-
1
-
-
59449095868
-
Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype
-
Akagi T, Ogawa S, Dugas M, Kawamata N, Yamamoto G, Nannya Y, Sanada M, Miller CW, Yung A, Schnittger S, Haferlach T, Haferlach C, Koeffler HP. 2009a. Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype. Haematologica 94: 213-223.
-
(2009)
Haematologica
, vol.94
, pp. 213-223
-
-
Akagi, T.1
Ogawa, S.2
Dugas, M.3
Kawamata, N.4
Yamamoto, G.5
Nannya, Y.6
Sanada, M.7
Miller, C.W.8
Yung, A.9
Schnittger, S.10
Haferlach, T.11
Haferlach, C.12
Koeffler, H.P.13
-
2
-
-
61849146788
-
Hidden abnormalities and novel classification of t(15;17) acute promyelocytic leukemia (APL) based on genomic alterations
-
Akagi T, Shih LY, Kato M, Kawamata N, Yamamoto G, Sanada M, Okamoto R, Miller CW, Liang DC, Ogawa S, Koeffler HP. 2009b. Hidden abnormalities and novel classification of t(15;17) acute promyelocytic leukemia (APL) based on genomic alterations. Blood 113: 1741-1748.
-
(2009)
Blood
, vol.113
, pp. 1741-1748
-
-
Akagi, T.1
Shih, L.Y.2
Kato, M.3
Kawamata, N.4
Yamamoto, G.5
Sanada, M.6
Okamoto, R.7
Miller, C.W.8
Liang, D.C.9
Ogawa, S.10
Koeffler, H.P.11
-
3
-
-
70349116956
-
Single nucleotide polymorphism genomic arrays analysis of t(8;21) acute myeloid leukemia cells
-
Akagi T, Shih LY, Ogawa S, Gerss J, Moore SR, Schreck R, Kawamata N, Liang DC, Sanada M, Nannya Y, Deneberg S, Zachariadis V, Nordgren A, Song JH, Dugas M, Lehmann S, Koeffler HP. 2009c. Single nucleotide polymorphism genomic arrays analysis of t(8;21) acute myeloid leukemia cells. Haematologica 94: 1301-1306.
-
(2009)
Haematologica
, vol.94
, pp. 1301-1306
-
-
Akagi, T.1
Shih, L.Y.2
Ogawa, S.3
Gerss, J.4
Moore, S.R.5
Schreck, R.6
Kawamata, N.7
Liang, D.C.8
Sanada, M.9
Nannya, Y.10
Deneberg, S.11
Zachariadis, V.12
Nordgren, A.13
Song, J.H.14
Dugas, M.15
Lehmann, S.16
Koeffler, H.P.17
-
4
-
-
77957923389
-
Broad copy neutral-loss of heterozygosity regions and rare recurring copy number abnormalities in normal karyotype-acute myeloid leukemia genomes
-
Barresi V, Romano A, Musso N, Capizzi C, Consoli C, Martelli MP, Palumbo G, Di Raimondo F, Condorelli DF. 2010. Broad copy neutral-loss of heterozygosity regions and rare recurring copy number abnormalities in normal karyotype-acute myeloid leukemia genomes. Genes Chromosomes Cancer 49: 1014-1023.
-
(2010)
Genes Chromosomes Cancer
, vol.49
, pp. 1014-1023
-
-
Barresi, V.1
Romano, A.2
Musso, N.3
Capizzi, C.4
Consoli, C.5
Martelli, M.P.6
Palumbo, G.7
Di Raimondo, F.8
Condorelli, D.F.9
-
5
-
-
77954583280
-
High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression
-
Boultwood J, Perry J, Zaman R, Fernandez-Santamaria C, Littlewood T, Kusec R, Pellagatti A, Wang L, Clark RE, Wainscoat JS. 2010. High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression. Leukemia 24: 1139-1145.
-
(2010)
Leukemia
, vol.24
, pp. 1139-1145
-
-
Boultwood, J.1
Perry, J.2
Zaman, R.3
Fernandez-Santamaria, C.4
Littlewood, T.5
Kusec, R.6
Pellagatti, A.7
Wang, L.8
Clark, R.E.9
Wainscoat, J.S.10
-
6
-
-
84856400546
-
Array-based cytogenetic approaches in acute myeloid leukemia: Clinical impact and biological insights
-
Bullinger L, Frohling S. 2012. Array-based cytogenetic approaches in acute myeloid leukemia: Clinical impact and biological insights. Semin Oncol 39: 37-46.
-
(2012)
Semin Oncol
, vol.39
, pp. 37-46
-
-
Bullinger, L.1
Frohling, S.2
-
7
-
-
76749153827
-
Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution single-nucleotide polymorphism analysis
-
Bullinger L, Kronke J, Schon C, Radtke I, Urlbauer K, Botzenhardt U, Gaidzik V, Cario A, Senger C, Schlenk RF, Downing JR, Holzmann K, Dohner K, Dohner H. 2010. Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution single-nucleotide polymorphism analysis. Leukemia 24: 438-449.
-
(2010)
Leukemia
, vol.24
, pp. 438-449
-
-
Bullinger, L.1
Kronke, J.2
Schon, C.3
Radtke, I.4
Urlbauer, K.5
Botzenhardt, U.6
Gaidzik, V.7
Cario, A.8
Senger, C.9
Schlenk, R.F.10
Downing, J.R.11
Holzmann, K.12
Dohner, K.13
Dohner, H.14
-
8
-
-
77954947022
-
Deletions of the derivative chromosome 9 do not influence the response and the outcome of chronic myeloid leukemia in early chronic phase treated with imatinib mesylate: GIMEMA CML Working Party analysis
-
Castagnetti F, Testoni N, Luatti S, Marzocchi G, Mancini M, Kerim S, Giugliano E, Albano F, Cuneo A, Abruzzese E, Martino B, Palandri F, Amabile M, Iacobucci I, Alimena G, Pane F, Martinelli G, Saglio G, Baccarani M, Rosti G. 2010. Deletions of the derivative chromosome 9 do not influence the response and the outcome of chronic myeloid leukemia in early chronic phase treated with imatinib mesylate: GIMEMA CML Working Party analysis. J Clin Oncol 28: 2748-2754.
-
(2010)
J Clin Oncol
, vol.28
, pp. 2748-2754
-
-
Castagnetti, F.1
Testoni, N.2
Luatti, S.3
Marzocchi, G.4
Mancini, M.5
Kerim, S.6
Giugliano, E.7
Albano, F.8
Cuneo, A.9
Abruzzese, E.10
Martino, B.11
Palandri, F.12
Amabile, M.13
Iacobucci, I.14
Alimena, G.15
Pane, F.16
Martinelli, G.17
Saglio, G.18
Baccarani, M.19
Rosti, G.20
more..
-
9
-
-
79955666046
-
Implementation of high resolution single nucleotide polymorphism array analysis as a clinical test for patients with hematologic malignancies
-
Dougherty MJ, Wilmoth DM, Tooke LS, Shaikh TH, Gai X, Hakonarson H, Biegel JA. 2011. Implementation of high resolution single nucleotide polymorphism array analysis as a clinical test for patients with hematologic malignancies. Cancer Genet 204: 26-38.
-
(2011)
Cancer Genet
, vol.204
, pp. 26-38
-
-
Dougherty, M.J.1
Wilmoth, D.M.2
Tooke, L.S.3
Shaikh, T.H.4
Gai, X.5
Hakonarson, H.6
Biegel, J.A.7
-
10
-
-
33845350493
-
Single nucleotide polymorphism array analysis of cancer
-
Dutt A, Beroukhim R. 2007. Single nucleotide polymorphism array analysis of cancer. Curr Opin Oncol 19: 43-49.
-
(2007)
Curr Opin Oncol
, vol.19
, pp. 43-49
-
-
Dutt, A.1
Beroukhim, R.2
-
11
-
-
84870981318
-
Near haploid acute lymphoblastic leukaemia. Atlas Genet Cytogenet Oncol Haematol
-
June 1999. URL:(access date Aug 28
-
Gibbons B. Near haploid acute lymphoblastic leukaemia. Atlas Genet Cytogenet Oncol Haematol. June 1999. URL: http://AtlasGeneticsOncology.org/Anomalies/nearhaploidID1145.html (access date Aug 28, 2012).
-
(2012)
-
-
Gibbons, B.1
-
12
-
-
35448931911
-
Detection of cryptic chromosomal lesions including acquired segmental uniparental disomy in advanced and low-risk myelodysplastic syndromes
-
Gondek LP, Haddad AS, O'Keefe CL, Tiu R, Wlodarski MW, Sekeres MA, Theil KS, Maciejewski JP. 2007. Detection of cryptic chromosomal lesions including acquired segmental uniparental disomy in advanced and low-risk myelodysplastic syndromes. Exp Hematol 35: 1728-1738.
-
(2007)
Exp Hematol
, vol.35
, pp. 1728-1738
-
-
Gondek, L.P.1
Haddad, A.S.2
O'Keefe, C.L.3
Tiu, R.4
Wlodarski, M.W.5
Sekeres, M.A.6
Theil, K.S.7
Maciejewski, J.P.8
-
13
-
-
25844451158
-
Frequent loss of heterozygosity without loss of genetic material in acute myeloid leukemia with a normal karyotype
-
Gorletta TA, Gasparini P, D'Elios MM, Trubia M, Pelicci PG, Di Fiore PP. 2005. Frequent loss of heterozygosity without loss of genetic material in acute myeloid leukemia with a normal karyotype. Genes Chromosomes Cancer 44: 334-337.
-
(2005)
Genes Chromosomes Cancer
, vol.44
, pp. 334-337
-
-
Gorletta, T.A.1
Gasparini, P.2
D'Elios, M.M.3
Trubia, M.4
Pelicci, P.G.5
Di Fiore, P.P.6
-
14
-
-
81255170298
-
Diagnostic and prognostic value of cytogenetics in acute myeloid leukemia
-
Grimwade D and Mrozek K. 2011. Diagnostic and prognostic value of cytogenetics in acute myeloid leukemia. Hematol Oncol Clin North Am 25: 1135-1161.
-
(2011)
Hematol Oncol Clin North Am
, vol.25
, pp. 1135-1161
-
-
Grimwade, D.1
Mrozek, K.2
-
15
-
-
44449151696
-
Novel regions of acquired uniparental disomy discovered in acute myeloid leukemia
-
Gupta M, Raghavan M, Gale RE, Chelala C, Allen C, Molloy G, Chaplin T, Linch DC, Cazier JB, Young BD. 2008. Novel regions of acquired uniparental disomy discovered in acute myeloid leukemia. Genes Chromosomes Cancer 47: 729-739.
-
(2008)
Genes Chromosomes Cancer
, vol.47
, pp. 729-739
-
-
Gupta, M.1
Raghavan, M.2
Gale, R.E.3
Chelala, C.4
Allen, C.5
Molloy, G.6
Chaplin, T.7
Linch, D.C.8
Cazier, J.B.9
Young, B.D.10
-
16
-
-
65549158870
-
The rewards and challenges of array-based karyotyping for clinical oncology applications
-
Hagenkord JM, Chang CC. 2009. The rewards and challenges of array-based karyotyping for clinical oncology applications. Leukemia 23: 829-833.
-
(2009)
Leukemia
, vol.23
, pp. 829-833
-
-
Hagenkord, J.M.1
Chang, C.C.2
-
18
-
-
70349306857
-
Accurate detection of uniparental disomy and microdeletions by SNP array analysis in myelodysplastic syndromes with normal cytogenetics
-
Heinrichs S, Kulkarni RV, Bueso-Ramos CE, Levine RL, Loh ML, Li C, Neuberg D, Kornblau SM, Issa JP, Gilliland DG, Garcia-Manero G, Kantarjian HM, Estey EH, Look AT. 2009. Accurate detection of uniparental disomy and microdeletions by SNP array analysis in myelodysplastic syndromes with normal cytogenetics. Leukemia 23: 1605-1613.
-
(2009)
Leukemia
, vol.23
, pp. 1605-1613
-
-
Heinrichs, S.1
Kulkarni, R.V.2
Bueso-Ramos, C.E.3
Levine, R.L.4
Loh, M.L.5
Li, C.6
Neuberg, D.7
Kornblau, S.M.8
Issa, J.P.9
Gilliland, D.G.10
Garcia-Manero, G.11
Kantarjian, H.M.12
Estey, E.H.13
Look, A.T.14
-
19
-
-
84855203185
-
Genome-wide high density single-nucleotide polymorphism array-based karyotyping improves detection of clonal aberrations including der(9) deletion, but does not predict treatment outcomes after imatinib therapy in chronic myeloid leukemia
-
Huh J, Jung CW, Kim JW, Kim HJ, Kim SH, Shin MG, Kim YK, Kim HJ, Suh JS, Moon JH, Sohn SK, Nam GH, Lee JE, Kim DH. 2011. Genome-wide high density single-nucleotide polymorphism array-based karyotyping improves detection of clonal aberrations including der(9) deletion, but does not predict treatment outcomes after imatinib therapy in chronic myeloid leukemia. Ann Hematol 90: 1255-1264.
-
(2011)
Ann Hematol
, vol.90
, pp. 1255-1264
-
-
Huh, J.1
Jung, C.W.2
Kim, J.W.3
Kim, H.J.4
Kim, S.H.5
Shin, M.G.6
Kim, Y.K.7
Kim, H.J.8
Suh, J.S.9
Moon, J.H.10
Sohn, S.K.11
Nam, G.H.12
Lee, J.E.13
Kim, D.H.14
-
20
-
-
84866752027
-
A genome-wide single-nucleotide polymorphism-array can improve the prognostic stratification of the core binding factor acute myeloid leukemia
-
on behalf of AML/MDS working party, Korean Society of Hematology. Jun 8. doi: 10.1002/ajh.23281.
-
Huh J, Kim HJ, Jung CW, Kim HJ, Kim SH, Kim YK, Kim HJ, Shin MG, Moon JH, Sohn SK, Kim SH, Lee WS, Won JH, Mun YC, Kim H, Park J, Min WS, Kim DH; on behalf of AML/MDS working party, Korean Society of Hematology. 2012. A genome-wide single-nucleotide polymorphism-array can improve the prognostic stratification of the core binding factor acute myeloid leukemia. Am J Hematol. Jun 8. doi: 10.1002/ajh.23281.
-
(2012)
Am J Hematol.
-
-
Huh, J.1
Kim, H.J.2
Jung, C.W.3
Kim, H.J.4
Kim, S.H.5
Kim, Y.K.6
Kim, H.J.7
Shin, M.G.8
Moon, J.H.9
Sohn, S.K.10
Kim, S.H.11
Lee, W.S.12
Won, J.H.13
Mun, Y.C.14
Kim, H.15
Park, J.16
Min, W.S.17
Kim, D.H.18
-
21
-
-
84870975879
-
-
Huret JL. 2012. Available at: http://atlasgeneticsoncology.org/Anomalies/nearhaploidID1145.html.
-
(2012)
-
-
Huret, J.L.1
-
22
-
-
38349177862
-
Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray
-
Kawamata N, Ogawa S, Zimmermann M, Kato M, Sanada M, Hemminki K, Yamatomo G, Nannya Y, Koehler R, Flohr T, Miller CW, Harbott J, Ludwig WD, Stanulla M, Schrappe M, Bartram CR, Koeffler HP. 2008. Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray. Blood 111: 776-784.
-
(2008)
Blood
, vol.111
, pp. 776-784
-
-
Kawamata, N.1
Ogawa, S.2
Zimmermann, M.3
Kato, M.4
Sanada, M.5
Hemminki, K.6
Yamatomo, G.7
Nannya, Y.8
Koehler, R.9
Flohr, T.10
Miller, C.W.11
Harbott, J.12
Ludwig, W.D.13
Stanulla, M.14
Schrappe, M.15
Bartram, C.R.16
Koeffler, H.P.17
-
23
-
-
84857232746
-
Older patients with normal karyotype acute myeloid leukemia have a higher rate of genomic changes compared to young patients as determined by SNP array analysis
-
Koren-Michowitz M, Sato-Otsubo A, Nagler A, Haferlach T, Ogawa S, Koeffler HP. 2012. Older patients with normal karyotype acute myeloid leukemia have a higher rate of genomic changes compared to young patients as determined by SNP array analysis. Leuk Res 36: 467-473.
-
(2012)
Leuk Res
, vol.36
, pp. 467-473
-
-
Koren-Michowitz, M.1
Sato-Otsubo, A.2
Nagler, A.3
Haferlach, T.4
Ogawa, S.5
Koeffler, H.P.6
-
24
-
-
84863399678
-
High-resolution genomic profiling of adult and pediatric core-binding factor acute myeloid leukemia reveals new recurrent genomic alterations
-
Kuhn MW, Radtke I, Bullinger L, Goorha S, Cheng J, Edelmann J, Gohlke J, Su X, Paschka P, Pounds S, Krauter J, Ganser A, Quessar A, Ribeiro R, Gaidzik VI, Shurtleff S, Kronke J, Holzmann K, Ma J, Schlenk RF, Rubnitz JE, Dohner K, Dohner H, Downing JR. 2012. High-resolution genomic profiling of adult and pediatric core-binding factor acute myeloid leukemia reveals new recurrent genomic alterations. Blood 119: e67-e75.
-
(2012)
Blood
, vol.119
-
-
Kuhn, M.W.1
Radtke, I.2
Bullinger, L.3
Goorha, S.4
Cheng, J.5
Edelmann, J.6
Gohlke, J.7
Su, X.8
Paschka, P.9
Pounds, S.10
Krauter, J.11
Ganser, A.12
Quessar, A.13
Ribeiro, R.14
Gaidzik, V.I.15
Shurtleff, S.16
Kronke, J.17
Holzmann, K.18
Ma, J.19
Schlenk, R.F.20
Rubnitz, J.E.21
Dohner, K.22
Dohner, H.23
Downing, J.R.24
more..
-
25
-
-
79959332080
-
The consequences of uniparental disomy and copy number neutral loss-of-heterozygosity during human development and cancer
-
Lapunzina P, Monk D. 2011. The consequences of uniparental disomy and copy number neutral loss-of-heterozygosity during human development and cancer. Biol Cell 103: 303-317.
-
(2011)
Biol Cell
, vol.103
, pp. 303-317
-
-
Lapunzina, P.1
Monk, D.2
-
26
-
-
68949213291
-
Application of array-based whole genome scanning technologies as a cytogenetic tool in haematological malignancies
-
Maciejewski JP, Tiu RV, O'Keefe C. 2009. Application of array-based whole genome scanning technologies as a cytogenetic tool in haematological malignancies. Br J Haematol 146: 479-488.
-
(2009)
Br J Haematol
, vol.146
, pp. 479-488
-
-
Maciejewski, J.P.1
Tiu, R.V.2
O'Keefe, C.3
-
27
-
-
79959214591
-
Pathogenesis and consequences of uniparental disomy in cancer
-
Makishima H, Maciejewski JP. 2011. Pathogenesis and consequences of uniparental disomy in cancer. Clin Cancer Res 17: 3913-3923.
-
(2011)
Clin Cancer Res
, vol.17
, pp. 3913-3923
-
-
Makishima, H.1
Maciejewski, J.P.2
-
28
-
-
76749133549
-
FISH and SNP-A karyotyping in myelodysplastic syndromes: Improving cytogenetic detection of del(5q), monosomy 7, del(7q), trisomy 8 and del(20q)
-
Makishima H, Rataul M, Gondek LP, Huh J, Cook JR, Theil KS, Sekeres MA, Kuczkowski E, O'Keefe C, Maciejewski JP. 2010. FISH and SNP-A karyotyping in myelodysplastic syndromes: Improving cytogenetic detection of del(5q), monosomy 7, del(7q), trisomy 8 and del(20q). Leuk Res 34: 447-453.
-
(2010)
Leuk Res
, vol.34
, pp. 447-453
-
-
Makishima, H.1
Rataul, M.2
Gondek, L.P.3
Huh, J.4
Cook, J.R.5
Theil, K.S.6
Sekeres, M.A.7
Kuczkowski, E.8
O'Keefe, C.9
Maciejewski, J.P.10
-
29
-
-
34547749829
-
The application of single nucleotide polymorphism microarrays in cancer research
-
Mao X, Young BD, Lu YJ. 2007. The application of single nucleotide polymorphism microarrays in cancer research. Curr Genomics 8: 219-228.
-
(2007)
Curr Genomics
, vol.8
, pp. 219-228
-
-
Mao, X.1
Young, B.D.2
Lu, Y.J.3
-
30
-
-
84857997094
-
From cryptic chromosomal lesions to pathologically relevant genes: Integration of SNP-array with gene expression profiling in myelodysplastic syndrome with normal karyotype
-
Merkerova MD, Bystricka D, Belickova M, Krejcik Z, Zemanova Z, Polak J, Hajkova H, Brezinova J, Michalova K, Cermak J. 2012. From cryptic chromosomal lesions to pathologically relevant genes: Integration of SNP-array with gene expression profiling in myelodysplastic syndrome with normal karyotype. Genes Chromosomes Cancer 51: 419-428.
-
(2012)
Genes Chromosomes Cancer
, vol.51
, pp. 419-428
-
-
Merkerova, M.D.1
Bystricka, D.2
Belickova, M.3
Krejcik, Z.4
Zemanova, Z.5
Polak, J.6
Hajkova, H.7
Brezinova, J.8
Michalova, K.9
Cermak, J.10
-
31
-
-
77952032690
-
Consensus statement: Chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies
-
Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, Church DM, Crolla JA, Eichler EE, Epstein CJ, Faucett WA, Feuk L, Friedman JM, Hamosh A, Jackson L, Kaminsky EB, Kok K, Krantz ID, Kuhn RM, Lee C, Ostell JM, Rosenberg C, Scherer SW, Spinner NB, Stavropoulos DJ, Tepperberg JH, Thorland EC, Vermeesch JR, Waggoner DJ, Watson MS, Martin CL, Ledbetter DH. 2010. Consensus statement: Chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am J Hum Genet 86: 749-764.
-
(2010)
Am J Hum Genet
, vol.86
, pp. 749-764
-
-
Miller, D.T.1
Adam, M.P.2
Aradhya, S.3
Biesecker, L.G.4
Brothman, A.R.5
Carter, N.P.6
Church, D.M.7
Crolla, J.A.8
Eichler, E.E.9
Epstein, C.J.10
Faucett, W.A.11
Feuk, L.12
Friedman, J.M.13
Hamosh, A.14
Jackson, L.15
Kaminsky, E.B.16
Kok, K.17
Krantz, I.D.18
Kuhn, R.M.19
Lee, C.20
Ostell, J.M.21
Rosenberg, C.22
Scherer, S.W.23
Spinner, N.B.24
Stavropoulos, D.J.25
Tepperberg, J.H.26
Thorland, E.C.27
Vermeesch, J.R.28
Waggoner, D.J.29
Watson, M.S.30
Martin, C.L.31
Ledbetter, D.H.32
more..
-
32
-
-
36148993604
-
Prevalence and prognostic significance of allelic imbalance by single-nucleotide polymorphism analysis in low-risk myelodysplastic syndromes
-
Mohamedali A, Gaken J, Twine NA, Ingram W, Westwood N, Lea NC, Hayden J, Donaldson N, Aul C, Gattermann N, Giagounidis A, Germing U, List AF, Mufti GJ. 2007. Prevalence and prognostic significance of allelic imbalance by single-nucleotide polymorphism analysis in low-risk myelodysplastic syndromes. Blood 110: 3365-3373.
-
(2007)
Blood
, vol.110
, pp. 3365-3373
-
-
Mohamedali, A.1
Gaken, J.2
Twine, N.A.3
Ingram, W.4
Westwood, N.5
Lea, N.C.6
Hayden, J.7
Donaldson, N.8
Aul, C.9
Gattermann, N.10
Giagounidis, A.11
Germing, U.12
List, A.F.13
Mufti, G.J.14
-
33
-
-
79551699535
-
New strategies in acute lymphoblastic leukemia: Translating advances in genomics into clinical practice
-
Mullighan CG. 2011. New strategies in acute lymphoblastic leukemia: Translating advances in genomics into clinical practice. Clin Cancer Res 17: 396-400.
-
(2011)
Clin Cancer Res
, vol.17
, pp. 396-400
-
-
Mullighan, C.G.1
-
34
-
-
34147224008
-
Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia
-
Mullighan CG, Goorha S, Radtke I, Miller CB, Coustan-Smith E, Dalton JD, Girtman K, Mathew S, Ma J, Pounds SB, Su X, Pui CH, Relling MV, Evans WE, Shurtleff SA, Downing JR. 2007. Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia. Nature 446: 758-764.
-
(2007)
Nature
, vol.446
, pp. 758-764
-
-
Mullighan, C.G.1
Goorha, S.2
Radtke, I.3
Miller, C.B.4
Coustan-Smith, E.5
Dalton, J.D.6
Girtman, K.7
Mathew, S.8
Ma, J.9
Pounds, S.B.10
Su, X.11
Pui, C.H.12
Relling, M.V.13
Evans, W.E.14
Shurtleff, S.A.15
Downing, J.R.16
-
35
-
-
58749109707
-
Deletion of IKZF1 and prognosis in acute lymphoblastic leukemia
-
Children's Oncology Group
-
Mullighan CG, Su X, Zhang J, Radtke I, Phillips LA, Miller CB, Ma J, Liu W, Cheng C, Schulman BA, Harvey RC, Chen IM, Clifford RJ, Carroll WL, Reaman G, Bowman WP, Devidas M, Gerhard DS, Yang W, Relling MV, Shurtleff SA, Campana D, Borowitz MJ, Pui CH, Smith M, Hunger SP, Willman CL, Downing JR, Children's Oncology Group. 2009. Deletion of IKZF1 and prognosis in acute lymphoblastic leukemia. New Engl J Med 360: 470-480.
-
(2009)
New Engl J Med
, vol.360
, pp. 470-480
-
-
Mullighan, C.G.1
Su, X.2
Zhang, J.3
Radtke, I.4
Phillips, L.A.5
Miller, C.B.6
Ma, J.7
Liu, W.8
Cheng, C.9
Schulman, B.A.10
Harvey, R.C.11
Chen, I.M.12
Clifford, R.J.13
Carroll, W.L.14
Reaman, G.15
Bowman, W.P.16
Devidas, M.17
Gerhard, D.S.18
Yang, W.19
Relling, M.V.20
Shurtleff, S.A.21
Campana, D.22
Borowitz, M.J.23
Pui, C.H.24
Smith, M.25
Hunger, S.P.26
Willman, C.L.27
Downing, J.R.28
more..
-
36
-
-
58149194736
-
Genome-wide DNA-mapping of CD34+ cells from patients with myelodysplastic syndrome using 500K SNP arrays identifies significant regions of deletion and uniparental disomy
-
Nowak D, Nolte F, Mossner M, Nowak V, Baldus CD, Hopfer O, Noll S, Thiel E, Wagner F, Hofmann WK. 2009. Genome-wide DNA-mapping of CD34+ cells from patients with myelodysplastic syndrome using 500K SNP arrays identifies significant regions of deletion and uniparental disomy. Exp Hematol 37: 215-224.
-
(2009)
Exp Hematol
, vol.37
, pp. 215-224
-
-
Nowak, D.1
Nolte, F.2
Mossner, M.3
Nowak, V.4
Baldus, C.D.5
Hopfer, O.6
Noll, S.7
Thiel, E.8
Wagner, F.9
Hofmann, W.K.10
-
37
-
-
77649222741
-
SNP array analysis of tyrosine kinase inhibitor-resistant chronic myeloid leukemia identifies heterogeneous secondary genomic alterations
-
Nowak D, Ogawa S, Muschen M, Kato M, Kawamata N, Meixel A, Nowak V, Kim HS, Kang S, Paquette R, Chang MS, Thoennissen NH, Mossner M, Hofmann WK, Kohlmann A, Weiss T, Haferlach T, Haferlach C, Koeffler HP. 2010. SNP array analysis of tyrosine kinase inhibitor-resistant chronic myeloid leukemia identifies heterogeneous secondary genomic alterations. Blood 115: 1049-1053.
-
(2010)
Blood
, vol.115
, pp. 1049-1053
-
-
Nowak, D.1
Ogawa, S.2
Muschen, M.3
Kato, M.4
Kawamata, N.5
Meixel, A.6
Nowak, V.7
Kim, H.S.8
Kang, S.9
Paquette, R.10
Chang, M.S.11
Thoennissen, N.H.12
Mossner, M.13
Hofmann, W.K.14
Kohlmann, A.15
Weiss, T.16
Haferlach, T.17
Haferlach, C.18
Koeffler, H.P.19
-
38
-
-
84861717511
-
SNP array analysis of acute promyelocytic leukemia may be of prognostic relevance and identifies a potential high risk group with recurrent deletions on chromosomal subband 1q31.3
-
Nowak D, Klaumuenzer M, Hanfstein B, Mossner M, Nolte F, Nowak V, Oblaender J, Hecht A, Hutter G, Ogawa S, Kohlmann A, Haferlach C, Schlegelberger B, Braess J, Seifarth W, Fabarius A, Erben P, Saussele S, Muller MC, Reiter A, Buechner T, Weiss C, Hofmann WK, Lengfelder E. 2012. SNP array analysis of acute promyelocytic leukemia may be of prognostic relevance and identifies a potential high risk group with recurrent deletions on chromosomal subband 1q31.3. Genes Chromosomes Cancer 51: 756-767.
-
(2012)
Genes Chromosomes Cancer
, vol.51
, pp. 756-767
-
-
Nowak, D.1
Klaumuenzer, M.2
Hanfstein, B.3
Mossner, M.4
Nolte, F.5
Nowak, V.6
Oblaender, J.7
Hecht, A.8
Hutter, G.9
Ogawa, S.10
Kohlmann, A.11
Haferlach, C.12
Schlegelberger, B.13
Braess, J.14
Seifarth, W.15
Fabarius, A.16
Erben, P.17
Saussele, S.18
Muller, M.C.19
Reiter, A.20
Buechner, T.21
Weiss, C.22
Hofmann, W.K.23
Lengfelder, E.24
more..
-
39
-
-
77956798455
-
Genomic profiling of adult acute lymphoblastic leukemia by single nucleotide polymorphism oligonucleotide microarray and comparison to pediatric acute lymphoblastic leukemia
-
Okamoto R, Ogawa S, Nowak D, Kawamata N, Akagi T, Kato M, Sanada M, Weiss T, Haferlach C, Dugas M, Ruckert C, Haferlach T, Koeffler HP. 2010. Genomic profiling of adult acute lymphoblastic leukemia by single nucleotide polymorphism oligonucleotide microarray and comparison to pediatric acute lymphoblastic leukemia. Haematologica 95: 1481-1488.
-
(2010)
Haematologica
, vol.95
, pp. 1481-1488
-
-
Okamoto, R.1
Ogawa, S.2
Nowak, D.3
Kawamata, N.4
Akagi, T.5
Kato, M.6
Sanada, M.7
Weiss, T.8
Haferlach, C.9
Dugas, M.10
Ruckert, C.11
Haferlach, T.12
Koeffler, H.P.13
-
40
-
-
77950990572
-
Copy neutral loss of heterozygosity: A novel chromosomal lesion in myeloid malignancies
-
O'Keefe C, McDevitt MA, Maciejewski JP. 2010. Copy neutral loss of heterozygosity: A novel chromosomal lesion in myeloid malignancies. Blood 115: 2731-2739.
-
(2010)
Blood
, vol.115
, pp. 2731-2739
-
-
O'Keefe, C.1
McDevitt, M.A.2
Maciejewski, J.P.3
-
41
-
-
78649753896
-
Acquired genomic copy number aberrations and survival in adult acute myelogenous leukemia
-
Parkin B, Erba H, Ouillette P, Roulston D, Purkayastha A, Karp J, Talpaz M, Kujawski L, Shakhan S, Li C, Shedden K, Malek SN. 2010. Acquired genomic copy number aberrations and survival in adult acute myelogenous leukemia. Blood 116: 4958-4967.
-
(2010)
Blood
, vol.116
, pp. 4958-4967
-
-
Parkin, B.1
Erba, H.2
Ouillette, P.3
Roulston, D.4
Purkayastha, A.5
Karp, J.6
Talpaz, M.7
Kujawski, L.8
Shakhan, S.9
Li, C.10
Shedden, K.11
Malek, S.N.12
-
42
-
-
84977552656
-
Monosomal karyotype (MK) in myeloid malignancies
-
Available at:(access date Aug 28, 2012).
-
Perdigão J, Gomes da Silva M. 2011. Monosomal karyotype (MK) in myeloid malignancies. Atlas Genet Cytogenet Oncol Haematol. Available at: http://AtlasGeneticsOncology.org/Anomalies/MonoKaryoID1574.html (access date Aug 28, 2012).
-
(2011)
Atlas Genet Cytogenet Oncol Haematol.
-
-
Perdigão, J.1
Gomes da Silva, M.2
-
43
-
-
50949113696
-
Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia
-
Raghavan M, Smith LL, Lillington DM, Chaplin T, Kakkas I, Molloy G, Chelala C, Cazier JB, Cavenagh JD, Fitzgibbon J, Lister TA, Young BD. 2008. Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia. Blood 112: 814-821.
-
(2008)
Blood
, vol.112
, pp. 814-821
-
-
Raghavan, M.1
Smith, L.L.2
Lillington, D.M.3
Chaplin, T.4
Kakkas, I.5
Molloy, G.6
Chelala, C.7
Cazier, J.B.8
Cavenagh, J.D.9
Fitzgibbon, J.10
Lister, T.A.11
Young, B.D.12
-
44
-
-
84856398561
-
Single-nucleotide polymorphism array karyotyping in clinical practice: Where, when, and how?
-
Sato-Otsubo A, Sanada M, Ogawa S. 2012. Single-nucleotide polymorphism array karyotyping in clinical practice: Where, when, and how? Semin Oncol 39: 13-25.
-
(2012)
Semin Oncol
, vol.39
, pp. 13-25
-
-
Sato-Otsubo, A.1
Sanada, M.2
Ogawa, S.3
-
46
-
-
80053632883
-
Microarray-based genomic profiling as a diagnostic tool in acute lymphoblastic leukemia
-
Simons A, Stevens-Kroef M, El Idrissi-Zaynoun N, van Gessel S, Weghuis DO, van den Berg E, Waanders E, Hoogerbrugge P, Kuiper R, van Kessel AG. 2011. Microarray-based genomic profiling as a diagnostic tool in acute lymphoblastic leukemia. Genes Chromosomes Cancer 50: 969-981.
-
(2011)
Genes Chromosomes Cancer
, vol.50
, pp. 969-981
-
-
Simons, A.1
Stevens-Kroef, M.2
El Idrissi-Zaynoun, N.3
van Gessel, S.4
Weghuis, D.O.5
van den Berg, E.6
Waanders, E.7
Hoogerbrugge, P.8
Kuiper, R.9
van Kessel, A.G.10
-
47
-
-
84865155258
-
Genome-wide arrays in routine diagnostics of hematological malignancies
-
Simons A, Sikkema-Raddatz B, de Leeuw N, Konrad NC, Hastings RJ, Schoumans J. 2012. Genome-wide arrays in routine diagnostics of hematological malignancies. Hum Mutat 33: 941-948.
-
(2012)
Hum Mutat
, vol.33
, pp. 941-948
-
-
Simons, A.1
Sikkema-Raddatz, B.2
de Leeuw, N.3
Konrad, N.C.4
Hastings, R.J.5
Schoumans, J.6
-
48
-
-
59449093453
-
A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups
-
Sulong S, Moorman AV, Irving JA, Strefford JC, Konn ZJ, Case MC, Minto L, Barber KE, Parker H, Wright SL, Stewart AR, Bailey S, Bown NP, Hall AG, Harrison CJ. 2009. A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups. Blood 113: 100-107.
-
(2009)
Blood
, vol.113
, pp. 100-107
-
-
Sulong, S.1
Moorman, A.V.2
Irving, J.A.3
Strefford, J.C.4
Konn, Z.J.5
Case, M.C.6
Minto, L.7
Barber, K.E.8
Parker, H.9
Wright, S.L.10
Stewart, A.R.11
Bailey, S.12
Bown, N.P.13
Hall, A.G.14
Harrison, C.J.15
-
49
-
-
53249123632
-
-
4th ed. Lyon: International Agency for Research on Cancer (IARC).
-
Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, Thiele J, Vardiman JW. 2008. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. 4th ed. Lyon: International Agency for Research on Cancer (IARC).
-
(2008)
WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues
-
-
Swerdlow, S.H.1
Campo, E.2
Harris, N.L.3
Jaffe, E.S.4
Pileri, S.A.5
Stein, H.6
Thiele, J.7
Vardiman, J.W.8
-
50
-
-
70449715477
-
New lesions detected by single nucleotide polymorphism array-based chromosomal analysis have important clinical impact in acute myeloid leukemia
-
Tiu RV, Gondek LP, O'Keefe CL, Huh J, Sekeres MA, Elson P, McDevitt MA, Wang XF, Levis MJ, Karp JE, Advani AS, Maciejewski JP. 2009. New lesions detected by single nucleotide polymorphism array-based chromosomal analysis have important clinical impact in acute myeloid leukemia. J Clin Oncol 27: 5219-5226.
-
(2009)
J Clin Oncol
, vol.27
, pp. 5219-5226
-
-
Tiu, R.V.1
Gondek, L.P.2
O'Keefe, C.L.3
Huh, J.4
Sekeres, M.A.5
Elson, P.6
McDevitt, M.A.7
Wang, X.F.8
Levis, M.J.9
Karp, J.E.10
Advani, A.S.11
Maciejewski, J.P.12
-
51
-
-
79955945973
-
Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and related myeloid malignancies
-
Tiu RV, Gondek LP, O'Keefe CL, Elson P, Huh J, Mohamedali A, Kulasekararaj A, Advani AS, Paquette R, List AF, Sekeres MA, McDevitt MA, Mufti GJ, Maciejewski JP. 2011. Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and related myeloid malignancies. Blood 117: 4552-4560.
-
(2011)
Blood
, vol.117
, pp. 4552-4560
-
-
Tiu, R.V.1
Gondek, L.P.2
O'Keefe, C.L.3
Elson, P.4
Huh, J.5
Mohamedali, A.6
Kulasekararaj, A.7
Advani, A.S.8
Paquette, R.9
List, A.F.10
Sekeres, M.A.11
McDevitt, M.A.12
Mufti, G.J.13
Maciejewski, J.P.14
-
53
-
-
69149100639
-
Acquired copy number alterations in adult acute myeloid leukemia genomes
-
Walter MJ, Payton JE, Ries RE, Shannon WD, Deshmukh H, Zhao Y, Baty J, Heath S, Westervelt P, Watson MA, Tomasson MH, Nagarajan R, O'Gara BP, Bloomfield CD, Mrozek K, Selzer RR, Richmond TA, Kitzman J, Geoghegan J, Eis PS, Maupin R, Fulton RS, McLellan M, Wilson RK, Mardis ER, Link DC, Graubert TA, DiPersio JF, Ley TJ. 2009. Acquired copy number alterations in adult acute myeloid leukemia genomes. Proc Natl Acad Sci USA 106: 12950-12955.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 12950-12955
-
-
Walter, M.J.1
Payton, J.E.2
Ries, R.E.3
Shannon, W.D.4
Deshmukh, H.5
Zhao, Y.6
Baty, J.7
Heath, S.8
Westervelt, P.9
Watson, M.A.10
Tomasson, M.H.11
Nagarajan, R.12
O'Gara, B.P.13
Bloomfield, C.D.14
Mrozek, K.15
Selzer, R.R.16
Richmond, T.A.17
Kitzman, J.18
Geoghegan, J.19
Eis, P.S.20
Maupin, R.21
Fulton, R.S.22
McLellan, M.23
Wilson, R.K.24
Mardis, E.R.25
Link, D.C.26
Graubert, T.A.27
DiPersio, J.F.28
Ley, T.J.29
more..
-
54
-
-
83255164849
-
Adverse prognostic impact of abnormal lesions detected by genome-wide single nucleotide polymorphism array-based karyotyping analysis in acute myeloid leukemia with normal karyotype
-
Yi JH, Huh J, Kim HJ, Kim SH, Kim HJ, Kim YK, Sohn SK, Moon JH, Kim SH, Kim KH, Won JH, Mun YC, Kim H, Park J, Jung CW, Kim DH. 2011. Adverse prognostic impact of abnormal lesions detected by genome-wide single nucleotide polymorphism array-based karyotyping analysis in acute myeloid leukemia with normal karyotype. J Clin Oncol 29: 4702-4708.
-
(2011)
J Clin Oncol
, vol.29
, pp. 4702-4708
-
-
Yi, J.H.1
Huh, J.2
Kim, H.J.3
Kim, S.H.4
Kim, H.J.5
Kim, Y.K.6
Sohn, S.K.7
Moon, J.H.8
Kim, S.H.9
Kim, K.H.10
Won, J.H.11
Mun, Y.C.12
Kim, H.13
Park, J.14
Jung, C.W.15
Kim, D.H.16
|