-
1
-
-
84891783452
-
The database of genomic variants: a curated collection of structural variation in the human genome
-
MacDonald J.R., Ziman R., Yuen R.K.C., Feuk L., Scherer S.W. The database of genomic variants: a curated collection of structural variation in the human genome. Nucleic Acids Res. 2014, 42:D986-D992.
-
(2014)
Nucleic Acids Res.
, vol.42
-
-
MacDonald, J.R.1
Ziman, R.2
Yuen, R.K.C.3
Feuk, L.4
Scherer, S.W.5
-
2
-
-
72949103929
-
A census of amplified and overexpressed human cancer genes
-
Santarius T., Shipley J., Brewer D., Stratton M.R., Cooper C.S. A census of amplified and overexpressed human cancer genes. Nat. Rev. Cancer 2010, 10:59-64.
-
(2010)
Nat. Rev. Cancer
, vol.10
, pp. 59-64
-
-
Santarius, T.1
Shipley, J.2
Brewer, D.3
Stratton, M.R.4
Cooper, C.S.5
-
3
-
-
84887992179
-
Cumulative haploinsufficiency and triplosensitivity drive aneuploidy patterns and shape the cancer genome
-
Davoli T., Xu A.W., Mengwasser K.E., Sack L.M., Yoon J.C., Park P.J., et al. Cumulative haploinsufficiency and triplosensitivity drive aneuploidy patterns and shape the cancer genome. Cell 2013, 155:948-962.
-
(2013)
Cell
, vol.155
, pp. 948-962
-
-
Davoli, T.1
Xu, A.W.2
Mengwasser, K.E.3
Sack, L.M.4
Yoon, J.C.5
Park, P.J.6
-
4
-
-
84981834288
-
The chromosome number of man
-
Tjio J.H., Levan A. The chromosome number of man. Hereditas 2010, 42:1-6.
-
(2010)
Hereditas
, vol.42
, pp. 1-6
-
-
Tjio, J.H.1
Levan, A.2
-
5
-
-
0038497542
-
Molecular structure of nucleic acids: A Structure for Deoxyribose Nucleic Acid
-
Watson J.D., Crick F. Molecular structure of nucleic acids: A Structure for Deoxyribose Nucleic Acid. Nature 1953, 171:737-738.
-
(1953)
Nature
, vol.171
, pp. 737-738
-
-
Watson, J.D.1
Crick, F.2
-
6
-
-
28444486962
-
Reappraisal of the Hansemann-Boveri hypothesis on the origin of tumors
-
Hardy P.A., Zacharias H. Reappraisal of the Hansemann-Boveri hypothesis on the origin of tumors. Cell Biol. Int. 2005, 12:983-992.
-
(2005)
Cell Biol. Int.
, vol.12
, pp. 983-992
-
-
Hardy, P.A.1
Zacharias, H.2
-
7
-
-
0015694748
-
A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and giemsa staining
-
Rowley J.D. A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and giemsa staining. Nature 1973, 243:290-293.
-
(1973)
Nature
, vol.243
, pp. 290-293
-
-
Rowley, J.D.1
-
8
-
-
72849159485
-
Chromosome studies on normal and leukemic human leukocytes
-
Nowell P.C., Hungerford D.A. Chromosome studies on normal and leukemic human leukocytes. J. Natl. Cancer Inst. 1960, 25:85-109.
-
(1960)
J. Natl. Cancer Inst.
, vol.25
, pp. 85-109
-
-
Nowell, P.C.1
Hungerford, D.A.2
-
9
-
-
0020416478
-
In situ hybridization of DNA sequences in human metaphase chromosomes visualized by an indirect fluorescent immunocytochemical procedure
-
Van Prooijen-Knegt A.C., Van Hoek J.F.M., Bauman J.G.J., Van Duijn P., Wool I.G., Van der Ploeg M. In situ hybridization of DNA sequences in human metaphase chromosomes visualized by an indirect fluorescent immunocytochemical procedure. Exp. Cell Res. 1982, 141:397-407.
-
(1982)
Exp. Cell Res.
, vol.141
, pp. 397-407
-
-
Van Prooijen-Knegt, A.C.1
Van Hoek, J.F.M.2
Bauman, J.G.J.3
Van Duijn, P.4
Wool, I.G.5
Van der Ploeg, M.6
-
10
-
-
0020037616
-
Double minutes in human tumor cells
-
Barker P.E. Double minutes in human tumor cells. Cancer Genet. Cytogenet. 1982, 5:81-94.
-
(1982)
Cancer Genet. Cytogenet.
, vol.5
, pp. 81-94
-
-
Barker, P.E.1
-
11
-
-
0017289341
-
Metaphase chromosome anomaly: association with drug resistance and cell-specific products
-
Biedler J.L., Spengler B.A. Metaphase chromosome anomaly: association with drug resistance and cell-specific products. Science 1976, 191:185-187.
-
(1976)
Science
, vol.191
, pp. 185-187
-
-
Biedler, J.L.1
Spengler, B.A.2
-
12
-
-
0030701970
-
Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances
-
Solinas-Toldo S., Lampel S., Stilgenbauer S., Nickolenko J., Benner A., Döhner H., et al. Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances. Genes Chromosom. Cancer 1997, 20:399-407.
-
(1997)
Genes Chromosom. Cancer
, vol.20
, pp. 399-407
-
-
Solinas-Toldo, S.1
Lampel, S.2
Stilgenbauer, S.3
Nickolenko, J.4
Benner, A.5
Döhner, H.6
-
13
-
-
0027537408
-
Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization
-
Manoir S., Speicher M., Joos S., Schröck E., Popp S., Döhner H., et al. Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization. Hum. Genet. 1993, 90:590-610.
-
(1993)
Hum. Genet.
, vol.90
, pp. 590-610
-
-
Manoir, S.1
Speicher, M.2
Joos, S.3
Schröck, E.4
Popp, S.5
Döhner, H.6
-
14
-
-
0026495364
-
Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
-
Kallioniemi A., Kallioniemi O.P., Sudar D., Rutovitz D., Gray J.W., Waldman F., et al. Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science 1992, 258:818-821.
-
(1992)
Science
, vol.258
, pp. 818-821
-
-
Kallioniemi, A.1
Kallioniemi, O.P.2
Sudar, D.3
Rutovitz, D.4
Gray, J.W.5
Waldman, F.6
-
15
-
-
0032823523
-
Genome-wide analysis of DNA copy-number changes using cDNA microarrays
-
Brown P.O., Pollack J.R., Perou C.M., Alizadeh A.A., Eisen M.B., Pergamenschikov A., et al. Genome-wide analysis of DNA copy-number changes using cDNA microarrays. Nat. Genet. 1999, 23:41-46.
-
(1999)
Nat. Genet.
, vol.23
, pp. 41-46
-
-
Brown, P.O.1
Pollack, J.R.2
Perou, C.M.3
Alizadeh, A.A.4
Eisen, M.B.5
Pergamenschikov, A.6
-
16
-
-
0035179871
-
Assembly of microarrays for genome-wide measurement of DNA copy number
-
Snijders A.M., Nowak N., Segraves R., Blackwood S., Brown N., Conroy J., et al. Assembly of microarrays for genome-wide measurement of DNA copy number. Nat. Genet. 2001, 29:263-264.
-
(2001)
Nat. Genet.
, vol.29
, pp. 263-264
-
-
Snijders, A.M.1
Nowak, N.2
Segraves, R.3
Blackwood, S.4
Brown, N.5
Conroy, J.6
-
17
-
-
17344371740
-
High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
-
Pinkel D., Segraves R., Sudar D., Clark S., Poole I., Kowbel D., et al. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nat. Genet. 1998, 20:207-211.
-
(1998)
Nat. Genet.
, vol.20
, pp. 207-211
-
-
Pinkel, D.1
Segraves, R.2
Sudar, D.3
Clark, S.4
Poole, I.5
Kowbel, D.6
-
18
-
-
10744230160
-
High-resolution analysis of DNA copy number using oligonucleotide microarrays
-
Bignell G.R. High-resolution analysis of DNA copy number using oligonucleotide microarrays. Genome Res. 2004, 14:287-295.
-
(2004)
Genome Res.
, vol.14
, pp. 287-295
-
-
Bignell, G.R.1
-
19
-
-
0031939328
-
Minimal sizes of deletions detected by comparative genomic hybridization
-
Bentz M., Plesch A., Stilgenbauer S., Döhner H., Lichter P. Minimal sizes of deletions detected by comparative genomic hybridization. Genes Chromosom. Cancer 1998, 21:172-175.
-
(1998)
Genes Chromosom. Cancer
, vol.21
, pp. 172-175
-
-
Bentz, M.1
Plesch, A.2
Stilgenbauer, S.3
Döhner, H.4
Lichter, P.5
-
20
-
-
32644441984
-
BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH)
-
Ylstra B., van den Ijssel P., Carvalho B., Brakenhoff R.H., Meijer G.A. BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH). Nucleic Acids Res. 2006, 34:445-450.
-
(2006)
Nucleic Acids Res.
, vol.34
, pp. 445-450
-
-
Ylstra, B.1
van den Ijssel, P.2
Carvalho, B.3
Brakenhoff, R.H.4
Meijer, G.A.5
-
21
-
-
79958162661
-
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
-
Pinto D., Darvishi K., Shi X., Rajan D., Rigler D., Fitzgerald T., et al. Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants. Nat. Biotechnol. 2011, 29:512-520.
-
(2011)
Nat. Biotechnol.
, vol.29
, pp. 512-520
-
-
Pinto, D.1
Darvishi, K.2
Shi, X.3
Rajan, D.4
Rigler, D.5
Fitzgerald, T.6
-
22
-
-
4444291843
-
Detection of large-scale variation in the human genome
-
Iafrate A.J., Feuk L., Rivera M.N., Listewnik M.L., Donahoe P.K., Qi Y., et al. Detection of large-scale variation in the human genome. Nat. Genet. 2004, 36:949-951.
-
(2004)
Nat. Genet.
, vol.36
, pp. 949-951
-
-
Iafrate, A.J.1
Feuk, L.2
Rivera, M.N.3
Listewnik, M.L.4
Donahoe, P.K.5
Qi, Y.6
-
23
-
-
20544462642
-
Segmental duplications and copy-number variation in the human genome
-
Sharp A.J., Locke D.P., McGrath S.D., Cheng Z., Bailey J.A., Vallente R.U., et al. Segmental duplications and copy-number variation in the human genome. Am. J. Hum. Genet. 2005, 77:78-88.
-
(2005)
Am. J. Hum. Genet.
, vol.77
, pp. 78-88
-
-
Sharp, A.J.1
Locke, D.P.2
McGrath, S.D.3
Cheng, Z.4
Bailey, J.A.5
Vallente, R.U.6
-
25
-
-
33644525896
-
High resolution analysis of non-small cell lung cancer cell lines by whole genome tiling path array CGH
-
Garnis C., Lockwood W.W., Vucic E., Ge Y., Girard L., Minna J.D., et al. High resolution analysis of non-small cell lung cancer cell lines by whole genome tiling path array CGH. Int. J. Cancer 2005, 118:1556-1564.
-
(2005)
Int. J. Cancer
, vol.118
, pp. 1556-1564
-
-
Garnis, C.1
Lockwood, W.W.2
Vucic, E.3
Ge, Y.4
Girard, L.5
Minna, J.D.6
-
26
-
-
36248980204
-
Characterizing the cancer genome in lung adenocarcinoma
-
Weir B.A., Woo M.S., Getz G., Perner S., Ding L., Beroukhim R., et al. Characterizing the cancer genome in lung adenocarcinoma. Nature 2007, 450:893-898.
-
(2007)
Nature
, vol.450
, pp. 893-898
-
-
Weir, B.A.1
Woo, M.S.2
Getz, G.3
Perner, S.4
Ding, L.5
Beroukhim, R.6
-
27
-
-
79955166265
-
GISTIC2.0 facilitates sensitive and confidentlocalization of the targets of focal somatic copy-number alteration in human cancers
-
Mermel C.H., Schumacher S.E., Hill B., Meyerson M.L., Beroukhim R., Getz G. GISTIC2.0 facilitates sensitive and confidentlocalization of the targets of focal somatic copy-number alteration in human cancers. Genome Biol. 2011, 12:R41.
-
(2011)
Genome Biol.
, vol.12
-
-
Mermel, C.H.1
Schumacher, S.E.2
Hill, B.3
Meyerson, M.L.4
Beroukhim, R.5
Getz, G.6
-
28
-
-
55849099654
-
Integrated analysis of homozygous deletions, focal amplifications, and sequence alterations in breast and colorectal cancers
-
Leary R.J., Lin J.C., Cummins J., Boca S., Wood L.D., Parsons D.W., et al. Integrated analysis of homozygous deletions, focal amplifications, and sequence alterations in breast and colorectal cancers. Proc. Natl. Acad. Sci. U. S. A. 2008, 105:16224-16229.
-
(2008)
Proc. Natl. Acad. Sci. U. S. A.
, vol.105
, pp. 16224-16229
-
-
Leary, R.J.1
Lin, J.C.2
Cummins, J.3
Boca, S.4
Wood, L.D.5
Parsons, D.W.6
-
29
-
-
77955778246
-
Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens
-
Wood H.M., Belvedere O., Conway C., Daly C., Chalkley R., Bickerdike M., et al. Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens. Nucleic Acids Res. 2010, 38:e151-e151.
-
(2010)
Nucleic Acids Res.
, vol.38
-
-
Wood, H.M.1
Belvedere, O.2
Conway, C.3
Daly, C.4
Chalkley, R.5
Bickerdike, M.6
-
30
-
-
79960988896
-
To DNA or not to DNA? That is the question, when it comes to molecular subtyping for the clinic!
-
Smeets S.J., Harjes U., van Wieringen W.N., Sie D., Brakenhoff R.H., Meijer G.A., et al. To DNA or not to DNA? That is the question, when it comes to molecular subtyping for the clinic!. Clin. Cancer Res. 2011, 17:4959-4964.
-
(2011)
Clin. Cancer Res.
, vol.17
, pp. 4959-4964
-
-
Smeets, S.J.1
Harjes, U.2
van Wieringen, W.N.3
Sie, D.4
Brakenhoff, R.H.5
Meijer, G.A.6
-
31
-
-
84871286330
-
Micro-scale genomic DNA copy number aberrations as another means of mutagenesis in breast cancer
-
Chao H.H., He X., Parker J.S., Zhao W., Perou C.M. Micro-scale genomic DNA copy number aberrations as another means of mutagenesis in breast cancer. PLoS ONE 2012, 7:e51719.
-
(2012)
PLoS ONE
, vol.7
-
-
Chao, H.H.1
He, X.2
Parker, J.S.3
Zhao, W.4
Perou, C.M.5
-
32
-
-
73349125417
-
Somatic mutations of the Parkinson's disease-associated gene PARK2 in glioblastoma and other human malignancies
-
Veeriah S., Taylor B.S., Meng S., Fang F., Yilmaz E., Vivanco I., et al. Somatic mutations of the Parkinson's disease-associated gene PARK2 in glioblastoma and other human malignancies. Nat. Genet. 2009, 42:77-82.
-
(2009)
Nat. Genet.
, vol.42
, pp. 77-82
-
-
Veeriah, S.1
Taylor, B.S.2
Meng, S.3
Fang, F.4
Yilmaz, E.5
Vivanco, I.6
-
33
-
-
77249123407
-
Signatures of mutation and selection in the cancer genome
-
Bignell G.R., Greenman C.D., Davies H., Butler A.P. Signatures of mutation and selection in the cancer genome. Nature 2010, 463:893-898.
-
(2010)
Nature
, vol.463
, pp. 893-898
-
-
Bignell, G.R.1
Greenman, C.D.2
Davies, H.3
Butler, A.P.4
-
34
-
-
84869862986
-
Focal aberrations indicate EYA2and hsa-miR-375as oncogene and tumor suppressor in cervical carcinogenesis
-
Bierkens M., Krijgsman O., Wilting S.M., Bosch L., Jaspers A., Meijer G.A., et al. Focal aberrations indicate EYA2and hsa-miR-375as oncogene and tumor suppressor in cervical carcinogenesis. Genes Chromosom. Cancer 2012, 52:56-68.
-
(2012)
Genes Chromosom. Cancer
, vol.52
, pp. 56-68
-
-
Bierkens, M.1
Krijgsman, O.2
Wilting, S.M.3
Bosch, L.4
Jaspers, A.5
Meijer, G.A.6
-
35
-
-
38049100456
-
Assessing the significance of chromosomal aberrations in cancer: methodology and application to glioma
-
Beroukhim R., Getz G., Nghiemphu L., Barretina J., Hsueh T., Linhart D., et al. Assessing the significance of chromosomal aberrations in cancer: methodology and application to glioma. Proc. Natl. Acad. Sci. 2007, 104:20007-20012.
-
(2007)
Proc. Natl. Acad. Sci.
, vol.104
, pp. 20007-20012
-
-
Beroukhim, R.1
Getz, G.2
Nghiemphu, L.3
Barretina, J.4
Hsueh, T.5
Linhart, D.6
-
36
-
-
77249119762
-
The landscape of somatic copy-number alteration across human cancers
-
Beroukhim R., Mermel C.H., Porter D., Wei G., Raychaudhuri S., Donovan J., et al. The landscape of somatic copy-number alteration across human cancers. Nature 2010, 463:899-905.
-
(2010)
Nature
, vol.463
, pp. 899-905
-
-
Beroukhim, R.1
Mermel, C.H.2
Porter, D.3
Wei, G.4
Raychaudhuri, S.5
Donovan, J.6
-
37
-
-
54549108740
-
Comprehensive genomic characterization defines human glioblastoma genes and core pathways
-
McLendon R., Friedman A., Bigner D., Van Meir E.G., Brat D.J., Mastrogianakis G.M., et al. Comprehensive genomic characterization defines human glioblastoma genes and core pathways. Nature 2008, 455:1061-1068.
-
(2008)
Nature
, vol.455
, pp. 1061-1068
-
-
McLendon, R.1
Friedman, A.2
Bigner, D.3
Van Meir, E.G.4
Brat, D.J.5
Mastrogianakis, G.M.6
-
38
-
-
84865238936
-
Gastrointestinal adenocarcinomas of the esophagus, stomach, and colon exhibit distinct patterns of genome instability and oncogenesis
-
Dulak A.M., Schumacher S.E., van Lieshout J., Imamura Y., Fox C., Shim B., et al. Gastrointestinal adenocarcinomas of the esophagus, stomach, and colon exhibit distinct patterns of genome instability and oncogenesis. Cancer Res. 2012, 72:4383-4393.
-
(2012)
Cancer Res.
, vol.72
, pp. 4383-4393
-
-
Dulak, A.M.1
Schumacher, S.E.2
van Lieshout, J.3
Imamura, Y.4
Fox, C.5
Shim, B.6
-
39
-
-
3543105225
-
Circular binary segmentation for the analysis of array-based DNA copy number data
-
Olshen A.B., Venkatraman E.S., Lucito R., Wigler M. Circular binary segmentation for the analysis of array-based DNA copy number data. Biostatistics 2004, 5:557-572.
-
(2004)
Biostatistics
, vol.5
, pp. 557-572
-
-
Olshen, A.B.1
Venkatraman, E.S.2
Lucito, R.3
Wigler, M.4
-
40
-
-
34248523183
-
CGHcall: calling aberrations for array CGH tumor profiles
-
van de Wiel M.A., Kim K.I., Vosse S.J., van Wieringen W.N., Wilting S.M., Ylstra B. CGHcall: calling aberrations for array CGH tumor profiles. Bioinformatics 2007, 23:892-894.
-
(2007)
Bioinformatics
, vol.23
, pp. 892-894
-
-
van de Wiel, M.A.1
Kim, K.I.2
Vosse, S.J.3
van Wieringen, W.N.4
Wilting, S.M.5
Ylstra, B.6
-
41
-
-
79551652532
-
Preprocessing and downstream analysis of microarray DNA copy number profiles
-
van de Wiel M.A., Picard F., van Wieringen W.N., Ylstra B. Preprocessing and downstream analysis of microarray DNA copy number profiles. Brief. Bioinform. 2011, 12:10-21.
-
(2011)
Brief. Bioinform.
, vol.12
, pp. 10-21
-
-
van de Wiel, M.A.1
Picard, F.2
van Wieringen, W.N.3
Ylstra, B.4
-
42
-
-
79955767473
-
Wavelet-based identification of DNA focal genomic aberrations from single nucleotide polymorphism arrays
-
Hur Y., Lee H. Wavelet-based identification of DNA focal genomic aberrations from single nucleotide polymorphism arrays. BMC Bioinforma. 2011, 12:146.
-
(2011)
BMC Bioinforma.
, vol.12
, pp. 146
-
-
Hur, Y.1
Lee, H.2
-
43
-
-
84885074034
-
The somatic genomic landscape of glioblastoma
-
Brennan C.W., Verhaak R.G.W., McKenna A., Campos B., Noushmehr H., Salama S.R., et al. The somatic genomic landscape of glioblastoma. Cell 2013, 155:462-477.
-
(2013)
Cell
, vol.155
, pp. 462-477
-
-
Brennan, C.W.1
Verhaak, R.G.W.2
McKenna, A.3
Campos, B.4
Noushmehr, H.5
Salama, S.R.6
-
44
-
-
78651339534
-
NCBI GEO: archive for functional genomics data sets-10years on
-
Barrett T., Troup D.B., Wilhite S.E., Ledoux P., Evangelista C., Kim I.F., et al. NCBI GEO: archive for functional genomics data sets-10years on. Nucleic Acids Res. 2011, 39:D1005-D1010.
-
(2011)
Nucleic Acids Res.
, vol.39
-
-
Barrett, T.1
Troup, D.B.2
Wilhite, S.E.3
Ledoux, P.4
Evangelista, C.5
Kim, I.F.6
-
45
-
-
84876097557
-
ArrayExpress update-trends in database growth and links to data analysis tools
-
Rustici G., Kolesnikov N., Brandizi M., Burdett T., Dylag M., Emam I., et al. ArrayExpress update-trends in database growth and links to data analysis tools. Nucleic Acids Res. 2013, 41:D987-D990.
-
(2013)
Nucleic Acids Res.
, vol.41
-
-
Rustici, G.1
Kolesnikov, N.2
Brandizi, M.3
Burdett, T.4
Dylag, M.5
Emam, I.6
-
46
-
-
39749145837
-
Array comparative genomic hybridization copy number profiling: a new tool for translational research in solid malignancies
-
Costa J.L., Meijer G., Ylstra B., Caldas C. Array comparative genomic hybridization copy number profiling: a new tool for translational research in solid malignancies. Semin. Radiat. Oncol. 2008, 18:98-104.
-
(2008)
Semin. Radiat. Oncol.
, vol.18
, pp. 98-104
-
-
Costa, J.L.1
Meijer, G.2
Ylstra, B.3
Caldas, C.4
-
47
-
-
79952284127
-
Hallmarks of cancer: the next generation
-
Hanahan D., Weinberg R.A. Hallmarks of cancer: the next generation. Cell 2011, 144:646-674.
-
(2011)
Cell
, vol.144
, pp. 646-674
-
-
Hanahan, D.1
Weinberg, R.A.2
-
48
-
-
77955484522
-
Candidate driver genes in focal chromosomal aberrations of stage II colon cancer
-
Brosens R.P., Haan J.C., Carvalho B., Rustenburg F., Grabsch H., Quirke P., et al. Candidate driver genes in focal chromosomal aberrations of stage II colon cancer. J. Pathol. 2010, 221:411-424.
-
(2010)
J. Pathol.
, vol.221
, pp. 411-424
-
-
Brosens, R.P.1
Haan, J.C.2
Carvalho, B.3
Rustenburg, F.4
Grabsch, H.5
Quirke, P.6
-
49
-
-
84889844937
-
Dissecting the gray zone between follicular lymphoma and marginal zone lymphoma using morphological and genetic features
-
Krijgsman O., Gonzalez P., Ponz O.B., Roemer M.G.M., Slot S., Broeks A., et al. Dissecting the gray zone between follicular lymphoma and marginal zone lymphoma using morphological and genetic features. Haematologica 2013, 98:1921-1929.
-
(2013)
Haematologica
, vol.98
, pp. 1921-1929
-
-
Krijgsman, O.1
Gonzalez, P.2
Ponz, O.B.3
Roemer, M.G.M.4
Slot, S.5
Broeks, A.6
-
50
-
-
84877921698
-
IRS2 is a candidate driver oncogene on 13q34 in colorectal cancer
-
Day E., Poulogiannis G., McCaughan F., Mulholland S., Arends M.J., Ibrahim A.E., et al. IRS2 is a candidate driver oncogene on 13q34 in colorectal cancer. Int. J. Exp. Pathol. 2013, 94:203-211.
-
(2013)
Int. J. Exp. Pathol.
, vol.94
, pp. 203-211
-
-
Day, E.1
Poulogiannis, G.2
McCaughan, F.3
Mulholland, S.4
Arends, M.J.5
Ibrahim, A.E.6
-
51
-
-
58149239686
-
Genomic loss of microRNA-101 leads to overexpression of histone methyltransferase EZH2 in cancer
-
Varambally S., Cao Q., Mani R.S., Shankar S., Wang X., Ateeq B., et al. Genomic loss of microRNA-101 leads to overexpression of histone methyltransferase EZH2 in cancer. Science 2008, 322:1695-1699.
-
(2008)
Science
, vol.322
, pp. 1695-1699
-
-
Varambally, S.1
Cao, Q.2
Mani, R.S.3
Shankar, S.4
Wang, X.5
Ateeq, B.6
-
52
-
-
77955084425
-
Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell lines
-
Mitsui J., Takahashi Y., Goto J., Tomiyama H., Ishikawa S., Yoshino H., et al. Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell lines. Am. J. Hum. Genet. 2010, 87:75-89.
-
(2010)
Am. J. Hum. Genet.
, vol.87
, pp. 75-89
-
-
Mitsui, J.1
Takahashi, Y.2
Goto, J.3
Tomiyama, H.4
Ishikawa, S.5
Yoshino, H.6
-
53
-
-
34347395733
-
Trastuzumab-mechanism of action and use in clinical practice
-
Hudis C.A. Trastuzumab-mechanism of action and use in clinical practice. N. Engl. J. Med. 2007, 357:39-51.
-
(2007)
N. Engl. J. Med.
, vol.357
, pp. 39-51
-
-
Hudis, C.A.1
-
54
-
-
27244450637
-
Favorable prognosis for patients 12 to 18 months of age with stage 4 nonamplified MYCN neuroblastoma: a Children's Cancer Group Study
-
Schmidt M.L. Favorable prognosis for patients 12 to 18 months of age with stage 4 nonamplified MYCN neuroblastoma: a Children's Cancer Group Study. J. Clin. Oncol. 2005, 23:6474-6480.
-
(2005)
J. Clin. Oncol.
, vol.23
, pp. 6474-6480
-
-
Schmidt, M.L.1
-
55
-
-
82755168803
-
Genomic dissection of the epidermal growth factor receptor (EGFR)/PI3K pathway reveals frequent deletion of the EGFR phosphatase PTPRS in head and neck cancers
-
Morris L.G., Taylor B.S., Bivona T.G., Gong Y., Eng S., Brennan C.W., et al. Genomic dissection of the epidermal growth factor receptor (EGFR)/PI3K pathway reveals frequent deletion of the EGFR phosphatase PTPRS in head and neck cancers. Proc. Natl. Acad. Sci. U. S. A. 2011, 108:19024-19029.
-
(2011)
Proc. Natl. Acad. Sci. U. S. A.
, vol.108
, pp. 19024-19029
-
-
Morris, L.G.1
Taylor, B.S.2
Bivona, T.G.3
Gong, Y.4
Eng, S.5
Brennan, C.W.6
-
56
-
-
84861625981
-
Integrated analysis of somatic mutations and focal copy-number changes identifies key genes and pathways in hepatocellular carcinoma
-
Guichard C., Amaddeo G., Imbeaud S., Ladeiro Y., Pelletier L., Maad I.B., et al. Integrated analysis of somatic mutations and focal copy-number changes identifies key genes and pathways in hepatocellular carcinoma. Nat. Genet. 2012, 44:694-698.
-
(2012)
Nat. Genet.
, vol.44
, pp. 694-698
-
-
Guichard, C.1
Amaddeo, G.2
Imbeaud, S.3
Ladeiro, Y.4
Pelletier, L.5
Maad, I.B.6
-
57
-
-
84874868907
-
Chromothripsis and focal copy number alterations determine poor outcome in malignant melanoma
-
Hirsch D., Kemmerling R., Davis S., Camps J., Meltzer P.S., Ried T., et al. Chromothripsis and focal copy number alterations determine poor outcome in malignant melanoma. Cancer Res. 2013, 73:1454-1460.
-
(2013)
Cancer Res.
, vol.73
, pp. 1454-1460
-
-
Hirsch, D.1
Kemmerling, R.2
Davis, S.3
Camps, J.4
Meltzer, P.S.5
Ried, T.6
-
58
-
-
84865134914
-
Passenger deletions generate therapeutic vulnerabilities in cancer
-
Müller F.L., Colla S., Aquilanti E., Manzo V.E., Genovese G., Lee J., et al. Passenger deletions generate therapeutic vulnerabilities in cancer. Nature 2012, 488:337-342.
-
(2012)
Nature
, vol.488
, pp. 337-342
-
-
Müller, F.L.1
Colla, S.2
Aquilanti, E.3
Manzo, V.E.4
Genovese, G.5
Lee, J.6
-
59
-
-
84877722178
-
Diverse mechanisms of somatic structural variations in human cancer genomes
-
Yang L., Luquette L.J., Gehlenborg N., Xi R., Haseley P.S., Hsieh C.H., et al. Diverse mechanisms of somatic structural variations in human cancer genomes. Cell 2013, 153:919-929.
-
(2013)
Cell
, vol.153
, pp. 919-929
-
-
Yang, L.1
Luquette, L.J.2
Gehlenborg, N.3
Xi, R.4
Haseley, P.S.5
Hsieh, C.H.6
-
60
-
-
77949676046
-
Hotspots of large rare deletions in the human genome
-
Bradley W.E., Raelson J.V., Dubois D.Y., Godin E., Fournier H., Privé C., et al. Hotspots of large rare deletions in the human genome. PLoS ONE 2010, 5:e9401.
-
(2010)
PLoS ONE
, vol.5
-
-
Bradley, W.E.1
Raelson, J.V.2
Dubois, D.Y.3
Godin, E.4
Fournier, H.5
Privé, C.6
-
61
-
-
84875135862
-
Criteria for inference of chromothripsis in cancer genomes
-
Korbel J.O., Campbell P.J. Criteria for inference of chromothripsis in cancer genomes. Cell 2013, 152:1226-1236.
-
(2013)
Cell
, vol.152
, pp. 1226-1236
-
-
Korbel, J.O.1
Campbell, P.J.2
-
62
-
-
84861576201
-
The landscape of cancer genes and mutational processes in breast cancer
-
Stephens P.J., Tarpey P.S., Davies H., Van Loo P., Greenman C., Wedge D.C., et al. The landscape of cancer genes and mutational processes in breast cancer. Nature 2012, 486:400-404.
-
(2012)
Nature
, vol.486
, pp. 400-404
-
-
Stephens, P.J.1
Tarpey, P.S.2
Davies, H.3
Van Loo, P.4
Greenman, C.5
Wedge, D.C.6
-
63
-
-
84875757638
-
Punctuated evolution of prostate cancer genomes
-
Baca S.C., Prandi D., Lawrence M.S., Mosquera J.M., Romanel A., Drier Y., et al. Punctuated evolution of prostate cancer genomes. Cell 2013, 153:666-677.
-
(2013)
Cell
, vol.153
, pp. 666-677
-
-
Baca, S.C.1
Prandi, D.2
Lawrence, M.S.3
Mosquera, J.M.4
Romanel, A.5
Drier, Y.6
-
64
-
-
30144442771
-
Common fragile sites, extremely large genes, neural development and cancer
-
Smith D.I., Zhu Y., McAvoy S., Kuhn R. Common fragile sites, extremely large genes, neural development and cancer. Cancer Lett. 2006, 232:48-57.
-
(2006)
Cancer Lett.
, vol.232
, pp. 48-57
-
-
Smith, D.I.1
Zhu, Y.2
McAvoy, S.3
Kuhn, R.4
-
65
-
-
84892833777
-
Discovery and saturation analysis of cancer genes across 21 tumour types
-
Lawrence M.S., Stojanov P., Mermel C.H., Robinson J.T., Garraway L.A., Golub T.R., et al. Discovery and saturation analysis of cancer genes across 21 tumour types. Nature 2015, 505:495-501.
-
(2015)
Nature
, vol.505
, pp. 495-501
-
-
Lawrence, M.S.1
Stojanov, P.2
Mermel, C.H.3
Robinson, J.T.4
Garraway, L.A.5
Golub, T.R.6
|