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Author Details
Full Name
Patrick G Buckley
Affiliation
Beaumont Hospital
ORCID
Career Start Year
2002
Papers
52
H Index
26
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36460769
Personalized health risk assessment based on single-cell RNA sequencing analysis of a male with 45, X/48, XYYY karyotype.
Sci Rep
2022
35768433
High prevalence of somatic PIK3CA and TP53 pathogenic variants in the normal mammary gland tissue of sporadic breast cancer patients revealed by duplex sequencing.
NPJ Breast Cancer
2022
32088416
Expansion of the phenotype of biallelic variants in TRIT1.
Eur J Med Genet
2020
29961873
Transcriptome Characterization of Matched Primary Breast and Brain Metastatic Tumors to Detect Novel Actionable Targets.
J Natl Cancer Inst
2019
29264834
Temporal stability of MGMT promoter methylation in glioblastoma patients undergoing STUPP protocol.
J Neurooncol
2018
30054533
Immunophenotyping and transcriptional profiling of in vitro cultured human adipose tissue derived stem cells.
Sci Rep
2018
29770897
Machine learning: a useful radiological adjunct in determination of a newly diagnosed glioma's grade and IDH status.
J Neurooncol
2018
29432475
High-Throughput Tabular Data Processor - Platform independent graphical tool for processing large data sets.
PLoS One
2018
29595124
Absence of 1p/19q codeletion in oligodendroglioma-like areas of pilocytic astrocytomas.
Clin Neuropathol
2018
29350171
The DNA copy number landscape of a collision tumor.
Clin Neuropathol
2018
32913965
Postmortem Examination of an Aggressive Case of Medullary Thyroid Carcinoma Characterized by Catastrophic Genomic Abnormalities.
JCO Precis Oncol
2017
25137037
Modulation of chemotherapeutic drug resistance in neuroblastoma SK-N-AS cells by the neural apoptosis inhibitory protein and miR-520f.
Int J Cancer
2015
26219265
Concurrent DNA Copy-Number Alterations and Mutations in Genes Related to Maintenance of Genome Stability in Uninvolved Mammary Glandular Tissue from Breast Cancer Patients.
Hum Mutat
2015
25960282
The development of cisplatin resistance in neuroblastoma is accompanied by epithelial to mesenchymal transition in vitro.
Cancer Lett
2015
24299514
miR-199a-5p silencing regulates the unfolded protein response in chronic obstructive pulmonary disease and α1-antitrypsin deficiency.
Am J Respir Crit Care Med
2014
24986208
Genetic features of oligodendrogliomas and presence of seizures. The relationship of seizures and genetics in LGOs.
Clin Neuropathol
2014
25085603
Rhabdoid tumor: the Irish experience 1986-2013.
Cancer Genet
2014
22797059
Modulation of neuroblastoma disease pathogenesis by an extensive network of epigenetically regulated microRNAs.
Oncogene
2013
21796619
Identification of a novel recurrent 1q42.2-1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas.
Int J Cancer
2012
22705586
Comparative genomic and proteomic analysis of high grade glioma primary cultures and matched tumor in situ.
Exp Cell Res
2012
22504026
Regeneration of comparative genomic hybridization oligonucleotide microarrays with dimethylurea.
Anal Biochem
2012
22302800
Differential DNA methylation patterns define status epilepticus and epileptic tolerance.
J Neurosci
2012
21860421
Oncogenic activation of FOXR1 by 11q23 intrachromosomal deletion-fusions in neuroblastoma.
Oncogene
2012
20669225
Genome-wide DNA methylation analysis of neuroblastic tumors reveals clinically relevant epigenetic events and large-scale epigenomic alterations localized to telomeric regions.
Int J Cancer
2011
21771658
MicroRNA and DNA methylation alterations mediating retinoic acid induced neuroblastoma cell differentiation.
Semin Cancer Biol
2011
21557326
Dissection of the oncogenic MYCN transcriptional network reveals a large set of clinically relevant cell cycle genes as drivers of neuroblastoma tumorigenesis.
Mol Carcinog
2011
21731748
Co-localization of the oncogenic transcription factor MYCN and the DNA methyl binding protein MeCP2 at genomic sites in neuroblastoma.
PLoS One
2011
21293300
Loss of chromosome 1p/19q in oligodendroglial tumors: refinement of chromosomal critical regions and evaluation of internexin immunostaining as a surrogate marker.
J Neuropathol Exp Neurol
2011
21266077
MicroRNA-34a is a potent tumor suppressor molecule in vivo in neuroblastoma.
BMC Cancer
2011
20406844
Chromosomal and microRNA expression patterns reveal biologically distinct subgroups of 11q- neuroblastoma.
Clin Cancer Res
2010
20841484
MicroRNA mediates DNA demethylation events triggered by retinoic acid during neuroblastoma cell differentiation.
Cancer Res
2010
20658962
Therapeutic targeting of miRNAs in neuroblastoma.
Expert Opin Ther Targets
2010
20398883
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
Am J Hum Genet
2010
20409325
MicroRNA-184 inhibits neuroblastoma cell survival through targeting the serine/threonine kinase AKT2.
Mol Cancer
2010
19672776
Genome-wide microarray-based comparative genomic hybridization analysis of lymphoplasmacytic lymphomas reveals heterogeneous aberrations.
Leuk Lymphoma
2009
19924232
Widespread dysregulation of MiRNAs by MYCN amplification and chromosomal imbalances in neuroblastoma: association of miRNA expression with survival.
PLoS One
2009
19997598
Global MYCN transcription factor binding analysis in neuroblastoma reveals association with distinct E-box motifs and regions of DNA hypermethylation.
PLoS One
2009
17222329
Comprehensive genetic and epigenetic analysis of sporadic meningioma for macro-mutations on 22q and micro-mutations within the NF2 locus.
BMC Genomics
2007
16161042
Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH.
Int J Cancer
2006
16713171
Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH.
Genomics
2006
16575877
Microarray-based survey of CpG islands identifies concurrent hyper- and hypomethylation patterns in tissues derived from patients with breast cancer.
Genes Chromosomes Cancer
2006
15805262
Comprehensive DNA copy number profiling of meningioma using a chromosome 1 tiling path microarray identifies novel candidate tumor suppressor loci.
Cancer Res
2005
16287142
Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2.
Hum Mutat
2005
15922827
Copy-number polymorphisms: mining the tip of an iceberg.
Trends Genet
2005
15880457
Localization of a putative low-penetrance ependymoma susceptibility locus to 22q11 using a chromosome 22 tiling-path genomic microarray.
Genes Chromosomes Cancer
2005
15578687
High-resolution gene copy number and expression profiling of human chromosome 22 in ovarian carcinomas.
Genes Chromosomes Cancer
2005
14746990
Genomic microarrays in the spotlight.
Trends Genet
2004
23573660
Genomic microarrays in the spotlight.
Drug Discov Today
2004
12830322
Development of NF2 gene specific, strictly sequence defined diagnostic microarray for deletion detection.
J Mol Med (Berl)
2003
14556248
Does chromosome 22 have anything to do with sex determination: further studies on a 46,XX,22q11.2 del male.
Am J Med Genet A
2003
1 - 50 of 52
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University of Alabama at Birmingham
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2
Chantal Depondt
Hopital Universitaire de Bruxelles - Hopital Erasme
Co-authored papers
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Guy A Rouleau
McGill University, Canada Montreal Neurological Institute and Hospital
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David B Goldstein
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Co-authored papers
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Medical University of Gdansk
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David M Beare
Co-authored papers
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Dongliang Ge
Department of Pharmacy, Liyang People's Hospital
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Claudia B Catarino
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William M Gallagher
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