Evidence map›Paper›PMID 24642830›Full record

ArticleEuropean journal of human genetics : EJHG2014

Common variant rs10033900 near the complement factor I gene is associated with age-related macular degeneration risk in Han Chinese population.

Dingguo Qian, Mengyuan Kan, Xiaoling Weng, Yugeng Huang, Changbo Zhou, Genlong Yu, Ting Wang, Daizhan Zhou, Zhou Zhang, Di Zhang and 2 more

Open access · bronzeAbstract readLetter
PubMed Full text at PMC Publisher
In one paragraph

Article in European journal of human genetics : EJHG, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Characterization of polymorphisms inMolecular biology research communications · 2022
    Article
  4. Article
  5. Haplotypes ofDisease markers · 2019
    Article
  6. Article
  7. 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

12 authors at 3 institutions in 1 country.

Dingguo QianDepartment of Ophthalmology, Putuo Peoples's Hospital, Zhoushan, China.
Mengyuan KanInstitute for Nutritional Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Graduate School of the Chinese Academy of Sciences, Shanghai, China.
Xiaoling WengInstitutes of Biomedical Sciences, Fudan University, Shanghai, China.
Yugeng HuangDepartment of Ophthalmology, Putuo Peoples's Hospital, Zhoushan, China.
Changbo ZhouDepartment of Ophthalmology, Putuo Peoples's Hospital, Zhoushan, China.
Genlong YuPutuo People's Hospital Laboratory, Zhoushan, China.
Ting WangInstitute for Nutritional Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Graduate School of the Chinese Academy of Sciences, Shanghai, China.
Daizhan ZhouBio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders, Ministry of Education, Shanghai Jiao Tong University, Shanghai, China.
Zhou ZhangBio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders, Ministry of Education, Shanghai Jiao Tong University, Shanghai, China.
Di ZhangBio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders, Ministry of Education, Shanghai Jiao Tong University, Shanghai, China.
Wei TangBio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders, Ministry of Education, Shanghai Jiao Tong University, Shanghai, China.
Yun LiuInstitutes of Biomedical Sciences, Fudan University, Shanghai, China.
Shanghai Jiao Tong University · CNChinese Academy of Sciences · CNFudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AgedAged, 80 and overAllelesAsian PeopleCase-Control StudiesComplement Factor IFemaleGene FrequencyGenetic VariationGenotypeGenotyping TechniquesHumansMacular DegenerationMaleMiddle AgedComplement Factor I

Identifiers

PMID24642830
PMCPMC4231406
OpenAlexW2055117406

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.