-
1
-
-
4944240144
-
Genetic predisposition to colorectal cancer
-
A. De La Chapelle, "Genetic predisposition to colorectal cancer," Nature Reviews Cancer, vol. 4, no. 10, pp. 769-780, 2004.
-
(2004)
Nature Reviews Cancer
, vol.4
, Issue.10
, pp. 769-780
-
-
De La Chapelle, A.1
-
2
-
-
64749094310
-
The cancer genome
-
M. R. Stratton, P. J. Campbell, and P. A. Futreal, "The cancer genome," Nature, vol. 458, no. 7239, pp. 719-724, 2009.
-
(2009)
Nature
, vol.458
, Issue.7239
, pp. 719-724
-
-
Stratton, M.R.1
Campbell, P.J.2
Futreal, P.A.3
-
3
-
-
4043181214
-
Cancer genes and the pathways they control
-
B. Vogelstein and K. W. Kinzler, "Cancer genes and the pathways they control," Nature Medicine, vol. 10, no. 8, pp. 789-799, 2004.
-
(2004)
Nature Medicine
, vol.10
, Issue.8
, pp. 789-799
-
-
Vogelstein, B.1
Kinzler, K.W.2
-
4
-
-
0037370476
-
The genetics and genomics of cancer
-
A. Balmain, J. Gray, and B. Ponder, "The genetics and genomics of cancer," Nature Genetics, vol. 33, supplement, pp. 238-244, 2003.
-
(2003)
Nature Genetics
, vol.33
, pp. 238-244
-
-
Balmain, A.1
Gray, J.2
Ponder, B.3
-
5
-
-
36248962105
-
The genomic landscapes of human breast and colorectal cancers
-
L. D. Wood, D. W. Parsons, S. Jones et al., "The genomic landscapes of human breast and colorectal cancers," Science, vol. 318, no. 5853, pp. 1108-1113, 2007.
-
(2007)
Science
, vol.318
, Issue.5853
, pp. 1108-1113
-
-
Wood, L.D.1
Parsons, D.W.2
Jones, S.3
-
6
-
-
33947101019
-
Patterns of somatic mutation in human cancer genomes
-
C. Greenman, P. Stephens, R. Smith et al., "Patterns of somatic mutation in human cancer genomes," Nature, vol. 446, pp. 153-158, 2007.
-
(2007)
Nature
, vol.446
, pp. 153-158
-
-
Greenman, C.1
Stephens, P.2
Smith, R.3
-
7
-
-
84856753045
-
The genetic basis for cancer treatment decisions
-
J. E. Dancey, P. L. Bedard, N. Onetto, and T. J. Hudson, "The genetic basis for cancer treatment decisions," Cell, vol. 148, no. 3, pp. 409-420, 2012.
-
(2012)
Cell
, vol.148
, Issue.3
, pp. 409-420
-
-
Dancey, J.E.1
Bedard, P.L.2
Onetto, N.3
Hudson, T.J.4
-
8
-
-
84873093569
-
Feasibility of real time next generation sequencing of cancer genes linked to drug response: Results from a clinical trial
-
B. Tran, A. M. K. Brown, P. L. Bedard et al., "Feasibility of real time next generation sequencing of cancer genes linked to drug response: results from a clinical trial," International Journal of Cancer, vol. 132, no. 7, pp. 1547-1555, 2013.
-
(2013)
International Journal of Cancer
, vol.132
, Issue.7
, pp. 1547-1555
-
-
Tran, B.1
Brown, A.M.K.2
Bedard, P.L.3
-
9
-
-
65349189958
-
American society of clinical oncology provisional clinical opinion: Testing for KRAS gene mutations in patients with metastatic colorectal carcinoma to predict response to anti-epidermal growth factor receptor monoclonal antibody therapy
-
C. J. Allegra, J. M. Jessup, M. R. Somerfield et al., "American society of clinical oncology provisional clinical opinion: testing for KRAS gene mutations in patients with metastatic colorectal carcinoma to predict response to anti-epidermal growth factor receptor monoclonal antibody therapy," Journal of Clinical Oncology, vol. 27, no. 12, pp. 2091-2096, 2009.
-
(2009)
Journal of Clinical Oncology
, vol.27
, Issue.12
, pp. 2091-2096
-
-
Allegra, C.J.1
Jessup, J.M.2
Somerfield, M.R.3
-
10
-
-
54949085398
-
K-ras mutations and benefit from cetuximab in advanced colorectal cancer
-
C. S. Karapetis, S. Khambata-Ford, D. J. Jonker et al., "K-ras mutations and benefit from cetuximab in advanced colorectal cancer," The New England Journal of Medicine, vol. 359, no. 17, pp. 1757-1765, 2008.
-
(2008)
The New England Journal of Medicine
, vol.359
, Issue.17
, pp. 1757-1765
-
-
Karapetis, C.S.1
Khambata-Ford, S.2
Jonker, D.J.3
-
11
-
-
84887491073
-
Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing
-
G. M. Frampton, A. Fichtenholtz, G. A. Otto et al., "Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing," Nature Biotechnology, vol. 31, no. 11, pp. 1023-1031, 2013.
-
(2013)
Nature Biotechnology
, vol.31
, Issue.11
, pp. 1023-1031
-
-
Frampton, G.M.1
Fichtenholtz, A.2
Otto, G.A.3
-
12
-
-
84855564475
-
Next-generation sequencing for cancer diagnostics: A practical perspective
-
C. Meldrum, M. A. Doyle, and R. W. Tothill, "Next-generation sequencing for cancer diagnostics: a practical perspective," Clinical Biochemist Reviews, vol. 32, no. 4, pp. 177-195, 2011.
-
(2011)
Clinical Biochemist Reviews
, vol.32
, Issue.4
, pp. 177-195
-
-
Meldrum, C.1
Doyle, M.A.2
Tothill, R.W.3
-
13
-
-
84871609389
-
Mutation detection by clonal sequencing of PCR amplicons and grouped read typing is applicable to clinical diagnostics
-
P. A. Chambers, L. F. Stead, J. E. Morgan et al., "Mutation detection by clonal sequencing of pcr amplicons and grouped read typing is applicable to clinical diagnostics," Human Mutation, vol. 34, no. 1, pp. 248-254, 2013.
-
(2013)
Human Mutation
, vol.34
, Issue.1
, pp. 248-254
-
-
Chambers, P.A.1
Stead, L.F.2
Morgan, J.E.3
-
14
-
-
77449121614
-
Target-enrichment strategies for next-generation sequencing
-
L. Mamanova, A. J. Coffey, C. E. Scott et al., "Target-enrichment strategies for next-generation sequencing,"NatureMethods, vol. 7, no. 2, pp. 111-118, 2010.
-
(2010)
NatureMethods
, vol.7
, Issue.2
, pp. 111-118
-
-
Mamanova, L.1
Coffey, A.J.2
Scott, C.E.3
-
15
-
-
84890409823
-
Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimens
-
C. C. Pritchard, S. J. Salipante, K. Koehler et al., "Validation and implementation of targeted capture and sequencing for the detection of actionable mutation, copy number variation, and gene rearrangement in clinical cancer specimens," Journal of Molecular Diagnostics, vol. 16, no. 1, pp. 56-67, 2014.
-
(2014)
Journal of Molecular Diagnostics
, vol.16
, Issue.1
, pp. 56-67
-
-
Pritchard, C.C.1
Salipante, S.J.2
Koehler, K.3
-
16
-
-
84893750117
-
Nextgeneration sequencing-based multi-gene mutation profiling of solid tumors using fine needle aspiration samples: Promises and challenges for routine clinical diagnostics
-
R. Kanagal-Shamanna, B. P. Portier, R. R. Singh et al., "Nextgeneration sequencing-based multi-gene mutation profiling of solid tumors using fine needle aspiration samples: promises and challenges for routine clinical diagnostics," Modern Pathology, vol. 27, no. 2, pp. 314-327, 2014.
-
(2014)
Modern Pathology
, vol.27
, Issue.2
, pp. 314-327
-
-
Kanagal-Shamanna, R.1
Portier, B.P.2
Singh, R.R.3
-
17
-
-
77955059918
-
Genetic diagnosis of familial breast cancer using clonal sequencing
-
J. E. Morgan, I. M. Carr, E. Sheridan et al., "Genetic diagnosis of familial breast cancer using clonal sequencing," Human Mutation, vol. 31, no. 4, pp. 484-491, 2010.
-
(2010)
Human Mutation
, vol.31
, Issue.4
, pp. 484-491
-
-
Morgan, J.E.1
Carr, I.M.2
Sheridan, E.3
-
18
-
-
84896137851
-
Robust diagnostic genetic testing using solution capture enrichment and a novel variant-filtering interface
-
C. M. Watson, L. A. Crinnion, J. E. Morgan et al., "Robust diagnostic genetic testing using solution capture enrichment and a novel variant-filtering interface," Human Mutation, vol. 35, no. 4, pp. 434-441, 2014.
-
(2014)
Human Mutation
, vol.35
, Issue.4
, pp. 434-441
-
-
Watson, C.M.1
Crinnion, L.A.2
Morgan, J.E.3
-
19
-
-
84897865695
-
Frequent inactivating mutations of STAG2 in bladder cancer are associated with low tumour grade and stage and inversely related to chromosomal copy number changes
-
C. F. Taylor, F. M. Platt, C. D. Hurst, H. H. Thygesen, and M. A. Knowles, "Frequent inactivating mutations of STAG2 in bladder cancer are associated with low tumour grade and stage and inversely related to chromosomal copy number changes," Human Molecular Genetics, vol. 23, no. 8, pp. 1964-1974, 2014.
-
(2014)
Human Molecular Genetics
, vol.23
, Issue.8
, pp. 1964-1974
-
-
Taylor, C.F.1
Platt, F.M.2
Hurst, C.D.3
Thygesen, H.H.4
Knowles, M.A.5
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