-
1
-
-
25444482801
-
Speeding disease gene discovery by sequence based candidate prioritization
-
Adie, E. A., Adams, R. R., Evans, K. L. et al. (2005). Speeding disease gene discovery by sequence based candidate prioritization. BMC Bioinformatics 6, 55.
-
(2005)
BMC Bioinformatics
, vol.6
, pp. 55
-
-
Adie, E.A.1
Adams, R.R.2
Evans, K.L.3
-
2
-
-
33745056414
-
Epigenetic inactivation of the premature aging Werner syndrome gene in human cancer
-
Agrelo, R., Cheng, W. H., Setien, F. et al. (2006). Epigenetic inactivation of the premature aging Werner syndrome gene in human cancer. Proc Natl Acad Sci USA 103(23), 8822-8827.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, Issue.23
, pp. 8822-8827
-
-
Agrelo, R.1
Cheng, W.H.2
Setien, F.3
-
3
-
-
0028962333
-
Detecting conserved regulatory elements with the model genome of the Japanese pufferfish, Fugu rubripes
-
Aparicio, S., Morrison, A., Gould, A. et al. (1995). Detecting conserved regulatory elements with the model genome of the Japanese pufferfish, Fugu rubripes. Proc Natl Acad Sci USA 92, 1684-1688.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 1684-1688
-
-
Aparicio, S.1
Morrison, A.2
Gould, A.3
-
4
-
-
0032544035
-
DNA strand breaking by the hydroxyl radical is governed by the accessible surface areas of the hydrogen atoms of the DNA backbone
-
Balasubramanian, B., Pogozelski, W. K. and Tullius, T. D. (1998). DNA strand breaking by the hydroxyl radical is governed by the accessible surface areas of the hydrogen atoms of the DNA backbone. Proc Natl Acad Sci USA 95(17), 9738-9743.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, Issue.17
, pp. 9738-9743
-
-
Balasubramanian, B.1
Pogozelski, W.K.2
Tullius, T.D.3
-
5
-
-
13444269543
-
Haploview: analysis and visualization of LD and haplotype maps
-
Barrett, J. C., Fry, B., Maller, J. et al. (2005). Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 21(2), 263-265.
-
(2005)
Bioinformatics
, vol.21
, Issue.2
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
-
6
-
-
3242663659
-
An integrated epigenetic and genetic approach to common human disease
-
Bjornsson, H. T., Fallin, M.D. and Feinberg, A. P. (2004). An integrated epigenetic and genetic approach to common human disease. Trends Genet 20(8), 350-358.
-
(2004)
Trends Genet
, vol.20
, Issue.8
, pp. 350-358
-
-
Bjornsson, H.T.1
Fallin, M.D.2
Feinberg, A.P.3
-
7
-
-
31344436263
-
ChIPOTle: a user-friendly tool for the analysis of ChIP-chip data
-
Buck, M. J., Nobel, A. B. and Lieb, J. D. (2005). ChIPOTle: a user-friendly tool for the analysis of ChIP-chip data. Genome Biol 6(11), R97.
-
(2005)
Genome Biol
, vol.6
, Issue.11
-
-
Buck, M.J.1
Nobel, A.B.2
Lieb, J.D.3
-
8
-
-
27644439141
-
Efficiency and power in genetic association studies
-
de Bakker, P. I., Yelensky, R., Pe'er, I. et al. (2005). Efficiency and power in genetic association studies. Nat Genet 37(11), 1217-1223.
-
(2005)
Nat Genet
, vol.37
, Issue.11
, pp. 1217-1223
-
-
De Bakker, P.I.1
Yelensky, R.2
Pe'er, I.3
-
9
-
-
33746407333
-
The emerging science of epigenomics
-
Callinan, P. A. and Feinberg, A. P. (2006). The emerging science of epigenomics. Hum Mol Genet 15 Spec No 1, R95-101.
-
(2006)
Hum Mol Genet
, vol.15 SPEC
, Issue.1
-
-
Callinan, P.A.1
Feinberg, A.P.2
-
10
-
-
29444441336
-
A high-resolution survey of deletion polymorphism in the human genome
-
Conrad, D. F., Andrews, T. D., Carter, N. P. et al. (2006). A high-resolution survey of deletion polymorphism in the human genome. Nat Genet 38(1), 75-81.
-
(2006)
Nat Genet
, vol.38
, Issue.1
, pp. 75-81
-
-
Conrad, D.F.1
Andrews, T.D.2
Carter, N.P.3
-
11
-
-
33745409293
-
DNase-chip: a high-resolutionmethod to identifyDNase I hypersensitive sites using tiled microarrays
-
Crawford, G. E., Davis, S., Scacheri, P. C. et al. (2006). DNase-chip: a high-resolutionmethod to identifyDNase I hypersensitive sites using tiled microarrays. NatMethods 3(7), 503-509.
-
(2006)
NatMethods
, vol.3
, Issue.7
, pp. 503-509
-
-
Crawford, G.E.1
Davis, S.2
Scacheri, P.C.3
-
12
-
-
0031458470
-
Naturally occurring antisense RNA
-
Dolnick, B. J. (1997). Naturally occurring antisense RNA. Pharmacol Ther 75, 179-184.
-
(1997)
Pharmacol Ther
, vol.75
, pp. 179-184
-
-
Dolnick, B.J.1
-
13
-
-
7444260846
-
The ENCODE (ENCyclopedia Of DNA Elements) Project
-
ENCODE Project Consortium
-
ENCODE Project Consortium (2004). The ENCODE (ENCyclopedia Of DNA Elements) Project. Science 306(5696), 636-640.
-
(2004)
Science
, vol.306
, Issue.5696
, pp. 636-640
-
-
-
14
-
-
33746363353
-
Structural variants: changing the landscape of chromosomes and design of disease studies
-
Feuk, L., Marshall, C. R., Wintle, R. F. et al. (2006). Structural variants: changing the landscape of chromosomes and design of disease studies. Hum Mol Genet 15 Suppl 1, R57-66.
-
(2006)
Hum Mol Genet
, vol.15
, Issue.SUPPL.1
-
-
Feuk, L.1
Marshall, C.R.2
Wintle, R.F.3
-
15
-
-
0034178257
-
Homology: a personal view on some of the problems
-
Fitch, W.M. (2000). Homology: a personal view on some of the problems. TrendsGenet 16(5), 227-231.
-
(2000)
TrendsGenet
, vol.16
, Issue.5
, pp. 227-231
-
-
Fitch, W.M.1
-
16
-
-
10644270827
-
Functional characterization of human organic cation transporter OCTN1 single nucleotide polymorphisms in the Japanese population
-
Kawasaki, Y., Kato, Y., Sai, Y. et al. (2004). Functional characterization of human organic cation transporter OCTN1 single nucleotide polymorphisms in the Japanese population. J Pharm Sci 93(12), 2920-2926.
-
(2004)
J Pharm Sci
, vol.93
, Issue.12
, pp. 2920-2926
-
-
Kawasaki, Y.1
Kato, Y.2
Sai, Y.3
-
17
-
-
19844367341
-
Exploring relationships and mining data with the UCSC Gene Sorter
-
Kent, W. J., Hsu, F., Karolchik, D. et al. (2005). Exploring relationships and mining data with the UCSC Gene Sorter. Genome Res 15(5), 737-741.
-
(2005)
Genome Res
, vol.15
, Issue.5
, pp. 737-741
-
-
Kent, W.J.1
Hsu, F.2
Karolchik, D.3
-
18
-
-
9444295337
-
Gene map of the extended human MHC
-
Horton, R., Wilming, L., Rand, V. et al. (2004). Gene map of the extended human MHC. Nat Rev Genet 5, 889-899.
-
(2004)
Nat Rev Genet
, vol.5
, pp. 889-899
-
-
Horton, R.1
Wilming, L.2
Rand, V.3
-
19
-
-
18444402182
-
The Ensembl genome database project
-
Hubbard, T., Barker, D., Birney, E. et al. (2002). The Ensembl genome database project. Nucleic Acids Res 30(1), 38-41.
-
(2002)
Nucleic Acids Res
, vol.30
, Issue.1
, pp. 38-41
-
-
Hubbard, T.1
Barker, D.2
Birney, E.3
-
20
-
-
0035978651
-
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn disease
-
Hugot, J. P., Chamaillard, M., Zouali, H. et al. (2001). Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn disease. Nature 411(6837), 599-603.
-
(2001)
Nature
, vol.411
, Issue.6837
, pp. 599-603
-
-
Hugot, J.P.1
Chamaillard, M.2
Zouali, H.3
-
21
-
-
4444291843
-
Detection of large-scale variation in the human genome
-
Iafrate, A. J., Feuk, L., Rivera, M. N. et al. (2004). Detection of large-scale variation in the human genome. Nat Genet 36(9), 949-951.
-
(2004)
Nat Genet
, vol.36
, Issue.9
, pp. 949-951
-
-
Iafrate, A.J.1
Feuk, L.2
Rivera, M.N.3
-
22
-
-
0037673656
-
Antisense transcripts with FANTOM2clone set and their implications for gene regulation
-
RIKEN GER Group; GSL Members
-
Kiyosawa, H., Yamanaka, I., Osato, N. et al. RIKEN GER Group; GSL Members. (2003). Antisense transcripts with FANTOM2clone set and their implications for gene regulation. Genome Res 13(6B), 1324-1334.
-
(2003)
Genome Res
, vol.13
, Issue.6 B
, pp. 1324-1334
-
-
Kiyosawa, H.1
Yamanaka, I.2
Osato, N.3
-
23
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
Lander, E. S., Linton, L. M., Birren, B.et al. (2001). 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
-
24
-
-
29444457877
-
Common deletion polymorphisms in the human genome
-
McCarroll, S. A., Hadnott, T. N., Perry, G. H. et al. (2006). Common deletion polymorphisms in the human genome. Nat Genet 38(1), 86-92.
-
(2006)
Nat Genet
, vol.38
, Issue.1
, pp. 86-92
-
-
McCarroll, S.A.1
Hadnott, T.N.2
Perry, G.H.3
-
25
-
-
33645118069
-
High-throughput genotyping of intermediate-size structural variation
-
Newman, T. L., Rieder, M. J., Morrison, V. A. et al. (2006). High-throughput genotyping of intermediate-size structural variation. Hum Mol Genet 15(7), 1159-1167.
-
(2006)
Hum Mol Genet
, vol.15
, Issue.7
, pp. 1159-1167
-
-
Newman, T.L.1
Rieder, M.J.2
Morrison, V.A.3
-
26
-
-
2442585704
-
Functional variants of OCTN cation transporter genes are associated with Crohn disease
-
Peltekova, V. D., Wintle, R. F., Rubin, L. A. et al. (2004). Functional variants of OCTN cation transporter genes are associated with Crohn disease. Nat Genet 36(5), 471-475.
-
(2004)
Nat Genet
, vol.36
, Issue.5
, pp. 471-475
-
-
Peltekova, V.D.1
Wintle, R.F.2
Rubin, L.A.3
-
27
-
-
26444581337
-
G2D: a tool for mining genes associated with disease
-
Perez-Iratxeta, C., Wjst, M., Bork, P. et al. (2005). G2D: a tool for mining genes associated with disease. BMC Genet 6, 45.
-
(2005)
BMC Genet
, vol.6
, pp. 45
-
-
Perez-Iratxeta, C.1
Wjst, M.2
Bork, P.3
-
28
-
-
20044390368
-
DNA methylation profiling of the humanmajor histocompatibility complex: a pilot study for theHumanEpigenome Project
-
Rakyan, V. K., Hildmann, T., Novik, K. L. et al. (2004). DNA methylation profiling of the humanmajor histocompatibility complex: a pilot study for theHumanEpigenome Project. PLoS Biol 2(12), e405.
-
(2004)
PLoS Biol
, vol.2
, Issue.12
-
-
Rakyan, V.K.1
Hildmann, T.2
Novik, K.L.3
-
29
-
-
33645098462
-
Role of the IBD5 susceptibility locus in the inflammatory bowel diseases
-
Reinhard, C. and Rioux, J.D. (2006). Role of the IBD5 susceptibility locus in the inflammatory bowel diseases. Inflamm Bowel Dis 12(3), 227-238.
-
(2006)
Inflamm Bowel Dis
, vol.12
, Issue.3
, pp. 227-238
-
-
Reinhard, C.1
Rioux, J.D.2
-
30
-
-
0034785352
-
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease
-
Rioux, J. D., Daly, M. J., Silverberg, M. S. et al. (2001). Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease. Nat Genet 29(2), 223-228.
-
(2001)
Nat Genet
, vol.29
, Issue.2
, pp. 223-228
-
-
Rioux, J.D.1
Daly, M.J.2
Silverberg, M.S.3
-
31
-
-
0034305821
-
DNA methylation in health and disease
-
Robertson, K. D. and Wolffe, A. P. (2000). DNA methylation in health and disease. Nat Rev Genet 1(1), 11-19.
-
(2000)
Nat Rev Genet
, vol.1
, Issue.1
, pp. 11-19
-
-
Robertson, K.D.1
Wolffe, A.P.2
-
32
-
-
27744495770
-
Tilling the chromatin landscape: emerging methods for the discovery and profiling of protein-DNA interactions
-
Rodriguez, B. A. and Huang, T.H. (2005). Tilling the chromatin landscape: emerging methods for the discovery and profiling of protein-DNA interactions. BiochemCell Biol 83(4), 525-534.
-
(2005)
BiochemCell Biol
, vol.83
, Issue.4
, pp. 525-534
-
-
Rodriguez, B.A.1
Huang, T.H.2
-
33
-
-
0035002807
-
Evaluation of gene-finding programs on mammalian sequences
-
Rogic, S., Mackworth, A. K. and Ouellette, F.B. F. (2001). Evaluation of gene-finding programs on mammalian sequences. Genome Res 11, 817-832.
-
(2001)
Genome Res
, vol.11
, pp. 817-832
-
-
Rogic, S.1
Mackworth, A.K.2
Ouellette, F.B.F.3
-
34
-
-
7244247384
-
Shotgun sequence assembly and recent segmental duplications within the human genome
-
She, X., Jiang, Z., Clark, R. A. et al. (2004). Shotgun sequence assembly and recent segmental duplications within the human genome. Nature 431(7011), 927-930.
-
(2004)
Nature
, vol.431
, Issue.7011
, pp. 927-930
-
-
She, X.1
Jiang, Z.2
Clark, R.A.3
-
35
-
-
2942750478
-
Incidental neurodevelopmental episodes in the etiology of schizophrenia: an expanded model involving epigenetics and development
-
Singh, S. M., McDonald, P., Murphy, B. et al. (2004). Incidental neurodevelopmental episodes in the etiology of schizophrenia: an expanded model involving epigenetics and development. Clin Genet 65(6), 435-440.
-
(2004)
Clin Genet
, vol.65
, Issue.6
, pp. 435-440
-
-
Singh, S.M.1
McDonald, P.2
Murphy, B.3
-
36
-
-
11144358198
-
A gene atlas of the mouse and human proteinencoding transcriptomes
-
Su, A. I., Wiltshire, T., Batalov, S. et al. (2004). A gene atlas of the mouse and human proteinencoding transcriptomes. Proc Natl Acad Sci 101, 6062-6067.
-
(2004)
Proc Natl Acad Sci
, vol.101
, pp. 6062-6067
-
-
Su, A.I.1
Wiltshire, T.2
Batalov, S.3
-
37
-
-
33344469939
-
Identification of frequent chromosome copy-number polymorphisms by use of high-resolution single-nucleotidepolymorphism arrays
-
Wirtenberger, M., Hemminki, K. and Burwinkel, B. (2006). Identification of frequent chromosome copy-number polymorphisms by use of high-resolution single-nucleotidepolymorphism arrays. Am J Hum Genet 78(3), 520-522.
-
(2006)
Am J Hum Genet
, vol.78
, Issue.3
, pp. 520-522
-
-
Wirtenberger, M.1
Hemminki, K.2
Burwinkel, B.3
|