| 1 |
tanakaFrequentIncidenceSomatic1992 |
Sanger |
1992-01-01 |
0 |
5 |
0 |
|
| 2 |
johnstonCmycHypermutationBurkitt1992 |
Sanger |
1992-12-01 |
0 |
0 |
9 |
|
| 3 |
pasqualucciHypermutationMultipleProtooncogenes2001 |
Sanger |
2001-07-19 |
11 |
28 |
0 |
|
| 4 |
wildaInactivationARFMDM2p53Pathway2004 |
Sanger |
2004-03-01 |
0 |
24 |
0 |
|
| 5 |
pasqualucciInactivationPRDM1BLIMP12006 |
Sanger |
2006-02-02 |
134 |
0 |
20 |
|
| 6 |
schollMutationsRegionFAS2007 |
Sanger |
2007-05-01 |
|
|
|
|
| 7 |
lenzOncogenicCARD11Mutations2008 |
Sanger |
2008-03-03 |
6 |
217 |
21 |
|
| 8 |
compagnoMutationsMultipleGenes2009 |
Sanger |
2009-06-04 |
0 |
101 |
Unclear |
|
| 9 |
morinSomaticMutationsAltering2010 |
RNA-seq/WGS |
2010-02-02 |
1 |
31 |
7 |
|
| 10 |
cheungAcquiredTNFRSF14Mutations2010 |
Sanger |
2010-11-15 |
11 |
251 |
0 |
|
| 11 |
ngoOncogenicallyActiveMYD882011 |
Sanger |
2011-02-03 |
0 |
382 |
20 |
|
| 12 |
pasqualucciInactivatingMutationsAcetyltransferase2011 |
exome/Sanger |
2011-03-10 |
7 |
134 |
0 |
|
| 13 |
tiacciBRAFMutationsHairycell2011 |
exome/Sanger |
2011-06-16 |
|
|
|
|
| 14 |
morinFrequentMutationHistonemodifying2011 |
WGS/RNA-seq |
2011-07-27 |
14 |
103 |
10 |
|
| 15 |
pasqualucciAnalysisCodingGenome2011 |
exome/Sanger |
2011-07-31 |
6 |
92 |
23 |
|
| 16 |
lohrDiscoveryPrioritizationSomatic2012 |
exome |
2012-03-06 |
55 |
0 |
0 |
|
| 17 |
bohleRoleEarlyBcell2013 |
Sanger |
2012-10-01 |
0 |
0 |
6 |
|
| 18 |
schmitzBurkittLymphomaPathogenesis2012 |
RNA-seq |
2012-10-04 |
0 |
41 |
0 |
|
| 19 |
kwanhianMicroRNA142Mutated202012 |
Sanger |
2012-10-1 |
unclear |
56 |
0 |
|
| 20 |
richterRecurrentMutationID32012 |
RNA-seq/WGS/exome |
2012-11-11 |
unclear |
53 |
|
|
| 21 |
khodabakhshiRecurrentTargetsAberrant2012 |
WGS |
2012-11-12 |
40 |
0 |
0 |
|
| 22 |
loveGeneticLandscapeMutations2012 |
exome |
2012-12-01 |
14 |
37 |
8 |
|
| 23 |
zhangGeneticHeterogeneityDiffuse2013 |
exome |
2013-01-01 |
34 |
39 |
21 |
|
| 24 |
morinMutationalStructuralAnalysis2013 |
WGS |
2013-08-15 |
40 |
0 |
13 |
|
| 25 |
muppidiLossSignalingGa132014 |
Sanger |
2014-12-11 |
unclear |
unclear |
|
|
| 26 |
yildizActivatingSTAT6Mutations2015 |
exome |
2015-01-22 |
24 |
0 |
0 |
|
| 27 |
novakWholeexomeAnalysisReveals2015 |
exome |
2015-08-01 |
51 |
0 |
|
|
| 28 |
shinBRAFV600EMAP2K12015 |
Sanger |
2015-03-01 |
unclear |
unclear |
unclear |
|
| 29 |
abateDistinctViralMutational2015 |
RNA-seq |
2015-10-15 |
0 |
20 |
0 |
|
| 30 |
okosunRecurrentMTORC1activatingRRAGC2016 |
exome |
2016-02-02 |
5 |
|
|
|
| 31 |
mareschalWholeExomeSequencing2016 |
exome |
2016-03-01 |
14 |
0 |
0 |
|
| 32 |
morinGeneticLandscapesRelapsed2016 |
exome |
2016-05-01 |
38 |
0 |
0 |
|
| 33 |
louissaintPediatrictypeNodalFollicular2016 |
exome/panel |
2016-08-25 |
22 |
0 |
0 |
|
| 34 |
krysiakRecurrentSomaticMutations2017 |
exome/panel |
2017-01-26 |
61 |
69 |
0 |
1716 gene panel described in Supplemental Table S4 from the study |
| 35 |
albuquerqueEnhancingKnowledgeDiscovery2017 |
exome |
2017-05-01 |
96 |
0 |
0 |
Exomes are from TCGA and Lohr et al |
| 36 |
reddyGeneticFunctionalDrivers2017 |
exome |
2017-10-10 |
400 |
601 |
0 |
Although normals were sequenced, the paired exomes were not analyzed as pairs and the identity of paired exomes was not included in the study |
| 37 |
schmitzGeneticsPathogenesisDiffuse2018 |
exome |
2018-04-12 |
48 |
526 |
|
|
| 38 |
chapuyMolecularSubtypesDiffuse2018 |
exome |
2018-05-01 |
137 |
167 |
|
|
| 39 |
arthurGenomewideDiscoverySomatic2018 |
WGS |
2018-10-01 |
153 |
0 |
0 |
|
| 40 |
grandeGenomewideDiscoverySomatic2019 |
WGS |
2019-03-21 |
106 |
0 |
0 |
Combination of endemic and sporadic BL and EBV+/EBV- BL |
| 41 |
zhouSporadicEndemicBurkitt2019 |
Sanger |
2019-07-23 |
0 |
74 |
0 |
All patients were sporadic BL |
| 42 |
paneaWholeGenomeLandscape2019 |
RNA-seq/exome |
2019-09-26 |
101 |
0 |
0 |
As per the errata, the study relied on a combination of RNA-seq and exome data https://doi.org/10.1182/blood.2023021419 |
| 43 |
barariaCathepsinAlterationsInduce2020 |
panel |
2020-05-05 |
0 |
305 |
|
Targeted sequencing panel covered all CTSS exons. Unclear if panel covered additional genes. |
| 44 |
fanComprehensiveCharacterizationDriver2020 |
exome |
2020-07-01 |
48 |
0 |
|
TCGA exomes |
| 45 |
rushtonGeneticEvolutionaryPatterns2020 |
exome/panel |
2020-07-14 |
135 |
0 |
0 |
63-gene panel |
| 46 |
pararajalingamCodingNoncodingDrivers2020 |
exome/WGS |
2020-07-30 |
85 |
0 |
0 |
|
| 47 |
hubschmannMutationalMechanismsShaping2021 |
WGS |
2021-05-05 |
179 |
2 |
0 |
ICGC MALY-DE |
| 48 |
dunsCharacterizationDLBCLPMBL2021 |
exome |
2021-07-15 |
7 |
8 |
0 |
|
| 49 |
maSubtypespecificCooccurringGenetic2022 |
panel |
2022-03-01 |
0 |
685 |
0 |
380-gene panel includes 79 Tier 1 genes |
| 50 |
burkhardtClinicalRelevanceMolecular2022 |
panel |
2022-07-06 |
0 |
298 |
10 |
134-gene panel includes 42 Tier 1 genes |
| 51 |
crouchMolecularSubclustersFollicular2022 |
panel |
2022-11-02 |
0 |
548 |
0 |
293-gene panel includes 97 Tier 1 genes |
| 52 |
thomasGeneticSubgroupsInform2023 |
WGS |
2023-02-03 |
193 |
82 |
22 |
Includes pediatric and adult BL cases as well as HIV+ DLBCLs |
| 53 |
russler-germainMutationsAssociatedProgression2023 |
exome |
2023-07-26 |
0 |
370 |
0 |
2595-gene panel covers 132 Tier 1 genes |
| 54 |
drevalGeneticSubdivisionsFollicular2023 |
WGS |
2023-08-10 |
423 |
0 |
0 |
|
Datasets
Models
