Evidence map›Paper›PMID 38932491›Full record

ArticleClinical and translational science2024

NF1

Vicki J Swier, Katherine A White, Pedro L Negrão de Assis, Tyler B Johnson, Hannah G Leppert, Mitchell J Rechtzigel, David K Meyerholz, Rebecca D Dodd, Dawn E Quelle, Rajesh Khanna and 2 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Clinical and translational science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Neurofibromin Deficiency Alters the Patterning and Prioritization of Motor Behaviors in a State-Dependent Manner.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  3. NF1Clinical and translational science · 2024
    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

12 authors.

Vicki J SwierPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, South Dakota, USA.ORCID 0000-0001-7509-9920
Katherine A WhitePediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, South Dakota, USA.ORCID 0000-0002-1663-1961
Pedro L Negrão de AssisPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, South Dakota, USA.ORCID 0000-0003-2096-2883
Tyler B JohnsonPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, South Dakota, USA.ORCID 0000-0002-6431-942X
Hannah G LeppertPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, South Dakota, USA.ORCID 0000-0002-5331-8499
Mitchell J RechtzigelPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, South Dakota, USA.ORCID 0000-0002-5298-7391
David K MeyerholzDepartment of Pathology, University of Iowa, Iowa City, Iowa, USA.ORCID 0000-0003-1552-3253
Rebecca D DoddDepartment of Internal Medicine, University of Iowa, Iowa City, Iowa, USA.ORCID 0000-0001-7295-1882
Dawn E QuelleDepartment of Neuroscience and Pharmacology, University of Iowa, Iowa City, Iowa, USA.ORCID 0000-0001-8776-0122
Rajesh KhannaDepartment of Pharmacology and Therapeutics, College of Medicine, University of Florida, Gainesville, Florida, USA.ORCID 0000-0002-9066-2969
Christopher S RogersExemplar Genetics, Coralville, Iowa, USA.ORCID 0000-0002-2980-2547
Jill M WeimerPediatrics and Rare Diseases Group, Sanford Research, Sioux Falls, South Dakota, USA.ORCID 0000-0003-2504-4942

Funding

Yeast 2 HybridP20GM103620 · NIGMS · SANFORD RESEARCH/USD · PI ROUX, KYLE J · 2013 to 2023
$24.2M
NIGMS NIH HHS P20 GM103620
6 · The paper itself

Abstract

Cognitive or motor impairment is common among individuals with neurofibromatosis type 1 (NF1), an autosomal dominant tumor-predisposition disorder. As many as 70% of children with NF1 report difficulties with spatial/working memory, attention, executive function, and fine motor movements. In contrast to the utilization of various Nf1 mouse models, here we employ an NF1

Indexed as

Disease Models, AnimalNeurofibromatosis 1AnimalsAstrocytesBehavior, AnimalCognitive DysfunctionFemaleHippocampusHumansMaleMiceNeurofibromin 1OligodendrogliaNeurofibromin 1

Identifiers

PMID38932491
PMCPMC11208292

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.