Seuraa
Eric Bareke, PhD
Eric Bareke, PhD
McGill University
Vahvistettu sähköpostiosoite verkkotunnuksessa mcgill.ca - Kotisivu
Nimike
Viittaukset
Viittaukset
Vuosi
The histone mark H3K36me2 recruits DNMT3A and shapes the intergenic DNA methylation landscape
DN Weinberg, S Papillon-Cavanagh, H Chen, Y Yue, X Chen, ...
Nature 573 (7773), 281-286, 2019
4862019
Germline and somatic FGFR1 abnormalities in dysembryoplastic neuroepithelial tumors
B Rivera, T Gayden, J Carrot-Zhang, J Nadaf, T Boshari, D Faury, ...
Acta neuropathologica 131, 847-863, 2016
1912016
Debunking Occam's razor: Diagnosing multiple genetic diseases in families by whole‐exome sequencing
TB Balci, T Hartley, Y Xi, DA Dyment, CL Beaulieu, FP Bernier, L Dupuis, ...
Clinical genetics 92 (3), 281-289, 2017
1192017
Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit
H Daoud, SM Luco, R Li, E Bareke, C Beaulieu, O Jarinova, N Carson, ...
Cmaj 188 (11), E254-E260, 2016
1102016
Whole-exome sequencing as a diagnostic tool: current challenges and future opportunities
M Tetreault, E Bareke, J Nadaf, N Alirezaie, J Majewski
Expert review of molecular diagnostics 15 (6), 749-760, 2015
1002015
A unique morphological phenotype in chemoresistant triple-negative breast cancer reveals metabolic reprogramming and PLIN4 expression as a molecular vulnerability
I Sirois, A Aguilar-Mahecha, J Lafleur, E Fowler, V Vu, M Scriver, ...
Molecular Cancer Research 17 (12), 2492-2507, 2019
872019
TRPV4 and KRAS and FGFR1 gain-of-function mutations drive giant cell lesions of the jaw
CC Gomes, T Gayden, A Bajic, OF Harraz, J Pratt, H Nikbakht, E Bareke, ...
Nature communications 9 (1), 4572, 2018
832018
H3K27M in gliomas causes a one-step decrease in H3K27 methylation and reduced spreading within the constraints of H3K36 methylation
AS Harutyunyan, H Chen, T Lu, C Horth, H Nikbakht, B Krug, C Russo, ...
Cell reports 33 (7), 2020
702020
Prognostic and predictive value of circulating tumor DNA during neoadjuvant chemotherapy for triple negative breast cancer
L Cavallone, A Aguilar-Mahecha, J Lafleur, S Brousse, M Aldamry, ...
Scientific reports 10 (1), 14704, 2020
702020
Chromatin dysregulation associated with NSD1 mutation in head and neck squamous cell carcinoma
N Farhangdoost, C Horth, B Hu, E Bareke, X Chen, Y Li, M Coradin, ...
Cell reports 34 (8), 2021
592021
Whole‐exome sequencing is a valuable diagnostic tool for inherited peripheral neuropathies: Outcomes from a cohort of 50 families
T Hartley, JD Wagner, J Warman‐Chardon, M Tétreault, L Brady, S Baker, ...
Clinical genetics 93 (2), 301-309, 2018
562018
Recessive mutations in the kinase ZAK cause a congenital myopathy with fibre type disproportion
N Vasli, E Harris, J Karamchandani, E Bareke, J Majewski, NB Romero, ...
Brain 140 (1), 37-48, 2017
402017
TDP-43 stabilizes G3BP1 mRNA: relevance to amyotrophic lateral sclerosis/frontotemporal dementia
H Sidibé, Y Khalfallah, S Xiao, NB Gómez, H Fakim, EMH Tank, ...
Brain 144 (11), 3461-3476, 2021
352021
A benchmark for statistical microarray data analysis that preserves actual biological and technical variance
B De Hertogh, B De Meulder, F Berger, M Pierre, E Bareke, A Gaigneaux, ...
BMC bioinformatics 11, 1-14, 2010
342010
H3K36 dimethylation shapes the epigenetic interaction landscape by directing repressive chromatin modifications in embryonic stem cells
H Chen, B Hu, C Horth, E Bareke, P Rosenbaum, SY Kwon, J Sirois, ...
Genome research 32 (5), 825-837, 2022
322022
Mutation in Eftud2 causes craniofacial defects in mice via mis-splicing of Mdm2 and increased P53
MC Beauchamp, A Djedid, E Bareke, F Merkuri, R Aber, AS Tam, ...
Human Molecular Genetics 30 (9), 739-757, 2021
312021
Fatty acids derived from the probiotic Lacticaseibacillus rhamnosus HA-114 suppress age-dependent neurodegeneration
A Labarre, E Guitard, G Tossing, A Forest, E Bareke, M Labrecque, ...
Communications Biology 5 (1), 1340, 2022
302022
POLR3A variants in hereditary spastic paraplegia and ataxia
L Gauquelin, M Tetreault, I Thiffault, E Farrow, N Miller, B Yoo, E Bareke, ...
Brain 141 (1), e1-e1, 2018
272018
SHORT syndrome due to a novel de novo mutation in PRKCE (Protein Kinase Cɛ) impairing TORC2-dependent AKT activation
D Alcantara, F Elmslie, M Tetreault, E Bareke, T Hartley, ...
Human Molecular Genetics 26 (19), 3713-3721, 2017
272017
Meconium ileus in a Lebanese family secondary to mutations in the GUCY2C gene
A Smith, DE Bulman, C Goldsmith, E Bareke, J Majewski, KM Boycott, ...
European Journal of Human Genetics 23 (7), 990-992, 2015
262015
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Artikkelit 1–20