1a27ec1d01c34fc538386ea217cd71425b42cdcc
Supplemental_Methods_and_Results.md
| ... | ... | @@ -9,6 +9,7 @@ csl: NLM.csl |
| 9 | 9 | ## Studies |
| 10 | 10 | |
| 11 | 11 | Any study that described at least one gene as recurrently mutated in DLBCL, FL or BL was eligible to contribute to the gene lists. This included 37 studies for DLBCL.@albuquerqueEnhancingKnowledgeDiscovery2017; @arthurGenomewideDiscoverySomatic2018; @bohleRoleEarlyBcell2013; @chapuyMolecularSubtypesDiffuse2018; @compagnoMutationsMultipleGenes2009; @davisChronicActiveBcellreceptor2010; @drevalGeneticSubdivisionsFollicular2023; @dunsCharacterizationDLBCLPMBL2021; @fanComprehensiveCharacterizationDriver2020; @hubschmannMutationalMechanismsShaping2021; @khodabakhshiRecurrentTargetsAberrant2012; @kwanhianMicroRNA142Mutated202012; @lenzOncogenicCARD11Mutations2008; @lohrDiscoveryPrioritizationSomatic2012; @mareschalWholeExomeSequencing2016; @morinFrequentMutationHistonemodifying2011; @morinGeneticLandscapesRelapsed2016; @morinMutationalStructuralAnalysis2013; @morinSomaticMutationsAltering2010; @ngoOncogenicallyActiveMYD882011; @novakWholeexomeAnalysisReveals2015; @okosunRecurrentMTORC1activatingRRAGC2016; @pararajalingamCodingNoncodingDrivers2020; @pasqualucciAnalysisCodingGenome2011; @pasqualucciHypermutationMultipleProtooncogenes2001; @pasqualucciInactivatingMutationsAcetyltransferase2011; @pasqualucciInactivationPRDM1BLIMP12006; @reddyGeneticFunctionalDrivers2017; @rushtonGeneticEvolutionaryPatterns2020; @schmitzGeneticsPathogenesisDiffuse2018; @schollMutationsRegionFAS2007; @shinBRAFV600EMAP2K12015; @tanakaFrequentIncidenceSomatic1992; @thomasMutationalAnalysisIkappaBalpha2004; @tiacciBRAFMutationsHairycell2011; @yildizActivatingSTAT6Mutations2015; @zhangGeneticHeterogeneityDiffuse2013 |
| 12 | +15 studies for FL.@barariaCathepsinAlterationsInduce2020,@cheungAcquiredTNFRSF14Mutations2010,@drevalGeneticSubdivisionsFollicular2023,@hubschmannMutationalMechanismsShaping2021,@krysiakRecurrentSomaticMutations2017,@laurentFollicularLymphomaComprises2024,@louissaintPediatrictypeNodalFollicular2016,@maSubtypespecificCooccurringGenetic2022,@morinFrequentMutationHistonemodifying2011,@morinSomaticMutationsAltering2010,@okosunRecurrentMTORC1activatingRRAGC2016,@pasqualucciInactivatingMutationsAcetyltransferase2011,@rossiAberrantSomaticHypermutation2006,@russler-germainMutationsAssociatedProgression2023,@yildizActivatingSTAT6Mutations2015 |
|
| 12 | 13 | |
| 13 | 14 | ## Procedure for gene retirement (Tier 3) |
| 14 | 15 |