Evidence map›Paper›PMID 21898125›Full record

ReviewJournal of molecular neuroscience : MN2011

Frontotemporal dementia: from Mendelian genetics towards genome wide association studies.

Raffaele Ferrari, John Hardy, Parastoo Momeni

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of molecular neuroscience : MN, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.4field-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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Genome-wide association studies in neurology.Annals of translational medicine · 2014
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. 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 at 3 institutions in 2 countries.

Raffaele FerrariDepartment of Internal Medicine, Texas Tech University Health Sciences Center, 3601 4th St. STOP 9410, Lubbock, TX 79430, USA. raffaele.ferrari@ttuhsc.edu
John Hardy
Parastoo Momeni
National Hospital for Neurology and Neurosurgery · GBTexas Tech University · USTexas Tech University Health Sciences Center · US

Funding

Medical Research Council G0701075
6 · The paper itself

Abstract

Frontotemporal lobar degeneration is the most common cause of dementia of non-Alzheimer's type worldwide. It manifests, clinically, with behavioural changes and language impairment and is pathologically associated with tau- or ubiquitin-positive inclusions detected in neurons and glial cells of the frontal and temporal lobes in the brain. Genetic variations in the microtubule-associated protein tau and progranulin genes explain almost 50% of familial cases, whilst variations in TAR DNA-binding protein, charged multivescicular body protein 2B, valosin-containing protein and fused in sarcoma genes contribute to <5% of cases. The rapidly developing investigative techniques available to geneticists such as genome-wide association studies, whole-exome sequencing and, soon, whole-genome sequencing promise to contribute to the unravelling of the genetic architecture of this complex disease and, in the future, to the development of more sensitive, accurate and effective diagnostic and treatment measures.

Indexed as

Genome-Wide Association StudyAdenosine TriphosphatasesCell Cycle ProteinsEndosomal Sorting Complexes Required for TransportExonsFrontotemporal DementiaFrontotemporal Lobar DegenerationHaplotypesHumansIntercellular Signaling Peptides and ProteinsMutationProgranulinstau ProteinsValosin Containing ProteinAdenosine TriphosphatasesCell Cycle ProteinsCHMP2B protein, humanEndosomal Sorting Complexes Required for TransportGRN protein, humanIntercellular Signaling Peptides and ProteinsMAPT protein, humanProgranulinstau ProteinsValosin Containing ProteinVCP protein, human

Identifiers

PMID21898125
OpenAlexW2008987424

What OpenQuestion holds

Textmetadata
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.