Evidence map›Paper›PMID 29681099›Full record

ArticleAmerican journal of medical genetics. Part A2018

2016 Children's Tumor Foundation conference on neurofibromatosis type 1, neurofibromatosis type 2, and schwannomatosis.

Michael J Fisher, Allan J Belzberg, Peter de Blank, Thomas De Raedt, Florent Elefteriou, Rosalie E Ferner, Marco Giovannini, Gordon J Harris, Michel Kalamarides, Matthias A Karajannis and 17 more

Open access · greenAbstract readConference ProceedingsLetter
In one paragraph

Article in American journal of medical genetics. Part A, 2018. 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
1.7field-weighted citation impact, top 17% 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, 18 citations in OpenAlex.

  1. Applications of organoid technology to brain tumors.CNS neuroscience & therapeutics · 2023
    Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. State of the Art and Advances in Peripheral Nerve Surgery.Advances and technical standards in neurosurgery · 2022
    Review
  7. Visceral plexiform schwannoma: A case series.Molecular and clinical oncology · 2021
    Article
  8. Article
  9. 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

27 authors at 20 institutions in 5 countries.

Michael J FisherDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.ORCID 0000-0003-3408-3839
Allan J BelzbergDepartment of Neurosurgery, The Johns Hopkins Hospital, Baltimore, Maryland.
Peter de BlankDivision of Oncology and Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Thomas De RaedtDivision of Genetics, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Florent ElefteriouCenter for Skeletal Medicine and Biology, Department of Molecular and Human Genetics and Orthopedic Surgery, Baylor College of Medicine, Houston, Texas.
Rosalie E FernerNeurofibromatosis Centre, Guy's and St. Thomas NHS Foundation Trust, London, United Kingdom.
Marco GiovanniniDepartment of Head and Neck Surgery, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California.
Gordon J HarrisDepartment of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
Michel KalamaridesDepartment of Neurosurgery, Hospital Pitie-Salpetriere, AP-HP, Paris, France; Université Pierre et Marie Curie, Sorbonne Universités, Paris, France.
Matthias A KarajannisDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, New York.
AeRang KimDivision of Oncology, Children's National Medical Center, Washington, District of Columbia.
Conxi LázaroHereditary Cancer Program, Catalan Institute of Oncology (ICO-IDIBELL-CIBERONC), L'Hospitalet de Llobregat, Barcelona, Spain.
Lu Q LeDepartment of Dermatology and Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, Texas.
Wei LiDepartment of Pediatrics, Department of Biochemistry & Molecular Biology, Penn State University College of Medicine, Hershey, Pennsylvania.
Robert ListernickDivision of Academic General Pediatrics, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois.
Staci MartinNational Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Helen MorrisonLeibniz Institute on Aging Research, Fritz Lipmann Institute, Jena, Germany.
Eric PasmantEA7331 and Cochin Hospital, Paris Descartes University, Faculty of Pharmacy of Paris, France.
Nancy RatnerDivision of Experimental Hematology and Cancer Biology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, Ohio.
Elisabeth SchorryDivision of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Nicole J UllrichDepartment of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
David ViskochilDivision of Medical Genetics, Department of Pediatrics, University of Utah, Salt Lake City, Utah.
Brian WeissDivision of Oncology, Cancer and Blood Diseases Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Brigitte C WidemannPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland.
Yuan ZhuThe Gilbert Family Neurofibromatosis Institute, Centers for Cancer and Immunology Research and Neuroscience Research, Children's National Medical Center, Washington, District of Columbia.
Annette BakkerChildren's Tumor Foundation, New York, New York.
Eduard SerraHereditary Cancer Group, The Institute for Health Science Research Germans Trias i Pujol (IGTP)-PMPPC, Barcelona, Spain.
Cincinnati Children's Hospital Medical Center · USChildren's National · USBaylor College of Medicine · USBoston Children's Hospital · USBrigham and Women's Hospital · USChildren's Hospital of Philadelphia · USChildren's Tumor Foundation · USDélégation Paris 5 · FRGuy's and St Thomas' NHS Foundation Trust · GBHarvard University · USInstitut d'Investigació Biomédica de Bellvitge · ESInstitut d'Investigació en Ciències de la Salut Germans Trias i Pujol · ESJohns Hopkins Hospital · USLeibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DEMemorial Sloan Kettering Cancer Center · USNational Cancer Institute · USNational Institutes of Health · USNorthwestern University · USPenn State Milton S. Hershey Medical Center · USSorbonne Université · FR

Funding

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
Children's Tumor Foundation 2016 Neurofibromatosis (NF) ConferenceR13NS084619 · NINDS · CHILDREN'S TUMOR FOUNDATION · PI FISHER, MICHAEL · 2013 to 2016
$63k
NINDS NIH HHS R13 NS084619
6 · The paper itself

Abstract

Organized and hosted by the Children's Tumor Foundation (CTF), the Neurofibromatosis (NF) conference is the premier annual gathering for clinicians and researchers interested in neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2), and schwannomatosis (SWN). The 2016 edition constituted a blend of clinical and basic aspects of NF research that helped in clarifying different advances in the field. The incorporation of next generation sequencing is changing the way genetic diagnostics is performed for NF and related disorders, providing solutions to problems like genetic heterogeneity, overlapping clinical manifestations, or the presence of mosaicism. The transformation from plexiform neurofibroma (PNF) to malignant peripheral nerve sheath tumor (MPNST) is being clarified, along with new management and treatments for benign and premalignant tumors. Promising new cellular and in vivo models for understanding the musculoskeletal abnormalities in NF1, the development of NF2 or SWN associated schwannomas, and clarifying the cells that give rise to NF1-associated optic pathway glioma were presented. The interaction of neurofibromin and SPRED1 was described comprehensively, providing functional insight that will help in the interpretation of pathogenicity of certain missense variants identified in NF1 and Legius syndrome patients. Novel promising imaging techniques are being developed, as well as new integrative and holistic management models for patients that take into account psychological, social, and biological factors. Importantly, new therapeutic approaches for schwannomas, meningiomas, ependymomas, PNF, and MPNST are being pursued. This report highlights the major advances that were presented at the 2016 CTF NF conference.

Indexed as

AnimalsDisease ManagementDisease Models, AnimalGenetic Association StudiesGenetic Predisposition to DiseaseHumansMolecular Diagnostic TechniquesNeurilemmomaNeurofibromatosesNeurofibromatosis 1Neurofibromatosis 2Skin NeoplasmsTranslational Research, Biomedicalautismconferenceependymomagliomamalignant peripheral nerve sheath tumormeningiomamerlinneurofibromaneurofibromatosisneurofibrominpseudoarthrosisschwannomaschwannomatosis

Identifiers

PMID29681099
PMCPMC5918269
OpenAlexW2801646849

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.