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20132020
most citedIntegrative Analysis of Prognosis Data on Multiple Cancer Subtypes using Penalization

2 citations · 4 across the 4 of their papers we have counts for

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7 papers · 1 filter

stat.ME20202 cited

Accounting for correlated horizontal pleiotropy in two-sample Mendelian randomization using correlated instrumental variants

Qing Cheng, Baoluo Sun, Yingcun Xia +1

Mendelian randomization (MR) is a powerful approach to examine the causal relationships between health risk factors and outcomes from observational studies. Due to the proliferatio…

stat.ME2019

BOLT-SSI: A Statistical Approach to Screening Interaction Effects for Ultra-High Dimensional Data

Min Zhou, Mingwei Dai, Yuan Yao +3

Detecting interaction effects among predictors on the response variable is a crucial step in various applications. In this paper, we first propose a simple method for sure screenin…

stat.ME2018

Bayesian Weighted Mendelian Randomization for Causal Inference based on Summary Statistics

Jia Zhao, Jingsi Ming, Xianghong Hu +3

The results from Genome-Wide Association Studies (GWAS) on thousands of phenotypes provide an unprecedented opportunity to infer the causal effect of one phenotype (exposure) on an…

stat.ME2018

VIMCO: Variational Inference for Multiple Correlated Outcomes in Genome-wide Association Studies

Xingjie Shi, Yuling Jiao, Yi Yang +4

In Genome-Wide Association Studies (GWAS) where multiple correlated traits have been measured on participants, a joint analysis strategy, whereby the traits are analyzed jointly, c…

stat.ME2017

LPG: a four-groups probabilistic approach to leveraging pleiotropy in genome-wide association studies

Yi Yang, Mingwei Dai, Jian Huang +4

To date, genome-wide association studies (GWAS) have successfully identified tens of thousands of genetic variants among a variety of traits/diseases, shedding a light on the genet…

stat.ME2017

LSMM: A statistical approach to integrating functional annotations with genome-wide association studies

Jingsi Ming, Mingwei Dai, Mingxuan Cai +3

Thousands of risk variants underlying complex phenotypes (quantitative traits and diseases) have been identified in genome-wide association studies (GWAS). However, there are still…