Evidence map›Paper›PMID 24895341›Full record

ArticleHaematologica2014

Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus.

Hannah Bogardus, Vincent P Schulz, Yelena Maksimova, Barbara A Miller, Peining Li, Bernard G Forget, Patrick G Gallagher

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

Article in Haematologica, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact, top 86% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Exome-Based Trio Analysis for Diagnosis of the Cause of Congenital Severe Hemolytic Anemia in a Child.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2022
    Article
  3. Review
  4. The Spectrum ofFrontiers in physiology · 2019
    Article
  5. Review
  6. Corrigendum: The Spectrum ofFrontiers in physiology
    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

7 authors at 2 institutions in 1 country.

Hannah BogardusDepartment of Pediatrics, Yale University School of Medicine, New Haven, CT.
Vincent P SchulzDepartment of Pediatrics, Yale University School of Medicine, New Haven, CT.
Yelena MaksimovaDepartment of Pediatrics, Yale University School of Medicine, New Haven, CT.
Barbara A MillerDepartments of Pediatrics and Biochemistry and Molecular Biology, Penn State University College of Medicine, Hershey, PA.
Peining LiDepartment of Genetics, Yale University School of Medicine, New Haven, CT, USA.
Bernard G ForgetDepartment of Genetics, Yale University School of Medicine, New Haven, CT, USA Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, USA.
Patrick G GallagherDepartment of Pediatrics, Yale University School of Medicine, New Haven, CT Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, USA Department of Pathology, Yale University School of Medicine, New Haven, CT, USA patrick.gallagher@yale.edu.
Yale University · USPenn State Milton S. Hershey Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Chromosomes, Human, Pair 1MutationAnkyrinsComparative Genomic HybridizationExonsFemaleGene DosageGenetic LociHumansIntronsMalePedigreeSeverity of Illness IndexSpectrinSpherocytosis, HereditaryUniparental DisomyAnkyrinsSpectrinanemiachromosome 1qerythrocyteisodisomymembranespectrinspherocytosisuniparental disomy

Identifiers

PMID24895341
PMCPMC4562552
OpenAlexW2069579506

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.