-
1
-
-
0033601201
-
Linkage disequilibrium and recombination in hominid mitochondrial DNA
-
Awadalla, P., Eyre-Walker, A., and Maynard Smith, J. 1999. Linkage disequilibrium and recombination in hominid mitochondrial DNA. Science 286: 2524-2525.
-
(1999)
Science
, vol.286
, pp. 2524-2525
-
-
Awadalla, P.1
Eyre-Walker, A.2
Maynard Smith, J.3
-
2
-
-
33745279056
-
Evaluating coverage of genome-wide association studies
-
Barrett, J.C. and Cardon, L.R. 2006. Evaluating coverage of genome-wide association studies. Nat. Genet. 38: 659-662.
-
(2006)
Nat. Genet
, vol.38
, pp. 659-662
-
-
Barrett, J.C.1
Cardon, L.R.2
-
3
-
-
33750471977
-
Transferability of tag SNPs in genetic association studies in multiple populations
-
de Bakker, P.I.W., Burtt, N.P., Graham, R.R., Cuiducci, C., Yelensky, R., Drake, J.A., Bersaglieri, T., Penney, K.L., Butler, J., Young, S., et al. 2006. Transferability of tag SNPs in genetic association studies in multiple populations. Nat. Genet. 38: 1298-1303.
-
(2006)
Nat. Genet
, vol.38
, pp. 1298-1303
-
-
de Bakker, P.I.W.1
Burtt, N.P.2
Graham, R.R.3
Cuiducci, C.4
Yelensky, R.5
Drake, J.A.6
Bersaglieri, T.7
Penney, K.L.8
Butler, J.9
Young, S.10
-
4
-
-
33846617194
-
A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation
-
Duffy, D.L., Montgomery, G.W., Chen, W., Zhao, Z.Z., Le, L., James, M.R., Hayward, N.K., Martin, N.G., and Sturm, R.A. 2007. A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation. Am. J. Hum. Genet. 80: 241-252.
-
(2007)
Am. J. Hum. Genet
, vol.80
, pp. 241-252
-
-
Duffy, D.L.1
Montgomery, G.W.2
Chen, W.3
Zhao, Z.Z.4
Le, L.5
James, M.R.6
Hayward, N.K.7
Martin, N.G.8
Sturm, R.A.9
-
5
-
-
33846625058
-
Associating mitochondrial DNA variation with complex traits
-
Elson, J.L., Majamaa, K., Howell, N., and Chinnery, P.F. 2007. Associating mitochondrial DNA variation with complex traits. Am. J. Hum. Genet. 80: 378-382.
-
(2007)
Am. J. Hum. Genet
, vol.80
, pp. 378-382
-
-
Elson, J.L.1
Majamaa, K.2
Howell, N.3
Chinnery, P.F.4
-
6
-
-
0034817685
-
Does human mtDNA recombine?
-
Eyre-Walker, A. and Awadalla, P. 2001. Does human mtDNA recombine? J. Mol. Evol. 53: 430-435.
-
(2001)
J. Mol. Evol
, vol.53
, pp. 430-435
-
-
Eyre-Walker, A.1
Awadalla, P.2
-
7
-
-
0002386913
-
2 from contingency tables, and the calculation of P
-
2 from contingency tables, and the calculation of P. J. R. Stat. Soc. [Ser A] 85: 87-94.
-
(1922)
J. R. Stat. Soc. [Ser A]
, vol.85
, pp. 87-94
-
-
Fisher, R.A.1
-
8
-
-
0028298036
-
Maximum-likelihood estimation of gene location by linkage disequilibrium
-
Hill, W.G. and Weir, B.S. 1994. Maximum-likelihood estimation of gene location by linkage disequilibrium. Am. J. Hum. Genet. 54: 705-714.
-
(1994)
Am. J. Hum. Genet
, vol.54
, pp. 705-714
-
-
Hill, W.G.1
Weir, B.S.2
-
9
-
-
0036184745
-
Generating samples under a Wright-Fisher neutral model of genetic variation
-
Hudson, R.R. 2002. Generating samples under a Wright-Fisher neutral model of genetic variation. Bioinformatics 18: 337-338.
-
(2002)
Bioinformatics
, vol.18
, pp. 337-338
-
-
Hudson, R.R.1
-
10
-
-
33644875533
-
mtDB: Human Mitochondrial Genome Database, a resource for population genetics and medical sciences
-
Ingman, M. and Gyllensten, U. 2006. mtDB: Human Mitochondrial Genome Database, a resource for population genetics and medical sciences. Nucleic Acids Res. 34: D749-D751.
-
(2006)
Nucleic Acids Res
, vol.34
-
-
Ingman, M.1
Gyllensten, U.2
-
11
-
-
0034619822
-
Mitochondrial genome variation and the origin of modern humans
-
Ingman, M., Kaessmann, H., Paabo, S., and Gyllensten, U. 2000. Mitochondrial genome variation and the origin of modern humans. Nature 408: 708-713.
-
(2000)
Nature
, vol.408
, pp. 708-713
-
-
Ingman, M.1
Kaessmann, H.2
Paabo, S.3
Gyllensten, U.4
-
12
-
-
79959524146
-
A haplotype map of the human genome
-
The International HapMap Consortium
-
The International HapMap Consortium. 2005. A haplotype map of the human genome. Nature 437: 1299-1320.
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
-
13
-
-
33745601940
-
Prevalence of mitochondrial DNA haplogroups in an Australian population
-
Manwaring, N., Jones, M.M., Wang, J.J., Rochtchina, E., Mitchell, P., and Sue, C.M. 2006. Prevalence of mitochondrial DNA haplogroups in an Australian population. Intern. Med. J. 36: 530-533.
-
(2006)
Intern. Med. J
, vol.36
, pp. 530-533
-
-
Manwaring, N.1
Jones, M.M.2
Wang, J.J.3
Rochtchina, E.4
Mitchell, P.5
Sue, C.M.6
-
14
-
-
0036199914
-
A coalescent-based method for detecting and estimating recombination from gene sequences
-
McVean, G., Awadalla, P., and Fearnhead, P. 2002. A coalescent-based method for detecting and estimating recombination from gene sequences. Genetics 160: 1231-1241.
-
(2002)
Genetics
, vol.160
, pp. 1231-1241
-
-
McVean, G.1
Awadalla, P.2
Fearnhead, P.3
-
15
-
-
0031731693
-
Does a common mitochondrial DNA polymorphism underlie susceptibility to diabetes and the thrifty genotype?
-
Poulton, J., Marchington, D.R., Scott-Brown, M., Phillips, D.I., and Hagelberg, E. 1998. Does a common mitochondrial DNA polymorphism underlie susceptibility to diabetes and the thrifty genotype? Trends Genet. 14: 387-389.
-
(1998)
Trends Genet
, vol.14
, pp. 387-389
-
-
Poulton, J.1
Marchington, D.R.2
Scott-Brown, M.3
Phillips, D.I.4
Hagelberg, E.5
-
16
-
-
33645474357
-
The power to detect disease associations with mitochondrial DNA haplogroups
-
Samuels, D.C., Carothers, A.D., Horton, R., and Chinnery, P.F. 2006. The power to detect disease associations with mitochondrial DNA haplogroups. Am. J. Hum. Genet. 78: 713-720.
-
(2006)
Am. J. Hum. Genet
, vol.78
, pp. 713-720
-
-
Samuels, D.C.1
Carothers, A.D.2
Horton, R.3
Chinnery, P.F.4
-
17
-
-
33745273048
-
Comprehensive association testing of common mitochondrial DNA variation in metabolic disease
-
Saxena, R., de Bakker, P.I.W., Singer, K., Mootha, V., Burtt, N., Hirschhorn, J.N., Gaudet, D., Isomaa, B., Daly, M.J., Groop, L., et al. 2006. Comprehensive association testing of common mitochondrial DNA variation in metabolic disease. Am. J. Hum. Genet. 79: 54-61.
-
(2006)
Am. J. Hum. Genet
, vol.79
, pp. 54-61
-
-
Saxena, R.1
de Bakker, P.I.W.2
Singer, K.3
Mootha, V.4
Burtt, N.5
Hirschhorn, J.N.6
Gaudet, D.7
Isomaa, B.8
Daly, M.J.9
Groop, L.10
-
18
-
-
0345399126
-
The probable error of a mean
-
Student
-
Student. 1908. The probable error of a mean. Biometrika 6: 1-25.
-
(1908)
Biometrika
, vol.6
, pp. 1-25
-
-
-
19
-
-
0033525773
-
Mitochondiral diseases in man and mouse
-
Wallace, D.C. 1999. Mitochondiral diseases in man and mouse. Science 283: 1482-1488.
-
(1999)
Science
, vol.283
, pp. 1482-1488
-
-
Wallace, D.C.1
-
20
-
-
6344225549
-
Genetic evidence for unequal effective population sizes of human females and males
-
Wilder, J.A., Mobasher, Z., and Hammer, M.F. 2004. Genetic evidence for unequal effective population sizes of human females and males. Mol. Biol. Evol. 21: 2047-2057.
-
(2004)
Mol. Biol. Evol
, vol.21
, pp. 2047-2057
-
-
Wilder, J.A.1
Mobasher, Z.2
Hammer, M.F.3
-
21
-
-
33845520278
-
A genome-wide scan for naevus count: Linkage to CDKN2A and to other chromosome regions
-
Zhu, G., Montgomery, G.W., James, M.R., Trent, J.M., Hayward, N.K., Martin, N.G., and Duffy, D.L. 2007. A genome-wide scan for naevus count: Linkage to CDKN2A and to other chromosome regions. Eur. J. Hum. Genet. 15: 94-102.
-
(2007)
Eur. J. Hum. Genet
, vol.15
, pp. 94-102
-
-
Zhu, G.1
Montgomery, G.W.2
James, M.R.3
Trent, J.M.4
Hayward, N.K.5
Martin, N.G.6
Duffy, D.L.7
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