ArticleApplied network science2016
Supporting novel biomedical research via multilayer collaboration networks.
Article in Applied network science, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- A Recommender for Research Collaborators Using Graph Neural Networks.Frontiers in artificial intelligence · 2022Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The value of research containing novel combinations of molecules can be seen in many innovative and award-winning research programs. Despite calls to use innovative approaches to address common diseases, an increasing majority of research funding goes toward "safe" incremental research. Counteracting this trend by nurturing novel and potentially transformative scientific research is challenging and it must be supported in competition with established research programs. Therefore, we propose a tool that helps to resolve the tension between safe/fundable research vs. high-risk/potentially transformational research. It does this by identifying hidden overlapping interests around novel molecular research topics. Specifically, it identifies paths of molecular interactions that connect research topics and hypotheses that would not typically be associated, as the basis for scientific collaboration. Because these collaborations are related to the scientists' present trajectory, they are low risk and can be initiated rapidly. Unlike most incremental steps, these collaborations have the potential for leaps in understanding, as they reposition research for novel disease applications. We demonstrate the use of this tool to identify scientists who could contribute to understanding the cellular role of genes with novel associations with Alzheimer's disease, which have not been thoroughly characterized, in part due to the funding emphasis on established research.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.