-
1
-
-
0242524432
-
Patterns of human genetic diversity: implications for human evolutionary history and disease
-
10.1146/annurev.genom.4.070802.110226, 14527305
-
Tishkoff SA, Verrelli BC. Patterns of human genetic diversity: implications for human evolutionary history and disease. Annu Rev Genomics Hum Genet 2003, 4:293-340. 10.1146/annurev.genom.4.070802.110226, 14527305.
-
(2003)
Annu Rev Genomics Hum Genet
, vol.4
, pp. 293-340
-
-
Tishkoff, S.A.1
Verrelli, B.C.2
-
2
-
-
33745121154
-
Positive natural selection in the human lineage
-
10.1126/science.1124309, 16778047
-
Sabeti PC, Schaffner SF, Fry B, Lohmueller J, Varilly P, Shamovsky O, Palma A, Mikkelsen TS, Altshuler D, Lander ES. Positive natural selection in the human lineage. Science 2006, 312:1614-20. 10.1126/science.1124309, 16778047.
-
(2006)
Science
, vol.312
, pp. 1614-1620
-
-
Sabeti, P.C.1
Schaffner, S.F.2
Fry, B.3
Lohmueller, J.4
Varilly, P.5
Shamovsky, O.6
Palma, A.7
Mikkelsen, T.S.8
Altshuler, D.9
Lander, E.S.10
-
3
-
-
0038315436
-
Entropy as a measure for linkage disequilibrium over multilocus haplotype blocks
-
10.1159/000070664, 12771551
-
Nothnagel M, Fürst R, Rohde K. Entropy as a measure for linkage disequilibrium over multilocus haplotype blocks. Hum Hered 2002, 54:186-98. 10.1159/000070664, 12771551.
-
(2002)
Hum Hered
, vol.54
, pp. 186-198
-
-
Nothnagel, M.1
Fürst, R.2
Rohde, K.3
-
4
-
-
0037167852
-
Detecting recent positive selection in the human genome from haplotype structure
-
10.1038/nature01140, 12397357
-
Sabeti PC, Reich DE, Higgins JM, Levine HZ, Richter DJ, Schaffner SF, Gabriel SB, Platko JV, Patterson NJ, McDonald GJ, Ackerman HC, Campbell SJ, Altshuler D, Cooper R, Kwiatkowski D, Ward R, Lander ES. Detecting recent positive selection in the human genome from haplotype structure. Nature 2002, 419:832-7. 10.1038/nature01140, 12397357.
-
(2002)
Nature
, vol.419
, pp. 832-837
-
-
Sabeti, P.C.1
Reich, D.E.2
Higgins, J.M.3
Levine, H.Z.4
Richter, D.J.5
Schaffner, S.F.6
Gabriel, S.B.7
Platko, J.V.8
Patterson, N.J.9
McDonald, G.J.10
Ackerman, H.C.11
Campbell, S.J.12
Altshuler, D.13
Cooper, R.14
Kwiatkowski, D.15
Ward, R.16
Lander, E.S.17
-
5
-
-
33644981509
-
A map of recent positive selection in the human genome
-
10.1371/journal.pbio.0040072, 1382018,1382018, 16494531
-
Voight BF, Kudaravalli S, Wen X, Pritchard JK. A map of recent positive selection in the human genome. PLoS Biol 2006, 4:e72. 10.1371/journal.pbio.0040072, 1382018,1382018, 16494531.
-
(2006)
PLoS Biol
, vol.4
-
-
Voight, B.F.1
Kudaravalli, S.2
Wen, X.3
Pritchard, J.K.4
-
6
-
-
35349012592
-
Genome-wide detection and characterization of positive selection in human populations
-
10.1038/nature06250, 2687721, 17943131, International HapMap Consortium
-
Sabeti PC, Varilly P, Fry B, Lohmueller J, Hostetter E, Cotsapas C, Xie X, Byrne EH, McCarroll SA, Gaudet R, Schaffner SF, Lander ES, . International HapMap Consortium Genome-wide detection and characterization of positive selection in human populations. Nature 2007, 449:913-8. 10.1038/nature06250, 2687721, 17943131, International HapMap Consortium.
-
(2007)
Nature
, vol.449
, pp. 913-918
-
-
Sabeti, P.C.1
Varilly, P.2
Fry, B.3
Lohmueller, J.4
Hostetter, E.5
Cotsapas, C.6
Xie, X.7
Byrne, E.H.8
McCarroll, S.A.9
Gaudet, R.10
Schaffner, S.F.11
Lander, E.S.12
-
7
-
-
27544437635
-
Genomic scans for selective sweeps using SNP data
-
10.1101/gr.4252305, 1310644, 16251466
-
Nielsen R, Williamson S, Kim Y, Hubisz MJ, Clark AG, Bustamante C. Genomic scans for selective sweeps using SNP data. Genome Res 2005, 15:1566-75. 10.1101/gr.4252305, 1310644, 16251466.
-
(2005)
Genome Res
, vol.15
, pp. 1566-1575
-
-
Nielsen, R.1
Williamson, S.2
Kim, Y.3
Hubisz, M.J.4
Clark, A.G.5
Bustamante, C.6
-
8
-
-
0035837267
-
Linkage disequilibrium in the human genome
-
10.1038/35075590, 11346797
-
Reich DE, Cargill M, Bolk S, Ireland J, Sabeti PC, Richter DJ, Lavery T, Kouyoumjian R, Farhadian SF, Ward R, Lander ES. Linkage disequilibrium in the human genome. Nature 2001, 411:199-204. 10.1038/35075590, 11346797.
-
(2001)
Nature
, vol.411
, pp. 199-204
-
-
Reich, D.E.1
Cargill, M.2
Bolk, S.3
Ireland, J.4
Sabeti, P.C.5
Richter, D.J.6
Lavery, T.7
Kouyoumjian, R.8
Farhadian, S.F.9
Ward, R.10
Lander, E.S.11
-
9
-
-
3042700117
-
Evidence for substantial fine-scale variation in recombination rates across the human genome
-
10.1038/ng1376, 15184900
-
Crawford DC, Bhangale T, Li N, Hellenthal G, Rieder MJ, Nickerson DA, Stephens M. Evidence for substantial fine-scale variation in recombination rates across the human genome. Nat Genet 2004, 36:700-6. 10.1038/ng1376, 15184900.
-
(2004)
Nat Genet
, vol.36
, pp. 700-706
-
-
Crawford, D.C.1
Bhangale, T.2
Li, N.3
Hellenthal, G.4
Rieder, M.J.5
Nickerson, D.A.6
Stephens, M.7
-
10
-
-
2342459066
-
Natural selection and population history in the human angiotensinogen gene (AGT): 736 complete AGT sequences in chromosomes from around the world
-
10.1086/420793, 1181984, 15077204
-
Nakajima T, Wooding S, Sakagami T, Emi M, Tokunaga K, Tamiya G, Ishigami T, Umemura S, Munkhbat B, Jin F, Guan-Jun J, Hayasaka I, Ishida T, Saitou N, Pavelka K, Lalouel JM, Jorde LB, Inoue I. Natural selection and population history in the human angiotensinogen gene (AGT): 736 complete AGT sequences in chromosomes from around the world. Am J Hum Genet 2004, 74:898-916. 10.1086/420793, 1181984, 15077204.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 898-916
-
-
Nakajima, T.1
Wooding, S.2
Sakagami, T.3
Emi, M.4
Tokunaga, K.5
Tamiya, G.6
Ishigami, T.7
Umemura, S.8
Munkhbat, B.9
Jin, F.10
Guan-Jun, J.11
Hayasaka, I.12
Ishida, T.13
Saitou, N.14
Pavelka, K.15
Lalouel, J.M.16
Jorde, L.B.17
Inoue, I.18
-
11
-
-
34248387347
-
Haplotype structure and selection of the MDM2 oncogene in humans
-
10.1073/pnas.0610998104, 1838634, 17360557
-
Atwal GS, Bond GL, Metsuyanim S, Papa M, Friedman E, Distelman-Menachem T, Ben Asher E, Lancet D, Ross DA, Sninsky J, White TJ, Levine AJ, Yarden R. Haplotype structure and selection of the MDM2 oncogene in humans. Proc Natl Acad Sci 2007, 104:4524-9. 10.1073/pnas.0610998104, 1838634, 17360557.
-
(2007)
Proc Natl Acad Sci
, vol.104
, pp. 4524-4529
-
-
Atwal, G.S.1
Bond, G.L.2
Metsuyanim, S.3
Papa, M.4
Friedman, E.5
Distelman-Menachem, T.6
Ben Asher, E.7
Lancet, D.8
Ross, D.A.9
Sninsky, J.10
White, T.J.11
Levine, A.J.12
Yarden, R.13
-
12
-
-
66049157487
-
Signals of recent positive selection in a worldwide sample of human populations
-
10.1101/gr.087577.108, 2675971, 19307593
-
Pickrell JK, Coop G, Novembre J, Kudaravalli S, Li JZ, Absher D, Srinivasan BS, Barsh GS, Myers RM, Feldman MW, Pritchard JK. Signals of recent positive selection in a worldwide sample of human populations. Genome Res 2009, 19:826-37. 10.1101/gr.087577.108, 2675971, 19307593.
-
(2009)
Genome Res
, vol.19
, pp. 826-837
-
-
Pickrell, J.K.1
Coop, G.2
Novembre, J.3
Kudaravalli, S.4
Li, J.Z.5
Absher, D.6
Srinivasan, B.S.7
Barsh, G.S.8
Myers, R.M.9
Feldman, M.W.10
Pritchard, J.K.11
-
13
-
-
0242438893
-
Genomewide distribution of high-frequency, completely mismatching SNP haplotype pairs observed to be common across human populations
-
10.1086/379154, 1180487, 14560401
-
Zhang J, Rowe WL, Clark AG, Buetow KH. Genomewide distribution of high-frequency, completely mismatching SNP haplotype pairs observed to be common across human populations. Am J Hum Genet 2003, 73:1073-81. 10.1086/379154, 1180487, 14560401.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 1073-1081
-
-
Zhang, J.1
Rowe, W.L.2
Clark, A.G.3
Buetow, K.H.4
-
14
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
10.1038/nature06258, 2689609, 17943122, International HapMap Consortium
-
International HapMap Consortium A second generation human haplotype map of over 3.1 million SNPs. Nature 2007, 449:851-61. 10.1038/nature06258, 2689609, 17943122, International HapMap Consortium.
-
(2007)
Nature
, vol.449
, pp. 851-861
-
-
-
15
-
-
33744815615
-
How reliable are empirical genomic scans for selective sweeps?
-
10.1101/gr.5105206, 1473181, 16687733
-
Teshima KM, Coop G, Przeworski M. How reliable are empirical genomic scans for selective sweeps?. Genome Res 2006, 16:702-12. 10.1101/gr.5105206, 1473181, 16687733.
-
(2006)
Genome Res
, vol.16
, pp. 702-712
-
-
Teshima, K.M.1
Coop, G.2
Przeworski, M.3
-
16
-
-
34347336584
-
Localizing recent adaptive evolution in the human genome
-
10.1371/journal.pgen.0030090, 1885279,1885279, 17542651
-
Williamson SH, Hubisz MJ, Clark AG, Payseur BA, Bustamante CD, Nielsen R. Localizing recent adaptive evolution in the human genome. PLoS Genet 2007, 3:e90. 10.1371/journal.pgen.0030090, 1885279,1885279, 17542651.
-
(2007)
PLoS Genet
, vol.3
-
-
Williamson, S.H.1
Hubisz, M.J.2
Clark, A.G.3
Payseur, B.A.4
Bustamante, C.D.5
Nielsen, R.6
-
17
-
-
38449113569
-
Human pigmentation variation: evolution, genetic basis, and implications for public health
-
10.1002/ajpa.20727, 18046745
-
Parra EJ. Human pigmentation variation: evolution, genetic basis, and implications for public health. Am J Phys Anthropol 2007, 45:85-105. 10.1002/ajpa.20727, 18046745.
-
(2007)
Am J Phys Anthropol
, vol.45
, pp. 85-105
-
-
Parra, E.J.1
-
18
-
-
0035964395
-
Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice
-
10.1073/pnas.181336698, 56945, 11504925
-
Matesic LE, Yip R, Reuss AE, Swing DA, O'Sullivan TN, Fletcher CF, Copeland NG, Jenkins NA. Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice. Proc Natl Acad Sci 2001, 98:10238-43. 10.1073/pnas.181336698, 56945, 11504925.
-
(2001)
Proc Natl Acad Sci
, vol.98
, pp. 10238-10243
-
-
Matesic, L.E.1
Yip, R.2
Reuss, A.E.3
Swing, D.A.4
O'Sullivan, T.N.5
Fletcher, C.F.6
Copeland, N.G.7
Jenkins, N.A.8
-
19
-
-
0042388106
-
Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)
-
166299, 12897212
-
Ménasché G, Ho CH, Sanal O, Feldmann J, Tezcan I, Ersoy F, Houdusse A, Fischer A, de Saint Basile G. Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1). J Clin Invest 2003, 112:450-6. 166299, 12897212.
-
(2003)
J Clin Invest
, vol.112
, pp. 450-456
-
-
Ménasché, G.1
Ho, C.H.2
Sanal, O.3
Feldmann, J.4
Tezcan, I.5
Ersoy, F.6
Houdusse, A.7
Fischer, A.8
de Saint Basile, G.9
-
20
-
-
38549115127
-
Genetic analysis of attractin homologs
-
10.1002/dvg.20351, 18064672
-
Walker WP, Aradhya S, Hu CL, Shen S, Zhang W, Azarani A, Lu X, Barsh GS, Gunn TM. Genetic analysis of attractin homologs. Genesis 2007, 45:744-56. 10.1002/dvg.20351, 18064672.
-
(2007)
Genesis
, vol.45
, pp. 744-756
-
-
Walker, W.P.1
Aradhya, S.2
Hu, C.L.3
Shen, S.4
Zhang, W.5
Azarani, A.6
Lu, X.7
Barsh, G.S.8
Gunn, T.M.9
-
21
-
-
62349119713
-
Ingenuity Pathway Analysis database
-
Ingenuity Pathway Analysis database. , http://www.ingenuity.com
-
-
-
-
22
-
-
4644367204
-
Positive selection on MMP3 regulation has shaped heart disease risk
-
10.1016/j.cub.2004.08.051, 15341739
-
Rockman MV, Hahn MW, Soranzo N, Loisel DA, Goldstein DB, Wray GA. Positive selection on MMP3 regulation has shaped heart disease risk. Curr Biol 2004, 14:1531-9. 10.1016/j.cub.2004.08.051, 15341739.
-
(2004)
Curr Biol
, vol.14
, pp. 1531-1539
-
-
Rockman, M.V.1
Hahn, M.W.2
Soranzo, N.3
Loisel, D.A.4
Goldstein, D.B.5
Wray, G.A.6
-
23
-
-
58049130325
-
A common haplotype of DRD3 affected by recent positive selection is associated with protection from schizophrenia
-
10.1007/s00439-008-0584-7, 18987889
-
Costas J, Carrera N, Domínguez E, Vilella E, Martorell L, Valero J, Gutiérrez-Zotes A, Labad A, Carracedo A. A common haplotype of DRD3 affected by recent positive selection is associated with protection from schizophrenia. Hum Genet 2009, 124:607-13. 10.1007/s00439-008-0584-7, 18987889.
-
(2009)
Hum Genet
, vol.124
, pp. 607-613
-
-
Costas, J.1
Carrera, N.2
Domínguez, E.3
Vilella, E.4
Martorell, L.5
Valero, J.6
Gutiérrez-Zotes, A.7
Labad, A.8
Carracedo, A.9
-
24
-
-
0033932291
-
Vitamin D receptor gene polymorphism: association with Crohn's disease susceptibility
-
10.1136/gut.47.2.211, 1728007, 10896912
-
Simmons JD, Mullighan C, Welsh KI, Jewell DP. Vitamin D receptor gene polymorphism: association with Crohn's disease susceptibility. Gut 2000, 47:211-4. 10.1136/gut.47.2.211, 1728007, 10896912.
-
(2000)
Gut
, vol.47
, pp. 211-214
-
-
Simmons, J.D.1
Mullighan, C.2
Welsh, K.I.3
Jewell, D.P.4
-
25
-
-
36749055773
-
TNFSF15 is an ethnic-specific IBD gene
-
10.1002/ibd.20223, 2552994, 17663424
-
Picornell Y, Mei L, Taylor K, Yang H, Targan SR, Rotter JI. TNFSF15 is an ethnic-specific IBD gene. Inflamm Bowel Dis 2007, 13:1333-8. 10.1002/ibd.20223, 2552994, 17663424.
-
(2007)
Inflamm Bowel Dis
, vol.13
, pp. 1333-1338
-
-
Picornell, Y.1
Mei, L.2
Taylor, K.3
Yang, H.4
Targan, S.R.5
Rotter, J.I.6
-
26
-
-
63749127623
-
Worldwide population differentiation at disease-associated SNPs
-
10.1186/1755-8794-1-22, 2440747, 18533027
-
Myles S, Davison D, Barrett J, Stoneking M, Timpson N. Worldwide population differentiation at disease-associated SNPs. BMC Med Genomics 2008, 1:22. 10.1186/1755-8794-1-22, 2440747, 18533027.
-
(2008)
BMC Med Genomics
, vol.1
, pp. 22
-
-
Myles, S.1
Davison, D.2
Barrett, J.3
Stoneking, M.4
Timpson, N.5
-
27
-
-
34247572104
-
Identification of a candidate genetic variant for the high prevalence of type II diabetes in Polynesians
-
10.1038/sj.ejhg.5201793, 17327880
-
Myles S, Hradetzky E, Engelken J, Lao O, Nürnberg P, Trent RJ, Wang X, Kayser M, Stoneking M. Identification of a candidate genetic variant for the high prevalence of type II diabetes in Polynesians. Eur J Hum Genet 2007, 15:584-9. 10.1038/sj.ejhg.5201793, 17327880.
-
(2007)
Eur J Hum Genet
, vol.15
, pp. 584-589
-
-
Myles, S.1
Hradetzky, E.2
Engelken, J.3
Lao, O.4
Nürnberg, P.5
Trent, R.J.6
Wang, X.7
Kayser, M.8
Stoneking, M.9
-
28
-
-
0035041203
-
Does 'imprinting' with low prenatal vitamin D contribute to the risk of various adult disorders?
-
10.1054/mehy.2000.1226, 11359362
-
McGrath J. Does 'imprinting' with low prenatal vitamin D contribute to the risk of various adult disorders?. Med Hypotheses 2001, 56:367-71. 10.1054/mehy.2000.1226, 11359362.
-
(2001)
Med Hypotheses
, vol.56
, pp. 367-371
-
-
McGrath, J.1
-
29
-
-
0033912992
-
The evolution of human skin coloration
-
10.1006/jhev.2000.0403, 10896812
-
Jablonski NG, Chaplin G. The evolution of human skin coloration. J Hum Evol 2000, 39:57-106. 10.1006/jhev.2000.0403, 10896812.
-
(2000)
J Hum Evol
, vol.39
, pp. 57-106
-
-
Jablonski, N.G.1
Chaplin, G.2
-
30
-
-
25844433784
-
Vitamin D endocrine system and the genetic susceptibility to diabetes, obesity and vascular disease
-
10.1016/S1262-3636(07)70200-8, 16369193
-
Reis AF, Hauache OM, Velho G. Vitamin D endocrine system and the genetic susceptibility to diabetes, obesity and vascular disease. Diabetes Metab 2005, 31:318-25. 10.1016/S1262-3636(07)70200-8, 16369193.
-
(2005)
Diabetes Metab
, vol.31
, pp. 318-325
-
-
Reis, A.F.1
Hauache, O.M.2
Velho, G.3
-
31
-
-
53849136271
-
Vitamin D and human health: lessons from vitamin D receptor null mice
-
10.1210/er.2008-0004, 2583388, 18694980
-
Bouillon R, Carmeliet G, Verlinden L, van Etten E, Verstuyf A, Luderer HF, Lieben L, Mathieu C, Demay M. Vitamin D and human health: lessons from vitamin D receptor null mice. Endocr Rev 2008, 29:726-76. 10.1210/er.2008-0004, 2583388, 18694980.
-
(2008)
Endocr Rev
, vol.29
, pp. 726-776
-
-
Bouillon, R.1
Carmeliet, G.2
Verlinden, L.3
van Etten, E.4
Verstuyf, A.5
Luderer, H.F.6
Lieben, L.7
Mathieu, C.8
Demay, M.9
-
32
-
-
0347362521
-
Genetic anthropology of the colorectal cancer-susceptibility allele APC I1307K: evidence of genetic drift within the Ashkenazim
-
10.1086/379926, 1180391, 14624392
-
Niell BL, Long JC, Rennert G, Gruber SB. Genetic anthropology of the colorectal cancer-susceptibility allele APC I1307K: evidence of genetic drift within the Ashkenazim. Am J Hum Genet 2003, 73:1250-60. 10.1086/379926, 1180391, 14624392.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 1250-1260
-
-
Niell, B.L.1
Long, J.C.2
Rennert, G.3
Gruber, S.B.4
-
33
-
-
38349165058
-
Haplotype patterns in cancer-related genes with long-range linkage disequilibrium: no evidence of association with breast cancer or positive selection
-
10.1038/sj.ejhg.5201953, 18000525
-
Ribas G, Milne RL, Gonzalez-Neira A, Benítez J. Haplotype patterns in cancer-related genes with long-range linkage disequilibrium: no evidence of association with breast cancer or positive selection. Eur J Hum Genet 2008, 16:252-60. 10.1038/sj.ejhg.5201953, 18000525.
-
(2008)
Eur J Hum Genet
, vol.16
, pp. 252-260
-
-
Ribas, G.1
Milne, R.L.2
Gonzalez-Neira, A.3
Benítez, J.4
-
34
-
-
33746669941
-
Vitamin D receptor polymorphisms and diseases
-
10.1016/j.cca.2006.02.016, 16563362
-
Valdivielso JM, Fernandez E. Vitamin D receptor polymorphisms and diseases. Clin Chim Acta 2006, 371:1-12. 10.1016/j.cca.2006.02.016, 16563362.
-
(2006)
Clin Chim Acta
, vol.371
, pp. 1-12
-
-
Valdivielso, J.M.1
Fernandez, E.2
-
35
-
-
34548051122
-
Association between vitamin D receptor gene polymorphism and Alzheimer's disease
-
10.1620/tjem.212.275, 17592215
-
Gezen-Ak D, Dursun E, Ertan T, Hanagasi H, Gürvit H, Emre M, Eker E, Oztürk M, Engin F, Yilmazer S. Association between vitamin D receptor gene polymorphism and Alzheimer's disease. Tohoku J Exp Med 2007, 212:275-82. 10.1620/tjem.212.275, 17592215.
-
(2007)
Tohoku J Exp Med
, vol.212
, pp. 275-282
-
-
Gezen-Ak, D.1
Dursun, E.2
Ertan, T.3
Hanagasi, H.4
Gürvit, H.5
Emre, M.6
Eker, E.7
Oztürk, M.8
Engin, F.9
Yilmazer, S.10
-
36
-
-
58549111852
-
VDR gene variants associate with cognitive function and depressive symptoms in old age
-
10.1016/j.neurobiolaging.2007.07.001, 17714831
-
Kuningas M, Mooijaart SP, Jolles J, Slagboom PE, Westendorp RG, van Heemst D. VDR gene variants associate with cognitive function and depressive symptoms in old age. Neurobiol Aging 2009, 30:466-73. 10.1016/j.neurobiolaging.2007.07.001, 17714831.
-
(2009)
Neurobiol Aging
, vol.30
, pp. 466-473
-
-
Kuningas, M.1
Mooijaart, S.P.2
Jolles, J.3
Slagboom, P.E.4
Westendorp, R.G.5
van Heemst, D.6
-
37
-
-
84874313360
-
International HapMap project web site
-
International HapMap project web site. , http://www.hapmap.org/
-
-
-
-
38
-
-
84874667657
-
NCBI FTP site
-
NCBI FTP site. , http://www.ncbi.nlm.nih.gov/Ftp/
-
-
-
-
39
-
-
77953338421
-
Haplotter database
-
Haplotter database. , http://hg-wen.uchicago.edu/selection/haplotter.htm
-
-
-
-
40
-
-
43849112140
-
GENOMEPOP: a program to simulate genomes in populations
-
10.1186/1471-2105-9-223, 2386491, 18447924
-
Carvajal-Rodríguez A. GENOMEPOP: a program to simulate genomes in populations. BMC Bioinformatics 2008, 9:223. 10.1186/1471-2105-9-223, 2386491, 18447924.
-
(2008)
BMC Bioinformatics
, vol.9
, pp. 223
-
-
Carvajal-Rodríguez, A.1
|