-
1
-
-
0021486666
-
Genetic epidemiology of coronary heart disease: Past, present, and future
-
Carter C, Havlik R, Feinleib M, Kuller LH, Elston R, Rao DC (1984) Genetic epidemiology of coronary heart disease: past, present, and future. Arteriosclerosis 4:510-516
-
(1984)
Arteriosclerosis
, vol.4
, pp. 510-516
-
-
Carter, C.1
Havlik, R.2
Feinleib, M.3
Kuller, L.H.4
Elston, R.5
Rao, D.C.6
-
2
-
-
0025269067
-
Inference of haplotypes from PCR-amplified samples of diploid populations
-
Clark AG (1990) Inference of haplotypes from PCR-amplified samples of diploid populations. Mol Biol Evol 7:111-122
-
(1990)
Mol Biol Evol
, vol.7
, pp. 111-122
-
-
Clark, A.G.1
-
3
-
-
0032231888
-
Haplotype structure and population genetic inferences from nucleotide sequence variation in human lipoprotein lipase
-
Clark AG, Weiss KM, Nickerson DA, Taylor SL, Buchanan A, Stengard J, Salomaa V, et al (1998) Haplotype structure and population genetic inferences from nucleotide sequence variation in human lipoprotein lipase. Am J Hum Genet 63: 595-612
-
(1998)
Am J Hum Genet
, vol.63
, pp. 595-612
-
-
Clark, A.G.1
Weiss, K.M.2
Nickerson, D.A.3
Taylor, S.L.4
Buchanan, A.5
Stengard, J.6
Salomaa, V.7
-
4
-
-
12044258905
-
Intraspecific cladogram estimation: Accuracy at higher levels of divergence
-
Crandall KA (1994) Intraspecific cladogram estimation: accuracy at higher levels of divergence. Syst Biol 43:222-235
-
(1994)
Syst Biol
, vol.43
, pp. 222-235
-
-
Crandall, K.A.1
-
5
-
-
0002437704
-
Applications of intraspecific phylogenetics
-
Harvey P, Brown AJL, Smith JM, Nee S (eds). Oxford University Press, Oxford
-
Crandall KA, Templeton AR (1996) Applications of intraspecific phylogenetics. In: Harvey P, Brown AJL, Smith JM, Nee S (eds) New uses for new phylogenies. Oxford University Press, Oxford, pp 81-99
-
(1996)
New Uses for New Phylogenies
, pp. 81-99
-
-
Crandall, K.A.1
Templeton, A.R.2
-
6
-
-
0000091731
-
Statistical approaches to detecting recombination
-
Johns Hopkins University Press, Baltimore
-
-(1999) Statistical approaches to detecting recombination. In: Crandall KA (ed) The evolution of HIV. Johns Hopkins University Press, Baltimore, pp 153-176
-
(1999)
The Evolution of HIV
, pp. 153-176
-
-
Crandall, K.A.1
-
8
-
-
0031470430
-
Common variation in the lipoprotein lipase gene: Effects on plasma lipids and risk of atherosclerosis
-
Fisher RM, Humphries SE, Talmud PJ (1997) Common variation in the lipoprotein lipase gene: effects on plasma lipids and risk of atherosclerosis. Atherosclerosis 135:145-159
-
(1997)
Atherosclerosis
, vol.135
, pp. 145-159
-
-
Fisher, R.M.1
Humphries, S.E.2
Talmud, P.J.3
-
9
-
-
0029046821
-
The low down on lipoprotein lipase
-
Funke H, Assmann G (1995) The low down on lipoprotein lipase. Nat Genet 10:6-7
-
(1995)
Nat Genet
, vol.10
, pp. 6-7
-
-
Funke, H.1
Assmann, G.2
-
10
-
-
0025299784
-
Reconstructing evolution of sequences subject to recombination using parsimony
-
Hein J (1990) Reconstructing evolution of sequences subject to recombination using parsimony. Math Biosci 98:185-200
-
(1990)
Math Biosci
, vol.98
, pp. 185-200
-
-
Hein, J.1
-
11
-
-
0027471670
-
A heuristic method to reconstruct the history of sequences subject to recombination
-
-(1993) A heuristic method to reconstruct the history of sequences subject to recombination. J Mol Evol 36: 396-405
-
(1993)
J Mol Evol
, vol.36
, pp. 396-405
-
-
-
12
-
-
0031035812
-
A coalescent estimator of the population recombination rate
-
Hey J, Wakeley J (1997) A coalescent estimator of the population recombination rate. Genetics 145:833-846
-
(1997)
Genetics
, vol.145
, pp. 833-846
-
-
Hey, J.1
Wakeley, J.2
-
13
-
-
0023612034
-
Estimating the recombination parameter of a finite population without selection
-
Hudson RR (1987) Estimating the recombination parameter of a finite population without selection. Genet Res 50:245-250
-
(1987)
Genet Res
, vol.50
, pp. 245-250
-
-
Hudson, R.R.1
-
14
-
-
0022211482
-
Statistical properties of the number of recombination events in the history of a sample of DNA sequences
-
Hudson RR, Kaplan NL (1985) Statistical properties of the number of recombination events in the history of a sample of DNA sequences. Genetics 111:147-164
-
(1985)
Genetics
, vol.111
, pp. 147-164
-
-
Hudson, R.R.1
Kaplan, N.L.2
-
15
-
-
0030994945
-
The partition matrix: Exploring variable phylogenetic signals along nucleotide sequence alignments
-
Jakobsen IB, Wilson SR, Easteal S (1997) The partition matrix: exploring variable phylogenetic signals along nucleotide sequence alignments. Mol Biol Evol 14:474-484
-
(1997)
Mol Biol Evol
, vol.14
, pp. 474-484
-
-
Jakobsen, I.B.1
Wilson, S.R.2
Easteal, S.3
-
16
-
-
0026443296
-
Methylation, mutation and cancer
-
Jones PA, Rideout WM, Shen JC, Spruck CH, Tsai YC (1992) Methylation, mutation and cancer. Bioessays 14:33-36
-
(1992)
Bioessays
, vol.14
, pp. 33-36
-
-
Jones, P.A.1
Rideout, W.M.2
Shen, J.C.3
Spruck, C.H.4
Tsai, Y.C.5
-
17
-
-
0031694075
-
Measured haplotype analysis of the Angiotensin-I Converting Enzyme gene
-
Keavney B, McKenzie CA, Connell JMC, Julier C, Ratcliffe PJ, Sobel E, Lathrop M, et al (1998) Measured haplotype analysis of the Angiotensin-I Converting Enzyme gene. Hum Mol Genet 7:1745-1751
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1745-1751
-
-
Keavney, B.1
McKenzie, C.A.2
Connell, J.M.C.3
Julier, C.4
Ratcliffe, P.J.5
Sobel, E.6
Lathrop, M.7
-
18
-
-
0025762012
-
Gene deletions causing human genetic disease: Mechanisms of mutagenesis and the role of the local DNA sequence environment
-
Krawczak M, Cooper DN (1991) Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment. Hum Genet 86: 425-441
-
(1991)
Hum Genet
, vol.86
, pp. 425-441
-
-
Krawczak, M.1
Cooper, D.N.2
-
19
-
-
0029029525
-
The mutational demography of protein C deficiency
-
Krawczak M, Reitsma PH, Cooper DN (1995) The mutational demography of protein C deficiency. Hum Genet 96: 142-146
-
(1995)
Hum Genet
, vol.96
, pp. 142-146
-
-
Krawczak, M.1
Reitsma, P.H.2
Cooper, D.N.3
-
20
-
-
0031747186
-
Two sites in the delta gene region contribute to naturally occurring variation in bristle number in Drosophila melanogaster
-
Long AD, Lyman RF, Langley CH, Mackay TFC (1998) Two sites in the delta gene region contribute to naturally occurring variation in bristle number in Drosophila melanogaster. Genetics 149:999-1017
-
(1998)
Genetics
, vol.149
, pp. 999-1017
-
-
Long, A.D.1
Lyman, R.F.2
Langley, C.H.3
Mackay, T.F.C.4
-
21
-
-
0031746544
-
Candidate quantitative trait loci and naturally occurring phenotypic variation for bristle number in Drosophila melanogaster - The Delta-Hairless gene region
-
Lyman RF, Mackay TFC (1998) Candidate quantitative trait loci and naturally occurring phenotypic variation for bristle number in Drosophila melanogaster - the Delta-Hairless gene region. Genetics 149:983-998
-
(1998)
Genetics
, vol.149
, pp. 983-998
-
-
Lyman, R.F.1
Mackay, T.F.C.2
-
23
-
-
0028333951
-
Ubiquitous and tenacious methylation of the CpG site in codon 248 of the p53 gene may explain its frequent appearance as a mutational hot spot in human cancer
-
Magewu AN, Jones PA (1994) Ubiquitous and tenacious methylation of the CpG site in codon 248 of the p53 gene may explain its frequent appearance as a mutational hot spot in human cancer. Mol Cell Biol 14:4225-4232
-
(1994)
Mol Cell Biol
, vol.14
, pp. 4225-4232
-
-
Magewu, A.N.1
Jones, P.A.2
-
25
-
-
0031662147
-
Nine novel germline mutations of Stk11 in ten families with Peutz-Jeghers syndrome
-
Nakagawa H, Koyama K, Miyoshi Y, Ando H, Baba S, Watatani M, Yasutomi M, et al (1998) Nine novel germline mutations of Stk11 in ten families with Peutz-Jeghers syndrome. Hum Genet 103:168-172
-
(1998)
Hum Genet
, vol.103
, pp. 168-172
-
-
Nakagawa, H.1
Koyama, K.2
Miyoshi, Y.3
Ando, H.4
Baba, S.5
Watatani, M.6
Yasutomi, M.7
-
26
-
-
17344364213
-
DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene
-
Nickerson DA, Taylor SL, Weiss KM, Clark AG, Hutchinson RG, Stengard J, Salomaa V, et al (1998) DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene. Nat Genet 19:233-240
-
(1998)
Nat Genet
, vol.19
, pp. 233-240
-
-
Nickerson, D.A.1
Taylor, S.L.2
Weiss, K.M.3
Clark, A.G.4
Hutchinson, R.G.5
Stengard, J.6
Salomaa, V.7
-
27
-
-
0025775435
-
Discrimination between recurrent mutation and identity by descent: Application to point mutations in exon 11 of the cystic fibrosis (CFTR) gene
-
Reiss J, Cooper DN, Bal J, Slomski R, Cutting GR, Krawczak M (1991) Discrimination between recurrent mutation and identity by descent: application to point mutations in exon 11 of the cystic fibrosis (CFTR) gene. Hum Genet 87: 457-461
-
(1991)
Hum Genet
, vol.87
, pp. 457-461
-
-
Reiss, J.1
Cooper, D.N.2
Bal, J.3
Slomski, R.4
Cutting, G.R.5
Krawczak, M.6
-
28
-
-
0025145277
-
5-Methylcytosine as an endogenous mutagen in the human LDL receptor and p53 gene
-
Rideout WM III, Coetzee GA, Olumi AF, Jones PA (1990) 5-Methylcytosine as an endogenous mutagen in the human LDL receptor and p53 gene. Science 249:1288-1290
-
(1990)
Science
, vol.249
, pp. 1288-1290
-
-
Rideout W.M. III1
Coetzee, G.A.2
Olumi, A.F.3
Jones, P.A.4
-
31
-
-
0030960257
-
DnaSP, version 2.0: A novel software package for extensive molecular population genetics analysis
-
Rozas J, Rozas R (1997) DnaSP, version 2.0: a novel software package for extensive molecular population genetics analysis. Comput Appl Biosci 13:307-311
-
(1997)
Comput Appl Biosci
, vol.13
, pp. 307-311
-
-
Rozas, J.1
Rozas, R.2
-
32
-
-
0031981810
-
Involvement of DNA methylation in human carcinogenesis
-
Schmutte C, Jones PA (1998) Involvement of DNA methylation in human carcinogenesis. Biol Chem 379:377-388
-
(1998)
Biol Chem
, vol.379
, pp. 377-388
-
-
Schmutte, C.1
Jones, P.A.2
-
33
-
-
0003019031
-
Alternative genetic strategies for predicting risk of atherosclerosis
-
Woodford FP, Davignon J, Sniderman AD (eds) Elsevier Science Publishers, Amsterdam
-
Sing CF, Haviland MB, Templeton AR, Reilly SL (1995) Alternative genetic strategies for predicting risk of atherosclerosis. In: Woodford FP, Davignon J, Sniderman AD (eds) Atherosclerosis X. Excerpta Medica International Congress Series. Elsevier Science Publishers, Amsterdam, pp 638-644
-
(1995)
Atherosclerosis X. Excerpta Medica International Congress Series
, pp. 638-644
-
-
Sing, C.F.1
Haviland, M.B.2
Templeton, A.R.3
Reilly, S.L.4
-
34
-
-
0008529861
-
Genetic analysis of common diseases: Applications to predictive factors in coronary disease
-
Alan R. Liss, New York
-
Sing CF, Skolnick M (eds) (1979) Genetic analysis of common diseases: applications to predictive factors in coronary disease. Progress in Clinical and Biological Research, Vol 32. Alan R. Liss, New York
-
(1979)
Progress in Clinical and Biological Research
, vol.32
-
-
Sing, C.F.1
Skolnick, M.2
-
36
-
-
0021084212
-
Phylogenetic inference from restriction endonuclease cleavage site maps with particular reference to the evolution of humans and the apes
-
Templeton AR (1983) Phylogenetic inference from restriction endonuclease cleavage site maps with particular reference to the evolution of humans and the apes. Evolution 37:221-244
-
(1983)
Evolution
, vol.37
, pp. 221-244
-
-
Templeton, A.R.1
-
37
-
-
0023338893
-
Nonparametric phylogenetic inference from restriction cleavage sites
-
-(1987) Nonparametric phylogenetic inference from restriction cleavage sites. Mol Biol Evol 4:315-319
-
(1987)
Mol Biol Evol
, vol.4
, pp. 315-319
-
-
-
38
-
-
0029683026
-
Cladistic approaches to identifying determinants of variability in multifactorial phenotypes and the evolutionary significance of variation in the human genome
-
Cardew G (ed). John Wiley & Sons, Chichester, England
-
-(1996) Cladistic approaches to identifying determinants of variability in multifactorial phenotypes and the evolutionary significance of variation in the human genome. In: Cardew G (ed) Variation in the human genome. John Wiley & Sons, Chichester, England, pp 259-283
-
(1996)
Variation in the Human Genome
, pp. 259-283
-
-
-
39
-
-
0023425198
-
A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping. I. Basic theory and an analysis of alcohol dehydrogenase activity in Drosophila
-
Templeton AR, Boerwinkle E, Sing CF (1987) A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping. I. Basic theory and an analysis of alcohol dehydrogenase activity in Drosophila. Genetics 117:343-351
-
(1987)
Genetics
, vol.117
, pp. 343-351
-
-
Templeton, A.R.1
Boerwinkle, E.2
Sing, C.F.3
-
40
-
-
0026662698
-
A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping and DNA sequence data. III. Cladogram estimation
-
Templeton AR, Crandall KA, Sing CF (1992) A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping and DNA sequence data. III. Cladogram estimation. Genetics 132:619-633
-
(1992)
Genetics
, vol.132
, pp. 619-633
-
-
Templeton, A.R.1
Crandall, K.A.2
Sing, C.F.3
-
41
-
-
0027278852
-
A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping. IV. Nested analyses with cladogram uncertainty and recombination
-
Templeton AR, Sing CF (1993) A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping. IV. Nested analyses with cladogram uncertainty and recombination. Genetics 134: 659-669
-
(1993)
Genetics
, vol.134
, pp. 659-669
-
-
Templeton, A.R.1
Sing, C.F.2
-
42
-
-
0030991489
-
Large majority of single-nucleotide mutations along the dystrophin gene can be explained by more than one mechanism of mutagenesis
-
Todorova A, Danieli GA (1997) Large majority of single-nucleotide mutations along the dystrophin gene can be explained by more than one mechanism of mutagenesis. Hum Mutat 9:537-547
-
(1997)
Hum Mutat
, vol.9
, pp. 537-547
-
-
Todorova, A.1
Danieli, G.A.2
-
43
-
-
0028298802
-
Myocardial infarction and coronary deaths in the World Health Organization MONICA project: Registration procedures, event rates, and case-fatality rates in 38 populations from 21 countries in four continents
-
Tunstall-Pedoe H, Kuulasmaa K, Amouyel P, Arveiler D, Rajakangas AM, Pajak A (1994) Myocardial infarction and coronary deaths in the World Health Organization MONICA project: registration procedures, event rates, and case-fatality rates in 38 populations from 21 countries in four continents. Circulation 90:583-612
-
(1994)
Circulation
, vol.90
, pp. 583-612
-
-
Tunstall-Pedoe, H.1
Kuulasmaa, K.2
Amouyel, P.3
Arveiler, D.4
Rajakangas, A.M.5
Pajak, A.6
-
44
-
-
0031656123
-
Molecular characterization of two deletion events involving Alu-sequences, one novel base substitution and two tentative hotspot mutations in the hypoxanthine phosphoribosyltransferase (HPRT) gene in five patients with Lesch-Nyhan syndrome
-
Tvrdik T, Marcus S, Hou SM, Falt S, Noori P, Podlutskaja N, Hanefeld F, et al (1998) Molecular characterization of two deletion events involving Alu-sequences, one novel base substitution and two tentative hotspot mutations in the hypoxanthine phosphoribosyltransferase (HPRT) gene in five patients with Lesch-Nyhan syndrome. Hum Genet 103:311-318
-
(1998)
Hum Genet
, vol.103
, pp. 311-318
-
-
Tvrdik, T.1
Marcus, S.2
Hou, S.M.3
Falt, S.4
Noori, P.5
Podlutskaja, N.6
Hanefeld, F.7
-
45
-
-
0026046333
-
African populations and the evolution of human mitochondrial DNA
-
Vigilant L, Stoneking M, Harpending H, Hawkes K, Wilson AC (1991) African populations and the evolution of human mitochondrial DNA. Science 253:1503-1507
-
(1991)
Science
, vol.253
, pp. 1503-1507
-
-
Vigilant, L.1
Stoneking, M.2
Harpending, H.3
Hawkes, K.4
Wilson, A.C.5
-
47
-
-
0029927415
-
The rate of CpG mutation in Alu repetitive elements within the p53 tumor suppressor gene in the primate germline
-
Yang AS, Gonzalgo ML, Zingg JM, Millar RP, Buckley JD, Jones PA (1996) The rate of CpG mutation in Alu repetitive elements within the p53 tumor suppressor gene in the primate germline. J Mol Biol 258:240-250
-
(1996)
J Mol Biol
, vol.258
, pp. 240-250
-
-
Yang, A.S.1
Gonzalgo, M.L.2
Zingg, J.M.3
Millar, R.P.4
Buckley, J.D.5
Jones, P.A.6
|