Margarita Raygada
Overview
Explore the profile of Margarita Raygada including associated specialties, affiliations and a list of published articles.
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31
Citations
1048
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Recent Articles
1.
Florou V, Jacobs M, Casey R, Evans D, Owens B, Raygada M, et al.
Cancer Med
. 2025 Feb;
14(3):e70669.
PMID: 39927693
Gastrointestinal Stromal Tumors (GISTs) have seen significant advancements in their diagnosis and management, driven by targeted therapeutic development and molecular testing. The identification of mutations in genes such as KIT...
2.
Raygada M, John L, Liu A, Schultz J, Thomas B, Bernstein D, et al.
J Cancer Res Clin Oncol
. 2024 May;
150(5):227.
PMID: 38700789
Introduction: Chordoma is a rare slow-growing tumor that occurs along the length of the spinal axis and arises from primitive notochordal remnants (Stepanek et al., Am J Med Genet 75:335-336,...
3.
Rogers J, Wall T, Acquaye-Mallory A, Boris L, Kim Y, Aldape K, et al.
J Neurooncol
. 2024 Mar;
167(2):349-359.
PMID: 38427131
Purpose: Multidisciplinary tumor boards (MTBs) integrate clinical, molecular, and radiological information and facilitate coordination of neuro-oncology care. During the COVID-19 pandemic, our MTB transitioned to a virtual and multi-institutional format....
4.
Ahmed S, Wedekind M, Del Rivero J, Raygada M, Lockridge R, Glod J, et al.
Cancer Res Commun
. 2023 Nov;
3(12):2468-2482.
PMID: 37966258
Significance: This study demonstrates that comprehensive, tumor-agnostic data and biospecimen collection is feasible to characterize different rare tumors, and speed progress in research. The findings will be foundational to developing...
5.
John L, Smith H, Ilanchezhian M, Lockridge R, Reilly K, Raygada M, et al.
Pediatr Blood Cancer
. 2023 Jun;
:e30358.
PMID: 37347686
Background: Chordomas are rare tumors arising from the skull base and spine, with approximately 20 pediatric chordoma cases in the Unitedn States per year. The natural history and optimal treatment...
6.
Wedekind M, Reilly K, Del Rivero J, Lockridge R, Allen T, Raygada M, et al.
Pediatr Blood Cancer
. 2023 Jun;
:e30495.
PMID: 37345354
Rare tumors across the world are lacking adequate knowledge, resources, and community. Through partnership with patients, advocacy organizations, researchers, and clinicians, we have developed a comprehensive, longitudinal, prospective, and retrospective...
7.
Merchant M, Raygada M, Pang Y, Quezado M, Raffeld M, Xi L, et al.
Front Oncol
. 2022 Aug;
12:954879.
PMID: 35982947
Most tumors, including brain tumors, are sporadic. However, a small subset of CNS tumors are associated with hereditary cancer conditions like Lynch Syndrome (LS). Here, we present a case of...
8.
Okafor C, Hogan J, Raygada M, Thomas B, Akshintala S, Glod J, et al.
Front Endocrinol (Lausanne)
. 2021 Sep;
12:708949.
PMID: 34489865
Medullary thyroid carcinoma (MTC) is a rare neuroendocrine tumor that accounts for 2-4% of all thyroid cancers. All inherited MTC and approximately 50% of sporadic cases are driven by mutations...
9.
Raygada M, Raffeld M, Bernstein A, Miettinen M, Glod J, Hughes M, et al.
Am J Med Genet A
. 2021 Feb;
185(4):1282-1287.
PMID: 33615670
Adrenocortical carcinoma (ACC) is a rare aggressive malignancy that originates in the outer layer of the adrenal gland. Most ACCs are sporadic, but a small percentage of cases are due...
10.
Penas-Prado M, Theeler B, Cordeiro B, Dunkel I, Hau P, Mahajan A, et al.
Neurooncol Adv
. 2020 Oct;
2(1):vdaa097.
PMID: 33005896
Background: Medulloblastoma (MB) is a rare brain tumor occurring more frequently in children in whom research has been primarily focused. Treatment recommendations in adults are mainly based on retrospective data...