Eric Bareke, PhD
Eric Bareke, PhD
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Cited by
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 (6), 847-863, 2016
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
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
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
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
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
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), 17, 2010
Meta-analysis of archived DNA microarrays identifies genes regulated by hypoxia and involved in a metastatic phenotype in cancer cells
M Pierre, B DeHertogh, A Gaigneaux, B DeMeulder, F Berger, E Bareke, ...
BMC cancer 10 (1), 176, 2010
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), 1-8, 2018
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
Enhanced meta-analysis highlights genes involved in metastasis from several microarray datasets
M Pierre, B De Hertogh, B De Meulder, E Bareke, S Depiereux, C Michiels, ...
Journal of Proteomics and Bioinformatics 4 (2), 36-43, 2011
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
Functional analysis: evaluation of response intensities-tailoring ANOVA for lists of expression subsets
F Berger, B De Meulder, A Gaigneaux, S Depiereux, E Bareke, M Pierre, ...
BMC bioinformatics 11 (1), 510, 2010
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
POLR3A variants in hereditary spastic paraplegia and ataxia
L Gauquelin, M Tétreault, I Thiffault, E Farrow, N Miller, B Yoo, E Bareke, ...
Brain 141 (1), e1-e1, 2018
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
Methylome analysis and whole-exome sequencing reveal that brain tumors associated with encephalocraniocutaneous lipomatosis are midline pilocytic astrocytomas
ET Valera, MK McConechy, T Gayden, B Rivera, DTW Jones, A Wittmann, ...
Acta neuropathologica 136 (4), 657-660, 2018
gViz, a novel tool for the visualization of co-expression networks
R Helaers, E Bareke, B De Meulder, M Pierre, S Depiereux, N Habra, ...
BMC Research Notes 4 (1), 452, 2011
PHOENIX, a web interface for (re) analysis of microarray data
F Berger, B Hertogh, M Pierre, E Bareke, A Gaigneaux, E Depiereux
Open Life Sciences 4 (4), 603-618, 2009
Autosomal dominant cutis laxa with progeroid features due to a novel, de novo mutation in ALDH18A1
PT Bhola, T Hartley, E Bareke, KM Boycott, SM Nikkel, DA Dyment
Journal of human genetics 62 (6), 661-663, 2017
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