Evidence map›Paper›PMID 21271647›Full record

ArticleAmerican journal of medical genetics. Part A2011

Back to the future: proceedings from the 2010 NF Conference.

Susan M Huson, Maria T Acosta, Allan J Belzberg, Andre Bernards, Jonathan Chernoff, Karen Cichowski, D Gareth Evans, Rosalie E Ferner, Marco Giovannini, Bruce R Korf and 14 more

Open access · greenAbstract readConference Proceedings
In one paragraph

Article in American journal of medical genetics. Part A, 2011. 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
3.3field-weighted citation impact, top 8% 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, 29 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Neurological diseases and pain.Brain : a journal of neurology · 2012
    Review
  8. Article
  9. Therapeutics for childhood neurofibromatosis type 1 and type 2.Current treatment options in neurology · 2011
    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

24 authors at 20 institutions in 4 countries.

Susan M HusonSt. Mary's Hospital, University of Manchester, Manchester, UK.
Maria T Acosta
Allan J Belzberg
Andre Bernards
Jonathan Chernoff
Karen Cichowski
D Gareth Evans
Rosalie E Ferner
Marco Giovannini
Bruce R Korf
Robert Listernick
Kathryn N North
Roger J Packer
Luis F Parada
Juha Peltonen
Vijaya Ramesh
Karlyne M Reilly
John W Risner
Elizabeth K Schorry
Meena Upadhyaya
David H Viskochil
Yuan Zhu
Kim Hunter-Schaedle
Filippo G Giancotti
Children's National · USChildren's Tumor Foundation · USSt Mary's Hospital · GBCardiff University · GBCincinnati Children's Hospital Medical Center · USFox Chase Cancer Center · USGuy's and St Thomas' NHS Foundation Trust · GBHarvard University · USHarvard University Press · USHouse Clinic · USJohns Hopkins Hospital · USLurie Children's Hospital · USMassachusetts General Hospital · USMemorial Sloan Kettering Cancer Center · USNational Cancer Institute · USThe University of Texas Southwestern Medical Center · USUniversity of Alabama at Birmingham · USUniversity of Helsinki · FIUniversity of Michigan–Ann Arbor · USUniversity of Sydney · AU

Funding

Mechanism of Merlin-mediated contact inhibition and tumor suppression.R01CA152975 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI GIANCOTTI, FILIPPO G · 2010 to 2014
$2.5M
Understanding Mechanisms Underlying Drosophila Neurofibromatosis-1 DefectsR01GM084220 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI BERNARDS, ANDRE · 2008 to 2011
$1.4M
2010 NF ConferenceR13NS070505 · NINDS · CHILDREN'S TUMOR FOUNDATION · PI GIANCOTTI, FILIPPO G · 2010 to 2010
$46k
NCI NIH HHS R01 CA152975NIGMS NIH HHS R01 GM084220NINDS NIH HHS 1R13NS070505-01NINDS NIH HHS R13 NS070505
6 · The paper itself

Abstract

The neurofibromatoses (NF) encompass the rare diseases NF1, NF2, and schwannomatosis. The NFs affect 100,000 Americans; over 2 million persons worldwide; and are caused by mutation of tumor suppressor genes. Individuals with NF1 in particular may develop tumors anywhere in the nervous system; additional manifestations can include learning disabilities, bone dysplasia, cardiovascular defects, unmanageable pain, and physical disfigurement. Ultimately, the NFs can cause blindness, deafness, severe morbidity, and increased mortality and NF1 includes a risk of malignant cancer. Today there is no treatment for the NFs (other than symptomatic); however, research efforts to understand these genetic conditions have made tremendous strides in the past few years. Progress is being made on all fronts, from discovery studies-understanding the molecular signaling deficits that cause the manifestations of NF-to the growth of preclinical drug screening initiatives and the emergence of a number of clinical trials. An important element in fuelling this progress is the sharing of knowledge, and to this end, for over 20 years the Children's Tumor Foundation has convened an annual NF Conference, bringing together NF professionals to share ideas and build collaborations. The 2010 NF Conference held in Baltimore, MD June 5-8, 2010 hosted over 300 NF researchers and clinicians. This paper provides a synthesis of the highlights presented at the Conference and as such, is a "state-of-the-field" for NF research in 2010.

Indexed as

Genes, Tumor SuppressorAnimalsDisease Models, AnimalGenes, rasHumansMitogen-Activated Protein KinasesNeurofibromatosesSignal TransductionMitogen-Activated Protein Kinases

Identifiers

PMID21271647
PMCPMC3079924
OpenAlexW1977763128

What OpenQuestion holds

Textmetadata
LicenceTDM
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.