|
| 36244574 | Recommendations for the Use of in Silico Approaches for Next-Generation Sequencing Bioinformatic Pipeline Validation: A Joint Report of the Association for Molecular Pathology, Association for Pathology Informatics, and College of American Pathologists. | J Mol Diagn | 2023 |
| 36787117 | Optimization of Genomewide CRISPR Screens Using AsCas12a and Multi-Guide Arrays. | CRISPR J | 2023 |
| 35189355 | Containers in Bioinformatics: Applications, Practical Considerations, and Best Practices in Molecular Pathology. | J Mol Diagn | 2022 |
| 35830791 | Unified classification of mouse retinal ganglion cells using function, morphology, and gene expression. | Cell Rep | 2022 |
| 36268089 | A performance evaluation study: Variant annotation tools - the enigma of clinical next generation sequencing (NGS) based genetic testing. | J Pathol Inform | 2022 |
| 33960872 | The RNA structurome in the asexual blood stages of malaria pathogen <i>plasmodium falciparum</i>. | RNA Biol | 2021 |
| 33608380 | Transcript analysis for variant classification resolution in a child with primary ciliary dyskinesia. | Cold Spring Harb Mol Case Stud | 2021 |
| 34379075 | Genomic Autopsy of Sudden Deaths in Young Individuals. | JAMA Cardiol | 2021 |
| 32276922 | Detailed Phenotypic and Functional Characterization of a Rare, Antibody-Dependent SLAM-Associated Protein Expression Pattern. | Immunohorizons | 2020 |
| 31783043 | Next-generation sequencing identifies 2 genomically distinct groups among pyloric gland adenomas. | Hum Pathol | 2020 |
| 32074275 | A phase 1 study of azacitidine with high-dose cytarabine and mitoxantrone in high-risk acute myeloid leukemia. | Blood Adv | 2020 |
| 32282345 | Follicular Thyroid Neoplasms: Comparison of Clinicopathologic and Molecular Features of Atypical Adenomas and Follicular Thyroid Carcinomas. | Am J Surg Pathol | 2020 |
| 30273779 | insiM: in silico Mutator Software for Bioinformatics Pipeline Validation of Clinical Next-Generation Sequencing Assays. | J Mol Diagn | 2019 |
| 31673932 | Clinical Validation and Implementation of a Measurable Residual Disease Assay for NPM1 in Acute Myeloid Leukemia by Error-Corrected Next-Generation Sequencing. | Mol Diagn Ther | 2019 |
| 31645901 | Fewer actionable mutations but higher tumor mutational burden characterizes NSCLC in black patients at an urban academic medical center. | Oncotarget | 2019 |
| 31658273 | Measurable residual disease monitoring for patients with acute myeloid leukemia following hematopoietic cell transplantation using error corrected hybrid capture next generation sequencing. | PLoS One | 2019 |
| 30176755 | Cribriform-Morular Variant of Papillary Thyroid Carcinoma With Poorly Differentiated Features: A Case Report With Immunohistochemical and Molecular Genetic Analysis. | Int J Surg Pathol | 2019 |
| 31186530 | Quantitative next-generation sequencing-based analysis indicates progressive accumulation of microsatellite instability between atypical hyperplasia/endometrial intraepithelial neoplasia and paired endometrioid endometrial carcinoma. | Mod Pathol | 2019 |
| 30986793 | Genetic Underpinnings of Renal Cell Carcinoma With Leiomyomatous Stroma. | Am J Surg Pathol | 2019 |
| 31054900 | Targeted mutational analysis of inflammatory bowel disease-associated colorectal cancers. | Hum Pathol | 2019 |
| 30698790 | Integrating a Large Next-Generation Sequencing Panel into the Clinical Diagnosis of Gliomas Provides a Comprehensive Platform for Classification from FFPE Tissue or Smear Preparations. | J Neuropathol Exp Neurol | 2019 |
| 30333224 | Cerdulatinib Pharmacodynamics and Relationships to Tumor Response Following Oral Dosing in Patients with Relapsed/Refractory B-cell Malignancies. | Clin Cancer Res | 2019 |
| 30557173 | Clinicopathologic and Molecular Features of Metastatic Follicular Thyroid Carcinoma in Patients Presenting With a Thyroid Nodule Versus a Distant Metastasis. | Am J Surg Pathol | 2019 |
| 30635337 | Autophagy Inhibition to Augment mTOR Inhibition: a Phase I/II Trial of Everolimus and Hydroxychloroquine in Patients with Previously Treated Renal Cell Carcinoma. | Clin Cancer Res | 2019 |
| 28710706 | Synchronous and Metastatic Papillary and Follicular Thyroid Carcinomas with Unique Molecular Signatures. | Endocr Pathol | 2018 |
| 35135165 | Clinical Activity of Olaparib in Urothelial Bladder Cancer With DNA Damage Response Gene Mutations. | JCO Precis Oncol | 2018 |
| 30113886 | Frequency of Germline Mutations in Cancer Susceptibility Genes in Malignant Mesothelioma. | J Clin Oncol | 2018 |
| 30425251 | Author Correction: Integrated molecular subtyping defines a curable oligometastatic state in colorectal liver metastasis. | Nat Commun | 2018 |
| 30510142 | XPO1 Inhibitor Selinexor Overcomes Intrinsic Ibrutinib Resistance in Mantle Cell Lymphoma via Nuclear Retention of IκB. | Mol Cancer Ther | 2018 |
| 28394804 | Risk factors, prevalence, and site concordance of human papillomavirus in high-risk Greek men. | Eur J Cancer Prev | 2018 |
| 29728604 | Integrated molecular subtyping defines a curable oligometastatic state in colorectal liver metastasis. | Nat Commun | 2018 |
| 29582677 | 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. | Arch Pathol Lab Med | 2018 |
| 29698836 | System for Informatics in the Molecular Pathology Laboratory: An Open-Source End-to-End Solution for Next-Generation Sequencing Clinical Data Management. | J Mol Diagn | 2018 |
| 29668487 | Are Sporadic Eosinophilic Solid and Cystic Renal Cell Carcinomas Characterized by Somatic Tuberous Sclerosis Gene Mutations? | Am J Surg Pathol | 2018 |
| 29365323 | Prognostic tumor sequencing panels frequently identify germ line variants associated with hereditary hematopoietic malignancies. | Blood Adv | 2018 |
| 27855558 | Diagnostic evaluation of RNA sequencing for the detection of genetic abnormalities associated with Ph-like acute lymphoblastic leukemia (ALL). | Leuk Lymphoma | 2017 |
| 28335028 | Defining the 5ο and 3ο landscape of the Drosophila transcriptome with Exo-seq and RNaseH-seq. | Nucleic Acids Res | 2017 |
| 28348046 | B-Cell Lymphoma Patient-Derived Xenograft Models Enable Drug Discovery and Are a Platform for Personalized Therapy. | Clin Cancer Res | 2017 |
| 29296715 | Clonal evolution underlying leukemia progression and Richter transformation in patients with ibrutinib-relapsed CLL. | Blood Adv | 2017 |
| 28009605 | Melanotic PEComa of the Sinonasal Mucosa With NONO-TFE3 Fusion: An Elusive Mimic of Sinonasal Melanoma. | Am J Surg Pathol | 2017 |
| 27926791 | High prevalence of MiTF staining in undifferentiated pleomorphic sarcoma: caution in the use of melanocytic markers in sarcoma. | Histopathology | 2017 |
| 27836695 | Clinical Validation of a Next-Generation Sequencing Genomic Oncology Panel via Cross-Platform Benchmarking against Established Amplicon Sequencing Assays. | J Mol Diagn | 2017 |
| 26838501 | Evolutionary analysis across mammals reveals distinct classes of long non-coding RNAs. | Genome Biol | 2016 |
| 26670585 | Polyglucosan bodies in intramuscular nerve branches are a poor predictor of GBE1 mutation and adult polyglucosan body disease. | Muscle Nerve | 2016 |
| 27626698 | Identification of a structurally novel BTK mutation that drives ibrutinib resistance in CLL. | Oncotarget | 2016 |
| 27173781 | Unclassified renal cell carcinoma with tubulopapillary architecture, clear cell phenotype, and chromosome 8 monosomy: a new kid on the block. | Virchows Arch | 2016 |
| 26319364 | Amplicon Indel Hunter Is a Novel Bioinformatics Tool to Detect Large Somatic Insertion/Deletion Mutations in Amplicon-Based Next-Generation Sequencing Data. | J Mol Diagn | 2015 |
| 24726434 | Reconstructing and reprogramming the tumor-propagating potential of glioblastoma stem-like cells. | Cell | 2014 |
| 25453760 | A negative feedback loop of transcription factors specifies alternative dendritic cell chromatin States. | Mol Cell | 2014 |
| 23828888 | The Xist lncRNA exploits three-dimensional genome architecture to spread across the X chromosome. | Science | 2013 |