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Samer K. Elbabaa

Researcher at Arnold Palmer Hospital for Children

Publications -  73
Citations -  2699

Samer K. Elbabaa is an academic researcher from Arnold Palmer Hospital for Children. The author has contributed to research in topics: Medicine & Endoscopic third ventriculostomy. The author has an hindex of 17, co-authored 66 publications receiving 2055 citations. Previous affiliations of Samer K. Elbabaa include University of Arkansas for Medical Sciences & Orlando Regional Medical Center.

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Journal ArticleDOI

Subgroup-specific structural variation across 1,000 medulloblastoma genomes

Paul A. Northcott, +139 more
- 02 Aug 2012 - 
TL;DR: Somatic copy number aberrations (SCNAs) in 1,087 unique medulloblastomas are reported, including recurrent events targeting TGF-β signalling in Group 3, and NF-κB signalling in Groups 4, which suggest future avenues for rational, targeted therapy.
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Intertumoral Heterogeneity within Medulloblastoma Subgroups

Florence M.G. Cavalli, +101 more
- 12 Jun 2017 - 
TL;DR: Similarity network fusion (SNF) applied to genome-wide DNA methylation and gene expression data across 763 primary samples identifies very homogeneous clusters of patients, supporting the presence of medulloblastoma subtypes.
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TERT promoter mutations are highly recurrent in SHH subgroup medulloblastoma

Marc Remke, +87 more
TL;DR: TERT mutations define a subset of SHH medulloblastoma with distinct demographics, cytogenetics, and outcomes, and are very highly enriched in adult SHH and WNT tumors.
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Therapeutic Impact of Cytoreductive Surgery and Irradiation of Posterior Fossa Ependymoma in the Molecular Era: A Retrospective Multicohort Analysis

Vijay Ramaswamy, +123 more
TL;DR: The most impactful biomarker for posterior fossa ependymoma is molecular subgroup affiliation, independent of other demographic or treatment variables, with the survival rates being particularly poor for subtotally resected EPN_PFA, even with adjuvant radiation therapy.
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The Dandy-Walker variant: a case series of 24 pediatric patients and evaluation of associated anomalies, incidence of hydrocephalus, and developmental outcomes.

TL;DR: Developmental outcome was solely affected by neurological deficits and that ventricular enlargement predicted the need for shunt placement, and the DWV was associated with both extra- and intracranial anomalies.