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Sanja Rogic

Showing results (11-20 of 30) with videos related to

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American Journal of Human Genetics|December 14, 2020
Multi-parametric analysis of 57 SYNGAP1 variants reveal impacts on GTPase signaling, localization, and protein stabilityFabian Meili, William J Wei, Wun-Chey Sin, et al.
The American Journal of Psychiatry|August 5, 2015
Transcriptome sequencing of the anterior cingulate in bipolar disorder: dysregulation of G protein-coupled receptorsCristiana Cruceanu, Powell Patrick Cheng Tan, Sanja Rogic, et al.
Biorxiv : the Preprint Server for Biology|March 31, 2025
Using semantic search to find publicly available gene-expression datasetsGrace S Brown, James Wengler, Aaron Joyce S Fabelico, et al.
Bioinformatics (Oxford, England)|February 2, 2026
Using semantic search to find publicly available gene-expression datasetsGrace S Brown, James Wengler, Aaron Joyce S Fabelico, et al.
Blood|February 15, 2013
The E3 ubiquitin ligase UBR5 is recurrently mutated in mantle cell lymphomaBarbara Meissner, Robert Kridel, Raymond S Lim, et al.
Human Mutation|February 28, 2022
ModelMatcher: A scientist-centric online platform to facilitate collaborations between stakeholders of rare and undiagnosed disease researchJ Michael Harnish, Lucian Li, Sanja Rogic, et al.
Blood|April 13, 2012
TBL1XR1/TP63: a novel recurrent gene fusion in B-cell non-Hodgkin lymphomaDavid W Scott, Karen L Mungall, Susana Ben-Neriah, et al.
Human Mutation|May 10, 2016
Interactive Exploration, Analysis, and Visualization of Complex Phenome-Genome Datasets with ASPIREdbPowell Patrick Cheng Tan, Sanja Rogic, Anton Zoubarev, et al.
Genetics|June 23, 2025
Revealing function-altering MECP2 mutations in individuals with autism spectrum disorder using yeast and DrosophilaEric Chen, Jessica Schmitt, Graeme McIntosh, et al.
Blood|January 3, 2012
Whole transcriptome sequencing reveals recurrent NOTCH1 mutations in mantle cell lymphomaRobert Kridel, Barbara Meissner, Sanja Rogic, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
American Journal of Human Genetics|December 14, 2020
Multi-parametric analysis of 57 SYNGAP1 variants reveal impacts on GTPase signaling, localization, and protein stabilityFabian Meili, William J Wei, Wun-Chey Sin, et al.
The American Journal of Psychiatry|August 5, 2015
Transcriptome sequencing of the anterior cingulate in bipolar disorder: dysregulation of G protein-coupled receptorsCristiana Cruceanu, Powell Patrick Cheng Tan, Sanja Rogic, et al.
Biorxiv : the Preprint Server for Biology|March 31, 2025
Using semantic search to find publicly available gene-expression datasetsGrace S Brown, James Wengler, Aaron Joyce S Fabelico, et al.
Bioinformatics (Oxford, England)|February 2, 2026
Using semantic search to find publicly available gene-expression datasetsGrace S Brown, James Wengler, Aaron Joyce S Fabelico, et al.
Blood|February 15, 2013
The E3 ubiquitin ligase UBR5 is recurrently mutated in mantle cell lymphomaBarbara Meissner, Robert Kridel, Raymond S Lim, et al.
Human Mutation|February 28, 2022
ModelMatcher: A scientist-centric online platform to facilitate collaborations between stakeholders of rare and undiagnosed disease researchJ Michael Harnish, Lucian Li, Sanja Rogic, et al.
Blood|April 13, 2012
TBL1XR1/TP63: a novel recurrent gene fusion in B-cell non-Hodgkin lymphomaDavid W Scott, Karen L Mungall, Susana Ben-Neriah, et al.
Human Mutation|May 10, 2016
Interactive Exploration, Analysis, and Visualization of Complex Phenome-Genome Datasets with ASPIREdbPowell Patrick Cheng Tan, Sanja Rogic, Anton Zoubarev, et al.
Genetics|June 23, 2025
Revealing function-altering MECP2 mutations in individuals with autism spectrum disorder using yeast and DrosophilaEric Chen, Jessica Schmitt, Graeme McIntosh, et al.
Blood|January 3, 2012
Whole transcriptome sequencing reveals recurrent NOTCH1 mutations in mantle cell lymphomaRobert Kridel, Barbara Meissner, Sanja Rogic, et al.
Pageof 3