-
1
-
-
35748951614
-
Direct selection of human genomic loci by microarray hybridization
-
Albert, T.J., Molla, M.N., Muzny, D.M., Nazareth, L., Wheeler, D., Song, X., Richmond, T.A., Middle, C.M., Rodesch, M.J., Packard, C.J., Weinstock, G.M. & Gibbs, R.A. (2007) Direct selection of human genomic loci by microarray hybridization. Nature Methods, 4, 903-905.
-
(2007)
Nature Methods
, vol.4
, pp. 903-905
-
-
Albert, T.J.1
Molla, M.N.2
Muzny, D.M.3
Nazareth, L.4
Wheeler, D.5
Song, X.6
Richmond, T.A.7
Middle, C.M.8
Rodesch, M.J.9
Packard, C.J.10
Weinstock, G.M.11
Gibbs, R.A.12
-
2
-
-
79952164235
-
Unraveling the molecular pathophysiology of myelodysplastic syndromes
-
Bejar, R., Levine, R. & Ebert, B.L. (2011a) Unraveling the molecular pathophysiology of myelodysplastic syndromes. Journal of Clinical Oncology, 29, 504-515.
-
(2011)
Journal of Clinical Oncology
, vol.29
, pp. 504-515
-
-
Bejar, R.1
Levine, R.2
Ebert, B.L.3
-
3
-
-
79959794787
-
Clinical effect of point mutations in myelodysplastic syndromes
-
Bejar, R., Stevenson, K., bdel-Wahab, O., Galili, N., Nilsson, B., Garcia-Manero, G., Kantarjian, H., Raza, A., Levine, R.L., Neuberg, D. & Ebert, B.L. (2011b) Clinical effect of point mutations in myelodysplastic syndromes. New England Journal of Medicine, 364, 2496-2506.
-
(2011)
New England Journal of Medicine
, vol.364
, pp. 2496-2506
-
-
Bejar, R.1
Stevenson, K.2
bdel-Wahab, O.3
Galili, N.4
Nilsson, B.5
Garcia-Manero, G.6
Kantarjian, H.7
Raza, A.8
Levine, R.L.9
Neuberg, D.10
Ebert, B.L.11
-
4
-
-
55549089660
-
Accurate whole human genome sequencing using reversible terminator chemistry
-
Bentley, D.R., Balasubramanian, S., Swerdlow, H.P., Smith, G.P., Milton, J., Brown, C.G., Hall, K.P., Evers, D.J., Barnes, C.L., Bignell, H.R., Boutell, J.M., Bryant, J., Carter, R.J., Keira, C.R., Cox, A.J., Ellis, D.J., Flatbush, M.R., Gormley, N.A., Humphray, S.J., Irving, L.J., Karbelashvili, M.S., Kirk, S.M., Li, H., Liu, X., Maisinger, K.S., Murray, L.J., Obradovic, B., Ost, T., Parkinson, M.L., Pratt, M.R., Rasolonjatovo, I.M., Reed, M.T., Rigatti, R., Rodighiero, C., Ross, M.T., Sabot, A., Sankar, S.V., Scally, A., Schroth, G.P., Smith, M.E., Smith, V.P., Spiridou, A., Torrance, P.E., Tzonev, S.S., Vermaas, E.H., Walter, K., Wu, X., Zhang, L., Alam, M.D., Anastasi, C., Aniebo, I.C., Bailey, D.M., Bancarz, I.R., Banerjee, S., Barbour, S.G., Baybayan, P.A., Benoit, V.A., Benson, K.F., Bevis, C., Black, P.J., Boodhun, A., Brennan, J.S., Bridgham, J.A., Brown, R.C., Brown, A.A., Buermann, D.H., Bundu, A.A., Burrows, J.C., Carter, N.P., Castillo, N., Chiara, E., Catenazzi, M., Chang, S., Neil, C.R., Crake, N.R., Dada, O.O., Diakoumakos, K.D., Dominguez-Fernandez, B., Earnshaw, D.J., Egbujor, U.C., Elmore, D.W., Etchin, S.S., Ewan, M.R., Fedurco, M., Fraser, L.J., Fuentes Fajardo, K.V., Scott, F.W., George, D., Gietzen, K.J., Goddard, C.P., Golda, G.S., Granieri, P.A., Green, D.E., Gustafson, D.L., Hansen, N.F., Harnish, K., Haudenschild, C.D., Heyer, N.I., Hims, M.M., Ho, J.T., Horgan, A.M., Hoschler, K., Hurwitz, S., Ivanov, D.V., Johnson, M.Q., James, T., Huw Jones, T.A., Kang, G.D., Kerelska, T.H., Kersey, A.D., Khrebtukova, I. & Kindwall, A.P., Kingsbury, Z., Kokko-Gonzales, P.I., Kumar, A., Laurent, M.A., Lawley, C.T., Lee, S.E., Lee, X., Liao, A.K., Loch, J.A., Lok, M., Luo, S., Mammen, R.M., Martin, J.W., McCauley, P.G., McNitt, P., Mehta, P., Moon, K.W., Mullens, J.W., Newington, T., Ning, Z., Ling, N.B., Novo, S.M., O'Neill, M.J., Osborne, M.A., Osnowski, A., Ostadan, O., Paraschos, L.L., Pickering, L., Pike, A.C., Pike, A.C., Chris, P.D., Pliskin, D.P., Podhasky, J., Quijano, V.J., Raczy, C., Rae, V.H., Rawlings, S.R., Chiva, R.A., Roe, P.M., Rogers, J., Rogert Bacigalupo, M.C., Romanov, N., Romieu, A., Roth, R.K., Rourke, N.J., Ruediger, S.T., Rusman, E., Sanches-Kuiper, R.M., Schenker, M.R., Seoane, J.M., Shaw, R.J., Shiver, M.K., Short, S.W., Sizto, N.L., Sluis, J.P., Smith, M.A., Ernest Sohna, S.J., Spence, E.J., Stevens, K., Sutton, N., Szajkowski, L., Tregidgo, C.L., Turcatti, G., Vandevondele, S., Verhovsky, Y., Virk, S.M., Wakelin, S., Walcott, G.C., Wang, J., Worsley, G.J., Yan, J., Yau, L., Zuerlein, M., Rogers, J., Mullikin, J.C., Hurles, M.E., McCooke, N.J., West, J.S., Oaks, F.L., Lundberg, P.L., Klenerman, D., Durbin, R. & Smith, A.J. (2008) Accurate whole human genome sequencing using reversible terminator chemistry. Nature, 456, 53-59.
-
(2008)
Nature
, vol.456
, pp. 53-59
-
-
Bentley, D.R.1
Balasubramanian, S.2
Swerdlow, H.P.3
Smith, G.P.4
Milton, J.5
Brown, C.G.6
Hall, K.P.7
Evers, D.J.8
Barnes, C.L.9
Bignell, H.R.10
Boutell, J.M.11
Bryant, J.12
Carter, R.J.13
Keira, C.R.14
Cox, A.J.15
Ellis, D.J.16
Flatbush, M.R.17
Gormley, N.A.18
Humphray, S.J.19
Irving, L.J.20
Karbelashvili, M.S.21
Kirk, S.M.22
Li, H.23
Liu, X.24
Maisinger, K.S.25
Murray, L.J.26
Obradovic, B.27
Ost, T.28
Parkinson, M.L.29
Pratt, M.R.30
Rasolonjatovo, I.M.31
Reed, M.T.32
Rigatti, R.33
Rodighiero, C.34
Ross, M.T.35
Sabot, A.36
Sankar, S.V.37
Scally, A.38
Schroth, G.P.39
Smith, M.E.40
Smith, V.P.41
Spiridou, A.42
Torrance, P.E.43
Tzonev, S.S.44
Vermaas, E.H.45
Walter, K.46
Wu, X.47
Zhang, L.48
Alam, M.D.49
Anastasi, C.50
Aniebo, I.C.51
Bailey, D.M.52
Bancarz, I.R.53
Banerjee, S.54
Barbour, S.G.55
Baybayan, P.A.56
Benoit, V.A.57
Benson, K.F.58
Bevis, C.59
Black, P.J.60
Boodhun, A.61
Brennan, J.S.62
Bridgham, J.A.63
Brown, R.C.64
Brown, A.A.65
Buermann, D.H.66
Bundu, A.A.67
Burrows, J.C.68
Carter, N.P.69
Castillo, N.70
Chiara, E.71
Catenazzi, M.72
Chang, S.73
Neil, C.R.74
Crake, N.R.75
Dada, O.O.76
Diakoumakos, K.D.77
Dominguez-Fernandez, B.78
Earnshaw, D.J.79
Egbujor, U.C.80
Elmore, D.W.81
Etchin, S.S.82
Ewan, M.R.83
Fedurco, M.84
Fraser, L.J.85
Fuentes Fajardo, K.V.86
Scott, F.W.87
George, D.88
Gietzen, K.J.89
Goddard, C.P.90
Golda, G.S.91
Granieri, P.A.92
Green, D.E.93
Gustafson, D.L.94
Hansen, N.F.95
Harnish, K.96
Haudenschild, C.D.97
Heyer, N.I.98
Hims, M.M.99
Ho, J.T.100
Horgan, A.M.101
Hoschler, K.102
Hurwitz, S.103
Ivanov, D.V.104
Johnson, M.Q.105
James, T.106
Huw Jones, T.A.107
Kang, G.D.108
Kerelska, T.H.109
Kersey, A.D.110
Khrebtukova, I.111
Kindwall, A.P.112
Kingsbury, Z.113
Kokko-Gonzales, P.I.114
Kumar, A.115
Laurent, M.A.116
Lawley, C.T.117
Lee, S.E.118
Lee, X.119
Liao, A.K.120
Loch, J.A.121
Lok, M.122
Luo, S.123
Mammen, R.M.124
Martin, J.W.125
McCauley, P.G.126
McNitt, P.127
Mehta, P.128
Moon, K.W.129
Mullens, J.W.130
Newington, T.131
Ning, Z.132
Ling, N.B.133
Novo, S.M.134
O'Neill, M.J.135
Osborne, M.A.136
Osnowski, A.137
Ostadan, O.138
Paraschos, L.L.139
Pickering, L.140
Pike, A.C.141
Pike, A.C.142
Chris, P.D.143
Pliskin, D.P.144
Podhasky, J.145
Quijano, V.J.146
Raczy, C.147
Rae, V.H.148
Rawlings, S.R.149
Chiva, R.A.150
Roe, P.M.151
Rogers, J.152
Rogert Bacigalupo, M.C.153
Romanov, N.154
Romieu, A.155
Roth, R.K.156
Rourke, N.J.157
Ruediger, S.T.158
Rusman, E.159
Sanches-Kuiper, R.M.160
Schenker, M.R.161
Seoane, J.M.162
Shaw, R.J.163
Shiver, M.K.164
Short, S.W.165
Sizto, N.L.166
Sluis, J.P.167
Smith, M.A.168
Ernest Sohna, S.J.169
Spence, E.J.170
Stevens, K.171
Sutton, N.172
Szajkowski, L.173
Tregidgo, C.L.174
Turcatti, G.175
Vandevondele, S.176
Verhovsky, Y.177
Virk, S.M.178
Wakelin, S.179
Walcott, G.C.180
Wang, J.181
Worsley, G.J.182
Yan, J.183
Yau, L.184
Zuerlein, M.185
Rogers, J.186
Mullikin, J.C.187
Hurles, M.E.188
McCooke, N.J.189
West, J.S.190
Oaks, F.L.191
Lundberg, P.L.192
Klenerman, D.193
Durbin, R.194
Smith, A.J.195
more..
-
5
-
-
79951494668
-
Initial genome sequencing and analysis of multiple myeloma
-
Chapman, M.A., Lawrence, M.S., Keats, J.J., Cibulskis, K., Sougnez, C., Schinzel, A.C., Harview, C.L., Brunet, J.P., Ahmann, G.J., Adli, M., Anderson, K.C., Ardlie, K.G., Auclair, D., Baker, A., Bergsagel, P.L., Bernstein, B.E., Drier, Y., Fonseca, R., Gabriel, S.B., Hofmeister, C.C., Jagannath, S., Jakubowiak, A.J., Krishnan, A., Levy, J., Liefeld, T., Lonial, S., Mahan, S., Mfuko, B., Monti, S., Perkins, L.M., Onofrio, R., Pugh, T.J., Rajkumar, S.V., Ramos, A.H., Siegel, D.S., Sivachenko, A., Stewart, A.K., Trudel, S., Vij, R., Voet, D., Winckler, W., Zimmerman, T., Carpten, J., Trent, J., Hahn, W.C., Garraway, L.A., Meyerson, M., Lander, E.S., Getz, G. & Golub, T.R. (2011) Initial genome sequencing and analysis of multiple myeloma. Nature, 471, 467-472.
-
(2011)
Nature
, vol.471
, pp. 467-472
-
-
Chapman, M.A.1
Lawrence, M.S.2
Keats, J.J.3
Cibulskis, K.4
Sougnez, C.5
Schinzel, A.C.6
Harview, C.L.7
Brunet, J.P.8
Ahmann, G.J.9
Adli, M.10
Anderson, K.C.11
Ardlie, K.G.12
Auclair, D.13
Baker, A.14
Bergsagel, P.L.15
Bernstein, B.E.16
Drier, Y.17
Fonseca, R.18
Gabriel, S.B.19
Hofmeister, C.C.20
Jagannath, S.21
Jakubowiak, A.J.22
Krishnan, A.23
Levy, J.24
Liefeld, T.25
Lonial, S.26
Mahan, S.27
Mfuko, B.28
Monti, S.29
Perkins, L.M.30
Onofrio, R.31
Pugh, T.J.32
Rajkumar, S.V.33
Ramos, A.H.34
Siegel, D.S.35
Sivachenko, A.36
Stewart, A.K.37
Trudel, S.38
Vij, R.39
Voet, D.40
Winckler, W.41
Zimmerman, T.42
Carpten, J.43
Trent, J.44
Hahn, W.C.45
Garraway, L.A.46
Meyerson, M.47
Lander, E.S.48
Getz, G.49
Golub, T.R.50
more..
-
6
-
-
33846515640
-
Myelodysplastic syndromes: the complexity of stem-cell diseases
-
Corey, S.J., Minden, M.D., Barber, D.L., Kantarjian, H., Wang, J.C. & Schimmer, A.D. (2007) Myelodysplastic syndromes: the complexity of stem-cell diseases. Nature Reviews Cancer, 7, 118-129.
-
(2007)
Nature Reviews Cancer
, vol.7
, pp. 118-129
-
-
Corey, S.J.1
Minden, M.D.2
Barber, D.L.3
Kantarjian, H.4
Wang, J.C.5
Schimmer, A.D.6
-
7
-
-
77954353060
-
Statistical analyses of next generation sequence data: a partial overview
-
Datta, S., Datta, S., Kim, S., Chakraborty, S. & Gill, R.S. (2010) Statistical analyses of next generation sequence data: a partial overview. Journal of Proteomics and Bioinformatics, 3, 183-190.
-
(2010)
Journal of Proteomics and Bioinformatics
, vol.3
, pp. 183-190
-
-
Datta, S.1
Datta, S.2
Kim, S.3
Chakraborty, S.4
Gill, R.S.5
-
8
-
-
0028820187
-
Solid-phase reversible immobilization for the isolation of PCR products
-
DeAngelis, M.M., Wang, D.G. & Hawkins, T.L. (1995) Solid-phase reversible immobilization for the isolation of PCR products. Nucleic Acids Research, 23, 4742-4743.
-
(1995)
Nucleic Acids Research
, vol.23
, pp. 4742-4743
-
-
DeAngelis, M.M.1
Wang, D.G.2
Hawkins, T.L.3
-
9
-
-
66249137734
-
Mutation in TET2 in myeloid cancers
-
Delhommeau, F., Dupont, S., Della, V., James, C., Trannoy, S., Masse, A., Kosmider, O., le Couedic, J.P., Robert, F., Alberdi, A., Lecluse, Y., Plo, I., Dreyfus, F.J., Marzac, C., Casadevall, N., Lacombe, C., Romana, S.P., Dessen, P., Soulier, J., Viguie, F., Fontenay, M., Vainchenker, W. & Bernard, O.A. (2009) Mutation in TET2 in myeloid cancers. New England Journal of Medicine, 360, 2289-2301.
-
(2009)
New England Journal of Medicine
, vol.360
, pp. 2289-2301
-
-
Delhommeau, F.1
Dupont, S.2
Della, V.3
James, C.4
Trannoy, S.5
Masse, A.6
Kosmider, O.7
le Couedic, J.P.8
Robert, F.9
Alberdi, A.10
Lecluse, Y.11
Plo, I.12
Dreyfus, F.J.13
Marzac, C.14
Casadevall, N.15
Lacombe, C.16
Romana, S.P.17
Dessen, P.18
Soulier, J.19
Viguie, F.20
Fontenay, M.21
Vainchenker, W.22
Bernard, O.A.23
more..
-
10
-
-
77955715121
-
Mutation analysis for RUNX1, MLL-PTD, FLT3-ITD, NPM1 and NRAS in 269 patients with MDS or secondary AML
-
Dicker, F., Haferlach, C., Sundermann, J., Wendland, N., Weiss, T., Kern, W., Haferlach, T. & Schnittger, S. (2010) Mutation analysis for RUNX1, MLL-PTD, FLT3-ITD, NPM1 and NRAS in 269 patients with MDS or secondary AML. Leukemia, 24, 1528-1532.
-
(2010)
Leukemia
, vol.24
, pp. 1528-1532
-
-
Dicker, F.1
Haferlach, C.2
Sundermann, J.3
Wendland, N.4
Weiss, T.5
Kern, W.6
Haferlach, T.7
Schnittger, S.8
-
11
-
-
84861417677
-
BRAF inhibition in refractory hairy-cell leukemia
-
Dietrich, S., Glimm, H., Andrulis, M., von, K.C., Ho, A.D. & Zenz, T. (2012) BRAF inhibition in refractory hairy-cell leukemia. New England Journal of Medicine, 366, 2038-2040.
-
(2012)
New England Journal of Medicine
, vol.366
, pp. 2038-2040
-
-
Dietrich, S.1
Glimm, H.2
Andrulis, M.3
von, K.C.4
Ho, A.D.5
Zenz, T.6
-
12
-
-
84862776906
-
Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing
-
Ding, L., Ley, T.J., Larson, D.E., Miller, C.A., Koboldt, D.C., Welch, J.S., Ritchey, J.K., Young, M.A., Lamprecht, T., McLellan, M.D., McMichael, J.F., Wallis, J.W., Lu, C., Shen, D., Harris, C.C., Dooling, D.J., Fulton, R.S., Fulton, L.L., Chen, K., Schmidt, H., Kalicki-Veizer, J., Magrini, V.J., Cook, L., McGrath, S.D., Vickery, T.L., Wendl, M.C., Heath, S., Watson, M.A., Link, D.C., Tomasson, M.H., Shannon, W.D., Payton, J.E., Kulkarni, S., Westervelt, P., Walter, M.J., Graubert, T.A., Mardis, E.R., Wilson, R.K. & Dipersio, J.F. (2012) Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing. Nature, 481, 506-510.
-
(2012)
Nature
, vol.481
, pp. 506-510
-
-
Ding, L.1
Ley, T.J.2
Larson, D.E.3
Miller, C.A.4
Koboldt, D.C.5
Welch, J.S.6
Ritchey, J.K.7
Young, M.A.8
Lamprecht, T.9
McLellan, M.D.10
McMichael, J.F.11
Wallis, J.W.12
Lu, C.13
Shen, D.14
Harris, C.C.15
Dooling, D.J.16
Fulton, R.S.17
Fulton, L.L.18
Chen, K.19
Schmidt, H.20
Kalicki-Veizer, J.21
Magrini, V.J.22
Cook, L.23
McGrath, S.D.24
Vickery, T.L.25
Wendl, M.C.26
Heath, S.27
Watson, M.A.28
Link, D.C.29
Tomasson, M.H.30
Shannon, W.D.31
Payton, J.E.32
Kulkarni, S.33
Westervelt, P.34
Walter, M.J.35
Graubert, T.A.36
Mardis, E.R.37
Wilson, R.K.38
Dipersio, J.F.39
more..
-
13
-
-
84868554484
-
Commonly altered genomic regions in acute myeloid leukemia are enriched for somatic mutations involved in chromatin remodeling and splicing
-
Dolnik, A., Engelmann, J.C., Scharfenberger-Schmeer, M., Mauch, J., Kelkenberg-Schade, S., Haldemann, B., Fries, T., Kronke, J., Kuhn, M.W., Paschka, P., Kayser, S., Wolf, S., Gaidzik, V.I., Schlenk, R.F., Rucker, F.G., Dohner, H., Lottaz, C., Dohner, K. & Bullinger, L. (2012) Commonly altered genomic regions in acute myeloid leukemia are enriched for somatic mutations involved in chromatin remodeling and splicing. Blood, 120, e83-e92.
-
(2012)
Blood
, vol.120
-
-
Dolnik, A.1
Engelmann, J.C.2
Scharfenberger-Schmeer, M.3
Mauch, J.4
Kelkenberg-Schade, S.5
Haldemann, B.6
Fries, T.7
Kronke, J.8
Kuhn, M.W.9
Paschka, P.10
Kayser, S.11
Wolf, S.12
Gaidzik, V.I.13
Schlenk, R.F.14
Rucker, F.G.15
Dohner, H.16
Lottaz, C.17
Dohner, K.18
Bullinger, L.19
-
14
-
-
84865772716
-
Genomics: ENCODE explained
-
Ecker, J.R., Bickmore, W.A., Barroso, I., Pritchard, J.K., Gilad, Y. & Segal, E. (2012) Genomics: ENCODE explained. Nature, 489, 52-55.
-
(2012)
Nature
, vol.489
, pp. 52-55
-
-
Ecker, J.R.1
Bickmore, W.A.2
Barroso, I.3
Pritchard, J.K.4
Gilad, Y.5
Segal, E.6
-
15
-
-
77955085750
-
Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders
-
Ernst, T., Chase, A.J., Score, J., Hidalgo-Curtis, C.E., Bryant, C., Jones, A.V., Waghorn, K., Zoi, K., Ross, F.M., Reiter, A., Hochhaus, A., Drexler, H.G., Duncombe, A., Cervantes, F., Oscier, D., Boultwood, J., Grand, F.H. & Cross, N.C. (2010) Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders. Nat.Genet., 42, 722-726.
-
(2010)
Nat.Genet.
, vol.42
, pp. 722-726
-
-
Ernst, T.1
Chase, A.J.2
Score, J.3
Hidalgo-Curtis, C.E.4
Bryant, C.5
Jones, A.V.6
Waghorn, K.7
Zoi, K.8
Ross, F.M.9
Reiter, A.10
Hochhaus, A.11
Drexler, H.G.12
Duncombe, A.13
Cervantes, F.14
Oscier, D.15
Boultwood, J.16
Grand, F.H.17
Cross, N.C.18
-
16
-
-
79960353160
-
Analysis of the chronic lymphocytic leukemia coding genome: role of NOTCH1 mutational activation
-
Fabbri, G., Rasi, S., Rossi, D., Trifonov, V., Khiabanian, H., Ma, J., Grunn, A., Fangazio, M., Capello, D., Monti, S., Cresta, S., Gargiulo, E., Forconi, F., Guarini, A., Arcaini, L., Paulli, M., Laurenti, L., Larocca, L.M., Marasca, R., Gattei, V., Oscier, D., Bertoni, F., Mullighan, C.G., Foa, R., Pasqualucci, L., Rabadan, R., la-Favera, R. & Gaidano, G. (2011) Analysis of the chronic lymphocytic leukemia coding genome: role of NOTCH1 mutational activation. The Journal of Experimental Medicine, 208, 1389-1401.
-
(2011)
The Journal of Experimental Medicine
, vol.208
, pp. 1389-1401
-
-
Fabbri, G.1
Rasi, S.2
Rossi, D.3
Trifonov, V.4
Khiabanian, H.5
Ma, J.6
Grunn, A.7
Fangazio, M.8
Capello, D.9
Monti, S.10
Cresta, S.11
Gargiulo, E.12
Forconi, F.13
Guarini, A.14
Arcaini, L.15
Paulli, M.16
Laurenti, L.17
Larocca, L.M.18
Marasca, R.19
Gattei, V.20
Oscier, D.21
Bertoni, F.22
Mullighan, C.G.23
Foa, R.24
Pasqualucci, L.25
Rabadan, R.26
la-Favera, R.27
Gaidano, G.28
more..
-
17
-
-
66849124925
-
Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia
-
Gelsi-Boyer, V., Trouplin, V., Adelaide, J., Bonansea, J., Cervera, N., Carbuccia, N., Lagarde, A., Prebet, T., Nezri, M., Sainty, D., Olschwang, S., Xerri, L., Chaffanet, M., Mozziconacci, M.J., Vey, N. & Birnbaum, D. (2009) Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia. British Journal of Haematology, 145, 788-800.
-
(2009)
British Journal of Haematology
, vol.145
, pp. 788-800
-
-
Gelsi-Boyer, V.1
Trouplin, V.2
Adelaide, J.3
Bonansea, J.4
Cervera, N.5
Carbuccia, N.6
Lagarde, A.7
Prebet, T.8
Nezri, M.9
Sainty, D.10
Olschwang, S.11
Xerri, L.12
Chaffanet, M.13
Mozziconacci, M.J.14
Vey, N.15
Birnbaum, D.16
-
18
-
-
80051688000
-
Field guide to next-generation DNA sequencers
-
Glenn, T.C. (2011) Field guide to next-generation DNA sequencers. Molecular Ecology Resources, 11, 759-769.
-
(2011)
Molecular Ecology Resources
, vol.11
, pp. 759-769
-
-
Glenn, T.C.1
-
19
-
-
59849113821
-
Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing
-
Gnirke, A., Melnikov, A., Maguire, J., Rogov, P., LeProust, E.M., Brockman, W., Fennell, T., Giannoukos, G., Fisher, S., Russ, C., Gabriel, S., Jaffe, D.B., Lander, E.S. & Nusbaum, C. (2009) Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing. Nature Biotechnology, 27, 182-189.
-
(2009)
Nature Biotechnology
, vol.27
, pp. 182-189
-
-
Gnirke, A.1
Melnikov, A.2
Maguire, J.3
Rogov, P.4
LeProust, E.M.5
Brockman, W.6
Fennell, T.7
Giannoukos, G.8
Fisher, S.9
Russ, C.10
Gabriel, S.11
Jaffe, D.B.12
Lander, E.S.13
Nusbaum, C.14
-
21
-
-
84866621729
-
Revised international prognostic scoring system for myelodysplastic syndromes
-
Greenberg, P.L., Tuechler, H., Schanz, J., Sanz, G., Garcia-Manero, G., Sole, F., Bennett, J.M., Bowen, D., Fenaux, P., Dreyfus, F., Kantarjian, H., Kuendgen, A., Levis, A., Malcovati, L., Cazzola, M., Cermak, J., Fonatsch, C., Le Beau, M.M., Slovak, M.L., Krieger, O., Luebbert, M., Maciejewski, J., Magalhaes, S.M., Miyazaki, Y., Pfeilstocker, M., Sekeres, M., Sperr, W.R., Stauder, R., Tauro, S., Valent, P., Vallespi, T., van de Loosdrecht, A.A., Germing, U. & Haase, D. (2012) Revised international prognostic scoring system for myelodysplastic syndromes. Blood, 120, 2454-2465.
-
(2012)
Blood
, vol.120
, pp. 2454-2465
-
-
Greenberg, P.L.1
Tuechler, H.2
Schanz, J.3
Sanz, G.4
Garcia-Manero, G.5
Sole, F.6
Bennett, J.M.7
Bowen, D.8
Fenaux, P.9
Dreyfus, F.10
Kantarjian, H.11
Kuendgen, A.12
Levis, A.13
Malcovati, L.14
Cazzola, M.15
Cermak, J.16
Fonatsch, C.17
Le Beau, M.M.18
Slovak, M.L.19
Krieger, O.20
Luebbert, M.21
Maciejewski, J.22
Magalhaes, S.M.23
Miyazaki, Y.24
Pfeilstocker, M.25
Sekeres, M.26
Sperr, W.R.27
Stauder, R.28
Tauro, S.29
Valent, P.30
Vallespi, T.31
van de Loosdrecht, A.A.32
Germing, U.33
Haase, D.34
more..
-
22
-
-
79954442305
-
Targeted next-generation sequencing detects point mutations, insertions, deletions and balanced chromosomal rearrangements as well as identifies novel leukemia-specific fusion genes in a single procedure
-
Grossmann, V., Kohlmann, A., Klein, H.U., Schindela, S., Schnittger, S., Dicker, F., Dugas, M., Kern, W., Haferlach, T. & Haferlach, C. (2011a) Targeted next-generation sequencing detects point mutations, insertions, deletions and balanced chromosomal rearrangements as well as identifies novel leukemia-specific fusion genes in a single procedure. Leukemia, 25, 671-680.
-
(2011)
Leukemia
, vol.25
, pp. 671-680
-
-
Grossmann, V.1
Kohlmann, A.2
Klein, H.U.3
Schindela, S.4
Schnittger, S.5
Dicker, F.6
Dugas, M.7
Kern, W.8
Haferlach, T.9
Haferlach, C.10
-
23
-
-
79952254129
-
Strategy for robust detection of insertions, deletions, and point mutations in CEBPA, a GC-rich content gene, using 454 next-generation deep-sequencing technology
-
Grossmann, V., Schnittger, S., Schindela, S., Klein, H.U., Eder, C., Dugas, M., Kern, W., Haferlach, T., Haferlach, C. & Kohlmann, A. (2011b) Strategy for robust detection of insertions, deletions, and point mutations in CEBPA, a GC-rich content gene, using 454 next-generation deep-sequencing technology. Journal of Molecular Diagnostics, 13, 129-136.
-
(2011)
Journal of Molecular Diagnostics
, vol.13
, pp. 129-136
-
-
Grossmann, V.1
Schnittger, S.2
Schindela, S.3
Klein, H.U.4
Eder, C.5
Dugas, M.6
Kern, W.7
Haferlach, T.8
Haferlach, C.9
Kohlmann, A.10
-
24
-
-
83055161507
-
Whole-exome sequencing identifies somatic mutations of BCOR in acute myeloid leukemia with normal karyotype
-
Grossmann, V., Tiacci, E., Holmes, A.B., Kohlmann, A., Martelli, M.P., Kern, W., Spanhol-Rosseto, A., Klein, H.U., Dugas, M., Schindela, S., Trifonov, V., Schnittger, S., Haferlach, C., Bassan, R., Wells, V.A., Spinelli, O., Chan, J., Rossi, R., Baldoni, S., De, C.L., Goetze, K., Serve, H., Peceny, R., Kreuzer, K.A., Oruzio, D., Specchia, G., Di, R.F., Fabbiano, F., Sborgia, M., Liso, A., Farinelli, L., Rambaldi, A., Pasqualucci, L., Rabadan, R., Haferlach, T. & Falini, B. (2011c) Whole-exome sequencing identifies somatic mutations of BCOR in acute myeloid leukemia with normal karyotype. Blood, 118, 6153-6163.
-
(2011)
Blood
, vol.118
, pp. 6153-6163
-
-
Grossmann, V.1
Tiacci, E.2
Holmes, A.B.3
Kohlmann, A.4
Martelli, M.P.5
Kern, W.6
Spanhol-Rosseto, A.7
Klein, H.U.8
Dugas, M.9
Schindela, S.10
Trifonov, V.11
Schnittger, S.12
Haferlach, C.13
Bassan, R.14
Wells, V.A.15
Spinelli, O.16
Chan, J.17
Rossi, R.18
Baldoni, S.19
De, C.L.20
Goetze, K.21
Serve, H.22
Peceny, R.23
Kreuzer, K.A.24
Oruzio, D.25
Specchia, G.26
Di, R.F.27
Fabbiano, F.28
Sborgia, M.29
Liso, A.30
Farinelli, L.31
Rambaldi, A.32
Pasqualucci, L.33
Rabadan, R.34
Haferlach, T.35
Falini, B.36
more..
-
25
-
-
79955810336
-
Molecular profiling of chronic myelomonocytic leukemia reveals diverse mutations in >80% of patients with TET2 and EZH2 being of high prognostic relevance
-
Grossmann, V., Kohlmann, A., Eder, C., Haferlach, C., Kern, W., Cross, N.C., Haferlach, T. & Schnittger, S. (2011d) Molecular profiling of chronic myelomonocytic leukemia reveals diverse mutations in >80% of patients with TET2 and EZH2 being of high prognostic relevance. Leukemia, 25, 877-879.
-
(2011)
Leukemia
, vol.25
, pp. 877-879
-
-
Grossmann, V.1
Kohlmann, A.2
Eder, C.3
Haferlach, C.4
Kern, W.5
Cross, N.C.6
Haferlach, T.7
Schnittger, S.8
-
26
-
-
84867806184
-
A novel hierarchical prognostic model of AML solely based on molecular mutations
-
Grossmann, V., Schnittger, S., Kohlmann, A., Eder, C., Roller, A., Dicker, F., Schmid, C., Wendtner, C.M., Staib, P., Serve, H., Kreuzer, K.A., Kern, W., Haferlach, T. & Haferlach, C. (2012) A novel hierarchical prognostic model of AML solely based on molecular mutations. Blood, 120, 2963-2972.
-
(2012)
Blood
, vol.120
, pp. 2963-2972
-
-
Grossmann, V.1
Schnittger, S.2
Kohlmann, A.3
Eder, C.4
Roller, A.5
Dicker, F.6
Schmid, C.7
Wendtner, C.M.8
Staib, P.9
Serve, H.10
Kreuzer, K.A.11
Kern, W.12
Haferlach, T.13
Haferlach, C.14
-
27
-
-
83655211930
-
Detection of low prevalence somatic mutations in solid tumors with ultra-deep targeted sequencing
-
Harismendy, O., Schwab, R.B., Bao, L., Olson, J., Rozenzhak, S., Kotsopoulos, S.K., Pond, S., Crain, B., Chee, M.S., Messer, K., Link, D.R. & Frazer, K.A. (2011) Detection of low prevalence somatic mutations in solid tumors with ultra-deep targeted sequencing. Genome Biology, 12, R124.
-
(2011)
Genome Biology
, vol.12
-
-
Harismendy, O.1
Schwab, R.B.2
Bao, L.3
Olson, J.4
Rozenzhak, S.5
Kotsopoulos, S.K.6
Pond, S.7
Crain, B.8
Chee, M.S.9
Messer, K.10
Link, D.R.11
Frazer, K.A.12
-
28
-
-
77952888699
-
De novo mutations of SETBP1 cause Schinzel-Giedion syndrome
-
Hoischen, A., van Bon, B.W., Gilissen, C., Arts, P., van Lier, B., Steehouwer, M., de Vries, P., de Reuver, R., Wieskamp, N., Mortier, G., Devriendt, K., Amorim, M.Z., Revencu, N., Kidd, A., Barbosa, M., Turner, A., Smith, J., Oley, C., Henderson, A., Hayes, I.M., Thompson, E.M., Brunner, H.G., de Vries, B.B. & Veltman, J.A. (2010) De novo mutations of SETBP1 cause Schinzel-Giedion syndrome. Nature Genetics, 42, 483-485.
-
(2010)
Nature Genetics
, vol.42
, pp. 483-485
-
-
Hoischen, A.1
van Bon, B.W.2
Gilissen, C.3
Arts, P.4
van Lier, B.5
Steehouwer, M.6
de Vries, P.7
de Reuver, R.8
Wieskamp, N.9
Mortier, G.10
Devriendt, K.11
Amorim, M.Z.12
Revencu, N.13
Kidd, A.14
Barbosa, M.15
Turner, A.16
Smith, J.17
Oley, C.18
Henderson, A.19
Hayes, I.M.20
Thompson, E.M.21
Brunner, H.G.22
de Vries, B.B.23
Veltman, J.A.24
more..
-
29
-
-
79956291339
-
TP53 mutations in low-risk myelodysplastic syndromes with del(5q) predict disease progression
-
Jadersten, M., Saft, L., Smith, A., Kulasekararaj, A., Pomplun, S., Gohring, G., Hedlund, A., Hast, R., Schlegelberger, B., Porwit, A., Hellstrom-Lindberg, E. & Mufti, G.J. (2011) TP53 mutations in low-risk myelodysplastic syndromes with del(5q) predict disease progression. Journal of Clinical Oncology, 29, 1971-1979.
-
(2011)
Journal of Clinical Oncology
, vol.29
, pp. 1971-1979
-
-
Jadersten, M.1
Saft, L.2
Smith, A.3
Kulasekararaj, A.4
Pomplun, S.5
Gohring, G.6
Hedlund, A.7
Hast, R.8
Schlegelberger, B.9
Porwit, A.10
Hellstrom-Lindberg, E.11
Mufti, G.J.12
-
30
-
-
79954500887
-
R453Plus1Toolbox: an R/Bioconductor package for analyzing Roche 454 Sequencing data
-
Klein, H.U., Bartenhagen, C., Kohlmann, A., Grossmann, V., Ruckert, C., Haferlach, T. & Dugas, M. (2011) R453Plus1Toolbox: an R/Bioconductor package for analyzing Roche 454 Sequencing data. Bioinformatics, 27, 1162-1163.
-
(2011)
Bioinformatics
, vol.27
, pp. 1162-1163
-
-
Klein, H.U.1
Bartenhagen, C.2
Kohlmann, A.3
Grossmann, V.4
Ruckert, C.5
Haferlach, T.6
Dugas, M.7
-
31
-
-
78650175023
-
Impaired hydroxylation of 5-methylcytosine in myeloid cancers with mutant TET2
-
Ko, M., Huang, Y., Jankowska, A.M., Pape, U.J., Tahiliani, M., Bandukwala, H.S., An, J., Lamperti, E.D., Koh, K.P., Ganetzky, R., Liu, X.S., Aravind, L., Agarwal, S., Maciejewski, J.P. & Rao, A. (2010) Impaired hydroxylation of 5-methylcytosine in myeloid cancers with mutant TET2. Nature, 468, 839-843.
-
(2010)
Nature
, vol.468
, pp. 839-843
-
-
Ko, M.1
Huang, Y.2
Jankowska, A.M.3
Pape, U.J.4
Tahiliani, M.5
Bandukwala, H.S.6
An, J.7
Lamperti, E.D.8
Koh, K.P.9
Ganetzky, R.10
Liu, X.S.11
Aravind, L.12
Agarwal, S.13
Maciejewski, J.P.14
Rao, A.15
-
32
-
-
77956237515
-
Next-generation sequencing technology reveals a characteristic pattern of molecular mutations in 72.8% of chronic myelomonocytic leukemia by detecting frequent alterations in TET2, CBL, RAS, and RUNX1
-
Kohlmann, A., Grossmann, V., Klein, H.U., Schindela, S., Weiss, T., Kazak, B., Dicker, F., Schnittger, S., Dugas, M., Kern, W., Haferlach, C. & Haferlach, T. (2010a) Next-generation sequencing technology reveals a characteristic pattern of molecular mutations in 72.8% of chronic myelomonocytic leukemia by detecting frequent alterations in TET2, CBL, RAS, and RUNX1. Journal of Clinical Oncology, 28, 3858-3865.
-
(2010)
Journal of Clinical Oncology
, vol.28
, pp. 3858-3865
-
-
Kohlmann, A.1
Grossmann, V.2
Klein, H.U.3
Schindela, S.4
Weiss, T.5
Kazak, B.6
Dicker, F.7
Schnittger, S.8
Dugas, M.9
Kern, W.10
Haferlach, C.11
Haferlach, T.12
-
33
-
-
83555160609
-
Ultra-deep next-generation sequencing detects RUNX1 mutations with unprecedented sensitivity and allows to monitor minimal residual disease in 116 samples from MDS and AML patients clinically relevant abstract
-
Kohlmann, A., Grossmann, V., Schindela, S., Kern, W., Haferlach, C., Haferlach, T. & Schnittger, S. (2010b) Ultra-deep next-generation sequencing detects RUNX1 mutations with unprecedented sensitivity and allows to monitor minimal residual disease in 116 samples from MDS and AML patients clinically relevant abstract. Blood, 116, 1691a.
-
(2010)
Blood
, vol.116
-
-
Kohlmann, A.1
Grossmann, V.2
Schindela, S.3
Kern, W.4
Haferlach, C.5
Haferlach, T.6
Schnittger, S.7
-
34
-
-
83555166249
-
The Interlaboratory RObustness of Next-generation sequencing (IRON) study: a deep sequencing investigation of TET2, CBL and KRAS mutations by an international consortium involving 10 laboratories
-
Kohlmann, A., Klein, H.U., Weissmann, S., Bresolin, S., Chaplin, T., Cuppens, H., Haschke-Becher, E., Garicochea, B., Grossmann, V., Hanczaruk, B., Hebestreit, K., Gabriel, C., Iacobucci, I., Jansen, J.H., Te, K.G., van de, L.L., Martinelli, G., McGowan, K., Schweiger, M.R., Timmermann, B., Vandenberghe, P., Young, B.D., Dugas, M. & Haferlach, T. (2011) The Interlaboratory RObustness of Next-generation sequencing (IRON) study: a deep sequencing investigation of TET2, CBL and KRAS mutations by an international consortium involving 10 laboratories. Leukemia, 25, 1840-1848.
-
(2011)
Leukemia
, vol.25
, pp. 1840-1848
-
-
Kohlmann, A.1
Klein, H.U.2
Weissmann, S.3
Bresolin, S.4
Chaplin, T.5
Cuppens, H.6
Haschke-Becher, E.7
Garicochea, B.8
Grossmann, V.9
Hanczaruk, B.10
Hebestreit, K.11
Gabriel, C.12
Iacobucci, I.13
Jansen, J.H.14
Te, K.G.15
van de, L.L.16
Martinelli, G.17
McGowan, K.18
Schweiger, M.R.19
Timmermann, B.20
Vandenberghe, P.21
Young, B.D.22
Dugas, M.23
Haferlach, T.24
more..
-
35
-
-
84874710238
-
The Interlaboratory Robustness of Next-generation sequencing (IRON) study phase II: deep-sequencing analyses of hematological malignancies performed by an international network involving 26 laboratories
-
Kohlmann, A., Martinelli, G., Hofmann, W.-K., Kronnie, G., Chiaretti, S., Preudhomme, C., Tagliafico, E., Hernandez, J., Gabriel, C., Lion, T., Vandenberghe, P., Polakova, K.M., Béné, M.-C., Brueggemann, M., Cazzaniga, G., Yeoh, A., Lehmann, S., Ernst, T., Oppliger Leibundgut, E., Ozbek, U., Mills, K.I., Dugas, M., Thiede, C., Spinelli, O., Foroni, L., Jansen, J.H., Hochhaus, A. & Haferlach, T. (2012) The Interlaboratory Robustness of Next-generation sequencing (IRON) study phase II: deep-sequencing analyses of hematological malignancies performed by an international network involving 26 laboratories. Blood (ASH Annual Meeting Abstracts), 120, abstract 1399.
-
(2012)
Blood (ASH Annual Meeting Abstracts)
, vol.120
-
-
Kohlmann, A.1
Martinelli, G.2
Hofmann, W.-K.3
Kronnie, G.4
Chiaretti, S.5
Preudhomme, C.6
Tagliafico, E.7
Hernandez, J.8
Gabriel, C.9
Lion, T.10
Vandenberghe, P.11
Polakova, K.M.12
Béné, M.-C.13
Brueggemann, M.14
Cazzaniga, G.15
Yeoh, A.16
Lehmann, S.17
Ernst, T.18
Oppliger Leibundgut, E.19
Ozbek, U.20
Mills, K.I.21
Dugas, M.22
Thiede, C.23
Spinelli, O.24
Foroni, L.25
Jansen, J.H.26
Hochhaus, A.27
Haferlach, T.28
more..
-
36
-
-
84861023172
-
Somatic STAT3 mutations in large granular lymphocytic leukemia
-
Koskela, H.L., Eldfors, S., Ellonen, P., van Adrichem, A.J., Kuusanmaki, H., Andersson, E.I., Lagstrom, S., Clemente, M.J., Olson, T., Jalkanen, S.E., Majumder, M.M., Almusa, H., Edgren, H., Lepisto, M., Mattila, P., Guinta, K., Koistinen, P., Kuittinen, T., Penttinen, K., Parsons, A., Knowles, J., Saarela, J., Wennerberg, K., Kallioniemi, O., Porkka, K., Loughran, T.P. Jr, Heckman, C.A., Maciejewski, J.P. & Mustjoki, S. (2012) Somatic STAT3 mutations in large granular lymphocytic leukemia. New England Journal of Medicine, 366, 1905-1913.
-
(2012)
New England Journal of Medicine
, vol.366
, pp. 1905-1913
-
-
Koskela, H.L.1
Eldfors, S.2
Ellonen, P.3
van Adrichem, A.J.4
Kuusanmaki, H.5
Andersson, E.I.6
Lagstrom, S.7
Clemente, M.J.8
Olson, T.9
Jalkanen, S.E.10
Majumder, M.M.11
Almusa, H.12
Edgren, H.13
Lepisto, M.14
Mattila, P.15
Guinta, K.16
Koistinen, P.17
Kuittinen, T.18
Penttinen, K.19
Parsons, A.20
Knowles, J.21
Saarela, J.22
Wennerberg, K.23
Kallioniemi, O.24
Porkka, K.25
Loughran Jr, T.P.26
Heckman, C.A.27
Maciejewski, J.P.28
Mustjoki, S.29
more..
-
37
-
-
55549101623
-
DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome
-
Ley, T.J., Mardis, E.R., Ding, L., Fulton, B., McLellan, M.D., Chen, K., Dooling, D., Dunford-Shore, B.H., McGrath, S., Hickenbotham, M., Cook, L., Abbott, R., Larson, D.E., Koboldt, D.C., Pohl, C., Smith, S., Hawkins, A., Abbott, S., Locke, D., Hillier, L.W., Miner, T., Fulton, L., Magrini, V., Wylie, T., Glasscock, J., Conyers, J., Sander, N., Shi, X., Osborne, J.R., Minx, P., Gordon, D., Chinwalla, A., Zhao, Y., Ries, R.E., Payton, J.E., Westervelt, P., Tomasson, M.H., Watson, M., Baty, J., Ivanovich, J., Heath, S., Shannon, W.D., Nagarajan, R., Walter, M.J., Link, D.C., Graubert, T.A., Dipersio, J.F. & Wilson, R.K. (2008) DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome. Nature, 456, 66-72.
-
(2008)
Nature
, vol.456
, pp. 66-72
-
-
Ley, T.J.1
Mardis, E.R.2
Ding, L.3
Fulton, B.4
McLellan, M.D.5
Chen, K.6
Dooling, D.7
Dunford-Shore, B.H.8
McGrath, S.9
Hickenbotham, M.10
Cook, L.11
Abbott, R.12
Larson, D.E.13
Koboldt, D.C.14
Pohl, C.15
Smith, S.16
Hawkins, A.17
Abbott, S.18
Locke, D.19
Hillier, L.W.20
Miner, T.21
Fulton, L.22
Magrini, V.23
Wylie, T.24
Glasscock, J.25
Conyers, J.26
Sander, N.27
Shi, X.28
Osborne, J.R.29
Minx, P.30
Gordon, D.31
Chinwalla, A.32
Zhao, Y.33
Ries, R.E.34
Payton, J.E.35
Westervelt, P.36
Tomasson, M.H.37
Watson, M.38
Baty, J.39
Ivanovich, J.40
Heath, S.41
Shannon, W.D.42
Nagarajan, R.43
Walter, M.J.44
Link, D.C.45
Graubert, T.A.46
Dipersio, J.F.47
Wilson, R.K.48
more..
-
38
-
-
78649906060
-
DNMT3A mutations in acute myeloid leukemia
-
Ley, T.J., Ding, L., Walter, M.J., McLellan, M.D., Lamprecht, T., Larson, D.E., Kandoth, C., Payton, J.E., Baty, J., Welch, J., Harris, C.C., Lichti, C.F., Townsend, R.R., Fulton, R.S., Dooling, D.J., Koboldt, D.C., Schmidt, H., Zhang, Q., Osborne, J.R., Lin, L., O'Laughlin, M., McMichael, J.F., Delehaunty, K.D., McGrath, S.D., Fulton, L.A., Magrini, V.J., Vickery, T.L., Hundal, J., Cook, L.L., Conyers, J.J., Swift, G.W., Reed, J.P., Alldredge, P.A., Wylie, T., Walker, J., Kalicki, J., Watson, M.A., Heath, S., Shannon, W.D., Varghese, N., Nagarajan, R., Westervelt, P., Tomasson, M.H., Link, D.C., Graubert, T.A., Dipersio, J.F., Mardis, E.R. & Wilson, R.K. (2010) DNMT3A mutations in acute myeloid leukemia. New England Journal of Medicine, 363, 2424-2433.
-
(2010)
New England Journal of Medicine
, vol.363
, pp. 2424-2433
-
-
Ley, T.J.1
Ding, L.2
Walter, M.J.3
McLellan, M.D.4
Lamprecht, T.5
Larson, D.E.6
Kandoth, C.7
Payton, J.E.8
Baty, J.9
Welch, J.10
Harris, C.C.11
Lichti, C.F.12
Townsend, R.R.13
Fulton, R.S.14
Dooling, D.J.15
Koboldt, D.C.16
Schmidt, H.17
Zhang, Q.18
Osborne, J.R.19
Lin, L.20
O'Laughlin, M.21
McMichael, J.F.22
Delehaunty, K.D.23
McGrath, S.D.24
Fulton, L.A.25
Magrini, V.J.26
Vickery, T.L.27
Hundal, J.28
Cook, L.L.29
Conyers, J.J.30
Swift, G.W.31
Reed, J.P.32
Alldredge, P.A.33
Wylie, T.34
Walker, J.35
Kalicki, J.36
Watson, M.A.37
Heath, S.38
Shannon, W.D.39
Varghese, N.40
Nagarajan, R.41
Westervelt, P.42
Tomasson, M.H.43
Link, D.C.44
Graubert, T.A.45
Dipersio, J.F.46
Mardis, E.R.47
Wilson, R.K.48
more..
-
39
-
-
82155183257
-
Somatic mutations in the transcriptional corepressor gene BCORL1 in adult acute myelogenous leukemia
-
Li, M., Collins, R., Jiao, Y., Ouillette, P., Bixby, D., Erba, H., Vogelstein, B., Kinzler, K.W., Papadopoulos, N. & Malek, S.N. (2011) Somatic mutations in the transcriptional corepressor gene BCORL1 in adult acute myelogenous leukemia. Blood, 118, 5914-5917.
-
(2011)
Blood
, vol.118
, pp. 5914-5917
-
-
Li, M.1
Collins, R.2
Jiao, Y.3
Ouillette, P.4
Bixby, D.5
Erba, H.6
Vogelstein, B.7
Kinzler, K.W.8
Papadopoulos, N.9
Malek, S.N.10
-
40
-
-
84860756398
-
Performance comparison of benchtop high-throughput sequencing platforms
-
Loman, N.J., Misra, R.V., Dallman, T.J., Constantinidou, C., Gharbia, S.E., Wain, J. & Pallen, M.J. (2012) Performance comparison of benchtop high-throughput sequencing platforms. Nature Biotechnology, 30, 434-439.
-
(2012)
Nature Biotechnology
, vol.30
, pp. 434-439
-
-
Loman, N.J.1
Misra, R.V.2
Dallman, T.J.3
Constantinidou, C.4
Gharbia, S.E.5
Wain, J.6
Pallen, M.J.7
-
41
-
-
75749096130
-
Cancer genome sequencing: a review
-
Mardis, E.R. & Wilson, R.K. (2009) Cancer genome sequencing: a review. Human etics, 18, R163-R168.
-
(2009)
Human etics
, vol.18
-
-
Mardis, E.R.1
Wilson, R.K.2
-
42
-
-
70149093912
-
Recurring mutations found by sequencing an acute myeloid leukemia genome
-
Mardis, E.R., Ding, L., Dooling, D.J., Larson, D.E., McLellan, M.D., Chen, K., Koboldt, D.C., Fulton, R.S., Delehaunty, K.D., McGrath, S.D., Fulton, L.A., Locke, D.P., Magrini, V.J., Abbott, R.M., Vickery, T.L., Reed, J.S., Robinson, J.S., Wylie, T., Smith, S.M., Carmichael, L., Eldred, J.M., Harris, C.C., Walker, J., Peck, J.B., Du, F., Dukes, A.F., Sanderson, G.E., Brummett, A.M., Clark, E., McMichael, J.F., Meyer, R.J., Schindler, J.K., Pohl, C.S., Wallis, J.W., Shi, X., Lin, L., Schmidt, H., Tang, Y., Haipek, C., Wiechert, M.E., Ivy, J.V., Kalicki, J., Elliott, G., Ries, R.E., Payton, J.E., Westervelt, P., Tomasson, M.H., Watson, M.A., Baty, J., Heath, S., Shannon, W.D., Nagarajan, R., Link, D.C., Walter, M.J., Graubert, T.A., Dipersio, J.F., Wilson, R.K. & Ley, T.J. (2009) Recurring mutations found by sequencing an acute myeloid leukemia genome. New England Journal of Medicine, 361, 1058-1066.
-
(2009)
New England Journal of Medicine
, vol.361
, pp. 1058-1066
-
-
Mardis, E.R.1
Ding, L.2
Dooling, D.J.3
Larson, D.E.4
McLellan, M.D.5
Chen, K.6
Koboldt, D.C.7
Fulton, R.S.8
Delehaunty, K.D.9
McGrath, S.D.10
Fulton, L.A.11
Locke, D.P.12
Magrini, V.J.13
Abbott, R.M.14
Vickery, T.L.15
Reed, J.S.16
Robinson, J.S.17
Wylie, T.18
Smith, S.M.19
Carmichael, L.20
Eldred, J.M.21
Harris, C.C.22
Walker, J.23
Peck, J.B.24
Du, F.25
Dukes, A.F.26
Sanderson, G.E.27
Brummett, A.M.28
Clark, E.29
McMichael, J.F.30
Meyer, R.J.31
Schindler, J.K.32
Pohl, C.S.33
Wallis, J.W.34
Shi, X.35
Lin, L.36
Schmidt, H.37
Tang, Y.38
Haipek, C.39
Wiechert, M.E.40
Ivy, J.V.41
Kalicki, J.42
Elliott, G.43
Ries, R.E.44
Payton, J.E.45
Westervelt, P.46
Tomasson, M.H.47
Watson, M.A.48
Baty, J.49
Heath, S.50
Shannon, W.D.51
Nagarajan, R.52
Link, D.C.53
Walter, M.J.54
Graubert, T.A.55
Dipersio, J.F.56
Wilson, R.K.57
Ley, T.J.58
more..
-
43
-
-
24044455869
-
Genome sequencing in microfabricated high-density picolitre reactors
-
Margulies, M., Egholm, M., Altman, W.E., Attiya, S., Bader, J.S., Bemben, L.A., Berka, J., Braverman, M.S., Chen, Y.J., Chen, Z., Dewell, S.B., Du, L., Fierro, J.M., Gomes, X.V., Godwin, B.C., He, W., Helgesen, S., Ho, C.H., Irzyk, G.P., Jando, S.C., Alenquer, M.L., Jarvie, T.P., Jirage, K.B., Kim, J.B., Knight, J.R., Lanza, J.R., Leamon, J.H., Lefkowitz, S.M., Lei, M., Li, J., Lohman, K.L., Lu, H., Makhijani, V.B., McDade, K.E., McKenna, M.P., Myers, E.W., Nickerson, E., Nobile, J.R., Plant, R., Puc, B.P., Ronan, M.T., Roth, G.T., Sarkis, G.J., Simons, J.F., Simpson, J.W., Srinivasan, M., Tartaro, K.R., Tomasz, A., Vogt, K.A., Volkmer, G.A., Wang, S.H., Wang, Y., Weiner, M.P., Yu, P., Begley, R.F. & Rothberg, J.M. (2005) Genome sequencing in microfabricated high-density picolitre reactors. Nature, 437, 376-380.
-
(2005)
Nature
, vol.437
, pp. 376-380
-
-
Margulies, M.1
Egholm, M.2
Altman, W.E.3
Attiya, S.4
Bader, J.S.5
Bemben, L.A.6
Berka, J.7
Braverman, M.S.8
Chen, Y.J.9
Chen, Z.10
Dewell, S.B.11
Du, L.12
Fierro, J.M.13
Gomes, X.V.14
Godwin, B.C.15
He, W.16
Helgesen, S.17
Ho, C.H.18
Irzyk, G.P.19
Jando, S.C.20
Alenquer, M.L.21
Jarvie, T.P.22
Jirage, K.B.23
Kim, J.B.24
Knight, J.R.25
Lanza, J.R.26
Leamon, J.H.27
Lefkowitz, S.M.28
Lei, M.29
Li, J.30
Lohman, K.L.31
Lu, H.32
Makhijani, V.B.33
McDade, K.E.34
McKenna, M.P.35
Myers, E.W.36
Nickerson, E.37
Nobile, J.R.38
Plant, R.39
Puc, B.P.40
Ronan, M.T.41
Roth, G.T.42
Sarkis, G.J.43
Simons, J.F.44
Simpson, J.W.45
Srinivasan, M.46
Tartaro, K.R.47
Tomasz, A.48
Vogt, K.A.49
Volkmer, G.A.50
Wang, S.H.51
Wang, Y.52
Weiner, M.P.53
Yu, P.54
Begley, R.F.55
Rothberg, J.M.56
more..
-
44
-
-
84867253750
-
SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML)
-
Meggendorfer, M., Roller, A., Haferlach, T., Eder, C., Dicker, F., Grossmann, V., Kohlmann, A., Alpermann, T., Yoshida, K., Ogawa, S., Koeffler, H.P., Kern, W., Haferlach, C. & Schnittger, S. (2012) SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML). Blood, 120, 3080-3088.
-
(2012)
Blood
, vol.120
, pp. 3080-3088
-
-
Meggendorfer, M.1
Roller, A.2
Haferlach, T.3
Eder, C.4
Dicker, F.5
Grossmann, V.6
Kohlmann, A.7
Alpermann, T.8
Yoshida, K.9
Ogawa, S.10
Koeffler, H.P.11
Kern, W.12
Haferlach, C.13
Schnittger, S.14
-
45
-
-
72849144434
-
Sequencing technologies - the next generation
-
Metzker, M.L. (2010) Sequencing technologies - the next generation. Nature Reviews. Genetics, 11, 31-46.
-
(2010)
Nature Reviews. Genetics
, vol.11
, pp. 31-46
-
-
Metzker, M.L.1
-
46
-
-
77955087290
-
Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes
-
Nikoloski, G., Langemeijer, S.M., Kuiper, R.P., Knops, R., Massop, M., Tonnissen, E.R., van der, H.A., Scheele, T.N., Vandenberghe, P., de, W.T., van der Reijden, B.A. & Jansen, J.H. (2010) Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes. Nature Genetics, 42, 665-667.
-
(2010)
Nature Genetics
, vol.42
, pp. 665-667
-
-
Nikoloski, G.1
Langemeijer, S.M.2
Kuiper, R.P.3
Knops, R.4
Massop, M.5
Tonnissen, E.R.6
van der, H.A.7
Scheele, T.N.8
Vandenberghe, P.9
de, W.T.10
van der Reijden, B.A.11
Jansen, J.H.12
-
47
-
-
84872469222
-
The clinical significance of NOTCH1 and SF3B1 mutations in the UK LRF CLL4 trial
-
doi: 10.1182/blood-2012-05-429282.
-
Oscier, D.G., Rose-Zerilli, M.J., Winkelmann, N., Gonzalez de, C.D., Gomez, B., Forster, J., Parker, H., Parker, A., Gardiner, A., Collins, A., Else, M., Cross, N.C., Catovsky, D. & Strefford, J.C. (2012) The clinical significance of NOTCH1 and SF3B1 mutations in the UK LRF CLL4 trial. Blood, doi: 10.1182/blood-2012-05-429282.
-
(2012)
Blood
-
-
Oscier, D.G.1
Rose-Zerilli, M.J.2
Winkelmann, N.3
Gonzalez de, C.D.4
Gomez, B.5
Forster, J.6
Parker, H.7
Parker, A.8
Gardiner, A.9
Collins, A.10
Else, M.11
Cross, N.C.12
Catovsky, D.13
Strefford, J.C.14
-
48
-
-
80054010617
-
Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts
-
Papaemmanuil, E., Cazzola, M., Boultwood, J., Malcovati, L., Vyas, P., Bowen, D., Pellagatti, A., Wainscoat, J.S., Hellstrom-Lindberg, E., Gambacorti-Passerini, C., Godfrey, A.L., Rapado, I., Cvejic, A., Rance, R., McGee, C., Ellis, P., Mudie, L.J., Stephens, P.J., McLaren, S., Massie, C.E., Tarpey, P.S., Varela, I., Nik-Zainal, S., Davies, H.R., Shlien, A., Jones, D., Raine, K., Hinton, J., Butler, A.P., Teague, J.W., Baxter, E.J., Score, J., Galli, A., la Porta, M.G., Travaglino, E., Groves, M., Tauro, S., Munshi, N.C., Anderson, K.C., El-Naggar, A., Fischer, A., Mustonen, V., Warren, A.J., Cross, N.C., Green, A.R., Futreal, P.A., Stratton, M.R. & Campbell, P.J. (2011) Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts. New England Journal of Medicine, 365, 1384-1395.
-
(2011)
New England Journal of Medicine
, vol.365
, pp. 1384-1395
-
-
Papaemmanuil, E.1
Cazzola, M.2
Boultwood, J.3
Malcovati, L.4
Vyas, P.5
Bowen, D.6
Pellagatti, A.7
Wainscoat, J.S.8
Hellstrom-Lindberg, E.9
Gambacorti-Passerini, C.10
Godfrey, A.L.11
Rapado, I.12
Cvejic, A.13
Rance, R.14
McGee, C.15
Ellis, P.16
Mudie, L.J.17
Stephens, P.J.18
McLaren, S.19
Massie, C.E.20
Tarpey, P.S.21
Varela, I.22
Nik-Zainal, S.23
Davies, H.R.24
Shlien, A.25
Jones, D.26
Raine, K.27
Hinton, J.28
Butler, A.P.29
Teague, J.W.30
Baxter, E.J.31
Score, J.32
Galli, A.33
la Porta, M.G.34
Travaglino, E.35
Groves, M.36
Tauro, S.37
Munshi, N.C.38
Anderson, K.C.39
El-Naggar, A.40
Fischer, A.41
Mustonen, V.42
Warren, A.J.43
Cross, N.C.44
Green, A.R.45
Futreal, P.A.46
Stratton, M.R.47
Campbell, P.J.48
more..
-
49
-
-
84863393263
-
Prognostic relevance of integrated genetic profiling in acute myeloid leukemia
-
Patel, J.P., Gonen, M., Figueroa, M.E., Fernandez, H., Sun, Z., Racevskis, J., Van, V.P., Dolgalev, I., Thomas, S., Aminova, O., Huberman, K., Cheng, J., Viale, A., Socci, N.D., Heguy, A., Cherry, A., Vance, G., Higgins, R.R., Ketterling, R.P., Gallagher, R.E., Litzow, M., van den Brink, M.R., Lazarus, H.M., Rowe, J.M., Luger, S., Ferrando, A., Paietta, E., Tallman, M.S., Melnick, A., bdel-Wahab, O. & Levine, R.L. (2012) Prognostic relevance of integrated genetic profiling in acute myeloid leukemia. New England Journal of Medicine, 366, 1079-1089.
-
(2012)
New England Journal of Medicine
, vol.366
, pp. 1079-1089
-
-
Patel, J.P.1
Gonen, M.2
Figueroa, M.E.3
Fernandez, H.4
Sun, Z.5
Racevskis, J.6
Van, V.P.7
Dolgalev, I.8
Thomas, S.9
Aminova, O.10
Huberman, K.11
Cheng, J.12
Viale, A.13
Socci, N.D.14
Heguy, A.15
Cherry, A.16
Vance, G.17
Higgins, R.R.18
Ketterling, R.P.19
Gallagher, R.E.20
Litzow, M.21
van den Brink, M.R.22
Lazarus, H.M.23
Rowe, J.M.24
Luger, S.25
Ferrando, A.26
Paietta, E.27
Tallman, M.S.28
Melnick, A.29
bdel-Wahab, O.30
Levine, R.L.31
more..
-
50
-
-
79960036578
-
Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia
-
Puente, X.S., Pinyol, M., Quesada, V., Conde, L., Ordonez, G.R., Villamor, N., Escaramis, G., Jares, P., Bea, S., Gonzalez-Diaz, M., Bassaganyas, L., Baumann, T., Juan, M., Lopez-Guerra, M., Colomer, D., Tubio, J.M., Lopez, C., Navarro, A., Tornador, C., Aymerich, M., Rozman, M., Hernandez, J.M., Puente, D.A., Freije, J.M., Velasco, G., Gutierrez-Fernandez, A., Costa, D., Carrio, A., Guijarro, S., Enjuanes, A., Hernandez, L., Yague, J., Nicolas, P., Romeo-Casabona, C.M., Himmelbauer, H., Castillo, E., Dohm, J.C., de, S.S., Piris, M.A., de, A.E., San, M.J., Royo, R., Gelpi, J.L., Torrents, D., Orozco, M., Pisano, D.G., Valencia, A., Guigo, R., Bayes, M., Heath, S., Gut, M., Klatt, P., Marshall, J., Raine, K., Stebbings, L.A., Futreal, P.A., Stratton, M.R., Campbell, P.J., Gut, I., Lopez-Guillermo, A., Estivill, X., Montserrat, E., Lopez-Otin, C. & Campo, E. (2011) Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia. Nature, 475, 101-105.
-
(2011)
Nature
, vol.475
, pp. 101-105
-
-
Puente, X.S.1
Pinyol, M.2
Quesada, V.3
Conde, L.4
Ordonez, G.R.5
Villamor, N.6
Escaramis, G.7
Jares, P.8
Bea, S.9
Gonzalez-Diaz, M.10
Bassaganyas, L.11
Baumann, T.12
Juan, M.13
Lopez-Guerra, M.14
Colomer, D.15
Tubio, J.M.16
Lopez, C.17
Navarro, A.18
Tornador, C.19
Aymerich, M.20
Rozman, M.21
Hernandez, J.M.22
Puente, D.A.23
Freije, J.M.24
Velasco, G.25
Gutierrez-Fernandez, A.26
Costa, D.27
Carrio, A.28
Guijarro, S.29
Enjuanes, A.30
Hernandez, L.31
Yague, J.32
Nicolas, P.33
Romeo-Casabona, C.M.34
Himmelbauer, H.35
Castillo, E.36
Dohm, J.C.37
de, S.S.38
Piris, M.A.39
de, A.E.40
San, M.J.41
Royo, R.42
Gelpi, J.L.43
Torrents, D.44
Orozco, M.45
Pisano, D.G.46
Valencia, A.47
Guigo, R.48
Bayes, M.49
Heath, S.50
Gut, M.51
Klatt, P.52
Marshall, J.53
Raine, K.54
Stebbings, L.A.55
Futreal, P.A.56
Stratton, M.R.57
Campbell, P.J.58
Gut, I.59
Lopez-Guillermo, A.60
Estivill, X.61
Montserrat, E.62
Lopez-Otin, C.63
Campo, E.64
more..
-
51
-
-
84865591846
-
A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers
-
Quail, M.A., Smith, M., Coupland, P., Otto, T.D., Harris, S.R., Connor, T.R., Bertoni, A., Swerdlow, H.P. & Gu, Y. (2012) A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers. BMC Genomics, 13, 341.
-
(2012)
BMC Genomics
, vol.13
, pp. 341
-
-
Quail, M.A.1
Smith, M.2
Coupland, P.3
Otto, T.D.4
Harris, S.R.5
Connor, T.R.6
Bertoni, A.7
Swerdlow, H.P.8
Gu, Y.9
-
52
-
-
84555171449
-
Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia
-
Quesada, V., Conde, L., Villamor, N., Ordonez, G.R., Jares, P., Bassaganyas, L., Ramsay, A.J., Bea, S., Pinyol, M., Martinez-Trillos, A., Lopez-Guerra, M., Colomer, D., Navarro, A., Baumann, T., Aymerich, M., Rozman, M., Delgado, J., Gine, E., Hernandez, J.M., Gonzalez-Diaz, M., Puente, D.A., Velasco, G., Freije, J.M., Tubio, J.M., Royo, R., Gelpi, J.L., Orozco, M., Pisano, D.G., Zamora, J., Vazquez, M., Valencia, A., Himmelbauer, H., Bayes, M., Heath, S., Gut, M., Gut, I., Estivill, X., Lopez-Guillermo, A., Puente, X.S., Campo, E. & Lopez-Otin, C. (2012) Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia. Nature Genetics, 44, 47-52.
-
(2012)
Nature Genetics
, vol.44
, pp. 47-52
-
-
Quesada, V.1
Conde, L.2
Villamor, N.3
Ordonez, G.R.4
Jares, P.5
Bassaganyas, L.6
Ramsay, A.J.7
Bea, S.8
Pinyol, M.9
Martinez-Trillos, A.10
Lopez-Guerra, M.11
Colomer, D.12
Navarro, A.13
Baumann, T.14
Aymerich, M.15
Rozman, M.16
Delgado, J.17
Gine, E.18
Hernandez, J.M.19
Gonzalez-Diaz, M.20
Puente, D.A.21
Velasco, G.22
Freije, J.M.23
Tubio, J.M.24
Royo, R.25
Gelpi, J.L.26
Orozco, M.27
Pisano, D.G.28
Zamora, J.29
Vazquez, M.30
Valencia, A.31
Himmelbauer, H.32
Bayes, M.33
Heath, S.34
Gut, M.35
Gut, I.36
Estivill, X.37
Lopez-Guillermo, A.38
Puente, X.S.39
Campo, E.40
Lopez-Otin, C.41
more..
-
53
-
-
79960597679
-
An integrated semiconductor device enabling non-optical genome sequencing
-
Rothberg, J.M., Hinz, W., Rearick, T.M., Schultz, J., Mileski, W., Davey, M., Leamon, J.H., Johnson, K., Milgrew, M.J., Edwards, M., Hoon, J., Simons, J.F., Marran, D., Myers, J.W., Davidson, J.F., Branting, A., Nobile, J.R., Puc, B.P., Light, D., Clark, T.A., Huber, M., Branciforte, J.T., Stoner, I.B., Cawley, S.E., Lyons, M., Fu, Y., Homer, N., Sedova, M., Miao, X., Reed, B., Sabina, J., Feierstein, E., Schorn, M., Alanjary, M., Dimalanta, E., Dressman, D., Kasinskas, R., Sokolsky, T., Fidanza, J.A., Namsaraev, E., McKernan, K.J., Williams, A., Roth, G.T. & Bustillo, J. (2011) An integrated semiconductor device enabling non-optical genome sequencing. Nature, 475, 348-352.
-
(2011)
Nature
, vol.475
, pp. 348-352
-
-
Rothberg, J.M.1
Hinz, W.2
Rearick, T.M.3
Schultz, J.4
Mileski, W.5
Davey, M.6
Leamon, J.H.7
Johnson, K.8
Milgrew, M.J.9
Edwards, M.10
Hoon, J.11
Simons, J.F.12
Marran, D.13
Myers, J.W.14
Davidson, J.F.15
Branting, A.16
Nobile, J.R.17
Puc, B.P.18
Light, D.19
Clark, T.A.20
Huber, M.21
Branciforte, J.T.22
Stoner, I.B.23
Cawley, S.E.24
Lyons, M.25
Fu, Y.26
Homer, N.27
Sedova, M.28
Miao, X.29
Reed, B.30
Sabina, J.31
Feierstein, E.32
Schorn, M.33
Alanjary, M.34
Dimalanta, E.35
Dressman, D.36
Kasinskas, R.37
Sokolsky, T.38
Fidanza, J.A.39
Namsaraev, E.40
McKernan, K.J.41
Williams, A.42
Roth, G.T.43
Bustillo, J.44
more..
-
54
-
-
78651310799
-
Database resources of the National Center for Biotechnology Information
-
Sayers, E.W., Barrett, T., Benson, D.A., Bolton, E., Bryant, S.H., Canese, K., Chetvernin, V., Church, D.M., Dicuccio, M., Federhen, S., Feolo, M., Fingerman, I.M., Geer, L.Y., Helmberg, W., Kapustin, Y., Landsman, D., Lipman, D.J., Lu, Z., Madden, T.L., Madej, T., Maglott, D.R., Marchler-Bauer, A., Miller, V., Mizrachi, I., Ostell, J., Panchenko, A., Phan, L., Pruitt, K.D., Schuler, G.D., Sequeira, E., Sherry, S.T., Shumway, M., Sirotkin, K., Slotta, D., Souvorov, A., Starchenko, G., Tatusova, T.A., Wagner, L., Wang, Y., Wilbur, W.J., Yaschenko, E. & Ye, J. (2011) Database resources of the National Center for Biotechnology Information. Nucleic Acids Research, 39, D38-D51.
-
(2011)
Nucleic Acids Research
, vol.39
-
-
Sayers, E.W.1
Barrett, T.2
Benson, D.A.3
Bolton, E.4
Bryant, S.H.5
Canese, K.6
Chetvernin, V.7
Church, D.M.8
Dicuccio, M.9
Federhen, S.10
Feolo, M.11
Fingerman, I.M.12
Geer, L.Y.13
Helmberg, W.14
Kapustin, Y.15
Landsman, D.16
Lipman, D.J.17
Lu, Z.18
Madden, T.L.19
Madej, T.20
Maglott, D.R.21
Marchler-Bauer, A.22
Miller, V.23
Mizrachi, I.24
Ostell, J.25
Panchenko, A.26
Phan, L.27
Pruitt, K.D.28
Schuler, G.D.29
Sequeira, E.30
Sherry, S.T.31
Shumway, M.32
Sirotkin, K.33
Slotta, D.34
Souvorov, A.35
Starchenko, G.36
Tatusova, T.A.37
Wagner, L.38
Wang, Y.39
Wilbur, W.J.40
Yaschenko, E.41
Ye, J.42
more..
-
55
-
-
79952134550
-
RUNX1 mutations are frequent in de novo AML with noncomplex karyotype and confer an unfavorable prognosis
-
Schnittger, S., Dicker, F., Kern, W., Wendland, N., Sundermann, J., Alpermann, T., Haferlach, C. & Haferlach, T. (2011) RUNX1 mutations are frequent in de novo AML with noncomplex karyotype and confer an unfavorable prognosis. Blood, 117, 2348-2357.
-
(2011)
Blood
, vol.117
, pp. 2348-2357
-
-
Schnittger, S.1
Dicker, F.2
Kern, W.3
Wendland, N.4
Sundermann, J.5
Alpermann, T.6
Haferlach, C.7
Haferlach, T.8
-
56
-
-
84859355494
-
Development and validation of a real-time quantification assay to detect and monitor BRAFV600E mutations in hairy cell leukemia
-
Schnittger, S., Bacher, U., Haferlach, T., Wendland, N., Ulke, M., Dicker, F., Grossmann, V., Haferlach, C. & Kern, W. (2012a) Development and validation of a real-time quantification assay to detect and monitor BRAFV600E mutations in hairy cell leukemia. Blood, 119, 3151-3154.
-
(2012)
Blood
, vol.119
, pp. 3151-3154
-
-
Schnittger, S.1
Bacher, U.2
Haferlach, T.3
Wendland, N.4
Ulke, M.5
Dicker, F.6
Grossmann, V.7
Haferlach, C.8
Kern, W.9
-
57
-
-
84873568769
-
ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an adverse outcome
-
doi: 10.1038/leu.2012.262.
-
Schnittger, S., Eder, C., Jeromin, S., Alpermann, T., Fasan, A., Grossmann, V., Kohlmann, A., Illig, T., Klopp, N., Wichmann, H.E., Kreuzer, K.A., Schmid, C., Staib, P., Peceny, R., Schmitz, N., Kern, W., Haferlach, C. & Haferlach, T. (2012b) ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an adverse outcome. Leukemia, doi: 10.1038/leu.2012.262.
-
(2012)
Leukemia
-
-
Schnittger, S.1
Eder, C.2
Jeromin, S.3
Alpermann, T.4
Fasan, A.5
Grossmann, V.6
Kohlmann, A.7
Illig, T.8
Klopp, N.9
Wichmann, H.E.10
Kreuzer, K.A.11
Schmid, C.12
Staib, P.13
Peceny, R.14
Schmitz, N.15
Kern, W.16
Haferlach, C.17
Haferlach, T.18
-
58
-
-
78649297854
-
Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing
-
Teer, J.K., Bonnycastle, L.L., Chines, P.S., Hansen, N.F., Aoyama, N., Swift, A.J., Abaan, H.O., Albert, T.J., Margulies, E.H., Green, E.D., Collins, F.S., Mullikin, J.C. & Biesecker, L.G. (2010) Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing. Genome Research, 20, 1420-1431.
-
(2010)
Genome Research
, vol.20
, pp. 1420-1431
-
-
Teer, J.K.1
Bonnycastle, L.L.2
Chines, P.S.3
Hansen, N.F.4
Aoyama, N.5
Swift, A.J.6
Abaan, H.O.7
Albert, T.J.8
Margulies, E.H.9
Green, E.D.10
Collins, F.S.11
Mullikin, J.C.12
Biesecker, L.G.13
-
59
-
-
70449339945
-
Microdroplet-based PCR enrichment for large-scale targeted sequencing
-
Tewhey, R., Warner, J.B., Nakano, M., Libby, B., Medkova, M., David, P.H., Kotsopoulos, S.K., Samuels, M.L., Hutchison, J.B., Larson, J.W., Topol, E.J., Weiner, M.P., Harismendy, O., Olson, J., Link, D.R. & Frazer, K.A. (2009) Microdroplet-based PCR enrichment for large-scale targeted sequencing. Nature Biotechnology, 27, 1025-1031.
-
(2009)
Nature Biotechnology
, vol.27
, pp. 1025-1031
-
-
Tewhey, R.1
Warner, J.B.2
Nakano, M.3
Libby, B.4
Medkova, M.5
David, P.H.6
Kotsopoulos, S.K.7
Samuels, M.L.8
Hutchison, J.B.9
Larson, J.W.10
Topol, E.J.11
Weiner, M.P.12
Harismendy, O.13
Olson, J.14
Link, D.R.15
Frazer, K.A.16
-
60
-
-
33745926178
-
Sensitive mutation detection in heterogeneous cancer specimens by massively parallel picoliter reactor sequencing
-
Thomas, R.K., Nickerson, E., Simons, J.F., Janne, P.A., Tengs, T., Yuza, Y., Garraway, L.A., LaFramboise, T., Lee, J.C., Shah, K., O'Neill, K., Sasaki, H., Lindeman, N., Wong, K.K., Borras, A.M., Gutmann, E.J., Dragnev, K.H., DeBiasi, R., Chen, T.H., Glatt, K.A., Greulich, H., Desany, B., Lubeski, C.K., Brockman, W., Alvarez, P., Hutchison, S.K., Leamon, J.H., Ronan, M.T., Turenchalk, G.S., Egholm, M., Sellers, W.R., Rothberg, J.M. & Meyerson, M. (2006) Sensitive mutation detection in heterogeneous cancer specimens by massively parallel picoliter reactor sequencing. Nature Medicine, 12, 852-855.
-
(2006)
Nature Medicine
, vol.12
, pp. 852-855
-
-
Thomas, R.K.1
Nickerson, E.2
Simons, J.F.3
Janne, P.A.4
Tengs, T.5
Yuza, Y.6
Garraway, L.A.7
LaFramboise, T.8
Lee, J.C.9
Shah, K.10
O'Neill, K.11
Sasaki, H.12
Lindeman, N.13
Wong, K.K.14
Borras, A.M.15
Gutmann, E.J.16
Dragnev, K.H.17
DeBiasi, R.18
Chen, T.H.19
Glatt, K.A.20
Greulich, H.21
Desany, B.22
Lubeski, C.K.23
Brockman, W.24
Alvarez, P.25
Hutchison, S.K.26
Leamon, J.H.27
Ronan, M.T.28
Turenchalk, G.S.29
Egholm, M.30
Sellers, W.R.31
Rothberg, J.M.32
Meyerson, M.33
more..
-
61
-
-
79959293462
-
BRAF mutations in hairy-cell leukemia
-
Tiacci, E., Trifonov, V., Schiavoni, G., Holmes, A., Kern, W., Martelli, M.P., Pucciarini, A., Bigerna, B., Pacini, R., Wells, V.A., Sportoletti, P., Pettirossi, V., Mannucci, R., Elliott, O., Liso, A., Ambrosetti, A., Pulsoni, A., Forconi, F., Trentin, L., Semenzato, G., Inghirami, G., Capponi, M., Di, R.F., Patti, C., Arcaini, L., Musto, P., Pileri, S., Haferlach, C., Schnittger, S., Pizzolo, G., Foa, R., Farinelli, L., Haferlach, T., Pasqualucci, L., Rabadan, R. & Falini, B. (2011) BRAF mutations in hairy-cell leukemia. New England Journal of Medicine, 364, 2305-2315.
-
(2011)
New England Journal of Medicine
, vol.364
, pp. 2305-2315
-
-
Tiacci, E.1
Trifonov, V.2
Schiavoni, G.3
Holmes, A.4
Kern, W.5
Martelli, M.P.6
Pucciarini, A.7
Bigerna, B.8
Pacini, R.9
Wells, V.A.10
Sportoletti, P.11
Pettirossi, V.12
Mannucci, R.13
Elliott, O.14
Liso, A.15
Ambrosetti, A.16
Pulsoni, A.17
Forconi, F.18
Trentin, L.19
Semenzato, G.20
Inghirami, G.21
Capponi, M.22
Di, R.F.23
Patti, C.24
Arcaini, L.25
Musto, P.26
Pileri, S.27
Haferlach, C.28
Schnittger, S.29
Pizzolo, G.30
Foa, R.31
Farinelli, L.32
Haferlach, T.33
Pasqualucci, L.34
Rabadan, R.35
Falini, B.36
more..
-
62
-
-
84855225601
-
The corepressors BCOR and BCORL1: two novel players in acute myeloid leukemia
-
Tiacci, E., Grossmann, V., Martelli, M.P., Kohlmann, A., Haferlach, T. & Falini, B. (2012) The corepressors BCOR and BCORL1: two novel players in acute myeloid leukemia. Haematologica, 97, 3-5.
-
(2012)
Haematologica
, vol.97
, pp. 3-5
-
-
Tiacci, E.1
Grossmann, V.2
Martelli, M.P.3
Kohlmann, A.4
Haferlach, T.5
Falini, B.6
-
63
-
-
84865475885
-
MYD88 L265P somatic mutation in Waldenstrom's macroglobulinemia
-
Treon, S.P., Xu, L., Yang, G., Zhou, Y., Liu, X., Cao, Y., Sheehy, P., Manning, R.J., Patterson, C.J., Tripsas, C., Arcaini, L., Pinkus, G.S., Rodig, S.J., Sohani, A.R., Harris, N.L., Laramie, J.M., Skifter, D.A., Lincoln, S.E. & Hunter, Z.R. (2012) MYD88 L265P somatic mutation in Waldenstrom's macroglobulinemia. New England Journal of Medicine, 367, 826-833.
-
(2012)
New England Journal of Medicine
, vol.367
, pp. 826-833
-
-
Treon, S.P.1
Xu, L.2
Yang, G.3
Zhou, Y.4
Liu, X.5
Cao, Y.6
Sheehy, P.7
Manning, R.J.8
Patterson, C.J.9
Tripsas, C.10
Arcaini, L.11
Pinkus, G.S.12
Rodig, S.J.13
Sohani, A.R.14
Harris, N.L.15
Laramie, J.M.16
Skifter, D.A.17
Lincoln, S.E.18
Hunter, Z.R.19
-
64
-
-
77950299929
-
PHF6 mutations in T-cell acute lymphoblastic leukemia
-
Van Vlierberghe, P., Palomero, T., Khiabanian, H., Van der, M.J., Castillo, M., Van, R.N., De, M.B., Philippe, J., Gonzalez-Garcia, S., Toribio, M.L., Taghon, T., Zuurbier, L., Cauwelier, B., Harrison, C.J., Schwab, C., Pisecker, M., Strehl, S., Langerak, A.W., Gecz, J., Sonneveld, E., Pieters, R., Paietta, E., Rowe, J.M., Wiernik, P.H., Benoit, Y., Soulier, J., Poppe, B., Yao, X., Cordon-Cardo, C., Meijerink, J., Rabadan, R., Speleman, F. & Ferrando, A. (2010) PHF6 mutations in T-cell acute lymphoblastic leukemia. Nature Genetics, 42, 338-342.
-
(2010)
Nature Genetics
, vol.42
, pp. 338-342
-
-
Van Vlierberghe, P.1
Palomero, T.2
Khiabanian, H.3
Van der, M.J.4
Castillo, M.5
Van, R.N.6
De, M.B.7
Philippe, J.8
Gonzalez-Garcia, S.9
Toribio, M.L.10
Taghon, T.11
Zuurbier, L.12
Cauwelier, B.13
Harrison, C.J.14
Schwab, C.15
Pisecker, M.16
Strehl, S.17
Langerak, A.W.18
Gecz, J.19
Sonneveld, E.20
Pieters, R.21
Paietta, E.22
Rowe, J.M.23
Wiernik, P.H.24
Benoit, Y.25
Soulier, J.26
Poppe, B.27
Yao, X.28
Cordon-Cardo, C.29
Meijerink, J.30
Rabadan, R.31
Speleman, F.32
Ferrando, A.33
more..
-
65
-
-
78649484216
-
A de novo paradigm for mental retardation
-
Vissers, L.E., de, L.J., Gilissen, C., Janssen, I., Steehouwer, M., de Vries, P., van Lier, B., Arts, P., Wieskamp, N., del Rosario, M., van Bon, B.W., Hoischen, A., de Vries, B.B., Brunner, H.G. & Veltman, J.A. (2010) A de novo paradigm for mental retardation. Nature Genetics, 42, 1109-1112.
-
(2010)
Nature Genetics
, vol.42
, pp. 1109-1112
-
-
Vissers, L.E.1
de, L.J.2
Gilissen, C.3
Janssen, I.4
Steehouwer, M.5
de Vries, P.6
van Lier, B.7
Arts, P.8
Wieskamp, N.9
del Rosario, M.10
van Bon, B.W.11
Hoischen, A.12
de Vries, B.B.13
Brunner, H.G.14
Veltman, J.A.15
-
66
-
-
77956792326
-
Next generation sequencing for clinical diagnostics-principles and application to targeted resequencing for hypertrophic cardiomyopathy: a paper from the 2009 William Beaumont Hospital Symposium on Molecular Pathology
-
Voelkerding, K.V., Dames, S. & Durtschi, J.D. (2010) Next generation sequencing for clinical diagnostics-principles and application to targeted resequencing for hypertrophic cardiomyopathy: a paper from the 2009 William Beaumont Hospital Symposium on Molecular Pathology. Journal of Molecular Diagnostics, 12, 539-551.
-
(2010)
Journal of Molecular Diagnostics
, vol.12
, pp. 539-551
-
-
Voelkerding, K.V.1
Dames, S.2
Durtschi, J.D.3
-
67
-
-
84863337617
-
Clonal architecture of secondary acute myeloid leukemia
-
Walter, M.J., Shen, D., Ding, L., Shao, J., Koboldt, D.C., Chen, K., Larson, D.E., McLellan, M.D., Dooling, D., Abbott, R., Fulton, R., Magrini, V., Schmidt, H., Kalicki-Veizer, J., O'Laughlin, M., Fan, X., Grillot, M., Witowski, S., Heath, S., Frater, J.L., Eades, W., Tomasson, M., Westervelt, P., Dipersio, J.F., Link, D.C., Mardis, E.R., Ley, T.J., Wilson, R.K. & Graubert, T.A. (2012) Clonal architecture of secondary acute myeloid leukemia. New England Journal of Medicine, 366, 1090-1098.
-
(2012)
New England Journal of Medicine
, vol.366
, pp. 1090-1098
-
-
Walter, M.J.1
Shen, D.2
Ding, L.3
Shao, J.4
Koboldt, D.C.5
Chen, K.6
Larson, D.E.7
McLellan, M.D.8
Dooling, D.9
Abbott, R.10
Fulton, R.11
Magrini, V.12
Schmidt, H.13
Kalicki-Veizer, J.14
O'Laughlin, M.15
Fan, X.16
Grillot, M.17
Witowski, S.18
Heath, S.19
Frater, J.L.20
Eades, W.21
Tomasson, M.22
Westervelt, P.23
Dipersio, J.F.24
Link, D.C.25
Mardis, E.R.26
Ley, T.J.27
Wilson, R.K.28
Graubert, T.A.29
more..
-
68
-
-
84855370035
-
SF3B1 and other novel cancer genes in chronic lymphocytic leukemia
-
Wang, L., Lawrence, M.S., Wan, Y., Stojanov, P., Sougnez, C., Stevenson, K., Werner, L., Sivachenko, A., DeLuca, D.S., Zhang, L., Zhang, W., Vartanov, A.R., Fernandes, S.M., Goldstein, N.R., Folco, E.G., Cibulskis, K., Tesar, B., Sievers, Q.L., Shefler, E., Gabriel, S., Hacohen, N., Reed, R., Meyerson, M., Golub, T.R., Lander, E.S., Neuberg, D., Brown, J.R., Getz, G. & Wu, C.J. (2011) SF3B1 and other novel cancer genes in chronic lymphocytic leukemia. New England Journal of Medicine, 365, 2497-2506.
-
(2011)
New England Journal of Medicine
, vol.365
, pp. 2497-2506
-
-
Wang, L.1
Lawrence, M.S.2
Wan, Y.3
Stojanov, P.4
Sougnez, C.5
Stevenson, K.6
Werner, L.7
Sivachenko, A.8
DeLuca, D.S.9
Zhang, L.10
Zhang, W.11
Vartanov, A.R.12
Fernandes, S.M.13
Goldstein, N.R.14
Folco, E.G.15
Cibulskis, K.16
Tesar, B.17
Sievers, Q.L.18
Shefler, E.19
Gabriel, S.20
Hacohen, N.21
Reed, R.22
Meyerson, M.23
Golub, T.R.24
Lander, E.S.25
Neuberg, D.26
Brown, J.R.27
Getz, G.28
Wu, C.J.29
more..
-
69
-
-
84864255882
-
The origin and evolution of mutations in acute myeloid leukemia
-
Welch, J.S., Ley, T.J., Link, D.C., Miller, C.A., Larson, D.E., Koboldt, D.C., Wartman, L.D., Lamprecht, T.L., Liu, F., Xia, J., Kandoth, C., Fulton, R.S., McLellan, M.D., Dooling, D.J., Wallis, J.W., Chen, K., Harris, C.C., Schmidt, H.K., Kalicki-Veizer, J.M., Lu, C., Zhang, Q., Lin, L., O'Laughlin, M.D., McMichael, J.F., Delehaunty, K.D., Fulton, L.A., Magrini, V.J., McGrath, S.D., Demeter, R.T., Vickery, T.L., Hundal, J., Cook, L.L., Swift, G.W., Reed, J.P., Alldredge, P.A., Wylie, T.N., Walker, J.R., Watson, M.A., Heath, S.E., Shannon, W.D., Varghese, N., Nagarajan, R., Payton, J.E., Baty, J.D., Kulkarni, S., Klco, J.M., Tomasson, M.H., Westervelt, P., Walter, M.J., Graubert, T.A., Dipersio, J.F., Ding, L., Mardis, E.R. & Wilson, R.K. (2012) The origin and evolution of mutations in acute myeloid leukemia. Cell, 150, 264-278.
-
(2012)
Cell
, vol.150
, pp. 264-278
-
-
Welch, J.S.1
Ley, T.J.2
Link, D.C.3
Miller, C.A.4
Larson, D.E.5
Koboldt, D.C.6
Wartman, L.D.7
Lamprecht, T.L.8
Liu, F.9
Xia, J.10
Kandoth, C.11
Fulton, R.S.12
McLellan, M.D.13
Dooling, D.J.14
Wallis, J.W.15
Chen, K.16
Harris, C.C.17
Schmidt, H.K.18
Kalicki-Veizer, J.M.19
Lu, C.20
Zhang, Q.21
Lin, L.22
O'Laughlin, M.D.23
McMichael, J.F.24
Delehaunty, K.D.25
Fulton, L.A.26
Magrini, V.J.27
McGrath, S.D.28
Demeter, R.T.29
Vickery, T.L.30
Hundal, J.31
Cook, L.L.32
Swift, G.W.33
Reed, J.P.34
Alldredge, P.A.35
Wylie, T.N.36
Walker, J.R.37
Watson, M.A.38
Heath, S.E.39
Shannon, W.D.40
Varghese, N.41
Nagarajan, R.42
Payton, J.E.43
Baty, J.D.44
Kulkarni, S.45
Klco, J.M.46
Tomasson, M.H.47
Westervelt, P.48
Walter, M.J.49
Graubert, T.A.50
Dipersio, J.F.51
Ding, L.52
Mardis, E.R.53
Wilson, R.K.54
more..
-
70
-
-
80053900941
-
Frequent pathway mutations of splicing machinery in myelodysplasia
-
Yoshida, K., Sanada, M., Shiraishi, Y., Nowak, D., Nagata, Y., Yamamoto, R., Sato, Y., Sato-Otsubo, A., Kon, A., Nagasaki, M., Chalkidis, G., Suzuki, Y., Shiosaka, M., Kawahata, R., Yamaguchi, T., Otsu, M., Obara, N., Sakata-Yanagimoto, M., Ishiyama, K., Mori, H., Nolte, F., Hofmann, W.K., Miyawaki, S., Sugano, S., Haferlach, C., Koeffler, H.P., Shih, L.Y., Haferlach, T., Chiba, S., Nakauchi, H., Miyano, S. & Ogawa, S. (2011) Frequent pathway mutations of splicing machinery in myelodysplasia. Nature, 478, 64-69.
-
(2011)
Nature
, vol.478
, pp. 64-69
-
-
Yoshida, K.1
Sanada, M.2
Shiraishi, Y.3
Nowak, D.4
Nagata, Y.5
Yamamoto, R.6
Sato, Y.7
Sato-Otsubo, A.8
Kon, A.9
Nagasaki, M.10
Chalkidis, G.11
Suzuki, Y.12
Shiosaka, M.13
Kawahata, R.14
Yamaguchi, T.15
Otsu, M.16
Obara, N.17
Sakata-Yanagimoto, M.18
Ishiyama, K.19
Mori, H.20
Nolte, F.21
Hofmann, W.K.22
Miyawaki, S.23
Sugano, S.24
Haferlach, C.25
Koeffler, H.P.26
Shih, L.Y.27
Haferlach, T.28
Chiba, S.29
Nakauchi, H.30
Miyano, S.31
Ogawa, S.32
more..
-
71
-
-
79551504914
-
TP53 mutation and survival in chronic lymphocytic leukemia
-
Zenz, T., Eichhorst, B., Busch, R., Denzel, T., Habe, S., Winkler, D., Buhler, A., Edelmann, J., Bergmann, M., Hopfinger, G., Hensel, M., Hallek, M., Dohner, H. & Stilgenbauer, S. (2010) TP53 mutation and survival in chronic lymphocytic leukemia. Journal of Clinical Oncology, 28, 4473-4479.
-
(2010)
Journal of Clinical Oncology
, vol.28
, pp. 4473-4479
-
-
Zenz, T.1
Eichhorst, B.2
Busch, R.3
Denzel, T.4
Habe, S.5
Winkler, D.6
Buhler, A.7
Edelmann, J.8
Bergmann, M.9
Hopfinger, G.10
Hensel, M.11
Hallek, M.12
Dohner, H.13
Stilgenbauer, S.14
-
72
-
-
84856077133
-
Analysis of the ABCA4 gene by next-generation sequencing
-
Zernant, J., Schubert, C., Im, K.M., Burke, T., Brown, C.M., Fishman, G.A., Tsang, S.H., Gouras, P., Dean, M. & Allikmets, R. (2011) Analysis of the ABCA4 gene by next-generation sequencing. Investigative Ophthalmology and Visual Science, 52, 8479-8487.
-
(2011)
Investigative Ophthalmology and Visual Science
, vol.52
, pp. 8479-8487
-
-
Zernant, J.1
Schubert, C.2
Im, K.M.3
Burke, T.4
Brown, C.M.5
Fishman, G.A.6
Tsang, S.H.7
Gouras, P.8
Dean, M.9
Allikmets, R.10
-
73
-
-
78649329196
-
Systematic detection of putative tumor suppressor genes through the combined use of exome and transcriptome sequencing
-
Zhao, Q., Kirkness, E.F., Caballero, O.L., Galante, P.A., Parmigiani, R.B., Edshall, L., Kuan, S., Ye, Z., Levy, S., Vasconcelos, A.T., Ren, B., de Souza, S.J., Camargo, A.A., Simpson, A.J. & Strausberg, R.L. (2010) Systematic detection of putative tumor suppressor genes through the combined use of exome and transcriptome sequencing. Genome Biology, 11, R114.
-
(2010)
Genome Biology
, vol.11
-
-
Zhao, Q.1
Kirkness, E.F.2
Caballero, O.L.3
Galante, P.A.4
Parmigiani, R.B.5
Edshall, L.6
Kuan, S.7
Ye, Z.8
Levy, S.9
Vasconcelos, A.T.10
Ren, B.11
de Souza, S.J.12
Camargo, A.A.13
Simpson, A.J.14
Strausberg, R.L.15
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