-
1
-
-
13144306071
-
Genome-wide association studies for common diseases and complex traits
-
Hirschhorn JN, Daly MJ. Genome-wide association studies for common diseases and complex traits. Nat Rev Genet 2005;6:95-108.
-
(2005)
Nat Rev Genet
, vol.6
, pp. 95-108
-
-
Hirschhorn, J.N.1
Daly, M.J.2
-
2
-
-
13144265739
-
Genome-wide association studies: Theoretical and practical concerns
-
Wang WY, Barratt BJ, Clayton DG, Todd JA. Genome-wide association studies: theoretical and practical concerns. Nat Rev Genet 2005;6:109-18.
-
(2005)
Nat Rev Genet
, vol.6
, pp. 109-118
-
-
Wang, W.Y.1
Barratt, B.J.2
Clayton, D.G.3
Todd, J.A.4
-
3
-
-
9244263625
-
The use of whole genome amplification in the study of human disease
-
Hughes S, Arneson N, Done S, Squire J. The use of whole genome amplification in the study of human disease. Prog Biophys Mol Biol 2005;88:173-89.
-
(2005)
Prog Biophys Mol Biol
, vol.88
, pp. 173-189
-
-
Hughes, S.1
Arneson, N.2
Done, S.3
Squire, J.4
-
4
-
-
0029966845
-
Whole genome amplification using a degenerate oligonucleotide primer allows hundreds of genotypes to be performed on less than one nanogram of genomic DNA
-
Cheung VG, Nelson SF. Whole genome amplification using a degenerate oligonucleotide primer allows hundreds of genotypes to be performed on less than one nanogram of genomic DNA. Proc Natl Acad Sci U S A 1996;93:14676-9.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 14676-14679
-
-
Cheung, V.G.1
Nelson, S.F.2
-
5
-
-
18344396798
-
Comprehensive human genome amplification using multiple displacement amplification
-
Dean FB, Hosono S, Fang L, et al. Comprehensive human genome amplification using multiple displacement amplification. Proc Natl Acad Sci U S A 2002;99:5261-6.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 5261-5266
-
-
Dean, F.B.1
Hosono, S.2
Fang, L.3
-
6
-
-
0242475336
-
Whole genome amplification: Abundant supplies of DNA from precious samples or clinical specimens
-
Lasken RS, Egholm M. Whole genome amplification: abundant supplies of DNA from precious samples or clinical specimens. Trends Biotechnol 2003;21:531-5.
-
(2003)
Trends Biotechnol
, vol.21
, pp. 531-535
-
-
Lasken, R.S.1
Egholm, M.2
-
7
-
-
33644760183
-
-
Zhang Y, Newcomb PA, Egan KM, et al. Genetic polymorphisms in base-excision repair pathway genes and risk of breast cancer. Cancer Epidemiol Biomarkers Prev2006;15:353-8.
-
Zhang Y, Newcomb PA, Egan KM, et al. Genetic polymorphisms in base-excision repair pathway genes and risk of breast cancer. Cancer Epidemiol Biomarkers Prev2006;15:353-8.
-
-
-
-
8
-
-
24344436666
-
Comparison of yield and genotyping performance of multiple displacement amplification and OmniPlex whole genome amplified DNA generated from multiple DNA sources
-
Bergen AW, Haque KA, Qi Y, et al. Comparison of yield and genotyping performance of multiple displacement amplification and OmniPlex whole genome amplified DNA generated from multiple DNA sources. Hum Mutat 2005;26:262-70.
-
(2005)
Hum Mutat
, vol.26
, pp. 262-270
-
-
Bergen, A.W.1
Haque, K.A.2
Qi, Y.3
-
9
-
-
0034904540
-
Collection of genomic DNA from adults in epidemiological studies by buccal cytobrush and mouthwash
-
Garcia-Closas M, Egan KM, Abruzzo J, et al. Collection of genomic DNA from adults in epidemiological studies by buccal cytobrush and mouthwash. Cancer Epidemiol Biomarkers Prev 2001; 10:687-96.
-
(2001)
Cancer Epidemiol Biomarkers Prev
, vol.10
, pp. 687-696
-
-
Garcia-Closas, M.1
Egan, K.M.2
Abruzzo, J.3
-
10
-
-
28844464294
-
A candidate gene approach to searching for low-penetrance breast and prostate cancer genes
-
Hunter DJ, Riboli E, Haiman CA, et al. A candidate gene approach to searching for low-penetrance breast and prostate cancer genes. Nat Rev Cancer 2005;5:977-85.
-
(2005)
Nat Rev Cancer
, vol.5
, pp. 977-985
-
-
Hunter, D.J.1
Riboli, E.2
Haiman, C.A.3
-
12
-
-
0038781878
-
Unbiased whole-genome amplification directly from clinical samples
-
Hosono S, Faruqi AF, Dean FB, et al. Unbiased whole-genome amplification directly from clinical samples. Genome Res 2003;13:954-64.
-
(2003)
Genome Res
, vol.13
, pp. 954-964
-
-
Hosono, S.1
Faruqi, A.F.2
Dean, F.B.3
-
13
-
-
3142617353
-
Assessment of multiple displacement amplification in molecular epidemiology
-
Yan J, Feng J, Hosono S, Sommer SS. Assessment of multiple displacement amplification in molecular epidemiology. Biotechniques 2004;37:136-8, 140- 3.
-
(2004)
Biotechniques
, vol.37
-
-
Yan, J.1
Feng, J.2
Hosono, S.3
Sommer, S.S.4
-
14
-
-
9144264420
-
High accuracy genotyping directly from genomic DNA using a rolling circle amplification based assay
-
Alsmadi OA, Bornarth CJ, Song W, et al. High accuracy genotyping directly from genomic DNA using a rolling circle amplification based assay. BMC Genomics 2003;4:21.
-
(2003)
BMC Genomics
, vol.4
, pp. 21
-
-
Alsmadi, O.A.1
Bornarth, C.J.2
Song, W.3
-
15
-
-
19944432329
-
Investigating the utility of combining phi29 whole genome amplification and highly multiplexed single nucleotide polymorphism Bead Array genotyping
-
Pask R, Rance HE, Barratt BJ, et al. Investigating the utility of combining phi29 whole genome amplification and highly multiplexed single nucleotide polymorphism Bead Array genotyping. BMC Biotechnol 2004;4:15.
-
(2004)
BMC Biotechnol
, vol.4
, pp. 15
-
-
Pask, R.1
Rance, H.E.2
Barratt, B.J.3
-
16
-
-
4344675709
-
Molecular typing of human leukocyte antigen and related polymorphisms following whole genome amplification
-
Shao W, Tang J, Dorak MT, et al. Molecular typing of human leukocyte antigen and related polymorphisms following whole genome amplification. Tissue Antigens 2004;64:286-92.
-
(2004)
Tissue Antigens
, vol.64
, pp. 286-292
-
-
Shao, W.1
Tang, J.2
Dorak, M.T.3
-
17
-
-
0023913194
-
Simple non-invasive method to obtain DNA for gene analysis
-
Lench N, Stanier P, Williamson R. Simple non-invasive method to obtain DNA for gene analysis. Lancet 1988;1:1356-8.
-
(1988)
Lancet
, vol.1
, pp. 1356-1358
-
-
Lench, N.1
Stanier, P.2
Williamson, R.3
-
18
-
-
0029084260
-
Utility of a "swish and spit" technique for the collection of buccal cells for TAP haplotype determination
-
Hayney MS, Dimanlig P, Lipsky JJ, Poland GA. Utility of a "swish and spit" technique for the collection of buccal cells for TAP haplotype determination. Mayo Clin Proc 1995;70:951-4.
-
(1995)
Mayo Clin Proc
, vol.70
, pp. 951-954
-
-
Hayney, M.S.1
Dimanlig, P.2
Lipsky, J.J.3
Poland, G.A.4
-
19
-
-
0031878156
-
A simple mouthwash method for obtaining genomic DNA in molecular epidemiological studies
-
Lum A, Le ML. A simple mouthwash method for obtaining genomic DNA in molecular epidemiological studies. Cancer Epidemiol Biomarkers Prev 1998;7:719-24.
-
(1998)
Cancer Epidemiol Biomarkers Prev
, vol.7
, pp. 719-724
-
-
Lum, A.1
ML, L.2
-
20
-
-
0034650164
-
Self-collection of oral epithelial cell DNA under instruction from epidemiologic interviewers
-
Harty LC, Shields PG, Winn DM, Caporaso NE, Hayes RB. Self-collection of oral epithelial cell DNA under instruction from epidemiologic interviewers. Am J Epidemiol 2000;151:199-205.
-
(2000)
Am J Epidemiol
, vol.151
, pp. 199-205
-
-
Harty, L.C.1
Shields, P.G.2
Winn, D.M.3
Caporaso, N.E.4
Hayes, R.B.5
-
21
-
-
34548094807
-
-
Sprague BL, Trentham-Dietz A, Garcia-Closas M, et al. Genetic variation in TP53 and risk of breast cancer in a population-based case-control study. Carcinogenesis 2007; Epub ahead of print.
-
Sprague BL, Trentham-Dietz A, Garcia-Closas M, et al. Genetic variation in TP53 and risk of breast cancer in a population-based case-control study. Carcinogenesis 2007; Epub ahead of print.
-
-
-
-
22
-
-
19944421744
-
Quantifying the percent increase in minimum sample size for SNP genotyping errors in genetic model-based association studies
-
Kang SJ, Finch SJ, Haynes C, Gordon D. Quantifying the percent increase in minimum sample size for SNP genotyping errors in genetic model-based association studies. Hum Hered 2004;58:139-44.
-
(2004)
Hum Hered
, vol.58
, pp. 139-144
-
-
Kang, S.J.1
Finch, S.J.2
Haynes, C.3
Gordon, D.4
-
23
-
-
0942276432
-
What SNP genotyping errors are most costly for genetic association studies?
-
Kang SJ, Gordon D, Finch SJ. What SNP genotyping errors are most costly for genetic association studies? Genet Epidemiol 2004;26:132-41.
-
(2004)
Genet Epidemiol
, vol.26
, pp. 132-141
-
-
Kang, S.J.1
Gordon, D.2
Finch, S.J.3
-
24
-
-
0033406444
-
Misclassification in case-control studies of gene-environment interactions: Assessment of bias and sample size
-
Garcia-Closas M, Rothman N, Lubin J. Misclassification in case-control studies of gene-environment interactions: assessment of bias and sample size. Cancer Epidemiol Biomarkers Prev 1999; 8:1043-50.
-
(1999)
Cancer Epidemiol Biomarkers Prev
, vol.8
, pp. 1043-1050
-
-
Garcia-Closas, M.1
Rothman, N.2
Lubin, J.3
-
25
-
-
33750286548
-
Quantifying bias due to allele misclassification in case-control studies of haplotypes
-
Govindarajulu US, Spiegelman D, Miller KL, Kraft P. Quantifying bias due to allele misclassification in case-control studies of haplotypes. Genet Epidemiol 2006;30:590-601.
-
(2006)
Genet Epidemiol
, vol.30
, pp. 590-601
-
-
Govindarajulu, U.S.1
Spiegelman, D.2
Miller, K.L.3
Kraft, P.4
-
26
-
-
22844436549
-
Assessment of multiple displacement amplification for polymorphism discovery and haplotype determination at a highly polymorphic locus, MC1R
-
Murthy KK, Mahboubi VS, Santiago A, et al. Assessment of multiple displacement amplification for polymorphism discovery and haplotype determination at a highly polymorphic locus, MC1R. Hum Mutat 2005;26:145-52.
-
(2005)
Hum Mutat
, vol.26
, pp. 145-152
-
-
Murthy, K.K.1
Mahboubi, V.S.2
Santiago, A.3
-
27
-
-
2442707739
-
Two methods of whole-genome amplification enable accurate genotyping across a 2320-SNP linkage panel
-
Barker DL, Hansen MS, Faruqi AF, et al. Two methods of whole-genome amplification enable accurate genotyping across a 2320-SNP linkage panel. Genome Res 2004;14:901-7.
-
(2004)
Genome Res
, vol.14
, pp. 901-907
-
-
Barker, D.L.1
Hansen, M.S.2
Faruqi, A.F.3
-
28
-
-
8844250780
-
STK15 polymorphism and breast cancer risk in a population-based study
-
Egan KM, Newcomb PA, Ambrosone CB, et al. STK15 polymorphism and breast cancer risk in a population-based study. Carcinogenesis 2004;25:2149-53.
-
(2004)
Carcinogenesis
, vol.25
, pp. 2149-2153
-
-
Egan, K.M.1
Newcomb, P.A.2
Ambrosone, C.B.3
-
29
-
-
33645744903
-
Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: Two population-based studies in USA and Poland, and meta-analyses
-
Garcia-Closas M, Egan KM, Newcomb PA, et al. Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: two population-based studies in USA and Poland, and meta-analyses. Hum Genet 2006;119:376-88.
-
(2006)
Hum Genet
, vol.119
, pp. 376-388
-
-
Garcia-Closas, M.1
Egan, K.M.2
Newcomb, P.A.3
-
30
-
-
34147115679
-
Genetic variation in tumor necrosis factor and lymphotoxin-α (TNF-LTA) and breast cancer risk
-
Gaudet MM, Egan KM, Lissowska J, et al. Genetic variation in tumor necrosis factor and lymphotoxin-α (TNF-LTA) and breast cancer risk. Hum Genet 2007;121:483-90.
-
(2007)
Hum Genet
, vol.121
, pp. 483-490
-
-
Gaudet, M.M.1
Egan, K.M.2
Lissowska, J.3
-
31
-
-
0042380119
-
MnSOD polymorphism and breast cancer in a population-based case-control study
-
Egan KM, Thompson PA, Titus-Ernstoff L, Moore JH, Ambrosone CB. MnSOD polymorphism and breast cancer in a population-based case-control study. Cancer Lett 2003;199:27-33.
-
(2003)
Cancer Lett
, vol.199
, pp. 27-33
-
-
Egan, K.M.1
Thompson, P.A.2
Titus-Ernstoff, L.3
Moore, J.H.4
Ambrosone, C.B.5
-
32
-
-
27744560561
-
Detection of genotyping errors and pseudo-SNPs via deviations from Hardy-Weinberg equilibrium
-
Leal SM. Detection of genotyping errors and pseudo-SNPs via deviations from Hardy-Weinberg equilibrium. Genet Epidemiol 2005;29:204-14.
-
(2005)
Genet Epidemiol
, vol.29
, pp. 204-214
-
-
Leal, S.M.1
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