-
1
-
-
84943171338
-
A global reference for human genetic variation
-
Genomes Project Consortium Auton, A., L. D. Brooks, R. M. Durbin, E. P. Garrison et al., 2015 A global reference for human genetic variation. Nature 526: 68–74.
-
(2015)
Nature
, vol.526
, pp. 68-74
-
-
Auton, A.1
Brooks, L.D.2
Durbin, R.M.3
Garrison, E.P.4
-
2
-
-
77951640946
-
A method and server for predicting damaging mis-sense mutations
-
Adzhubei, I. A., S. Schmidt, L. Peshkin, V. E. Ramensky, A. Gerasimova et al., 2010 A method and server for predicting damaging mis-sense mutations. Nat. Methods 7: 248–249.
-
(2010)
Nat. Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
Ramensky, V.E.4
Gerasimova, A.5
-
3
-
-
33745626459
-
Improved scoring of functional groups from gene expression data by decorrelating GO graph structure
-
Alexa, A., J. Rahnenfuhrer, and T. Lengauer, 2006 Improved scoring of functional groups from gene expression data by decorrelating GO graph structure. Bioinformatics 22: 1600–1607.
-
(2006)
Bioinformatics
, vol.22
, pp. 1600-1607
-
-
Alexa, A.1
Rahnenfuhrer, J.2
Lengauer, T.3
-
4
-
-
0032410933
-
Social transmission of reproductive behavior increases frequency of inherited disorders in a young-expanding population
-
Austerlitz, F., and E. Heyer, 1998 Social transmission of reproductive behavior increases frequency of inherited disorders in a young-expanding population. Proc. Natl. Acad. Sci. USA 95: 15140–15144.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 15140-15144
-
-
Austerlitz, F.1
Heyer, E.2
-
5
-
-
84878835954
-
Cohort profile of the CARTaGENE study: Quebec’s population-based biobank for public health and personalized genomics
-
Awadalla, P., C. Boileau, Y. Payette, Y. Idaghdour, J. P. Goulet et al., 2013 Cohort profile of the CARTaGENE study: Quebec’s population-based biobank for public health and personalized genomics. Int. J. Epidemiol. 42: 1285–1299.
-
(2013)
Int. J. Epidemiol.
, vol.42
, pp. 1285-1299
-
-
Awadalla, P.1
Boileau, C.2
Payette, Y.3
Idaghdour, Y.4
Goulet, J.P.5
-
6
-
-
0030467524
-
Evaluating loci for use in the genetic analysis of population structure
-
Beaumont, M. A., and R. A. Nichols, 1996 Evaluating loci for use in the genetic analysis of population structure. Proc. Biol. Sci. 263: 1619–1626.
-
(1996)
Proc. Biol. Sci
, vol.263
, pp. 1619-1626
-
-
Beaumont, M.A.1
Nichols, R.A.2
-
7
-
-
79951500671
-
Admixed ancestry and stratification of Quebec regional populations
-
Bherer, C., D. Labuda, M. H. Roy-Gagnon, L. Houde, M. Tremblay et al., 2011 Admixed ancestry and stratification of Quebec regional populations. Am. J. Phys. Anthropol. 144: 432–441.
-
(2011)
Am. J. Phys. Anthropol.
, vol.144
, pp. 432-441
-
-
Bherer, C.1
Labuda, D.2
Roy-Gagnon, M.H.3
Houde, L.4
Tremblay, M.5
-
8
-
-
44949129000
-
Assessing the evolutionary impact of amino acid mutations in the human genome
-
Boyko, A. R., S. H. Williamson, A. R. Indap, J. D. Degenhardt, R. D. Hernandez et al., 2008 Assessing the evolutionary impact of amino acid mutations in the human genome. PLoS Genet. 4: e1000083.
-
(2008)
Plos Genet
, vol.4
-
-
Boyko, A.R.1
Williamson, S.H.2
Indap, A.R.3
Degenhardt, J.D.4
Hernandez, R.D.5
-
9
-
-
84884681237
-
Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans
-
Casals, F., A. Hodgkinson, J. Hussin, Y. Idaghdour, V. Bruat et al., 2013 Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans. PLoS Genet. 9: e1003815.
-
(2013)
Plos Genet
, vol.9
-
-
Casals, F.1
Hodgkinson, A.2
Hussin, J.3
Idaghdour, Y.4
Bruat, V.5
-
10
-
-
4444265263
-
The population of the St. Lawrence Valley, 1608–1760
-
M. R. Haines, and R. H. Steckel. Cambridge University Press, New York
-
Charbonneau, H., B. Desjardins, J. Légaré, and H. Denis, 2000 The population of the St. Lawrence Valley, 1608–1760, pp. 99–142 in A Population History of North America, edited by M. R. Haines, and R. H. Steckel. Cambridge University Press, New York.
-
(2000)
A Population History of North America
, pp. 99-142
-
-
Charbonneau, H.1
Desjardins, B.2
Légaré, J.3
Denis, H.4
-
11
-
-
22244452677
-
Distribution and intensity of constraint in mammalian genomic sequence
-
Cooper, G. M., E. A. Stone, G. Asimenos, N. C. S. Program, E. D. Green et al., 2005 Distribution and intensity of constraint in mammalian genomic sequence. Genome Res. 15: 901–913.
-
(2005)
Genome Res
, vol.15
, pp. 901-913
-
-
Cooper, G.M.1
Stone, E.A.2
Asimenos, G.3
Program, N.C.S.4
Green, E.D.5
-
12
-
-
78651237647
-
Identifying a high fraction of the human genome to be under selective constraint using GERP++
-
Davydov, E. V., D. L. Goode, M. Sirota, G. M. Cooper, A. Sidow et al., 2010 Identifying a high fraction of the human genome to be under selective constraint using GERP++. PLoS Comput. Biol. 6: e1001025.
-
(2010)
Plos Comput. Biol.
, vol.6
-
-
Davydov, E.V.1
Goode, D.L.2
Sirota, M.3
Cooper, G.M.4
Sidow, A.5
-
13
-
-
0025756913
-
Hereditary disorders in Saguenay-Lac-St-Jean (Quebec, Canada)
-
De Braekeleer, M., 1991 Hereditary disorders in Saguenay-Lac-St-Jean (Quebec, Canada). Hum. Hered. 41: 141–146.
-
(1991)
Hum. Hered.
, vol.41
, pp. 141-146
-
-
De Braekeleer, M.1
-
14
-
-
84926169268
-
No evidence that selection has been less effective at removing deleterious mutations in Europeans than in Africans
-
Do, R., D. Balick, H. Li, I. Adzhubei, S. Sunyaev et al., 2015 No evidence that selection has been less effective at removing deleterious mutations in Europeans than in Africans. Nat. Genet. 47: 126–131.
-
(2015)
Nat. Genet
, vol.47
, pp. 126-131
-
-
Do, R.1
Balick, D.2
Li, H.3
Adzhubei, I.4
Sunyaev, S.5
-
15
-
-
68449101067
-
Mapping identifiers for the integration of genomic data- sets with the R/Bioconductor package biomaRt
-
Durinck, S., P. T. Spellman, E. Birney, and W. Huber, 2009 Mapping identifiers for the integration of genomic data- sets with the R/Bioconductor package biomaRt. Nat. Protoc. 4: 1184–1191.
-
(2009)
Nat. Protoc.
, vol.4
, pp. 1184-1191
-
-
Durinck, S.1
Spellman, P.T.2
Birney, E.3
Huber, W.4
-
16
-
-
77953032930
-
Arlequin suite ver 3.5: A new series of programs to perform population genetics analyses under Linux and Windows
-
Excoffier, L., and H. E. Lischer, 2010 Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows. Mol. Ecol. Resour. 10: 564–567.
-
(2010)
Mol. Ecol. Resour.
, vol.10
, pp. 564-567
-
-
Excoffier, L.1
Lischer, H.E.2
-
17
-
-
84887312794
-
Robust demographic inference from genomic and SNP data
-
Excoffier, L., I. Dupanloup, E. Huerta-Sánchez, V. C. Sousa, and M. Foll, 2013 Robust demographic inference from genomic and SNP data. PLoS Genet. 9: e1003905.
-
(2013)
Plos Genet
, vol.9
-
-
Excoffier, L.1
Dupanloup, I.2
Huerta-Sánchez, E.3
Sousa, V.C.4
Foll, M.5
-
18
-
-
34447546660
-
The distribution of fitness effects of new mutations
-
Eyre-Walker, A., and P. D. Keightley, 2007 The distribution of fitness effects of new mutations. Nat. Rev. Genet. 8: 610–618.
-
(2007)
Nat. Rev. Genet.
, vol.8
, pp. 610-618
-
-
Eyre-Walker, A.1
Keightley, P.D.2
-
19
-
-
84872143942
-
Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants
-
Fu, W., T. D. O’Connor, G. Jun, H. M. Kang, G. Abecasis et al., 2013 Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants. Nature 493: 216–220.
-
(2013)
Nature
, vol.493
, pp. 216-220
-
-
Fu, W.1
O’Connor, T.D.2
Jun, G.3
Kang, H.M.4
Abecasis, G.5
-
20
-
-
84921818763
-
Characteristics of neutral and deleterious protein-coding variation among individuals and populations
-
Fu, W., R. M. Gittelman, M. J. Bamshad, and J. M. Akey, 2014 Characteristics of neutral and deleterious protein-coding variation among individuals and populations. Am. J. Hum. Genet. 95: 421–436.
-
(2014)
Am. J. Hum. Genet.
, vol.95
, pp. 421-436
-
-
Fu, W.1
Gittelman, R.M.2
Bamshad, M.J.3
Akey, J.M.4
-
21
-
-
84887109646
-
Population growth inflates the per-individual number of deleterious mutations and reduces their mean effect
-
Gazave, E., D. Chang, A. G. Clark, and A. Keinan, 2013 Population growth inflates the per-individual number of deleterious mutations and reduces their mean effect. Genetics 195: 969–978.
-
(2013)
Genetics
, vol.195
, pp. 969-978
-
-
Gazave, E.1
Chang, D.2
Clark, A.G.3
Keinan, A.4
-
22
-
-
77649255315
-
Evolutionary constraint facilitates interpretation of genetic variation in resequenced human genomes
-
Goode, D. L., G. M. Cooper, J. Schmutz, M. Dickson, E. Gonzales et al., 2010 Evolutionary constraint facilitates interpretation of genetic variation in resequenced human genomes. Genome Res. 20: 301–310.
-
(2010)
Genome Res
, vol.20
, pp. 301-310
-
-
Goode, D.L.1
Cooper, G.M.2
Schmutz, J.3
Dickson, M.4
Gonzales, E.5
-
23
-
-
84979887636
-
When is selection effective?
-
Gravel, S., 2016 When is selection effective? Genetics 203: 451– 462.
-
(2016)
Genetics
, vol.203
, pp. 451-462
-
-
Gravel, S.1
-
24
-
-
79961091828
-
Demographic history and rare allele sharing among human populations
-
Gravel, S., B. M. Henn, R. N. Gutenkunst, A. R. Indap, G. T. Marth et al., 2011 Demographic history and rare allele sharing among human populations. Proc. Natl. Acad. Sci. USA 108: 11983–11988.
-
(2011)
Proc. Natl. Acad. Sci. USA
, vol.108
, pp. 11983-11988
-
-
Gravel, S.1
Henn, B.M.2
Gutenkunst, R.N.3
Indap, A.R.4
Marth, G.T.5
-
25
-
-
84929509878
-
Estimating the mutation load in human genomes
-
Henn, B. M., L. R. Botigue, C. D. Bustamante, A. G. Clark, and S. Gravel, 2015 Estimating the mutation load in human genomes. Nat. Rev. Genet. 16: 333–343.
-
(2015)
Nat. Rev. Genet.
, vol.16
, pp. 333-343
-
-
Henn, B.M.1
Botigue, L.R.2
Bustamante, C.D.3
Clark, A.G.4
Gravel, S.5
-
26
-
-
84955508579
-
Distance from sub-Saharan Africa predicts mutational load in diverse human genomes
-
Henn, B. M., L. R. Botigue, S. Peischl, I. Dupanloup, M. Lipatov et al., 2016 Distance from sub-Saharan Africa predicts mutational load in diverse human genomes. Proc. Natl. Acad. Sci. USA 113: E440–E449.
-
(2016)
Proc. Natl. Acad. Sci. USA
, vol.113
, pp. E440-E449
-
-
Henn, B.M.1
Botigue, L.R.2
Peischl, S.3
Dupanloup, I.4
Lipatov, M.5
-
27
-
-
0029151236
-
Genetic consequences of differential demographic behavior in the Saguenay region, Quebec
-
Heyer, E., 1995 Genetic consequences of differential demographic behavior in the Saguenay region, Quebec. Am. J. Phys. Anthropol. 98: 1–11.
-
(1995)
Am. J. Phys. Anthropol
, vol.98
, pp. 1-11
-
-
Heyer, E.1
-
28
-
-
0033083369
-
One founder/one gene hypothesis in a new expanding population: Saguenay (Quebec, Canada)
-
Heyer, E., 1999 One founder/one gene hypothesis in a new expanding population: Saguenay (Quebec, Canada). Hum. Biol. 71: 99–109.
-
(1999)
Hum. Biol.
, vol.71
, pp. 99-109
-
-
Heyer, E.1
-
29
-
-
5844400942
-
-
Les Presses de l’Université de Montréal, Montréal
-
Jetté, R., 1991 Traité de Généalogie. Les Presses de l’Université de Montréal, Montréal.
-
(1991)
Traité De Généalogie
-
-
Jetté, R.1
-
30
-
-
84860817223
-
Recent explosive human population growth has resulted in an excess of rare genetic variants
-
Keinan, A., and A. G. Clark, 2012 Recent explosive human population growth has resulted in an excess of rare genetic variants. Science 336: 740–743.
-
(2012)
Science
, vol.336
, pp. 740-743
-
-
Keinan, A.1
Clark, A.G.2
-
31
-
-
84874773677
-
Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequency
-
Kiezun, A., S. L. Pulit, L. C. Francioli, F. van Dijk, M. Swertz et al., 2013 Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequency. PLoS Genet. 9: e1003301.
-
(2013)
Plos Genet
, vol.9
-
-
Kiezun, A.1
Pulit, S.L.2
Francioli, L.C.3
Van Dijk, F.4
Swertz, M.5
-
32
-
-
85020727089
-
Inference of the distribution of selection coefficients for new nonsynonymous mutations using large samples
-
Kim, B. Y., C. D. Huber, and K. E. Lohmueller, 2017 Inference of the distribution of selection coefficients for new nonsynonymous mutations using large samples. Genetics 206: 345–361.
-
(2017)
Genetics
, vol.206
, pp. 345-361
-
-
Kim, B.Y.1
Huber, C.D.2
Lohmueller, K.E.3
-
33
-
-
84895858942
-
A general framework for estimating the relative pathogenicity of human genetic variants
-
Kircher, M., D. M. Witten, P. Jain, B. J. O’Roak, G. M. Cooper et al., 2014 A general framework for estimating the relative pathogenicity of human genetic variants. Nat. Genet. 46: 310–315.
-
(2014)
Nat. Genet
, vol.46
, pp. 310-315
-
-
Kircher, M.1
Witten, D.M.2
Jain, P.3
O’Roak, B.J.4
Cooper, G.M.5
-
34
-
-
0034127251
-
The effects of a bottleneck on inbreeding depression and the genetic load
-
Kirkpatrick, M., and P. Jarne, 2000 The effects of a bottleneck on inbreeding depression and the genetic load. Am. Nat. 155: 154–167.
-
(2000)
Am. Nat.
, vol.155
, pp. 154-167
-
-
Kirkpatrick, M.1
Jarne, P.2
-
35
-
-
33244467305
-
The fate of mutations surfing on the wave of a range expansion
-
Klopfstein, S., M. Currat, and L. Excoffier, 2006 The fate of mutations surfing on the wave of a range expansion. Mol. Biol. Evol. 23: 482–490.
-
(2006)
Mol. Biol. Evol.
, vol.23
, pp. 482-490
-
-
Klopfstein, S.1
Currat, M.2
Excoffier, L.3
-
36
-
-
25144485002
-
Population history and its impact on medical genetics in Quebec
-
Laberge, A. M., J. Michaud, A. Richter, E. Lemyre, M. Lambert et al., 2005 Population history and its impact on medical genetics in Quebec. Clin. Genet. 68: 287–301.
-
(2005)
Clin. Genet.
, vol.68
, pp. 287-301
-
-
Laberge, A.M.1
Michaud, J.2
Richter, A.3
Lemyre, E.4
Lambert, M.5
-
37
-
-
84891809093
-
ClinVar: Public archive of relationships among sequence variation and human phenotype
-
Landrum, M. J., J. M. Lee, G. R. Riley, W. Jang, W. S. Rubinstein et al., 2014 ClinVar: public archive of relationships among sequence variation and human phenotype. Nucleic Acids Res. 42: D980–D985.
-
(2014)
Nucleic Acids Res
, vol.42
, pp. D980-D985
-
-
Landrum, M.J.1
Lee, J.M.2
Riley, G.R.3
Jang, W.4
Rubinstein, W.S.5
-
38
-
-
84906497659
-
The distribution of deleterious genetic variation in human populations
-
Lohmueller, K. E., 2014 The distribution of deleterious genetic variation in human populations. Curr. Opin. Genet. Dev. 29: 139–146.
-
(2014)
Curr. Opin. Genet. Dev
, vol.29
, pp. 139-146
-
-
Lohmueller, K.E.1
-
39
-
-
39749139577
-
Proportionally more deleterious genetic variation in European than in African populations
-
Lohmueller, K. E., A. R. Indap, S. Schmidt, A. R. Boyko, R. D. Hernandez et al., 2008 Proportionally more deleterious genetic variation in European than in African populations. Nature 451: 994–997.
-
(2008)
Nature
, vol.451
, pp. 994-997
-
-
Lohmueller, K.E.1
Indap, A.R.2
Schmidt, S.3
Boyko, A.R.4
Hernandez, R.D.5
-
40
-
-
82255175508
-
Deep human genealogies reveal a selective advantage to be on an expanding wave front
-
Moreau, C., C. Bherer, H. Vezina, M. Jomphe, D. Labuda et al., 2011 Deep human genealogies reveal a selective advantage to be on an expanding wave front. Science 334: 1148–1150.
-
(2011)
Science
, vol.334
, pp. 1148-1150
-
-
Moreau, C.1
Bherer, C.2
Vezina, H.3
Jomphe, M.4
Labuda, D.5
-
41
-
-
84863541347
-
An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people
-
Nelson, M. R., D. Wegmann, M. G. Ehm, D. Kessner, P. St Jean et al., 2012 An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people. Science 337: 100–104.
-
(2012)
Science
, vol.337
, pp. 100-104
-
-
Nelson, M.R.1
Wegmann, D.2
Ehm, M.G.3
Kessner, D.4
St Jean, P.5
-
42
-
-
84928546633
-
Expansion load: Recessive mutations and the role of standing genetic variation
-
Peischl, S., and L. Excoffier, 2015 Expansion load: recessive mutations and the role of standing genetic variation. Mol. Ecol. 24: 2084–2094.
-
(2015)
Mol. Ecol.
, vol.24
, pp. 2084-2094
-
-
Peischl, S.1
Excoffier, L.2
-
43
-
-
84890120078
-
On the accumulation of deleterious mutations during range expansions
-
Peischl, S., I. Dupanloup, M. Kirkpatrick, and L. Excoffier, 2013 On the accumulation of deleterious mutations during range expansions. Mol. Ecol. 22: 5972–5982.
-
(2013)
Mol. Ecol.
, vol.22
, pp. 5972-5982
-
-
Peischl, S.1
Dupanloup, I.2
Kirkpatrick, M.3
Excoffier, L.4
-
44
-
-
84928251107
-
Expansion load and the evolutionary dynamics of a species range
-
Peischl, S., M. Kirkpatrick, and L. Excoffier, 2015 Expansion load and the evolutionary dynamics of a species range. Am. Nat. 185: E81–E93.
-
(2015)
Am. Nat.
, vol.185
, pp. E81-E93
-
-
Peischl, S.1
Kirkpatrick, M.2
Excoffier, L.3
-
45
-
-
84983784726
-
Genetic surfing in human populations: From genes to genomes
-
Peischl, S., I. Dupanloup, L. Bosshard, and L. Excoffier, 2016 Genetic surfing in human populations: from genes to genomes. Curr. Opin. Genet. Dev. 41: 53–61.
-
(2016)
Curr. Opin. Genet. Dev
, vol.41
, pp. 53-61
-
-
Peischl, S.1
Dupanloup, I.2
Bosshard, L.3
Excoffier, L.4
-
46
-
-
74949092081
-
Detection of nonneutral substitution rates on mammalian phylogenies
-
Pollard, K. S., M. J. Hubisz, K. R. Rosenbloom, and A. Siepel, 2010 Detection of nonneutral substitution rates on mammalian phylogenies. Genome Res. 20: 110–121.
-
(2010)
Genome Res
, vol.20
, pp. 110-121
-
-
Pollard, K.S.1
Hubisz, M.J.2
Rosenbloom, K.R.3
Siepel, A.4
-
47
-
-
84912075546
-
Approximation to the distribution of fitness effects across functional categories in human segregating polymorphisms
-
Racimo, F., and J. G. Schraiber, 2014 Approximation to the distribution of fitness effects across functional categories in human segregating polymorphisms. PLoS Genet. 10: e1004697.
-
(2014)
Plos Genet
, vol.10
-
-
Racimo, F.1
Schraiber, J.G.2
-
48
-
-
84928209346
-
Standards and guidelines for the interpretation of sequence variants: A joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
-
Richards, S., N. Aziz, S. Bale, D. Bick, S. Das et al., 2015 Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet. Med. 17: 405–424.
-
(2015)
Genet. Med.
, vol.17
, pp. 405-424
-
-
Richards, S.1
Aziz, N.2
Bale, S.3
Bick, D.4
Das, S.5
-
49
-
-
83455176994
-
A method for inferring the rate of occurrence and fitness effects of advantageous mutations
-
Schneider, A., B. Charlesworth, A. Eyre-Walker, and P. D. Keightley, 2011 A method for inferring the rate of occurrence and fitness effects of advantageous mutations. Genetics 189: 1427–1437.
-
(2011)
Genetics
, vol.189
, pp. 1427-1437
-
-
Schneider, A.1
Charlesworth, B.2
Eyre-Walker, A.3
Keightley, P.D.4
-
50
-
-
0036727404
-
Wright-Fisher revisited: The case of fertility correlation
-
Sibert, A., F. Austerlitz, and E. Heyer, 2002 Wright-Fisher revisited: the case of fertility correlation. Theor. Popul. Biol. 62: 181– 197.
-
(2002)
Theor. Popul. Biol.
, vol.62
, pp. 181-197
-
-
Sibert, A.1
Austerlitz, F.2
Heyer, E.3
-
51
-
-
84895867277
-
The deleterious mutation load is insensitive to recent population history
-
Simons, Y. B., M. C. Turchin, J. K. Pritchard, and G. Sella, 2014 The deleterious mutation load is insensitive to recent population history. Nat. Genet. 46: 220–224.
-
(2014)
Nat. Genet.
, vol.46
, pp. 220-224
-
-
Simons, Y.B.1
Turchin, M.C.2
Pritchard, J.K.3
Sella, G.4
-
52
-
-
84906493593
-
Impact of range expansions on current human genomic diversity
-
Sousa, V., S. Peischl, and L. Excoffier, 2014 Impact of range expansions on current human genomic diversity. Curr. Opin. Genet. Dev. 29: 22–30.
-
(2014)
Curr. Opin. Genet. Dev.
, vol.29
, pp. 22-30
-
-
Sousa, V.1
Peischl, S.2
Excoffier, L.3
-
53
-
-
0001507896
-
Coefficients of inbreeding and relationship
-
Wright, S., 1922 Coefficients of inbreeding and relationship. Am. Nat. 56: 330–338.
-
(1922)
Am. Nat
, vol.56
, pp. 330-338
-
-
Wright, S.1
-
54
-
-
26944468325
-
Anatomy of a founder effect: Myotonic dystrophy in Northeastern Quebec
-
Yotova, V., D. Labuda, E. Zietkiewicz, D. Gehl, A. Lovell et al., 2005 Anatomy of a founder effect: myotonic dystrophy in Northeastern Quebec. Hum. Genet. 117: 177–187.
-
(2005)
Hum. Genet.
, vol.117
, pp. 177-187
-
-
Yotova, V.1
Labuda, D.2
Zietkiewicz, E.3
Gehl, D.4
Lovell, A.5
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