-
1
-
-
69249117494
-
The causation of childhood leukemia: a paradox of progress?
-
Greaves M. The causation of childhood leukemia: a paradox of progress?. Discov Med 2006, 6:24-28.
-
(2006)
Discov Med
, vol.6
, pp. 24-28
-
-
Greaves, M.1
-
2
-
-
84876442551
-
Children's Oncology Group's 2013 blueprint for research: acute lymphoblastic leukemia
-
Committee COGALL
-
Hunger S.P., Loh M.L., Whitlock J.A., et al. Children's Oncology Group's 2013 blueprint for research: acute lymphoblastic leukemia. Pediatr Blood Cancer 2013, 60:957-963. Committee COGALL.
-
(2013)
Pediatr Blood Cancer
, vol.60
, pp. 957-963
-
-
Hunger, S.P.1
Loh, M.L.2
Whitlock, J.A.3
-
3
-
-
84867145464
-
Molecular genetics of B-precursor acute lymphoblastic leukemia
-
Mullighan C.G. Molecular genetics of B-precursor acute lymphoblastic leukemia. JClin Invest 2012, 122:3407-3415.
-
(2012)
JClin Invest
, vol.122
, pp. 3407-3415
-
-
Mullighan, C.G.1
-
4
-
-
34249733805
-
High-resolution genomic profiling of childhood ALL reveals novel recurrent genetic lesions affecting pathways involved in lymphocyte differentiation and cell cycle progression
-
Kuiper R.P., Schoenmakers E.F., van Reijmersdal S.V., et al. High-resolution genomic profiling of childhood ALL reveals novel recurrent genetic lesions affecting pathways involved in lymphocyte differentiation and cell cycle progression. Leukemia 2007, 21:1258-1266.
-
(2007)
Leukemia
, vol.21
, pp. 1258-1266
-
-
Kuiper, R.P.1
Schoenmakers, E.F.2
van Reijmersdal, S.V.3
-
5
-
-
34249668665
-
Genome complexity in acute lymphoblastic leukemia is revealed by array-based comparative genomic hybridization
-
Strefford J.C., Worley H., Barber K., et al. Genome complexity in acute lymphoblastic leukemia is revealed by array-based comparative genomic hybridization. Oncogene 2007, 26:4306-4318.
-
(2007)
Oncogene
, vol.26
, pp. 4306-4318
-
-
Strefford, J.C.1
Worley, H.2
Barber, K.3
-
6
-
-
34147224008
-
Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia
-
Mullighan C.G., Goorha S., Radtke I., et al. Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia. Nature 2007, 446:758-764.
-
(2007)
Nature
, vol.446
, pp. 758-764
-
-
Mullighan, C.G.1
Goorha, S.2
Radtke, I.3
-
7
-
-
38349177862
-
Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray
-
Kawamata N., Ogawa S., Zimmermann M., et al. Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray. Blood 2008, 111:776-784.
-
(2008)
Blood
, vol.111
, pp. 776-784
-
-
Kawamata, N.1
Ogawa, S.2
Zimmermann, M.3
-
8
-
-
78649742010
-
Identification of novel cluster groups in pediatric high-risk B-precursor acute lymphoblastic leukemia with gene expression profiling: correlation with genome-wide DNA copy number alterations, clinical characteristics, and outcome
-
Harvey R.C., Mullighan C.G., Wang X., et al. Identification of novel cluster groups in pediatric high-risk B-precursor acute lymphoblastic leukemia with gene expression profiling: correlation with genome-wide DNA copy number alterations, clinical characteristics, and outcome. Blood 2010, 116:4874-4884.
-
(2010)
Blood
, vol.116
, pp. 4874-4884
-
-
Harvey, R.C.1
Mullighan, C.G.2
Wang, X.3
-
9
-
-
80053632883
-
Microarray-based genomic profiling as a diagnostic tool in acute lymphoblastic leukemia
-
Simons A., Stevens-Kroef M., El Idrissi-Zaynoun N., et al. Microarray-based genomic profiling as a diagnostic tool in acute lymphoblastic leukemia. Genes Chromosomes Cancer 2011, 50:969-981.
-
(2011)
Genes Chromosomes Cancer
, vol.50
, pp. 969-981
-
-
Simons, A.1
Stevens-Kroef, M.2
El Idrissi-Zaynoun, N.3
-
10
-
-
79955666046
-
Implementation of high resolution single nucleotide polymorphism array analysis as a clinical test for patients with hematologic malignancies
-
Dougherty M.J., Wilmoth D.M., Tooke L.S., et al. Implementation of high resolution single nucleotide polymorphism array analysis as a clinical test for patients with hematologic malignancies. Cancer Genet 2011, 204:26-38.
-
(2011)
Cancer Genet
, vol.204
, pp. 26-38
-
-
Dougherty, M.J.1
Wilmoth, D.M.2
Tooke, L.S.3
-
11
-
-
84865118132
-
Genetic alterations activating kinase and cytokine receptor signaling in high-risk acute lymphoblastic leukemia
-
Roberts K.G., Morin R.D., Zhang J., et al. Genetic alterations activating kinase and cytokine receptor signaling in high-risk acute lymphoblastic leukemia. Cancer Cell 2012, 22:153-166.
-
(2012)
Cancer Cell
, vol.22
, pp. 153-166
-
-
Roberts, K.G.1
Morin, R.D.2
Zhang, J.3
-
12
-
-
67249146555
-
JAK mutations in high-risk childhood acute lymphoblastic leukemia
-
Mullighan C.G., Zhang J., Harvey R.C., et al. JAK mutations in high-risk childhood acute lymphoblastic leukemia. Proc Natl Acad Sci USA 2009, 106:9414-9418.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 9414-9418
-
-
Mullighan, C.G.1
Zhang, J.2
Harvey, R.C.3
-
13
-
-
58749097408
-
Asubtype of childhood acute lymphoblastic leukaemia with poor treatment outcome: a genome-wide classification study
-
Den Boer M.L., van Slegtenhorst M., De Menezes R.X., et al. Asubtype of childhood acute lymphoblastic leukaemia with poor treatment outcome: a genome-wide classification study. Lancet Oncol 2009, 10:125-134.
-
(2009)
Lancet Oncol
, vol.10
, pp. 125-134
-
-
Den Boer, M.L.1
van Slegtenhorst, M.2
De Menezes, R.X.3
-
14
-
-
82355181594
-
Diagnostic implications of excessive homozygosity detected by SNP-based microarrays: consanguinity, uniparental disomy, and recessive single-gene mutations
-
ix
-
Kearney H.M., Kearney J.B., Conlin L.K. Diagnostic implications of excessive homozygosity detected by SNP-based microarrays: consanguinity, uniparental disomy, and recessive single-gene mutations. Clin Lab Med 2011, 31:595-613. ix.
-
(2011)
Clin Lab Med
, vol.31
, pp. 595-613
-
-
Kearney, H.M.1
Kearney, J.B.2
Conlin, L.K.3
-
15
-
-
69649109364
-
Circos: an information aesthetic for comparative genomics
-
Krzywinski M., Schein J., Birol I., et al. Circos: an information aesthetic for comparative genomics. Genome Res 2009, 19:1639-1645.
-
(2009)
Genome Res
, vol.19
, pp. 1639-1645
-
-
Krzywinski, M.1
Schein, J.2
Birol, I.3
-
16
-
-
78650745577
-
Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia
-
Paulsson K., Forestier E., Lilljebjorn H., et al. Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia. Proc Natl Acad Sci USA 2010, 107:21719-21724.
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, pp. 21719-21724
-
-
Paulsson, K.1
Forestier, E.2
Lilljebjorn, H.3
-
17
-
-
34249065493
-
Specific extra chromosomes occur in a modal number dependent pattern in pediatric acute lymphoblastic leukemia
-
Heerema N.A., Raimondi S.C., Anderson J.R., et al. Specific extra chromosomes occur in a modal number dependent pattern in pediatric acute lymphoblastic leukemia. Genes Chromosomes Cancer 2007, 46:684-693.
-
(2007)
Genes Chromosomes Cancer
, vol.46
, pp. 684-693
-
-
Heerema, N.A.1
Raimondi, S.C.2
Anderson, J.R.3
-
18
-
-
79958724230
-
Analysis of a breakpoint cluster reveals insight into the mechanism of intrachromosomal amplification in a lymphoid malignancy
-
Sinclair P.B., Parker H., An Q., et al. Analysis of a breakpoint cluster reveals insight into the mechanism of intrachromosomal amplification in a lymphoid malignancy. Hum Mol Genet 2011, 20:2591-2602.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 2591-2602
-
-
Sinclair, P.B.1
Parker, H.2
An, Q.3
-
19
-
-
79959510774
-
Genomic characterization implicates iAMP21 as a likely primary genetic event in childhood B-cell precursor acute lymphoblastic leukemia
-
Rand V., Parker H., Russell L.J., et al. Genomic characterization implicates iAMP21 as a likely primary genetic event in childhood B-cell precursor acute lymphoblastic leukemia. Blood 2011, 117:6848-6855.
-
(2011)
Blood
, vol.117
, pp. 6848-6855
-
-
Rand, V.1
Parker, H.2
Russell, L.J.3
-
20
-
-
84897568967
-
Intrachromosomal amplification of chromosome 21 is associated with inferior outcomes in children with acute lymphoblastic leukemia treated in contemporary standard-risk children's oncology group studies: a report from the children's oncology group
-
Heerema N.A., Carroll A.J., Devidas M., et al. Intrachromosomal amplification of chromosome 21 is associated with inferior outcomes in children with acute lymphoblastic leukemia treated in contemporary standard-risk children's oncology group studies: a report from the children's oncology group. JClin Oncol 2013, 31:3397-3402.
-
(2013)
JClin Oncol
, vol.31
, pp. 3397-3402
-
-
Heerema, N.A.1
Carroll, A.J.2
Devidas, M.3
-
21
-
-
33947131584
-
Intrachromosomal amplification of chromosome 21 (iAMP21) may arise from a breakage-fusion-bridge cycle
-
Robinson H.M., Harrison C.J., Moorman A.V., et al. Intrachromosomal amplification of chromosome 21 (iAMP21) may arise from a breakage-fusion-bridge cycle. Genes Chromosomes Cancer 2007, 46:318-326.
-
(2007)
Genes Chromosomes Cancer
, vol.46
, pp. 318-326
-
-
Robinson, H.M.1
Harrison, C.J.2
Moorman, A.V.3
-
22
-
-
33947257508
-
Prognosis of children with acute lymphoblastic leukemia (ALL) and intrachromosomal amplification of chromosome 21 (iAMP21)
-
Party UKMRCNCRICLW
-
Moorman A.V., Richards S.M., Robinson H.M., et al. Prognosis of children with acute lymphoblastic leukemia (ALL) and intrachromosomal amplification of chromosome 21 (iAMP21). Blood 2007, 109:2327-2330. Party UKMRCNCRICLW.
-
(2007)
Blood
, vol.109
, pp. 2327-2330
-
-
Moorman, A.V.1
Richards, S.M.2
Robinson, H.M.3
-
23
-
-
33744474290
-
Complex genomic alterations and gene expression in acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21
-
Strefford J.C., van Delft F.W., Robinson H.M., et al. Complex genomic alterations and gene expression in acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21. Proc Natl Acad Sci USA 2006, 103:8167-8172.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 8167-8172
-
-
Strefford, J.C.1
van Delft, F.W.2
Robinson, H.M.3
-
24
-
-
84899979360
-
An international study of intrachromosomal amplification of chromosome 21 (iAMP21): cytogenetic characterization and outcome
-
Harrison C.J., Moorman A.V., Schwab C., et al. An international study of intrachromosomal amplification of chromosome 21 (iAMP21): cytogenetic characterization and outcome. Leukemia 2014, 28:1015-1021.
-
(2014)
Leukemia
, vol.28
, pp. 1015-1021
-
-
Harrison, C.J.1
Moorman, A.V.2
Schwab, C.3
-
25
-
-
84897528140
-
Constitutional and somatic rearrangement of chromosome 21 in acute lymphoblastic leukaemia
-
Li Y., Schwab C., Ryan S.L., et al. Constitutional and somatic rearrangement of chromosome 21 in acute lymphoblastic leukaemia. Nature 2014, 508:98-102.
-
(2014)
Nature
, vol.508
, pp. 98-102
-
-
Li, Y.1
Schwab, C.2
Ryan, S.L.3
-
26
-
-
84874647204
-
The genomic landscape of hypodiploid acute lymphoblastic leukemia
-
Holmfeldt L., Wei L., Diaz-Flores E., et al. The genomic landscape of hypodiploid acute lymphoblastic leukemia. Nat Genet 2013, 45:242-252.
-
(2013)
Nat Genet
, vol.45
, pp. 242-252
-
-
Holmfeldt, L.1
Wei, L.2
Diaz-Flores, E.3
-
27
-
-
84873566348
-
Loss of chromosomes is the primary event in near-haploid and low-hypodiploid acute lymphoblastic leukemia
-
Safavi S., Forestier E., Golovleva I., et al. Loss of chromosomes is the primary event in near-haploid and low-hypodiploid acute lymphoblastic leukemia. Leukemia 2013, 27:248-250.
-
(2013)
Leukemia
, vol.27
, pp. 248-250
-
-
Safavi, S.1
Forestier, E.2
Golovleva, I.3
-
28
-
-
2942563738
-
Three distinct subgroups of hypodiploidy in acute lymphoblastic leukaemia
-
Childhood and Adult Leukaemia Working Parties
-
Harrison C.J., Moorman A.V., Broadfield Z.J., et al. Three distinct subgroups of hypodiploidy in acute lymphoblastic leukaemia. Br J Haematol 2004, 125:552-559. Childhood and Adult Leukaemia Working Parties.
-
(2004)
Br J Haematol
, vol.125
, pp. 552-559
-
-
Harrison, C.J.1
Moorman, A.V.2
Broadfield, Z.J.3
-
29
-
-
58749109707
-
Deletion of IKZF1 and prognosis in acute lymphoblastic leukemia
-
Children's Oncology Group
-
Mullighan C.G., Su X., Zhang J., et al. Deletion of IKZF1 and prognosis in acute lymphoblastic leukemia. NEngl J Med 2009, 360:470-480. Children's Oncology Group.
-
(2009)
NEngl J Med
, vol.360
, pp. 470-480
-
-
Mullighan, C.G.1
Su, X.2
Zhang, J.3
-
30
-
-
84891850778
-
An intragenic ERG deletion is a marker of an oncogenic subtype of B-cell precursor acute lymphoblastic leukemia with a favorable outcome despite frequent IKZF1 deletions
-
Clappier E., Auclerc M.F., Rapion J., et al. An intragenic ERG deletion is a marker of an oncogenic subtype of B-cell precursor acute lymphoblastic leukemia with a favorable outcome despite frequent IKZF1 deletions. Leukemia 2014, 28:70-77.
-
(2014)
Leukemia
, vol.28
, pp. 70-77
-
-
Clappier, E.1
Auclerc, M.F.2
Rapion, J.3
-
31
-
-
84872457525
-
Tyrosine kinome sequencing of pediatric acute lymphoblastic leukemia: a report from the Children's Oncology Group TARGET Project
-
Loh M.L., Zhang J., Harvey R.C., et al. Tyrosine kinome sequencing of pediatric acute lymphoblastic leukemia: a report from the Children's Oncology Group TARGET Project. Blood 2013, 121:485-488.
-
(2013)
Blood
, vol.121
, pp. 485-488
-
-
Loh, M.L.1
Zhang, J.2
Harvey, R.C.3
-
32
-
-
33947430093
-
Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: a Nordic series of 245 cases and review of the literature
-
Nordic Society of Pediatric Hematology and Oncology (NOPHO); Swedish Cytogenetic Leukemia Study Group (SCLSG); NOPHO Leukemia Cytogenetic Study Group (NLCSG)
-
Forestier E., Andersen M.K., Autio K., et al. Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: a Nordic series of 245 cases and review of the literature. Genes Chromosomes Cancer 2007, 46:440-450. Nordic Society of Pediatric Hematology and Oncology (NOPHO); Swedish Cytogenetic Leukemia Study Group (SCLSG); NOPHO Leukemia Cytogenetic Study Group (NLCSG).
-
(2007)
Genes Chromosomes Cancer
, vol.46
, pp. 440-450
-
-
Forestier, E.1
Andersen, M.K.2
Autio, K.3
-
33
-
-
79959463542
-
Clonal origins of relapse in ETV6-RUNX1 acute lymphoblastic leukemia
-
van Delft F.W., Horsley S., Colman S., et al. Clonal origins of relapse in ETV6-RUNX1 acute lymphoblastic leukemia. Blood 2011, 117:6247-6254.
-
(2011)
Blood
, vol.117
, pp. 6247-6254
-
-
van Delft, F.W.1
Horsley, S.2
Colman, S.3
-
34
-
-
77954516863
-
Rearrangement of CRLF2 is associated with mutation of JAK kinases, alteration of IKZF1, Hispanic/Latino ethnicity, and a poor outcome in pediatric B-progenitor acute lymphoblastic leukemia
-
Harvey R.C., Mullighan C.G., Chen I.M., et al. Rearrangement of CRLF2 is associated with mutation of JAK kinases, alteration of IKZF1, Hispanic/Latino ethnicity, and a poor outcome in pediatric B-progenitor acute lymphoblastic leukemia. Blood 2010, 115:5312-5321.
-
(2010)
Blood
, vol.115
, pp. 5312-5321
-
-
Harvey, R.C.1
Mullighan, C.G.2
Chen, I.M.3
-
35
-
-
70350680415
-
Rearrangement of CRLF2 in B-progenitor- and Down syndrome-associated acute lymphoblastic leukemia
-
Mullighan C.G., Collins-Underwood J.R., Phillips L.A., et al. Rearrangement of CRLF2 in B-progenitor- and Down syndrome-associated acute lymphoblastic leukemia. Nat Genet 2009, 41:1243-1246.
-
(2009)
Nat Genet
, vol.41
, pp. 1243-1246
-
-
Mullighan, C.G.1
Collins-Underwood, J.R.2
Phillips, L.A.3
-
36
-
-
77954659221
-
IKZF1 deletions predict relapse in uniformly treated pediatric precursor B-ALL
-
Kuiper R.P., Waanders E., van der Velden V.H., et al. IKZF1 deletions predict relapse in uniformly treated pediatric precursor B-ALL. Leukemia 2010, 24:1258-1264.
-
(2010)
Leukemia
, vol.24
, pp. 1258-1264
-
-
Kuiper, R.P.1
Waanders, E.2
van der Velden, V.H.3
|