Evidence map›Paper›PMID 20087399›Full record

ArticleEuropean journal of human genetics : EJHG2010

Additional evidence to support the role of a common variant near the complement factor I gene in susceptibility to age-related macular degeneration.

Naoshi Kondo, Hiroaki Bessho, Shigeru Honda, Akira Negi

Abstract readCommentLetter
In one paragraph

Article in European journal of human genetics : EJHG, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
–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

21 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Characterization of polymorphisms inMolecular biology research communications · 2022
    Article
  4. Article
  5. Haplotypes ofDisease markers · 2019
    Article
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  9. Tag SNPs of CFI contributed to the susceptibility for non-small cell lung cancer in Chinese population.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
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  12. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Naoshi Kondo
Hiroaki Bessho
Shigeru Honda
Akira Negi

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAgedAged, 80 and overChromosomes, Human, Pair 4Complement Factor IFemaleGene FrequencyGenetic LociGenome-Wide Association StudyHumansMacular DegenerationMaleMiddle AgedComplement Factor I

Identifiers

PMID20087399
PMCPMC2987347

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.