Evidence map›Paper›PMID 30948487›Full record

ArticleHaematologica2019

Compound heterozygosity in

Shruti Bagla, Kanta Bhambhani, Manisha Gadgeel, Steven Buck, Jian-Ping Jin, Yaddanapudi Ravindranath

Abstract readCase Reports
In one paragraph

Article in Haematologica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Case report: Compound heterozygosity inFrontiers in pediatrics · 2022
    Article
  5. Pyruvate kinase deficiency in children.Pediatric blood & cancer · 2021
    Article
  6. Article
  7. Review
  8. 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

6 authors.

Shruti BaglaDivision of Hematology/Oncology, Department of Pediatrics, Wayne State University - School of Medicine, and Children's Hospital of Michigan.
Kanta BhambhaniDivision of Hematology/Oncology, Department of Pediatrics, Wayne State University - School of Medicine, and Children's Hospital of Michigan.
Manisha GadgeelDivision of Hematology/Oncology, Department of Pediatrics, Wayne State University - School of Medicine, and Children's Hospital of Michigan.
Steven BuckDivision of Hematology/Oncology, Department of Pediatrics, Wayne State University - School of Medicine, and Children's Hospital of Michigan.
Jian-Ping JinDepartment of Physiology, Wayne State University, School of Medicine, Detroit, MI, USA.
Yaddanapudi RavindranathDivision of Hematology/Oncology, Department of Pediatrics, Wayne State University - School of Medicine, and Children's Hospital of Michigan ravi@med.wayne.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

HeterozygoteMutation, Missense5' Untranslated RegionsAllelesAnemia, HemolyticAnemia, Hemolytic, Congenital NonspherocyticBinding SitesBlood TransfusionChildExonsFemaleGATA1 Transcription FactorHumansIntronsMutationPyruvate Kinase5' Untranslated RegionsGATA1 protein, humanGATA1 Transcription FactorPKLR protein, humanPyruvate Kinase

Identifiers

PMID30948487
PMCPMC6717571

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.