Evidence map›Paper›PMID 35645283›Full record

ArticleInternational journal of neonatal screening2022

Newborn Screening for X-Linked Adrenoleukodystrophy in Nebraska: Initial Experiences and Challenges.

Craig V Baker, Alyssa Cady Keller, Richard Lutz, Karen Eveans, Krystal Baumert, James C DiPerna, William B Rizzo

Open access · goldAbstract read
In one paragraph

Article in International journal of neonatal screening, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 20% 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, 17 citations in OpenAlex.

  1. Article
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  8. Review
  9. Sex-specific newborn screening for X-linked adrenoleukodystrophy.Journal of inherited metabolic disease · 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

7 authors at 4 institutions in 1 country.

Craig V BakerMunroe-Meyer Institute for Genetics and Rehabilitation, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Alyssa Cady KellerMunroe-Meyer Institute for Genetics and Rehabilitation, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Richard LutzMunroe-Meyer Institute for Genetics and Rehabilitation, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Karen EveansNebraska Newborn Screening Program, Department of Health and Human Services, Lincoln, NE 68509, USA.
Krystal BaumertNebraska Newborn Screening Program, Department of Health and Human Services, Lincoln, NE 68509, USA.
James C DiPernaPerkin Elmer Genetics, Pittsburgh, PA 15275, USA.
William B RizzoDepartment of Pediatrics and Child Health Research Institute, University of Nebraska Medical Center, Omaha, NE 68198, USA.ORCID 0000-0002-3686-0518
Nebraska Medical Center · USNebraska Department of Health and Human Services · USPerkinElmer (United States) · USUniversity of Nebraska Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

X-linked adrenoleukodystrophy (X-ALD) is a neurodegenerative disease caused by pathogenic variants in

Indexed as

ABCD1adrenoleukodystrophyadrenomyeloneuropathynewborn screeningperoxisomal fatty acid oxidationX-ALD

Identifiers

PMID35645283
PMCPMC9149921
OpenAlexW4224780977

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.