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Author Details
Full Name
Marilyn M Li
Affiliation
Children's Hospital of Philadelphia
ORCID
Career Start Year
2000
Papers
88
H Index
23
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36759776
Model performance and interpretability of semi-supervised generative adversarial networks to predict oncogenic variants with unlabeled data.
BMC Bioinformatics
2023
35604410
Multi-institutional study of the frequency, genomic landscape, and outcome of IDH-mutant glioma in pediatrics.
Neuro Oncol
2023
37645778
Alternative splicing of its 5'-UTR limits CD20 mRNA translation and enables resistance to CD20-directed immunotherapies.
bioRxiv
2023
36655517
First-time identification of a KIF5B-NTRK2 fusion in extraventricular neurocytoma.
J Neuropathol Exp Neurol
2023
36503149
Assessments of Somatic Variant Classification Using the Association for Molecular Pathology/American Society of Clinical Oncology/College of American Pathologists Guidelines: A Report from the Association for Molecular Pathology.
J Mol Diagn
2023
36759776
Model performance and interpretability of semi-supervised generative adversarial networks to predict oncogenic variants with unlabeled data.
BMC Bioinformatics
2023
37259034
Correction: Model performance and interpretability of semi-supervised generative adversarial networks to predict oncogenic variants with unlabeled data.
BMC Bioinformatics
2023
36541551
Alternative lengthening of telomeres (ALT) in pediatric high-grade gliomas can occur without ATRX mutation and is enriched in patients with pathogenic germline mismatch repair (MMR) variants.
Neuro Oncol
2023
37645778
Alternative splicing of its 5'-UTR limits CD20 mRNA translation and enables resistance to CD20-directed immunotherapies.
bioRxiv
2023
35604410
Multi-institutional study of the frequency, genomic landscape, and outcome of IDH-mutant glioma in pediatrics.
Neuro Oncol
2023
37259034
Correction: Model performance and interpretability of semi-supervised generative adversarial networks to predict oncogenic variants with unlabeled data.
BMC Bioinformatics
2023
36655517
First-time identification of a KIF5B-NTRK2 fusion in extraventricular neurocytoma.
J Neuropathol Exp Neurol
2023
36541551
Alternative lengthening of telomeres (ALT) in pediatric high-grade gliomas can occur without ATRX mutation and is enriched in patients with pathogenic germline mismatch repair (MMR) variants.
Neuro Oncol
2023
36503149
Assessments of Somatic Variant Classification Using the Association for Molecular Pathology/American Society of Clinical Oncology/College of American Pathologists Guidelines: A Report from the Association for Molecular Pathology.
J Mol Diagn
2023
34338561
Mammary-type Myofibroblastoma with Leiomyomatous Differentiation: A Rare Variant with Potential Pitfalls.
Int J Surg Pathol
2022
36307212
Discovery and functional characterization of the oncogenicity and targetability of a novel <i>NOTCH1-ROS1</i> gene fusion in pediatric angiosarcoma.
Cold Spring Harb Mol Case Stud
2022
36108156
Serial Profiling of Circulating Tumor DNA Identifies Dynamic Evolution of Clinically Actionable Genomic Alterations in High-Risk Neuroblastoma.
Cancer Discov
2022
35836290
Novel ATXN1/ATXN1L::NUTM2A fusions identified in aggressive infant sarcomas with gene expression and methylation patterns similar to CIC-rearranged sarcoma.
Acta Neuropathol Commun
2022
36150821
Best Practice for Clinical Somatic Variant Interpretation and Reporting.
Clin Lab Med
2022
35366592
Standardized evidence-based approach for assessment of oncogenic and clinical significance of NTRK fusions.
Cancer Genet
2022
35794233
Defining the spatial landscape of KRAS mutated congenital pulmonary airway malformations: a distinct entity with a spectrum of histopathologic features.
Mod Pathol
2022
35923098
Looking closely at overgrowth: Constitutional mosaicism in PTEN hamartoma tumor syndrome.
Clin Genet
2022
35544644
CancerVar: An artificial intelligence-empowered platform for clinical interpretation of somatic mutations in cancer.
Sci Adv
2022
34291746
Mesenchymal PLAG1 Tumor With PCMTD1-PLAG1 Fusion in an Infant: A New Type of "Plagoma".
Am J Dermatopathol
2022
34338561
Mammary-type Myofibroblastoma with Leiomyomatous Differentiation: A Rare Variant with Potential Pitfalls.
Int J Surg Pathol
2022
35278038
Neuroblastoma and cutaneous angiosarcoma in a child with PTEN hamartoma tumor syndrome.
Pediatr Blood Cancer
2022
34979564
Tiered Somatic Variant Classification Adoption Has Increased Worldwide With Some Practice Differences Based on Location and Institutional Setting.
Arch Pathol Lab Med
2022
34972035
Atypical teratoid rhabdoid tumor in a child with neurofibromatosis type 2: A novel dual diagnosis.
Cancer Genet
2022
34907337
Correction to: Recommendations for future extensions to the HGNC gene fusion nomenclature.
Leukemia
2022
35232817
A novel <i>TP53</i> tandem duplication in a child with Li-Fraumeni syndrome.
Cold Spring Harb Mol Case Stud
2022
34550633
KMT2A-MAML2 rearrangement emerged and regressed during neuroblastoma therapy without leukemia after 12.8-year follow-up.
Pediatr Blood Cancer
2022
35015563
Fusion Oncogenes Are Associated With Increased Metastatic Capacity and Persistent Disease in Pediatric Thyroid Cancers.
J Clin Oncol
2022
34937317
Rational drug combinations with CDK4/6 inhibitors in acute lymphoblastic leukemia.
Haematologica
2022
35544644
CancerVar: An artificial intelligence-empowered platform for clinical interpretation of somatic mutations in cancer.
Sci Adv
2022
35836290
Novel ATXN1/ATXN1L::NUTM2A fusions identified in aggressive infant sarcomas with gene expression and methylation patterns similar to CIC-rearranged sarcoma.
Acta Neuropathol Commun
2022
35794233
Defining the spatial landscape of KRAS mutated congenital pulmonary airway malformations: a distinct entity with a spectrum of histopathologic features.
Mod Pathol
2022
35366592
Standardized evidence-based approach for assessment of oncogenic and clinical significance of NTRK fusions.
Cancer Genet
2022
36150821
Best Practice for Clinical Somatic Variant Interpretation and Reporting.
Clin Lab Med
2022
36108156
Serial Profiling of Circulating Tumor DNA Identifies Dynamic Evolution of Clinically Actionable Genomic Alterations in High-Risk Neuroblastoma.
Cancer Discov
2022
36307212
Discovery and functional characterization of the oncogenicity and targetability of a novel <i>NOTCH1-ROS1</i> gene fusion in pediatric angiosarcoma.
Cold Spring Harb Mol Case Stud
2022
35923098
Looking closely at overgrowth: Constitutional mosaicism in PTEN hamartoma tumor syndrome.
Clin Genet
2022
35015563
Fusion Oncogenes Are Associated With Increased Metastatic Capacity and Persistent Disease in Pediatric Thyroid Cancers.
J Clin Oncol
2022
34979564
Tiered Somatic Variant Classification Adoption Has Increased Worldwide With Some Practice Differences Based on Location and Institutional Setting.
Arch Pathol Lab Med
2022
35278038
Neuroblastoma and cutaneous angiosarcoma in a child with PTEN hamartoma tumor syndrome.
Pediatr Blood Cancer
2022
34972035
Atypical teratoid rhabdoid tumor in a child with neurofibromatosis type 2: A novel dual diagnosis.
Cancer Genet
2022
34937317
Rational drug combinations with CDK4/6 inhibitors in acute lymphoblastic leukemia.
Haematologica
2022
34907337
Correction to: Recommendations for future extensions to the HGNC gene fusion nomenclature.
Leukemia
2022
35232817
A novel <i>TP53</i> tandem duplication in a child with Li-Fraumeni syndrome.
Cold Spring Harb Mol Case Stud
2022
34550633
KMT2A-MAML2 rearrangement emerged and regressed during neuroblastoma therapy without leukemia after 12.8-year follow-up.
Pediatr Blood Cancer
2022
34291746
Mesenchymal PLAG1 Tumor With PCMTD1-PLAG1 Fusion in an Infant: A New Type of "Plagoma".
Am J Dermatopathol
2022
1 - 50 of 176
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Children's Hospital of Philadelphia
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Angela N Viaene
Perelman School of Medicine, University of Pennsylvania
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Kristina A Cole
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