-
1
-
-
23744469394
-
Region-specific detection of neuroblastoma loss of heterozygosity at multiple loci simultaneously using a SNP-based tag-array platform
-
Maris JM, Hii G, Gelfand CA, Varde S, White PS, Rappaport E, Surrey S, Fortina P: Region-specific detection of neuroblastoma loss of heterozygosity at multiple loci simultaneously using a SNP-based tag-array platform. Genome Res 2005, 15:1168-1176.
-
(2005)
Genome Res
, vol.15
, pp. 1168-1176
-
-
Maris, J.M.1
Hii, G.2
Gelfand, C.A.3
Varde, S.4
White, P.S.5
Rappaport, E.6
Surrey, S.7
Fortina, P.8
-
2
-
-
0037370466
-
Chromosome-wide distribution of haplotype blocks and the role of recombination hot spots
-
Phillips MS, Lawrence R, Sachidanandam R, Morris AP, Balding DJ, Donaldson MA, Studebaker JF, Ankener WM, Alfisi SV, Kuo FS, Camisa AL, Pazorov V, Scott KE, Carey BJ, Faith J, Katari G, Bhatti HA, Cyr JM, Derohannessian V, Elosua C, Forman AM, Grecco NM, Hock CR, Kuebler JM, Lathrop JA, Mockler MA, Nachtman EP, Restine SL, Varde SA, Hozza MJ, Gelfand CA, Broxholme J, Abecasis GR, Boyce-Jacino MT, Cardon LR: Chromosome-wide distribution of haplotype blocks and the role of recombination hot spots. Nat Genet 2003, 33:382-387.
-
(2003)
Nat Genet
, vol.33
, pp. 382-387
-
-
Phillips, M.S.1
Lawrence, R.2
Sachidanandam, R.3
Morris, A.P.4
Balding, D.J.5
Donaldson, M.A.6
Studebaker, J.F.7
Ankener, W.M.8
Alfisi, S.V.9
Kuo, F.S.10
Camisa, A.L.11
Pazorov, V.12
Scott, K.E.13
Carey, B.J.14
Faith, J.15
Katari, G.16
Bhatti, H.A.17
Cyr, J.M.18
Derohannessian, V.19
Elosua, C.20
Forman, A.M.21
Grecco, N.M.22
Hock, C.R.23
Kuebler, J.M.24
Lathrop, J.A.25
Mockler, M.A.26
Nachtman, E.P.27
Restine, S.L.28
Varde, S.A.29
Hozza, M.J.30
Gelfand, C.A.31
Broxholme, J.32
Abecasis, G.R.33
Boyce-Jacino, M.T.34
Cardon, L.R.35
more..
-
3
-
-
2342453338
-
An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays
-
Zhao X, Li C, Paez JG, Chin K, Janne PA, Chen TH, Girard L, Minna J, Christiani D, Leo C, Gray JW, Sellers WR, Meyerson M: An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays. Cancer Res 2004, 64:3060-3071.
-
(2004)
Cancer Res
, vol.64
, pp. 3060-3071
-
-
Zhao, X.1
Li, C.2
Paez, J.G.3
Chin, K.4
Janne, P.A.5
Chen, T.H.6
Girard, L.7
Minna, J.8
Christiani, D.9
Leo, C.10
Gray, J.W.11
Sellers, W.R.12
Meyerson, M.13
-
4
-
-
2342647468
-
High-resolution single-nucleotide polymorphism array and clustering analysis of loss of heterozygosity in human lung cancer cell lines
-
Janne PA, Li C, Zhao X, Girard L, Chen TH, Minna J, Christiani DC, Johnson BE, Meyerson M: High-resolution single-nucleotide polymorphism array and clustering analysis of loss of heterozygosity in human lung cancer cell lines. Oncogene 2004, 23:2716-2726.
-
(2004)
Oncogene
, vol.23
, pp. 2716-2726
-
-
Janne, P.A.1
Li, C.2
Zhao, X.3
Girard, L.4
Chen, T.H.5
Minna, J.6
Christiani, D.C.7
Johnson, B.E.8
Meyerson, M.9
-
5
-
-
2442671820
-
Allelic imbalance analysis by high-density single-nucleotide polymorphic allele (SNP) array with whole genome amplified DNA
-
Wong KK, Tsang YT, Shen J, Cheng RS, Chang YM, Man TK, Lau CC: Allelic imbalance analysis by high-density single-nucleotide polymorphic allele (SNP) array with whole genome amplified DNA. Nucleic Acids Res 2004, 32:e69.
-
(2004)
Nucleic Acids Res
, vol.32
-
-
Wong, K.K.1
Tsang, Y.T.2
Shen, J.3
Cheng, R.S.4
Chang, Y.M.5
Man, T.K.6
Lau, C.C.7
-
6
-
-
23944476059
-
A high-density SNP genomewide linkage scan for chronic lymphocytic leukemia-susceptibility loci
-
Sellick GS, Webb EL, Allinson R, Matutes E, Dyer MJ, Jonsson V, Langerak AW, Mauro FR, Fuller S, Wiley J, Lyttelton M, Callea V, Yuille M, Catovsky D, Houlston RS: A high-density SNP genomewide linkage scan for chronic lymphocytic leukemia-susceptibility loci. Am J Hum Genet 2005, 77:420-429.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 420-429
-
-
Sellick, G.S.1
Webb, E.L.2
Allinson, R.3
Matutes, E.4
Dyer, M.J.5
Jonsson, V.6
Langerak, A.W.7
Mauro, F.R.8
Fuller, S.9
Wiley, J.10
Lyttelton, M.11
Callea, V.12
Yuille, M.13
Catovsky, D.14
Houlston, R.S.15
-
7
-
-
2342635193
-
Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: A comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22
-
Middleton FA, Pato MT, Gentile KL, Morley CP, Zhao X, Eisener AF, Brown A, Petryshen TL, Kirby AN, Medeiros H, Carvalho C, Macedo A, Dourado A, Coelho I, Valente J, Soares MJ, Ferreira CP, Lei M, Azevedo MH, Kennedy JL, Daly MJ, Sklar P, Pato CN: Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22. Am J Hum Genet 2004, 74:886-897.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 886-897
-
-
Middleton, F.A.1
Pato, M.T.2
Gentile, K.L.3
Morley, C.P.4
Zhao, X.5
Eisener, A.F.6
Brown, A.7
Petryshen, T.L.8
Kirby, A.N.9
Medeiros, H.10
Carvalho, C.11
Macedo, A.12
Dourado, A.13
Coelho, I.14
Valente, J.15
Soares, M.J.16
Ferreira, C.P.17
Lei, M.18
Azevedo, M.H.19
Kennedy, J.L.20
Daly, M.J.21
Sklar, P.22
Pato, C.N.23
more..
-
8
-
-
4544354302
-
Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping array
-
Zhou X, Mok SC, Chen Z, Li Y, Wong DT: Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping array. Hum Genet 2004, 115:327-330.
-
(2004)
Hum Genet
, vol.115
, pp. 327-330
-
-
Zhou, X.1
Mok, S.C.2
Chen, Z.3
Li, Y.4
Wong, D.T.5
-
9
-
-
13844299266
-
High-resolution analysis of chromosomal imbalances using the Affymetrix 10K SNP genotyping chip
-
Herr A, Grutzmann R, Matthaei A, Artelt J, Schrock E, Rump A, Pilarsky C: High-resolution analysis of chromosomal imbalances using the Affymetrix 10K SNP genotyping chip. Genomics 2005, 85:392-400.
-
(2005)
Genomics
, vol.85
, pp. 392-400
-
-
Herr, A.1
Grutzmann, R.2
Matthaei, A.3
Artelt, J.4
Schrock, E.5
Rump, A.6
Pilarsky, C.7
-
10
-
-
11244298063
-
High-density single nucleotide polymorphism array defines novel stage and location-dependent allelic imbalances in human bladder tumors
-
von der MH
-
Koed K, Wiuf C, Christensen LL, Wikman FP, Zieger K, Moller K, von der MH, Orntoft TF: High-density single nucleotide polymorphism array defines novel stage and location-dependent allelic imbalances in human bladder tumors. Cancer Res 2005, 65:34-45.
-
(2005)
Cancer Res
, vol.65
, pp. 34-45
-
-
Koed, K.1
Wiuf, C.2
Christensen, L.L.3
Wikman, F.P.4
Zieger, K.5
Moller, K.6
Orntoft, T.F.7
-
11
-
-
17144422895
-
Loss of heterozygosity in childhood acute lymphoblastic leukemia detected by genome-wide microarray single nucleotide polymorphism analysis
-
Irving JA, Bloodworth L, Bown NP, Case MC, Hogarth LA, Hall AG: Loss of heterozygosity in childhood acute lymphoblastic leukemia detected by genome-wide microarray single nucleotide polymorphism analysis. Cancer Res 2005, 65:3053-3058.
-
(2005)
Cancer Res
, vol.65
, pp. 3053-3058
-
-
Irving, J.A.1
Bloodworth, L.2
Bown, N.P.3
Case, M.C.4
Hogarth, L.A.5
Hall, A.G.6
-
12
-
-
25444510786
-
Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event
-
Teh MT, Blaydon D, Chaplin T, Foot NJ, Skoulakis S, Raghavan M, Harwood CA, Proby CM, Philpott MP, Young BD, Kelsell DP: Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event. Cancer Res 2005, 65:8597-8603.
-
(2005)
Cancer Res
, vol.65
, pp. 8597-8603
-
-
Teh, M.T.1
Blaydon, D.2
Chaplin, T.3
Foot, N.J.4
Skoulakis, S.5
Raghavan, M.6
Harwood, C.A.7
Proby, C.M.8
Philpott, M.P.9
Young, B.D.10
Kelsell, D.P.11
-
13
-
-
0020331835
-
Epidemiology of esophageal cancer in China
-
Li JY: Epidemiology of esophageal cancer in China. Natl Cancer Inst Monogr 1982, 62:113-120.
-
(1982)
Natl Cancer Inst Monogr
, vol.62
, pp. 113-120
-
-
Li, J.Y.1
-
14
-
-
0009545696
-
The trends and preventive strategies of esophageal cancer in high-risk areas of Taihang Mountains, China
-
Qiao YL, Hou J, Yang L, He YT, Liu YY, Li LD, Li SS, Lian SY, Dong ZW: [The trends and preventive strategies of esophageal cancer in high-risk areas of Taihang Mountains, China]. Zhongguo Yi Xue Ke Xue Yuan Xue Bao 2001, 23:10-14.
-
(2001)
Zhongguo Yi Xue Ke Xue Yuan Xue Bao
, vol.23
, pp. 10-14
-
-
Qiao, Y.L.1
Hou, J.2
Yang, L.3
He, Y.T.4
Liu, Y.Y.5
Li, L.D.6
Li, S.S.7
Lian, S.Y.8
Dong, Z.W.9
-
15
-
-
0033974187
-
Identification of novel regions of allelic loss from a genomewide scan of esophageal squamous-cell carcinoma in a high-risk Chinese population
-
Hu N, Roth MJ, Polymeropolous M, Tang ZZ, Emmert-Buck MR, Wang QH, Goldstein AM, Feng SS, Dawsey SM, Ding T, Zhuang ZP, Han XY, Ried T, Giffen C, Taylor PR: Identification of novel regions of allelic loss from a genomewide scan of esophageal squamous-cell carcinoma in a high-risk Chinese population. Genes Chromosomes Cancer 2000, 27:217-228.
-
(2000)
Genes Chromosomes Cancer
, vol.27
, pp. 217-228
-
-
Hu, N.1
Roth, M.J.2
Polymeropolous, M.3
Tang, Z.Z.4
Emmert-Buck, M.R.5
Wang, Q.H.6
Goldstein, A.M.7
Feng, S.S.8
Dawsey, S.M.9
Ding, T.10
Zhuang, Z.P.11
Han, X.Y.12
Ried, T.13
Giffen, C.14
Taylor, P.R.15
-
16
-
-
0035872450
-
Genetic progression and heterogeneity associated with the development of esophageal squamous cell carcinoma 471
-
Roth MJ, Hu N, Emmert-Buck MR, Wang QH, Dawsey SM, Li G, Guo WJ, Zhang YZ, Taylor PR: Genetic progression and heterogeneity associated with the development of esophageal squamous cell carcinoma 471. Cancer Res 2001, 61:4098-4104.
-
(2001)
Cancer Res
, vol.61
, pp. 4098-4104
-
-
Roth, M.J.1
Hu, N.2
Emmert-Buck, M.R.3
Wang, Q.H.4
Dawsey, S.M.5
Li, G.6
Guo, W.J.7
Zhang, Y.Z.8
Taylor, P.R.9
-
17
-
-
0033737598
-
High frequency allelic loss on chromosome 17p13.3-p11.1 in esophageal squamous cell carcinomas from a high incidence area in northern China
-
Huang J, Hu N, Goldstein AM, Emmert-Buck MR, Tang ZZ, Roth MJ, Wang QH, Dawsey SM, Han XY, Ding T, Li G, Giffen C, Taylor PR: High frequency allelic loss on chromosome 17p13.3-p11.1 in esophageal squamous cell carcinomas from a high incidence area in northern China. Carcinogenesis 2000, 21:2019-2026.
-
(2000)
Carcinogenesis
, vol.21
, pp. 2019-2026
-
-
Huang, J.1
Hu, N.2
Goldstein, A.M.3
Emmert-Buck, M.R.4
Tang, Z.Z.5
Roth, M.J.6
Wang, Q.H.7
Dawsey, S.M.8
Han, X.Y.9
Ding, T.10
Li, G.11
Giffen, C.12
Taylor, P.R.13
-
18
-
-
0034895906
-
Frequent inactivation of the TP53 gene in esophageal squamous cell carcinoma from a high-risk population in China
-
Hu N, Huang J, Emmert-Buck MR, Tang ZZ, Roth MJ, Wang C, Dawsey SM, Li G, Li WJ, Wang QH, Han XY, Ding T, Giffen C, Goldstein AM, Taylor PR: Frequent inactivation of the TP53 gene in esophageal squamous cell carcinoma from a high-risk population in China. Clin Cancer Res 2001, 7:883-891.
-
(2001)
Clin Cancer Res
, vol.7
, pp. 883-891
-
-
Hu, N.1
Huang, J.2
Emmert-Buck, M.R.3
Tang, Z.Z.4
Roth, M.J.5
Wang, C.6
Dawsey, S.M.7
Li, G.8
Li, W.J.9
Wang, Q.H.10
Han, X.Y.11
Ding, T.12
Giffen, C.13
Goldstein, A.M.14
Taylor, P.R.15
-
19
-
-
0036682298
-
Identification of somatic mutations of the RNF6 gene in human esophageal squamous cell carcinoma
-
Lo HS, Hu N, Gere S, Lu N, Su H, Goldstein AM, Taylor PR, Lee MP: Identification of somatic mutations of the RNF6 gene in human esophageal squamous cell carcinoma. Cancer Res 2002, 62:4191-4193.
-
(2002)
Cancer Res
, vol.62
, pp. 4191-4193
-
-
Lo, H.S.1
Hu, N.2
Gere, S.3
Lu, N.4
Su, H.5
Goldstein, A.M.6
Taylor, P.R.7
Lee, M.P.8
-
20
-
-
0037254305
-
Common genetic variants of TP53 and BRCA2 in esophageal cancer patients and healthy individuals from low and high risk areas of northern China
-
Hu N, Li WJ, Su H, Wang C, Goldstein AM, Albert PS, Emmert-Buck MR, Kong LH, Roth MJ, Dawsey SM, He LJ, Cao SF, Ding T, Giffen C, Taylor PR: Common genetic variants of TP53 and BRCA2 in esophageal cancer patients and healthy individuals from low and high risk areas of northern China. Cancer Detect Prev 2003, 27:132-138.
-
(2003)
Cancer Detect Prev
, vol.27
, pp. 132-138
-
-
Hu, N.1
Li, W.J.2
Su, H.3
Wang, C.4
Goldstein, A.M.5
Albert, P.S.6
Emmert-Buck, M.R.7
Kong, L.H.8
Roth, M.J.9
Dawsey, S.M.10
He, L.J.11
Cao, S.F.12
Ding, T.13
Giffen, C.14
Taylor, P.R.15
-
21
-
-
0032712720
-
Allelic loss in esophageal squamous cell carcinoma patients with and without family history of upper gastrointestinal tract cancer
-
Hu N, Roth MJ, Emmert-Buck MR, Tang ZZ, Polymeropolous M, Wang QH, Goldstein AM, Han XY, Dawsey SM, Ding T, Giffen C, Taylor PR: Allelic loss in esophageal squamous cell carcinoma patients with and without family history of upper gastrointestinal tract cancer. Clin Cancer Res 1999, 5:3476-3482.
-
(1999)
Clin Cancer Res
, vol.5
, pp. 3476-3482
-
-
Hu, N.1
Roth, M.J.2
Emmert-Buck, M.R.3
Tang, Z.Z.4
Polymeropolous, M.5
Wang, Q.H.6
Goldstein, A.M.7
Han, X.Y.8
Dawsey, S.M.9
Ding, T.10
Giffen, C.11
Taylor, P.R.12
-
22
-
-
25844434735
-
Allelotyping of esophageal squamous-cell carcinoma on chromosome 13 defines deletions related to family history
-
Hu N, Su H, Li WJ, Giffen C, Goldstein AM, Hu Y, Wang C, Roth MJ, Li G, Dawsey SM, Xu Y, Taylor PR, Emmert-Buck MR: Allelotyping of esophageal squamous-cell carcinoma on chromosome 13 defines deletions related to family history. Genes Chromosomes Cancer 2005, 44:271-278.
-
(2005)
Genes Chromosomes Cancer
, vol.44
, pp. 271-278
-
-
Hu, N.1
Su, H.2
Li, W.J.3
Giffen, C.4
Goldstein, A.M.5
Hu, Y.6
Wang, C.7
Roth, M.J.8
Li, G.9
Dawsey, S.M.10
Xu, Y.11
Taylor, P.R.12
Emmert-Buck, M.R.13
-
23
-
-
0030575911
-
Laser capture microdissection
-
Emmert-Buck MR, Bonner RF, Smith PD, Chuaqui RF, Zhuang Z, Goldstein SR, Weiss RA, Liotta LA: Laser capture microdissection. Science 1996, 274:998-1001.
-
(1996)
Science
, vol.274
, pp. 998-1001
-
-
Emmert-Buck, M.R.1
Bonner, R.F.2
Smith, P.D.3
Chuaqui, R.F.4
Zhuang, Z.5
Goldstein, S.R.6
Weiss, R.A.7
Liotta, L.A.8
-
24
-
-
10744221619
-
Large-scale genotyping of complex DNA
-
Kennedy GC, Matsuzaki H, Dong S, Liu WM, Huang J, Liu G, Su X, Cao M, Chen W, Zhang J, Liu W, Yang G, Di X, Ryder T, He Z, Surti U, Phillips MS, Boyce-Jacino MT, Fodor SP, Jones KW: Large-scale genotyping of complex DNA. Nat Biotechnol 2003, 21:1233-1237.
-
(2003)
Nat Biotechnol
, vol.21
, pp. 1233-1237
-
-
Kennedy, G.C.1
Matsuzaki, H.2
Dong, S.3
Liu, W.M.4
Huang, J.5
Liu, G.6
Su, X.7
Cao, M.8
Chen, W.9
Zhang, J.10
Liu, W.11
Yang, G.12
Di, X.13
Ryder, T.14
He, Z.15
Surti, U.16
Phillips, M.S.17
Boyce-Jacino, M.T.18
Fodor, S.P.19
Jones, K.W.20
more..
-
25
-
-
0141557460
-
Algorithms for large-scale genotyping microarrays
-
Liu WM, Di X, Yang G, Matsuzaki H, Huang J, Mei R, Ryder TB, Webster TA, Dong S, Liu G, Jones KW, Kennedy GC, Kulp D: Algorithms for large-scale genotyping microarrays. Bioinformatics 2003, 19:2397-2403.
-
(2003)
Bioinformatics
, vol.19
, pp. 2397-2403
-
-
Liu, W.M.1
Di, X.2
Yang, G.3
Matsuzaki, H.4
Huang, J.5
Mei, R.6
Ryder, T.B.7
Webster, T.A.8
Dong, S.9
Liu, G.10
Jones, K.W.11
Kennedy, G.C.12
Kulp, D.13
-
26
-
-
20144388722
-
Genome-wide association study in esophageal cancer using GeneChip mapping 10K array
-
Hu N, Wang C, Hu Y, Yang HH, Giffen C, Tang ZZ, Han XY, Goldstein AM, Emmert-Buck MR, Buetow KH, Taylor PR, Lee MP: Genome-wide association study in esophageal cancer using GeneChip mapping 10K array. Cancer Res 2005, 65:2542-2546.
-
(2005)
Cancer Res
, vol.65
, pp. 2542-2546
-
-
Hu, N.1
Wang, C.2
Hu, Y.3
Yang, H.H.4
Giffen, C.5
Tang, Z.Z.6
Han, X.Y.7
Goldstein, A.M.8
Emmert-Buck, M.R.9
Buetow, K.H.10
Taylor, P.R.11
Lee, M.P.12
-
27
-
-
10844232112
-
Whole genome DNA copy number changes identified by high density oligonucleotide arrays
-
Huang J, Wei W, Zhang J, Liu G, Bignell GR, Stratton MR, Futreal PA, Wooster R, Jones KW, Shapero MH: Whole genome DNA copy number changes identified by high density oligonucleotide arrays. Hum Genomics 2004, 1:287-299.
-
(2004)
Hum Genomics
, vol.1
, pp. 287-299
-
-
Huang, J.1
Wei, W.2
Zhang, J.3
Liu, G.4
Bignell, G.R.5
Stratton, M.R.6
Futreal, P.A.7
Wooster, R.8
Jones, K.W.9
Shapero, M.H.10
|