-
1
-
-
0036338150
-
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR. 2002. Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 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
-
2
-
-
0033362231
-
Direct power comparisons between simple LOD scores and NPL scores for linkage analysis in complex diseases
-
Abreu PC, Greenberg DA, Hodge SE. 1999. Direct power comparisons between simple LOD scores and NPL scores for linkage analysis in complex diseases. Am J Hum Genet 65:847-857.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 847-857
-
-
Abreu, P.C.1
Greenberg, D.A.2
Hodge, S.E.3
-
3
-
-
0033358545
-
Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure
-
Allison DB, Neale MC, Zannolli R, Schork NJ, Amos CI, Blangero J. 1999. Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure. Am J Hum Genet 65:531-544.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 531-544
-
-
Allison, D.B.1
Neale, M.C.2
Zannolli, R.3
Schork, N.J.4
Amos, C.I.5
Blangero, J.6
-
4
-
-
0031966959
-
Multipoint quantitative trait linkage analysis in general pedigrees
-
Almasy L, Blangero J. 1998. Multipoint quantitative trait linkage analysis in general pedigrees. Am J Hum Genet 62:1198-1211.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1198-1211
-
-
Almasy, L.1
Blangero, J.2
-
5
-
-
0034758045
-
Genomewide scans of complex human diseases: True linkage is hard to find
-
Altmuller J, Palmer LJ, Fischer G, Scherb H, Wjst M. 2001. Genomewide scans of complex human diseases: true linkage is hard to find. Am J Hum Genet 69:936-950.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 936-950
-
-
Altmuller, J.1
Palmer, L.J.2
Fischer, G.3
Scherb, H.4
Wjst, M.5
-
6
-
-
0037308728
-
Limits of fine-mapping a quantitative trait
-
Atwood LD, Heard-Costa NL. 2003. Limits of fine-mapping a quantitative trait. Genet Epidemiol 24:99-106.
-
(2003)
Genet Epidemiol
, vol.24
, pp. 99-106
-
-
Atwood, L.D.1
Heard-Costa, N.L.2
-
7
-
-
30344450278
-
The role of parametric linkage methods in complex trait analyses using microsatellites
-
Badzioch MD, Goode EL, Jarvik GP. 2005. The role of parametric linkage methods in complex trait analyses using microsatellites. BMC Genet 30(Suppl. 1):S48.
-
(2005)
BMC Genet
, vol.30
, Issue.SUPPL. 1
-
-
Badzioch, M.D.1
Goode, E.L.2
Jarvik, G.P.3
-
9
-
-
11144290045
-
Simultaneous localization of two linked disease susceptibility genes
-
Biernacka JM, Sun L, Bull SB. 2005. Simultaneous localization of two linked disease susceptibility genes. Genet Epidemiol 28:33-47.
-
(2005)
Genet Epidemiol
, vol.28
, pp. 33-47
-
-
Biernacka, J.M.1
Sun, L.2
Bull, S.B.3
-
10
-
-
34248682654
-
Linkage analysis of the simulated data - evaluations and comparisons of methods
-
Biswas S, Papachristou C, Irwin ME, Lin S. 2003. Linkage analysis of the simulated data - evaluations and comparisons of methods. BMC Genet 4(Suppl. 1):S70.
-
(2003)
BMC Genet
, vol.4
, Issue.SUPPL. 1
-
-
Biswas, S.1
Papachristou, C.2
Irwin, M.E.3
Lin, S.4
-
11
-
-
22044455177
-
A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia
-
Cader MZ, Steckley JL, Dyment DA, McLachlan RS, Ebers GC. 2005. A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia. Neurology 65:156-158.
-
(2005)
Neurology
, vol.65
, pp. 156-158
-
-
Cader, M.Z.1
Steckley, J.L.2
Dyment, D.A.3
McLachlan, R.S.4
Ebers, G.C.5
-
13
-
-
0015183542
-
A general model for the genetic analysis of pedigree data
-
Elston RC, Stewart J. 1971. A general model for the genetic analysis of pedigree data. Hum Hered 21:523-542.
-
(1971)
Hum Hered
, vol.21
, pp. 523-542
-
-
Elston, R.C.1
Stewart, J.2
-
14
-
-
0033925884
-
Composite statistics for QTL mapping with moderately discordant sibling pairs
-
Forrest WF, Feingold E. 2000. Composite statistics for QTL mapping with moderately discordant sibling pairs. Am J Hum Genet 66:1642-1660.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1642-1660
-
-
Forrest, W.F.1
Feingold, E.2
-
16
-
-
24144469193
-
Genome scan for quantitative trait loci influencing HDL levels: Evidence for multilocus inheritance in familial combined hyperlipidemia
-
Gagnon F, Jarvik GP, Badzioch MD, Motulsky AG, Brunzell JD, Wijsman EM. 2005. Genome scan for quantitative trait loci influencing HDL levels: evidence for multilocus inheritance in familial combined hyperlipidemia. Hum Genet 117:494-505.
-
(2005)
Hum Genet
, vol.117
, pp. 494-505
-
-
Gagnon, F.1
Jarvik, G.P.2
Badzioch, M.D.3
Motulsky, A.G.4
Brunzell, J.D.5
Wijsman, E.M.6
-
18
-
-
21044459378
-
MCMC multilocus lod scores: Application of a new approach
-
George AW, Wijsman EM, Thompson EA. 2005. MCMC multilocus lod scores: application of a new approach. Hum Hered 59:98-108.
-
(2005)
Hum Hered
, vol.59
, pp. 98-108
-
-
George, A.W.1
Wijsman, E.M.2
Thompson, E.A.3
-
19
-
-
0037146578
-
Finding genes that underlie complex traits
-
Glazier AM, Nadeau JH, Aitman TJ. 2002. Finding genes that underlie complex traits. Science 298:2345-2349.
-
(2002)
Science
, vol.298
, pp. 2345-2349
-
-
Glazier, A.M.1
Nadeau, J.H.2
Aitman, T.J.3
-
20
-
-
0032231937
-
The power to detect linkage in complex disease by means of simple LOD-score analyses
-
Greenberg DA, Abreu P, Hodge SE. 1998. The power to detect linkage in complex disease by means of simple LOD-score analyses. Am J Hum Genet 63:870-879.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 870-879
-
-
Greenberg, D.A.1
Abreu, P.2
Hodge, S.E.3
-
21
-
-
0034098774
-
Allegro, a new computer program for multipoint linkage analysis
-
Gudbjartsson DF, Jonasson K, Frigge M, Kong A. 2000. Allegro, a new computer program for multipoint linkage analysis. Nat Genet 25:12-13.
-
(2000)
Nat Genet
, vol.25
, pp. 12-13
-
-
Gudbjartsson, D.F.1
Jonasson, K.2
Frigge, M.3
Kong, A.4
-
23
-
-
0019996201
-
A mixed model likelihood approximation for large pedigrees
-
Hasstedt SJ. 1982. A mixed model likelihood approximation for large pedigrees. Comput Biomed Res 15:295-307.
-
(1982)
Comput Biomed Res
, vol.15
, pp. 295-307
-
-
Hasstedt, S.J.1
-
24
-
-
0030833349
-
Markov chain Monte Carlo segregation and Linkage analysis for oligogenic models
-
Heath SC. 1997. Markov chain Monte Carlo segregation and Linkage analysis for oligogenic models. Am J Hum Genet 61:748-760.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 748-760
-
-
Heath, S.C.1
-
25
-
-
0017288665
-
A simple method for computing the inverse of a numerator relationship matrix used in prediction of breeding values
-
Henderson CR. 1976. A simple method for computing the inverse of a numerator relationship matrix used in prediction of breeding values. Biometrics 32:69-83.
-
(1976)
Biometrics
, vol.32
, pp. 69-83
-
-
Henderson, C.R.1
-
26
-
-
13444306425
-
Mapping of psoriasis to 17q terminus
-
Hwu WL, Yang CF, Fann CS, Chen CL, Tsai TF, Chien YH, Chiang SC, Chen CH, Hung SI, Wu JY, Chen YT. 2005. Mapping of psoriasis to 17q terminus. J Med Genet 42:152-158.
-
(2005)
J Med Genet
, vol.42
, pp. 152-158
-
-
Hwu, W.L.1
Yang, C.F.2
Fann, C.S.3
Chen, C.L.4
Tsai, T.F.5
Chien, Y.H.6
Chiang, S.C.7
Chen, C.H.8
Hung, S.I.9
Wu, J.Y.10
Chen, Y.T.11
-
27
-
-
30344454660
-
Genomewide scan for real-word reading subphenotypes of dyslexia: Novel chromosome 13 locus and genetic complexity
-
Igo RP Jr, Chapman NH, Berninger VW, Matsushita M, Brkanac Z, Rothstein JH, Holzman T, Nielsen K, Raskind WH, Wijsman EM. 2006. Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity. Am J Med Genet B Neuropsychiatr Genet 141:15-27.
-
(2006)
Am J Med Genet B Neuropsychiatr Genet
, vol.141
, pp. 15-27
-
-
Igo Jr, R.P.1
Chapman, N.H.2
Berninger, V.W.3
Matsushita, M.4
Brkanac, Z.5
Rothstein, J.H.6
Holzman, T.7
Nielsen, K.8
Raskind, W.H.9
Wijsman, E.M.10
-
28
-
-
0030305457
-
R: Language for data analysis and graphics
-
Stat
-
Ihaka R, Gentleman R. 1996. R: language for data analysis and graphics. J Comput Graph Stat 5:299-314.
-
(1996)
J Comput Graph
, vol.5
, pp. 299-314
-
-
Ihaka, R.1
Gentleman, R.2
-
29
-
-
0028030120
-
Two-locus disease models with two marker loci: The power of affected-sib-pair tests
-
Knapp M, Seuchter SA, Baur MP. 1994. Two-locus disease models with two marker loci: the power of affected-sib-pair tests. Am J Hum Genet 55:1030-1041.
-
(1994)
Am J Hum Genet
, vol.55
, pp. 1030-1041
-
-
Knapp, M.1
Seuchter, S.A.2
Baur, M.P.3
-
30
-
-
0029886532
-
Parametric and non-parametric linkage analysis: Unified multipoint approach
-
Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES. 1996. Parametric and non-parametric linkage analysis: unified multipoint approach. Am J Hum Genet 58:1347-1363.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1347-1363
-
-
Kruglyak, L.1
Daly, M.J.2
Reeve-Daly, M.P.3
Lander, E.S.4
-
31
-
-
0000803318
-
Construction of multilocus linkage maps in humans
-
Lander ES, Green P. 1987. Construction of multilocus linkage maps in humans. Proc Natl Acad Sci USA 84:2363-2367.
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 2363-2367
-
-
Lander, E.S.1
Green, P.2
-
32
-
-
0026329112
-
A random walk method for computing genetic location scores
-
Lange K, Sobel E. 1991. A random walk method for computing genetic location scores. Am J Hum Genet 49:1320-1334.
-
(1991)
Am J Hum Genet
, vol.49
, pp. 1320-1334
-
-
Lange, K.1
Sobel, E.2
-
33
-
-
0021344005
-
Easy calculations of lod scores and genetic risks on small computers
-
Lathrop GM, Lalouel JM. 1984. Easy calculations of lod scores and genetic risks on small computers. Am J Hum Genet 36:460-465.
-
(1984)
Am J Hum Genet
, vol.36
, pp. 460-465
-
-
Lathrop, G.M.1
Lalouel, J.M.2
-
34
-
-
0000827658
-
Analysis of complex diseases under oligogenic models and intrafamilial heterogeneity by the LINKAGE programs
-
Lathrop GM, Ott J. 1990. Analysis of complex diseases under oligogenic models and intrafamilial heterogeneity by the LINKAGE programs. Am J Hum Genet 47(Suppl.):A188.
-
(1990)
Am J Hum Genet
, vol.47
, Issue.SUPPL.
-
-
Lathrop, G.M.1
Ott, J.2
-
35
-
-
0034473857
-
Monte Carlo methods for linkage analysis of two-locus disease models
-
Lin S. 2000. Monte Carlo methods for linkage analysis of two-locus disease models. Ann Hum Genet 64:519-532.
-
(2000)
Ann Hum Genet
, vol.64
, pp. 519-532
-
-
Lin, S.1
-
36
-
-
0029611014
-
Simulation of a common oligogenic disease with quantitative risk factors. GAW9 problem 2: The answers
-
MacCluer JW, Blangero J, Dyer TD, Kammerer CM. 1995. Simulation of a common oligogenic disease with quantitative risk factors. GAW9 problem 2: the answers. Genet Epidemiol 12:707-712.
-
(1995)
Genet Epidemiol
, vol.12
, pp. 707-712
-
-
MacCluer, J.W.1
Blangero, J.2
Dyer, T.D.3
Kammerer, C.M.4
-
37
-
-
15944368228
-
The power to detect genetic linkage for quantitative traits in the Utah CEPH pedigrees
-
Malhotra A, Cromer K, Leppert MF, Hasstedt SJ. 2005. The power to detect genetic linkage for quantitative traits in the Utah CEPH pedigrees. J Hum Genet 50:69-75.
-
(2005)
J Hum Genet
, vol.50
, pp. 69-75
-
-
Malhotra, A.1
Cromer, K.2
Leppert, M.F.3
Hasstedt, S.J.4
-
38
-
-
0035071608
-
Efficient multipoint linkage analysis through reduction of inheritance space
-
Markianos K, Daly MJ, Kruglyak L. 2001. Efficient multipoint linkage analysis through reduction of inheritance space. Am J Hum Genet 68:963-977.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 963-977
-
-
Markianos, K.1
Daly, M.J.2
Kruglyak, L.3
-
39
-
-
0028790963
-
The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype and set-recoding and fuzzy inheritance
-
O'Connell JR, Weeks DE. 1995. The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype and set-recoding and fuzzy inheritance. Nat Genet 11:402-408.
-
(1995)
Nat Genet
, vol.11
, pp. 402-408
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
40
-
-
0035095150
-
Rapid multipoint linkage analysis via inheritance vectors in the Elston-Stewart algorithm
-
O'Connell JR. 2001. Rapid multipoint linkage analysis via inheritance vectors in the Elston-Stewart algorithm. Hum Hered 51:226-240.
-
(2001)
Hum Hered
, vol.51
, pp. 226-240
-
-
O'Connell, J.R.1
-
41
-
-
24644469037
-
New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1
-
Orlacchio A, Kawarai T, Gaudiello F, St George-Hyslop PH, Floris R, Bernardi G. 2005. New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1. Ann Neurol 58:423-429.
-
(2005)
Ann Neurol
, vol.58
, pp. 423-429
-
-
Orlacchio, A.1
Kawarai, T.2
Gaudiello, F.3
St George-Hyslop, P.H.4
Floris, R.5
Bernardi, G.6
-
42
-
-
0016302483
-
Estimation of the recombination fraction in human pedigrees: Efficient computation of the likelihood for human linkage studies
-
Ott J. 1974. Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies. Am J Hum Genet 26:588-597.
-
(1974)
Am J Hum Genet
, vol.26
, pp. 588-597
-
-
Ott, J.1
-
43
-
-
0017027786
-
Computing the diagonal elements and inverse of a large numerator relationship matrix
-
Quaas RL. 1976. Computing the diagonal elements and inverse of a large numerator relationship matrix. Biometrics 32: 949-953.
-
(1976)
Biometrics
, vol.32
, pp. 949-953
-
-
Quaas, R.L.1
-
45
-
-
0020132583
-
Batch size effects in the analysis of simulation output
-
Schmeiser B. 1982. Batch size effects in the analysis of simulation output. Oper Res 30:556-568.
-
(1982)
Oper Res
, vol.30
, pp. 556-568
-
-
Schmeiser, B.1
-
46
-
-
0027430716
-
Two-trait-locus linkage analysis: A powerful strategy for mapping complex genetic traits
-
Schork NJ, Boehnke M, Terwilliger JD, Ott J. 1993. Two-trait-locus linkage analysis: a powerful strategy for mapping complex genetic traits. Am J Hum Genet 53:1127-1136.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 1127-1136
-
-
Schork, N.J.1
Boehnke, M.2
Terwilliger, J.D.3
Ott, J.4
-
47
-
-
0033911219
-
Power comparison of parametric and nonparametric linkage tests in small pedigrees
-
Sham PC, Lin MW, Zhao JH, Curtis D. 2000. Power comparison of parametric and nonparametric linkage tests in small pedigrees. Am J Hum Genet 66:1661-1668.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1661-1668
-
-
Sham, P.C.1
Lin, M.W.2
Zhao, J.H.3
Curtis, D.4
-
48
-
-
30344457465
-
Comparison of marker types and map assumptions using Markov chain Monte Carlo-based linkage analysis of COGA data
-
Sieh W, Basu S, Fu AQ, Rothstein JH, Scheet PA, Stewart WC, Sung YJ, Thompson EA, Wijsman EM. 2005. Comparison of marker types and map assumptions using Markov chain Monte Carlo-based linkage analysis of COGA data. BMC Genet 6(Suppl. 1):S11.
-
(2005)
BMC Genet
, vol.6
, Issue.SUPPL. 1
-
-
Sieh, W.1
Basu, S.2
Fu, A.Q.3
Rothstein, J.H.4
Scheet, P.A.5
Stewart, W.C.6
Sung, Y.J.7
Thompson, E.A.8
Wijsman, E.M.9
-
49
-
-
0029945706
-
Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics
-
Sobel E, Lange K. 1996. Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics. Am J Hum Genet 58:1323-1337.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
-
50
-
-
0033911385
-
Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: Application to mite sensitization
-
Strauch K, Fimmers R, Kurz T, Deichmann KA, Wienker TF, Baur MP. 2000. Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization. Am J Hum Genet 66:1945-1957.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1945-1957
-
-
Strauch, K.1
Fimmers, R.2
Kurz, T.3
Deichmann, K.A.4
Wienker, T.F.5
Baur, M.P.6
-
51
-
-
1642588402
-
How to model a complex trait. 2. Analysis with two disease loci
-
Strauch K, Fimmers R, Baur MP, Wienker TF. 2003. How to model a complex trait. 2. Analysis with two disease loci. Hum Hered 56:200-211.
-
(2003)
Hum Hered
, vol.56
, pp. 200-211
-
-
Strauch, K.1
Fimmers, R.2
Baur, M.P.3
Wienker, T.F.4
-
52
-
-
33846407807
-
Accounting for Epistasis in Linkage Analysis of General Pedigrees
-
In press
-
Sung YJ, Wijsman EM. 2007. Accounting for Epistasis in Linkage Analysis of General Pedigrees. Hum Hered, In press.
-
(2007)
Hum Hered
-
-
Sung, Y.J.1
Wijsman, E.M.2
-
54
-
-
33846444186
-
-
Thompson EA. 2005. Chapter 4: MCMC in the analysis of genetic data on pedigrees. In: Liang F, Wang J-S, Kendall W, editors. Lecture Note Series of the IMS, National University of Singapore. Singapore: World Scientific Co Pvt. Ltd. p 183-216.
-
Thompson EA. 2005. Chapter 4: MCMC in the analysis of genetic data on pedigrees. In: Liang F, Wang J-S, Kendall W, editors. Lecture Note Series of the IMS, National University of Singapore. Singapore: World Scientific Co Pvt. Ltd. p 183-216.
-
-
-
-
56
-
-
0002531916
-
Estimation of conditional multilocus gene identity among relatives
-
Statistics in Molecular Biology and Genetics: Selected Proceedings of a 1997 Joint AMS-IMS-SIAM Summer Conference on Statistics in Molecular Biology
-
Thompson EA, Heath SC. 1999. Estimation of conditional multilocus gene identity among relatives. Statistics in Molecular Biology and Genetics: Selected Proceedings of a 1997 Joint AMS-IMS-SIAM Summer Conference on Statistics in Molecular Biology, IMS Lecture Note-Monograph Series 33, p 95-113.
-
(1999)
IMS Lecture Note-Monograph Series
, vol.33
, pp. 95-113
-
-
Thompson, E.A.1
Heath, S.C.2
-
57
-
-
0031469587
-
Genetic analysis of simulated oligogenic traits in nuclear and extended pedigrees: Summary of GAW10 contributions
-
Wijsman EM, Amos CI. 1997. Genetic analysis of simulated oligogenic traits in nuclear and extended pedigrees: summary of GAW10 contributions. Genet Epidemiol 14:719-735.
-
(1997)
Genet Epidemiol
, vol.14
, pp. 719-735
-
-
Wijsman, E.M.1
Amos, C.I.2
|