Ryan Morin
Ryan Morin
Associate Professor, Simon Fraser University; Scientist at Genome Sciences Centre, BC Cancer Agency
Verified email at sfu.ca - Homepage
TitleCited byYear
Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin
RD Morin, NA Johnson, TM Severson, AJ Mungall, J An, R Goya, JE Paul, ...
Nature genetics 42 (2), 181, 2010
12462010
Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma
RD Morin, M Mendez-Lago, AJ Mungall, R Goya, KL Mungall, RD Corbett, ...
Nature 476 (7360), 298-303, 2011
11342011
Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution
SP Shah, RD Morin, J Khattra, L Prentice, T Pugh, A Burleigh, A Delaney, ...
Nature 461 (7265), 809, 2009
10562009
Application of massively parallel sequencing to microRNA profiling and discovery in human embryonic stem cells
RD Morin, MD O’Connor, M Griffith, F Kuchenbauer, A Delaney, ...
Genome research 18 (4), 610-621, 2008
10322008
The complete genome of Rhodococcus sp. RHA1 provides insights into a catabolic powerhouse
MP McLeod, RL Warren, WWL Hsiao, N Araki, M Myhre, C Fernandes, ...
Proceedings of the National Academy of Sciences 103 (42), 15582, 2006
5882006
Identification of miR-145 and miR-146a as mediators of the 5q–syndrome phenotype
DT Starczynowski, F Kuchenbauer, B Argiropoulos, S Sung, R Morin, ...
Nature medicine 16 (1), 49, 2010
5862010
Mutation of FOXL2 in granulosa-cell tumors of the ovary
SP Shah, M Köbel, J Senz, RD Morin, BA Clarke, KC Wiegand, G Leung, ...
New England Journal of Medicine 360 (26), 2719-2729, 2009
5202009
Genetic Alterations Activating Kinase and Cytokine Receptor Signaling in High-Risk Acute Lymphoblastic Leukemia
KG Roberts, RD Morin, J Zhang, M Hirst, Y Zhao, X Su, SC Chen, ...
Cancer Cell 22 (2), 153-166, 2012
5122012
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
DS Gerhard, L Wagner, EA Feingold, CM Shenmen, LH Grouse, ...
Genome research 14 (10B), 2121-2127, 2004
5112004
Profiling the HeLa S3 transcriptome using randomly primed cDNA and massively parallel short-read sequencing
RD Morin, M Bainbridge, A Fejes, M Hirst, M Krzywinski, TJ Pugh, ...
Biotechniques 45 (1), 81-94, 2008
4482008
Somatic mutations at EZH2 Y641 act dominantly through a mechanism of selectively altered PRC2 catalytic activity, to increase H3K27 trimethylation
DB Yap, J Chu, T Berg, M Schapira, SWG Cheng, A Moradian, RD Morin, ...
Blood 117 (8), 2451-2459, 2011
4412011
De novo transcriptome assembly with ABySS
I Birol, SD Jackman, CB Nielsen, JQ Qian, R Varhol, G Stazyk, RD Morin, ...
Bioinformatics 25 (21), 2872-2877, 2009
4142009
Next-generation tag sequencing for cancer gene expression profiling
AS Morrissy, RD Morin, A Delaney, T Zeng, H McDonald, S Jones, Y Zhao, ...
Genome research 19 (10), 1825-1835, 2009
3152009
Comparative analysis of the small RNA transcriptomes of Pinus contorta and Oryza sativa
RD Morin, G Aksay, E Dolgosheina, HA Ebhardt, V Magrini, ER Mardis, ...
Genome research 18 (4), 571-584, 2008
2862008
Alternative expression analysis by RNA sequencing
M Griffith, OL Griffith, J Mwenifumbo, R Goya, AS Morrissy, RD Morin, ...
Nature methods 7 (10), 843, 2010
2822010
Mutational and structural analysis of diffuse large B-cell lymphoma using whole-genome sequencing
RD Morin, K Mungall, E Pleasance, AJ Mungall, R Goya, RD Huff, ...
Blood 122 (7), 1256-1265, 2013
2642013
Whole transcriptome sequencing reveals recurrent NOTCH1 mutations in mantle cell lymphoma
R Kridel, B Meissner, S Rogic, M Boyle, A Telenius, B Woolcock, ...
Blood 119 (9), 1963-1971, 2012
2482012
SNVMix: predicting single nucleotide variants from next-generation sequencing of tumors
R Goya, MGF Sun, RD Morin, G Leung, G Ha, KC Wiegand, J Senz, ...
Bioinformatics 26 (6), 730-736, 2010
2202010
In-depth characterization of the microRNA transcriptome in a leukemia progression model
F Kuchenbauer, RD Morin, B Argiropoulos, OI Petriv, M Griffith, M Heuser, ...
Genome research 18 (11), 1787, 2008
1862008
JointSNVMix: a probabilistic model for accurate detection of somatic mutations in normal/tumour paired next-generation sequencing data
A Roth, J Ding, R Morin, A Crisan, G Ha, R Giuliany, A Bashashati, M Hirst, ...
Bioinformatics 28 (7), 907-913, 2012
1582012
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Articles 1–20