Evidence map›Paper›PMID 25488329›Full record

ArticleScientific reports2014

Next-generation sequencing of the mitochondrial genome and association with IgA nephropathy in a renal transplant population.

Adam P Douglas, Dwaine R Vance, Elaine M Kenny, Derek W Morris, Alexander P Maxwell, Amy Jayne McKnight

Abstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–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

13 citing papers in PubMed.

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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

6 authors.

Adam P DouglasCentre for Public Health, Queen's University Belfast, United Kingdom.
Dwaine R VanceCentre for Public Health, Queen's University Belfast, United Kingdom.
Elaine M KennyTrinSeq, Trinity Genome Sequencing Lab, Department of Psychiatry, Institute of Molecular Medicine, Trinity College, Dublin, Ireland.
Derek W MorrisTrinSeq, Trinity Genome Sequencing Lab, Department of Psychiatry, Institute of Molecular Medicine, Trinity College, Dublin, Ireland.
Alexander P Maxwell1] Centre for Public Health, Queen's University Belfast, United Kingdom [2] Regional Nephrology Unit, Belfast City Hospital, Belfast, United Kingdom.
Amy Jayne McKnightCentre for Public Health, Queen's University Belfast, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kidneys are highly aerobic organs that are critically dependent on the normal functioning of mitochondria. Genetic variations disrupting mitochondrial function are associated with multifactorial disorders including kidney disease. This study sequenced the entire mitochondrial genome in a renal transplant cohort of 64 individuals, using next-generation sequencing, to evaluate the association of genetic variants with IgA nephropathy and end-stage renal disease (ESRD, n = 100).

Indexed as

Genetic Association StudiesGenome, MitochondrialKidney TransplantationAllelesGene FrequencyGenes, MitochondrialGenomicsGenotypeGlomerulonephritis, IGAHigh-Throughput Nucleotide SequencingHumansKidney Failure, ChronicLinkage DisequilibriumPolymorphism, Single NucleotideReproducibility of Results

Identifiers

PMID25488329
PMCPMC4260226

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.