Simon Papillon-Cavanagh
Simon Papillon-Cavanagh
Bristol Myers Squibb
Verified email at mail.mcgill.ca
Title
Cited by
Cited by
Year
Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytoma
AM Fontebasso, S Papillon-Cavanagh, J Schwartzentruber, H Nikbakht, ...
Nature genetics 46 (5), 462-466, 2014
2912014
Histone H3K36 mutations promote sarcomagenesis through altered histone methylation landscape
C Lu, SU Jain, D Hoelper, D Bechet, RC Molden, L Ran, D Murphy, ...
Science 352 (6287), 844-849, 2016
1772016
Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR
CL Kleinman, N Gerges, S Papillon-Cavanagh, P Sin-Chan, ...
Nature genetics 46 (1), 39-44, 2014
1432014
Spatial and temporal homogeneity of driver mutations in diffuse intrinsic pontine glioma
H Nikbakht, E Panditharatna, LG Mikael, R Li, T Gayden, M Osmond, ...
Nature communications 7 (1), 1-8, 2016
1252016
Mutations in C5ORF42 cause Joubert syndrome in the French Canadian population
M Srour, J Schwartzentruber, FF Hamdan, LH Ospina, L Patry, D Labuda, ...
The American Journal of Human Genetics 90 (4), 693-700, 2012
1052012
Impaired H3K36 methylation defines a subset of head and neck squamous cell carcinomas
S Papillon-Cavanagh, C Lu, T Gayden, LG Mikael, D Bechet, ...
Nature genetics 49 (2), 180-185, 2017
962017
mRMRe: an R package for parallelized mRMR ensemble feature selection
N De Jay, S Papillon-Cavanagh, C Olsen, N El-Hachem, G Bontempi, ...
Bioinformatics 29 (18), 2365-2368, 2013
942013
Spatial heterogeneity in medulloblastoma
AS Morrissy, FMG Cavalli, M Remke, V Ramaswamy, DJH Shih, ...
Nature genetics 49 (5), 780-788, 2017
762017
Mutation in The Nuclear‐Encoded Mitochondrial Isoleucyl–tRNA Synthetase IARS2 in Patients with Cataracts, Growth Hormone Deficiency with Short Stature …
J Schwartzentruber, D Buhas, J Majewski, F Sasarman, ...
Human mutation 35 (11), 1285-1289, 2014
682014
De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development
CT Gordon, S Xue, G Yigit, H Filali, K Chen, N Rosin, K Yoshiura, ...
Nature genetics 49 (2), 249-255, 2017
662017
Comparison and validation of genomic predictors for anticancer drug sensitivity
S Papillon-Cavanagh, N De Jay, N Hachem, C Olsen, G Bontempi, ...
Journal of the American Medical Informatics Association 20 (4), 597-602, 2013
642013
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
512019
H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis
AS Harutyunyan, B Krug, H Chen, S Papillon-Cavanagh, M Zeinieh, ...
Nature communications 10 (1), 1-13, 2019
512019
Mutations in a novel serine protease PRSS56 in families with nanophthalmos
A Orr, MP Dubé, JC Zenteno, H Jiang, G Asselin, SC Evans, A Caqueret, ...
Molecular vision 17, 1850, 2011
402011
Epigenetic dysregulation: a novel pathway of oncogenesis in pediatric brain tumors
AM Fontebasso, T Gayden, H Nikbakht, M Neirinck, S Papillon-Cavanagh, ...
Acta neuropathologica 128 (5), 615-627, 2014
322014
The molecular landscape of ETMR at diagnosis and relapse
S Lambo, SN Gröbner, T Rausch, SM Waszak, C Schmidt, A Gorthi, ...
Nature 576 (7786), 274-280, 2019
132019
STK11 and KEAP1 mutations as prognostic biomarkers in an observational real-world lung adenocarcinoma cohort
S Papillon-Cavanagh, P Doshi, R Dobrin, J Szustakowski, AM Walsh
ESMO open 5 (2), e000706, 2020
62020
A probabilistic assessment of cycle life of GTE disks made of granular materials
MS Nikhamkin, DA Vyatchanin
Russian Aeronautics (Iz VUZ) 51 (1), 94-96, 2008
42008
Mutation in The Nuclear‐Encoded Mitochondrial Isoleucyl–tRNA Synthetase IARS2 in Patients with Cataracts, Growth Hormone Deficiency with Short Stature …
J Schwartzentruber, D Buhas, J Majewski, F Sasarman, ...
Human Mutation 36 (2), 281-281, 2015
12015
32 Airway hyperresponsiveness in FVB/N DF508 cystic fibrosis transmembrane conductance regulator mice
M Bazett, CK Haston
Journal of Cystic Fibrosis 11, S64, 2012
12012
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