Evidence map›Paper›PMID 40127956›Full record

ArticleGenes & development2025

Cognition and behavior in neurofibromatosis type 1: report and perspective from the Cognition and Behavior in NF1 (CABIN) Task Force.

David H Gutmann, Corina Anastasaki, Aditi Gupta, Yang Hou, Stephanie M Morris, Jonathan M Payne, Jacob Raber, Seth M Tomchik, Linda Van Aelst, James A Walker and 2 more

Abstract read
In one paragraph

Article in Genes & development, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Trial
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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.

David H GutmannDepartment of Neurology, Data Science, and Biostatistics, Washington University School of Medicine, St. Louis, Missouri 63110, USA; gutmannd@wustl.edu kaleb.yohay@nyulangone.org.ORCID 0000-0002-3127-5045
Corina AnastasakiDepartment of Neurology, Data Science, and Biostatistics, Washington University School of Medicine, St. Louis, Missouri 63110, USA.ORCID 0000-0002-9928-6488
Aditi GuptaInstitute for Informatics, Data Science, and Biostatistics, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Yang HouDepartment of Behavioral Sciences and Social Medicine, Florida State University, Tallahassee, Florida 32306, USA.ORCID 0000-0002-7360-5751
Stephanie M MorrisCenter for Autism Services, Science, and Innovation (CASSI), Kennedy Krieger Institute, Baltimore, Maryland 21211, USA.ORCID 0000-0003-0461-1098
Jonathan M PayneMurdoch Children's Research Institute, Department of Paediatrics, Faculty of Medicine, Dentistry, and Health Sciences, University of Melbourne, Parkville, Victoria 3052, Australia.ORCID 0000-0001-9565-3845
Jacob RaberDepartment of Behavioral Neuroscience, Division of Neuroscience, Oregon National Primate Research Center (ONPRC), Oregon Health Sciences University, Portland, Oregon 97296, USA.ORCID 0000-0002-9861-9893
Seth M TomchikDepartment of Neuroscience and Pharmacology, University of Iowa, Iowa City, Iowa 52242, USA.ORCID 0000-0001-5686-0833
Linda Van AelstCold Spring Harbor Laboratory, Cold Spring Harbor, New York 11724, USA.ORCID 0000-0002-0870-012X
James A WalkerCenter for Genomic Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 12114, USA.ORCID 0000-0001-5585-698X
Kaleb H YohayDepartment of Neurology, New York University Langone, New York, New York 10017, USA gutmannd@wustl.edu kaleb.yohay@nyulangone.org.ORCID 0000-0001-5560-3392
CABIN Task Force

Funding

Single-Cell Biology Shared ResourceP30CA045508 · NCI · COLD SPRING HARBOR LABORATORY · PI David A Tuveson · 1987 to 2026
$118.9M
NCI NIH HHS P30 CA045508
6 · The paper itself

Abstract

Individuals with neurofibromatosis type 1 (NF1) are prone to the evolution of neurodevelopmental symptomatology including motor delays, learning disabilities, autism, and attention deficits. Caused by heterozygous germline mutations in the

Indexed as

CognitionNeurofibromatosis 1AnimalsDisease Models, AnimalHumansNeurofibromin 1Neurofibromin 1attention deficitautismclinical translationcognitioninformaticsNF1preclinical modeling

Identifiers

PMID40127956
PMCPMC12047663

What OpenQuestion holds

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LicenceCC BY-NC
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.