Evidence map›Paper›PMID 33816073›Full record

ArticleBalkan journal of medical genetics : BJMG2020

Pros and Cons for Fluorescent

E Ikbal Atli, H Gurkan, H Onur Kirkizlar, E Atli, S Demir, S Yalcintepe, R Kalkan, A M Demir

Abstract read
In one paragraph

Article in Balkan journal of medical genetics : BJMG, 2020. 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
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.

  1. Solitary Bone Plasmacytoma of Left Wrist Joint - A Case Report.Journal of orthopaedic case reports · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Review
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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

8 authors.

E Ikbal AtliDepartment of Medical Genetics, Faculty of Medicine, Edirne, Trakya University, Edirne, Turkey.
H GurkanDepartment of Medical Genetics, Faculty of Medicine, Edirne, Trakya University, Edirne, Turkey.
H Onur KirkizlarDepartment of Hematology, Faculty of Medicine, Trakya University, Edirne, Turkey.
E AtliDepartment of Medical Genetics, Faculty of Medicine, Edirne, Trakya University, Edirne, Turkey.
S DemirDepartment of Medical Genetics, Faculty of Medicine, Edirne, Trakya University, Edirne, Turkey.
S YalcintepeDepartment of Medical Genetics, Faculty of Medicine, Edirne, Trakya University, Edirne, Turkey.
R KalkanDepartment of Medical Genetics, Faculty of Medicine, Near East University, North Nicosia, Northern Cyprus.
A M DemirDepartment of Hematology, Faculty of Medicine, Trakya University, Edirne, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is one of the plasma cell-related hematological malignancies exceeding 10.0% of all marrow cells, and they make a paraprotein that is a marker of the disease. Myeloma is one of the most common types of hematological malignancies in humans. Genetic bio-markers have been used for prognostic markers in patients diagnosed with MM. The genetic and genomic changes have been identified using karyotyping, fluorescent

Indexed as

CytogeneticsFluorescent in situ hybridization (FISH)Multiple myelomaNext generation sequencing (NGS)

Identifiers

PMID33816073
PMCPMC8009570

What OpenQuestion holds

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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.