Demo Data from EDBT 2026 / reviewers in the wild / expert
Satoshi Yoshiji
dblp:426/4594
· DBLP profile ↗
1ranked-venue papers
0as first author
1since 2021 · last 2024
—ORCID · unresolved
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1 · 1 since 2021
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Interdisciplinary, comprehensive, and emerging computing
1 paper |
Bioinformatics and computational biology · 70% Computational science and engineering · 30% |
Topics — the 4 heaviest of 4, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › statistical genetics › genetic study design
mendelian randomization |
0.8 | 1 | 2024 | MR Corge: sensitivity analysis of Mendelian randomization based on the core gene hypothesis for polygenic exposures · Bioinform. 2024 |
Computational science and engineering
sensitivity analysis |
0.8 | 1 | 2024 | MR Corge: sensitivity analysis of Mendelian randomization based on the core gene hypothesis for polygenic exposures · Bioinform. 2024 |
Bioinformatics and computational biology
statistical genetics |
0.8 | 1 | 2024 | MR Corge: sensitivity analysis of Mendelian randomization based on the core gene hypothesis for polygenic exposures · Bioinform. 2024 |
Bioinformatics and computational biology
genetic epidemiology |
0.2 | 1 | 2024 | MR Corge: sensitivity analysis of Mendelian randomization based on the core gene hypothesis for polygenic exposures · Bioinform. 2024 |
Methods — techniques the papers use, named apart from their topics
instrumental variable analysis · 0.8core gene hypothesis · 0.8
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2024 | MR Corge: sensitivity analysis of Mendelian randomization based on the core gene hypothesis for polygenic exposuresabstractSUMMARY: Mendelian randomization is being utilized to assess causal effects of polygenic exposures, where many genetic instruments are subject to horizontal pleiotropy. Existing methods for detecting and correcting for horizontal pleiotropy have important assumptions that may not be fulfilled. Built upon the core gene hypothesis, we developed MR Corge for performing sensitivity analysis of Mendelian randomization. MR Corge identifies a small number of putative core instruments that are more likely to affect genes with a direct biological role in an exposure and obtains causal effect estimates based on these instruments, thereby reducing the risk of horizontal pleiotropy. Using positive and negative controls, we demonstrated that MR Corge estimates aligned with established biomedical knowledge and the results of randomized controlled trials. MR Corge may be widely applied to investigate polygenic exposure-outcome relationships. AVAILABILITY AND IMPLEMENTATION: An open-sourced R package is available at https://github.com/zhwm/MRCorge. Wenmin Zhang, Chen-Yang Su, Satoshi Yoshiji, Tianyuan Lu |
Bioinform. | 3 |