Jüri Reimand
Molecular Biology · 2007–2020
A researcher in the Science corpus: 12 papers; trusts 4 researchers and is trusted by 8 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 259 citations into it; #5,336 of 17,773 by trust here, #4,843 by citations
Whom Jüri Reimand trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Minoru Kanehisa
- Purvesh Khatri
- Sorin Draghici
- Jaak Vilo
- Tauno Metsalu
- Daniele Merico
- Fátima Al-Shahrour
- Yoav Benjamini
- Gordon K. Smyth
- Meelis Kull
Who trusts Jüri Reimand overall
- Fran Supek
- Tauno Metsalu
- Jaak Vilo
- Tambet Arak
- Jing Wang
- Liis Kolberg
- Guangyan Zhou
- Oliver Stegle
- Ronan C. O’Malley
- Nives Skunca
Papers from Jüri Reimand's perspective
Ordered by how strongly the researchers Jüri Reimand trusts endorse each paper. Same corpus, a different order for every researcher.
- Controlling the false discovery rate: a practical and powerful approach to multiple testing
- dbSNP: the NCBI database of genetic variation
- NCBI GEO: mining tens of millions of expression profiles—database and tools update
- Ontological analysis of gene expression data: current tools, limitations, and open problems (Bioinform.)
- Integration of biological networks and gene expression data using Cytoscape (Nature Protocols)
- THE CONTROL OF THE FALSE DISCOVERY RATE IN MULTIPLE TESTING UNDER DEPENDENCY
- PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes (Nature Genetics)
- Reactome: a knowledgebase of biological pathways (Nucleic Acids Res.)
- Onto-Tools, the toolkit of the modern biologist: Onto-Express, Onto-Compare, Onto-Design and Onto-Translate (Nucleic Acids Res.)
- DAVID: Database for Annotation, Visualization, and Integrated Discovery (Genome Biology)
Their papers
- g:Profiler—a web-based toolset for functional profiling of gene lists from large-scale experiments (2007) — 1,334 citations
- Pathway and Network Analysis of Cancer Genomes (2015) — 319 citations
- Impact of outdated gene annotations on pathway enrichment analysis (2016) — 121 citations
- g:Profiler—a web server for functional interpretation of gene lists (2011 update) (2011) — 1,588 citations
- Pathway enrichment analysis and visualization of omics data using g:Profiler, GSEA, Cytoscape and EnrichmentMap (2019) — 1,618 citations
- Subgroup-specific structural variation across 1,000 medulloblastoma genomes (2012) — 871 citations
- Analyses of non-coding somatic drivers in 2,658 cancer whole genomes (2020) — 508 citations
- Pathogenic germline variants in 10,389 adult cancers (2018) — 734 citations
- g:Profiler—a web server for functional interpretation of gene lists (2016 update) (2016) — 326 citations
- New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs (2016) — 819 citations
- Molecular Classification of Ependymal Tumors across All CNS Compartments, Histopathological Grades, and Age Groups. (2015) — 1,015 citations
- Genome Sequencing of SHH Medulloblastoma Predicts Genotype-Related Response to Smoothened Inhibition (2014) — 693 citations