-
1
-
-
0039513062
-
Computer-simulation methods in human linkage analysis
-
Ott J: Computer-simulation methods in human linkage analysis. Proc Natl Acad Sci USA 1989;86:4175-1758.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 4175-11758
-
-
Ott, J.1
-
4
-
-
0022792421
-
Estimating the power of a proposed linkage study: A practical computer simulation approach
-
Boehnke M: Estimating the power of a proposed linkage study: A practical computer simulation approach. Am J Hum Genet 1986;39:513-527.
-
(1986)
Am J Hum Genet
, vol.39
, pp. 513-527
-
-
Boehnke, M.1
-
5
-
-
0000801438
-
SLINK: A general simulation program for linkage analysis
-
Weeks DE, Ott J, M LG: SLINK: A general simulation program for linkage analysis. Am J Hum Genet 1990;47:A204 (supplement).
-
(1990)
Am J Hum Genet
, vol.47
, Issue.SUPPL.
-
-
Weeks, D.E.1
Ott, J.2
M, L.G.3
-
6
-
-
0002907949
-
The interaction of selection and linkage. I. General considerations; heterotic models
-
Lewontin RC: The interaction of selection and linkage. I. General considerations; heterotic models. Genetics 1964;49:49-67.
-
(1964)
Genetics
, vol.49
, pp. 49-67
-
-
Lewontin, R.C.1
-
7
-
-
12244264435
-
Genetic power calculator: Design of linkage and association genetic mapping studies of complex traits
-
Purcell S, Cherny SS, Sham PC: Genetic power calculator: design of linkage and association genetic mapping studies of complex traits. Bioinformatics 2003;19:149-150.
-
(2003)
Bioinformatics
, vol.19
, pp. 149-150
-
-
Purcell, S.1
Cherny, S.S.2
Sham, P.C.3
-
8
-
-
1842859051
-
Power and sample size calculations for case-control genetic association tests when errors are present: Application to single nucleotide polymorphisms
-
Gordon D, Finch SJ, Nothnagel M, Ott J: Power and sample size calculations for case-control genetic association tests when errors are present: Application to single nucleotide polymorphisms. Hum Hered 2002;54:22-33.
-
(2002)
Hum Hered
, vol.54
, pp. 22-33
-
-
Gordon, D.1
Finch, S.J.2
Nothnagel, M.3
Ott, J.4
-
9
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch N, Merikangas K: The future of genetic studies of complex human diseases. Science 1996;273:1516-1517.
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
10
-
-
79959503826
-
The International HapMap Project
-
HapMap Consortium: The International HapMap Project. Nature 2003;426:789-796.
-
(2003)
Nature
, vol.426
, pp. 789-796
-
-
-
11
-
-
0032429154
-
A DNA polymorphism discovery resource for research on human genetic variation
-
Collins FS, Brooks LD, Chakravarti A: A DNA polymorphism discovery resource for research on human genetic variation. Genome Res 1998;8:1229-1231.
-
(1998)
Genome Res
, vol.8
, pp. 1229-1231
-
-
Collins, F.S.1
Brooks, L.D.2
Chakravarti, A.3
-
12
-
-
0033039497
-
Prospects for whole-genome linkage disequilibrium mapping of common disease genes
-
Kruglyak L: Prospects for whole-genome linkage disequilibrium mapping of common disease genes. Nat Genet 1999;22:139-144.
-
(1999)
Nat Genet
, vol.22
, pp. 139-144
-
-
Kruglyak, L.1
-
13
-
-
0035214299
-
Trimming, weighting, and grouping SNPs in human case-control association studies
-
Hoh J, Wille A, Ott J: Trimming, weighting, and grouping SNPs in human case-control association studies. Genome Res 2001;11:2115-2119.
-
(2001)
Genome Res
, vol.11
, pp. 2115-2119
-
-
Hoh, J.1
Wille, A.2
Ott, J.3
-
14
-
-
0034527775
-
Selecting SNPs in two-stage analysis of disease association data: A model-free approach
-
Hoh J, Wille A, Zee R, Cheng S, Reynolds R, Lindpaintner K, Ott J: Selecting SNPs in two-stage analysis of disease association data: A model-free approach. Ann Hum Genet 2000;64(Pt 5):413-417.
-
(2000)
Ann Hum Genet
, vol.64
, Issue.5 PART
, pp. 413-417
-
-
Hoh, J.1
Wille, A.2
Zee, R.3
Cheng, S.4
Reynolds, R.5
Lindpaintner, K.6
Ott, J.7
-
15
-
-
0033810469
-
Single nucleotide polymorphisms and the future of genetic epidemiology
-
Schork NJ, Fallin D, Lanchbury JS: Single nucleotide polymorphisms and the future of genetic epidemiology. Clin Genet 2000;58:250-264.
-
(2000)
Clin Genet
, vol.58
, pp. 250-264
-
-
Schork, N.J.1
Fallin, D.2
Lanchbury, J.S.3
-
16
-
-
0035220161
-
The future of genetic case-control studies
-
Schork NJ, Fallin D, Thiel B, Xu X, Broeckel U, Jacob HJ, Cohen D: The future of genetic case-control studies. Adv Genet 2001;42:191-212.
-
(2001)
Adv Genet
, vol.42
, pp. 191-212
-
-
Schork, N.J.1
Fallin, D.2
Thiel, B.3
Xu, X.4
Broeckel, U.5
Jacob, H.J.6
Cohen, D.7
-
17
-
-
0033863391
-
SNPing away at complex diseases: Analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease
-
Martin ER, Lai EH, Gilbert JR, Rogala AR, Afshari AJ, Riley J, Finch KL, et al: SNPing away at complex diseases: Analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease. Am J Hum Genet 2000;67:383-394.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 383-394
-
-
Martin, E.R.1
Lai, E.H.2
Gilbert, J.R.3
Rogala, A.R.4
Afshari, A.J.5
Riley, J.6
Finch, K.L.7
-
19
-
-
0037386186
-
Genome association studies of complex diseases by case-control designs
-
Fan R, Knapp M: Genome association studies of complex diseases by case-control designs. Am J Hum Genet 2003;72:850-868.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 850-868
-
-
Fan, R.1
Knapp, M.2
-
20
-
-
0036918575
-
Haplotype block structure and its applications to association studies: Power and study designs
-
Zhang K, Calabrese P, Nordborg M, Sun F: Haplotype block structure and its applications to association studies: Power and study designs. Am J Hum Genet 2002;71:1386-1394.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1386-1394
-
-
Zhang, K.1
Calabrese, P.2
Nordborg, M.3
Sun, F.4
-
21
-
-
0036011273
-
Generalized T2 test for genome association studies
-
Xiong M, Zhao J, Boerwinkle E: Generalized T2 test for genome association studies. Am J Hum Genet 2002;70:1257-1268.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1257-1268
-
-
Xiong, M.1
Zhao, J.2
Boerwinkle, E.3
-
22
-
-
0036094731
-
Power calculations for genetic association studies using estimated probability distributions
-
Schork NJ: Power calculations for genetic association studies using estimated probability distributions. Am J Hum Genet 2002;70:1480-1489.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1480-1489
-
-
Schork, N.J.1
-
23
-
-
0034890791
-
The power of genomewide association studies of complex disease genes: Statistical limitations of indirect approaches using SNP markers
-
Ohashi J, Tokunaga K: The power of genomewide association studies of complex disease genes: Statistical limitations of indirect approaches using SNP markers. J Hum Genet 2001;46:478-482.
-
(2001)
J Hum Genet
, vol.46
, pp. 478-482
-
-
Ohashi, J.1
Tokunaga, K.2
-
24
-
-
0035154452
-
Genetic analysis of case/control data using estimated haplotype frequencies: Application to APOE locus variation and Alzheimer's disease
-
Fallin D, Cohen A, Essioux L, Chumakov I, Blumenfeld M, Cohen D, Schork NJ: Genetic analysis of case/control data using estimated haplotype frequencies: Application to APOE locus variation and Alzheimer's disease. Genome Res 2001;11:143-151.
-
(2001)
Genome Res
, vol.11
, pp. 143-151
-
-
Fallin, D.1
Cohen, A.2
Essioux, L.3
Chumakov, I.4
Blumenfeld, M.5
Cohen, D.6
Schork, N.J.7
-
25
-
-
0037312921
-
Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease
-
Lohmueller KE, Pearce CL, Pike M, Lander ES, Hirschhorn JN: Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease. Nat Genet 2003;33:177-182.
-
(2003)
Nat Genet
, vol.33
, pp. 177-182
-
-
Lohmueller, K.E.1
Pearce, C.L.2
Pike, M.3
Lander, E.S.4
Hirschhorn, J.N.5
-
26
-
-
2342597140
-
A high-density admixture map for disease gene discovery in African americans
-
Smith MW, Patterson N, Lautenberger JA, Truelove AL, McDonald GJ, Waliszewska A, Kessing BD, et al: A high-density admixture map for disease gene discovery in African americans. Am J Hum Genet 2004;74:1001-1013.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 1001-1013
-
-
Smith, M.W.1
Patterson, N.2
Lautenberger, J.A.3
Truelove, A.L.4
McDonald, G.J.5
Waliszewska, A.6
Kessing, B.D.7
-
27
-
-
0036594903
-
New generation pharmacogenomic tools: A SNP linkage disequilibrium Map, validated SNP assay resource, and high-throughput instrumentation system for large-scale genetic studies
-
De La Vega FM, Dailey D, Ziegle J, Williams J, Madden D, Gilbert DA: New generation pharmacogenomic tools: A SNP linkage disequilibrium Map, validated SNP assay resource, and high-throughput instrumentation system for large-scale genetic studies. Biotechniques 2002;Suppl:48-50, 52, 54.
-
(2002)
Biotechniques
, Issue.SUPPL.
, pp. 48-50
-
-
De La Vega, F.M.1
Dailey, D.2
Ziegle, J.3
Williams, J.4
Madden, D.5
Gilbert, D.A.6
-
28
-
-
17144371712
-
The linkage disequilibrium maps of three human chromosomes across four populations reflect their demographic history and a common underlying recombination pattern
-
De La Vega FM, Isaac H, Collins A, Scafe CR, Halldorsson BV, Su X, Lippert RA, et al: The linkage disequilibrium maps of three human chromosomes across four populations reflect their demographic history and a common underlying recombination pattern. Genome Res 2005;15:454-462.
-
(2005)
Genome Res
, vol.15
, pp. 454-462
-
-
De La Vega, F.M.1
Isaac, H.2
Collins, A.3
Scafe, C.R.4
Halldorsson, B.V.5
Su, X.6
Lippert, R.A.7
-
29
-
-
0036359893
-
An automated computer system to support ultra high throughput SNP genotyping
-
Heil J, Glanowski S, Scott J, Winn-Deen E, McMullen I, Wu L, Gire C, et al: An automated computer system to support ultra high throughput SNP genotyping. Pac Symp Biocomput 2002:30-40.
-
(2002)
Pac Symp Biocomput
, pp. 30-40
-
-
Heil, J.1
Glanowski, S.2
Scott, J.3
Winn-Deen, E.4
McMullen, I.5
Wu, L.6
Gire, C.7
-
30
-
-
0036338150
-
Merlin - Rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR: Merlin - rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 2002;30:97-101.
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
31
-
-
0042629677
-
Errors and linkage disequilibrium interact multiplicatively when computing sample sizes for genetic case-control association studies
-
Gordon D, Levenstien MA, Finch SJ, Ott J: Errors and linkage disequilibrium interact multiplicatively when computing sample sizes for genetic case-control association studies. Pac Symp Biocomput 2003:490-501.
-
(2003)
Pac Symp Biocomput
, pp. 490-501
-
-
Gordon, D.1
Levenstien, M.A.2
Finch, S.J.3
Ott, J.4
-
33
-
-
84856043672
-
A mathematical theory of communication
-
Shannon CE: A mathematical theory of communication. Bell Syst Tech J 1948;27:379-423, 623-656.
-
(1948)
Bell Syst Tech J
, vol.27
, pp. 379-423
-
-
Shannon, C.E.1
-
34
-
-
0742288585
-
The complex interplay among factors that influence allelic association
-
Zondervan KT, Cardon LR: The complex interplay among factors that influence allelic association. Nat Rev Genet 2004;5:89-100.
-
(2004)
Nat Rev Genet
, vol.5
, pp. 89-100
-
-
Zondervan, K.T.1
Cardon, L.R.2
-
35
-
-
0034017850
-
GOLD - Graphical overview of linkage disequilibrium
-
Abecasis GR, Cookson WO: GOLD - graphical overview of linkage disequilibrium. Bioinformatics 2000;16:182-183.
-
(2000)
Bioinformatics
, vol.16
, pp. 182-183
-
-
Abecasis, G.R.1
Cookson, W.O.2
-
36
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, Higgins J, et al: The structure of haplotype blocks in the human genome. Science 2002;296:2225-2229.
-
(2002)
Science
, vol.296
, pp. 2225-2229
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
Moore, J.M.4
Roy, J.5
Blumenstiel, B.6
Higgins, J.7
-
37
-
-
0001174368
-
On the limiting power function of the frequency chi-square test
-
Mitra SK: On the limiting power function of the frequency chi-square test. Ann Math Stat 1958;29:1221-1233.
-
(1958)
Ann Math Stat
, vol.29
, pp. 1221-1233
-
-
Mitra, S.K.1
-
39
-
-
0035451780
-
On the allelic spectrum of human disease
-
Reich DE, Lander ES: On the allelic spectrum of human disease. Trends Genet 2001;17:502-510.
-
(2001)
Trends Genet
, vol.17
, pp. 502-510
-
-
Reich, D.E.1
Lander, E.S.2
-
40
-
-
0040175649
-
The powers and strengths of tests for multinomials and contingency tables
-
Crook JF, Good IJ: The powers and strengths of tests for multinomials and contingency tables. J Am Stat Assoc 1982;77:793-802.
-
(1982)
J Am Stat Assoc
, vol.77
, pp. 793-802
-
-
Crook, J.F.1
Good, I.J.2
-
41
-
-
0042358733
-
Sample size calculations for population - and family-based case-control association studies on marker genotypes
-
Pfeiffer RM, Gail MH: Sample size calculations for population - and family-based case-control association studies on marker genotypes. Genet Epidemiol 2003;25:136-148.
-
(2003)
Genet Epidemiol
, vol.25
, pp. 136-148
-
-
Pfeiffer, R.M.1
Gail, M.H.2
-
42
-
-
0036250657
-
The public health impact of Alzheimer's Disease, 2000-2050: Potential implication of treatment advances
-
Sloane PD, Zimmerman S, Suchindran C, Reed P, Wang L, Boustani M, Sudha S: The public health impact of Alzheimer's Disease, 2000-2050: potential implication of treatment advances. Annu Rev Public Health 2002;23:213-231.
-
(2002)
Annu Rev Public Health
, vol.23
, pp. 213-231
-
-
Sloane, P.D.1
Zimmerman, S.2
Suchindran, C.3
Reed, P.4
Wang, L.5
Boustani, M.6
Sudha, S.7
-
43
-
-
0036285796
-
Bipolar disorder in the general population in The Netherlands (prevalence, consequences and care utilisation): Results from The Netherlands Mental Health Survey and Incidence Study (NEMESIS)
-
ten Have M, Vollebergh W, Bijl R, Nolen WA: Bipolar disorder in the general population in The Netherlands (prevalence, consequences and care utilisation): results from The Netherlands Mental Health Survey and Incidence Study (NEMESIS). J Affect Disord 2002;68:203-213.
-
(2002)
J Affect Disord
, vol.68
, pp. 203-213
-
-
Ten Have, M.1
Vollebergh, W.2
Bijl, R.3
Nolen, W.A.4
-
44
-
-
0031878501
-
Familial psoriasis and HLA-B: Unambiguous support for linkage in 97 published families
-
Leder RO, Mansbridge JN, Hallmayer J, Hodge SE: Familial psoriasis and HLA-B: unambiguous support for linkage in 97 published families. Hum Hered 1998;48:198-211.
-
(1998)
Hum Hered
, vol.48
, pp. 198-211
-
-
Leder, R.O.1
Mansbridge, J.N.2
Hallmayer, J.3
Hodge, S.E.4
-
45
-
-
18544383722
-
Family-based analysis using a dense single-nucleotide polymorphism-based map defines genetic variation at PSORS1, the major psoriasis-susceptibility locus
-
Veal CD, Capon F, Allen MH, Heath EK, Evans JC, Jones A, Patel S, et al: Family-based analysis using a dense single-nucleotide polymorphism-based map defines genetic variation at PSORS1, the major psoriasis-susceptibility locus. Am J Hum Genet 2002;71:554-564.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 554-564
-
-
Veal, C.D.1
Capon, F.2
Allen, M.H.3
Heath, E.K.4
Evans, J.C.5
Jones, A.6
Patel, S.7
-
46
-
-
0033927713
-
Localization of psoriasis-susceptibility locus PSORS1 to a 60-kb interval telomeric to HLA-C
-
Nair RP, Stuart P, Henseler T, Jenisch S, Chia NV, Westphal E, Schork NJ, et al: Localization of psoriasis-susceptibility locus PSORS1 to a 60-kb interval telomeric to HLA-C. Am J Hum Genet 2000;66:1833-1844.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1833-1844
-
-
Nair, R.P.1
Stuart, P.2
Henseler, T.3
Jenisch, S.4
Chia, N.V.5
Westphal, E.6
Schork, N.J.7
-
47
-
-
0024788805
-
Man bites dog? The validity of maximizing lod scores to determine mode of inheritance
-
Elston RC: Man bites dog? The validity of maximizing lod scores to determine mode of inheritance. Am J Med Genet 1989;34:487-488.
-
(1989)
Am J Med Genet
, vol.34
, pp. 487-488
-
-
Elston, R.C.1
-
48
-
-
0024828416
-
Inferring mode of inheritance by comparison of lod scores
-
Greenberg DA: Inferring mode of inheritance by comparison of lod scores. Am J Med Genet 1989;34:480-486.
-
(1989)
Am J Med Genet
, vol.34
, pp. 480-486
-
-
Greenberg, D.A.1
-
49
-
-
0035283148
-
The genome-wide distribution of background linkage disequilibrium in a population isolate
-
Service SK, Ophoff RA, Freimer NB: The genome-wide distribution of background linkage disequilibrium in a population isolate. Hum Mol Genet 2001;10:545-551.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 545-551
-
-
Service, S.K.1
Ophoff, R.A.2
Freimer, N.B.3
-
50
-
-
0035257236
-
Association study designs for complex diseases
-
Cardon LR ,Bell JI: Association study designs for complex diseases. Nat Rev Genet 2001;2:91-99.
-
(2001)
Nat Rev Genet
, vol.2
, pp. 91-99
-
-
Cardon, L.R.1
Bell, J.I.2
-
51
-
-
0034789532
-
Haplotype tagging for the identification of common disease genes
-
Johnson GC, Esposito L, Barratt BJ, Smith AN, Heward J, Di Genova G, Ueda H, et al: Haplotype tagging for the identification of common disease genes. Nat Genet 2001;29:233-237.
-
(2001)
Nat Genet
, vol.29
, pp. 233-237
-
-
Johnson, G.C.1
Esposito, L.2
Barratt, B.J.3
Smith, A.N.4
Heward, J.5
Di Genova, G.6
Ueda, H.7
-
52
-
-
18444396271
-
A first-generation linkage disequilibrium map of human chromosome 22
-
Dawson E, Abecasis GR, Bumpstead S, Chen Y, Hunt S, Beare DM, Pabial J, et al: A first-generation linkage disequilibrium map of human chromosome 22. Nature 2002;418:544-548.
-
(2002)
Nature
, vol.418
, pp. 544-548
-
-
Dawson, E.1
Abecasis, G.R.2
Bumpstead, S.3
Chen, Y.4
Hunt, S.5
Beare, D.M.6
Pabial, J.7
-
53
-
-
0037373275
-
Discovering genotypes underlying human phenotypes: Past successes for mendelian disease, future approaches for complex disease
-
Botstein D, Risch N: Discovering genotypes underlying human phenotypes: Past successes for mendelian disease, future approaches for complex disease. Nat Genet 2003;33(suppl):228-237.
-
(2003)
Nat Genet
, vol.33
, Issue.SUPPL.
, pp. 228-237
-
-
Botstein, D.1
Risch, N.2
-
54
-
-
20444495264
-
Factors affecting statistical power in the detection of genetic association
-
Gordon D, Finch SJ: Factors affecting statistical power in the detection of genetic association. J Clin Invest 2005;115:1408-1418.
-
(2005)
J Clin Invest
, vol.115
, pp. 1408-1418
-
-
Gordon, D.1
Finch, S.J.2
-
55
-
-
0034800188
-
GAW12: Simulated genome scan, sequence, and family data for a common disease
-
Almasy L, Terwilliger JD, Nielsen D, Dyer TD, Zaykin D, Blangero J: GAW12: Simulated genome scan, sequence, and family data for a common disease. Genet Epidemiol 2001;21(suppl 1):S332-338.
-
(2001)
Genet Epidemiol
, vol.21
, Issue.1 SUPPL.
-
-
Almasy, L.1
Terwilliger, J.D.2
Nielsen, D.3
Dyer, T.D.4
Zaykin, D.5
Blangero, J.6
-
56
-
-
0033794938
-
Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype data
-
Fallin D, Schork NJ: Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype data. Am J Hum Genet 2000;67:947-959.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 947-959
-
-
Fallin, D.1
Schork, N.J.2
-
57
-
-
0027194791
-
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families
-
Corder EH, Saunders AM, Strittmatter WJ, Schmechel DE, Gaskell PC, Small GW, Roses AD, et al: Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. Science 1993;261:921-923.
-
(1993)
Science
, vol.261
, pp. 921-923
-
-
Corder, E.H.1
Saunders, A.M.2
Strittmatter, W.J.3
Schmechel, D.E.4
Gaskell, P.C.5
Small, G.W.6
Roses, A.D.7
-
58
-
-
0001400362
-
The chi-square test of goodness of fit
-
Cochran WG: The chi-square test of goodness of fit. Ann Math Stat 1952;23:315-345.
-
(1952)
Ann Math Stat
, vol.23
, pp. 315-345
-
-
Cochran, W.G.1
-
59
-
-
1542315614
-
Patterns of linkage disequilibrium in the MHC region on human chromosome 6p
-
Stenzel A, Lu T, Koch WA, Hampe J, Guenther SM, De La Vega FM, Krawczak M, et al: Patterns of linkage disequilibrium in the MHC region on human chromosome 6p. Hum Genet 2004;114:377-385.
-
(2004)
Hum Genet
, vol.114
, pp. 377-385
-
-
Stenzel, A.1
Lu, T.2
Koch, W.A.3
Hampe, J.4
Guenther, S.M.5
De La Vega, F.M.6
Krawczak, M.7
-
60
-
-
0037133218
-
The first linkage disequilibrium (LD) maps: Delineation of hot and cold blocks by diplotype analysis
-
Maniatis N, Collins A, Xu CF, McCarthy LC, Hewett DR, Tapper W, Ennis S, et al: The first linkage disequilibrium (LD) maps: delineation of hot and cold blocks by diplotype analysis. Proc Natl Acad Sci USA 2002;99:2228-2233.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 2228-2233
-
-
Maniatis, N.1
Collins, A.2
Xu, C.F.3
McCarthy, L.C.4
Hewett, D.R.5
Tapper, W.6
Ennis, S.7
-
61
-
-
11244313872
-
Reconstituting the frequency spectrum of ascertained single-nucleotide polymorphism data
-
Nielsen R, Hubisz MJ, Clark AG: Reconstituting the frequency spectrum of ascertained single-nucleotide polymorphism data. Genetics 2004;168:2373-2382.
-
(2004)
Genetics
, vol.168
, pp. 2373-2382
-
-
Nielsen, R.1
Hubisz, M.J.2
Clark, A.G.3
-
62
-
-
1842435224
-
Power for genetic association studies with random allele frequencies and genotype distributions
-
Ambrosius WT, Lange EM, Langefeld CD: Power for genetic association studies with random allele frequencies and genotype distributions. Am J Hum Genet 2004;74:683-693.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 683-693
-
-
Ambrosius, W.T.1
Lange, E.M.2
Langefeld, C.D.3
-
63
-
-
3042591234
-
Linkage disequilibrium mapping via cladistic analysis of single-nucleotide polymorphism haplotypes
-
Durrant C, Zondervan KT, Cardon LR, Hunt S, Deloukas P, Morris AP: Linkage disequilibrium mapping via cladistic analysis of single-nucleotide polymorphism haplotypes. Am J Hum Genet 2004;75:35-43.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 35-43
-
-
Durrant, C.1
Zondervan, K.T.2
Cardon, L.R.3
Hunt, S.4
Deloukas, P.5
Morris, A.P.6
-
64
-
-
0038449167
-
Evolutionary-based association analysis using haplotype data
-
Seltman H, Roeder K, Devlin B: Evolutionary-based association analysis using haplotype data. Genet Epidemiol 2003;25:48-58.
-
(2003)
Genet Epidemiol
, vol.25
, pp. 48-58
-
-
Seltman, H.1
Roeder, K.2
Devlin, B.3
-
65
-
-
0029130796
-
Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population
-
Excoffier L, Slatkin M: Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population. Mol Biol Evol 1995;12:921-927.
-
(1995)
Mol Biol Evol
, vol.12
, pp. 921-927
-
-
Excoffier, L.1
Slatkin, M.2
-
66
-
-
0001200144
-
Testing linkage disequilibrium between a disease gene and marker loci
-
abstract
-
Xie X, Ott J: Testing linkage disequilibrium between a disease gene and marker loci. Am J Hum Genet 1993;53:1107 (abstract).
-
(1993)
Am J Hum Genet
, vol.53
, pp. 1107
-
-
Xie, X.1
Ott, J.2
-
67
-
-
0035071957
-
A new statistical method for haplotype reconstruction from population data
-
Stephens M, Smith NJ, Donnelly P: A new statistical method for haplotype reconstruction from population data. Am J Hum Genet 2001;68:978-989.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 978-989
-
-
Stephens, M.1
Smith, N.J.2
Donnelly, P.3
-
68
-
-
18544362940
-
Increasing power for tests of genetic association in the presence of phenotype and/or genotype error by use of double-sampling
-
Article 26
-
Gordon D, Yang Y, Haynes C, Finch SJ, Mendell NR, Brown AM, Haroutunian V: Increasing power for tests of genetic association in the presence of phenotype and/or genotype error by use of double-sampling. Stat Appl Genet and Mol Biol 2004;3:Article 26.
-
(2004)
Stat Appl Genet and Mol Biol
, vol.3
-
-
Gordon, D.1
Yang, Y.2
Haynes, C.3
Finch, S.J.4
Mendell, N.R.5
Brown, A.M.6
Haroutunian, V.7
-
70
-
-
0344826588
-
Haplotype tagging single nucleotide polymorphisms and association studies
-
Thompson D, Stram D, Goldgar D, Witte JS: Haplotype tagging single nucleotide polymorphisms and association studies. Hum Hered 2003;56:48-55.
-
(2003)
Hum Hered
, vol.56
, pp. 48-55
-
-
Thompson, D.1
Stram, D.2
Goldgar, D.3
Witte, J.S.4
-
71
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander E, Kruglyak L: Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results. Nat Genet 1995;11:241-247.
-
(1995)
Nat Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
73
-
-
0003633894
-
-
Ames, Iowa, Iowa State University Press
-
Snedecor GW, Cochran WG: Statistical Methods, ed 8. Ames, Iowa, Iowa State University Press, 1989.
-
(1989)
Statistical Methods, Ed 8
-
-
Snedecor, G.W.1
Cochran, W.G.2
-
74
-
-
0001677717
-
Controlling the false discovery rate: A practical and powerful approach to multiple testing
-
Benjamini Y, Hochberg Y: Controlling the false discovery rate: A practical and powerful approach to multiple testing. J R Stat Soc B 1995;57:289-300.
-
(1995)
J R Stat Soc B
, vol.57
, pp. 289-300
-
-
Benjamini, Y.1
Hochberg, Y.2
-
76
-
-
10844228016
-
Mapping genes for common diseases: The case for genetic (LD) maps
-
Collins A, Lau W, De La Vega FM: Mapping genes for common diseases: the case for genetic (LD) maps. Hum Hered 2004;58:2-9.
-
(2004)
Hum Hered
, vol.58
, pp. 2-9
-
-
Collins, A.1
Lau, W.2
De La Vega, F.M.3
|