemic control are associated with past adenovirus infection, Diabetes Care, 3, pp701-707
2012 Lin W-Y, Yi N, Zhi D, Zhang K, Gao G, Tiwari HK, Liu N*, Haplotype-based methods for detecting uncommon causal variants with common SNPs, Genetic Epidemiology, 6, pp572-582
2012 Lin W-Y, Tiwari HK, Gao G, Zhang K, Arcaroli JJ, Abraham E, Liu N*, Similarity-based multimarker association tests for continuous traits, Annals of Human Genetics, 3, pp246-260
2012 Lin W-Y*, Lee W-C, Improving power of genome-wide association studies with weighted false discovery rate control and prioritized subset analysis, PLoS ONE, 4, ppe33716-0
2012 Lin W-Y, Liu N*, Reducing bias of allele frequency estimates by modeling SNP genotype data with informative missingness, Frontiers in Genetics, pp107-0
2012 Lin W-Y, Lee W-C*, Presenting the uncertainties of odds ratios using empirical-Bayes prediction intervals, PLoS ONE, 2, ppe32022-0
2011 Lin W-Y, Zhang B, Yi N, Gao G, Liu N*, Evaluation of pooled association tests for rare variant identification, BMC Proceedings, Supp9, ppS118-0
2011 Lin W-Y, Lee W-C*, Floating prioritized subset analysis: a powerful method to detect differentially expressed genes, Computational Statistics and Data Analysis, 1, pp903-913
2010 Lin W-Y*, Lee W-C, Discovering joint associations between disease and gene pairs with a novel similarity test, BMC Genetics, pp86-0
2010 Lin W-Y, Lee W-C*, Incorporating prior knowledge to facilitate discoveries in a genome-wide association study on age-related macular degeneration, BMC Research Notes, pp26-0
2009 Lin W-Y, Schaid DJ*, Power comparisons between similarity-based multilocus association methods, logistic regression, and score tests for haplotypes, Genetic Epidemiology, 3, pp183-197
2007 Schaid DJ*, Lin W-Y, One- and two-locus models for mapping rheumatoid arthritis-susceptibility genes on chromosome 6, BMC Proceedings, Supp1, ppS103-0
2007 Lin W-Y, Schaid DJ*, Robust multipoint simultaneous identical-by-descent mapping for two linked loci, Human Heredity, 1, pp35-46
2007 Lin W-Y, Schaid DJ*, Identifying single-nucleotide polymorphisms responsible for the linkage signal of rheumatoid arthritis on chromosome 6 by joint modeling of linkage and association, BMC Proceedings, Supp1, ppS40-0
2007 Yang Q*, Biernacka JM, Chen M-H, Houwing-Duistermaat JJ, Bergemann TL, Basu S, Fan R, Liu L, Bourgey M, Clerget-Darpoux F, Lin W-Y, Elston RC, Cupples LA*, Using linkage and association to identify and model genetic effects: Summary of GAW 15 Group 4, Genetic Epidemiology, S1, ppS34-S42
2007 Ghosh S*, Babron MC, Amos CI, Briollais L, Chen P, Chen WV, Chiu WF, Drigalenko E, Etzel CJ, Hamshere ML, Holmans PA, Margaritte-Jeannin P, Lebrec JJ, Lin S, Lin W-Y, Mandhyan DD, Nishchenko I, Schaid DJ, Seguardo R, Shete S, Taylor K, Tayo BO, Wan S, Wei LY, Wu CO, Yang XR, Linkage analyses of rheumatoid arthritis and related quantitative phenotypes: the GAW15 experience, Genetic Epidemiology, S1, ppS86-S95