Evidence map›Paper›PMID 24443315›Full record

ArticleAmerican journal of medical genetics. Part A2014

CTF meeting 2012: Translation of the basic understanding of the biology and genetics of NF1, NF2, and schwannomatosis toward the development of effective therapies.

Brigitte C Widemann, Maria T Acosta, Sylvia Ammoun, Allan J Belzberg, Andre Bernards, Jaishri Blakeley, Antony Bretscher, Karen Cichowski, D Wade Clapp, Eva Dombi and 29 more

Open access · bronzeAbstract readConference Proceedings
In one paragraph

Article in American journal of medical genetics. Part A, 2014. 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
3.0field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Neurofibromatosis type I in children: a case report and literature review.International journal of clinical and experimental pathology · 2020
    Article
  4. Diagnosis and Management of Subcutaneous Soft Tissue Sarcoma.Current treatment options in oncology · 2019
    Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
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

39 authors at 20 institutions in 5 countries.

Brigitte C WidemannPediatric Oncology Branch, NIH-National Cancer Institute, Bethesda, Maryland.
Maria T Acosta
Sylvia Ammoun
Allan J Belzberg
Andre Bernards
Jaishri Blakeley
Antony Bretscher
Karen Cichowski
D Wade Clapp
Eva Dombi
Gareth D Evans
Rosalie Ferner
Cristina Fernandez-Valle
Michael J Fisher
Marco Giovannini
David H Gutmann
C Oliver Hanemann
Robert Hennigan
Susan Huson
David Ingram
Joe Kissil
Bruce R Korf
Eric Legius
Roger J Packer
Andrea I McClatchey
Frank McCormick
Kathryn North
Minja Pehrsson
Scott R Plotkin
Vijaya Ramesh
Nancy Ratner
Susann Schirmer
Larry Sherman
Elizabeth Schorry
David Stevenson
Douglas R Stewart
Nicole Ullrich
Annette C Bakker
Helen Morrison
Cincinnati Children's Hospital Medical Center · USChildren's National · USHarvard University · USJohns Hopkins University · USLeibniz Association · DEMassachusetts General Hospital · USNational Cancer Institute · USPeninsula College of Medicine and Dentistry · GBSt Mary's Hospital · GBBoston Children's Museum · USBrigham and Women's Hospital · USChildren's Hospital at Westmead · AUChildren's Hospital of Philadelphia · USChildren's Tumor Foundation · USCornell University · USDivision of Cancer Epidemiology and GeneticsGuy's and St Thomas' NHS Foundation Trust · GBHouse Clinic · USIndiana University – Purdue University Indianapolis · USIndiana University School of Medicine

Funding

Clinical Genetic Studies of Familial and Hereditary Cancer SyndromesZIACP010144 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI SAVAGE, SHARON A. · 2009 to 2025
$111.8M
SYNAPTIC MECHANISMS IN HIPPOCAMPAL EPILEPTOGENESISP30HD018655 · NICHD · CHILDREN'S HOSPITAL BOSTON · PI POMEROY, SCOTT LOREN · 1985 to 2015
$26.2M
Therapy for NF1-Related Tumors and other Genetic Tumor Predisposition SyndromesZIABC010801 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI WIDEMANN, BRIGITTE · 2009 to 2020
$13.8M
MICROFILAMENT ORGANIZATION AND REGULATIONR01GM036652 · NIGMS · CORNELL UNIVERSITY ITHACA · PI BRETSCHER, ANTHONY P. · 1986 to 2018
$8.7M
Identification of Novel Drug Targets For Use in Preventing Deafness Caused by NF2R01DC010189 · NIDCD · UNIVERSITY OF CENTRAL FLORIDA · PI FERNANDEZ-VALLE, CRISTINA MARIA · 2009 to 2013
$1.4M
2010 NF ConferenceR13NS070505 · NINDS · CHILDREN'S TUMOR FOUNDATION · PI GIANCOTTI, FILIPPO G · 2010 to 2010
$46k
NICHD NIH HHS P30 HD018655NIDCD NIH HHS R01 DC010189NIGMS NIH HHS R01 GM036652NINDS NIH HHS 1R13NS070505-01NINDS NIH HHS R13 NS070505
6 · The paper itself

Abstract

The neurofibromatoses (NF) are autosomal dominant genetic disorders that encompass the rare diseases NF1, NF2, and schwannomatosis. The NFs affect more people worldwide than Duchenne muscular dystrophy and Huntington's disease combined. NF1 and NF2 are caused by mutations of known tumor suppressor genes (NF1 and NF2, respectively). For schwannomatosis, although mutations in SMARCB1 were identified in a subpopulation of schwannomatosis patients, additional causative gene mutations are still to be discovered. Individuals with NF1 may demonstrate manifestations in multiple organ systems, including tumors of the nervous system, learning disabilities, and physical disfigurement. NF2 ultimately can cause deafness, cranial nerve deficits, and additional severe morbidities caused by tumors of the nervous system. Unmanageable pain is a key finding in patients with schwannomatosis. Although today there is no marketed treatment for NF-related tumors, a significant number of clinical trials have become available. In addition, significant preclinical efforts have led to a more rational selection of potential drug candidates for NF trials. An important element in fueling this progress is the sharing of knowledge. For over 20 years the Children's Tumor Foundation has convened an annual NF Conference, bringing together NF professionals to share novel findings, ideas, and build collaborations. The 2012 NF Conference held in New Orleans hosted over 350 NF researchers and clinicians. This article provides a synthesis of the highlights presented at the conference and as such, is a "state-of-the-field" for NF research in 2012.

Indexed as

HumansNeurilemmomaNeurofibromatosesNeurofibromatosis 1Neurofibromatosis 2Skin Neoplasmsmerlin neurofibrominneurofibromatosis type 1neurofibromatosis type 2NF1NF2preclinical modelsschwannomatosisSMARCB1tumor suppressor

Identifiers

PMID24443315
PMCPMC4150212
OpenAlexW2037189803

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.