Evidence map›Paper›PMID 25583407›Full record

ArticleExpert review of molecular diagnostics2015

The development of next-generation screening and diagnostic platforms will change diabetes care.

Rajiv B Kumar, Mihir Gupta, Brian J Feldman

Abstract readEditorial
In one paragraph

Article in Expert review of molecular diagnostics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Rajiv B KumarDepartment of Pediatrics, Stanford School of Medicine, Stanford University, Stanford, CA, USA.
Mihir Gupta
Brian J Feldman

Funding

Using Components of the Circadian Clock to Regulate Stem Cell Fate DecisionsDP2OD006740 · OD · STANFORD UNIVERSITY · PI FELDMAN, BRIAN J · 2010 to 2010
$2.4M
NIH HHS DP2 OD006740
6 · The paper itself

Abstract

Diabetes mellitus is a common disease with a rising incidence and the findings of hyperglycemia and glucosuria. However, there are multiple types of diabetes, each with distinct etiologies. The two major types of diabetes are type 1, which is caused by an autoimmune process, and type 2, which is thought to be primarily metabolic, resulting from insulin resistance, often in the setting of obesity. Historically, the distinction between these two types was obvious. Here, we discuss how this paradigm has dramatically changed because of both the evolving epidemiology of diabetes mellitus and new and emerging tools, and therapies to diagnose and treat diabetes. As we believe that understanding these changes is critical to providing optimal care to patients with diabetes, we have developed a novel plasmonic gold chip platform that is able to meet the new and emerging demands of modern diabetes care.

Indexed as

Diagnostic Techniques and ProceduresDiabetes MellitusDisease ManagementHumansautoantibodiesdiabetesdiabetes mellitusplasmonic gold chip

Identifiers

PMID25583407
PMCPMC4627787

What OpenQuestion holds

Textmetadata
LicenceTDM
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Registered trials

None linked

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.