Evidence map›Paper›PMID 19285134›Full record

ReviewNeurobiology of disease2009

Chipping away at diagnostics for neurodegenerative diseases.

Clemens R Scherzer

Open access · greenAbstract readReview
In one paragraph

Review in Neurobiology of disease, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Transcriptional modulator H2A histone family, member Y (H2AFY) marks Huntington disease activity in man and mouse.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Neurodegeneration as an RNA disorder.Progress in neurobiology · 2012
    Review
  8. Article
  9. Article
  10. Pilot study: peripheral biomarkers for diagnosing sporadic Parkinson's disease.Journal of neural transmission (Vienna, Austria : 1996) · 2010
    Article
  11. Article
  12. Review
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

1 author at 1 institution in 1 country.

Clemens R ScherzerLaboratory for Neurogenomics, Center for Neurologic Diseases, Harvard Medical School and Brigham and Women's Hospital, 65 Landsdowne Street, Suite 307A, Cambridge, MA 02139, USA. cscherzer@rics.bwh.harvard.edu
Harvard University · US

Funding

Neuroimaging Biomarkers for disease-modyfying therapies in Hintington's diseaseP01NS058793 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI HERSCH, STEVEN M · 2008 to 2012
$6.6M
Risk Marker for Parkinson's Disease: Enabling Novel TherapiesR01NS064155 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI SCHERZER, CLEMENS R · 2008 to 2011
$1.7M
Genomic and Genetic Analysis of Parkinson's DiseaseK08AG024816 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI SCHERZER, CLEMENS R · 2004 to 2008
$840k
Multigene Marker of Progression in Parkinson's DiseaseR21NS060227 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI SCHERZER, CLEMENS R · 2007 to 2008
$421k
NIA NIH HHS K08 AG024816NIA NIH HHS K08AG024816NINDS NIH HHS NS058793NINDS NIH HHS NS060227NINDS NIH HHS NS064155NINDS NIH HHS P01 NS058793NINDS NIH HHS R01 NS064155NINDS NIH HHS R21 NS060227
6 · The paper itself

Abstract

Biomarkers are needed to overcome critical roadblocks in the development of disease-modifying therapeutics for neurodegenerative diseases. Evolving genome-wide expression technologies can comprehensively search for molecular biomarkers and allow fascinating insights into the expanding complexity of the human transcriptome. The technology has matured to the point where some applications are deemed reliable enough for use in patient care. In the neurosciences, it has led to the discoveries of osteopontin in multiple sclerosis and SORL1/LR11 in Alzheimer's, and recent studies indicate its potential for identifying neurogenomic biomarkers. Advances in pre-analytical and analytical methods are improving search efficiency and reproducibility and may lead to a pipeline of biomarker candidates suitable for development into future neurologic diagnostics.

Indexed as

Gene ExpressionAlzheimer DiseaseAnimalsBiomarkersBrainClinical Trials as TopicGenetic Predisposition to DiseaseHumansLDL-Receptor Related ProteinsMembrane Transport ProteinsMultiple SclerosisNeurodegenerative DiseasesOligonucleotide Array Sequence AnalysisOsteopontinRNABiomarkersLDL-Receptor Related ProteinsMembrane Transport ProteinsOsteopontinRNASORL1 protein, human

Identifiers

PMID19285134
PMCPMC2753504
OpenAlexW2084210959

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.