-
1
-
-
0034800188
-
GAW12: Simulated genome scan, sequence, and family data for a common disease
-
Almasy, L., Terwilliger, J. D., Nielsen, D., Dyer, T. D., Zaykin, D. & Blangero, J. (2001) GAW12: simulated genome scan, sequence, and family data for a common disease. Genet Epidemiol 21 Suppl 1, S332-8.
-
(2001)
Genet. Epidemiol.
, vol.21
, Issue.SUPPL. 1
-
-
Almasy, L.1
Terwilliger, J.D.2
Nielsen, D.3
Dyer, T.D.4
Zaykin, D.5
Blangero, J.6
-
2
-
-
0037373275
-
Discovering genotypes underlying human phenotypes: Past successes for mendelian disease, future approaches for complex disease
-
Borstein, D. & Risch, N. (2003) Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease. Nat Genet 33 Suppl, 228-37.
-
(2003)
Nat. Genet.
, vol.33
, Issue.SUPPL.
, pp. 228-237
-
-
Borstein, D.1
Risch, N.2
-
3
-
-
0041707972
-
Nonparametric disequilibrium mapping of functional sites using haplotypes of multiple tightly linked single-nucleotide polymorphism markers
-
Cheng, R., Ma, J. Z., Wright, F. A., Lin, S., Gao, X., Wang, D., Elston, R. C. & Li, M. D. (2003) Nonparametric disequilibrium mapping of functional sites using haplotypes of multiple tightly linked single-nucleotide polymorphism markers. Genetics 164, 1175-87.
-
(2003)
Genetics
, vol.164
, pp. 1175-1187
-
-
Cheng, R.1
Ma, J.Z.2
Wright, F.A.3
Lin, S.4
Gao, X.5
Wang, D.6
Elston, R.C.7
Li, M.D.8
-
4
-
-
0031823031
-
Fine genetic mapping using haplotype analysis and the missing data problem
-
Chiano, M. N. & Clayton, D. G. (1998) Fine genetic mapping using haplotype analysis and the missing data problem. Ann Hum Genet 62 (Pt 1), 55-60.
-
(1998)
Ann. Hum. Genet.
, vol.62
, Issue.PART 1
, pp. 55-60
-
-
Chiano, M.N.1
Clayton, D.G.2
-
5
-
-
0025269067
-
Inference of haplotypes from PCR-amplified samples of diploid populations
-
Clark, A. G. (1990) Inference of haplotypes from PCR-amplified samples of diploid populations. Mol Biol Evol 7 111-22.
-
(1990)
Mol. Biol. Evol.
, vol.7
, pp. 111-122
-
-
Clark, A.G.1
-
6
-
-
0033237335
-
A generalization of the transmission/disequilibrium test for uncertain haplotype transmission
-
Clayton, D. G. (1999) A generalization of the transmission/disequilibrium test for uncertain haplotype transmission. Am J Hum Genet 65, 1170-1177.
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 1170-1177
-
-
Clayton, D.G.1
-
7
-
-
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, H. J. & Clayton, D. G. (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, 124-41.
-
(2002)
Am. J. Hum. Genet.
, vol.70
, pp. 124-141
-
-
Cordell, H.J.1
Clayton, D.G.2
-
8
-
-
0037165976
-
Genomics. New mapping project splits the community
-
Couzin, J. (2002) Genomics. New mapping project splits the community. Science 296, 1391-3.
-
(2002)
Science
, vol.296
, pp. 1391-1393
-
-
Couzin, J.1
-
9
-
-
0002629270
-
Maximum likelihood from incomplete data via the EM algorithm
-
Dempster, A., Laird, N. & Rubin, D. (1977) Maximum likelihood from incomplete data via the EM algorithm. J Roy Stat. Soc B 39 1-38.
-
(1977)
J. Roy. Stat. Soc. B
, vol.39
, pp. 1-38
-
-
Dempster, A.1
Laird, N.2
Rubin, D.3
-
10
-
-
0344410771
-
Inference on haplotype effects in case-control studies using unphased genotype data
-
Epstein, M. P. & Satten, G. A. (2003) Inference on haplotype effects in case-control studies using unphased genotype data. Am J Hum Genet 73, 1316-29.
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 1316-1329
-
-
Epstein, M.P.1
Satten, G.A.2
-
11
-
-
0029130796
-
Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population
-
Excoffier, L. & Slatkin, M. (1995) Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population. Mol Biol Evol 12, 921-7.
-
(1995)
Mol. Biol. Evol.
, vol.12
, pp. 921-927
-
-
Excoffier, L.1
Slatkin, M.2
-
12
-
-
0031915985
-
Incorporating genotypes of relatives into a test of linkage disequilibrium
-
Excoffier, L. & Slatkin, M. (1998) Incorporating genotypes of relatives into a test of linkage disequilibrium. Am J Hum Genet 62, 171-80.
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 171-180
-
-
Excoffier, L.1
Slatkin, M.2
-
13
-
-
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, N. J. (2001) Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease. Genome Res 11, 143-51.
-
(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
-
14
-
-
4243448613
-
Nonparametric disequilibrium mapping when haplotypes are available
-
Gao, X. & Wright, F. A. (1999) Nonparametric disequilibrium mapping when haplotypes are available. Am J Hum Genet 65, A250.
-
(1999)
Am. J. Hum. Genet.
, vol.65
-
-
Gao, X.1
Wright, F.A.2
-
16
-
-
0029372419
-
HAPLO: A program using the EM algorithm to estimate the frequencies of multi-site haplotypes
-
Hawley, M. E. & Kidd, K. K. (1995) HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes. J Hered 86, 409-11.
-
(1995)
J. Hered.
, vol.86
, pp. 409-411
-
-
Hawley, M.E.1
Kidd, K.K.2
-
17
-
-
0031955802
-
Lipoprotein lipase gene variation is associated with a paternal history of premature coronary artery disease and fasting and postprandial plasma triglycerides: The European Atherosclerosis Research Study (EARS)
-
Humphries, S. E., Nicaud, V., Margalef, J., Tiret, L. & Talmud, P. J. (1998) Lipoprotein lipase gene variation is associated with a paternal history of premature coronary artery disease and fasting and postprandial plasma triglycerides: the European Atherosclerosis Research Study (EARS). Arterioscler Thromb Vasc Biol 18, 526-34.
-
(1998)
Arterioscler. Thromb. Vasc. Biol.
, vol.18
, pp. 526-534
-
-
Humphries, S.E.1
Nicaud, V.2
Margalef, J.3
Tiret, L.4
Talmud, P.J.5
-
18
-
-
0028913523
-
An E-M algorithm and testing strategy for multiple-locus haplotypes
-
Long, J. C., Williams, R. C. & Urbanek, M. (1995) An E-M algorithm and testing strategy for multiple-locus haplotypes. Am J Hum Genet 56, 799-810.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 799-810
-
-
Long, J.C.1
Williams, R.C.2
Urbanek, M.3
-
19
-
-
9844227496
-
Chi-square tests with one degree of freedom: Extension of the Mantel-Haenszel procedure
-
Mantel, N. (1963) Chi-square tests with one degree of freedom: extension of the Mantel-Haenszel procedure. J Am Stat Assoc 58, 799-810.
-
(1963)
J. Am. Stat. Assoc.
, vol.58
, pp. 799-810
-
-
Mantel, N.1
-
20
-
-
84959801619
-
Statistical sapects of the analysis of data from retrospective studies of disease
-
Mantel, N. & Haenszel, W. (1959) Statistical sapects of the analysis of data from retrospective studies of disease. J Natl Cancer Ins 22, 719-748.
-
(1959)
J. Natl. Cancer Ins.
, vol.22
, pp. 719-748
-
-
Mantel, N.1
Haenszel, W.2
-
21
-
-
0037739943
-
Association between lipoprotein lipase (LPL) gene and blood lipids: A common variant for a common trait?
-
Morabia, A., Cayanis, E., Costanza, M. C., Ross, B. M., Bernstein, M. S., Flaherty, M. S., Alvin, G. B., Das, K., Morris, M. A., Penchaszadeh, G. K., Zhang, P. & Gilliam, T. C. (2003) Association between lipoprotein lipase (LPL) gene and blood lipids: a common variant for a common trait? Genet Epidemiol 24, 309-21.
-
(2003)
Genet. Epidemiol.
, vol.24
, pp. 309-321
-
-
Morabia, A.1
Cayanis, E.2
Costanza, M.C.3
Ross, B.M.4
Bernstein, M.S.5
Flaherty, M.S.6
Alvin, G.B.7
Das, K.8
Morris, M.A.9
Penchaszadeh, G.K.10
Zhang, P.11
Gilliam, T.C.12
-
22
-
-
0032231375
-
Detecting marker-disease association by testing for Hardy-Weinberg disequilibrium at a marker locus
-
Nielsen, D. A., Ehm, M. G. & Weir, B. S. (1999) Detecting marker-disease association by testing for Hardy-Weinberg disequilibrium at a marker locus. Am J Hum Genet 63, 1531-40.
-
(1999)
Am. J. Hum. Genet.
, vol.63
, pp. 1531-1540
-
-
Nielsen, D.A.1
Ehm, M.G.2
Weir, B.S.3
-
23
-
-
0036138183
-
Bayesian haplotype inference for multiple linked single-nucleotide polymorphisms
-
Niu, T., Qin, Z. S., Xu, X. & Liu, J. S. (2002) Bayesian haplotype inference for multiple linked single-nucleotide polymorphisms. Am J Hum Genet 70, 157-69.
-
(2002)
Am. J. Hum. Genet.
, vol.70
, pp. 157-169
-
-
Niu, T.1
Qin, Z.S.2
Xu, X.3
Liu, J.S.4
-
24
-
-
0036844521
-
Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphisms
-
Qin, Z. S., Niu, T. & Liu, J. S. (2002) Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphisms. Am J Hum Genet 71, 1242-7.
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 1242-1247
-
-
Qin, Z.S.1
Niu, T.2
Liu, J.S.3
-
25
-
-
0035865322
-
A map of human genome sequence variation containing 1.42 million single nucleoticle polymorphisms
-
Sachidanandam, R., Weissman, D., Schmidt, S. C., Kakol, J. M., Stein, L. D., Marth, G., Sherry, S., Mullikin, J. C., Mortimore, B. J., Willey, D. L., Hunt, S. E., Cole, C. G., Coggill, P. C., Rice, C. M., Ning, Z., Rogers, J., Bentley, D. R., Kwok, P. Y., Mardis, E. R., Yeh, R. T., Schultz, B., Cook, L., Davenport, R., Dante, M., Fulton, L., Hillier, L., Waterston, R. H., McPherson, J. D., Gilman, B., Schaffner, S., Van Etten, W.J., Reich, D., Higgins, J., Daly, M. J., Blumenstiel, B., Baldwin, J., Stange-Thomann, N., Zody, M. C., Linton, L., Lander, E. S. & Altshuler, D. (2001) A map of human genome sequence variation containing 1.42 million single nucleoticle polymorphisms. Nature 409, 928-33.
-
(2001)
Nature
, vol.409
, pp. 928-933
-
-
Sachidanandam, R.1
Weissman, D.2
Schmidt, S.C.3
Kakol, J.M.4
Stein, L.D.5
Marth, G.6
Sherry, S.7
Mullikin, J.C.8
Mortimore, B.J.9
Willey, D.L.10
Hunt, S.E.11
Cole, C.G.12
Coggill, P.C.13
Rice, C.M.14
Ning, Z.15
Rogers, J.16
Bentley, D.R.17
Kwok, P.Y.18
Mardis, E.R.19
Yeh, R.T.20
Schultz, B.21
Cook, L.22
Davenport, R.23
Dante, M.24
Fulton, L.25
Hillier, L.26
Waterston, R.H.27
McPherson, J.D.28
Gilman, B.29
Schaffner, S.30
Van Etten, W.J.31
Reich, D.32
Higgins, J.33
Daly, M.J.34
Blumenstiel, B.35
Baldwin, J.36
Stange-Thomann, N.37
Zody, M.C.38
Linton, L.39
Lander, E.S.40
Altshuler, D.41
more..
-
26
-
-
0029956803
-
General score tests for associations of genetic markers with disease using cases and their parents
-
Schaid, D. J. (1996) General score tests for associations of genetic markers with disease using cases and their parents. Genet Epidemiol 13, 423-49.
-
(1996)
Genet. Epidemiol.
, vol.13
, pp. 423-449
-
-
Schaid, D.J.1
-
27
-
-
0036155283
-
Score tests for association between traits and haplotypes when linkage phase is ambiguous
-
Schaid, D. J., Rowland, C. M., Tines, D. E., Jacobson, R. M. & Poland, G. A. (2002) Score tests for association between traits and haplotypes when linkage phase is ambiguous. Am J Hum Genet 70 425-34.
-
(2002)
Am. J. Hum. Genet.
, vol.70
, pp. 425-434
-
-
Schaid, D.J.1
Rowland, C.M.2
Tines, D.E.3
Jacobson, R.M.4
Poland, G.A.5
-
28
-
-
0037261235
-
HapMap: Building a database with blocks
-
Schmidt, C. W. (2003) HapMap: building a database with blocks. EHP Toxicogenomics 111, A16.
-
(2003)
EHP Toxicogenomics
, vol.111
-
-
Schmidt, C.W.1
-
29
-
-
0030131165
-
Testing for linkage disequilibrium in genotypic data using the Expectation-Maximization algorithm
-
Slarkin, M. & Excoffier, L. (1996) Testing for linkage disequilibrium in genotypic data using the Expectation-Maximization algorithm. Heredity 76 (Pt 4), 377-83.
-
(1996)
Heredity
, vol.76
, Issue.PART 4
, pp. 377-383
-
-
Slarkin, M.1
Excoffier, L.2
-
30
-
-
0036284203
-
Testing association of statistically inferred haplotypes with discrete and continuous traits in samples of unrelated individuals
-
Zaykin, D. V., Westfall, P. H., Young, S. S., Karnoub, M. A., Wagner, M. J. & Ehm, M. G. (2002) Testing association of statistically inferred haplotypes with discrete and continuous traits in samples of unrelated individuals. Hum Hered 53, 79-91.
-
(2002)
Hum. Hered.
, vol.53
, pp. 79-91
-
-
Zaykin, D.V.1
Westfall, P.H.2
Young, S.S.3
Karnoub, M.A.4
Wagner, M.J.5
Ehm, M.G.6
-
31
-
-
0036918575
-
Haplotype block structure and its applications to association studies: Power and study designs
-
Zhang, K., Calabrese, P., Nordborg, M. & Sun, F. (2002) Haplotype block structure and its applications to association studies: power and study designs. Am J Hum Genet 71, 1386-94.
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 1386-1394
-
-
Zhang, K.1
Calabrese, P.2
Nordborg, M.3
Sun, F.4
-
32
-
-
0033990339
-
Model-free analysis and permutation tests for allelic associations
-
Zhao, J. H., Curtis, D. & Sham, P. C. (2000) Model-free analysis and permutation tests for allelic associations. Hum Hered 50, 133-9.
-
(2000)
Hum. Hered.
, vol.50
, pp. 133-139
-
-
Zhao, J.H.1
Curtis, D.2
Sham, P.C.3
-
33
-
-
0038406155
-
A method for the assessment of disease associations with single-nucleotide polymorphism haplotypes and environmental variables in case-control studies
-
Zhao, L. P., Li, S. S. & Khalid, N. (2003) A method for the assessment of disease associations with single-nucleotide polymorphism haplotypes and environmental variables in case-control studies. Am J Hum Genet 72, 1231-50.
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 1231-1250
-
-
Zhao, L.P.1
Li, S.S.2
Khalid, N.3
|