Evidence map›Paper›PMID 31309534›Full record

ArticleClinical genetics2019

Bioinformatic detection of copy number variation in HNF4A causing maturity onset diabetes of the young.

Amanda J Berberich, Arati Mokashi, Adam D McIntyre, John F Robinson, Henian Cao, Jian Wang, Robert A Hegele

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

Article in Clinical genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Trial
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 2 institutions in 1 country.

Amanda J BerberichDepartment of Medicine and Robarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, N6A 5B7, Canada.ORCID 0000-0002-9461-9036
Arati MokashiDivision of Endocrinology, Department of Pediatrics, IWK Health Centre, Dalhousie University, Faculty of Medicine, Halifax B3K 6R8, Canada.
Adam D McIntyreDepartment of Medicine and Robarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, N6A 5B7, Canada.
John F RobinsonDepartment of Medicine and Robarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, N6A 5B7, Canada.
Henian CaoDepartment of Medicine and Robarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, N6A 5B7, Canada.
Jian WangDepartment of Medicine and Robarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, N6A 5B7, Canada.
Robert A HegeleDepartment of Medicine and Robarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, N6A 5B7, Canada.ORCID 0000-0003-2861-5325
Western University · CADalhousie University · CA

Funding

CIHR
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Computational BiologyDNA Copy Number VariationsGenetic Association StudiesGenetic Predisposition to DiseaseAdolescentComparative Genomic HybridizationDiabetes Mellitus, Type 2FemaleHepatocyte Nuclear Factor 4High-Throughput Nucleotide SequencingHumansHepatocyte Nuclear Factor 4HNF4A protein, human

Identifiers

PMID31309534
PMCPMC6899894
OpenAlexW2961051363

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.