Follow
Sanja Rogic
Sanja Rogic
Unknown affiliation
Verified email at ubc.ca
Title
Cited by
Cited by
Year
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
19512011
Concurrent expression of MYC and BCL2 in diffuse large B-cell lymphoma treated with rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone
NA Johnson, GW Slack, KJ Savage, JM Connors, S Ben-Neriah, S Rogic, ...
Journal of clinical oncology 30 (28), 3452-3459, 2012
11442012
A physical map of the human genome.
JD McPherson, M Marra, LD Hillier, RH Waterston, A Chinwalla, J Wallis, ...
Nature 409 (6822), 2001
8722001
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, The Journal of the American Society of Hematology 122 (7), 1256-1265, 2013
4712013
Whole transcriptome sequencing reveals recurrent NOTCH1 mutations in mantle cell lymphoma
R Kridel, B Meissner, S Rogic, M Boyle, A Telenius, B Woolcock, ...
Blood, The Journal of the American Society of Hematology 119 (9), 1963-1971, 2012
4242012
A physical map of the human genome
M Marra, L Hillier, RH Waterston, A Chinwalla, J Wallis, M Sekhon, ...
Nature 409 (6822), 934-941, 2001
4022001
Evaluation of gene-finding programs on mammalian sequences
S Rogic, AK Mackworth, FBF Ouellette
Genome research 11 (5), 817-832, 2001
3972001
Recurrent somatic mutations of PTPN1 in primary mediastinal B cell lymphoma and Hodgkin lymphoma
J Gunawardana, FC Chan, A Telenius, B Woolcock, R Kridel, KL Tan, ...
Nature genetics 46 (4), 329-335, 2014
2482014
Gene expression–based model using formalin-fixed paraffin-embedded biopsies predicts overall survival in advanced-stage classical Hodgkin lymphoma
DW Scott, FC Chan, F Hong, S Rogic, KL Tan, B Meissner, S Ben-Neriah, ...
Journal of Clinical Oncology 31 (6), 692-700, 2013
1982013
The E3 ubiquitin ligase UBR5 is recurrently mutated in mantle cell lymphoma
B Meissner, R Kridel, RS Lim, S Rogic, K Tse, DW Scott, R Moore, ...
Blood, The Journal of the American Society of Hematology 121 (16), 3161-3164, 2013
1572013
Improving gene recognition accuracy by combining predictions from two gene-finding programs
S Rogic, BFF Ouellette, AK Mackworth
Bioinformatics 18 (8), 1034-1045, 2002
822002
TBL1XR1/TP63: a novel recurrent gene fusion in B-cell non-Hodgkin lymphoma
DW Scott, KL Mungall, S Ben-Neriah, S Rogic, RD Morin, GW Slack, ...
Blood, The Journal of the American Society of Hematology 119 (21), 4949-4952, 2012
742012
Correlation between the secondary structure of pre-mRNA introns and the efficiency of splicing in Saccharomyces cerevisiae
S Rogic, B Montpetit, HH Hoos, AK Mackworth, BFF Ouellette, P Hieter
BMC genomics 9, 1-19, 2008
592008
Meta‐analysis of gene expression in autism spectrum disorder
C Ch'ng, W Kwok, S Rogic, P Pavlidis
Autism Research 8 (5), 593-608, 2015
562015
Transcriptome sequencing of the anterior cingulate in bipolar disorder: dysregulation of G protein-coupled receptors
C Cruceanu, PPC Tan, S Rogic, JP Lopez, SG Torres-Platas, CO Gigek, ...
American Journal of Psychiatry 172 (11), 1131-1140, 2015
502015
Multi-model functionalization of disease-associated PTEN missense mutations identifies multiple molecular mechanisms underlying protein dysfunction
KL Post, M Belmadani, P Ganguly, F Meili, R Dingwall, TA McDiarmid, ...
Nature communications 11 (1), 2073, 2020
462020
GeneComber: combining outputs of gene prediction programs for improved results
SP Shah, GP McVicker, AK Mackworth, S Rogic, BFF Ouellette
Bioinformatics 19 (10), 1296-1297, 2003
452003
The Canadian rare diseases models and mechanisms (RDMM) network: connecting understudied genes to model organisms
KM Boycott, PM Campeau, HE Howley, P Pavlidis, S Rogic, C Oriel, ...
The American Journal of Human Genetics 106 (2), 143-152, 2020
432020
An RCOR1 loss–associated gene expression signature identifies a prognostically significant DLBCL subgroup
FC Chan, A Telenius, S Healy, S Ben-Neriah, A Mottok, R Lim, M Drake, ...
Blood, The Journal of the American Society of Hematology 125 (6), 959-966, 2015
342015
VariCarta: a comprehensive database of harmonized genomic variants found in autism spectrum disorder sequencing studies
M Belmadani, M Jacobson, N Holmes, M Phan, T Nguyen, P Pavlidis, ...
Autism Research 12 (12), 1728-1736, 2019
312019
The system can't perform the operation now. Try again later.
Articles 1–20