-
2
-
-
13844313862
-
Whole-genome patterns of common DNA variation in three human populations
-
Hinds DA, Stuve LL, Nilsen GB, Halperin E, Eskin E, et al.(2005) Whole-genome patterns of common DNA variation in three human populations. Science 307: 1072-9.
-
(2005)
Science
, vol.307
, pp. 1072-1079
-
-
Hinds, D.A.1
Stuve, L.L.2
Nilsen, G.B.3
Halperin, E.4
Eskin, E.5
-
3
-
-
33745148197
-
Processes of copy-number change in human DNA: the dynamics of α-globin gene deletion
-
Lam KW, Jeffreys AJ, (2006) Processes of copy-number change in human DNA: the dynamics of α-globin gene deletion. Proc Natl Acad Sci U S A 103: 8921-7.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 8921-8927
-
-
Lam, K.W.1
Jeffreys, A.J.2
-
4
-
-
33751329250
-
Global variation in copy number in the human genome
-
Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, et al.(2006) Global variation in copy number in the human genome. Nature 444: 444-54.
-
(2006)
Nature
, vol.444
, pp. 444-454
-
-
Redon, R.1
Ishikawa, S.2
Fitch, K.R.3
Feuk, L.4
Perry, G.H.5
-
5
-
-
34347335669
-
The population genetics of structural variation
-
Conrad DF, Hurles ME, (2007) The population genetics of structural variation. Nat Genet 39: S30-6.
-
(2007)
Nat Genet
, vol.39
-
-
Conrad, D.F.1
Hurles, M.E.2
-
6
-
-
33847697015
-
Copy-number variations add a new layer of complexity in the human genome
-
Hegele RA, (2007) Copy-number variations add a new layer of complexity in the human genome. Cmaj 176: 441-2.
-
(2007)
Cmaj
, vol.176
, pp. 441-442
-
-
Hegele, R.A.1
-
7
-
-
33846006596
-
A comprehensive analysis of common copy-number variations in the human genome
-
Wong KK, deLeeuw RJ, Dosanjh NS, Kimm LR, Cheng Z, et al.(2007) A comprehensive analysis of common copy-number variations in the human genome. Am J Hum Genet 80: 91-104.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 91-104
-
-
Wong, K.K.1
deLeeuw, R.J.2
Dosanjh, N.S.3
Kimm, L.R.4
Cheng, Z.5
-
8
-
-
33846978695
-
Relative impact of nucleotide and copy number variation on gene expression phenotypes
-
Stranger BE, Forrest MS, Dunning M, Ingle CE, Beazley C, et al.(2007) Relative impact of nucleotide and copy number variation on gene expression phenotypes. Science 315: 848-53.
-
(2007)
Science
, vol.315
, pp. 848-853
-
-
Stranger, B.E.1
Forrest, M.S.2
Dunning, M.3
Ingle, C.E.4
Beazley, C.5
-
9
-
-
20044377204
-
The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility
-
Gonzalez E, Kulkarni H, Bolivar H, Mangano A, Sanchez R, et al.(2005) The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility. Science 307: 1434-40.
-
(2005)
Science
, vol.307
, pp. 1434-1440
-
-
Gonzalez, E.1
Kulkarni, H.2
Bolivar, H.3
Mangano, A.4
Sanchez, R.5
-
10
-
-
32844460938
-
Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans
-
Aitman TJ, Dong R, Vyse TJ, Norsworthy PJ, Johnson MD, et al.(2006) Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans. Nature 439: 851-5.
-
(2006)
Nature
, vol.439
, pp. 851-855
-
-
Aitman, T.J.1
Dong, R.2
Vyse, T.J.3
Norsworthy, P.J.4
Johnson, M.D.5
-
11
-
-
41449113254
-
X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation
-
Madrigal I, Rodriguez-Revenga L, Armengol L, Gonzalez E, Rodriguez B, et al.(2007) X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation. BMC Genomics 8: 443.
-
(2007)
BMC Genomics
, vol.8
, pp. 443
-
-
Madrigal, I.1
Rodriguez-Revenga, L.2
Armengol, L.3
Gonzalez, E.4
Rodriguez, B.5
-
12
-
-
34247481814
-
Strong association of de novo copy number mutations with autism
-
Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, et al.(2007) Strong association of de novo copy number mutations with autism. Science 316: 445-9.
-
(2007)
Science
, vol.316
, pp. 445-449
-
-
Sebat, J.1
Lakshmi, B.2
Malhotra, D.3
Troge, J.4
Lese-Martin, C.5
-
13
-
-
35548992257
-
Identification of cryptic microaberrations in osteosarcoma by high-definition oligonucleotide array comparative genomic hybridization
-
Selvarajah S, Yoshimoto M, Maire G, Paderova J, Bayani J, et al.(2007) Identification of cryptic microaberrations in osteosarcoma by high-definition oligonucleotide array comparative genomic hybridization. Cancer Genet Cytogenet 179: 52-61.
-
(2007)
Cancer Genet Cytogenet
, vol.179
, pp. 52-61
-
-
Selvarajah, S.1
Yoshimoto, M.2
Maire, G.3
Paderova, J.4
Bayani, J.5
-
14
-
-
57149123783
-
Genome-wide Copy-Number-Variation Study Identified a Susceptibility Gene, UGT2B17, for Osteoporosis
-
Yang TL, Chen XD, Guo Y, Lei SF, Wang JT, et al.(2008) Genome-wide Copy-Number-Variation Study Identified a Susceptibility Gene, UGT2B17, for Osteoporosis. Am J Hum Genet 83: 663-674.
-
(2008)
Am J Hum Genet
, vol.83
, pp. 663-674
-
-
Yang, T.L.1
Chen, X.D.2
Guo, Y.3
Lei, S.F.4
Wang, J.T.5
-
15
-
-
35448992970
-
Germ-line DNA copy number variation frequencies in a large North American population
-
Zogopoulos G, Ha KC, Naqib F, Moore S, Kim H, et al.(2007) Germ-line DNA copy number variation frequencies in a large North American population. Hum Genet 122: 345-353.
-
(2007)
Hum Genet
, vol.122
, pp. 345-353
-
-
Zogopoulos, G.1
Ha, K.C.2
Naqib, F.3
Moore, S.4
Kim, H.5
-
16
-
-
4444291843
-
Detection of large-scale variation in the human genome
-
Iafrate AJ, Feuk L, Rivera MN, Listewnik ML, Donahoe PK, et al.(2004) Detection of large-scale variation in the human genome. Nat Genet 36: 949-51.
-
(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
-
17
-
-
36148993604
-
Prevalence and prognostic significance of allelic imbalance by single-nucleotide polymorphism analysis in low-risk myelodysplastic syndromes
-
Mohamedali A, Gaken J, Twine NA, Ingram W, Westwood N, et al.(2007) Prevalence and prognostic significance of allelic imbalance by single-nucleotide polymorphism analysis in low-risk myelodysplastic syndromes. Blood 110: 3365-73.
-
(2007)
Blood
, vol.110
, pp. 3365-3373
-
-
Mohamedali, A.1
Gaken, J.2
Twine, N.A.3
Ingram, W.4
Westwood, N.5
-
18
-
-
34047245312
-
Genome-wide, high-resolution detection of copy number, loss of heterozygosity, and genotypes from formalin-fixed, paraffin-embedded tumor tissue using microarrays
-
Jacobs S, Thompson ER, Nannya Y, Yamamoto G, Pillai R, et al.(2007) Genome-wide, high-resolution detection of copy number, loss of heterozygosity, and genotypes from formalin-fixed, paraffin-embedded tumor tissue using microarrays. Cancer Res 67: 2544-51.
-
(2007)
Cancer Res
, vol.67
, pp. 2544-2551
-
-
Jacobs, S.1
Thompson, E.R.2
Nannya, Y.3
Yamamoto, G.4
Pillai, R.5
-
19
-
-
33846883741
-
Genome-wide analysis of DNA copy number changes and LOH in CLL using high-density SNP arrays
-
Pfeifer D, Pantic M, Skatulla I, Rawluk J, Kreutz C, et al.(2007) Genome-wide analysis of DNA copy number changes and LOH in CLL using high-density SNP arrays. Blood 109: 1202-10.
-
(2007)
Blood
, vol.109
, pp. 1202-1210
-
-
Pfeifer, D.1
Pantic, M.2
Skatulla, I.3
Rawluk, J.4
Kreutz, C.5
-
20
-
-
38549158349
-
Comprehensive analysis of loss of heterozygosity events in glioblastoma using the 100K SNP mapping arrays and comparison with copy number abnormalities defined by BAC array comparative genomic hybridization
-
Lo KC, Bailey D, Burkhardt T, Gardina P, Turpaz Y, et al.(2008) Comprehensive analysis of loss of heterozygosity events in glioblastoma using the 100K SNP mapping arrays and comparison with copy number abnormalities defined by BAC array comparative genomic hybridization. Genes Chromosomes Cancer 47: 221-37.
-
(2008)
Genes Chromosomes Cancer
, vol.47
, pp. 221-237
-
-
Lo, K.C.1
Bailey, D.2
Burkhardt, T.3
Gardina, P.4
Turpaz, Y.5
-
21
-
-
33845678584
-
Genome-wide loss of heterozygosity and copy number alteration in esophageal squamous cell carcinoma using the Affymetrix GeneChip Mapping 10 K array
-
Hu N, Wang C, Hu Y, Yang HH, Kong LH, et al.(2006) Genome-wide loss of heterozygosity and copy number alteration in esophageal squamous cell carcinoma using the Affymetrix GeneChip Mapping 10 K array. BMC Genomics 7: 299.
-
(2006)
BMC Genomics
, vol.7
, pp. 299
-
-
Hu, N.1
Wang, C.2
Hu, Y.3
Yang, H.H.4
Kong, L.H.5
-
22
-
-
22244453416
-
A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays
-
Nannya Y, Sanada M, Nakazaki K, Hosoya N, Wang L, et al.(2005) A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays. Cancer Res 65: 6071-9.
-
(2005)
Cancer Res
, vol.65
, pp. 6071-6079
-
-
Nannya, Y.1
Sanada, M.2
Nakazaki, K.3
Hosoya, N.4
Wang, L.5
-
23
-
-
33644942486
-
CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays
-
Huang J, Wei W, Chen J, Zhang J, Liu G, et al.(2006) CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays. BMC Bioinformatics 7: 83.
-
(2006)
BMC Bioinformatics
, vol.7
, pp. 83
-
-
Huang, J.1
Wei, W.2
Chen, J.3
Zhang, J.4
Liu, G.5
-
24
-
-
20844440702
-
Dynamic model based algorithms for screening and genotyping over 100 K SNPs on oligonucleotide microarrays
-
Di X, Matsuzaki H, Webster TA, Hubbell E, Liu G, et al.(2005) Dynamic model based algorithms for screening and genotyping over 100 K SNPs on oligonucleotide microarrays. Bioinformatics 21: 1958-63.
-
(2005)
Bioinformatics
, vol.21
, pp. 1958-1963
-
-
Di, X.1
Matsuzaki, H.2
Webster, T.A.3
Hubbell, E.4
Liu, G.5
-
25
-
-
30344454706
-
A genotype calling algorithm for affymetrix SNP arrays
-
Rabbee N, Speed TP, (2006) A genotype calling algorithm for affymetrix SNP arrays. Bioinformatics 22: 7-12.
-
(2006)
Bioinformatics
, vol.22
, pp. 7-12
-
-
Rabbee, N.1
Speed, T.P.2
-
26
-
-
0037316303
-
A comparison of normalization methods for high density oligonucleotide array data based on variance and bias
-
Bolstad BM, Irizarry RA, Astrand M, Speed TP, (2003) A comparison of normalization methods for high density oligonucleotide array data based on variance and bias. Bioinformatics 19: 185-93.
-
(2003)
Bioinformatics
, vol.19
, pp. 185-193
-
-
Bolstad, B.M.1
Irizarry, R.A.2
Astrand, M.3
Speed, T.P.4
-
27
-
-
0034118493
-
Inference of population structure using multilocus genotype data
-
Pritchard JK, Stephens M, Donnelly P, (2000) Inference of population structure using multilocus genotype data. Genetics 155: 945-59.
-
(2000)
Genetics
, vol.155
, pp. 945-959
-
-
Pritchard, J.K.1
Stephens, M.2
Donnelly, P.3
-
28
-
-
33847287196
-
Visualization of genomic aberrations using Affymetrix SNP arrays
-
Muller A, Holzmann K, Kestler HA, (2007) Visualization of genomic aberrations using Affymetrix SNP arrays. Bioinformatics 23: 496-7.
-
(2007)
Bioinformatics
, vol.23
, pp. 496-497
-
-
Muller, A.1
Holzmann, K.2
Kestler, H.A.3
|