-
1
-
-
0032868141
-
Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA
-
Andrews RM, Kubacka I, Chinnery PF, Lightowlers RN, Turnbull DM, Howell N (1999) Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA. Nat Genet 23:147
-
(1999)
Nat Genet
, vol.23
, pp. 147
-
-
Andrews, R.M.1
Kubacka, I.2
Chinnery, P.F.3
Lightowlers, R.N.4
Turnbull, D.M.5
Howell, N.6
-
2
-
-
20744439437
-
Phylogeography of the human mitochondrial haplogroup L3e: A snapshot of African prehistory and Atlantic slave trade
-
Bandelt H-J, Alves-Silva J, Guimaraes PEM, Santos MS, Brehm A, Pereira L, Coppa A, Larruga JM, Rengo C, Scozzari R, Torroni A, Prata MJ, Amorim A, Prado VF, Pena SDJ (2001) Phylogeography of the human mitochondrial haplogroup L3e: a snapshot of African prehistory and Atlantic slave trade. Ann Hum Genet 65:549-563
-
(2001)
Ann Hum Genet
, vol.65
, pp. 549-563
-
-
Bandelt, H.-J.1
Alves-Silva, J.2
Guimaraes, P.E.M.3
Santos, M.S.4
Brehm, A.5
Pereira, L.6
Coppa, A.7
Larruga, J.M.8
Rengo, C.9
Scozzari, R.10
Torroni, A.11
Prata, M.J.12
Amorim, A.13
Prado, V.F.14
Pena, S.D.J.15
-
4
-
-
0033901422
-
mtDNA substitution rate and segregation of heteroplasmy in coding and noncoding regions
-
Cavelier L, Jazin E, Jalonen P, Gyllensten U (2000) mtDNA substitution rate and segregation of heteroplasmy in coding and noncoding regions. Hum Genet 107:45-50
-
(2000)
Hum Genet
, vol.107
, pp. 45-50
-
-
Cavelier, L.1
Jazin, E.2
Jalonen, P.3
Gyllensten, U.4
-
5
-
-
0034333230
-
The inheritance of mitochondrial DNA heteroplasmy: Random drift, selection or both?
-
Chinnery PF, Thorburn DR, Samuels DC, White SL, Dahl HHM, Turnbull DM, Lightowlers RN, Howell N (2000) The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both? Trends Genet 16:500-505
-
(2000)
Trends Genet
, vol.16
, pp. 500-505
-
-
Chinnery, P.F.1
Thorburn, D.R.2
Samuels, D.C.3
White, S.L.4
Dahl, H.H.M.5
Turnbull, D.M.6
Lightowlers, R.N.7
Howell, N.8
-
6
-
-
0034730598
-
High direct estimate of the mutation rate in the mitochondrial genome of Caenorhabditis elegans
-
Denver DR, Morris K, Lynch M, Vassilieva LL, Thomas WK (2000) High direct estimate of the mutation rate in the mitochondrial genome of Caenorhabditis elegans. Science 289:2342-2344
-
(2000)
Science
, vol.289
, pp. 2342-2344
-
-
Denver, D.R.1
Morris, K.2
Lynch, M.3
Vassilieva, L.L.4
Thomas, W.K.5
-
7
-
-
84972507817
-
Comment on the growth and stabilization of populations
-
Donnelly P (1991) Comment on the growth and stabilization of populations. Stat Sci 6:277-279
-
(1991)
Stat Sci
, vol.6
, pp. 277-279
-
-
Donnelly, P.1
-
8
-
-
0032873641
-
Substitution rate variation among sites in mitochondrial hypervariable region I of humans and chimpanzees
-
Excoffier L, Yang Z (1999) Substitution rate variation among sites in mitochondrial hypervariable region I of humans and chimpanzees. Mol Biol Evol 16:1357-1368
-
(1999)
Mol Biol Evol
, vol.16
, pp. 1357-1368
-
-
Excoffier, L.1
Yang, Z.2
-
9
-
-
0035542729
-
Does nonneutral evolution shape observed patterns of DNA variation in animal mitochondrial genomes?
-
Gerber AS, Loggins R, Kumar S, Dowling TE (2001) Does nonneutral evolution shape observed patterns of DNA variation in animal mitochondrial genomes? Ann Rev Genet 35:539-566
-
(2001)
Ann Rev Genet
, vol.35
, pp. 539-566
-
-
Gerber, A.S.1
Loggins, R.2
Kumar, S.3
Dowling, T.E.4
-
10
-
-
0027428406
-
Toward a more accurate estimate for the human mitochondrial DNA tree
-
Hasegawa M, DiRenzo A, Kocher TD, Wilson AC (1993) Toward a more accurate estimate for the human mitochondrial DNA tree. J Mol Evol 37:347-354
-
(1993)
J Mol Evol
, vol.37
, pp. 347-354
-
-
Hasegawa, M.1
DiRenzo, A.2
Kocher, T.D.3
Wilson, A.C.4
-
11
-
-
18344366125
-
Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups
-
Herrnstadt C, Elson JL, Fahy E, Preston G, Turnbull DM, Anderson C, Ghosh SS, Olefsky JM, Beal MF, Davis RE, Howell N (2002a) Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups. Am J Hum Genet 70:1152-1171
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1152-1171
-
-
Herrnstadt, C.1
Elson, J.L.2
Fahy, E.3
Preston, G.4
Turnbull, D.M.5
Anderson, C.6
Ghosh, S.S.7
Olefsky, J.M.8
Beal, M.F.9
Davis, R.E.10
Howell, N.11
-
12
-
-
0037171660
-
A high frequency of polymorphisms in HeLa cell sublines
-
Herrnstadt C, Preston G, Andrews R, Chinnery PF, Lightowlers R, Turnbull DM, Kubacka I, Howell N (2002b) A high frequency of polymorphisms in HeLa cell sublines. Mutat Res 501:19-28
-
(2002)
Mutat Res
, vol.501
, pp. 19-28
-
-
Herrnstadt, C.1
Preston, G.2
Andrews, R.3
Chinnery, P.F.4
Lightowlers, R.5
Turnbull, D.M.6
Kubacka, I.7
Howell, N.8
-
13
-
-
0029002151
-
Mitochondrial and nuclear genetic contribution of female founders to a contemporary population in northeast Quebec
-
Heyer E (1995) Mitochondrial and nuclear genetic contribution of female founders to a contemporary population in northeast Quebec. Am J Hum Genet 56:1450-1455
-
(1995)
Am J Hum Genet
, vol.56
, pp. 1450-1455
-
-
Heyer, E.1
-
14
-
-
0030940879
-
Estimating Y chromosome specific microsatellite mutation frequencies using deep rooting pedigrees
-
Heyer E, Puymirat J, Dieltjes P, Bakker E, de Knijff P (1997) Estimating Y chromosome specific microsatellite mutation frequencies using deep rooting pedigrees. Hum Mol Genet 6:799-803
-
(1997)
Hum Mol Genet
, vol.6
, pp. 799-803
-
-
Heyer, E.1
Puymirat, J.2
Dieltjes, P.3
Bakker, E.4
De Knijff, P.5
-
15
-
-
0034764948
-
Phylogenetic and familial estimates of mitochondrial substitution rates: Study of control region mutations in deep-rooting pedigrees
-
Heyer E, Zietkiewicz E, Rochowski A, Yotova V, Puymirat J, Labuda D (2001) Phylogenetic and familial estimates of mitochondrial substitution rates: study of control region mutations in deep-rooting pedigrees. Am J Hum Genet 69:1113-1126
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1113-1126
-
-
Heyer, E.1
Zietkiewicz, E.2
Rochowski, A.3
Yotova, V.4
Puymirat, J.5
Labuda, D.6
-
16
-
-
0031893037
-
mtDNA mutations that cause optic neuropathy: How do we know?
-
Howell N, Bogolin C, Jamieson R, Marenda DR, Mackey DA (1998) mtDNA mutations that cause optic neuropathy: how do we know? Am J Hum Genet 62:196-202
-
(1998)
Am J Hum Genet
, vol.62
, pp. 196-202
-
-
Howell, N.1
Bogolin, C.2
Jamieson, R.3
Marenda, D.R.4
Mackey, D.A.5
-
17
-
-
0033646619
-
Transmission of the human mitochondrial genome
-
Howell N, Chinnery PF, Ghosh SS, Fahy E, Turnbull DM (2000) Transmission of the human mitochondrial genome. Hum Reprod Suppl 15:235-245
-
(2000)
Hum Reprod Suppl
, vol.15
, pp. 235-245
-
-
Howell, N.1
Chinnery, P.F.2
Ghosh, S.S.3
Fahy, E.4
Turnbull, D.M.5
-
18
-
-
0028928397
-
Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees
-
Howell N, Kubacka I, Halvorson S, Howell B, McCullough DA, Mackey D (1995) Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees. Genetics 140:285-302
-
(1995)
Genetics
, vol.140
, pp. 285-302
-
-
Howell, N.1
Kubacka, I.2
Halvorson, S.3
Howell, B.4
McCullough, D.A.5
Mackey, D.6
-
19
-
-
0029759163
-
How rapidly does the human mitochondrial genome evolve?
-
Howell N, Kubacka I, Mackey DA (1996) How rapidly does the human mitochondrial genome evolve? Am J Hum Genet 59:501-509
-
(1996)
Am J Hum Genet
, vol.59
, pp. 501-509
-
-
Howell, N.1
Kubacka, I.2
Mackey, D.A.3
-
21
-
-
0032231349
-
Low-penetrance branches in matrilineal pedigrees with Leber hereditary optic neuropathy
-
_ (1998) Low-penetrance branches in matrilineal pedigrees with Leber hereditary optic neuropathy. Am J Hum Genet 63:1220-1224
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1220-1224
-
-
-
22
-
-
0033911276
-
Persistent heteroplasmy of a mutation in the human mtDNA control region: Hypermutation as an apparent consequence of simple-repeat expansion/contraction
-
Howell N, Smejkal CB (2000) Persistent heteroplasmy of a mutation in the human mtDNA control region: hypermutation as an apparent consequence of simple-repeat expansion/contraction. Am J Hum Genet 66:1589-1598
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1589-1598
-
-
Howell, N.1
Smejkal, C.B.2
-
23
-
-
0025897119
-
Leber hereditary optic neuropathy: Involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation
-
Howell N, Kubacka I, Xu M, McCullough DA (1991) Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation. Am J Hum Genet 48:935-942
-
(1991)
Am J Hum Genet
, vol.48
, pp. 935-942
-
-
Howell, N.1
Kubacka, I.2
Xu, M.3
McCullough, D.A.4
-
24
-
-
0028100561
-
A heteroplasmic LHON family: Tissue distribution and transmission of the 11778 mutation
-
Howell N, Xu M, Halvorson S, Bodis-Wollner I, Sherman J (1994) A heteroplasmic LHON family: tissue distribution and transmission of the 11778 mutation. Am J Hum Genet 55:203-206
-
(1994)
Am J Hum Genet
, vol.55
, pp. 203-206
-
-
Howell, N.1
Xu, M.2
Halvorson, S.3
Bodis-Wollner, I.4
Sherman, J.5
-
25
-
-
0034619822
-
Mitochondrial genome variation and the origin of modern humans
-
Ingman M, Kaessmann H, Pääbo S, Gyllensten U (2000) Mitochondrial genome variation and the origin of modern humans. Nature 408:708-712
-
(2000)
Nature
, vol.408
, pp. 708-712
-
-
Ingman, M.1
Kaessmann, H.2
Pääbo, S.3
Gyllensten, U.4
-
26
-
-
0013355748
-
The bottleneck: Gamete and embryo mitochondria in humans
-
Jansen RPS (ed) (2000) The bottleneck: gamete and embryo mitochondria in humans. Hum Reprod volume 15, supplement 2
-
(2000)
Hum Reprod
, vol.15
, Issue.SUPPL. 2
-
-
Jansen, R.P.S.1
-
27
-
-
0031992675
-
Mitochondrial mutation rate revisited: Hot spots and polymorphism
-
Jazin E, Soodyall H, Jalonen P, Lindholm E, Stoneking M, Gyllensten U (1998) Mitochondrial mutation rate revisited: hot spots and polymorphism. Nat Genet 18:109-110
-
(1998)
Nat Genet
, vol.18
, pp. 109-110
-
-
Jazin, E.1
Soodyall, H.2
Jalonen, P.3
Lindholm, E.4
Stoneking, M.5
Gyllensten, U.6
-
28
-
-
0347231556
-
Characteristics and frequency of germline mutations at microsatellite loci from the human Y chromosome, as revealed by direct observation in father/son pairs
-
Kayser M, Roewer L, Hedman M, Henke L, Henke J, Brauer S, Kruger C, Krawczak M, Nagy M, Dobosz T, Szibor R, de Knijff P, Stoneking M, Sajantila A (2000) Characteristics and frequency of germline mutations at microsatellite loci from the human Y chromosome, as revealed by direct observation in father/son pairs. Am J Hum Genet 66:1580-1588
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1580-1588
-
-
Kayser, M.1
Roewer, L.2
Hedman, M.3
Henke, L.4
Henke, J.5
Brauer, S.6
Kruger, C.7
Krawczak, M.8
Nagy, M.9
Dobosz, T.10
Szibor, R.11
De Knijff, P.12
Stoneking, M.13
Sajantila, A.14
-
29
-
-
0037155593
-
Rates of evolution in ancient DNA from Adélie penguins
-
Lambert DM, Ritchie PA, Millar CD, Holland B, Drummond AJ, Baroni C (2002) Rates of evolution in ancient DNA from Adélie penguins. Science 295:2270-2273
-
(2002)
Science
, vol.295
, pp. 2270-2273
-
-
Lambert, D.M.1
Ritchie, P.A.2
Millar, C.D.3
Holland, B.4
Drummond, A.J.5
Baroni, C.6
-
30
-
-
0030870985
-
mtDNA mutation rates: No need to panic
-
Macaulay VA, Richards MB, Forster P, Bendall KE, Watson E, Sykes BC, Bandelt H-J (1997) mtDNA mutation rates: no need to panic. Am J Hum Genet 61:983-986
-
(1997)
Am J Hum Genet
, vol.61
, pp. 983-986
-
-
Macaulay, V.A.1
Richards, M.B.2
Forster, P.3
Bendall, K.E.4
Watson, E.5
Sykes, B.C.6
Bandelt, H.-J.7
-
31
-
-
0026989344
-
Leber hereditary optic neuropathy in Australia
-
Mackey DA, Buttery RG (1992) Leber hereditary optic neuropathy in Australia. Aust N Z J Ophthalmol 20:177-184
-
(1992)
Aust N Z J Ophthalmol
, vol.20
, pp. 177-184
-
-
Mackey, D.A.1
Buttery, R.G.2
-
32
-
-
0032779612
-
Pattern of nucleotide substitutions and rate heterogeneity in the hypervariable regions I and II of human mtDNA
-
Meyer S, Weiss G, von Haeseler A (1999) Pattern of nucleotide substitutions and rate heterogeneity in the hypervariable regions I and II of human mtDNA. Genetics 152:1103-1110
-
(1999)
Genetics
, vol.152
, pp. 1103-1110
-
-
Meyer, S.1
Weiss, G.2
Von Haeseler, A.3
-
33
-
-
0031035505
-
mtDNA analysis shows common ancestry in two kindreds with X-linked recessive hypoparathyroidism and reveals a heteroplasmic silent mutation
-
Mumm S, Whyte MP, Thakker RV, Buetow KH, Schlessinger D (1997) mtDNA analysis shows common ancestry in two kindreds with X-linked recessive hypoparathyroidism and reveals a heteroplasmic silent mutation. Am J Hum Genet 60:153-159
-
(1997)
Am J Hum Genet
, vol.60
, pp. 153-159
-
-
Mumm, S.1
Whyte, M.P.2
Thakker, R.V.3
Buetow, K.H.4
Schlessinger, D.5
-
34
-
-
0029738581
-
Mutational hot spots in the mitochondrial microcosm
-
Pääbo S (1996) Mutational hot spots in the mitochondrial microcosm. Am J Hum Genet 59:493-496
-
(1996)
Am J Hum Genet
, vol.59
, pp. 493-496
-
-
Pääbo, S.1
-
35
-
-
0031992675
-
Mitochondrial mutation rate revisited: Hot spots and polymorphism
-
Parsons TJ, Holland MM (1998) Mitochondrial mutation rate revisited: hot spots and polymorphism. Nat Genet 18:110
-
(1998)
Nat Genet
, vol.18
, pp. 110
-
-
Parsons, T.J.1
Holland, M.M.2
-
36
-
-
0030898192
-
A high observed substitution rate in the human mitochondrial DNA control region
-
Parsons TJ, Muniec DS, Sullivan K, Woodyatt N, Alliston-Grenier R, Wilson MR, Berry DL, Holland KA, Weedn VW, Gill P, Holland MM (1997) A high observed substitution rate in the human mitochondrial DNA control region. Nat Genet 15:363-368
-
(1997)
Nat Genet
, vol.15
, pp. 363-368
-
-
Parsons, T.J.1
Muniec, D.S.2
Sullivan, K.3
Woodyatt, N.4
Alliston-Grenier, R.5
Wilson, M.R.6
Berry, D.L.7
Holland, K.A.8
Weedn, V.W.9
Gill, P.10
Holland, M.M.11
-
37
-
-
0035673444
-
The units of selection on mitochondrial DNA
-
Rand DM (2001) The units of selection on mitochondrial DNA. Ann Rev Ecol Syst 32:415-448
-
(2001)
Ann Rev Ecol Syst
, vol.32
, pp. 415-448
-
-
Rand, D.M.1
-
38
-
-
0034897603
-
Using linked markers to infer the age of a mutation
-
Rannala B, Bertorelle G (2001) Using linked markers to infer the age of a mutation. Hum Mutat 18:87-100
-
(2001)
Hum Mutat
, vol.18
, pp. 87-100
-
-
Rannala, B.1
Bertorelle, G.2
-
39
-
-
0035895204
-
Ancient DNA and the origin of modern humans
-
Relethford JH (2001) Ancient DNA and the origin of modern humans. Proc Natl Acad Sci USA 98:390-391
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 390-391
-
-
Relethford, J.H.1
-
40
-
-
0033764821
-
Tracing European founder lineages in the Near Eastern mtDNA pool
-
Richards M, Macaulay V, Hickey E, Vega E, Sykes B, Guida V, Rengo C, et al (2000) Tracing European founder lineages in the Near Eastern mtDNA pool. Am J Hum Genet 67:1251-1277
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1251-1277
-
-
Richards, M.1
Macaulay, V.2
Hickey, E.3
Vega, E.4
Sykes, B.5
Guida, V.6
Rengo, C.7
-
41
-
-
0346455087
-
The mutation rate in the human mtDNA control region
-
Siguroardóttir S, Helgason A, Gulcher JR, Stefansson K, Donnelly P (2000) The mutation rate in the human mtDNA control region. Am J Hum Genet 66:1599-1609
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1599-1609
-
-
Siguroardóttir, S.1
Helgason, A.2
Gulcher, J.R.3
Stefansson K.Donnelly, P.4
-
42
-
-
0030696709
-
The founding mitochondrial DNA lineages of Tristan da Cunha
-
Soodyall H, Jenkins T, Mukherjee A, Du Toit E, Roberts DF, Stoneking M (1997) The founding mitochondrial DNA lineages of Tristan da Cunha. Am J Phys Anthropol 104:157-166
-
(1997)
Am J Phys Anthropol
, vol.104
, pp. 157-166
-
-
Soodyall, H.1
Jenkins, T.2
Mukherjee, A.3
Du Toit, E.4
Roberts, D.F.5
Stoneking, M.6
-
44
-
-
0034707211
-
On the estimation of the rate of nucleotide substitution for the control region of human mitochondrial DNA
-
Tamura K (2000) On the estimation of the rate of nucleotide substitution for the control region of human mitochondrial DNA. Gene 259:189-197
-
(2000)
Gene
, vol.259
, pp. 189-197
-
-
Tamura, K.1
-
45
-
-
0027157960
-
Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees
-
Tamura K, Nei M (1993) Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees. Mol Biol Evol 10:512-526
-
(1993)
Mol Biol Evol
, vol.10
, pp. 512-526
-
-
Tamura, K.1
Nei, M.2
-
46
-
-
0034822098
-
A signal, from human mtDNA, of postglacial recolonization in Europe
-
Torroni A, Bandelt H-J, Macaulay V, Richards M, Cruciani F, Rengo C, Martinez-Cabrera V, et al (2001a) A signal, from human mtDNA, of postglacial recolonization in Europe. Am J Hum Genet 69:844-852
-
(2001)
Am J Hum Genet
, vol.69
, pp. 844-852
-
-
Torroni, A.1
Bandelt, H.-J.2
Macaulay, V.3
Richards, M.4
Cruciani, F.5
Rengo, C.6
Martinez-Cabrera, V.7
-
47
-
-
0035205417
-
Do the four clades of the mtDNA haplogroup L2 evolve at different rates?
-
Torroni A, Rengo R, Guida V, Cruciani F, Sellitto D, Coppa A, Calderon FL, Simionati B, Valle G, Richards M, Macaulay V, Scozzari R (2001b) Do the four clades of the mtDNA haplogroup L2 evolve at different rates? Am J Hum Genet 69:1348-1356
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1348-1356
-
-
Torroni, A.1
Rengo, R.2
Guida, V.3
Cruciani, F.4
Sellitto, D.5
Coppa, A.6
Calderon, F.L.7
Simionati, B.8
Valle, G.9
Richards, M.10
Macaulay, V.11
Scozzari, R.12
-
48
-
-
0033851835
-
A sensitive denaturing gradient-gel electrophoresis assay reveals a high frequency of heteroplasmy in hypervariable region 1 of the human mtDNA control region
-
Tully LA, Parsons TJ, Steighner RJ, Holland MM, Marino MA, Prenger VL (2000) A sensitive denaturing gradient-gel electrophoresis assay reveals a high frequency of heteroplasmy in hypervariable region 1 of the human mtDNA control region. Am J Hum Genet 67:432-443
-
(2000)
Am J Hum Genet
, vol.67
, pp. 432-443
-
-
Tully, L.A.1
Parsons, T.J.2
Steighner, R.J.3
Holland, M.M.4
Marino, M.A.5
Prenger, V.L.6
-
49
-
-
0014706751
-
A new manifestation of Leber's disease and a new explanation for the agency responsible for its unusual pattern of inheritance
-
Wallace DC (1970) A new manifestation of Leber's disease and a new explanation for the agency responsible for its unusual pattern of inheritance. Brain 93:121-132
-
(1970)
Brain
, vol.93
, pp. 121-132
-
-
Wallace, D.C.1
-
50
-
-
0035546221
-
Statistical inference of sequence-dependent mutation rates
-
Zavolan M, Kepler TB (2001) Statistical inference of sequence-dependent mutation rates. Curr Opin Genet Devel 11:612-615
-
(2001)
Curr Opin Genet Devel
, vol.11
, pp. 612-615
-
-
Zavolan, M.1
Kepler, T.B.2
|