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Author Details
Full Name
Payal Jain
Affiliation
Maharaja Agrasen Medical College
ORCID
Career Start Year
2009
Papers
22
H Index
13
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37397046
Adult Brainstem Astroblastoma: Unusual Presentation of a Rare Tumor.
Asian J Neurosurg
2023
37397046
Adult Brainstem Astroblastoma: Unusual Presentation of a Rare Tumor.
Asian J Neurosurg
2023
37492101
OpenPBTA: The Open Pediatric Brain Tumor Atlas.
Cell Genom
2023
37492101
OpenPBTA: The Open Pediatric Brain Tumor Atlas.
Cell Genom
2023
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
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
35852795
Upfront Biology-Guided Therapy in Diffuse Intrinsic Pontine Glioma: Therapeutic, Molecular, and Biomarker Outcomes from PNOC003.
Clin Cancer Res
2022
35852795
Upfront Biology-Guided Therapy in Diffuse Intrinsic Pontine Glioma: Therapeutic, Molecular, and Biomarker Outcomes from PNOC003.
Clin Cancer Res
2022
33565241
BRAF fusions in pediatric histiocytic neoplasms define distinct therapeutic responsiveness to RAF paradox breakers.
Pediatr Blood Cancer
2021
33565241
BRAF fusions in pediatric histiocytic neoplasms define distinct therapeutic responsiveness to RAF paradox breakers.
Pediatr Blood Cancer
2021
32160911
Smarcad1 mediates microbiota-induced inflammation in mouse and coordinates gene expression in the intestinal epithelium.
Genome Biol
2020
32160911
Smarcad1 mediates microbiota-induced inflammation in mouse and coordinates gene expression in the intestinal epithelium.
Genome Biol
2020
32155117
PHF19 mediated regulation of proliferation and invasiveness in prostate cancer cells.
Elife
2020
33317447
annoFuse: an R Package to annotate, prioritize, and interactively explore putative oncogenic RNA fusions.
BMC Bioinformatics
2020
33317447
annoFuse: an R Package to annotate, prioritize, and interactively explore putative oncogenic RNA fusions.
BMC Bioinformatics
2020
32155117
PHF19 mediated regulation of proliferation and invasiveness in prostate cancer cells.
Elife
2020
30861105
A pilot precision medicine trial for children with diffuse intrinsic pontine glioma-PNOC003: A report from the Pacific Pediatric Neuro-Oncology Consortium.
Int J Cancer
2019
31617914
Genomic Analysis of Dysembryoplastic Neuroepithelial Tumor Spectrum Reveals a Diversity of Molecular Alterations Dysregulating the MAPK and PI3K/mTOR Pathways.
J Neuropathol Exp Neurol
2019
30024272
Purification of mRNA Encoding Chimeric Antigen Receptor Is Critical for Generation of a Robust T-Cell Response.
Hum Gene Ther
2019
30861105
A pilot precision medicine trial for children with diffuse intrinsic pontine glioma-PNOC003: A report from the Pacific Pediatric Neuro-Oncology Consortium.
Int J Cancer
2019
31335288
Sclerosing Epithelioid Fibrosarcoma of the Bone With Rare EWSR1-CREB3L3 Translocation Driving Upregulation of the PI3K/mTOR Signaling Pathway.
Pediatr Dev Pathol
2019
30024272
Purification of mRNA Encoding Chimeric Antigen Receptor Is Critical for Generation of a Robust T-Cell Response.
Hum Gene Ther
2019
31335288
Sclerosing Epithelioid Fibrosarcoma of the Bone With Rare EWSR1-CREB3L3 Translocation Driving Upregulation of the PI3K/mTOR Signaling Pathway.
Pediatr Dev Pathol
2019
31617914
Genomic Analysis of Dysembryoplastic Neuroepithelial Tumor Spectrum Reveals a Diversity of Molecular Alterations Dysregulating the MAPK and PI3K/mTOR Pathways.
J Neuropathol Exp Neurol
2019
28780023
Shared ACVR1 mutations in FOP and DIPG: Opportunities and challenges in extending biological and clinical implications across rare diseases.
Bone
2018
28780023
Shared ACVR1 mutations in FOP and DIPG: Opportunities and challenges in extending biological and clinical implications across rare diseases.
Bone
2018
29767381
Novel FGFR2-INA fusion identified in two low-grade mixed neuronal-glial tumors drives oncogenesis via MAPK and PI3K/mTOR pathway activation.
Acta Neuropathol
2018
29317660
Microbiota derived short chain fatty acids promote histone crotonylation in the colon through histone deacetylases.
Nat Commun
2018
29767381
Novel FGFR2-INA fusion identified in two low-grade mixed neuronal-glial tumors drives oncogenesis via MAPK and PI3K/mTOR pathway activation.
Acta Neuropathol
2018
29317660
Microbiota derived short chain fatty acids promote histone crotonylation in the colon through histone deacetylases.
Nat Commun
2018
27973981
MYB-QKI drives childhood brain tumors via tripartite mechanism.
Cell Cycle
2017
28806393
CRAF gene fusions in pediatric low-grade gliomas define a distinct drug response based on dimerization profiles.
Oncogene
2017
29156677
Overcoming resistance to single-agent therapy for oncogenic <i>BRAF</i> gene fusions <i>via</i> combinatorial targeting of MAPK and PI3K/mTOR signaling pathways.
Oncotarget
2017
27973981
MYB-QKI drives childhood brain tumors via tripartite mechanism.
Cell Cycle
2017
29156677
Overcoming resistance to single-agent therapy for oncogenic <i>BRAF</i> gene fusions <i>via</i> combinatorial targeting of MAPK and PI3K/mTOR signaling pathways.
Oncotarget
2017
28806393
CRAF gene fusions in pediatric low-grade gliomas define a distinct drug response based on dimerization profiles.
Oncogene
2017
27000413
Mutations and deletions of PRC2 in prostate cancer.
Bioessays
2016
27000413
Mutations and deletions of PRC2 in prostate cancer.
Bioessays
2016
26829751
MYB-QKI rearrangements in angiocentric glioma drive tumorigenicity through a tripartite mechanism.
Nat Genet
2016
26829751
MYB-QKI rearrangements in angiocentric glioma drive tumorigenicity through a tripartite mechanism.
Nat Genet
2016
22126247
Combinatorial assembly and function of chromatin regulatory complexes.
Epigenomics
2011
22126247
Combinatorial assembly and function of chromatin regulatory complexes.
Epigenomics
2011
19361779
Null mutations in LTBP2 cause primary congenital glaucoma.
Am J Hum Genet
2009
19361779
Null mutations in LTBP2 cause primary congenital glaucoma.
Am J Hum Genet
2009
1 - 44 of 44
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Children's Hospital of Philadelphia
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Joshua Straka
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University Children's Hospital Zurich
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Children's Hospital of Philadelphia
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Children's Hospital of Philadelphia
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Anna Maria Buccoliero
Co-authored papers
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Co-authored papers
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Pichai Raman
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Javad Nazarian
USA University of Zurich
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Krutika S Gaonkar
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Namrata Choudhari
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