Evidence map›Paper›PMID 40321317›Full record

ArticleInternational journal of genomics2025

An Oxford Nanopore Technologies-Based Sequencing Assay for Molecular Diagnosis of Phenylketonuria and Variant Frequencies in a Turkish Cohort.

Gülten Tuncel, Mehmet Cihan Balcı, Gökçe Akan, Hasan Hüseyin Kazan, Özge Özgen, Ahmet Çağlar Özketen, Meryem Karaca, Asuman Gedikbaşı, Fatmahan Atalar, Gülden Fatma Gökçay

Abstract read
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Article in International journal of genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Gülten TuncelDESAM Research Institute, Near East University, Mersin, Türkiye.ORCID https://orcid.org/0000-0002-3332-471X
Mehmet Cihan BalcıDivision of Paediatric Nutrition and Metabolism, Istanbul Medical Faculty, Istanbul University, Istanbul, Türkiye.ORCID https://orcid.org/0000-0003-2167-8139
Gökçe AkanDESAM Research Institute, Near East University, Mersin, Türkiye.ORCID https://orcid.org/0000-0002-3878-1135
Hasan Hüseyin KazanDepartment of Medical Biology, Gulhane Faculty of Medicine, University of Health Sciences, Ankara, Türkiye.ORCID https://orcid.org/0000-0001-7936-8606
Özge ÖzgenRare Diseases Research Laboratory, Istanbul Medical Faculty, Istanbul University, Istanbul, Türkiye.ORCID https://orcid.org/0000-0002-1859-3962
Ahmet Çağlar ÖzketenDESAM Research Institute, Near East University, Mersin, Türkiye.ORCID https://orcid.org/0000-0001-6482-6918
Meryem KaracaDivision of Paediatric Nutrition and Metabolism, Istanbul Medical Faculty, Istanbul University, Istanbul, Türkiye.
Asuman GedikbaşıDepartment of Paediatric Basic Sciences, Institute of Child Health, Istanbul Medical Faculty, Istanbul University, Istanbul, Türkiye.ORCID https://orcid.org/0000-0001-7121-6077
Fatmahan AtalarRare Diseases Research Laboratory, Istanbul Medical Faculty, Istanbul University, Istanbul, Türkiye.ORCID https://orcid.org/0000-0002-1793-9220
Gülden Fatma GökçayDivision of Paediatric Nutrition and Metabolism, Istanbul Medical Faculty, Istanbul University, Istanbul, Türkiye.ORCID https://orcid.org/0000-0003-3726-5726

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

molecular diagnostic techniquesnanopore sequencingneonatal screeningphenylalanine hydroxylasephenylketonurias

Identifiers

PMID40321317
PMCPMC12048195

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.