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Lu Wang

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Medical Director, Molecular Pathology

St. Jude Children's Research Hospital

United States

Research Interests

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Recent Grants

Grant: Close

The PDGF/PI3K/AKT Axis in Mesenchymal Chondrosarcoma: Functional Characterization and Implications for Anticancer Therapy

Open Date: 2022-06-01

Close Date: 2023-05-31

Articles (17)

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2025

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Assistant Professor

Cooper University Hospital

UNITED STATES

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ApplyKite TwinLearns as you apply

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Lu Wang

Research Interests

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Recent Grants

Articles (17)

Genomic landscape and clonal architecture in pediatric myeloid neoplasms with chromosome 7 deletions

Validation of target‐enriched enzymatic methylation sequencing for brain tumor classification from formalin‐fixed paraffin embedded‐derived DNA

Cytarabine‐Related Neurotoxicity in an Infant With Acute Lymphoblastic Leukemia

Clinical experience of using integrated whole genome and transcriptome sequencing as a framework for pediatric and adolescent acute myeloid leukemia diagnosis and risk assessment

Reduced-Intensity Chemotherapy With Immunotherapy for Children With Down Syndrome and B-Cell Acute Lymphoblastic Leukemia.

Chromothripsis-Mediated Small Cell Lung Carcinoma.

Outcomes in patients with ETV6::RUNX1 or high-hyperdiploid B-ALL treated in the St. Jude Total Therapy XV/XVI studies.

DNA Mutational and Copy Number Variation Profiling of Primary Craniofacial Osteosarcomas by Next-Generation Sequencing

Evaluation of Bayesian point-based system on the variant classification of hereditary cancer predisposition genes.

SJPedPanel: A Pan-Cancer Gene Panel for Childhood Malignancies to Enhance Cancer Monitoring and Early Detection.

SMARCA4-deficient primary bone sarcoma with "teratoid" features in a rhabdoid tumor predisposition syndrome patient.

Atypical teratoid/rhabdoid tumour-TYR subtype arising in the setting of germline ring chromosome 22: An uncommon form of tumour predisposition.

Concurrent peripheral T-cell lymphoma and T-cell lymphoblastic leukemia/lymphoma with identical STIL::TAL1 fusion events.

Genomic and global gene expression profiling in pediatric and young adult acute leukemia with PICALM::MLLT10 Fusion.

A new genomic framework to categorize pediatric acute myeloid leukemia.

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

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

Collaborators (6)

Raja Khan

Brent Orr

Mignon L. Loh

Stephanie Dixon

Kim Erika Nichols

Gord Zhu

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