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Author Details
Full Name
Francine B de Abreu
Affiliation
Center for Cancer Research, National Cancer Institute, National Institutes of Health
ORCID
Career Start Year
2007
Papers
42
H Index
18
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
32228502
The first pancreatic neuroendocrine tumor in Li-Fraumeni syndrome: a case report.
BMC Cancer
2020
32613070
Molecular matching and treatment strategies for advanced stage lung cancer at Dartmouth-Hitchcock Medical Center: A three-year review of a Molecular Tumor Board.
Pract Lab Med
2020
30360665
Synchronous Pulmonary Adenofibroma and Solitary Fibrous Tumor: Case Report and Review of the Literature.
Int J Surg Pathol
2019
30085960
Undifferentiated Sarcoma as Intermediate Step in the Progression of Malignant Melanoma to Rhabdomyosarcoma: Histologic, Immunohistochemical, and Molecular Studies of a New Case of Malignant Melanoma With Rhabdomyosarcomatous Differentiation.
Am J Dermatopathol
2019
30950098
A novel MAP3K7CL-ERG fusion in a molecularly confirmed case of dermatofibrosarcoma protuberans with fibrosarcomatous transformation.
J Cutan Pathol
2019
30997856
Variant allele frequencies do not correlate well with myeloblast counts in a clinically validated gene sequencing panel for routine acute myeloid leukemia workup.
Leuk Lymphoma
2019
29621832
Identifying Associations between Somatic Mutations and Clinicopathologic Findings in Lung Cancer Pathology Reports.
Methods Inf Med
2018
30141999
Impact of Molecular Sequencing Information as Related to 2008 and 2016 World Health Organization Classification of Acute Myeloid Leukemia and Myelodysplasia.
Arch Pathol Lab Med
2018
30376129
MicroRNAs involved in the HMGA2 deregulation and its co-occurrence with MED12 mutation in uterine leiomyoma.
Mol Hum Reprod
2018
29727697
Central xanthoma of the jaw in association with Noonan syndrome.
Hum Pathol
2018
29723602
Non-small cell lung cancers with isocitrate dehydrogenase 1 or 2 (IDH1/2) mutations.
Hum Pathol
2018
29454261
Frequency of Somatic TP53 Mutations in Combination with Known Pathogenic Mutations in Colon Adenocarcinoma, Non-Small Cell Lung Carcinoma, and Gliomas as Identified by Next-Generation Sequencing.
Neoplasia
2018
27763790
Improving Adequacy of Small Biopsy and Fine-Needle Aspiration Specimens for Molecular Testing by Next-Generation Sequencing in Patients With Lung Cancer: A Quality Improvement Study at Dartmouth-Hitchcock Medical Center.
Arch Pathol Lab Med
2017
32630970
Use of Biosynthetic Controls as Performance Standards for Next-Generation Sequencing Assays of Somatic Tumors: A Multilaboratory Study.
J Appl Lab Med
2017
28192086
Variant call concordance between two laboratory-developed, solid tumor targeted genomic profiling assays using distinct workflows and sequencing instruments.
Exp Mol Pathol
2017
28343174
miRNA analysis in pancreatic cancer: the Dartmouth experience.
Clin Chem Lab Med
2017
28822769
Somatic mutation analysis in melanoma using targeted next generation sequencing.
Exp Mol Pathol
2017
28734944
Triple-Negative Breast Cancer: Next-Generation Sequencing for Target Identification.
Am J Pathol
2017
27932416
A Phase II Trial of Dovitinib in BCG-Unresponsive Urothelial Carcinoma with <i>FGFR3</i> Mutations or Overexpression: Hoosier Cancer Research Network Trial HCRN 12-157.
Clin Cancer Res
2017
26923179
The Pitfalls of Companion Diagnostics: Evaluation of Discordant EGFR Mutation Results from a Clinical Laboratory and a Central Laboratory.
J Mol Diagn
2016
26427657
ROBO1 deletion as a novel germline alteration in breast and colorectal cancer patients.
Tumour Biol
2016
27659017
Clinical Genotyping of Non-Small Cell Lung Cancers Using Targeted Next-Generation Sequencing: Utility of Identifying Rare and Co-mutations in Oncogenic Driver Genes.
Neoplasia
2016
27686171
Detection of CALR Mutation in Clonal and Nonclonal Hematologic Diseases Using Fragment Analysis and Next-Generation Sequencing.
Am J Clin Pathol
2016
27498048
The genomic profile of pancreatic adenocarcinoma and its relationship to metastatic disease.
Exp Mol Pathol
2016
27095739
Targeted next-generation sequencing detects a high frequency of potentially actionable mutations in metastatic breast cancers.
Exp Mol Pathol
2016
27068338
The potential utility of re-mining results of somatic mutation testing: KRAS status in lung adenocarcinoma.
Cancer Genet
2016
26934555
Genomic characterization of patient-derived xenograft models established from fine needle aspirate biopsies of a primary pancreatic ductal adenocarcinoma and from patient-matched metastatic sites.
Oncotarget
2016
26872315
Effective quality management practices in routine clinical next-generation sequencing.
Clin Chem Lab Med
2016
25476122
Benign phyllodes tumor of the breast recurring as a malignant phyllodes tumor and spindle cell metaplastic carcinoma.
Hum Pathol
2015
27051784
Rat-bite fever: An uncommon cause of fever and rash in a 9-year-old patient.
JAAD Case Rep
2015
26189129
Molecular profiling of intrahepatic and extrahepatic cholangiocarcinoma using next generation sequencing.
Exp Mol Pathol
2015
26205736
Implementation of a Molecular Tumor Board: The Impact on Treatment Decisions for 35 Patients Evaluated at Dartmouth-Hitchcock Medical Center.
Oncologist
2015
25618892
Regulatory T cells are not a strong predictor of survival for patients with glioblastoma.
Neuro Oncol
2015
24334431
Routine use of the Ion Torrent AmpliSeqâ¿¢ Cancer Hotspot Panel for identification of clinically actionable somatic mutations.
Clin Chem Lab Med
2014
26150933
Determining methylation status of methylguanine DNA methyl transferase (MGMT) from formalin-fixed, paraffin embedded tumor tissue.
MethodsX
2014
24821835
Molecular profiling of appendiceal epithelial tumors using massively parallel sequencing to identify somatic mutations.
Clin Chem
2014
24635704
Personalized therapy for breast cancer.
Clin Genet
2014
23545277
A clinical PCR fragment analysis assay for TA repeat sizing in the UGT1A1 promoter region.
Clin Chim Acta
2013
23920325
The emerging role of the molecular diagnostics laboratory in breast cancer personalized medicine.
Am J Pathol
2013
23404580
Genomic and phenotypic profiles of two Brazilian breast cancer cell lines derived from primary human tumors.
Oncol Rep
2013
21668474
Recurrent copy number gains of ACVR1 and corresponding transcript overexpression are associated with survival in head and neck squamous cell carcinomas.
Histopathology
2011
17465263
Shorter CAG repeat in the AR gene is associated with atypical hyperplasia and breast carcinoma.
Anticancer Res
2007
1 - 42 of 42
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