Evidence map›Paper›PMID 31264897›Full record

ReviewInternational journal of audiology2019

Genetic screening as an adjunct to universal newborn hearing screening: literature review and implications for non-congenital pre-lingual hearing loss.

Christine D'Aguillo, Sara Bressler, Denise Yan, Rahul Mittal, Robert Fifer, Susan H Blanton, Xuezhong Liu

Open access · greenAbstract readReview
In one paragraph

Review in International journal of audiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 32% 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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Hearing loss in neonates and infants.Clinical and experimental pediatrics · 2023
    Article
  7. Various aspects of hearing loss in newborns: A narrative review.World journal of clinical pediatrics · 2023
    Review
  8. Review
  9. 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

7 authors at 1 institution in 2 countries.

Christine D'AguilloDepartment of Otolaryngology, University of Miami Miller School of Medicine, Miami, FL, USA.
Sara BresslerDepartment of Otolaryngology, University of Miami Miller School of Medicine, Miami, FL, USA.
Denise YanDepartment of Otolaryngology, University of Miami Miller School of Medicine, Miami, FL, USA.
Rahul MittalDepartment of Otolaryngology, University of Miami Miller School of Medicine, Miami, FL, USA.ORCID 0000-0003-0894-237X
Robert FiferDepartment of Pediatrics, University of Miami Miller School of Medicine, Miami, FL, USA.
Susan H BlantonDepartment of Otolaryngology, University of Miami Miller School of Medicine, Miami, FL, USA.
Xuezhong LiuDepartment of Otolaryngology, University of Miami Miller School of Medicine, Miami, FL, USA.
University of Miami · US

Funding

Molecular Genetics on Non Syndromic Hearing Loss (NSHL)R01DC005575 · NIDCD · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI LIU, XUE Z · 2001 to 2024
$10.6M
Sensory disorders in COVID -19 as an early identifier and healthcare worker protectionR01DC012115 · NIDCD · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI LIU, XUE Z · 2013 to 2022
$7.2M
Preclinical Testing of PI3K Inhibitors for Vestibular SchwannomasR01DC017264 · NIDCD · UNIVERSITY OF CENTRAL FLORIDA · PI FERNANDEZ-VALLE, CRISTINA MARIA, LIU, XUE Z · 2018 to 2022
$3.1M
Interdisciplinary Research Training in OtolaryngologyT32DC015995 · NIDCD · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI LIU, XUE Z · 2018 to 2022
$330k
NIDCD NIH HHS R01 DC005575NIDCD NIH HHS R01 DC012115NIDCD NIH HHS R01 DC017264NIDCD NIH HHS T32 DC015995
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genetic TestingHearing TestsNeonatal ScreeningHearing LossHumansInfant, NewbornCongenital hearing lossgenetic screenhereditary hearing lossnewborn hearing screennon-congenital pre-lingual hearing losspre-lingual hearing loss

Identifiers

PMID31264897
PMCPMC7244215
OpenAlexW2955325273

What OpenQuestion holds

Textmetadata
LicenceTDM
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.