Evidence map›Paper›PMID 20508730›Full record

ArticleMolecular vision2010

A new locus for autosomal dominant congenital coronary cataract in a Chinese family maps to chromosome 3q.

Guishun Liu, Yunbo Li, Yanfei Ruan, Wenping Cao, Li Xin, Jiangyuan Qian, Jingzhi Gu

Open access · greenAbstract read
In one paragraph

Article in Molecular vision, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 1 institution in 1 country.

Guishun LiuDepartment of Ophthalmology, the Port Hospital of Tianjin, Tianjin, China.
Yunbo Li
Yanfei Ruan
Wenping Cao
Li Xin
Jiangyuan Qian
Jingzhi Gu
Tianjin Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo identify the genetic defect in an autosomal dominant congenital coronary cataract family (ADCCC).

methodsA Chinese family with ADCC was identified and characterized. All the members were genotyped with microsatellite markers at genes and loci that were considered to be associated with hereditary cataracts. Linkage analysis was performed after genotyping. Two-point Logarithm of odds (LOD) scores were calculated using MLINK software, from the LINKAGE program package. Multipoint parametric and non-parametric linkage were performed via the program MERLIN.

resultsLinkage analysis provided evidence for a genetic locus for the ADCC on chromosome 3q. The maximum Two-point LOD score was 3.01 (theta=0) for two close markers.

conclusionsThe mapping of the congenital cataracts in a Chinese family locus to chromosome 3q.

Indexed as

Chromosome MappingChromosomes, Human, Pair 3Genes, DominantAsian PeopleCataractFemaleGenetic LinkageGenotypeHumansLod ScoreMaleMicrosatellite RepeatsRare Diseases

Identifiers

PMID20508730
PMCPMC2874577
OpenAlexW174230100

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.