Evidence map›Paper›PMID 37273678›Full record

ArticleCureus2023

Supratentorial Sporadic Hemangioblastoma: A Case Report With Mutation Profiling Using Next-Generation DNA Sequencing.

Mohiuddin M Taher, Najwa A Bantan, Mustafa H Alwalily, Muhammad Saeed, Nuha M Taher, Meriem Bouzidi, Raid A Jastania, Kamal B Balkhoyour

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Cureus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Primary hemangioblastoma of rectum: a rare case report and review of literature.Journal of cancer research and clinical oncology · 2025
    Review
  2. 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

8 authors at 2 institutions in 2 countries.

Mohiuddin M TaherScience and Technology Unit, Deanship of Scientific Research, Umm Al-Qura University, Makkah, SAU.
Najwa A BantanDepartment of Radiology, Al-Noor Specialty Hospital, Makkah, SAU.
Mustafa H AlwalilyDepartment of Neurosurgery, Al-Noor Specialty Hospital, Makkah, SAU.
Muhammad SaeedDepartment of Radiology, Al-Noor Specialty Hospital, Makkah, SAU.
Nuha M TaherDepartment of Medical Genetics, Umm Al-Qura University College of Medicine, Makkah, SAU.
Meriem BouzidiDepartment of Laboratory Medicine, Division of Histopathology, Al-Noor Specialty Hospital, Makkah, SAU.
Raid A JastaniaDepartment of Pathology, Umm Al-Qura University College of Medicine, Makkah, SAU.
Kamal B BalkhoyourDepartment of Neurosurgery, Al-Noor Specialty Hospital, Makkah, SAU.
Al Noor Hospitals · AEUmm al-Qura University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study aimed to determine genomic changes in sporadic intracranial hemangioblastoma (HBL), and the mutation patterns were analyzed using next-generation DNA sequencing (NGS). In this NGS analysis of the HBL tumor, 67 variants of 41 genes were identified. Of these, 64 were single-nucleotide variants (SNVs), two were exonic insertions and deletions (INDEL), and one was an intronic INDEL. In total, 15 were missense exonic variants, including an insertion variant in the

Indexed as

brain tumorhemangioblastomaintracranial tumorsion protonion torrentnext-generation dna sequencingngssupratentorial lesionstargeted therapyvhl-related syndrome

Identifiers

PMID37273678
PMCPMC10233511
OpenAlexW4379053014

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.