Evidence map›Paper›PMID 22735669›Full record

ReviewExperimental gerontology2012

Genetics of subcortical vascular dementia.

Helena Schmidt, Paul Freudenberger, Stephan Seiler, Reinhold Schmidt

Open access · hybridAbstract readReview
In one paragraph

Review in Experimental gerontology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.5field-weighted citation impact, top 12% of its field
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

18 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Research and development prospects of TRIM65.Journal of cancer research and clinical oncology · 2025
    Review
  3. Article
  4. The Magic and Mystery of TRIM65 in Diseases.Current medicinal chemistry · 2025
    Review
  5. Article
  6. Review
  7. Prostaglandin EFrontiers in aging neuroscience · 2021
    Article
  8. Article
  9. Article
  10. Article
  11. Stroke Risk and Vascular Dementia in South Asians.Current atherosclerosis reports · 2018
    Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. 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

4 authors at 1 institution in 1 country.

Helena SchmidtInstitute of Molecular Biology and Biochemistry, Centre for Molecular Medicine, Medical University of Graz, Harrachgasse 21, A-8010 Graz, Austria. helena.schmidt@meduni-graz.at
Paul Freudenberger
Stephan Seiler
Reinhold Schmidt
Medical University of Graz · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Subcortical vascular dementia or cerebral small vessel disease is a common cause of disability in the elderly. On magnetic resonance imaging the disease is manifested as white matter lesions, lacunes and microbleeds. Its etiology is complex, with age and hypertension as established risk factors. The heritability of white matter lesions is constantly high over different populations. Linkage studies identified several loci for these lesions however no genes responsible for the linkage signals had been identified so far. Results from genetic association studies using the candidate gene approach support the role of APOE, the renin-angiotensin system, as well as the Notch3 signaling pathway in the development of subcortical vascular dementia. The recent genomegenome wide association study on white matter lesions identified a novel locus on chromosome 17q25 harboring several genes such as TRIM65 and TRIM47 which pinpoints to possible novel mechanisms leading to these lesions.

Indexed as

Genetic Predisposition to DiseaseAdaptor Proteins, Signal TransducingAgedAged, 80 and overAge FactorsApolipoproteins EChromosomes, Human, Pair 17Dementia, VascularGenetic LinkageGenome-Wide Association StudyHumansHypertensionMagnetic Resonance ImagingMembrane ProteinsReceptor, Notch3Receptors, NotchAdaptor Proteins, Signal TransducingApolipoproteins EMembrane ProteinsNOTCH3 protein, humanReceptor, Notch3Receptors, NotchTRAT1 protein, human

Identifiers

PMID22735669
PMCPMC3490100
OpenAlexW2055845014

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.