Evidence map›Paper›PMID 30846498›Full record

ArticleHaematologica2019

Hereditary platelet function disorder from

Jae Won Yun, Ki-O Lee, Chul Won Jung, Soo-Young Oh, Sun-Hee Kim, Chul Won Choi, Hee-Jin Kim

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Observational
  2. Article
  3. Review
  4. Review
  5. 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 4 institutions in 2 countries.

Jae Won YunDepartment of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul.
Ki-O LeeSamsung Biomedical Research Institute, Samsung Medical Center.
Chul Won JungDepartment of Internal Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine.
Soo-Young OhDepartment of Obstetrics and Gynecology, Samsung Medical Center, Sungkyunkwan University School of Medicine.
Sun-Hee KimDepartment of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul.
Chul Won ChoiDivision of Hematology and Oncology, Department of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Hee-Jin KimDepartment of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul heejinkim@skku.edu.
Sungkyunkwan University · KRSamsung Medical Center · KRBiomedical Research Institute · USKorea University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseMutationAdultAllelesAmino Acid SubstitutionBlood Platelet DisordersDisease ManagementDNA Mutational AnalysisExome SequencingFemaleGenotypeGuanine Nucleotide Exchange FactorsHemorrhageHumansPregnancyGuanine Nucleotide Exchange FactorsRASGRP2 protein, human

Identifiers

PMID30846498
PMCPMC6545837
OpenAlexW2922311520

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.