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Author Details
Full Name
Ninad Oak
Affiliation
St. Jude Children's Research Hospital
ORCID
Career Start Year
2014
Papers
17
H Index
7
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36693186
Pathogenic Variants in Adult-Onset Cancer Predisposition Genes in Pediatric Cancer: Prevalence and Impact on Tumor Molecular Features and Clinical Management.
Clin Cancer Res
2023
37522715
ETV6 represses inflammatory response genes and regulates HSPC function during stress hematopoiesis in mice.
Blood Adv
2023
37620322
Immune stress suppresses innate immune signaling in preleukemic precursor B-cells to provoke leukemia in predisposed mice.
Nat Commun
2023
37869077
Germline landscape of <i>RPA1, RPA2 and RPA3</i> variants in pediatric malignancies: identification of <i>RPA1</i> as a novel cancer predisposition candidate gene.
Front Oncol
2023
36993649
The Genetic and Epigenetic Features of Bilateral Wilms Tumor Predisposition: A Report from the Children's Oncology Group AREN18B5-Q Study.
Res Sq
2023
37228616
Cellular and transcriptional impacts of Janus kinase and/or IFN-gamma inhibition in a mouse model of primary hemophagocytic lymphohistiocytosis.
Front Immunol
2023
34996063
Development of BRAFV600E-positive acute myeloid leukemia in a patient on long-term dabrafenib for multisystem LCH.
Blood Adv
2022
35131871
Transient Inhibition of the JAK/STAT Pathway Prevents B-ALL Development in Genetically Predisposed Mice.
Cancer Res
2022
32693409
Molecular basis of ETV6-mediated predisposition to childhood acute lymphoblastic leukemia.
Blood
2021
32412586
Recent advances in Wilms' tumor predisposition.
Hum Mol Genet
2020
30302893
Framework for microRNA variant annotation and prioritization using human population and disease datasets.
Hum Mutat
2019
31604778
Enrichment of heterozygous germline <i>RECQL4</i> loss-of-function variants in pediatric osteosarcoma.
Cold Spring Harb Mol Case Stud
2019
29625052
Pathogenic Germline Variants in 10,389 Adult Cancers.
Cell
2018
30266087
Insights from the 2018 Biology of Genomes meeting.
Genome Biol
2018
29179779
Evaluation of in silico algorithms for use with ACMG/AMP clinical variant interpretation guidelines.
Genome Biol
2017
26572163
Integrated genomics approach to identify biologically relevant alterations in fewer samples.
BMC Genomics
2015
23855664
Identification of ligand binding pockets on nuclear receptors by machine learning methods.
Protein Pept Lett
2014
1 - 17 of 17
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row(s) 1 - 30 of 30
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Changhai Hospital, Second Military Medical University
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3
Zhaoming Wang
St Jude Children's Research Hospital
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David A Wheeler
Baylor College of Medicine
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2
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McDonnell Genome Institute, Washington University School of Medicine
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Institute for Systems Biology
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1
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University of Texas MD Anderson Cancer Center
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1
Charles G Mullighan
St Jude Children's Research Hospital
Co-authored papers
1
Mignon L Loh
University of Washington
Co-authored papers
1
Olivier Lichtarge
Baylor College of Medicine
Co-authored papers
1
Alexander J Lazar
The University of Texas MD Anderson Cancer Center
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1
Feng Chen
Washington University in St Louis
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1
Yige Wu
Washington University in St. Louis, USA McDonnell Genome Institute
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1
Amanda Koire
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Vishwanathan Hucthagowder
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