Evidence map›Paper›PMID 40350211›Full record

ReviewClinics in perinatology2025

Advances in Genetic Testing of Neurologically Abnormal Neonates in the Neonatal Intensive Care Unit.

William Burns, Darrah Haffner, Bimal P Chaudhari

Abstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Clinics in perinatology, 2025. 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
–field-weighted citation impact
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

3 authors.

William BurnsDivision of Genetics and Genomic Medicine, Nationwide Children's Hospital, 700 Children's Drive, Columbus, OH 43215, USA.
Darrah HaffnerDivision of Neurology, Nationwide Children's Hospital, 700 Children's Drive, Columbus, OH 43215, USA.
Bimal P ChaudhariDivision of Genetics and Genomic Medicine, Nationwide Children's Hospital, 700 Children's Drive, Columbus, OH 43215, USA; Division of Neonatology, Nationwide Children's Hospital, 700 Children's Drive, Columbus, OH, USA; Steve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children's Hospital, Research Building 3, 575 Children's Xroads WB 3151, Columbus, OH 43205, USA; Clinical and Translational Sciences Institute, Nationwide Children's Hospital and The Ohio State University, Columbus, OH, USA. Electronic address: Bimal.Chaudhari@NationwideChildrens.org.

Funding

The OSU Center for Clinical and Translational Science: Advancing Today's Discoveries to Improve HealthUM1TR004548 · NCATS · OHIO STATE UNIVERSITY · PI CYNTHIA A GERHARDT, JULIE A. JOHNSON · 2023 to 2026
$22.0M
NCATS NIH HHS UM1 TR004548
6 · The paper itself

Abstract

Recent advances in cost and speed with which genome sequencing can be achieved have changed the approach to genetic testing in neonatal intensive care units (NICUs). In this article, we review the impact of these changes on the genetic evaluation of the neurologically abnormal neonate admitted to a NICU and share our center's approach to this important patient population, developed through multidisciplinary collaboration and reflective of a growing body of literature. We emphasize the importance of early identification of treatable disorders and other actionable findings.

Indexed as

Genetic TestingIntensive Care Units, NeonatalNervous System DiseasesHumansInfant, NewbornNeonatal ScreeningNeonatal neurologyNeurocritical careRapid genome sequencing

Identifiers

PMID40350211
PMCPMC13652047

What OpenQuestion holds

Textmetadata
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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.