-
1
-
-
0033539168
-
CpG islands as genomic footprints of promoters that are associated with replication origins
-
Antequera, F. and Bird, A. 1999. CpG islands as genomic footprints of promoters that are associated with replication origins. Curr. Biol. 9: R661-R667.
-
(1999)
Curr. Biol
, vol.9
-
-
Antequera, F.1
Bird, A.2
-
2
-
-
0038365277
-
CpG methylation of human papillomavirus type 16 DNA in cervical cancer cell lines and in clinical specimens: Genomic hypomethylation correlates with carcinogenic progression
-
Badal, V., Chuang, L.S., Tan, E.H., Badal, S., Villa, L.L., Wheeler, C.M., Li, B.F., and Bernard, H.U. 2003. CpG methylation of human papillomavirus type 16 DNA in cervical cancer cell lines and in clinical specimens: Genomic hypomethylation correlates with carcinogenic progression. J. Virol. 77: 6227-6234.
-
(2003)
J. Virol
, vol.77
, pp. 6227-6234
-
-
Badal, V.1
Chuang, L.S.2
Tan, E.H.3
Badal, S.4
Villa, L.L.5
Wheeler, C.M.6
Li, B.F.7
Bernard, H.U.8
-
3
-
-
0019322245
-
DNA methylation and the frequency of CpG in animal DNA
-
Bird, A.P. 1980. DNA methylation and the frequency of CpG in animal DNA. Nucleic Acids Res. 8: 1499-1504.
-
(1980)
Nucleic Acids Res
, vol.8
, pp. 1499-1504
-
-
Bird, A.P.1
-
4
-
-
0022540321
-
CpG-rich islands and the function of DNA methylation
-
Bird, A.P. 1986. CpG-rich islands and the function of DNA methylation. Nature 321: 209-213.
-
(1986)
Nature
, vol.321
, pp. 209-213
-
-
Bird, A.P.1
-
5
-
-
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: 350-358.
-
(2004)
Trends Genet
, vol.20
, pp. 350-358
-
-
Bjornsson, H.T.1
Fallin, M.D.2
Feinberg, A.P.3
-
6
-
-
33644873001
-
Transposon-derived repeats in the human genome and 5-methylcytosine-associated mutations in adjacent genes
-
Bjornsson, H.T., Ellingsen, L.M., andJonsson, J.J. 2006. Transposon-derived repeats in the human genome and 5-methylcytosine-associated mutations in adjacent genes. Gene 370: 43-50.
-
(2006)
Gene
, vol.370
, pp. 43-50
-
-
Bjornsson, H.T.1
Ellingsen, L.M.2
andJonsson, J.J.3
-
7
-
-
45849127657
-
Intra-individual change over time in DNA methylation with familial clustering
-
Bjornsson, H.T., Sigurdsson, M.I., Fallin, M.D., Irizarry, R.A., Aspelund, T., Cui, H., Yu, W., Rongione, M.A., Ekstrom, T.J., Harris, T.B., et al. 2008. Intra-individual change over time in DNA methylation with familial clustering. JAMA 299: 2877-2883.
-
(2008)
JAMA
, vol.299
, pp. 2877-2883
-
-
Bjornsson, H.T.1
Sigurdsson, M.I.2
Fallin, M.D.3
Irizarry, R.A.4
Aspelund, T.5
Cui, H.6
Yu, W.7
Rongione, M.A.8
Ekstrom, T.J.9
Harris, T.B.10
-
8
-
-
4544223707
-
Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L
-
Bourc'his, D. and Bestor, T.H. 2004. Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L. Nature 431: 96-99.
-
(2004)
Nature
, vol.431
, pp. 96-99
-
-
Bourc'his, D.1
Bestor, T.H.2
-
9
-
-
0032231877
-
Comprehensive human genetic maps: Individual and sex-specific variation in recombination
-
Broman, K.W., Murray, J.C., Sheffield, V.C., White, R.L., and Weber, J.L. 1998. Comprehensive human genetic maps: Individual and sex-specific variation in recombination. Am. J. Hum. Genet. 63: 861-869.
-
(1998)
Am. J. Hum. Genet
, vol.63
, pp. 861-869
-
-
Broman, K.W.1
Murray, J.C.2
Sheffield, V.C.3
White, R.L.4
Weber, J.L.5
-
10
-
-
39449116116
-
High- resolution mapping of crossovers reveals extensive variation in fine- scale recombination patterns among humans
-
Coop, G., Wen, X., Ober, C., Pritchard, J.K., and Przeworski, M. 2008. High- resolution mapping of crossovers reveals extensive variation in fine- scale recombination patterns among humans. Science 319: 1395-1398.
-
(2008)
Science
, vol.319
, pp. 1395-1398
-
-
Coop, G.1
Wen, X.2
Ober, C.3
Pritchard, J.K.4
Przeworski, M.5
-
11
-
-
0023853921
-
The CpG dinucleotide and human genetic disease
-
Cooper, D.N. and Youssoufian, H. 1988. The CpG dinucleotide and human genetic disease. Hum. Genet. 78: 151-155.
-
(1988)
Hum. Genet
, vol.78
, pp. 151-155
-
-
Cooper, D.N.1
Youssoufian, H.2
-
12
-
-
0018185292
-
Molecular basis of base substitution hotspots in Escherichia coli
-
Coulondre, C., Miller, J.H., Farabaugh, P.J., and Gilbert, W. 1978. Molecular basis of base substitution hotspots in Escherichia coli. Nature 274: 775-780.
-
(1978)
Nature
, vol.274
, pp. 775-780
-
-
Coulondre, C.1
Miller, J.H.2
Farabaugh, P.J.3
Gilbert, W.4
-
13
-
-
0033562954
-
Acquisition of the H19 methylation imprint occurs differentially on the parental alleles during spermatogenesis
-
Davis, T.L., Trasler, J.M., Moss, S.B., Yang, G.J., and Bartolomei, M.S. 1999. Acquisition of the H19 methylation imprint occurs differentially on the parental alleles during spermatogenesis. Genomics 58: 18-28.
-
(1999)
Genomics
, vol.58
, pp. 18-28
-
-
Davis, T.L.1
Trasler, J.M.2
Moss, S.B.3
Yang, G.J.4
Bartolomei, M.S.5
-
14
-
-
33751505540
-
DNA methylation profiling of human chromosomes 6, 20 and 22
-
Eckhardt, F., Lewin, J., Cortese, R., Rakyan, V.K., Attwood, J., Burger, M., Burton, J., Cox, T.V., Davies, R., Down, T.A., et al. 2006. DNA methylation profiling of human chromosomes 6, 20 and 22. Nat. Genet. 38: 1378-1385.
-
(2006)
Nat. Genet
, vol.38
, pp. 1378-1385
-
-
Eckhardt, F.1
Lewin, J.2
Cortese, R.3
Rakyan, V.K.4
Attwood, J.5
Burger, M.6
Burton, J.7
Cox, T.V.8
Davies, R.9
Down, T.A.10
-
15
-
-
7444260846
-
The ENCODE (ENCyclopedia Of DNA Elements) Project
-
The ENCODE Project Consortium
-
The ENCODE Project Consortium. 2004. The ENCODE (ENCyclopedia Of DNA Elements) Project. Science 306: 636-640.
-
(2004)
Science
, vol.306
, pp. 636-640
-
-
-
16
-
-
0020699979
-
Hypomethylation distinguishes genes of some human cancers from their normal counterparts
-
Feinberg, A.P. and Vogelstein, B. 1983. Hypomethylation distinguishes genes of some human cancers from their normal counterparts. Nature 301: 89-92.
-
(1983)
Nature
, vol.301
, pp. 89-92
-
-
Feinberg, A.P.1
Vogelstein, B.2
-
17
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
Frazer, K.A., Ballinger, D.G., Cox, D.R., Hinds, D.A., Stuve, L.L., Gibbs, R.A., Belmont, J.W., Boudreau, A., Hardenbol, P., Leal, S.M., et al. 2007. A second generation human haplotype map of over 3.1 million SNPs. Nature 449: 851-861.
-
(2007)
Nature
, vol.449
, pp. 851-861
-
-
Frazer, K.A.1
Ballinger, D.G.2
Cox, D.R.3
Hinds, D.A.4
Stuve, L.L.5
Gibbs, R.A.6
Belmont, J.W.7
Boudreau, A.8
Hardenbol, P.9
Leal, S.M.10
-
18
-
-
0023216891
-
CpG islands in vertebrate genomes
-
Gardiner-Garden, M. and Frommer, M. 1987. CpG islands in vertebrate genomes. J. Mol. Biol. 196: 261-282.
-
(1987)
J. Mol. Biol
, vol.196
, pp. 261-282
-
-
Gardiner-Garden, M.1
Frommer, M.2
-
19
-
-
1842536305
-
The DNA sequence and biology ofhuman chromosome 19
-
Grimwood, J., Gordon, L.A., Olsen, A., Terry, A., Schmutz, J., Lamerdin, J., Hellsten, U., Goodstein, D., Couronne, O., Tran-Gyamfi, M., et al. 2004. The DNA sequence and biology ofhuman chromosome 19. Nature 428:529-535.
-
(2004)
Nature
, vol.428
, pp. 529-535
-
-
Grimwood, J.1
Gordon, L.A.2
Olsen, A.3
Terry, A.4
Schmutz, J.5
Lamerdin, J.6
Hellsten, U.7
Goodstein, D.8
Couronne, O.9
Tran-Gyamfi, M.10
-
20
-
-
33847304609
-
Gene body-specific methylation on the active X chromosome
-
Hellman, A. and Chess, A. 2007. Gene body-specific methylation on the active X chromosome. Science 315: 1141-1143.
-
(2007)
Science
, vol.315
, pp. 1141-1143
-
-
Hellman, A.1
Chess, A.2
-
21
-
-
33646133653
-
The UCSC known genes
-
Hsu, F., Kent, W.J., Clawson, H., Kuhn, R.M., Diekhans, M., and Haussler, D. 2006. The UCSC known genes. Bioinformatics 22: 1036-1046.
-
(2006)
Bioinformatics
, vol.22
, pp. 1036-1046
-
-
Hsu, F.1
Kent, W.J.2
Clawson, H.3
Kuhn, R.M.4
Diekhans, M.5
Haussler, D.6
-
22
-
-
79959524146
-
A haplotype map of the human genome
-
The International HapMap Consortium
-
The International HapMap Consortium. 2005. A haplotype map of the human genome. Nature 437: 1299-1320.
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
-
23
-
-
0034795550
-
Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex
-
Jeffreys, A.J., Kauppi, L., and Neumann, R. 2001. Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex. Nat. Genet. 29: 217-222.
-
(2001)
Nat. Genet
, vol.29
, pp. 217-222
-
-
Jeffreys, A.J.1
Kauppi, L.2
Neumann, R.3
-
24
-
-
1842717957
-
Comparative recombination rates in the rat, mouse, and human genomes
-
Jensen-Seaman, M.I., Furey, T.S., Payseur, B.A., Lu, Y., Roskin, K.M., Chen, C.F., Thomas, M.A., Haussler, D., and Jacob, H.J. 2004. Comparative recombination rates in the rat, mouse, and human genomes. Genome Res. 14: 528-538.
-
(2004)
Genome Res
, vol.14
, pp. 528-538
-
-
Jensen-Seaman, M.I.1
Furey, T.S.2
Payseur, B.A.3
Lu, Y.4
Roskin, K.M.5
Chen, C.F.6
Thomas, M.A.7
Haussler, D.8
Jacob, H.J.9
-
25
-
-
23844525077
-
Repbase Update, a database of eukaryotic repetitive elements
-
Jurka, J., Kapitonov, V.V., Pavlicek, A., Klonowski, P., Kohany, O., and Walichiewicz, J. 2005. Repbase Update, a database of eukaryotic repetitive elements. Cytogenet. Genome Res. 110: 462-467.
-
(2005)
Cytogenet. Genome Res
, vol.110
, pp. 462-467
-
-
Jurka, J.1
Kapitonov, V.V.2
Pavlicek, A.3
Klonowski, P.4
Kohany, O.5
Walichiewicz, J.6
-
26
-
-
0347755531
-
The UCSC table browser data retrieval tool
-
Karolchik, D., Hinrichs, A.S., Furey, T.S., Roskin, K.M., Sugnet, C.W., Haussler, D., and Kent, W.J. 2004. The UCSC table browser data retrieval tool. Nucleic Acids Res. 32: D493-D496.
-
(2004)
Nucleic Acids Res
, vol.32
-
-
Karolchik, D.1
Hinrichs, A.S.2
Furey, T.S.3
Roskin, K.M.4
Sugnet, C.W.5
Haussler, D.6
Kent, W.J.7
-
27
-
-
0036079158
-
The human genome browser at UCSC
-
Kent, W.J., Sugnet, C.W., Furey, T.S., Roskin, K.M., Pringle, T.H., Zahler, A.M., and Haussler, D. 2002. The human genome browser at UCSC. Genome Res. 12: 996-1006.
-
(2002)
Genome Res
, vol.12
, pp. 996-1006
-
-
Kent, W.J.1
Sugnet, C.W.2
Furey, T.S.3
Roskin, K.M.4
Pringle, T.H.5
Zahler, A.M.6
Haussler, D.7
-
28
-
-
0024356362
-
The neutral theory of molecular evolution and the world view of the neutralists
-
Kimura, M. 1989. The neutral theory of molecular evolution and the world view of the neutralists. Genome 31: 24-31.
-
(1989)
Genome
, vol.31
, pp. 24-31
-
-
Kimura, M.1
-
29
-
-
0025912824
-
Recent development of the neutral theory viewed from the Wrightian tradition of theoretical population genetics
-
Kimura, M. 1991. Recent development of the neutral theory viewed from the Wrightian tradition of theoretical population genetics. Proc. Natl. Acad. Sci. 88: 5969-5973.
-
(1991)
Proc. Natl. Acad. Sci
, vol.88
, pp. 5969-5973
-
-
Kimura, M.1
-
30
-
-
18544381909
-
A high-resolution recombination map of the human genome
-
Kong, A., Gudbjartsson, D.F., Sainz, J., Jonsdottir, G.M., Gudjonsson, S.A., Richardsson, B., Sigurdardottir, S., Barnard, J., Hallbeck, B., Masson, G., et al. 2002. A high-resolution recombination map of the human genome. Nat. Genet. 31: 241-247.
-
(2002)
Nat. Genet
, vol.31
, pp. 241-247
-
-
Kong, A.1
Gudbjartsson, D.F.2
Sainz, J.3
Jonsdottir, G.M.4
Gudjonsson, S.A.5
Richardsson, B.6
Sigurdardottir, S.7
Barnard, J.8
Hallbeck, B.9
Masson, G.10
-
31
-
-
0032231701
-
Neighboring-nucleotide effects on the rates of germ-line single-base-pair substitution in human genes
-
Krawczak, M., Ball, E.V., and Cooper, D.N. 1998. Neighboring-nucleotide effects on the rates of germ-line single-base-pair substitution in human genes. Am. J. Hum. Genet. 63: 474-488.
-
(1998)
Am. J. Hum. Genet
, vol.63
, pp. 474-488
-
-
Krawczak, M.1
Ball, E.V.2
Cooper, D.N.3
-
32
-
-
0347622761
-
Imprinted chromosomal regions of the human genome have unusually high recombination rates
-
Lercher, M.J. and Hurst, L.D. 2003. Imprinted chromosomal regions of the human genome have unusually high recombination rates. Genetics 165:1629-1632.
-
(2003)
Genetics
, vol.165
, pp. 1629-1632
-
-
Lercher, M.J.1
Hurst, L.D.2
-
33
-
-
33645814398
-
CTCF mediates interchromosomal colocalization between Igf2/H19 and Wsb1/Nf1
-
Ling, J.Q., Li, T., Hu, J.F., Vu, T.H., Chen, H.L., Qiu, X.W., Cherry, A.M., and Hoffman, A.R. 2006. CTCF mediates interchromosomal colocalization between Igf2/H19 and Wsb1/Nf1. Science 312: 269-272.
-
(2006)
Science
, vol.312
, pp. 269-272
-
-
Ling, J.Q.1
Li, T.2
Hu, J.F.3
Vu, T.H.4
Chen, H.L.5
Qiu, X.W.6
Cherry, A.M.7
Hoffman, A.R.8
-
34
-
-
0019510628
-
Reactivation of an inactive human X chromosome: Evidence for X inactivation by DNA methylation
-
Mohandas, T., Sparkes, R.S., and Shapiro, L.J. 1981. Reactivation of an inactive human X chromosome: Evidence for X inactivation by DNA methylation. Science 211: 393-396.
-
(1981)
Science
, vol.211
, pp. 393-396
-
-
Mohandas, T.1
Sparkes, R.S.2
Shapiro, L.J.3
-
35
-
-
26844482093
-
A fine-scale map of recombination rates and hotspots across the human genome
-
Myers, S., Bottolo, L., Freeman, C., McVean, G., and Donnelly, P. 2005. A fine-scale map of recombination rates and hotspots across the human genome. Science 310: 321-324.
-
(2005)
Science
, vol.310
, pp. 321-324
-
-
Myers, S.1
Bottolo, L.2
Freeman, C.3
McVean, G.4
Donnelly, P.5
-
36
-
-
33747189181
-
The distribution and causes of meiotic recombination in the human genome
-
Myers, S., Spencer, C.C., Auton, A., Bottolo, L., Freeman, C., Donnelly, P., and McVean, G. 2006. The distribution and causes of meiotic recombination in the human genome. Biochem. Soc. Trans. 34:526-530.
-
(2006)
Biochem. Soc. Trans
, vol.34
, pp. 526-530
-
-
Myers, S.1
Spencer, C.C.2
Auton, A.3
Bottolo, L.4
Freeman, C.5
Donnelly, P.6
McVean, G.7
-
37
-
-
33646130166
-
Polymorphism in the activity of human crossover hotspots independent of local DNA sequence variation
-
Neumann, R. and Jeffreys, A.J. 2006. Polymorphism in the activity of human crossover hotspots independent of local DNA sequence variation. Hum. Mol. Genet. 15: 1401-1411.
-
(2006)
Hum. Mol. Genet
, vol.15
, pp. 1401-1411
-
-
Neumann, R.1
Jeffreys, A.J.2
-
38
-
-
34347213437
-
Developmental acquisition of genome-wide DNA methylation occurs prior to meiosis in male germ cells
-
Oakes, C.C., La Salle, S., Smiraglia, D.J., Robaire, B., and Trasler, J.M. 2007. Developmental acquisition of genome-wide DNA methylation occurs prior to meiosis in male germ cells. Dev. Biol. 307: 368-379.
-
(2007)
Dev. Biol
, vol.307
, pp. 368-379
-
-
Oakes, C.C.1
La Salle, S.2
Smiraglia, D.J.3
Robaire, B.4
Trasler, J.M.5
-
39
-
-
50849104569
-
-
O'Hagan, H.M., Mohammad, H.P., and Baylin, S.B. 2008. Double-strand breaks can initiate gene silencing and SIRT1-dependent onset of DNA methylation in an exogenous promoter CpG island. PLoS Genet. 4: e1000155. doi: 10.1371/journal.pgen.1000155.
-
O'Hagan, H.M., Mohammad, H.P., and Baylin, S.B. 2008. Double-strand breaks can initiate gene silencing and SIRT1-dependent onset of DNA methylation in an exogenous promoter CpG island. PLoS Genet. 4: e1000155. doi: 10.1371/journal.pgen.1000155.
-
-
-
-
40
-
-
20044390368
-
DNA methylation profiling of the human major histocompatibility complex: A pilot study for the Human Epigenome Project
-
doi:10.1371/journal. pbio.0020405
-
Rakyan, V.K., Hildmann, T., Novik, K.L., Lewin, J., Tost, J., Cox, A.V., Andrews, T.D., Howe, K.L., Otto, T., Olek, A., et al. 2004. DNA methylation profiling of the human major histocompatibility complex: A pilot study for the Human Epigenome Project. PLoS Biol. 2: e405. doi:10.1371/journal. pbio.0020405.
-
(2004)
PLoS Biol
, vol.2
-
-
Rakyan, V.K.1
Hildmann, T.2
Novik, K.L.3
Lewin, J.4
Tost, J.5
Cox, A.V.6
Andrews, T.D.7
Howe, K.L.8
Otto, T.9
Olek, A.10
-
41
-
-
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: 11-19.
-
(2000)
Nat. Rev. Genet
, vol.1
, pp. 11-19
-
-
Robertson, K.D.1
Wolffe, A.P.2
-
42
-
-
33746626111
-
Human imprinted chromosomal regions are historical hot-spots of recombination
-
doi: 10.1371/journal.pgen.0020101
-
Sandovici, I., Kassovska-Bratinova, S., Vaughan, J.E., Stewart, R., Leppert, M., and Sapienza, C. 2006. Human imprinted chromosomal regions are historical hot-spots of recombination. PLoS Genet. 2: e101. doi: 10.1371/journal.pgen.0020101.
-
(2006)
PLoS Genet
, vol.2
-
-
Sandovici, I.1
Kassovska-Bratinova, S.2
Vaughan, J.E.3
Stewart, R.4
Leppert, M.5
Sapienza, C.6
-
43
-
-
27544435335
-
Sequence features in regions of weak and strong linkage disequilibrium
-
Smith, A.V., Thomas, D.J., Munro, H.M., and Abecasis, G.R. 2005. Sequence features in regions of weak and strong linkage disequilibrium. Genome Res. 15: 1519-1534.
-
(2005)
Genome Res
, vol.15
, pp. 1519-1534
-
-
Smith, A.V.1
Thomas, D.J.2
Munro, H.M.3
Abecasis, G.R.4
-
44
-
-
14744267496
-
Association of tissue-specific differentially methylated regions (TDMs) with differential gene expression
-
Song, F., Smith, J.F., Kimura, M.T., Morrow, A.D., Matsuyama, T., Nagase, H., and Held, W.A. 2005. Association of tissue-specific differentially methylated regions (TDMs) with differential gene expression. Proc. Natl. Acad. Sci. 102: 3336-3341.
-
(2005)
Proc. Natl. Acad. Sci
, vol.102
, pp. 3336-3341
-
-
Song, F.1
Smith, J.F.2
Kimura, M.T.3
Morrow, A.D.4
Matsuyama, T.5
Nagase, H.6
Held, W.A.7
-
45
-
-
33846101990
-
Variation resources at UC Santa Cruz
-
Thomas, D.J., Trumbower, H., Kern, A.D., Rhead, B.L., Kuhn, R.M., Haussler, D., and Kent, W.J. 2007. Variation resources at UC Santa Cruz. Nucleic Acids Res. 35: D716-D720.
-
(2007)
Nucleic Acids Res
, vol.35
-
-
Thomas, D.J.1
Trumbower, H.2
Kern, A.D.3
Rhead, B.L.4
Kuhn, R.M.5
Haussler, D.6
Kent, W.J.7
-
46
-
-
0020027521
-
Transformation with DNA from 5-azacytidine- reactivated X chromosomes
-
Venolia, L., Gartler, S.M., Wassman, E.R., Yen, P., Mohandas, T., and Shapiro, L.J. 1982. Transformation with DNA from 5-azacytidine- reactivated X chromosomes. Proc. Natl. Acad. Sci. 79: 2352-2354.
-
(1982)
Proc. Natl. Acad. Sci
, vol.79
, pp. 2352-2354
-
-
Venolia, L.1
Gartler, S.M.2
Wassman, E.R.3
Yen, P.4
Mohandas, T.5
Shapiro, L.J.6
-
47
-
-
33644981509
-
A map of recent positive selection in the human genome
-
doi:10.1371/journal.pbio.0040072
-
Voight, B.F., Kudaravalli, S., Wen, X., and Pritchard, J.K. 2006. A map of recent positive selection in the human genome. PLoS Biol. 4: e72. doi:10.1371/journal.pbio.0040072.
-
(2006)
PLoS Biol
, vol.4
-
-
Voight, B.F.1
Kudaravalli, S.2
Wen, X.3
Pritchard, J.K.4
-
48
-
-
48749119888
-
Sperm cross-over activity in regions of the human genome showing extreme breakdown of marker association
-
Webb, A.J., Berg, I.L., and Jeffreys, A. 2008. Sperm cross-over activity in regions of the human genome showing extreme breakdown of marker association. Proc. Natl. Acad. Sci. 105: 10471-10476.
-
(2008)
Proc. Natl. Acad. Sci
, vol.105
, pp. 10471-10476
-
-
Webb, A.J.1
Berg, I.L.2
Jeffreys, A.3
-
49
-
-
34047116826
-
Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome
-
Weber, M., Hellmann, I., Stadler, M.B., Ramos, L., Paabo, S., Rebhan, M., and Schubeler, D. 2007. Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome. Nat. Genet. 39: 457-466.
-
(2007)
Nat. Genet
, vol.39
, pp. 457-466
-
-
Weber, M.1
Hellmann, I.2
Stadler, M.B.3
Ramos, L.4
Paabo, S.5
Rebhan, M.6
Schubeler, D.7
-
50
-
-
29244490041
-
Analysis of repetitive element DNA methylation by Methy Light
-
Weisenberger, D.J., Campan, M., Long, T.I., Kim, M., Woods, C., Fiala, E., Ehrlich, M., and Laird, P.W. 2005. Analysis of repetitive element DNA methylation by Methy Light. Nucleic Acids Res. 33: 6823-6836.
-
(2005)
Nucleic Acids Res
, vol.33
, pp. 6823-6836
-
-
Weisenberger, D.J.1
Campan, M.2
Long, T.I.3
Kim, M.4
Woods, C.5
Fiala, E.6
Ehrlich, M.7
Laird, P.W.8
-
51
-
-
20144387806
-
Comparison of fine-scale recombination rates in humans and chimpanzees
-
Winckler, W., Myers, S.R., Richter, D.J., Onofrio, R.C., McDonald, G.J., Bontrop, R.E., McVean, G.A., Gabriel, S.B., Reich, D., Donnelly, P., et al. 2005. Comparison of fine-scale recombination rates in humans and chimpanzees. Science 308: 107-111.
-
(2005)
Science
, vol.308
, pp. 107-111
-
-
Winckler, W.1
Myers, S.R.2
Richter, D.J.3
Onofrio, R.C.4
McDonald, G.J.5
Bontrop, R.E.6
McVean, G.A.7
Gabriel, S.B.8
Reich, D.9
Donnelly, P.10
-
52
-
-
0033547330
-
Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene
-
Xu, G.L., Bestor, T.H., Bourc'his, D., Hsieh, C.L., Tommerup, N., Bugge, M., Hulten, M., Qu, X., Russo, J.J., and Viegas-Pequignot, E. 1999. Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene. Nature 402: 187-191.
-
(1999)
Nature
, vol.402
, pp. 187-191
-
-
Xu, G.L.1
Bestor, T.H.2
Bourc'his, D.3
Hsieh, C.L.4
Tommerup, N.5
Bugge, M.6
Hulten, M.7
Qu, X.8
Russo, J.J.9
Viegas-Pequignot, E.10
-
53
-
-
0030840954
-
Cytosine methylation and the ecology of intragenomic parasites
-
Yoder, J.A., Walsh, C.P., and Bestor, T.H. 1997. Cytosine methylation and the ecology of intragenomic parasites. Trends Genet. 13: 335-340.
-
(1997)
Trends Genet
, vol.13
, pp. 335-340
-
-
Yoder, J.A.1
Walsh, C.P.2
Bestor, T.H.3
-
54
-
-
32444436681
-
Sequence context analysis of 8.2 million single nucleotide polymorphisms in the human genome
-
Zhao, Z. and Zhang, F. 2006. Sequence context analysis of 8.2 million single nucleotide polymorphisms in the human genome. Gene 366: 316-324.
-
(2006)
Gene
, vol.366
, pp. 316-324
-
-
Zhao, Z.1
Zhang, F.2
|