-
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: The theoretical and practical concerns
-
Wang WYS, Barratt BJ, Clayton DG, Todd JA: Genome-wide association studies: The theoretical and practical concerns. Nat Rev 2005, 6:109-118.
-
(2005)
Nat Rev
, vol.6
, pp. 109-118
-
-
Wang, W.Y.S.1
Barratt, B.J.2
Clayton, D.G.3
Todd, J.A.4
-
3
-
-
0345350737
-
Use of pooled DNA samples to detect linkage disequilibrium of polymorphic restriction fragments and human disease: Studies of the HLA class II loci
-
Arnheim N, Strange C, Erlich H: Use of pooled DNA samples to detect linkage disequilibrium of polymorphic restriction fragments and human disease: Studies of the HLA class II loci. Proc Natl Acad Sci USA 1985, 82:6970-6974.
-
(1985)
Proc Natl Acad Sci USA
, vol.82
, pp. 6970-6974
-
-
Arnheim, N.1
Strange, C.2
Erlich, H.3
-
4
-
-
0037168559
-
High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools
-
Mohlke KL, Erdos MR, Scott LJ, Fingerlin TE, Jackson AU, Silander K, Hollstein P, Boehnke M, Collins FS: High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools. Proc Natl Acad Sci USA 2002, 99:16928-16933.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 16928-16933
-
-
Mohlke, K.L.1
Erdos, M.R.2
Scott, L.J.3
Fingerlin, T.E.4
Jackson, A.U.5
Silander, K.6
Hollstein, P.7
Boehnke, M.8
Collins, F.S.9
-
5
-
-
0037404767
-
High-resolution SNP scan of chromosome 6p21 in pooled samples from patients with complex diseases
-
Herbon N, Werner M, Braig C, Gohlke H, Dütsch G, Illig T, Altmüller J, Hampe J, Lantermann A, Schreiber S, Bonifacio E, Ziegler A, Schwab S, Wildenauer D, van den Boom D, Braun A, Knapp M, Reitmeir P, Wjst M: High-resolution SNP scan of chromosome 6p21 in pooled samples from patients with complex diseases. Genomics 2003, 81:510-518.
-
(2003)
Genomics
, vol.81
, pp. 510-518
-
-
Herbon, N.1
Werner, M.2
Braig, C.3
Gohlke, H.4
Dütsch, G.5
Illig, T.6
Altmüller, J.7
Hampe, J.8
Lantermann, A.9
Schreiber, S.10
Bonifacio, E.11
Ziegler, A.12
Schwab, S.13
Wildenauer, D.14
van den Boom, D.15
Braun, A.16
Knapp, M.17
Reitmeir, P.18
Wjst, M.19
-
6
-
-
0035895258
-
Highthroughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
-
Buetow KH, Edmonson M, MacDonald R, Clifford R, Yip P, Kelley J, Little DP, Strausberg R, Koester H, Cantor CR, Braun A: Highthroughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Proc Natl Acad Sci USA 2001, 98:581-584.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 581-584
-
-
Buetow, K.H.1
Edmonson, M.2
MacDonald, R.3
Clifford, R.4
Yip, P.5
Kelley, J.6
Little, D.P.7
Strausberg, R.8
Koester, H.9
Cantor, C.R.10
Braun, A.11
-
7
-
-
4444312513
-
Large-scale validation of single nucleotide polymorphisms in gene regions
-
Nelson MR, Marnellos G, Kammerer S, Hoyal CR, Shi MM, Cantor CR, Braun A: Large-scale validation of single nucleotide polymorphisms in gene regions. Genome Res 2004, 14:1664-1668.
-
(2004)
Genome Res
, vol.14
, pp. 1664-1668
-
-
Nelson, M.R.1
Marnellos, G.2
Kammerer, S.3
Hoyal, C.R.4
Shi, M.M.5
Cantor, C.R.6
Braun, A.7
-
8
-
-
84874661850
-
Polymorphism validation using DNA pools prior to conducting large-scale genetic studies
-
in press
-
Yang HC, Lin CH, Hung SI, Fann CSJ: Polymorphism validation using DNA pools prior to conducting large-scale genetic studies. Ann Hum Genet in press.
-
Ann Hum Genet
-
-
Yang, H.C.1
Lin, C.H.2
Hung, S.I.3
Fann, C.S.J.4
-
9
-
-
0036844881
-
DNA pooling: A tool for large-scale association studies
-
Sham P, Bader JS, Craig I, O'Donovan M, Owen M: DNA pooling: A tool for large-scale association studies. Nat Rev Genet 2002, 3 862-871.
-
(2002)
Nat Rev Genet
, vol.3
, pp. 862-871
-
-
Sham, P.1
Bader, J.S.2
Craig, I.3
O'Donovan, M.4
Owen, M.5
-
10
-
-
33749627970
-
Association mapping using pooled DNA
-
Edited by: Collins A. New Jersey: The Humana Press Inc;
-
Yang HC, Fann CSJ: Association mapping using pooled DNA. In Linkage Disequilibrium and Association Mapping Edited by: Collins A. New Jersey: The Humana Press Inc; 2006.
-
(2006)
Linkage Disequilibrium and Association Mapping
-
-
Yang, H.C.1
Fann, C.S.J.2
-
11
-
-
13744260170
-
New adjustment factors and sample size calculation in a DNA-pooling experiment with preferential amplification
-
Yang HC, Pan CC, Lu RCY, Fann CSJ: New adjustment factors and sample size calculation in a DNA-pooling experiment with preferential amplification. Genetics 2005, 169:399-410.
-
(2005)
Genetics
, vol.169
, pp. 399-410
-
-
Yang, H.C.1
Pan, C.C.2
Lu, R.C.Y.3
Fann, C.S.J.4
-
12
-
-
17744380449
-
Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools
-
Hoogendoorn B, Norton N, Kirov G, Williams N, Hamshere ML, Spurlock G, Austin J, Stephens MK, Buckland PR, Owen MJ, O'Donovan MC: Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools. Hum Genet 2000, 107:488-493.
-
(2000)
Hum Genet
, vol.107
, pp. 488-493
-
-
Hoogendoorn, B.1
Norton, N.2
Kirov, G.3
Williams, N.4
Hamshere, M.L.5
Spurlock, G.6
Austin, J.7
Stephens, M.K.8
Buckland, P.R.9
Owen, M.J.10
O'Donovan, M.C.11
-
13
-
-
0037739946
-
Simple method to analyze SNPbased association studies using DNA pools
-
Visscher PM, Le Hellard S: Simple method to analyze SNPbased association studies using DNA pools. Genet Epidemiol 2003, 24:291-296.
-
(2003)
Genet Epidemiol
, vol.24
, pp. 291-296
-
-
Visscher, P.M.1
Le Hellard, S.2
-
14
-
-
0037320552
-
Estimation of haplotype frequencies, linkage-disequilibrium measures, and combination of haplotype copies in each pool by use of pooled DNA data
-
Ito T, Chiku S, Inoue E, Tomita M, Morisaki T, Morisaki H, Kamatani N: Estimation of haplotype frequencies, linkage-disequilibrium measures, and combination of haplotype copies in each pool by use of pooled DNA data. Am J Hum Genet 2003, 72:384-398.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 384-398
-
-
Ito, T.1
Chiku, S.2
Inoue, E.3
Tomita, M.4
Morisaki, T.5
Morisaki, H.6
Kamatani, N.7
-
15
-
-
0037226556
-
On the use of DNA pooling to estimate haplotype frequencies
-
Wang S, Kidd KK, Zhao H: On the use of DNA pooling to estimate haplotype frequencies. Genet Epidemiol 2003, 24:74-82.
-
(2003)
Genet Epidemiol
, vol.24
, pp. 74-82
-
-
Wang, S.1
Kidd, K.K.2
Zhao, H.3
-
16
-
-
0038472056
-
Efficiency of single-nucleotide polymorphism haplotype estimation from pooled DNA
-
Yang Y, Zhang J, Hoh J, Matsuda F, Xu P, Lathrop M, Ott J: Efficiency of single-nucleotide polymorphism haplotype estimation from pooled DNA Proc Natl Acad Sci USA 2003, 100:7225-7230.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 7225-7230
-
-
Yang, Y.1
Zhang, J.2
Hoh, J.3
Matsuda, F.4
Xu, P.5
Lathrop, M.6
Ott, J.7
-
17
-
-
11144314695
-
Estimating haplotype-disease associations with pooled genotype data
-
Zeng D, Lin DY: Estimating haplotype-disease associations with pooled genotype data. Genet Epidemiol 2005, 28:70-82.
-
(2005)
Genet Epidemiol
, vol.28
, pp. 70-82
-
-
Zeng, D.1
Lin, D.Y.2
-
18
-
-
0036866635
-
Identification of the sources of error in allele frequency estimations from pooled DNA indicates an optimal experimental design
-
Barratt BJ, Payne F, Rance HE, Nutland S, Todd JA, Clayton DG: Identification of the sources of error in allele frequency estimations from pooled DNA indicates an optimal experimental design. Ann Hum Genet 2002, 66:393-405.
-
(2002)
Ann Hum Genet
, vol.66
, pp. 393-405
-
-
Barratt, B.J.1
Payne, F.2
Rance, H.E.3
Nutland, S.4
Todd, J.A.5
Clayton, D.G.6
-
19
-
-
2442474313
-
SNP allele frequency estimation in DNA pools and variance components analysis
-
Downes K, Barratt BJ, Akan P, Bumpstead SJ, Taylor SD, Clayton DG, Deloukas P: SNP allele frequency estimation in DNA pools and variance components analysis. Biotechniques 2004, 36:840-845.
-
(2004)
Biotechniques
, vol.36
, pp. 840-845
-
-
Downes, K.1
Barratt, B.J.2
Akan, P.3
Bumpstead, S.J.4
Taylor, S.D.5
Clayton, D.G.6
Deloukas, P.7
-
20
-
-
0036143307
-
Truncated product method for combing p-values
-
Zaykin DV, Zhivotovsky LA, Westfall PH, Weir BS: Truncated product method for combing p-values. Genet Epidemiol 2002, 22 170-185.
-
(2002)
Genet Epidemiol
, vol.22
, pp. 170-185
-
-
Zaykin, D.V.1
Zhivotovsky, L.A.2
Westfall, P.H.3
Weir, B.S.4
-
21
-
-
0000561875
-
An additive model for combining probability values from independent experiments
-
Edgington ES: An additive model for combining probability values from independent experiments. J Psychol 1972, 80:351-363.
-
(1972)
J Psychol
, vol.80
, pp. 351-363
-
-
Edgington, E.S.1
-
22
-
-
0042567474
-
Use of max and min scores for trend tests for association when the genetic model is unknown
-
Zheng G: Use of max and min scores for trend tests for association when the genetic model is unknown. Stat Med 2003, 22 2657-2666.
-
(2003)
Stat Med
, vol.22
, pp. 2657-2666
-
-
Zheng, G.1
-
23
-
-
7444256665
-
Genetic association mapping under founder heterogeneity via weighted haplotype similarity analysis in candidate genes
-
Yu K, Gu CC, Province M, Xiong CJ, Rao DC: Genetic association mapping under founder heterogeneity via weighted haplotype similarity analysis in candidate genes. Genet Epidemiol 2004, 27 182-191.
-
(2004)
Genet Epidemiol
, vol.27
, pp. 182-191
-
-
Yu, K.1
Gu, C.C.2
Province, M.3
Xiong, C.J.4
Rao, D.C.5
-
24
-
-
0344826563
-
Rank truncated product of p-values, with application to genomewide association scans
-
Dudbridge F, Koeleman BPC: Rank truncated product of p-values, with application to genomewide association scans. Genet Epidemiol 2003, 25:360-366.
-
(2003)
Genet Epidemiol
, vol.25
, pp. 360-366
-
-
Dudbridge, F.1
Koeleman, B.P.C.2
-
25
-
-
26444564724
-
A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays
-
Simpson CL, Knight J, Butcher LM, Hansen VK, Meaburn E, Schalkwyk LC, Craig IW, Powell JF, Sham PC, AL-Chalabi A: A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays. Nucleic Acids Res 2005, 33:e25.
-
(2005)
Nucleic Acids Res
, vol.33
-
-
Simpson, C.L.1
Knight, J.2
Butcher, L.M.3
Hansen, V.K.4
Meaburn, E.5
Schalkwyk, L.C.6
Craig, I.W.7
Powell, J.F.8
Sham, P.C.9
AL-Chalabi, A.10
-
27
-
-
0036792816
-
On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles
-
Morris RW, Kaplan NL: On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles. Genet Epidemiol 2002, 23:221-233.
-
(2002)
Genet Epidemiol
, vol.23
, pp. 221-233
-
-
Morris, R.W.1
Kaplan, N.L.2
-
28
-
-
13844262641
-
Rapid simulation of p values for product methods and multiple-testing adjustment in association studies
-
Seaman SR, Müller-Myhsok B: Rapid simulation of p values for product methods and multiple-testing adjustment in association studies Am J Hum Genet 2005, 76:399-408.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 399-408
-
-
Seaman, S.R.1
Müller-Myhsok, B.2
-
30
-
-
13844306901
-
Application of pooled genotyping to scan candidate regions for association with HDL cholesterol levels
-
Hinds DA, Seymour AB, Durham LK, Banerjee P, Ballinger DG, Milos PM, Cox DR, Thompson JF, Frazer KA: Application of pooled genotyping to scan candidate regions for association with HDL cholesterol levels. Human Genomics 2004, 1:421-434.
-
(2004)
Human Genomics
, vol.1
, pp. 421-434
-
-
Hinds, D.A.1
Seymour, A.B.2
Durham, L.K.3
Banerjee, P.4
Ballinger, D.G.5
Milos, P.M.6
Cox, D.R.7
Thompson, J.F.8
Frazer, K.A.9
-
31
-
-
0038728035
-
Selection of genetic markers for association analyses, using linkage disequilibrium and haplotypes
-
Meng Z, Zaykin DV, Xu CF, Wagner M, Ehm MG: Selection of genetic markers for association analyses, using linkage disequilibrium and haplotypes. Am J Hum Genet 2003, 73:115-130.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 115-130
-
-
Meng, Z.1
Zaykin, D.V.2
Xu, C.F.3
Wagner, M.4
Ehm, M.G.5
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