Evidence map›Paper›PMID 28944295›Full record

ArticleExpert review of precision medicine and drug development2017

Towards precision medicine in Alzheimer's disease: deciphering genetic data to establish informative biomarkers.

Ornit Chiba-Falek, Michael W Lutz

Abstract read
In one paragraph

Article in Expert review of precision medicine and drug development, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. International journal of molecular sciences · 2021
    Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Alzheimer's & dementia (Amsterdam, Netherlands)
    Article
  8. 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

2 authors.

Ornit Chiba-FalekDepartment of Neurology, Duke University Medical Center, Durham, NC 27710, USA.
Michael W LutzDepartment of Neurology, Duke University Medical Center, Durham, NC 27710, USA.

Funding

Role of the TOMM40 poly-T variant in the pathogenesis of Alzheimer's diseaseR01AG040370 · NIA · DUKE UNIVERSITY · PI CHIBA-FALEK, ORNIT · 2013 to 2017
$2.2M
NIA NIH HHS R01 AG040370
6 · The paper itself

Abstract

introductionDeveloping biomarker tools for identification of individuals at high-risk for late-onset Alzheimer's disease (LOAD) is important for prognosis and early treatment. This review focuses on genetic factors and their potential role for precision medicine in LOAD. AREAS COVERED: EXPERT COMMENTARY: Deciphering the precise causal genetic-variants within LOAD-GWAS regions will advance the development of genetic-biomarkers to complement and refine the

Indexed as

APOEgenetic-based LOAD prediction modelsgenetic biomarkersLate-Onset Alzheimer’s disease (LOAD)precision medicineTOMM40 poly-T

Identifiers

PMID28944295
PMCPMC5605187

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.