-
1
-
-
77950349542
-
Proteomics and breast cancer: A search for novel diagnostic and theragnostic biomarkers
-
Gilabert M, Audebert S, Viens P, Borg JP, Bertucci F, Goncalves A. Proteomics and breast cancer: a search for novel diagnostic and theragnostic biomarkers. Bull Cancer 2010; 97 : 321-39.
-
(2010)
Bull Cancer
, vol.97
, pp. 321-339
-
-
Gilabert, M.1
Audebert, S.2
Viens, P.3
Borg, J.P.4
Bertucci, F.5
Goncalves, A.6
-
2
-
-
78650129338
-
Search for new genes involved in breast tumorigenesis by "omics" analysis
-
Bieche I. Search for new genes involved in breast tumorigenesis by "Omics" analysis. Bull Cancer 2010; 97 : 1365-80.
-
(2010)
Bull Cancer
, vol.97
, pp. 1365-1380
-
-
Bieche, I.1
-
3
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
DOI 10.1038/35057062
-
Lander ES, Linton LM, Birren B, et al. Initial sequencing and analysis of the human genome. Nature 2001; 409 : 860-921. (Pubitemid 32165345)
-
(2001)
Nature
, vol.409
, Issue.6822
, pp. 860-921
-
-
Lander, E.S.1
Linton, L.M.2
Birren, B.3
Nusbaum, C.4
Zody, M.C.5
Baldwin, J.6
Devon, K.7
Dewar, K.8
Doyle, M.9
Fitzhugh, W.10
Funke, R.11
Gage, D.12
Harris, K.13
Heaford, A.14
Howland, J.15
Kann, L.16
Lehoczky, J.17
Levine, R.18
McEwan, P.19
McKernan, K.20
Meldrim, J.21
Mesirov, J.P.22
Miranda, C.23
Morris, W.24
Naylor, J.25
Raymond, C.26
Rosetti, M.27
Santos, R.28
Sheridan, A.29
Sougnez, C.30
Stange-Thomann, N.31
Stojanovic, N.32
Subramanian, A.33
Wyman, D.34
Rogers, J.35
Sulston, J.36
Ainscough, R.37
Beck, S.38
Bentley, D.39
Burton, J.40
Clee, C.41
Carter, N.42
Coulson, A.43
Deadman, R.44
Deloukas, P.45
Dunham, A.46
Dunham, I.47
Durbin, R.48
French, L.49
Grafham, D.50
Gregory, S.51
Hubbard, T.52
Humphray, S.53
Hunt, A.54
Jones, M.55
Lloyd, C.56
McMurray, A.57
Matthews, L.58
Mercer, S.59
Milne, S.60
Mullikin, J.C.61
Mungall, A.62
Plumb, R.63
Ross, M.64
Shownkeen, R.65
Sims, S.66
Waterston, R.H.67
Wilson, R.K.68
Hillier, L.W.69
McPherson, J.D.70
Marra, M.A.71
Mardis, E.R.72
Fulton, L.A.73
Chinwalla, A.T.74
Pepin, K.H.75
Gish, W.R.76
Chissoe, S.L.77
more..
-
4
-
-
79960597679
-
An integrated semiconductor device enabling non-optical genome sequencing
-
Rothberg JM, Hinz W, Rearick TM, et al. An integrated semiconductor device enabling non-optical genome sequencing. Nature 2011; 475 : 348-52.
-
(2011)
Nature
, vol.475
, pp. 348-352
-
-
Rothberg, J.M.1
Hinz, W.2
Rearick, T.M.3
-
5
-
-
84860756398
-
Performance comparison of benchtop high-Throughput sequencing platforms
-
Loman NJ, Misra RV, Dallman TJ, et al. Performance comparison of benchtop high-Throughput sequencing platforms. Nat Biotechnol 2012; 30 : 434-9.
-
(2012)
Nat Biotechnol
, vol.30
, pp. 434-439
-
-
Loman, N.J.1
Misra, R.V.2
Dallman, T.J.3
-
6
-
-
77955868506
-
Computational solutions to large-scale data management and analysis
-
Schadt EE, Linderman MD, Sorenson J, Lee L, Nolan GP. Computational solutions to large-scale data management and analysis. Nat Rev Genet 2010; 11 : 647-57.
-
(2010)
Nat Rev Genet
, vol.11
, pp. 647-657
-
-
Schadt, E.E.1
Linderman, M.D.2
Sorenson, J.3
Lee, L.4
Nolan, G.P.5
-
7
-
-
67649406102
-
Mutation of foxl2 in granulosa-cell tumors of the ovary
-
Shah SP, Kobel M, Senz J, et al. Mutation of FOXL2 in granulosa-cell tumors of the ovary. N Engl J Med 2009; 360 : 2719-29.
-
(2009)
N Engl J Med
, vol.360
, pp. 2719-2729
-
-
Shah, S.P.1
Kobel, M.2
Senz, J.3
-
8
-
-
78650046221
-
Complete characterization of the micrornaome in a patient with acute myeloid leukemia
-
Ramsingh G, Koboldt DC, Trissal M, et al. Complete characterization of the microRNAome in a patient with acute myeloid leukemia. Blood 2010; 116 : 5316-26.
-
(2010)
Blood
, vol.116
, pp. 5316-5326
-
-
Ramsingh, G.1
Koboldt, D.C.2
Trissal, M.3
-
9
-
-
59849113821
-
Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing
-
Gnirke A, Melnikov A, Maguire J, et al. Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing. Nat Biotechnol 2009; 27 : 182-9.
-
(2009)
Nat Biotechnol
, vol.27
, pp. 182-189
-
-
Gnirke, A.1
Melnikov, A.2
Maguire, J.3
-
10
-
-
73149123343
-
Genetic diagnosis by whole exome capture and massively parallel dna sequencing
-
Choi M, Scholl UI, Ji W, et al. Genetic diagnosis by whole exome capture and massively parallel DNA sequencing. Proc Natl Acad Sci U S A 2009; 106 : 19096-101.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 19096-19101
-
-
Choi, M.1
Scholl, U.I.2
Ji, W.3
-
11
-
-
79953766940
-
Tumour evolution inferred by single-cell sequencing
-
Navin N, Kendall J, Troge J, et al. Tumour evolution inferred by single-cell sequencing. Nature 2011; 472 : 90-4.
-
(2011)
Nature
, vol.472
, pp. 90-94
-
-
Navin, N.1
Kendall, J.2
Troge, J.3
-
12
-
-
84863637922
-
Accuratewhole-genome sequencing and haplotyping from 10 to 20 human cells
-
Peters BA, Kermani BG, Sparks AB, et al. Accuratewhole-genome sequencing and haplotyping from 10 to 20 human cells. Nature 2012; 487 : 190-5.
-
(2012)
Nature
, vol.487
, pp. 190-195
-
-
Peters, B.A.1
Kermani, B.G.2
Sparks, A.B.3
-
13
-
-
84863393080
-
Intratumor heterogeneity and branched evolution revealed by multiregion sequencing
-
Gerlinger M, Rowan AJ, Horswell S, et al. Intratumor heterogeneity and branched evolution revealed by multiregion sequencing. N Engl J Med 2012; 366 : 883-92.
-
(2012)
N Engl J Med
, vol.366
, pp. 883-892
-
-
Gerlinger, M.1
Rowan, A.J.2
Horswell, S.3
-
14
-
-
34547834963
-
The use of coded pcr primers enables high-Throughput sequencing of multiple homolog amplification products by 454 parallel sequencing
-
Binladen J, Gilbert MT, Bollback JP, et al. The use of coded PCR primers enables high-Throughput sequencing of multiple homolog amplification products by 454 parallel sequencing. PLoS One 2007; 2 : e197.
-
(2007)
PLoS One
, vol.2
-
-
Binladen, J.1
Gilbert, M.T.2
Bollback, J.P.3
-
15
-
-
63349090507
-
The oncogenic ews-fli1 protein binds in vivo ggaa microsatellite sequences with potential transcriptional activation function
-
Guillon N, Tirode F, Boeva V, Zynovyev A, Barillot E, Delattre O. The oncogenic EWS-FLI1 protein binds in vivo GGAA microsatellite sequences with potential transcriptional activation function. PLoS One 2009; 4 : e4932.
-
(2009)
PLoS One
, vol.4
-
-
Guillon, N.1
Tirode, F.2
Boeva, V.3
Zynovyev, A.4
Barillot, E.5
Delattre, O.6
-
16
-
-
77957322330
-
Whole methylome analysis by ultra-deep sequencing using two-base encoding
-
Bormann Chung CA, Boyd VL, McKernan KJ, et al. Whole methylome analysis by ultra-deep sequencing using two-base encoding. PLoS One 2010; 5 : e9320.
-
(2010)
PLoS One
, vol.5
-
-
Bormann Chung, C.A.1
Boyd, V.L.2
McKernan, K.J.3
-
18
-
-
70149093912
-
Recurring mutations found by sequencing an acute myeloid leukemia genome
-
Mardis ER, Ding L, Dooling DJ, et al. Recurring mutations found by sequencing an acute myeloid leukemia genome. N Engl J Med 2009; 361 : 1058-66.
-
(2009)
N Engl J Med
, vol.361
, pp. 1058-1066
-
-
Mardis, E.R.1
Ding, L.2
Dooling, D.J.3
-
19
-
-
84857985225
-
Ret, ros1 and alk fusions in lung cancer
-
Takeuchi K, Soda M, Togashi Y, et al. RET, ROS1 and ALK fusions in lung cancer. Nat Med 2012; 18 : 378-81.
-
(2012)
Nat Med
, vol.18
, pp. 378-381
-
-
Takeuchi, K.1
Soda, M.2
Togashi, Y.3
-
21
-
-
78649906060
-
Dnmt3a mutations in acute myeloid leukemia
-
Ley TJ, Ding L, Walter MJ, et al. DNMT3A mutations in acute myeloid leukemia. N Engl J Med 2010; 363 : 2424-33.
-
(2010)
N Engl J Med
, vol.363
, pp. 2424-2433
-
-
Ley, T.J.1
Ding, L.2
Walter, M.J.3
-
22
-
-
60849115270
-
Idh1 and idh2 mutations in gliomas
-
Yan H, Parsons DW, Jin G, et al. IDH1 and IDH2 mutations in gliomas. N Engl J Med 2009; 360 : 765-73.
-
(2009)
N Engl J Med
, vol.360
, pp. 765-773
-
-
Yan, H.1
Parsons, D.W.2
Jin, G.3
-
23
-
-
82555205202
-
A sumoylationdefective mitf germline mutation predisposes to melanoma and renal carcinoma
-
Bertolotto C, Lesueur F, Giuliano S, et al. A SUMOylationdefective MITF germline mutation predisposes to melanoma and renal carcinoma. Nature 2011; 480 : 94-8.
-
(2011)
Nature
, vol.480
, pp. 94-98
-
-
Bertolotto, C.1
Lesueur, F.2
Giuliano, S.3
-
24
-
-
70350072363
-
Cancer genetics: Estimation of the needs of the population in france for the next ten years
-
Bonaiti-Pellie C, Andrieu N, Arveux P, et al. Cancer genetics: estimation of the needs of the population in France for the next ten years. Bull Cancer 2009; 96 : 875-900.
-
(2009)
Bull Cancer
, vol.96
, pp. 875-900
-
-
Bonaiti-Pellie, C.1
Andrieu, N.2
Arveux, P.3
-
25
-
-
84861429390
-
Birth notice: A new bone sarcoma has been born
-
Orbach D. Birth notice: a new bone sarcoma has been born. Bull Cancer 2012; 99 : 512.
-
(2012)
Bull Cancer
, vol.99
, pp. 512
-
-
Orbach, D.1
-
26
-
-
84859430312
-
A new subtype of bone sarcoma defined by bcor-ccnb3 gene fusion
-
Pierron G, Tirode F, Lucchesi C, et al. A new subtype of bone sarcoma defined by BCOR-CCNB3 gene fusion. Nat Genet 2012; 44 : 461-6.
-
(2012)
Nat Genet
, vol.44
, pp. 461-466
-
-
Pierron, G.1
Tirode, F.2
Lucchesi, C.3
-
27
-
-
79951906119
-
Pilot study using molecular profiling of patients' tumors to find potential targets and select treatments for their refractory cancers
-
von Hoff DD, Stephenson Jr. JJ, Rosen P, et al. Pilot study using molecular profiling of patients' tumors to find potential targets and select treatments for their refractory cancers. J Clin Oncol 2010; 28 : 4877-83.
-
(2010)
J Clin Oncol
, vol.28
, pp. 4877-4883
-
-
Von Hoff, D.D.1
Stephenson Jr., J.J.2
Rosen, P.3
-
28
-
-
51349141191
-
Circulating mutant dna to assess tumor dynamics
-
Diehl F, Schmidt K, Choti MA, et al. Circulating mutant DNA to assess tumor dynamics. Nat Med 2008; 14 : 985-90.
-
(2008)
Nat Med
, vol.14
, pp. 985-990
-
-
Diehl, F.1
Schmidt, K.2
Choti, M.A.3
-
29
-
-
74449085934
-
A small-cell lung cancer genome with complex signatures of tobacco exposure
-
Pleasance ED, Stephens PJ, O'Meara S, et al. A small-cell lung cancer genome with complex signatures of tobacco exposure. Nature 2010; 463 : 184-90.
-
(2010)
Nature
, vol.463
, pp. 184-190
-
-
Pleasance, E.D.1
Stephens, P.J.2
O'Meara, S.3
|