J. Segal

发表

Quantitation of HIV-1-specific cytotoxic T lymphocytes and plasma load of viral RNA.

M A Nowak, M. Nowak, D. Ho, 1998, Science.

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.

Human Organoids Share Structural and Genetic Features with Primary Pancreatic Adenocarcinoma Tumors

Andrey Rzhetsky, Kevin P. White, Christopher R. Weber, 2018, Molecular Cancer Research.

Direct in Vivo RNAi Screen Unveils Myosin IIa as a Tumor Suppressor of Squamous Cell Carcinomas

Elaine Fuchs, Boris Reva, Jeremy P. Segal, 2014, Science.

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.

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.

Fewer actionable mutations but higher tumor mutational burden characterizes NSCLC in black patients at an urban academic medical center

Lauren L. Ritterhouse, Sabah Kadri, A. Husain, 2019, Oncotarget.

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.

Secondary resistance to immunotherapy associated with β-catenin pathway activation or PTEN loss in metastatic melanoma

Lauren L. Ritterhouse, J. Luke, T. Gajewski, 2019, Journal of Immunotherapy for Cancer.

NF2-mutated Renal Carcinomas Have Common Morphologic Features Which Overlap With Biphasic Hyalinizing Psammomatous Renal Cell Carcinoma

T. Antic, W. Stadler, A. Gallan, 2022, The American journal of surgical pathology.

A Tale of 2 Morphologies: Diagnostic Pitfalls in TFEB-Associated Renal Cell Carcinomas, Including a Novel NEAT1-TFEB Fusion

T. Antic, J. Segal, M. Parilla, 2020, International journal of surgical pathology.

1 Title: Autophagy inhibition to augment mTOR inhibition: A phase I/II trial of everolimus and hydroxychloroquine in patients with previously treated renal cell carcinoma

Kim, Ravi, P. Gimotty, 2019 .

Circulating Tumor DNA Testing for Liver Cancer

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

Feasibility and limitations of cultured skin fibroblasts for germline genetic testing in hematologic disorders

Soma Das, D. del Gaudio, L. Godley, 2020, Human mutation.

Dihydropyrimidine dehydrogenase deficiency as a cause of fatal 5-Fluorouracil toxicity

Aarti Sharma, J. Segal, R. Lastra, 2018, Autopsy & case reports.

Identifying Inherited and Acquired Genetic Factors Involved in Poor Stem Cell Mobilization and Donor-Derived Malignancy.

T. Walsh, M. King, R. Larson, 2016, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Next generation sequencing identifies two Genomically distinct groups among pyloric gland adenomas.

Lauren L. Ritterhouse, Sabah Kadri, N. Niu, 2019, Human pathology.

MUC4 expression by immunohistochemistry is a specific marker for BCR-ABL1+ and BCR-ABL1-like B-lymphoblastic leukemia

G. Raca, W. Stock, K. Yap, 2022, Leukemia & lymphoma.

Heterozygous germ line CSF3R variants as risk alleles for development of hematologic malignancies.

Soma Das, L. Godley, L. Druhan, 2020, Blood advances.

Synchronous and Metastatic Papillary and Follicular Thyroid Carcinomas with Unique Molecular Signatures

N. Cipriani, Sabah Kadri, N. Niu, 2018, Endocrine Pathology.

Measurable residual disease monitoring for patients with acute myeloid leukemia following hematopoietic cell transplantation using error corrected hybrid capture next generation sequencing

Lauren L. Ritterhouse, Sabah Kadri, W. Stock, 2019, PloS one.

The phenotypic profile of dermatomyositis and lupus erythematosus: a comparative analysis

C. Magro, J. Segal, A. Crowson, 2010, Journal of cutaneous pathology.

Author Correction: Integrated molecular subtyping defines a curable oligometastatic state in colorectal liver metastasis

K. White, R. Weichselbaum, M. Talamonti, 2018, Nature Communications.

Eosinophilic Renal Cell Tumors With a TSC and MTOR Gene Mutations Are Morphologically and Immunohistochemically Heterogenous

T. Antic, J. Segal, M. Parilla, 2020, The American journal of surgical pathology.

Cerdulatinib Pharmacodynamics and Relationships to Tumor Response Following Oral Dosing in Patients with Relapsed/Refractory B-cell Malignancies

Sabah Kadri, Y. L. Wang, J. Leeds, 2017, Clinical Cancer Research.

B-cell lymphoma-2 (BCL2) downregulation is a useful feature -supporting a neoplastic phenotype in mature T-cell lymphomas.

K. Karube, D. Arber, G. Venkataraman, 2022, Human pathology.

I. Helenowski, J. Altman, H. Tariq, 2022, British journal of haematology.

Fulminant and accelerated presentation of dermatomyositis in two previously healthy young adult males: a potential role for endotheliotropic viral infection

G. Nuovo, C. Magro, J. Segal, 2009, Journal of cutaneous pathology.

NPM1 exon 5 mutations in acute myeloid leukemia: Implications in diagnosis and minimal residual monitoring

D. Arber, G. Venkataraman, J. Segal, 2022, EJHaem.

Clinical outcomes of IDH2‐mutated advanced‐phase Ph‐negative myeloproliferative neoplasms treated with enasidenib

R. Larson, W. Stock, Kirk Cahill, 2020, British journal of haematology.

Recurrent Loss of Heterozygosity in Pancreatic Neuroendocrine Tumors

Lauren L. Ritterhouse, J. Hechtman, D. Klimstra, 2022, The American journal of surgical pathology.

Melanotic PEComa of the Sinonasal Mucosa With NONO-TFE3 Fusion: An Elusive Mimic of Sinonasal Melanoma.

Sabah Kadri, T. Krausz, J. Bridge, 2017, The American journal of surgical pathology.

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.

Unified classification of mouse retinal ganglion cells using function, morphology, and gene expression

Zachary F. Jessen, J. Sanes, K. Shekhar, 2021, bioRxiv.

by Monoclonal Antibodies to CCR5 gp120 Binding, and CC-Chemokine Activity Immunodeficiency Virus Type 1 Fusion, Differential Inhibition of Human

John P. Moore, G. Rabut, Paul J Maddon, 2012 .

Differential Inhibition of Human Immunodeficiency Virus Type 1 Fusion, gp120 Binding, and CC-Chemokine Activity by Monoclonal Antibodies to CCR5

William C. Olson, Yong Guo, Jeremy P. Segal, 1999, Journal of Virology.

High Rates of Ultraviolet-Signature Mutations in Squamous Cell Carcinomas of the Parotid Gland and Prognostic Implications

N. Cipriani, G. Steinhardt, J. Segal, 2021, Head and Neck Pathology.

Integrated molecular subtyping defines a curable oligometastatic state in colorectal liver metastasis

Jorge Andrade, Sabha Ganai, Samuel Hellman, 2018, Nature Communications.

Frequency of Germline Mutations in Cancer Susceptibility Genes in Malignant Mesothelioma.

Lauren L. Ritterhouse, D. Huo, Sabah Kadri, 2018, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Unique Growth Pattern in Papillary Carcinoma of the Thyroid Gland Mimicking Adenoid Cystic Carcinoma

Z. Baloch, V. Livolsi, J. Segal, 2011, Endocrine pathology.

Pancreatic adenocarcinoma human organoids share structural and genetic features with primary tumors

K. White, R. Weichselbaum, A. Rzhetsky, 2018, bioRxiv.

TITLE: Human Organoids Share Structural and Genetic Features with Primary Pancreatic Adenocarcinoma Tumors AUTHOR AND AFFILIATIONS:

Qiang, R. Weichselbaum, A. Rzhetsky, 2018 .

Germline BRCA-Associated Endometrial Carcinoma Is a Distinct Clinicopathologic Entity

Lauren L. Ritterhouse, H. Hollema, C. V. van Asperen, 2019, Clinical Cancer Research.

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

Lauren L. Ritterhouse, Sushant A. Patil, Sabah Kadri, 2019, Journal of neuropathology and experimental neurology.

STK11 Inactivation Predicts Rapid Recurrence in Inoperable Early-Stage Non-Small-Cell Lung Cancer.

B. Loo, M. Diehn, E. Vokes, 2023, JCO precision oncology.

CDKN2A loss-of-function predicts immunotherapy resistance in non-small cell lung cancer

R. Weichselbaum, E. Vokes, J. Donington, 2021, Scientific Reports.

Practical, ethical and regulatory considerations for the evolving medical and research genomics landscape☆

G. Lyon, J. Segal, 2013, Applied & translational genomics.

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.

High NPM1 mutant allele burden at diagnosis correlates with minimal residual disease at first remission in de novo acute myeloid leukemia

Lauren L. Ritterhouse, P. D. Dal Cin, G. Pinkus, 2019, American journal of hematology.

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 .

Molecular Testing in Pediatric Oncology Practice

Jeremy P. Segal, Lauren L. Ritterhouse, L. Ritterhouse, 2018 .

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.

Quantitative next-generation sequencing-based analysis indicates progressive accumulation of microsatellite instability between atypical hyperplasia/endometrial intraepithelial neoplasia and paired endometrioid endometrial carcinoma

Lauren L. Ritterhouse, Sushant A. Patil, Sabah Kadri, 2019, Modern Pathology.

insiM: in silico Mutator Software for Bioinformatics Pipeline Validation of Clinical Next-Generation Sequencing Assays.

Sabah Kadri, Ibro Mujacic, Jeremy P. Segal, 2019, The Journal of molecular diagnostics : JMD.

Prognostic tumor sequencing panels frequently identify germ line variants associated with hereditary hematopoietic malignancies.

Sushant A. Patil, G. Raca, Sabah Kadri, 2018, Blood advances.

Sensitive detection and quantification of SARS-CoV-2 in saliva

C. Bethel, S. Tay, E. Izumchenko, 2021, Scientific Reports.

Sensitive detection and quantification of SARS-CoV-2 in saliva

C. Bethel, S. Tay, E. Izumchenko, 2020, medRxiv.

Follicular Thyroid Neoplasms

Lauren L. Ritterhouse, N. Cipriani, Sabah Kadri, 2020, The American journal of surgical pathology.

Identification of Molecular Alterations Challenging Initial Pathologic Classification in Cases of Clinician-Initiated Next-Generation Sequencing Testing.

P. Pytel, J. Segal, Joseph H Cho, 2021, American journal of clinical pathology.

Aggressive morphologic variants of mantle cell lymphoma characterized with high genomic instability showing frequent chromothripsis, CDKN2A/B loss, and TP53 mutations: A multi‐institutional study

L. Gordon, G. Venkataraman, A. Behdad, 2020, Genes, chromosomes & cancer.

Diagnosis and treatment of mixed phenotype (T-myeloid/lymphoid) acute leukemia with novel ETV6-FGFR2 rearrangement.

D. Arber, E. Hyjek, J. Segal, 2020, Blood advances.

Autophagy Inhibition to Augment mTOR Inhibition: a Phase I/II Trial of Everolimus and Hydroxychloroquine in Patients with Previously Treated Renal Cell Carcinoma

P. Gimotty, Sabah Kadri, L. Appleman, 2019, Clinical Cancer Research.

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.

Telomere biology disorder prevalence and phenotypes in adults with familial hematologic and/or pulmonary presentations.

T. Walsh, M. King, R. Collins, 2020, Blood advances.

Melanotic Translocation Renal Cell Carcinoma With a Novel ARID1B-TFE3 Gene Fusion

T. Antic, J. Taxy, J. Segal, 2017, The American journal of surgical pathology.

Clinical Activity of Olaparib in Urothelial Bladder Cancer With DNA Damage Response Gene Mutations.

Lauren L. Ritterhouse, N. Smith, Sabah Kadri, 2018, JCO precision oncology.

Decay Kinetics of Human Immunodeficiency Virus-Specific Effector Cytotoxic T Lymphocytes after Combination Antiretroviral Therapy

M. Nowak, D. Ho, Y. Cao, 1999, Journal of Virology.

EZR-ROS1 fusion renal cell carcinoma mimicking urothelial carcinoma: report of a previously undescribed gene fusion in renal cell carcinoma

S. Eggener, P. Agarwal, J. Segal, 2021, Virchows Archiv.

Clinicopathologic and Molecular Features of Metastatic Follicular Thyroid Carcinoma in Patients Presenting With a Thyroid Nodule Versus a Distant Metastasis

Lauren L. Ritterhouse, N. Cipriani, Sabah Kadri, 2019, The American journal of surgical pathology.

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.

Nfatc1 orchestrates aging in hair follicle stem cells

D. Zheng, E. Fuchs, Wen-Hui Lien, 2013, Proceedings of the National Academy of Sciences.

TSC/MTOR Mutated Renal Cell Carcinoma with Leiomyomatous Stroma is a Distinct Entity: A Comprehensive Study of 12 Cases.

T. Antic, J. Segal, P. Wanjari, 2022, Human pathology.

Genetic Underpinnings of Renal Cell Carcinoma With Leiomyomatous Stroma

Lauren L. Ritterhouse, Sushant A. Patil, T. Antic, 2019, The American journal of surgical pathology.

Are Sporadic Eosinophilic Solid and Cystic Renal Cell Carcinomas Characterized by Somatic Tuberous Sclerosis Gene Mutations?

Lauren L. Ritterhouse, Sushant A. Patil, T. Antic, 2018, The American journal of surgical pathology.

Eosinophilic renal cell carcinoma with isolated MTOR mutation metastatic to the liver: a novel case.

T. Antic, W. Stadler, J. Segal, 2021, Pathology.

TSC/MTOR mutated eosinophilic renal tumors are a distinct entity that are CK7+/CK20-/vimentin-: a validation study.

T. Antic, J. Segal, P. Wanjari, 2020, Human pathology.

EWSR1-PATZ1 fusion renal cell carcinoma: a recurrent gene fusion characterizing thyroid-like follicular renal cell carcinoma

D. Grignon, V. Reuter, Liang Cheng, 2021, Modern Pathology.

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.

BAP1-Mutated Clear Cell Renal Cell Carcinoma.

Lauren L. Ritterhouse, T. Antic, A. Gallan, 2020, American journal of clinical pathology.

Evaluation of SWI/SNF Protein Expression by Immunohistochemistry in Ovarian Clear Cell Carcinoma.

E. Oliva, J. Segal, J. Bennett, 2020, International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.

TCEB1-mutated renal cell carcinoma in relation to renal cell carcinoma with smooth muscle stroma in tuberous sclerosis complex.

T. Antic, Sabah Kadri, J. Segal, 2018 .

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.

Clonal evolution underlying leukemia progression and Richter transformation in patients with ibrutinib-relapsed CLL.

Sonali M. Smith, Sabah Kadri, W. Stock, 2017, Blood advances.

B-Cell Lymphoma Patient-Derived Xenograft Models Enable Drug Discovery and Are a Platform for Personalized Therapy

Michael L. Wang, Shouhao Zhou, Sabah Kadri, 2017, Clinical Cancer Research.

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

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

Use of Laser-Capture Microdissection for the Identification of Marker Genes for the Ventromedial Hypothalamic Nucleus

Thomas M. Harris, Thomas M Harris, Jeremy P Segal, 2005, The Journal of Neuroscience.