-
1
-
-
0141994858
-
Genomic microarrays in human genetic disease and cancer
-
Albertson, D. G., and Pinkel, D. (2003). Genomic microarrays in human genetic disease and cancer. Hum. Mol. Genet. 12(Spec. no. 2), R145-R152.
-
(2003)
Hum. Mol. Genet.
, vol.12
, Issue.SPEC. NO. 2
-
-
Albertson, D.G.1
Pinkel, D.2
-
2
-
-
18144445946
-
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications
-
Buckley, P. G., Mantripragada, K. K., Benetkiewicz, M., Tapia-Paez, I., Diaz De Stahl, T., Rosenquist, M., Ali, H., Jarbo, C., De Bustos, C., Hirvela, C., Sinder Wilen, B., Fransson, I., Thyr, C., Johnsson, B. I., Bruder, C. E., Menzel, U., Hergersberg, M., Mandahl, N., Blennow, E., Wedell, A., Beare, D. M., Collins, J. E., Dunham, I., Albertson, D., Pinkel, D., Bastian, B. C., Faruqi, A. F., Lasken, R. S., Ichimura, K., Collins, V. P., and Dumanski, J. P. (2002). A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications. Hum. Mol. Genet. 11, 3221-3229.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 3221-3229
-
-
Buckley, P.G.1
Mantripragada, K.K.2
Benetkiewicz, M.3
Tapia-Paez, I.4
Diaz De Stahl, T.5
Rosenquist, M.6
Ali, H.7
Jarbo, C.8
De Bustos, C.9
Hirvela, C.10
Sinder Wilen, B.11
Fransson, I.12
Thyr, C.13
Johnsson, B.I.14
Bruder, C.E.15
Menzel, U.16
Hergersberg, M.17
Mandahl, N.18
Blennow, E.19
Wedell, A.20
Beare, D.M.21
Collins, J.E.22
Dunham, I.23
Albertson, D.24
Pinkel, D.25
Bastian, B.C.26
Faruqi, A.F.27
Lasken, R.S.28
Ichimura, K.29
Collins, V.P.30
Dumanski, J.P.31
more..
-
4
-
-
0344441890
-
A DNA damage checkpoint response in telomere-initiated senescence
-
Fagagna Fd, F., Reaper, P. M., Clay-Farrace, L., Fiegler, H., Carr, P., Von Zglinicki, T., Saretzki, G., Carter, N. P., and Jackson, S. P. (2003a). A DNA damage checkpoint response in telomere-initiated senescence. Nature 426, 194-198.
-
(2003)
Nature
, vol.426
, pp. 194-198
-
-
Fagagna, Fd.F.1
Reaper, P.M.2
Clay-Farrace, L.3
Fiegler, H.4
Carr, P.5
Von Zglinicki, T.6
Saretzki, G.7
Carter, N.P.8
Jackson, S.P.9
-
5
-
-
0037376804
-
DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones
-
Fiegler, H., Carr, P., Douglas, E. J., Burford, D. C., Hunt, S., Scott, C. E., Smith, J., Vetrie, D., Gorman, P., Tomlinson, I. P., and Carter, N. P. (2003a). DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones. Genes Chromosomes Cancer 36, 361-374.
-
(2003)
Genes Chromosomes Cancer
, vol.36
, pp. 361-374
-
-
Fiegler, H.1
Carr, P.2
Douglas, E.J.3
Burford, D.C.4
Hunt, S.5
Scott, C.E.6
Smith, J.7
Vetrie, D.8
Gorman, P.9
Tomlinson, I.P.10
Carter, N.P.11
-
6
-
-
0041328509
-
Array painting: A method for the rapid analysis of aberrant chromosomes using DNA microarrays
-
Fiegler, H., Gribble, S. M., Burford, D. C., Carr, P., Prigmore, E., Porter, K. M., Clegg, S., Crolla, J. A., Dennis, N. R., Jacobs, P., and Carter, N. P. (2003b). Array painting: A method for the rapid analysis of aberrant chromosomes using DNA microarrays. J. Med. Genet. 40, 664-670.
-
(2003)
J. Med. Genet.
, vol.40
, pp. 664-670
-
-
Fiegler, H.1
Gribble, S.M.2
Burford, D.C.3
Carr, P.4
Prigmore, E.5
Porter, K.M.6
Clegg, S.7
Crolla, J.A.8
Dennis, N.R.9
Jacobs, P.10
Carter, N.P.11
-
7
-
-
0033813580
-
Real-time PCR-based method for assaying the purity of bacterial artificial chromosome preparations
-
Foreman, P. K., and Davis, R. W. (2000). Real-time PCR-based method for assaying the purity of bacterial artificial chromosome preparations. Biotechniques 29, 410-412.
-
(2000)
Biotechniques
, vol.29
, pp. 410-412
-
-
Foreman, P.K.1
Davis, R.W.2
-
8
-
-
18344392245
-
Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas
-
Hodgson, G., Hager, J. H., Volik, S., Hariono, S., Wernick, M., Moore, D., Nowak, N., Albertson, D. G., Pinkel, D., Collins, C., Hanahan, D., and Gray, J. W. (2001). Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas. Nat. Genet. 29, 459-464.
-
(2001)
Nat. Genet.
, vol.29
, pp. 459-464
-
-
Hodgson, G.1
Hager, J.H.2
Volik, S.3
Hariono, S.4
Wernick, M.5
Moore, D.6
Nowak, N.7
Albertson, D.G.8
Pinkel, D.9
Collins, C.10
Hanahan, D.11
Gray, J.W.12
-
9
-
-
1842591164
-
High-resolution analysis of genomic copy number alterations in bladder cancer by microarray-based comparative genomic hybridization
-
Hurst, C. D., Fiegler, H., Carr, P., Williams, S., Carter, N. P., and Knowles, M. A. (2004). High-resolution analysis of genomic copy number alterations in bladder cancer by microarray-based comparative genomic hybridization. Oncogene. 23, 2250-2263.
-
(2004)
Oncogene
, vol.23
, pp. 2250-2263
-
-
Hurst, C.D.1
Fiegler, H.2
Carr, P.3
Williams, S.4
Carter, N.P.5
Knowles, M.A.6
-
10
-
-
0028341315
-
Down syndrome phenotypes: The consequences of chromosomal imbalance
-
Korenberg, J. R., Chen, X., Schipper, R., Sun, Z., Gonsky, R., Gerwehr, S., Carpenter, N., Daumer, C., Dignan, P., Disteche, C., Graham Jr, J. M., Hudgins, L., McGillivray, B., Miyazaki, K., Ogasawara, N., Park, J. P., Pagon, R., Pueschel, S., Sack, G., Say, B., Schuffenhauer, S., Soukup, S., and Yamanaka, T. (1994). Down syndrome phenotypes: The consequences of chromosomal imbalance. Proc. Natl. Acad. Sci. USA 91, 4997-5001.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 4997-5001
-
-
Korenberg, J.R.1
Chen, X.2
Schipper, R.3
Sun, Z.4
Gonsky, R.5
Gerwehr, S.6
Carpenter, N.7
Daumer, C.8
Dignan, P.9
Disteche, C.10
Graham Jr., J.M.11
Hudgins, L.12
McGillivray, B.13
Miyazaki, K.14
Ogasawara, N.15
Park, J.P.16
Pagon, R.17
Pueschel, S.18
Sack, G.19
Say, B.20
Schuffenhauer, S.21
Soukup, S.22
Yamanaka, T.23
more..
-
11
-
-
2042437650
-
International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome
-
Lander, E. S., Linton, L. M., Birren, B., Nusbaum, C., Zody, M. C., Baldwin, J., Devon, K., Dewar, K., Doyle, M., FitzHugh, W., Funke, R., Gage, D., Harris, K., Heaford, A., Howland, J., Kann, L., Lehoczky, J., LeVine, R., McEwan, P., McKernan, K., Meldrim, J., Mesirov, J. P., Miranda, C., Morris, W., Naylor, J., Raymond, C., Rosetti, M., Santos, R., Sheridan, A., Spugnez, C., Stange-Thomann, N., Stojanovic, N., Subramanian, A., Wyman, D., Rogers, J., Sulston, J., Ainscough, R., Beck, S., Bentley, D., Burton, J., Clee, C., Carter, N., Coulson, A., Deadman, R., Deloukas, P., Dunham, A., Dunham, I., Durbin, R., French, L., Grafham, D., Gregory, S., Hubbard, T., Humphrey, S., Hunt, A., Jones, M., Lloyd, C., McMurray, A., Matthews, L., Mercer, S., Milne, S., Mullikin, J. C., Mungall, A., Plumb, R., Ross, M., Shownkeen, R., Sims, S., Waterston, R. H., Wilson, R. K., Hillier, L. W., McPherson, J. D., Marra, M. A., Mardis, E. R., Fulton, L. A., Chinwalla, A. T., Pepin, K. H., Gish, W. R., Chissoe, S. L., Wendl, M. C., Delehaunty, K. D., Miner, T. L., Delehaunty, A., Kramer, J. B., Cook, L. L., Fulton, R. S., Johnson, D. L., Minx, P. J., Clifton, S. W., Hawkins, T., Branscomb, E., Predki, P., Richardson, P., Wenning, S., Slezak, T., Doggett, N., Cheng, J. F., Olsen, A., Lucas, S., Elkin, C., Uberbacher, E., Frazier, M., Gibbs, R. A., Muzny, D. M., Scherer, S. E., Bouck, J. B., Sodergren, E. J., Worley, K. C., Rives, C. M., Gorrell, J. H., Metzker, M. L., Naylor, S. L., Kucherlapati, R. S., Nelson, D. L., Weinstock, G. M., Sakaki, Y., Fujiyama, A., Hattori, M., Yada, T., Toyoda, A., Itoh, T., Kawagoe, C., Watanabe, H., Totoki, Y., Taylor, T., Weissenbach, J., Heilig, R., Saurin, W., Artiguenave, F., Brottier, P., Bruls, T., Pelletier, E., Robert, C., Wincker, P., Smith, D. R., Doucette-Stamm, L., Rubenfield, M., Weinstock, K., Lee, H. M., Dubois, J., Rosenthal, A., Platzer, M., Nyakatura, G., Taudien, S., Rump, A., Yang, H., Yu, J., Wang, J., Huang, G., Gu, J., Hood, L., Rowen, L., Madan, A., Qin, S., Davis, R. W., Federspiel, N. A., Abola, A. P., Proctor, M. J., Myers, R. M., Schmutz, J., Dickson, M., Grimwood, J., Cox, D. R., Olson, M. V., Kaul, R., Raymond, C., Shimizu, N., Kawasaki, K., Minoshima, S., Evans, G. A., Athanasiou, M., Schultz, R., Roe, B. A., Chen, F., Pan, H., Ramser, J., Lehrach, H., Reinhardt, R., McCombie, W. R., de la Bastide, M., Dedhia, N., Blocker, H., Kornischer, K., Nordsiek, G., Agarwala, R., Aravind, L., Bailey, J. A., Bateman, A., Batzoglou, S., Birney, E., Bork, P., Brown, D. G., Burge, C. B., Cerutti, L., Chen, H. C., Church, D., Clamp, M., Copley, R. R., Doerks, T., Eddy, S. R., Eichler, E. E., Furey, T. S., Galagan, J., Gilbert, J. G., Harmon, C., Hayashizaki, Y., Haussler, D., Hermjakob, H., Hokamp, K., Jang, W., Johnson, L. S., Jones, T. A., Kasif, S., Kaspryzk, A., Kennedy, S., Kent, W. J., Kitts, P., Koonin, E. V., Korf, I., Kulp, D., Lancet, D., Lowe, T. M., McLysaght, A., Mikkelsen, T., Moran, J. V., Mulder, N., Pollara, V. J., Ponting, C. P., Schuler, G., Schultz, J., Slater, G., Smit, A. F., Stupka, E., Szustakowski, J., Thierry-Mieg, D., Thierry-Mieg, J., Wagner, L., Wallis, J., Wheeler, R., Williams, A., Wolf, Y. I., Wolfe, K. H., Yang, S. P., Yeh, R. F., Collins, F., Guyer, M. S., Peterson, J., Felsenfeld, A., Wetterstrand, K. A., Patrinos, A., Morgan, M. J., Szustakowki, J., de Jong, P., Catanese, J. J., Osoegawa, K., Shizuya, H., Choi, S., and Chen, Y. J. (2001). International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome. Nature 409, 860-921.
-
(2001)
Nature
, vol.409
, 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
Spugnez, 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
Humphrey, 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
Wendl, M.C.78
Delehaunty, K.D.79
Miner, T.L.80
Delehaunty, A.81
Kramer, J.B.82
Cook, L.L.83
Fulton, R.S.84
Johnson, D.L.85
Minx, P.J.86
Clifton, S.W.87
Hawkins, T.88
Branscomb, E.89
Predki, P.90
Richardson, P.91
Wenning, S.92
Slezak, T.93
Doggett, N.94
Cheng, J.F.95
Olsen, A.96
Lucas, S.97
Elkin, C.98
Uberbacher, E.99
more..
-
12
-
-
0033785455
-
Comparative genomic hybridization: Uses and limitations
-
Lichter, P., Joos, S., Bentz, M., and Lampel, S. (2000). Comparative genomic hybridization: Uses and limitations. Semin. Hematol. 37, 348-357.
-
(2000)
Semin. Hematol.
, vol.37
, pp. 348-357
-
-
Lichter, P.1
Joos, S.2
Bentz, M.3
Lampel, S.4
-
13
-
-
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., Collins, C., Kuo, W. L., Chen, C., Zhai, Y., Dairkee, S. H., Ljung, B. M., Gray, J. W., and Albertson, D. G. (1998). High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nat. Genet. 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
Collins, C.7
Kuo, W.L.8
Chen, C.9
Zhai, Y.10
Dairkee, S.H.11
Ljung, B.M.12
Gray, J.W.13
Albertson, D.G.14
-
14
-
-
2942583149
-
Tetrasomy 21pter->q21.2 in a male infant without typical Down's syndrome dysmorphic features but moderate mental retardation
-
Rost, I., Fiegler, H., Fauth, C., Carr, P., Bettecken, T., Kraus, J., Meyer, C., Enders, A., Wirtz, A., Meitinger, T., Carter, N. P., and Speicher, M. R. (2004). Tetrasomy 21pter->q21.2 in a male infant without typical Down's syndrome dysmorphic features but moderate mental retardation. J Med Genet. 41, e26.
-
(2004)
J Med Genet.
, vol.41
-
-
Rost, I.1
Fiegler, H.2
Fauth, C.3
Carr, P.4
Bettecken, T.5
Kraus, J.6
Meyer, C.7
Enders, A.8
Wirtz, A.9
Meitinger, T.10
Carter, N.P.11
Speicher, M.R.12
-
15
-
-
0035179871
-
Assembly of microarrays for genomewide measurement of DNA copy number
-
Snijders, A. M., Nowak, N., Segraves, R., Blackwood, S., Brown, N., Conroy, J., Hamilton, G., Hindle, A. K., Huey, B., Kimura, K., Law, S., Myambo, K., Palmer, J., Ylstra, B., Yue, J. P., Gray, J. W., Jain, A. N., Pinkel, D., and Albertson, D. G. (2001). Assembly of microarrays for genomewide measurement of DNA copy number. Nat. Genet. 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
Hamilton, G.7
Hindle, A.K.8
Huey, B.9
Kimura, K.10
Law, S.11
Myambo, K.12
Palmer, J.13
Ylstra, B.14
Yue, J.P.15
Gray, J.W.16
Jain, A.N.17
Pinkel, D.18
Albertson, D.G.19
-
16
-
-
0030701970
-
Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalances
-
Solinas-Toldo, S., Lampel, S., Stilgenbauer, S., Nickolenko, J., Benner, A., Dohner, H., Cremer, T., and Lichter, P. (1997). Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalances. Genes Chromosomes Cancer 20, 399-407.
-
(1997)
Genes Chromosomes Cancer
, vol.20
, pp. 399-407
-
-
Solinas-Toldo, S.1
Lampel, S.2
Stilgenbauer, S.3
Nickolenko, J.4
Benner, A.5
Dohner, H.6
Cremer, T.7
Lichter, P.8
-
17
-
-
0026736251
-
Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer
-
Telenius, H., Carter, N. P., Bebb, C. E., Nordenskjold, M., Ponder, B. A., and Tunnacliffe, A. (1992a). Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer. Genomics 13, 718-725.
-
(1992)
Genomics
, vol.13
, pp. 718-725
-
-
Telenius, H.1
Carter, N.P.2
Bebb, C.E.3
Nordenskjold, M.4
Ponder, B.A.5
Tunnacliffe, A.6
-
18
-
-
0026587345
-
Cytogenetic analysis by chromosome painting using DOP-PCR amplified flow-sorted chromosomes
-
Telenius, H., Pelmear, A. H., Tunnacliffe, A., Carter, N. P., Behmel, A., Ferguson-Smith, M. A., Nordenskjold, M., Pfragner, R., and Ponder, B. A. (1992b). Cytogenetic analysis by chromosome painting using DOP-PCR amplified flow-sorted chromosomes. Genes Chromosomes Cancer 4, 257-263.
-
(1992)
Genes Chromosomes Cancer
, vol.4
, pp. 257-263
-
-
Telenius, H.1
Pelmear, A.H.2
Tunnacliffe, A.3
Carter, N.P.4
Behmel, A.5
Ferguson-Smith, M.A.6
Nordenskjold, M.7
Pfragner, R.8
Ponder, B.A.9
-
19
-
-
0036143687
-
Automated screening for genomic imbalances using matrix-based comparative genomic hybridization
-
Wessendorf, S., Fritz, B., Wrobel, G., Nessling, M., Lampel, S., Goettel, D., Kuepper, M., Joos, S., Hopman, T., Kokocinski, F., Dohner, H., Bentz, M., Schwaenen, C., and Lichter, P. (2002). Automated screening for genomic imbalances using matrix-based comparative genomic hybridization. Lab. Invest. 82, 47-60.
-
(2002)
Lab. Invest.
, vol.82
, pp. 47-60
-
-
Wessendorf, S.1
Fritz, B.2
Wrobel, G.3
Nessling, M.4
Lampel, S.5
Goettel, D.6
Kuepper, M.7
Joos, S.8
Hopman, T.9
Kokocinski, F.10
Dohner, H.11
Bentz, M.12
Schwaenen, C.13
Lichter, P.14
|