Evidence map›Paper›PMID 37265977›Full record

ArticleBalkan journal of medical genetics : BJMG2023

High Risk of Gestational Trophoblastic Neoplasia Development in Recurrent Hydatidiform Moles with

M Kocabey, I Gulhan, A Koc, T Cankaya, V Karatasli, A Ileri

Open access · goldAbstract read
In one paragraph

Article in Balkan journal of medical genetics : BJMG, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Advances in the genetic etiology of female infertility.Journal of assisted reproduction and genetics · 2024
    Review
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 at 3 institutions in 1 country.

M KocabeyDepartment of Medical Genetics, Faculty of Medicine, Dokuz Eylul University, Izmir, Turkey, 35330.
I GulhanDepartment of Gynecologic Oncology, Izmir Tepecik Training and Research Hospital, Izmir, Turkey, 35020.
A KocDepartment of Medical Genetics, Faculty of Medicine, Dokuz Eylul University, Izmir, Turkey, 35330.
T CankayaDepartment of Medical Genetics, Faculty of Medicine, Dokuz Eylul University, Izmir, Turkey, 35330.
V KaratasliDepartment of Gynecologic Oncology, Izmir Tepecik Training and Research Hospital, Izmir, Turkey, 35020.
A IleriDepartment of Obstetrics and Gynecology, Izmir Tepecik Training and Research Hospital, Izmir, Turkey, 35020.
Dokuz Eylül University · TRIzmir Tepecik Eğitim ve Araştırma Hastanesi · TRIzmir University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Pathogenic variations of the Material and Methods: Three unrelated cases with recurrent molar pregnancies are included in this study. None of the patients had a known family history of molar pregnancy. Clinical findings and follow-up results are documented. Sanger sequencing is used to reveal genetic defects in exons and exon-intron boundaries of Results: Conclusions: We found that defects of the

Indexed as

GeneticKHDC3LNLRP7Recurrent hydatidiform mole

Identifiers

PMID37265977
PMCPMC10230829
OpenAlexW4368282579

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.