Evidence map›Paper›PMID 22821737›Full record

ReviewAmerican journal of medical genetics. Part A2012

The Learning Disabilities Network (LeaDNet): using neurofibromatosis type 1 (NF1) as a paradigm for translational research.

Maria T Acosta, Carrie E Bearden, F Xavier Castellanos, Xavier F Castellanos, Laurie Cutting, Ype Elgersma, Gerard Gioia, David H Gutmann, Yong-Seok Lee, Eric Legius and 6 more

Erratum issued 2 registry-linked trialsOpen access · greenAbstract readReview
In one paragraph

Review in American journal of medical genetics. Part A, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to 2 registered trials, which are not on this map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 14% 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.

NCT04481035 phase2completednot on this mapstarted 2019, after this paper: background citation

Antioxidant Therapy With N-acetylcysteine for Learning and Motor Behavior in Children With Neurofibromatosis Type 1

TypeinterventionalSponsorChildren's Hospital Medical Center, CincinnatiRan2019 to 2021Enrolled5ConditionsNeurofibromatosis 1ArmsN-acetylcysteine (NAC), Placebo
NCT04481048 phase2completednot on this mapstarted 2021, after this paper: background citation

Antioxidant Therapy With N-acetylcysteine for Motor Behavior and/or Learning in Children With Neurofibromatosis Type 1

TypeinterventionalSponsorChildren's Hospital Medical Center, CincinnatiRan2021 to 2024Enrolled25ConditionsNeurofibromatosis 1ArmsN-Acetyl cysteine, Placebo
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Review
  7. An executive functioning perspective in neurofibromatosis type 1: from ADHD and autism spectrum disorder to research domains.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2020
    Review
  8. Review
  9. Examination of the genetic factors underlying the cognitive variability associated with neurofibromatosis type 1.Genetics in medicine : official journal of the American College of Medical Genetics · 2020
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. The RASopathies.Annual review of genomics and human genetics · 2013
    Review
4 · The record

Corrections and comments

  • Erratum issued
    Castellanos, Xavier F [corrected to Castellanos, F Xavier]
5 · Who and what money

Authors and funding

16 authors at 12 institutions in 4 countries.

Maria T AcostaThe Gilbert Neurofibromatosis Institute, Children's National Medical Center, Washington, District of Columbia 20010, USA. macosta@childrensnational.org
Carrie E Bearden
F Xavier Castellanos
Xavier F Castellanos
Laurie Cutting
Ype Elgersma
Gerard Gioia
David H Gutmann
Yong-Seok Lee
Eric Legius
Maximillian Muenke
Kathryn North
Luis F Parada
Nancy Ratner
Kim Hunter-Schaedle
Alcino J Silva
Children's Hospital at Westmead · AUNational Human Genome Research Institute · USUniversity of California, Los Angeles · USChildren's National · USChildren's Tumor Foundation · USCincinnati Children's Hospital Medical Center · USErasmus University Rotterdam · NLKU Leuven · BENew York University · USThe University of Texas Southwestern Medical Center · USVanderbilt University · USWashington University in St. Louis · US

Funding

NHGRI/DIR Medical Genetics Training ProgramsZIEHG200354 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI SHCHELOCHKOV, OLEG · 2009 to 2025
$50.9M
Genetic Analysis of Attention Deficit Hyperactivity DisorderZIAHG000175 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI SHAW, PHILIP · 2009 to 2025
$13.4M
Neurofibromatosis Type I as a Model for Therapeutic NeuroadaptationR34MH089299 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BEARDEN, CARRIE E · 2009 to 2011
$691k
NIMH NIH HHS R34 MH089299
6 · The paper itself

Abstract

Learning disabilities and other cognitive disorders represent one of the most important unmet medical needs and a significant source of lifelong disability. To accelerate progress in this area, an international consortium of researchers and clinicians, the Learning Disabilities Network (LeaDNet), was established in 2006. Initially, LeaDNet focused on neurofibromatosis type 1 (NF1), a common single gene disorder with a frequency of 1:3,000. Although NF1 is best recognized as an inherited tumor predisposition syndrome, learning, cognitive, and neurobehavioral deficits account for significant morbidity in this condition and can have a profound impact on the quality of life of affected individuals. Recently, there have been groundbreaking advances in our understanding of the molecular, cellular, and neural systems underpinnings of NF1-associated learning deficits in animal models, which precipitated clinical trials using a molecularly targeted treatment for these deficits. However, much remains to be learned about the spectrum of cognitive, neurological, and psychiatric phenotypes associated with the NF1 clinical syndrome. In addition, there is a pressing need to accelerate the identification of specific clinical targets and treatments for these phenotypes. The successes with NF1 have allowed LeaDNet investigators to broaden their initial focus to other genetic disorders characterized by learning disabilities and cognitive deficits including other RASopathies (caused by changes in the Ras signaling pathway). The ultimate mission of LeaDNet is to leverage an international translational consortium of clinicians and neuroscientists to integrate bench-to-bedside knowledge across a broad range of cognitive genetic disorders, with the goal of accelerating the development of rational and biologically based treatments.

Indexed as

Translational Research, BiomedicalAnimalsHumansLearning DisabilitiesMiceNeurofibromatosis 1

Identifiers

PMID22821737
PMCPMC4074877
OpenAlexW2096701673

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.