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Recurrent somatic mutations of PTPN1 in primary mediastinal B cell lymphoma and Hodgkin lymphoma.
Published in:
Nature Genetics, 2014, v. 46, n. 4, p. 329, doi. 10.1038/ng.2900
By:
- Gunawardana, Jay;
- Chan, Fong Chun;
- Telenius, Adèle;
- Woolcock, Bruce;
- Kridel, Robert;
- Tan, King L;
- Ben-Neriah, Susana;
- Mottok, Anja;
- Lim, Raymond S;
- Boyle, Merrill;
- Rogic, Sanja;
- Rimsza, Lisa M;
- Guiter, Chrystelle;
- Leroy, Karen;
- Gaulard, Philippe;
- Haioun, Corinne;
- Marra, Marco A;
- Savage, Kerry J;
- Connors, Joseph M;
- Shah, Sohrab P
Publication type:
Article
VariCarta: A Comprehensive Database of Harmonized Genomic Variants Found in Autism Spectrum Disorder Sequencing Studies.
Published in:
Autism Research: Official Journal of the International Society for Autism Research, 2019, v. 12, n. 12, p. 1728, doi. 10.1002/aur.2236
By:
- Belmadani, Manuel;
- Jacobson, Matthew;
- Holmes, Nathan;
- Phan, Minh;
- Nguyen, Tue;
- Pavlidis, Paul;
- Rogic, Sanja
Publication type:
Article
Meta-Analysis of Gene Expression in Autism Spectrum Disorder.
Published in:
Autism Research: Official Journal of the International Society for Autism Research, 2015, v. 8, n. 5, p. 593, doi. 10.1002/aur.1475
By:
- Ch'ng, Carolyn;
- Kwok, Willie;
- Rogic, Sanja;
- Pavlidis, Paul
Publication type:
Article
Correlation between the secondary structure of pre-mRNA introns and the efficiency of splicing in Saccharomyces cerevisiae.
Published in:
BMC Genomics, 2008, v. 9, p. 1, doi. 10.1186/1471-2164-9-355
By:
- Rogic, Sanja;
- Montpetit, Ben;
- Hoos, Holger H.;
- Mackworth, Alan K.;
- Ouellette, B. F. Francis;
- Hieter, Philip
Publication type:
Article
Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma.
Published in:
Nature, 2011, v. 476, n. 7360, p. 298, doi. 10.1038/nature10351
By:
- Morin, Ryan D.;
- Mendez-Lago, Maria;
- Mungall, Andrew J.;
- Goya, Rodrigo;
- Mungall, Karen L.;
- Corbett, Richard D.;
- Johnson, Nathalie A.;
- Severson, Tesa M.;
- Chiu, Readman;
- Field, Matthew;
- Jackman, Shaun;
- Krzywinski, Martin;
- Scott, David W.;
- Trinh, Diane L.;
- Tamura-Wells, Jessica;
- Li, Sa;
- Firme, Marlo R.;
- Rogic, Sanja;
- Griffith, Malachi;
- Chan, Susanna
Publication type:
Article
3D-QSAR-Based Pharmacophore Determination and Design of Novel DPP-4 Inhibitors.
Published in:
Scripta Medica, 2022, v. 53, n. 4, p. 271, doi. 10.5937/scriptamed53-40866
By:
- Rogić, Sanja;
- Gagić, Žarko
Publication type:
Article
Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort.
Published in:
Clinical Genetics, 2019, v. 96, n. 3, p. 199, doi. 10.1111/cge.13556
By:
- Callaghan, Daniel Benjamin;
- Rogic, Sanja;
- Tan, Powell Patrick Cheng;
- Calli, Kristina;
- Qiao, Ying;
- Baldwin, Robert;
- Jacobson, Matthew;
- Belmadani, Manuel;
- Holmes, Nathan;
- Yu, Chang;
- Li, Yanchen;
- Li, Yingrui;
- Kurtzke, Franz‐Edward;
- Kuzeljevic, Boris;
- Yu, An Yi;
- Hudson, Melissa;
- Mcaughton, Amy J.M.;
- Xu, Yuchen;
- Dionne‐Laporte, Alexandre;
- Girard, Simon
Publication type:
Article
Improving gene recognition accuracy by combining predictions from two gene-finding programs.
Published in:
Bioinformatics, 2002, v. 18, n. 8, p. 1034, doi. 10.1093/bioinformatics/18.8.1034
By:
- Rogic, Sanja;
- Ouellette, B.F. Francis;
- Mackworth, Alan K.
Publication type:
Article
ModelMatcher: A scientist‐centric online platform to facilitate collaborations between stakeholders of rare and undiagnosed disease research.
Published in:
Human Mutation, 2022, v. 43, n. 6, p. 743, doi. 10.1002/humu.24364
By:
- Harnish, J. Michael;
- Li, Lucian;
- Rogic, Sanja;
- Poirier‐Morency, Guillaume;
- Kim, Seon‐Young;
- Boycott, Kym M.;
- Wangler, Michael F.;
- Bellen, Hugo J.;
- Hieter, Philip;
- Pavlidis, Paul;
- Liu, Zhandong;
- Yamamoto, Shinya
Publication type:
Article
Interactive Exploration, Analysis, and Visualization of Complex Phenome-Genome Datasets with ASPIREdb.
Published in:
Human Mutation, 2016, v. 37, n. 8, p. 719, doi. 10.1002/humu.23011
By:
- Tan, Powell Patrick Cheng;
- Rogic, Sanja;
- Zoubarev, Anton;
- McDonald, Cameron;
- Lui, Frances;
- Charathsandran, Gayathiri;
- Jacobson, Matthew;
- Belmadani, Manuel;
- Leong, Justin;
- Rossum, Thea;
- Portales‐Casamar, Elodie;
- Qiao, Ying;
- Calli, Kristina;
- Liu, Xudong;
- Hudson, Melissa;
- Rajcan‐Separovic, Evica;
- Lewis, ME Suzanne;
- Pavlidis, Paul
Publication type:
Article
Multi-model functionalization of disease-associated PTEN missense mutations identifies multiple molecular mechanisms underlying protein dysfunction.
Published in:
Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-15943-0
By:
- Post, Kathryn L.;
- Belmadani, Manuel;
- Ganguly, Payel;
- Meili, Fabian;
- Dingwall, Riki;
- McDiarmid, Troy A.;
- Meyers, Warren M.;
- Herrington, Caitlin;
- Young, Barry P.;
- Callaghan, Daniel B.;
- Rogic, Sanja;
- Edwards, Matthew;
- Niciforovic, Ana;
- Cau, Alessandro;
- Rankin, Catharine H.;
- O'Connor, Timothy P.;
- Bamji, Shernaz X.;
- Loewen, Christopher J. R.;
- Allan, Douglas W.;
- Pavlidis, Paul
Publication type:
Article

Found: 11