-
1
-
-
0038618794
-
Genebanks: A comparison of eight proposed international genetic databases
-
Austin MA, Harding S, McElroy C (2003) Genebanks: a comparison of eight proposed international genetic databases. Community Genet 6:37-45
-
(2003)
Community Genet
, vol.6
, pp. 37-45
-
-
Austin, M.A.1
Harding, S.2
McElroy, C.3
-
2
-
-
0032676163
-
Classifying proteins by family using the product of correlated p-values
-
Paper presented, Lyon, France, April
-
Bailey TL, Grundy WN (1999) Classifying proteins by family using the product of correlated p-values. Paper presented at the Third International Conference on Computational Molecular Biology, Lyon, France, April 11-14
-
(1999)
Third International Conference on Computational Molecular Biology
, pp. 11-14
-
-
Bailey, T.L.1
Grundy, W.N.2
-
3
-
-
0001677717
-
Controlling the false discovery rate: A practical and powerful approach to multiple testing
-
Benjamini Y, Hochberg Y (1995) Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Stat Soc B 57:289-300
-
(1995)
J R Stat Soc B
, vol.57
, pp. 289-300
-
-
Benjamini, Y.1
Hochberg, Y.2
-
4
-
-
0030671078
-
Methods of correcting for multiple testing: Operating characteristics
-
Brown BW, Russell K (1997) Methods of correcting for multiple testing: operating characteristics. Stat Med 16:2511-2528
-
(1997)
Stat Med
, vol.16
, pp. 2511-2528
-
-
Brown, B.W.1
Russell, K.2
-
5
-
-
0344033602
-
Detecting disease associations due to linkage disequilibrium using haplotype tags: A class of tests and the determinants of statistical power
-
Chapman JM, Cooper JD, Todd JA, Clayton DG (2003) Detecting disease associations due to linkage disequilibrium using haplotype tags: a class of tests and the determinants of statistical power. Hum Hered 56:18-31
-
(2003)
Hum Hered
, vol.56
, pp. 18-31
-
-
Chapman, J.M.1
Cooper, J.D.2
Todd, J.A.3
Clayton, D.G.4
-
6
-
-
0034781050
-
A simple correction for multiple comparisons in interval mapping genome scans
-
Cheverud JM (2001) A simple correction for multiple comparisons in interval mapping genome scans. Heredity 87:52-58
-
(2001)
Heredity
, vol.87
, pp. 52-58
-
-
Cheverud, J.M.1
-
7
-
-
0028151261
-
Empirical threshold values for quantitative trait mapping
-
Churchill GA, Doerge RW (1994) Empirical threshold values for quantitative trait mapping. Genetics 138:963-971
-
(1994)
Genetics
, vol.138
, pp. 963-971
-
-
Churchill, G.A.1
Doerge, R.W.2
-
9
-
-
0036137030
-
A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: Application to HLA in type 1 diabetes
-
Cordell HJ, Clayton DG (2002) A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes. Am J Hum Genet 70:124-141
-
(2002)
Am J Hum Genet
, vol.70
, pp. 124-141
-
-
Cordell, H.J.1
Clayton, D.G.2
-
10
-
-
0041857847
-
Pedigree disequilibrium tests for multilocus haplotypes
-
Dudbridge F (2003) Pedigree disequilibrium tests for multilocus haplotypes. Genet Epidemiol 25:115-121
-
(2003)
Genet Epidemiol
, vol.25
, pp. 115-121
-
-
Dudbridge, F.1
-
11
-
-
0344826563
-
Rank truncated product of P-values, with application to genomewide association scans
-
Dudbridge F, Koeleman BP (2003) Rank truncated product of P-values, with application to genomewide association scans. Genet Epidemiol 25:360-366
-
(2003)
Genet Epidemiol
, vol.25
, pp. 360-366
-
-
Dudbridge, F.1
Koeleman, B.P.2
-
14
-
-
0346101571
-
Power estimation of multiple SNP association test of case-control study and application
-
Hao K, Xu X, Laird N, Wang X, Xu X (2004) Power estimation of multiple SNP association test of case-control study and application. Genet Epidemiol 26:22-30
-
(2004)
Genet Epidemiol
, vol.26
, pp. 22-30
-
-
Hao, K.1
Xu, X.2
Laird, N.3
Wang, X.4
Xu, X.5
-
15
-
-
0042881041
-
Mathematical multi-locus approaches to localizing complex human trait genes
-
Hoh J, Ott J (2003) Mathematical multi-locus approaches to localizing complex human trait genes. Nat Rev Genet 4:701-709
-
(2003)
Nat Rev Genet
, vol.4
, pp. 701-709
-
-
Hoh, J.1
Ott, J.2
-
16
-
-
0035214299
-
Trimming, weighting, and grouping SNPs in human case-control association studies
-
Hoh J, Wille A, Ott J (2001) Trimming, weighting, and grouping SNPs in human case-control association studies. Genome Res 11:2115-2119
-
(2001)
Genome Res
, vol.11
, pp. 2115-2119
-
-
Hoh, J.1
Wille, A.2
Ott, J.3
-
17
-
-
79959503826
-
-
The International HapMap Project
-
International HapMap Consortium (2003) The International HapMap Project. Nature 426:789-796
-
(2003)
Nature
, vol.426
, pp. 789-796
-
-
-
18
-
-
0037159470
-
Limitations of stratifying sib-pair data in common disease linkage studies: An example using chromosome 10p14-10q11 in type 1 diabetes
-
Johnson GC, Koeleman BP, Todd JA (2002) Limitations of stratifying sib-pair data in common disease linkage studies: an example using chromosome 10p14-10q11 in type 1 diabetes. Am J Med Genet 113:158-166
-
(2002)
Am J Med Genet
, vol.113
, pp. 158-166
-
-
Johnson, G.C.1
Koeleman, B.P.2
Todd, J.A.3
-
19
-
-
0038038678
-
Gene selection criterion for discriminant microarray data analysis based on extreme value distributions
-
Paper presented, Berlin, April
-
Li W, Grosse I (2003) Gene selection criterion for discriminant microarray data analysis based on extreme value distributions. Paper presented at the Seventh International Conference on Computational Molecular Biology, Berlin, April 10-13
-
(2003)
Seventh International Conference on Computational Molecular Biology
, pp. 10-13
-
-
Li, W.1
Grosse, I.2
-
20
-
-
0025259313
-
Methods for assessing the statistical significance of molecular sequence features by using general scoring schemes
-
Karlin S, Altschul SF (1990) Methods for assessing the statistical significance of molecular sequence features by using general scoring schemes. Proc Natl Acad Sci USA 87:2264-2268
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 2264-2268
-
-
Karlin, S.1
Altschul, S.F.2
-
21
-
-
1842539516
-
A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other
-
Nyholt DR (2004) A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other. Am J Hum Genet 74:765-769
-
(2004)
Am J Hum Genet
, vol.74
, pp. 765-769
-
-
Nyholt, D.R.1
-
22
-
-
18544365654
-
Genomewide linkage disequilibrium mapping of severe bipolar disorder in a population isolate
-
Ophoff RA, Escamilla MA, Service SK, Spesny M, Meshi DB, Poon W, Molina J, Fournier E, Gallegos A, Mathews C, Neylan T, Batki SL, Roche E, Ramirez M, Silva S, De Mille MC, Dong P, Leon PE, Reus VI, Sandkuijl LA, Freimer NB (2002) Genomewide linkage disequilibrium mapping of severe bipolar disorder in a population isolate. Am J Hum Genet 71:565-574
-
(2002)
Am J Hum Genet
, vol.71
, pp. 565-574
-
-
Ophoff, R.A.1
Escamilla, M.A.2
Service, S.K.3
Spesny, M.4
Meshi, D.B.5
Poon, W.6
Molina, J.7
Fournier, E.8
Gallegos, A.9
Mathews, C.10
Neylan, T.11
Batki, S.L.12
Roche, E.13
Ramirez, M.14
Silva, S.15
De Mille, M.C.16
Dong, P.17
Leon, P.E.18
Reus, V.I.19
Sandkuijl, L.A.20
Freimer, N.B.21
more..
-
23
-
-
18744407845
-
Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarction
-
Ozaki K, Ohnishi Y, Iida A, Sekine A, Yamada R, Tsunoda T, Sato H, Sato H, Hori M, Nakamura Y, Tanaka T (2002) Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarction. Nat Genet 32:650-654
-
(2002)
Nat Genet
, vol.32
, pp. 650-654
-
-
Ozaki, K.1
Ohnishi, Y.2
Iida, A.3
Sekine, A.4
Yamada, R.5
Tsunoda, T.6
Sato, H.7
Sato, H.8
Hori, M.9
Nakamura, Y.10
Tanaka, T.11
-
25
-
-
0038156106
-
Estimating the occurrence of false positives and false negatives in microarray studies by approximating and partitioning the empirical distribution of p-values
-
Pounds S, Morris SW (2003) Estimating the occurrence of false positives and false negatives in microarray studies by approximating and partitioning the empirical distribution of p-values. Bioinformatics 19:1236-1242
-
(2003)
Bioinformatics
, vol.19
, pp. 1236-1242
-
-
Pounds, S.1
Morris, S.W.2
-
26
-
-
0034969437
-
Are rare variants responsible for susceptibility to complex diseases?
-
Pritchard JK (2001) Are rare variants responsible for susceptibility to complex diseases? Am J Hum Genet 69:124-137
-
(2001)
Am J Hum Genet
, vol.69
, pp. 124-137
-
-
Pritchard, J.K.1
-
28
-
-
0035837267
-
Linkage disequilibrium in the human genome
-
Reich DE, Cargill M, Bolk S, Ireland J, Sabeti PC, Richter DJ, Lavery T, Kouyoumjian R, Farhadian SF Ward R, Lander ES (2001) Linkage disequilibrium in the human genome. Nature 411:199-204
-
(2001)
Nature
, vol.411
, pp. 199-204
-
-
Reich, D.E.1
Cargill, M.2
Bolk, S.3
Ireland, J.4
Sabeti, P.C.5
Richter, D.J.6
Lavery, T.7
Kouyoumjian, R.8
Farhadian, S.F.9
Ward, R.10
Lander, E.S.11
-
29
-
-
0034660559
-
Searching for genetic determinants in the new millennium
-
Risch NJ (2000) Searching for genetic determinants in the new millennium. Nature 405:847-856
-
(2000)
Nature
, vol.405
, pp. 847-856
-
-
Risch, N.J.1
-
30
-
-
0029741063
-
The future of genetic studies of complex human disease
-
Risch NJ, Merikangas KR (1996) The future of genetic studies of complex human disease. Science 273:1516-1517
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.J.1
Merikangas, K.R.2
-
31
-
-
0037786658
-
False discovery rate in linkage and association genome screens for complex disorders
-
Sabatti C, Service S, Freimer N (2003) False discovery rate in linkage and association genome screens for complex disorders. Genetics 164:829-833
-
(2003)
Genetics
, vol.164
, pp. 829-833
-
-
Sabatti, C.1
Service, S.2
Freimer, N.3
-
32
-
-
0036188784
-
Two-stage designs for gene-disease association studies
-
Satagopan JM, Verbel DA, Venkatraman ES, Offit KE, Begg CB (2002) Two-stage designs for gene-disease association studies. Biometrics 58:163-170
-
(2002)
Biometrics
, vol.58
, pp. 163-170
-
-
Satagopan, J.M.1
Verbel, D.A.2
Venkatraman, E.S.3
Offit, K.E.4
Begg, C.B.5
-
33
-
-
0036263896
-
A whole genome screen for linkage disequilibrium in multiple sclerosis confirms disease associations with regions previously linked to susceptibility
-
Sawcer S, Maranian M, Setakis E, Curwen V, Akesson E, Hensiek A, Coraddu F, Roxburgh R, Sawcer D, Gray J, Deans J, Goodfellow PN, Walker N, Clayton D, Compston A (2002) A whole genome screen for linkage disequilibrium in multiple sclerosis confirms disease associations with regions previously linked to susceptibility. Brain 125:1337-1347
-
(2002)
Brain
, vol.125
, pp. 1337-1347
-
-
Sawcer, S.1
Maranian, M.2
Setakis, E.3
Curwen, V.4
Akesson, E.5
Hensiek, A.6
Coraddu, F.7
Roxburgh, R.8
Sawcer, D.9
Gray, J.10
Deans, J.11
Goodfellow, P.N.12
Walker, N.13
Clayton, D.14
Compston, A.15
-
34
-
-
0036908801
-
Multiplex relative risk and estimation of the number of loci underlying an inherited disease
-
Schliekelman P, Slatkin M (2002) Multiplex relative risk and estimation of the number of loci underlying an inherited disease. Am J Hum Genet 71:1369-1385
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1369-1385
-
-
Schliekelman, P.1
Slatkin, M.2
-
35
-
-
0034910345
-
Navigating gene expression using microarrays: A technology review
-
Schulze A, Downward J (2001) Navigating gene expression using microarrays: a technology review. Nat Cell Biol 3:E190-E195
-
(2001)
Nat Cell Biol
, vol.3
-
-
Schulze, A.1
Downward, J.2
-
36
-
-
0038067802
-
Cost-effective designs for linkage disequilibrium mapping of complex traits
-
Service SK, Sandkuijl LA, Freimer NB (2003) Cost-effective designs for linkage disequilibrium mapping of complex traits. Am J Hum Genet 72:1213-1220
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1213-1220
-
-
Service, S.K.1
Sandkuijl, L.A.2
Freimer, N.B.3
-
37
-
-
0036844881
-
DNA pooling: A tool for large-scale association studies
-
Sham PC, Bader JS, Craig I, O'Donovan M, Owen M (2002) DNA pooling: a tool for large-scale association studies. Nat Rev Genet 3:862-871
-
(2002)
Nat Rev Genet
, vol.3
, pp. 862-871
-
-
Sham, P.C.1
Bader, J.S.2
Craig, I.3
O'Donovan, M.4
Owen, M.5
-
38
-
-
84947402121
-
Rectangular confidence regions for the means of multivariate normal distributions
-
Šidák Z (1967) Rectangular confidence regions for the means of multivariate normal distributions. J Am Stat Assoc 78:626-633
-
(1967)
J Am Stat Assoc
, vol.78
, pp. 626-633
-
-
Šidák, Z.1
-
39
-
-
67649345185
-
An improved Bonferroni procedure for multiple tests of significance
-
Simes RJ (1986) An improved Bonferroni procedure for multiple tests of significance. Biometrika 73:751-754
-
(1986)
Biometrika
, vol.73
, pp. 751-754
-
-
Simes, R.J.1
-
40
-
-
4143082554
-
EVD: Extreme value distributions
-
Stephenson AG (2002) EVD: extreme value distributions. R-News 2:31-32
-
(2002)
R-News
, vol.2
, pp. 31-32
-
-
Stephenson, A.G.1
-
41
-
-
0042424602
-
Statistical significance for genome-wide studies
-
Storey JD, Tibshirani R (2003) Statistical significance for genome-wide studies. Proc Natl Acad Sci USA 100:9440-9445
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 9440-9445
-
-
Storey, J.D.1
Tibshirani, R.2
-
42
-
-
0042387804
-
Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: Implications for linkage-disequilibrium gene mapping
-
Weale ME, Depondt C, Macdonald SJ, Smith A, Lai PS, Shorvon SD, Wood NW, Goldstein DB (2003) Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping. Am J Hum Genet 73:551-565
-
(2003)
Am J Hum Genet
, vol.73
, pp. 551-565
-
-
Weale, M.E.1
Depondt, C.2
Macdonald, S.J.3
Smith, A.4
Lai, P.S.5
Shorvon, S.D.6
Wood, N.W.7
Goldstein, D.B.8
-
43
-
-
0345689434
-
Sum statistics for the joint detection of multiple disease loci in case-control association studies with SNP markers
-
Wille A, Hoh J, Ott J (2003) Sum statistics for the joint detection of multiple disease loci in case-control association studies with SNP markers. Genet Epidemiol 25:350-359
-
(2003)
Genet Epidemiol
, vol.25
, pp. 350-359
-
-
Wille, A.1
Hoh, J.2
Ott, J.3
|