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Author Details
Full Name
Adrian M Dubuc
Affiliation
Dana-Farber Cancer Institute
ORCID
Career Start Year
2008
Papers
82
H Index
36
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36780194
ALK Amplification and Rearrangements Are Recurrent Targetable Events in Congenital and Adult Glioblastoma.
Clin Cancer Res
2023
37532182
ROS1 Alterations as a Potential Driver of Gliomas in Infant, Pediatric, and Adult Patients.
Mod Pathol
2023
34508644
A molecularly integrated grade for meningioma.
Neuro Oncol
2022
36150823
Copy Number Analysis in Cancer Diagnostic Testing.
Clin Lab Med
2022
36063163
Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).
Genet Med
2022
36219398
Dormant SOX9-Positive Cells Facilitate MYC-Driven Recurrence of Medulloblastoma.
Cancer Res
2022
35101336
Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).
Genet Med
2022
35167654
Guiding the global evolution of cytogenetic testing for hematologic malignancies.
Blood
2022
33387364
Correlation of methylthioadenosine phosphorylase (MTAP) protein expression with MTAP and CDKN2A copy number in malignant pleural mesothelioma.
Histopathology
2021
34074652
Twists and turns from "tumor in tumor" profiling: surveillance of chronic lymphocytic leukemia (CLL) leads to detection of a lung adenocarcinoma, whose genomic characterization alters the original hematologic diagnosis.
Cold Spring Harb Mol Case Stud
2021
33986460
Re-evaluating tumors of purported specialized prostatic stromal origin reveals molecular heterogeneity, including non-recurring gene fusions characteristic of uterine and soft tissue sarcoma subtypes.
Mod Pathol
2021
33247715
Quantification of aneuploidy in targeted sequencing data using ASCETS.
Bioinformatics
2021
30839344
Differential Expression of PLAG1 in Apocrine and Eccrine Cutaneous Mixed Tumors: Evidence for Distinct Molecular Pathogenesis.
Am J Dermatopathol
2020
31905241
Clinical response to larotrectinib in adult Philadelphia chromosome-like ALL with cryptic ETV6-NTRK3 rearrangement.
Blood Adv
2020
33392505
Near haploidization is a genomic hallmark which defines a molecular subgroup of giant cell glioblastoma.
Neurooncol Adv
2020
32615168
A Role for Chromosomal Microarray Testing in the Workup of Male Infertility.
J Mol Diagn
2020
32389271
From Banding to BAM Files: Genomics Informs Diagnosis and Precision Medicine for Brain Tumors.
Surg Pathol Clin
2020
32286280
Modeling germline mutations in pineoblastoma uncovers lysosome disruption-based therapy.
Nat Commun
2020
31375768
Characterization of molecular signatures of supratentorial ependymomas.
Mod Pathol
2020
31371807
Molecular characterization of localized pleural mesothelioma.
Mod Pathol
2020
30674530
<i>Sleeping Beauty</i> Insertional Mutagenesis Reveals Important Genetic Drivers of Central Nervous System Embryonal Tumors.
Cancer Res
2019
31650892
A Novel <i>ALK</i> Fusion in Pediatric Medullary Thyroid Carcinoma.
Thyroid
2019
30160587
ZMYM2-FGFR1 fusion as secondary change in acute myeloid leukemia.
Leuk Lymphoma
2019
31355086
Clinical Importance of CDKN2A Loss and Monosomy 10 in Pilocytic Astrocytoma.
Cureus
2019
31138931
Technical laboratory standards for interpretation and reporting of acquired copy-number abnormalities and copy-neutral loss of heterozygosity in neoplastic disorders: a joint consensus recommendation from the American College of Medical Genetics and Genomics (ACMG) and the Cancer Genomics Consortium (CGC).
Genet Med
2019
30816933
Recurrent EP300-BCOR Fusions in Pediatric Gliomas With Distinct Clinicopathologic Features.
J Neuropathol Exp Neurol
2019
29758594
PHOX2B is a reliable immunomarker in distinguishing peripheral neuroblastic tumours from CNS embryonal tumours.
Histopathology
2018
29915380
Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Genet Med
2018
30801050
Mismatch repair deficiency in high-grade meningioma: a rare but recurrent event associated with dramatic immune activation and clinical response to PD-1 blockade.
JCO Precis Oncol
2018
28719464
Nuclear CRX and FOXJ1 Expression Differentiates Non-Germ Cell Pineal Region Tumors and Supports the Ependymal Differentiation of Papillary Tumor of the Pineal Region.
Am J Surg Pathol
2017
28104717
Clinical targeted exome-based sequencing in combination with genome-wide copy number profiling: precision medicine analysis of 203 pediatric brain tumors.
Neuro Oncol
2017
28157586
The current state of clinical interpretation of sequence variants.
Curr Opin Genet Dev
2017
29212025
Convergence of BMI1 and CHD7 on ERK Signaling in Medulloblastoma.
Cell Rep
2017
26226092
Integrated Genomic Characterization of a Pineal Parenchymal Tumor of Intermediate Differentiation.
World Neurosurg
2016
26518543
Somatic cell transfer of c-Myc and Bcl-2 induces large-cell anaplastic medulloblastomas in mice.
J Neurooncol
2016
27882345
Institutional implementation of clinical tumor profiling on an unselected cancer population.
JCI Insight
2016
27823583
Norrin/Frizzled4 signalling in the preneoplastic niche blocks medulloblastoma initiation.
Elife
2016
27425854
Genomic characterization of recurrent high-grade astroblastoma.
Cancer Genet
2016
27199251
Clonal evolution in patients with chronic lymphocytic leukaemia developing resistance to BTK inhibition.
Nat Commun
2016
27341486
FISHing in the dark: How the combination of FISH and conventional karyotyping improves the diagnostic yield in CpG-stimulated chronic lymphocytic leukemia.
Am J Hematol
2016
27037490
Reporting of Diagnostic Cytogenetic Results.
Curr Protoc Hum Genet
2016
25391241
Foretinib is effective therapy for metastatic sonic hedgehog medulloblastoma.
Cancer Res
2015
26258683
EAG2 potassium channel with evolutionarily conserved function as a brain tumor target.
Nat Neurosci
2015
25689980
Medulloblastoma subgroups remain stable across primary and metastatic compartments.
Acta Neuropathol
2015
25754088
Clinical implementation of integrated whole-genome copy number and mutation profiling for glioblastoma.
Neuro Oncol
2015
25576913
A microRNA-1280/JAG2 network comprises a novel biological target in high-risk medulloblastoma.
Oncotarget
2015
24460684
Polycomb group gene BMI1 controls invasion of medulloblastoma cells and inhibits BMP-regulated cell adhesion.
Acta Neuropathol Commun
2014
25059231
Genetic drivers of metastatic dissemination in sonic hedgehog medulloblastoma.
Acta Neuropathol Commun
2014
24553142
Epigenomic alterations define lethal CIMP-positive ependymomas of infancy.
Nature
2014
24661910
Integrated genomic analysis identifies the mitotic checkpoint kinase WEE1 as a novel therapeutic target in medulloblastoma.
Mol Cancer
2014
1 - 50 of 82
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Keith L Ligon
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David J H Shih
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William A Weiss
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Livia Garzia
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Cynthia Hawkins
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Marcel Kool
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