Larissa V Furtado

发表

System for Informatics in the Molecular Pathology Laboratory: An Open-Source End-to-End Solution for Next-Generation Sequencing Clinical Data Management.

Jorge Andrade, Samuel L Volchenboum, Dara L Aisner, 2018, The Journal of molecular diagnostics : JMD.

Multi-Institutional Evaluation of Inter-rater Agreement of Variant Classification Based on the 2017 AMP, ASCO and CAP Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer.

Robert L Schmidt, Dara L Aisner, Susan J Hsiao, 2019, The Journal of molecular diagnostics : JMD.

Septin 9 methylated DNA is a sensitive and specific blood test for colorectal cancer

Larissa V Furtado, W. Samowitz, C. Vaughn, 2011, BMC medicine.

Do circulating tumor cells, exosomes, and circulating tumor nucleic acids have clinical utility? A report of the association for molecular pathology.

Larissa V Furtado, Milena Cankovic, Christopher D Gocke, 2015, The Journal of molecular diagnostics : JMD.

The RSH/“Smith–Lemli–Opitz” Syndrome: Historical footnote

Larissa V Furtado, J. Opitz, Larissa V. Furtado, 2012, American journal of medical genetics. Part C, Seminars in medical genetics.

Frequency of KRAS, BRAF, and NRAS mutations in colorectal cancer

Larissa V Furtado, W. Samowitz, C. Vaughn, 2011, Genes, chromosomes & cancer.

Disorders of sterol biosynthesis

Larissa V Furtado, J. Opitz, R. Kelley, 2016 .

Metastatic HPV-Associated Oropharyngeal Versus Primary Pulmonary Squamous Cell Carcinoma: is p16 Immunostain Useful?

Larissa V Furtado, N. Cipriani, Jefree J. Schulte, 2020, Head and Neck Pathology.

Should the qualitative serum pregnancy test be considered obsolete?

Larissa V Furtado, C. M. Lehman, Larissa V. Furtado, 2012, American journal of clinical pathology.

Yolk Sac Tumor of the Thyroid Gland: A Case Report

Larissa V Furtado, T. Pysher, L. Layfield, 2011, Pediatric and Developmental Pathology.

Epithelioid Trophoblastic Tumor: Expanding the Clinicopathologic Spectrum of a Rare Malignancy

Larissa V Furtado, A. Montag, R. Lastra, 2020, International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.

Precision Molecular Pathology of Neoplastic Pediatric Diseases

Larissa V Furtado, P. Cagle, A. Husain, 2018, Molecular Pathology Library.

Denys-Drash Syndrome with Neonatal Renal Failure in Monozygotic Twins Due to C.1097G>A Mutation in the WT1 Gene

Larissa V Furtado, J. Opitz, T. Pysher, 2011, Fetal and pediatric pathology.

Correlation of age-specific phenylalanine levels with intellectual outcome in patients with phenylketonuria

Larissa V Furtado, N. Longo, H. Wengreen, 2011, Journal of Inherited Metabolic Disease.

A novel X‐linked multiple congenital anomaly syndrome associated with an EBP mutation

Larissa V Furtado, A. Rope, J. Carey, 2010, American journal of medical genetics. Part A.

Lorlatinib in a Child with ALK-Fusion-Positive High-Grade Glioma.

Sandeep Kumar Dhanda, Larissa V Furtado, A. Gajjar, 2021, The New England journal of medicine.

High prevalence of somatic MAP2K1 mutations in BRAF V600E-negative Langerhans cell histiocytosis.

Larissa V Furtado, K. Elenitoba-Johnson, M. Lim, 2014, Blood.

Diagnostic evaluation of RNA sequencing for the detection of genetic abnormalities associated with Ph-like acute lymphoblastic leukemia (ALL)

Larissa V Furtado, Yusuke Nakamura, M. L. Le Beau, 2017, Leukemia & lymphoma.

Colorectal cancer molecular profiling: from IHC to NGS in search of optimal algorithm

Larissa V Furtado, W. Samowitz, 2017, Virchows Archiv.

Diagnostic utility of microsatellite genotyping for molar pregnancy testing.

Larissa V Furtado, E. Lyon, S. Tripp, 2013, Archives of Pathology & Laboratory Medicine.

Multi-Institutional Evaluation of Interrater Agreement of Variant Classification Based on the 2017 Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Ca

Larissa V Furtado, Lauren L. Ritterhouse, S. Murray, 2020 .

Unilateral Sclerocornea and Tracheal Stenosis: Unusual Findings in a Patient with Goldenhar Anomaly

Larissa V Furtado, J. Opitz, D. Viskochil, 2011, Fetal and pediatric pathology.

Female adnexal tumors of probable Wolffian origin: morphological, immunohistochemical, and molecular analysis of 15 cases

Larissa V Furtado, Lauren L. Ritterhouse, A. Félix, 2019, Modern Pathology.

Clinical performance of endobronchial ultrasound‐guided transbronchial needle aspiration for assessing programmed death ligand‐1 expression in nonsmall cell lung cancer

Larissa V Furtado, M. Jantz, Marino E. Leon, 2018, Diagnostic cytopathology.

Tumor PD-L1 expression in malignant pleural and peritoneal mesothelioma by Dako PD-L1 22C3 pharmDx and Dako PD-L1 28-8 pharmDx assays.

Larissa V Furtado, A. Husain, T. Krausz, 2019, Human pathology.

Clinical Validation of a Next-Generation Sequencing Genomic Oncology Panel via Cross-Platform Benchmarking against Established Amplicon Sequencing Assays.

Michelle N Wurst, Larissa V Furtado, Megan E. McNerney, 2017, The Journal of molecular diagnostics : JMD.

A Phase I trial assessing the safety and tolerability of a therapeutic DNA vaccination against HPV16 and HPV18 E6/E7 oncogenes after chemoradiation for cervical cancer.

Larissa V Furtado, S. Jolly, R. Weichselbaum, 2020, International journal of radiation oncology, biology, physics.

Detection of MPL mutations by a novel allele-specific PCR-based strategy.

Larissa V Furtado, K. Elenitoba-Johnson, B. Betz, 2013, The Journal of molecular diagnostics : JMD.

Do Circulating Tumor Cells, Exosomes, and Circulating Tumor Nucleic Acids Have Clinical Utility?: A Report of the Association for Molecular Pathology.

Larissa V Furtado, B. Gold, C. Gocke, 2015, The Journal of molecular diagnostics : JMD.

A direct comparison of next generation sequencing enrichment methods using an aortopathy gene panel- clinical diagnostics perspective

Brendan D. O'Fallon, Larissa V Furtado, A. Rope, 2012, BMC Medical Genomics.

Amplicon Indel Hunter Is a Novel Bioinformatics Tool to Detect Large Somatic Insertion/Deletion Mutations in Amplicon-Based Next-Generation Sequencing Data.

Michelle N Wurst, Larissa V Furtado, Sabah Kadri, 2015, The Journal of molecular diagnostics : JMD.

Characterization of large genomic deletions in the FBN1 gene using multiplex ligation-dependent probe amplification

Larissa V Furtado, A. Rope, P. Bayrak-Toydemir, 2011, BMC Medical Genetics.

Unclassified renal cell carcinoma with tubulopapillary architecture, clear cell phenotype, and chromosome 8 monosomy: a new kid on the block

Larissa V Furtado, T. Antic, Sabah Kadri, 2016, Virchows Archiv.

A CTNNB1‐altered medulloblastoma shows the immunophenotypic, DNA methylation and transcriptomic profiles of SHH‐activated, and not WNT‐activated, medulloblastoma

Larissa V Furtado, P. Blackburn, Larissa V. Furtado, 2022, Neuropathology and applied neurobiology.

Adrenocortical carcinoma is a lynch syndrome-associated cancer.

Larissa V Furtado, S. Gruber, T. Giordano, 2013, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Cribriform-Morular Variant of Papillary Thyroid Carcinoma With Poorly Differentiated Features: A Case Report With Immunohistochemical and Molecular Genetic Analysis

Larissa V Furtado, Sabah Kadri, J. Segal, 2018, International journal of surgical pathology.

Identification of a structurally novel BTK mutation that drives ibrutinib resistance in CLL

Larissa V Furtado, Sabah Kadri, W. Stock, 2016, Oncotarget.

Molecular Testing in Myeloproliferative Neoplasms

Larissa V Furtado, B. Betz, Larissa V. Furtado, 2017 .

A multiplexed fragment analysis-based assay for detection of JAK2 exon 12 mutations.

Larissa V Furtado, K. Elenitoba-Johnson, B. Betz, 2013, The Journal of molecular diagnostics : JMD.

Treatment outcomes and HPV characteristics for an institutional cohort of patients with anal cancer receiving concurrent chemotherapy and intensity-modulated radiation therapy

Larissa V Furtado, N. Hyman, S. Xiao, 2018, PloS one.

High prevalence of MiTF staining in undifferentiated pleomorphic sarcoma: caution in the use of melanocytic markers in sarcoma

Larissa V Furtado, A. Montag, N. Cipriani, 2017, Histopathology.

Cervical Ribs Are More Prevalent in Stillborn Fetuses than in Live-Born Infants and Are Strongly Associated with Fetal Aneuploidy

Larissa V Furtado, J. Opitz, B. Shirts, 2011, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Characterization of Molecular Alterations in an Unusual Case of Lynch Syndrome–Associated Adrenocortical Carcinoma

Larissa V Furtado, T. Antic, Sabah Kadri, 2017, AJSP: Reviews and Reports.

Feasibility of Endobronchial Ultrasound‐guided Transbronchial Needle Aspiration Cytology Specimens for Next Generation Sequencing in Non–small‐cell Lung Cancer

Larissa V Furtado, S. Murgu, E. Vokes, 2017, Clinical lung cancer.

Successful lung Cancer EGFR sequencing from DNA extracted from TTF-1 immunohistochemistry slides: a new means to extend insufficient tissue.

Larissa V Furtado, M. Bronner, Georgios Deftereos, 2020, Human pathology.

Standardized evidence-based approach for assessment of oncogenic and clinical significance of NTRK fusions.

Marilyn M. Li, Larissa V Furtado, O. Griffith, 2022, Cancer genetics.

Noninvasive Follicular Thyroid Neoplasms With Papillary-like Nuclear Features Are Genetically and Biologically Similar to Adenomatous Nodules and Distinct From Papillary Thyroid Carcinomas With Extensive Follicular Growth.

Michelle N Wurst, Larissa V Furtado, N. Cipriani, 2018, Archives of pathology & laboratory medicine.

PD-L1 Tumor Cell Expression in Upper Tract Urothelial Carcinomas is Associated With Higher Pathologic Stage

Larissa V Furtado, D. Albertson, Georgios Deftereos, 2020, Applied immunohistochemistry & molecular morphology : AIMM.

Polyglucosan bodies in intramuscular nerve branches are a poor predictor of GBE1 mutation and adult polyglucosan body disease

Larissa V Furtado, Sabah Kadri, P. Pytel, 2016, Muscle & nerve.

Progressive metastatic infantile fibrosarcoma with multiple acquired mutations

Larissa V Furtado, A. Pappo, B. Shulkin, 2023, Cold Spring Harbor molecular case studies.

Molecular Testing Strategies for Pulmonary Adenocarcinoma: An Optimal Approach With Cost Analysis.

Larissa V Furtado, L. Layfield, R. Schmidt, 2019, Archives of pathology & laboratory medicine.

Clinical Validation and Implementation of a Measurable Residual Disease Assay for NPM1 in Acute Myeloid Leukemia by Error-Corrected Next-Generation Sequencing

Michelle N Wurst, Larissa V Furtado, Lauren L. Ritterhouse, 2019, Molecular Diagnosis & Therapy.

Premature Closure of the Foramen Ovale Secondary to Congenital Aortic Valvular Stenosis in a Stillborn

Larissa V Furtado, J. Opitz, Lance K. Erickson, 2012, Fetal and pediatric pathology.

Histologic and Molecular Characterization of Non−Small Cell Lung Carcinoma With Discordant ROS1 Immunohistochemistry and Fluorescence In Situ Hybridization

Larissa V Furtado, R. Schmidt, D. Sirohi, 2021, Applied immunohistochemistry & molecular morphology : AIMM.

Novel HNRNPM::LEUTX fusion resulting from chromothripsis of chromosome 19 in a pediatric undifferentiated small round cell neoplasm.

Larissa V Furtado, Zonggao Shi, T. Santiago, 2023, Genes, chromosomes & cancer.

Circulating Tumor DNA Testing for Liver Cancer

Larissa V Furtado, J. Segal, Larissa V. Furtado, 2015, Cellular and molecular gastroenterology and hepatology.

Risk factors, prevalence, and site concordance of human papillomavirus in high-risk Greek men

Larissa V Furtado, Sabah Kadri, Shruti Sharma, 2017, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

Four-Year Laboratory Performance of the First College of American Pathologists In Silico Next-Generation Sequencing Bioinformatics Proficiency Testing Surveys.

Larissa V Furtado, J. Merker, Rhona J. Souers, 2022, Archives of Pathology & Laboratory Medicine.

Prognostic significance of chromosome arm 1q gain and methylation class in molecularly defined diffuse leptomeningeal glioneuronal tumor

Larissa V Furtado, Xiaoyu Li, J. Chiang, 2022, Acta Neuropathologica.

In silico approaches to proficiency testing: Considerations for continued feasibility.

Larissa V Furtado, A. Zehir, I. Hagemann, 2023, The Journal of molecular diagnostics : JMD.

CBFA2T3::GLIS2‐positive acute leukemia with RAM and mixed T/megakaryocytic phenotype

Larissa V Furtado, J. Klco, Laura Key, 2023, EJHaem.

Principles of Molecular Biology and Oncogenesis

Larissa V Furtado, Selene C. Koo, R. Stewart, 2018 .

Constitutional balanced translocations involving SMARCB1: A rare cause of rhabdoid tumor predisposition syndrome.

Larissa V Furtado, G. Armstrong, P. Blackburn, 2023, Genes, chromosomes & cancer.

Clinical and genomic characterization of an ATRA‐insensitive acute promyelocytic leukemia variant with a FNDC3B::RARB fusion

Larissa V Furtado, J. Klco, P. Blackburn, 2023, Genes, chromosomes & cancer.