Brent Orr
Overview
Explore the profile of Brent Orr including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
12
Citations
130
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Norrie J, Nityanandam A, Lai K, Chen X, Wilson M, Stewart E, et al.
Nat Commun
. 2021 Jul;
12(1):4535.
PMID: 34315877
Retinoblastoma is a childhood cancer of the developing retina that initiates with biallelic inactivation of the RB1 gene. Children with germline mutations in RB1 have a high likelihood of developing...
2.
Pujadas E, Chen L, Weingart J, Orr B, Ozer B, Holdhoff M, et al.
Clin Neuropathol
. 2020 Feb;
39(4):179-187.
PMID: 32017698
Ependymosarcomas are rare, biphasic tumors composed of ependymal and sarcomatous components. Due to their rarity, their biologic basis is not well understood. We report the case of a 38-year-old male...
3.
El Ahmadieh T, Plitt A, Kafka B, Aoun S, Raisanen J, Orr B, et al.
World Neurosurg
. 2019 Jan;
124:87-92.
PMID: 30639498
Background: The revised World Health Organization classification of central nervous system tumors, published in 2016, has recognized the H3 K27M mutation as a critical genetic signature defining a new group...
4.
Rodriguez F, Brosnan-Cashman J, Allen S, Vizcaino M, Giannini C, Camelo-Piragua S, et al.
Brain Pathol
. 2018 Sep;
29(1):126-140.
PMID: 30192422
Anaplasia may be identified in a subset of tumors with a presumed pilocytic astrocytoma (PA) component or piloid features, which may be associated with aggressive behavior, but the biologic basis...
5.
Murdock T, Orr B, Allen S, Ibrahim J, Sharma R, Ronnett B, et al.
Am J Surg Pathol
. 2018 Aug;
42(11):1429-1444.
PMID: 30074494
Central nervous system (CNS)-type tumors and tumor-like proliferations arising in the gynecologic tract and pelvis are rare. Clinicopathologic features of 23 cases are reported using the current WHO classification system...
6.
Lucas Jr J, Cooper D, Hwang S, Tinkle C, Li X, Li Y, et al.
Int J Radiat Oncol Biol Phys
. 2017 Sep;
99(2):450-458.
PMID: 28871996
Purpose: We sought to investigate the pattern of treatment failure with respect to anatomic extent, radiation dose, and criteria for failure according to the Response Assessment in Neuro-Oncology (RANO). We...
7.
Lee R, Foster K, Lillard J, Klimo Jr P, Ellison D, Orr B, et al.
J Neurosurg Pediatr
. 2017 Jul;
20(3):247-255.
PMID: 28686121
OBJECTIVE Thalamopeduncular tumors are a group of pediatric low-grade gliomas that arise at the interface of the thalamus and brainstem peduncle. They typically occur within the first 2 decades of...
8.
McAbee J, Modica J, Thompson C, Broniscer A, Orr B, Choudhri A, et al.
J Neurosurg Pediatr
. 2015 Jun;
16(4):357-66.
PMID: 26114990
Object: Cervicomedullary tumors (CMTs) represent a heterogeneous group of intrinsic neoplasms that are typically low grade and generally carry a good prognosis. This single-institution study was undertaken to document the...
9.
Tse B, Kaste S, Brennan R, Orr B, Wilson M
Ophthalmology
. 2014 Dec;
122(2):435-7.
PMID: 25439599
No abstract available.
10.
Mehta V, Kretzer R, Orr B, Jallo G
World Neurosurg
. 2011 Dec;
76(5):478.e1-6.
PMID: 22152582
Background: Intramedullary spinal germ cell tumors are rare lesions, with germinomas being the most common variant. Methods: To date, there have been 23 reports of primary intramedullary germ cell tumors...