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Enhancing systems medicine beyond genotype data by dynamic patient signatures: having information and using it too

Overview of attention for article published in Frontiers in Genetics, January 2013
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Title
Enhancing systems medicine beyond genotype data by dynamic patient signatures: having information and using it too
Published in
Frontiers in Genetics, January 2013
DOI 10.3389/fgene.2013.00241
Pubmed ID
Authors

Frank Emmert-Streib, Matthias Dehmer

Abstract

In order to establish systems medicine, based on the results and insights from basic biological research applicable for a medical and a clinical patient care, it is essential to measure patient-based data that represent the molecular and cellular state of the patient's pathology. In this paper, we discuss potential limitations of the sole usage of static genotype data, e.g., from next-generation sequencing, for translational research. The hypothesis advocated in this paper is that dynOmics data, i.e., high-throughput data that are capable of capturing dynamic aspects of the activity of samples from patients, are important for enabling personalized medicine by complementing genotype data.

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The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 18 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 18 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 28%
Student > Ph. D. Student 3 17%
Professor 2 11%
Other 1 6%
Professor > Associate Professor 1 6%
Other 0 0%
Unknown 6 33%
Readers by discipline Count As %
Medicine and Dentistry 5 28%
Computer Science 3 17%
Agricultural and Biological Sciences 2 11%
Chemistry 1 6%
Design 1 6%
Other 0 0%
Unknown 6 33%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 19 November 2013.
All research outputs
#20,210,424
of 22,731,677 outputs
Outputs from Frontiers in Genetics
#8,548
of 11,757 outputs
Outputs of similar age
#248,807
of 280,774 outputs
Outputs of similar age from Frontiers in Genetics
#263
of 319 outputs
Altmetric has tracked 22,731,677 research outputs across all sources so far. This one is in the 1st percentile – i.e., 1% of other outputs scored the same or lower than it.
So far Altmetric has tracked 11,757 research outputs from this source. They receive a mean Attention Score of 3.7. This one is in the 1st percentile – i.e., 1% of its peers scored the same or lower than it.
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We're also able to compare this research output to 319 others from the same source and published within six weeks on either side of this one. This one is in the 1st percentile – i.e., 1% of its contemporaries scored the same or lower than it.