-
1
-
-
0035849821
-
Genetics group targets disease markers in the human sequence
-
Adam D: Genetics group targets disease markers in the human sequence. Nature 2001; 412: 105.
-
(2001)
Nature
, vol.412
, pp. 105
-
-
Adam, D.1
-
2
-
-
0035458416
-
Racially defined haplotype project debated
-
Robertson D: Racially defined haplotype project debated. Nat Biotechnol 2001; 19: 795-796.
-
(2001)
Nat. Biotechnol
, vol.19
, pp. 795-796
-
-
Robertson, D.1
-
3
-
-
0034795550
-
Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex
-
Jeffreys AJ, Kauppi L, Neumann R: Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex. Nat Genet 2001; 29: 217-222.
-
(2001)
Nat. Genet
, vol.29
, pp. 217-222
-
-
Jeffreys, A.J.1
Kauppi, L.2
Neumann, R.3
-
4
-
-
0034701292
-
High resolution analysis of haplotype diversity and meiotic crossover in the human TAP2 recombination hotspot
-
Jeffreys AJ, Ritchie A, Neumann R: High resolution analysis of haplotype diversity and meiotic crossover in the human TAP2 recombination hotspot. Hum Mol Genet 2000; 9: 725-733.
-
(2000)
Hum. Mol. Genet
, vol.9
, pp. 725-733
-
-
Jeffreys, A.J.1
Ritchie, A.2
Neumann, R.3
-
5
-
-
0034791035
-
High-resolution haplotype structure in the human genome
-
Daly MJ, Rioux JD, Schaffner SP, Hudson TJ, Lander ES: High-resolution haplotype structure in the human genome. Nat Genet 2001; 29: 229-232.
-
(2001)
Nat. Genet
, vol.29
, pp. 229-232
-
-
Daly, M.J.1
Rioux, J.D.2
Schaffner, S.P.3
Hudson, T.J.4
Lander, E.S.5
-
6
-
-
0033930144
-
Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28
-
Taillon-Miller P, Bauer-Sardina I, Saccone NL et al: Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28. Nat Genet 2000; 25: 324-328.
-
(2000)
Nat. Genet
, vol.25
, pp. 324-328
-
-
Taillon-Miller, P.1
Bauer-Sardina, I.2
Saccone, N.L.3
-
7
-
-
0033918564
-
The genetically isolated populations of Finland and Sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes
-
Eaves IA, Merriman TR, Barber RA et al: The genetically isolated populations of Finland and Sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes. Nat Genet 2000; 25: 320-323.
-
(2000)
Nat. Genet
, vol.25
, pp. 320-323
-
-
Eaves, I.A.1
Merriman, T.R.2
Barber, R.A.3
-
8
-
-
0035163547
-
Extent and distribution of linkage disequilibrium in three genomic regions
-
Abecasis GR, Noguchi E, Heinzmann A et al: Extent and distribution of linkage disequilibrium in three genomic regions. Am J Hum Genet 2001; 68: 191-197.
-
(2001)
Am. J. Hum. Genet
, vol.68
, pp. 191-197
-
-
Abecasis, G.R.1
Noguchi, E.2
Heinzmann, A.3
-
9
-
-
0035837267
-
Linkage disequillbrium in the human genome
-
Reich DE, Cargill M, Bolk S et al: Linkage disequillbrium in the human genome. Nature 2001; 411: 199-204.
-
(2001)
Nature
, vol.411
, pp. 199-204
-
-
Reich, D.E.1
Cargill, M.2
Bolk, S.3
-
10
-
-
0034934775
-
Experimentally-derived haplotypes substantially increase the efficiency of linkage disequilibrium studies
-
Douglas JA, Boehnke M, Gillanders E, Trent JM, Gruber SB: Experimentally-derived haplotypes substantially increase the efficiency of linkage disequilibrium studies. Nat Genet 2001; 28: 361-364.
-
(2001)
Nat. Genet
, vol.28
, pp. 361-364
-
-
Douglas, J.A.1
Boehnke, M.2
Gillanders, E.3
Trent, J.M.4
Gruber, S.B.5
-
11
-
-
0029803735
-
Molecular haplotyping of genetic markers 10 kb apart by allele-specific long-range PCR
-
Michalatos-Beloin S, Tishkoff SA, Bentley KL, Kidd KK, Ruano G: Molecular haplotyping of genetic markers 10 kb apart by allele-specific long-range PCR. Nucleic Acids Res 1996; 24: 4841-4843.
-
(1996)
Nucleic Acids Res
, vol.24
, pp. 4841-4843
-
-
Michalatos-Beloin, S.1
Tishkoff, S.A.2
Bentley, K.L.3
Kidd, K.K.4
Ruano, G.5
-
12
-
-
0025269067
-
Inference of haplotypes from PCR-amplified samples of diploid populations
-
Clark AG: Inference of haplotypes from PCR-amplified samples of diploid populations. Mol Biol Evol 1990; 7: 111-122.
-
(1990)
Mol. Biol. Evol
, vol.7
, pp. 111-122
-
-
Clark, A.G.1
-
13
-
-
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
-
14
-
-
0029372419
-
HAPLO: A program using the EM algorithm to estimate the frequencies of multi-site haplotypes
-
Hawley ME, Kidd KK: HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes. J Hered 1995; 86: 409-411.
-
(1995)
J. Hered
, vol.86
, pp. 409-411
-
-
Hawley, M.E.1
Kidd, K.K.2
-
15
-
-
0028913523
-
An E-M algorithm and testing strategy for multiple-locus haplotypes
-
Long JC, Williams RC, Urbanek M: An E-M algorithm and testing strategy for multiple-locus haplotypes. Am J Hum Genet 1995; 56: 799-810.
-
(1995)
Am. J. Hum. Genet
, vol.56
, pp. 799-810
-
-
Long, J.C.1
Williams, R.C.2
Urbanek, M.3
-
16
-
-
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
-
17
-
-
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
-
18
-
-
0033855750
-
The accuracy of statistical methods for estimation of haplotype frequencies: An example from the CD4 locus
-
Tishkoff SA, Pakstis AJ, Ruano G, Kidd KK: The accuracy of statistical methods for estimation of haplotype frequencies: an example from the CD4 locus. Am J Hum Genet 2000; 67: 518-522.
-
(2000)
Am. J. Hum. Genet
, vol.67
, pp. 518-522
-
-
Tishkoff, S.A.1
Pakstis, A.J.2
Ruano, G.3
Kidd, K.K.4
-
19
-
-
0033941023
-
Multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data
-
Douglas JA, Boehnke M, Lange KA: multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data. Am J Hum Genet 2000; 66: 1287-1297.
-
(2000)
Am. J. Hum. Genet
, vol.66
, pp. 1287-1297
-
-
Douglas, J.A.1
Boehnke, M.2
Lange, K.A.3
-
20
-
-
0035131982
-
The impact of genotype error on family-based analysis of quantitative traits
-
Abecasis GR, Cherny SS, Cardon LR: The impact of genotype error on family-based analysis of quantitative traits. Euro J Hum Genet 2001; 9: 130-134.
-
(2001)
Euro. J. Hum. Genet
, vol.9
, pp. 130-134
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cardon, L.R.3
-
21
-
-
0034981387
-
The effect that genotyping errors have on the robustness of common linkage-disequilibrium measures
-
Akey JM, Zhang K, Xiong M, Doris P, Jin L: The effect that genotyping errors have on the robustness of common linkage-disequilibrium measures. Am J Hum Genet 2001; 68: 1447-1456.
-
(2001)
Am. J. Hum. Genet
, vol.68
, pp. 1447-1456
-
-
Akey, J.M.1
Zhang, K.2
Xiong, M.3
Doris, P.4
Jin, L.5
-
22
-
-
0033643184
-
An analytic solution to single nucleotide polymorphism error-detection rates in nuclear families: Implications for study design
-
Gordon D, Leal SM, Heath SC, Ott J: An analytic solution to single nucleotide polymorphism error-detection rates in nuclear families: implications for study design. Pac Symp Biocomput 2000; 663-674.
-
(2000)
Pac. Symp. Biocomput
, pp. 663-674
-
-
Gordon, D.1
Leal, S.M.2
Heath, S.C.3
Ott, J.4
-
23
-
-
0000951097
-
The evolutionary dynamics of complex polymorphisms
-
Lewontin RC, Kojima K: The evolutionary dynamics of complex polymorphisms. Evolution 1960; 14: 450-472.
-
(1960)
Evolution
, vol.14
, pp. 450-472
-
-
Lewontin, R.C.1
Kojima, K.2
-
24
-
-
0036157589
-
Detection and integration of genotyping errors in statistical genetics
-
Sobel E, Papp JC, Lange K: Detection and integration of genotyping errors in statistical genetics. Am J Hum Genet 2002; 70: 496-508.
-
(2002)
Am. J. Hum. Genet
, vol.70
, pp. 496-508
-
-
Sobel, E.1
Papp, J.C.2
Lange, K.3
-
25
-
-
0026563916
-
Systematic detection of errors in genetic linkage data
-
Lincoln SE, Lander ES: Systematic detection of errors in genetic linkage data. Genomics 1992; 14: 604-610.
-
(1992)
Genomics
, vol.14
, pp. 604-610
-
-
Lincoln, S.E.1
Lander, E.S.2
-
26
-
-
0027406460
-
Detecting marker inconsistencies in human gene mapping
-
Ott J: Detecting marker inconsistencies in human gene mapping. Human Heredity 1993; 43: 25-30.
-
(1993)
Human Heredity
, vol.43
, pp. 25-30
-
-
Ott, J.1
-
27
-
-
84966140178
-
Estimation of linkage disequilibrium in randomly mating populations
-
Weir BS, Cockerham CC: Estimation of linkage disequilibrium in randomly mating populations. Heredity 1979; 42: 105-111.
-
(1979)
Heredity
, vol.42
, pp. 105-111
-
-
Weir, B.S.1
Cockerham, C.C.2
-
28
-
-
0000803318
-
Construction of multilocus genetic linkage maps in humans
-
Lander ES, Green P: Construction of multilocus genetic linkage maps in humans. Proc Natl Acad Sci USA 1987; 84: 2363-2367.
-
(1987)
Proc. Natl. Acad. Sci. USA
, vol.84
, pp. 2363-2367
-
-
Lander, E.S.1
Green, P.2
-
29
-
-
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
-
30
-
-
0035865322
-
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
-
Sachidanandam R, Weissman D, Schmidt SC et al: A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature 2001; 409: 928-933.
-
(2001)
Nature
, vol.409
, pp. 928-933
-
-
Sachidanandam, R.1
Weissman, D.2
Schmidt, S.C.3
-
31
-
-
0035065577
-
Single-nucleotide polymorphisms in the public domain: How useful are they?
-
Marth G, Yeh R, Minton M et al: Single-nucleotide polymorphisms in the public domain: how useful are they? Nat Genet 2001; 27: 371-372.
-
(2001)
Nat. Genet
, vol.27
, pp. 371-372
-
-
Marth, G.1
Yeh, R.2
Minton, M.3
-
32
-
-
0032992242
-
True pedigree errors more frequent than apparent errors for single nucleotide polymorphisms
-
Gordon D, Heath SC, Ott J: True pedigree errors more frequent than apparent errors for single nucleotide polymorphisms. Hum Hered 1999; 49: 65-70.
-
(1999)
Hum. Hered
, vol.49
, pp. 65-70
-
-
Gordon, D.1
Heath, S.C.2
Ott, J.3
-
33
-
-
0036154960
-
Probability of detection of genotyping errors and mutations as inheritance inconsistencies in nuclear-family data
-
Douglas JA, Skol AD, Boehnke M: Probability of detection of genotyping errors and mutations as inheritance inconsistencies in nuclear-family data. Am J Hum Genet 2002; 70: 487-495.
-
(2002)
Am. J. Hum. Genet
, vol.70
, pp. 487-495
-
-
Douglas, J.A.1
Skol, A.D.2
Boehnke, M.3
-
34
-
-
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
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