Evidence map›Paper›PMID 35682719›Full record

ArticleInternational journal of molecular sciences2022

Searching for the Molecular Basis of Partial Deafness.

Dominika Oziębło, Natalia Bałdyga, Marcin L Leja, Henryk Skarżyński, Monika Ołdak

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 52% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

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

5 authors at 2 institutions in 1 country.

Dominika OziębłoDepartment of Genetics, Institute of Physiology and Pathology of Hearing, 02-042 Warsaw, Poland.ORCID 0000-0002-3454-8002
Natalia BałdygaDepartment of Genetics, Institute of Physiology and Pathology of Hearing, 02-042 Warsaw, Poland.ORCID 0000-0002-3140-8821
Marcin L LejaDepartment of Genetics, Institute of Physiology and Pathology of Hearing, 02-042 Warsaw, Poland.ORCID 0000-0002-3856-8377
Henryk SkarżyńskiOto-Rhino-Laryngology Surgery Clinic, Institute of Physiology and Pathology of Hearing, 02-042 Warsaw, Poland.ORCID 0000-0001-7141-9851
Monika OłdakDepartment of Genetics, Institute of Physiology and Pathology of Hearing, 02-042 Warsaw, Poland.ORCID 0000-0002-4216-9141
Institute of Physiology and Pathology of Hearing · PLMedical University of Warsaw · PL

Funding

National Science Center 2016/22/E/NZ5/00470National Science Center 2017/27/N/NZ5/02369
6 · The paper itself

Abstract

Hearing is an important human sense for communicating and connecting with others. Partial deafness (PD) is a common hearing problem, in which there is a down-sloping audiogram. In this study, we apply a practical system for classifying PD patients, used for treatment purposes, to distinguish two groups of patients: one with almost normal hearing thresholds at low frequencies (PDT-EC,

Indexed as

Cochlear ImplantationDeafnessHearing LossHearing Loss, SensorineuralReceptors, SteroidGenes, RecessiveHumansOxysterol Binding ProteinsOSBPL2 protein, humanOxysterol Binding ProteinsReceptors, Steroidcochlear implantationgenegeneticshearing losshigh-throughput sequencingpartial deafnesspathogenic variantPDT-EASPDT-EC

Identifiers

PMID35682719
PMCPMC9181477
OpenAlexW4281735300

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.