Origins of BL genes

Tier 1 BL genes

29 total

Gene Tier First BL evidence Other entities
ARID1A 1 Love et al1 2,wienandGenomicAnalysesFlowsorted2019b?,rossiCodingGenomeSplenic2012c?,krysiakRecurrentSomaticMutations2017b?
BCL7A 1, aSHM Grande et al3 4,reichelFlowSortingExome2015a?,krysiakRecurrentSomaticMutations2017b?
BMP7 1 Panea et al5
CCND3 1 Richter et alrichterRecurrentMutationID32012a? 68
CHD8 1 Grande et al3 9
DDX3X 1 Schmitz et al10 schmitzGeneticsPathogenesisDiffuse2018a?,mottokIntegrativeGenomicAnalysis2019b?
EIF4A1 1 Panea et al5
EPPK1 1 Panea et al5
FBXO11 1 Richter et alrichterRecurrentMutationID32012a? 11,hubschmannMutationalMechanismsShaping2021b?
FOXO1 1 Schmitz et al10 7,dunsCharacterizationDLBCLPMBL2021b?
GNA13 1 Love et al1 7,reichelFlowSortingExome2015a?
GNAI2 1 Grande et al3 12
HNRNPU 1, aSHM Panea et al5 9
ID3 1 Richter et alrichterRecurrentMutationID32012a? 10,spinaGeneticsNodalMarginal2016b?
KMT2D 1 Grande et al3 6,7,13,rossiCodingGenomeSplenic2012c?
MYC 1, aSHM Johnston et al14 8,pasqualucciHypermutationMultipleProtooncogenes2001a?,dunsCharacterizationDLBCLPMBL2021b?
P2RY8 1 Muppidi et almuppidiLossSignalingGa132014b? lohrDiscoveryPrioritizationSomatic2012a?
PHF6 1 Thomas et al15 9
PTEN 1 Love et al1
RFX7 1 Grande et al3
RHOA 1 Richter et alrichterRecurrentMutationID32012a?
SIN3A 1 Grande et al3 rossiCodingGenomeSplenic2012c?
SMARCA4 1 Richter et alrichterRecurrentMutationID32012a? krysiakRecurrentSomaticMutations2017b?,nadeuGenomicEpigenomicInsights2020b?,lohrDiscoveryPrioritizationSomatic2012a?
TCF3 1 Schmitz et al10
TCL1A 1, aSHM Grande et al3
TFAP4 1 Grande et al3
TP53 1 Wilda et al16 7,13,rossiCodingGenomeSplenic2012c?,lohrDiscoveryPrioritizationSomatic2012a?,tiacciPervasiveMutationsJAKSTAT2018b?
USP7 1 Grande et al3
WNK1 1 Thomas et al15 8,hubschmannMutationalMechanismsShaping2021b?

Tier 2 BL genes

152 total

This includes *70 genes failed QC (2-F)

Gene Tier First BL evidence Other entities
ADAMTS5 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
ADNP 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
AGO4 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
ARHGEF1 2 Muppidi et almuppidiLossSignalingGa132014b?
BACH2 2, aSHM Grande et al3
BCL2 2, aSHM Burkhardt et alburkhardtClinicalRelevanceMolecular2022b? 7,17,sarkozyMutationalLandscapeGray2021a?
BCL6 2, aSHM Love et al1 7
BTG1 2, aSHM Burkhardt et alburkhardtClinicalRelevanceMolecular2022b? 7,sarkozyMutationalLandscapeGray2021a?
C16orf48 2 Schmitz et al10
CARD11 2 Panea et al5 7,18,19,yanBCRTLRSignaling2012a?
CARD4 2 Love et al1
CCNF 2 Abate et alabateDistinctViralMutational2015a?
CD79A 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b? rossiCodingGenomeSplenic2012c?
CD83 2, aSHM Panea et al5 12,dunsCharacterizationDLBCLPMBL2021b?,russler-germainMutationsAssociatedProgression2023b?
CDC73 2 Love et al1 9
CDKN2A 2 Grande et al3 12,spinaGeneticsNodalMarginal2016b?
CDKN2C 2 Thomas et al15
CHD4 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
CPXM2 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
CREBBP 2 Love et al1 11,dunsCharacterizationDLBCLPMBL2021b?,pasqualucciInactivatingMutationsAcetyltransferase2011a?
CXCR4 2, aSHM Panea et al5 20,krysiakRecurrentSomaticMutations2017b?
DHCR7 2 Schmitz et al10
E2F2 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
EBF1 2, aSHM Thomas et al15 21,reichelFlowSortingExome2015a?
EDNRB 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
EHD1 2 Thomas et al15
ELP2 2 Schmitz et al10
EP300 2 Panea et al5 rossiCodingGenomeSplenic2012c?,pasqualucciInactivatingMutationsAcetyltransferase2011a?
ERAP1 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
EXOSC6 2 Schmitz et al10
EZH2 2 Love et al1 mottokIntegrativeGenomicAnalysis2019b?,morinSomaticMutationsAltering2010a?
FLYWCH1 2 Schmitz et al10
GGTLA4 2 Love et al1
GRB2 2 Panea et al5 22
GTSE1 2 Schmitz et al10
HIST1H1E 2, aSHM Grande et al3 krysiakRecurrentSomaticMutations2017b?,reichelFlowSortingExome2015a?,lohrDiscoveryPrioritizationSomatic2012a?
HIST1H3D 2, aSHM Panea et al5
HIST1H3I 2, aSHM Panea et al5 krysiakRecurrentSomaticMutations2017b?
HIST1H4J 2, aSHM Panea et al5 mottokIntegrativeGenomicAnalysis2019b?
HLA-DQB1 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
IGLL5 2, aSHM Panea et al5 6,russler-germainMutationsAssociatedProgression2023b?
IKZF3 2, aSHM Panea et al5 12
IRF8 2, aSHM Panea et al5 7,mottokIntegrativeGenomicAnalysis2019b?
KANK2 2 Schmitz et al10
KLHL26 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
KLHL6 2, aSHM Panea et al5 7,23
KMT2C 2 Zhou et al24 2,25,sarkozyMutationalLandscapeGray2021a?
LTB 2, aSHM Panea et al5 6,chapuyMolecularSubtypesDiffuse2018b?
MCL1 2 Panea et al5 9,dunsCharacterizationDLBCLPMBL2021b?
MIR142 2, aSHM Grande et al3 kwanhianMicroRNA142Mutated202012b?
MKI67 2 Schmitz et al10 russler-germainMutationsAssociatedProgression2023b?
MYO18A 2 Schmitz et al10
NBEAL1 2 Love et al1
NCOR2 2 Schmitz et al10 sarkozyMutationalLandscapeGray2021a?,spinaGeneticsNodalMarginal2016b?
NOA1 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
NOTCH2 2 Panea et al5 13,26,rossiCodingGenomeSplenic2012c?
P2RY2 2 Love et al1
PCBP1 2 Schmitz et al10
PDCD11 2 Schmitz et al10
PIM1 2, aSHM Burkhardt et alburkhardtClinicalRelevanceMolecular2022b? pasqualucciHypermutationMultipleProtooncogenes2001a?,dunsCharacterizationDLBCLPMBL2021b?
PLCG2 2 Panea et al5
PPP6R2 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
PREX1 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
RAC2 2 Panea et al5 hubschmannMutationalMechanismsShaping2021b?
RANBP6 2 Love et al1
REV3L 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
RNF144B 2 Panea et al5
RPL10 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
S1PR2 2, aSHM Muppidi et almuppidiLossSignalingGa132014b? 7
SAL3 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
TET2 2 Panea et al5 albuquerqueEnhancingKnowledgeDiscovery2017a?
TOP2A 2 Schmitz et al10
TTN 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
VWA7 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
WDR90 2 Schmitz et al10
WHAMM 2 Schmitz et al10
WNK2 2 Panea et al5
YY1AP1 2 Schmitz et al10
ZAN 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
ZBTB7A 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b? 9
ZFP36L1 2, aSHM Panea et al5 7,reichelFlowSortingExome2015a?
ZNF85 2 Burkhardt et alburkhardtClinicalRelevanceMolecular2022b?
ACAD9 2-F Love et al1
ACE 2-F Love et al1
ALPK2 2-F Panea et al5
ATP2C2 2-F Love et al1
BRAF 2-F Love et al1 tiacciBRAFMutationsHairycell2011a?
BRD4 2-F Love et al1
BTG2 2-F Love et al1 7
C6orf27 2-F Love et al1
CAD 2-F Love et al1
CCT6B 2-F Love et al1
CD79B 2-F Panea et al5 7
CDH17 2-F Love et al1
COL4A2 2-F Love et al1
CTCF 2-F Panea et al5
CYB5D1 2-F Love et al1
CYP4F22 2-F Love et al1
DLGAP1 2-F Love et al1
DNMT1 2-F Panea et al5
DTX1 2-F Love et al1 27,rossiCodingGenomeSplenic2012c?,schmitzGeneticsPathogenesisDiffuse2018a?
EIF2C4 2-F Love et al1
EML2 2-F Love et al1
ENTPD3 2-F Love et al1
EPHB2 2-F Love et al1
ETS1 2-F Panea et al5 7
FAM129B 2-F Love et al1
FGFR3 2-F Love et al1
FTCD 2-F Love et al1
FZD3 2-F Panea et al5
GRIK5 2-F Love et al1
HIST1H1C 2-F Panea et al5 7
HIST1H2AG 2-F Panea et al5 12,krysiakRecurrentSomaticMutations2017b?,rossiCodingGenomeSplenic2012c?
HIST1H2AM 2-F Panea et al5 krysiakRecurrentSomaticMutations2017b?
HIST1H2BK 2-F Panea et al5 rossiCodingGenomeSplenic2012c?
HIST1H3H 2-F Panea et al5
HIST1H3J 2-F Panea et al5
ICK 2-F Love et al1
ITPR3 2-F Love et al1 tiacciPervasiveMutationsJAKSTAT2018b?
KCNK10 2-F Panea et al5
KIFC3 2-F Love et al1
MAP3K6 2-F Love et al1
MME 2-F Panea et al5
MTOR 2-F Panea et al5 2
MYH10 2-F Love et al1
NOTCH1 2-F Love et al1 13,22,rossiCodingGenomeSplenic2012c?
NRXN2 2-F Love et al1
PABPC4L 2-F Panea et al5
PC 2-F Love et al1
PCDHA11 2-F Panea et al5
PDZRN3 2-F Panea et al5
PIK3R1 2-F Panea et al5 2
POLRMT 2-F Love et al1
POR 2-F Love et al1
PRSS22 2-F Love et al1
PTPRN 2-F Love et al1
PXDNL 2-F Panea et al5
RBP3 2-F Love et al1
RET 2-F Love et al1
SALL3 2-F Love et al1 25
SAPS2 2-F Love et al1
SBF1 2-F Love et al1
SF3B1 2-F Love et al1
SHANK1 2-F Love et al1
SLC29A2 2-F Love et al1
SNTB2 2-F Panea et al5
SYNGAP1 2-F Love et al1
TBC1D9B 2-F Love et al1
TIGD6 2-F Love et al1
TPST2 2-F Love et al1
WDR7 2-F Panea et al5
ZNF229 2-F Love et al1

References

1.
Love C, Sun Z, Jima D, Li G, Zhang J, Miles R, Richards KL, Dunphy CH, Choi WWL, Srivastava G, Lugar PL, Rizzieri DA, Lagoo AS, Bernal-Mizrachi L, Mann KP, Flowers CR, Naresh KN, Evens AM, Chadburn A, Gordon LI, Czader MB, Gill JI, Hsi ED, Greenough A, Moffitt AB, McKinney M, Banerjee A, Grubor V, Levy S, Dunson DB, Dave SS. The genetic landscape of mutations in Burkitt lymphoma. Nat Genet. 2012 Dec;44(12):1321–1325. PMCID: PMC3674561
2.
Zhang J, Grubor V, Love CL, Banerjee A, Richards KL, Mieczkowski PA, Dunphy C, Choi W, Au WY, Srivastava G, Lugar PL, Rizzieri DA, Lagoo AS, Bernal-Mizrachi L, Mann KP, Flowers C, Naresh K, Evens A, Gordon LI, Czader M, Gill JI, Hsi ED, Liu Q, Fan A, Walsh K, Jima D, Smith LL, Johnson AJ, Byrd JC, Luftig MA, Ni T, Zhu J, Chadburn A, Levy S, Dunson D, Dave SS. Genetic heterogeneity of diffuse large B-cell lymphoma. Proceedings of the National Academy of Sciences of the United States of America. 2013;110:1398–1403. PMCID: PMC3557051
3.
Grande BM, Gerhard DS, Jiang A, Griner NB, Abramson JS, Alexander TB, Allen H, Ayers LW, Bethony JM, Bhatia K, Bowen J, Casper C, Choi JK, Culibrk L, Davidsen TM, Dyer MA, Gastier-Foster JM, Gesuwan P, Greiner TC, Gross TG, Hanf B, Harris NL, He Y, Irvin JD, Jaffe ES, Jones SJM, Kerchan P, Knoetze N, Leal FE, Lichtenberg TM, Ma Y, Martin JP, Martin MR, Mbulaiteye SM, Mullighan CG, Mungall AJ, Namirembe C, Novik K, Noy A, Ogwang MD, Omoding A, Orem J, Reynolds SJ, Rushton CK, Sandlund JT, Schmitz R, Taylor C, Wilson WH, Wright GW, Zhao EY, Marra MA, Morin RD, Staudt LM. Genome-wide discovery of somatic coding and noncoding mutations in pediatric endemic and sporadic Burkitt lymphoma. Blood. 2019;133(12):1313–1324. PMCID: PMC6428665
4.
Arthur SE, Jiang A, Grande BM, Alcaide M, Cojocaru R, Rushton CK, Mottok A, Hilton LK, Lat PK, Zhao EY, Culibrk L, Ennishi D, Jessa S, Chong L, Thomas N, Pararajalingam P, Meissner B, Boyle M, Davidson J, Bushell KR, Lai D, Farinha P, Slack GW, Morin GB, Shah S, Sen D, Jones SJM, Mungall AJ, Gascoyne RD, Audas TE, Unrau P, Marra MA, Connors JM, Steidl C, Scott DW, Morin RD. Genome-wide discovery of somatic regulatory variants in diffuse large B-cell lymphoma. Nat Commun. 2018 Oct 1;9(1):4001. PMCID: PMC6167379
5.
Panea R, Love C, Shingleton JR, Reddy A, Bailey J, Moormann A, Otieno J, Ong’echa J, Oduor C, Schroêder K, Masalu N, Chao N, Agajanian M, Major M, Fedoriw Y, Richards K, Rymkiewicz G, Miles R, Alobeid B, Bhagat G, Flowers C, Ondrejka S, Hsi E, Choi W, Au-Yeung R, Hartmann W, Lenz G, Meyerson H, Lin YY, Zhuang Y, Luftig M, Waldrop A, Dave T, Thakkar D, Sahay H, Li G, Palus B, Seshadri V, Kim S, Gascoyne R, Levy S, Mukhopadhyay M, Dunson D, Dave S. The whole genome landscape of Burkitt lymphoma subtypes. Blood. 2019;
6.
Desch AK, Hartung K, Botzen A, Brobeil A, Rummel M, Kurch L, Georgi T, Jox T, Bielack S, Burdach S, Classen CF, Claviez A, Debatin KM, Ebinger M, Eggert A, Faber J, Flotho C, Frühwald M, Graf N, Jorch N, Kontny U, Kramm C, Kulozik A, Kühr J, Sykora KW, Metzler M, Müller HL, Nathrath M, Nüßlein T, Paulussen M, Pekrun A, Reinhardt D, Reinhard H, Rössig C, Sauerbrey A, Schlegel PG, Schneider DT, Scheurlen W, Schweigerer L, Simon T, Suttorp M, Vorwerk P, Schmitz R, Kluge R, Mauz-Körholz C, Körholz D, Gattenlöhner S, Bräuninger A. Genotyping circulating tumor DNA of pediatric Hodgkin lymphoma. Leukemia. 2020 Jan;34(1):151–166.
7.
Morin RD, Mendez-Lago M, Mungall AJ, Goya R, Mungall KL, Corbett RD, Johnson NA, Severson TM, Chiu R, Field M, Jackman S, Krzywinski M, Scott DW, Trinh DL, Tamura-Wells J, Li S, Firme MR, Rogic S, Griffith M, Chan S, Yakovenko O, Meyer IM, Zhao EY, Smailus D, Moksa M, Chittaranjan S, Rimsza L, Brooks-Wilson A, Spinelli JJ, Ben-Neriah S, Meissner B, Woolcock B, Boyle M, McDonald H, Tam A, Zhao Y, Delaney A, Zeng T, Tse K, Butterfield Y, Birol I, Holt R, Schein J, Horsman DE, Moore R, Jones SJM, Connors JM, Hirst M, Gascoyne RD, Marra MA. Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma. Nature. 2011 Jul 27;476(7360):298–303. PMCID: PMC3210554
8.
Jallades L, Baseggio L, Sujobert P, Huet S, Chabane K, Callet-Bauchu E, Verney A, Hayette S, Desvignes JP, Salgado D, Levy N, Béroud C, Felman P, Berger F, Magaud JP, Genestier L, Salles G, Traverse-Glehen A. Exome sequencing identifies recurrent BCOR alterations and the absence of KLF2, TNFAIP3 and MYD88 mutations in splenic diffuse red pulp small B-cell lymphoma. Haematologica. 2017 Oct;102(10):1758–1766. PMCID: PMC5622860
9.
Reddy A, Zhang J, Davis NS, Moffitt AB, Love CL, Waldrop A, Leppa S, Pasanen A, Meriranta L, Karjalainen-Lindsberg ML, Nørgaard P, Pedersen M, Gang AO, Høgdall E, Heavican TB, Lone W, Iqbal J, Qin Q, Li G, Kim SY, Healy J, Richards KL, Fedoriw Y, Bernal-Mizrachi L, Koff JL, Staton AD, Flowers CR, Paltiel O, Goldschmidt N, Calaminici M, Clear A, Gribben J, Nguyen E, Czader MB, Ondrejka SL, Collie A, Hsi ED, Tse E, Au-Yeung RKH, Kwong YL, Srivastava G, Choi WWL, Evens AM, Pilichowska M, Sengar M, Reddy N, Li S, Chadburn A, Gordon LI, Jaffe ES, Levy S, Rempel R, Tzeng T, Happ LE, Dave T, Rajagopalan D, Datta J, Dunson DB, Dave SS. Genetic and Functional Drivers of Diffuse Large B Cell Lymphoma. Cell. 2017 Oct;171(2):481–494.e15. PMCID: PMC5659841
10.
Schmitz R, Young RM, Ceribelli M, Jhavar S, Xiao W, Zhang M, Wright G, Shaffer AL, Hodson DJ, Buras E, Liu X, Powell J, Yang Y, Xu W, Zhao H, Kohlhammer H, Rosenwald A, Kluin P, Müller-Hermelink HK, Ott G, Gascoyne RD, Connors JM, Rimsza LM, Campo E, Jaffe ES, Delabie J, Smeland EB, Ogwang MD, Reynolds SJ, Fisher RI, Braziel RM, Tubbs RR, Cook JR, Weisenburger DD, Chan WC, Pittaluga S, Wilson W, Waldmann TA, Rowe M, Mbulaiteye SM, Rickinson AB, Staudt LM. Burkitt lymphoma pathogenesis and therapeutic targets from structural and functional genomics. Nature. 2012 Oct 4;490(7418):116–120. PMCID: PMC3609867
11.
Parry M, Rose-Zerilli MJJ, Gibson J, Ennis S, Walewska R, Forster J, Parker H, Davis Z, Gardiner A, Collins A, Oscier DG, Strefford JC. Whole exome sequencing identifies novel recurrently mutated genes in patients with splenic marginal zone lymphoma. PLoS One. 2013;8(12):e83244. PMCID: PMC3862727
12.
Morin RD, Mungall K, Pleasance E, Mungall AJ, Goya R, Huff RD, Scott DW, Ding J, Roth A, Chiu R, Corbett RD, Chan FC, Mendez-Lago M, Trinh DL, Bolger-Munro M, Taylor G, Hadj Khodabakhshi A, Ben-Neriah S, Pon J, Meissner B, Woolcock B, Farnoud N, Rogic S, Lim EL, Johnson NA, Shah S, Jones S, Steidl C, Holt R, Birol I, Moore R, Connors JM, Gascoyne RD, Marra MA. Mutational and structural analysis of diffuse large B-cell lymphoma using whole-genome sequencing. Blood. 2013 Aug 15;122(7):1256–1265. PMCID: PMC3744992
13.
Beà S, Valdés-Mas R, Navarro A, Salaverria I, Martín-Garcia D, Jares P, Giné E, Pinyol M, Royo C, Nadeu F, Conde L, Juan M, Clot G, Vizán P, Croce LD, Puente DA, López-Guerra M, Moros A, Roue G, Aymerich M, Villamor N, Colomo L, Martínez A, Valera A, Martín-Subero JI, Amador V, Hernández L, Rozman M, Enjuanes A, Forcada P, Muntañola A, Hartmann EM, Calasanz MJ, Rosenwald A, Ott G, Hernández-Rivas JM, Klapper W, Siebert R, Wiestner A, Wilson WH, Colomer D, López-Guillermo A, López-Otín C, Puente XS, Campo E. Landscape of somatic mutations and clonal evolution in mantle cell lymphoma. PNAS. 2013;110(45):18250–18255.
14.
Johnston JM, Carroll WL. C-myc hypermutation in Burkitt’s lymphoma. Leuk Lymphoma. 1992 Dec;8(6):431–439.
15.
Thomas N, Dreval K, Gerhard DS, Hilton LK, Abramson JS, Ambinder RF, Barta S, Bartlett NL, Bethony J, Bhatia K, Bowen J, Bryan AC, Cesarman E, Casper C, Chadburn A, Cruz M, Dittmer DP, Dyer MA, Farinha P, Gastier-Foster JM, Gerrie AS, Grande BM, Greiner T, Griner NB, Gross TG, Harris NL, Irvin JD, Jaffe ES, Henry D, Huppi R, Leal FE, Lee MS, Martin JP, Martin MR, Mbulaiteye SM, Mitsuyasu R, Morris V, Mullighan CG, Mungall AJ, Mungall K, Mutyaba I, Nokta M, Namirembe C, Noy A, Ogwang MD, Omoding A, Orem J, Ott G, Petrello H, Pittaluga S, Phelan JD, Ramos JC, Ratner L, Reynolds SJ, Rubinstein PG, Sissolak G, Slack G, Soudi S, Swerdlow SH, Traverse-Glehen A, Wilson WH, Wong J, Yarchoan R, ZenKlusen JC, Marra MA, Staudt LM, Scott DW, Morin RD. Genetic subgroups inform on pathobiology in adult and pediatric Burkitt lymphoma. Blood. 2023 Feb 23;141(8):904–916. PMCID: PMC10023728
16.
Wilda M, Bruch J, Harder L, Rawer D, Reiter A, Borkhardt A, Woessmann W. Inactivation of the ARF-MDM-2-p53 pathway in sporadic Burkitt’s lymphoma in children. Leukemia. 2004 Mar;18(3):584–588.
17.
Tanaka S, Louie DC, Kant JA, Reed JC. Frequent incidence of somatic mutations in translocated BCL2 oncogenes of non-Hodgkin’s lymphomas. Blood. 1992 Jan 1;79(1):229–237.
18.
Wu C, de Miranda NF, Chen L, Wasik AM, Mansouri L, Jurczak W, Galazka K, Dlugosz-Danecka M, Machaczka M, Zhang H, Peng R, Morin RD, Rosenquist R, Sander B, Pan-Hammarström Q. Genetic heterogeneity in primary and relapsed mantle cell lymphomas: Impact of recurrent CARD11 mutations. Oncotarget. 2016 Jun 21;7(25):38180–38190. PMCID: PMC5122381
19.
Lenz G, Davis RE, Ngo VN, Lam L, George TC, Wright GW, Dave SS, Zhao H, Xu W, Rosenwald A, Ott G, Müller-Hermelink HK, Gascoyne RD, Connors JM, Rimsza LM, Campo E, Jaffe ES, Delabie J, Smeland EB, Fisher RI, Chan WC, Staudt LM. Oncogenic CARD11 mutations in human diffuse large B cell lymphoma. Science. 2008 Mar;319(5870):1676–1679.
20.
Khodabakhshi AH, Morin RD, Fejes AP, Mungall AJ, Mungall KL, Bolger-Munro M, Johnson NA, Connors JM, Gascoyne RD, Marra MA, Birol I, Jones SJM. Recurrent targets of aberrant somatic hypermutation in lymphoma. Oncotarget. 2012;3(11):1308–1319. PMCID: PMC3717795
21.
Bohle V, Döring C, Hansmann M-L, Küppers R. Role of early B-cell factor 1 (EBF1) in Hodgkin lymphoma. Leukemia. 2013 Mar;27(3):671–679.
22.
Pasqualucci L, Trifonov V, Fabbri G, Ma J, Rossi D, Chiarenza A, Wells VA, Grunn A, Messina M, Elliot O, Chan J, Bhagat G, Chadburn A, Gaidano G, Mullighan CG, Rabadan R, Dalla-Favera R. Analysis of the coding genome of diffuse large B-cell lymphoma. Nat Genet. 2011 Jul 31;43(9):830–837. PMCID: PMC3297422
23.
Ganapathi KA, Jobanputra V, Iwamoto F, Jain P, Chen J, Cascione L, Nahum O, Levy B, Xie Y, Khattar P, Hoehn D, Bertoni F, Murty VV, Pittaluga S, Jaffe ES, Alobeid B, Mansukhani MM, Bhagat G. The genetic landscape of dural marginal zone lymphomas. Oncotarget. Impact Journals; 2016 May 27;7(28):43052–43061.
24.
Zhou P, Blain AE, Newman AM, Zaka M, Chagaluka G, Adlar FR, Offor UT, Broadbent C, Chaytor L, Whitehead A, Hall A, O’Connor H, Van Noorden S, Lampert I, Bailey S, Molyneux E, Bacon CM, Bomken S, Rand V. Sporadic and endemic Burkitt lymphoma have frequent FOXO1 mutations but distinct hotspots in the AKT recognition motif. Blood Adv. 2019 Jul 23;3(14):2118–2127. PMCID: PMC6650741
25.
Zhang J, Jima D, Moffitt AB, Liu Q, Czader M, Hsi ED, Fedoriw Y, Dunphy CH, Richards KL, Gill JI, Sun Z, Love C, Scotland P, Lock E, Levy S, Hsu DS, Dunson D, Dave SS. The genomic landscape of mantle cell lymphoma is related to the epigenetically determined chromatin state of normal B cells. Blood. 2014 May 8;123(19):2988–2996.
26.
Trøen G, Wlodarska I, Warsame A, Hernández Llodrà S, De Wolf-Peeters C, Delabie J. NOTCH2 mutations in marginal zone lymphoma. Haematologica. 2008 Jul;93(7):1107–1109.
27.
Gomez F, Fisk B, McMichael JF, Mosior M, Foltz JA, Skidmore ZL, Duncavage EJ, Miller CA, Abel H, Li YS, Russler-Germain DA, Krysiak K, Watkins MP, Ramirez CA, Schmidt A, Martins Rodrigues F, Trani L, Khanna A, Wagner JA, Fulton RS, Fronick CC, O’Laughlin MD, Schappe T, Cashen AF, Mehta-Shah N, Kahl BS, Walker J, Bartlett NL, Griffith M, Fehniger TA, Griffith OL. Ultra-Deep Sequencing Reveals the Mutational Landscape of Classical Hodgkin Lymphoma. Cancer Res Commun. 2023 Nov 15;3(11):2312–2330. PMCID: PMC10648575