Evidence map›Paper›PMID 31439644›Full record

ArticleDiabetes2019

Nadja Vuori, Niina Sandholm, Anmol Kumar, Kustaa Hietala, Anna Syreeni, Carol Forsblom, Kati Juuti-Uusitalo, Heli Skottman, Minako Imamura, Shiro Maeda and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  5. Observational
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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

14 authors at 4 institutions in 3 countries.

Nadja VuoriFolkhälsan Institute of Genetics, Folkhälsan Research Center, Helsinki, Finland.ORCID 0000-0003-4322-6942
Niina SandholmFolkhälsan Institute of Genetics, Folkhälsan Research Center, Helsinki, Finland.
Anmol KumarFolkhälsan Institute of Genetics, Folkhälsan Research Center, Helsinki, Finland.
Kustaa HietalaCentral Finland Central Hospital, Jyväskylä, Finland.
Anna SyreeniFolkhälsan Institute of Genetics, Folkhälsan Research Center, Helsinki, Finland.ORCID 0000-0003-1857-2560
Carol ForsblomFolkhälsan Institute of Genetics, Folkhälsan Research Center, Helsinki, Finland.
Kati Juuti-UusitaloFaculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Heli SkottmanFaculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Minako ImamuraLaboratory for Endocrinology, Metabolism and Kidney Diseases, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan.
Shiro MaedaLaboratory for Endocrinology, Metabolism and Kidney Diseases, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan.ORCID 0000-0001-6688-9875
Paula A SummanenOphthalmology, University of Helsinki, Helsinki University Hospital, Helsinki, Finland.
Markku LehtoFolkhälsan Institute of Genetics, Folkhälsan Research Center, Helsinki, Finland.
FinnDiane Study
University of Helsinki · FITampere University · FIUniversity of the Ryukyus · JPCentral Finland Health Care District · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic retinopathy is a common diabetes complication that threatens the eyesight and may eventually lead to acquired visual impairment or blindness. While a substantial heritability has been reported for proliferative diabetic retinopathy (PDR), only a few genetic risk factors have been identified. Using genome-wide sib pair linkage analysis including 361 individuals with type 1 diabetes, we found suggestive evidence of linkage with PDR at chromosome 10p12 overlapping the

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAdultAllelesCalcium Channels, L-TypeCase-Control StudiesDiabetes Mellitus, Type 1Diabetic RetinopathyFemaleGenetic LinkageGenotypeHumansMaleMiddle AgedRetinal Pigment EpitheliumVascular Endothelial Growth Factor ACACNB2 protein, humanCalcium Channels, L-TypeVascular Endothelial Growth Factor A

Identifiers

PMID31439644
PMCPMC6804633
OpenAlexW2969415620

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.