Robert Daber
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Explore the profile of Robert Daber including associated specialties, affiliations and a list of published articles.
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20
Citations
487
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Recent Articles
1.
Garcia-Murillas I, Cutts R, Walsh-Crestani G, Phillips E, Hrebien S, Dunne K, et al.
Breast Cancer Res Treat
. 2024 Oct;
209(3):493-502.
PMID: 39424680
Purpose: Detection of molecular residual disease (MRD) allows for the identification of breast cancer patients at high-risk of recurrence, with the potential that early initiation of treatment at early stages...
2.
Zhao J, Reuther J, Scozzaro K, Hawley M, Metzger E, Emery M, et al.
Mol Diagn Ther
. 2023 Aug;
27(6):753-768.
PMID: 37632661
Background: Highly sensitive molecular assays have been developed to detect plasma-based circulating tumor DNA (ctDNA), and emerging evidence suggests their clinical utility for monitoring minimal residual disease and recurrent disease,...
3.
De Abreu F, Peterson J, Deharvengt S, Daber R, Sarsani V, Spotlow V, et al.
J Appl Lab Med
. 2020 Jul;
2(2):138-149.
PMID: 32630970
Background: Next-generation sequencing (NGS) assays are highly complex tests that can vary substantially in both their design and intended application. Despite their innumerous advantages, NGS assays present some unique challenges...
4.
Maxwell K, Wubbenhorst B, Wenz B, De Sloover D, Pluta J, Emery L, et al.
Nat Commun
. 2017 Aug;
8(1):319.
PMID: 28831036
Complete loss of BRCA1 or BRCA2 function is associated with sensitivity to DNA damaging agents. However, not all BRCA1 and BRCA2 germline mutation-associated tumors respond. Herein we report analyses of...
5.
Azzato E, Deshpande C, Aikawa V, Aggarwal C, Alley E, Jacobs B, et al.
Anticancer Res
. 2015 May;
35(5):3007-12.
PMID: 25964588
Testing for somatic alterations, including anaplastic lymphoma receptor tyrosine kinase gene (ALK) rearrangements and epidermal growth factor receptor gene (EGFR) mutations, is standard practice in the diagnostic evaluation and therapeutic...
6.
Sehgal A, Gimotty P, Zhao J, Hsu J, Daber R, Morrissette J, et al.
Clin Cancer Res
. 2015 Jan;
21(7):1614-20.
PMID: 25609058
Purpose: DNA methyltransferase 3A (DNMT3A) is one of the commonly mutated genes in acute myelogenous leukemia (AML). Reports on the prognostic significance of DNMT3A mutations have been inconsistent, and most...
7.
Fishbein L, Khare S, Wubbenhorst B, DeSloover D, DAndrea K, Merrill S, et al.
Nat Commun
. 2015 Jan;
6:6140.
PMID: 25608029
Pheochromocytomas and paragangliomas (PCC/PGL) are the solid tumour type most commonly associated with an inherited susceptibility syndrome. However, very little is known about the somatic genetic changes leading to tumorigenesis...
8.
Oshrine B, Olsen M, Heneghan M, Wertheim G, Daber R, Wilmoth D, et al.
Cancer Genet
. 2014 May;
207(4):153-9.
PMID: 24831771
Previous reports have described an association between hematologic malignancies (HMs) and extragonadal germ cell tumor (GCT). Most patients have been adolescent males with mediastinal nonseminomatous GCT. Although a variety of...
9.
Daber R, Sukhadia S, Morrissette J
Cancer Genet
. 2014 Feb;
206(12):441-8.
PMID: 24528889
The advantages of massively parallel sequencing are quickly being realized through the adoption of comprehensive genomic panels across the spectrum of genetic testing. Despite such widespread utilization of next generation...
10.
Luskin M, Wertheim G, Morrissette J, Daber R, Biegel J, Wilmoth D, et al.
Pediatr Blood Cancer
. 2013 Nov;
61(6):1107-10.
PMID: 24281971
Chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) is a disease of older adults. Pediatric CLL/SLL is vanishingly rare in the literature. We present a case of CLL/SLL diagnosed in a 17-year-old...