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Profil bibliographique

Jennifer R. Shingleton

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

17Publications signalées
329Citations signalées
2Affiliations récentes

Les institutions déclarées

Les domaines associés

Lymphoma Diagnosis and TreatmentChronic Lymphocytic Leukemia ResearchAcute Myeloid Leukemia ResearchCancer Genomics and DiagnosticsCutaneous lymphoproliferative disorders research

Les publications récentes

Accès ouvert 2025 conference-abstract OpenAlex

Genomic landscape of mycosis fungoides

Fadzai Chinyengetere, Leonardo P. A. Biral, Veronica S. Russell, Kikkeri N. Naresh et autres

Abstract Introduction: Cutaneous T-cell lymphomas (CTCLs) are a rare, clinically heterogenous group of extranodal lymphomas that arise from mature skin-resident T cells. Mycosis fungoides (MF) is the most common primary CTCL, accounting for >50% of all cases. MF occurs on a spectrum …

us, gb, Afrique du Sud, dk, fi, sg, qa, Égypte (code pays fourni par la source)

0 citations Blood
2025 conference-abstract OpenAlex

Identifying biological differences between two clinical risk groups of cutaneous CD30+ T cell lymphoproliferative disorders

Leonardo P. A. Biral, Veronica S. Russell, Chee Leong Cheng, Andrew Evans et autres

Abstract Background Cutaneous CD30+ T cell lymphoproliferative disorders (CD30+ T LPD) comprise a group of diseases that share overlapping dermato-histopathologic features with variable clinical outcomes. These diagnoses include lymphomatoid papulosis (LYP), primary cutaneous anaplastic large cell lymphoma (cALCL), CD30+ mycosis fungoides (MF), …

us, gb, sg, fi (code pays fourni par la source)

0 citations Blood
2024 conference-abstract OpenAlex

Abstract 3910: The Atlas of Blood Cancer Genomes: A resource for therapeutic and biomarker development

Jennifer R. Shingleton, Raju K. Pillai, Sarah Lynn Ondrejka, Govind Bhagat et autres

Abstract Developing a novel cancer therapy is an expensive, time-consuming, high-risk endeavor that involves identifying a molecular target as well as target indications. This process could be accelerated by a comprehensive interrogation of driver variants and gene expression profiles across cancer types. …

us, qa, sg, dk, fi, cn, hk, ca (code pays fourni par la source)

1 citation Cancer Research
Accès ouvert 2023 conference-abstract OpenAlex

Analytical and Clinical Validation of Duoseq, a Novel Assay for Rapid, on-Site Clinical DNA and RNA Sequencing of Hematologic Malignancies

Eric D. Hsi, Magdalena Czader, Brian Thomas Hill, Elizabeth Thacker et autres

Introduction: Next generation sequencing (NGS) has become a critical component of the workup of malignancies. NGS can provide important diagnostic information including mutations, chromosomal copy number alterations and translocations (from DNAseq) as well as gene expression and fusions (from RNAseq). Incorporation of …

us (code pays fourni par la source)

0 citations Blood
2023 other OpenAlex

Identifying Molecular Drivers of Lymphomagenesis

Jennifer R. Shingleton, Sandeep S. Davé

Genomic technologies have revolutionized the study of molecular drivers of lymphoma development. These studies have uncovered common as well as disease-specific lymphoma drivers that represent promising therapeutic targets; however, significant barriers to clinical translation still remain. In this chapter, we review the …

1 citation
2021 other OpenAlex

Enteropathy‐Associated and Monomorphic Epitheliotropic Intestinal T‐cell Lymphomas

Craig R. Soderquist, Jennifer R. Shingleton, Sandeep S. Davé, Govind Bhagat

This chapter describes the clinical, pathological, and genetic characteristics of enteropathy-associated T-cell lymphoma (EATL), monomorphic epitheliotropic intestinal T-cell lymphoma, and refractory celiac disease (RCD), a rare lymphoproliferative disorder that is a precursor to a subset of EATLs. It discusses current and emerging …

us (code pays fourni par la source)

0 citations
Accès ouvert 2020 preprint OpenAlex

Non-Hodgkin Lymphomas: Malignancies Arising from Mature B Cells

Jennifer R. Shingleton, Jie Wang, Carolyn Baloh, Tushar Dave et autres

Non-Hodgkin lymphomas (NHLs) are a diverse group of entities, both clinically and molecularly. Here, we review the evolution of classification schemes in B-cell lymphoma, noting the now standard WHO classification system that is based on immune cell-of-origin and molecular phenotypes. We review …

us (code pays fourni par la source)

19 citations Cold Spring Harbor Perspectives in Medicine
2019 article OpenAlex

Polatuzumab Vedotin: Honing in on Relapsed or Refractory Diffuse Large B-Cell Lymphoma

Jennifer R. Shingleton, Sandeep S. Davé

Article Tools UNDERSTANDING THE PATHWAY Article Tools OPTIONS & TOOLS Export Citation Track Citation Add To Favorites Rights & Permissions COMPANION ARTICLES Polatuzumab Vedotin in Relapsed or Refractory Diffuse Large B-Cell Lymphoma. November 06, 2019 ARTICLE CITATION DOI: 10.1200/JCO.19.02587 Journal of Clinical …

us (code pays fourni par la source)

10 citations Journal of Clinical Oncology
Accès ouvert 2019 article OpenAlex

The whole-genome landscape of Burkitt lymphoma subtypes

Razvan Panea, Cassandra Love, Jennifer R. Shingleton, Anupama Reddy et autres

Burkitt lymphoma (BL) is an aggressive, MYC-driven lymphoma comprising 3 distinct clinical subtypes: sporadic BLs that occur worldwide, endemic BLs that occur predominantly in sub-Saharan Africa, and immunodeficiency-associated BLs that occur primarily in the setting of HIV. In this study, we comprehensively …

us, Kenya, Tanzanie, pl, hk, cn, de, ca (code pays fourni par la source)

203 citations Blood
2018 article OpenAlex

Genetic convergence of rare lymphomas

Jennifer R. Shingleton, Sandeep S. Davé

PURPOSE OF REVIEW: We review the genetic foundations of different rare lymphomas to examine their shared origins. These data indicate the potential application of genomics to improve the diagnosis and treatment of these rare diseases. RECENT FINDINGS: Next generation sequencing technologies have …

us (code pays fourni par la source)

2 citations Current Opinion in Hematology

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