Kenny Ye

Affiliations: 
Stony Brook University, Stony Brook, NY, United States 
Area:
Statistics
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"Kenny Ye"
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Publications

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Wang T, Xue X, Xie X, et al. (2018) Adjustment for covariates using summary statistics of genome-wide association studies. Genetic Epidemiology
Loudig O, Wang T, Ye K, et al. (2017) Evaluation and Adaptation of a Laboratory-Based cDNA Library Preparation Protocol for Retrospective Sequencing of Archived MicroRNAs from up to 35-Year-Old Clinical FFPE Specimens. International Journal of Molecular Sciences. 18
Iossifov I, O'Roak BJ, Sanders SJ, et al. (2014) The contribution of de novo coding mutations to autism spectrum disorder. Nature. 515: 216-21
Cheng G, Tang CS, Wong EH, et al. (2013) Common genetic variants regulating ADD3 gene expression alter biliary atresia risk. Journal of Hepatology. 59: 1285-91
Iossifov I, Ronemus M, Levy D, et al. (2012) De novo gene disruptions in children on the autistic spectrum. Neuron. 74: 285-99
Huffman DM, Deelen J, Ye K, et al. (2012) Distinguishing between longevity and buffered-deleterious genotypes for exceptional human longevity: the case of the MTP gene. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. 67: 1153-60
Lee YH, Ronemus M, Kendall J, et al. (2012) Reducing system noise in copy number data using principal components of self-self hybridizations. Proceedings of the National Academy of Sciences of the United States of America. 109: E103-10
Pradhan K, Yoon SC, Wang T, et al. (2011) Identification of genes and variants associated with quantitative traits using Bayesian factor screening. Bmc Proceedings. 5: S4
Wang T, Pradhan K, Ye K, et al. (2011) Estimating allele frequency from next-generation sequencing of pooled mitochondrial DNA samples. Frontiers in Genetics. 2: 51
Ye KQ, Engelman CD. (2011) Detecting multiple causal rare variants in exome sequence data. Genetic Epidemiology. 35: S18-21
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