Evidence map›Paper›PMID 32125967›Full record

ArticleTurkish journal of urology2020

Evaluation of chromosomal abnormalities and Y-chromosome microdeletions in 1696 Turkish cases with primary male infertility: A single-center study.

Taha Reşid Özdemir, Berk Özyılmaz, Özgür Çakmak, Özge Özer Kaya, Can Köse, Özgür Kırbıyık, Mehmet Zeynel Keskin, Altuğ Koç, Tuğba Zeyrek, Yaşar Bekir Kutbay and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Turkish journal of urology, 2020. 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
1.1field-weighted citation impact, top 19% 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, 17 citations in OpenAlex.

  1. Article
  2. Gene Polymorphism, Microdeletion, and Gene Expression ofReports of biochemistry & molecular biology · 2023
    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

12 authors at 1 institution in 1 country.

Taha Reşid ÖzdemirGenetic Diagnostic Center, Health Sciences University, İzmir Tepecik Training and Research Hospital, İzmir, Turkey.ORCID http://orcid.org/0000-0003-4870-6945
Berk ÖzyılmazGenetic Diagnostic Center, Health Sciences University, İzmir Tepecik Training and Research Hospital, İzmir, Turkey.ORCID http://orcid.org/0000-0003-2654-3698
Özgür ÇakmakDepartment of Urology, Health Sciences University, İzmir Tepecik Training and Research Hospital, İzmir, Turkey.ORCID http://orcid.org/0000-0002-4618-9465
Özge Özer KayaGenetic Diagnostic Center, Health Sciences University, İzmir Tepecik Training and Research Hospital, İzmir, Turkey.ORCID http://orcid.org/0000-0001-6731-2461
Can KöseDepartment of Histology and Embryology, Health Sciences University, İzmir Tepecik Training and Research Hospital, İzmir, Turkey.ORCID http://orcid.org/0000-0001-7351-7981
Özgür KırbıyıkGenetic Diagnostic Center, Health Sciences University, İzmir Tepecik Training and Research Hospital, İzmir, Turkey.ORCID http://orcid.org/0000-0003-1333-2007
Mehmet Zeynel KeskinDepartment of Urology, Health Sciences University, İzmir Tepecik Training and Research Hospital, İzmir, Turkey.ORCID http://orcid.org/0000-0002-9206-5586
Altuğ KoçGenetic Diagnostic Center, Health Sciences University, İzmir Tepecik Training and Research Hospital, İzmir, Turkey.ORCID http://orcid.org/0000-0002-8366-6806
Tuğba ZeyrekDepartment of Histology and Embryology, Health Sciences University, İzmir Tepecik Training and Research Hospital, İzmir, Turkey.ORCID http://orcid.org/0000-0002-1427-6863
Yaşar Bekir KutbayGenetic Diagnostic Center, Health Sciences University, İzmir Tepecik Training and Research Hospital, İzmir, Turkey.ORCID http://orcid.org/0000-0002-9006-5072
Kadri Murat ErdoğanGenetic Diagnostic Center, Health Sciences University, İzmir Tepecik Training and Research Hospital, İzmir, Turkey.ORCID http://orcid.org/0000-0003-0097-1424
Merve Saka GüvençGenetic Diagnostic Center, Health Sciences University, İzmir Tepecik Training and Research Hospital, İzmir, Turkey.ORCID http://orcid.org/0000-0001-8842-0381
Izmir University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe aim of this study was to determine the frequencies of chromosomal abnormalities and Y-chromosome microdeletions in Turkish cases with primary male infertility in a single center. MATERIAL AND

methodsChromosomal abnormalities and Y-chromosome microdeletions were investigated in 1696 cases with primary male infertility between 2012 and 2017. Karyotype analyzes and Y-chromosome microdeletions analyzes [azoospermia factor (AZF) regions] were performed in all cases by using standard cytogenetic methods and the multiplex polymerase chain reaction method, respectively.

resultsChromosomal abnormalities were found in 142 cases (8.4%; 142/1696). Y-chromosome microdeletions were detected in 46 cases (2.7%; 46/1696). Y-chromosome microdeletions in the AZFc region were found in 20 of 46 cases (43%).

conclusionThis study is one of the few were a large number of cases was studied in Turkey. It indicates that cytogenetic and Y-chromosome microdeletion studies should be conducted in cases with primary male infertility prior to selecting assisted reproductive techniques.

Identifiers

PMID32125967
PMCPMC7053983
OpenAlexW2996462405

What OpenQuestion holds

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Registered trials

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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.