-
2
-
-
84874782510
-
The population genetics of the Jewish people
-
Ostrer, H. & Skorecki, K. The population genetics of the Jewish people. Hum. Genet. 132, 119-127 (2013).
-
(2013)
Hum. Genet.
, vol.132
, pp. 119-127
-
-
Ostrer, H.1
Skorecki, K.2
-
3
-
-
31344439221
-
LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews
-
Ozelius, L. J. et al. LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews. N. Engl. J. Med. 354, 424-425 (2006).
-
(2006)
N. Engl. J. Med.
, vol.354
, pp. 424-425
-
-
Ozelius, L.J.1
-
4
-
-
0030910022
-
The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews
-
Struewing, J. P. et al. The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews. N. Engl. J. Med. 336, 1401-1408 (1997).
-
(1997)
N. Engl. J. Med.
, vol.336
, pp. 1401-1408
-
-
Struewing, J.P.1
-
5
-
-
77953231974
-
Abraham's children in the genome era: Major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry
-
Atzmon, G. et al. Abraham's children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry. Am. J. Hum. Genet. 86, 850-859 (2010).
-
(2010)
Am. J. Hum. Genet.
, vol.86
, pp. 850-859
-
-
Atzmon, G.1
-
6
-
-
77957999545
-
Signatures of founder effects, admixture, and selection in the Ashkenazi Jewish population
-
Bray, S. M. et al. Signatures of founder effects, admixture, and selection in the Ashkenazi Jewish population. Proc. Natl Acad. Sci. USA 107, 16222-16227 (2010).
-
(2010)
Proc. Natl Acad. Sci. USA
, vol.107
, pp. 16222-16227
-
-
Bray, S.M.1
-
7
-
-
60849097246
-
A genome-wide genetic signature of Jewish ancestry perfectly separates individuals with and without full Jewish ancestry in a large random sample of European Americans
-
Need, A. C., Kasperaviciute, D., Cirulli, E. T. & Goldstein, D. B. A genome-wide genetic signature of Jewish ancestry perfectly separates individuals with and without full Jewish ancestry in a large random sample of European Americans. Genome Biol. 10, R7 (2009).
-
(2009)
Genome Biol.
, vol.10
, pp. R7
-
-
Need, A.C.1
Kasperaviciute, D.2
Cirulli, E.T.3
Goldstein, D.B.4
-
8
-
-
38949104183
-
Discerning the ancestry of European Americans in genetic association studies
-
Price, A. L. et al. Discerning the ancestry of European Americans in genetic association studies. PLoS Genet. 4, e236 (2008).
-
(2008)
PLoS Genet.
, vol.4
, pp. e236
-
-
Price, A.L.1
-
9
-
-
77954542018
-
The genome-wide structure of the Jewish people
-
Behar, D. M. et al. The genome-wide structure of the Jewish people. Nature 466, 238-242 (2010).
-
(2010)
Nature
, vol.466
, pp. 238-242
-
-
Behar, D.M.1
-
10
-
-
73249132603
-
Genomic microsatellites identify shared Jewish ancestry intermediate between Middle Eastern and European populations
-
Kopelman, N. M. et al. Genomic microsatellites identify shared Jewish ancestry intermediate between Middle Eastern and European populations. BMC Genet. 10, 80 (2009).
-
(2009)
BMC Genet.
, vol.10
, pp. 80
-
-
Kopelman, N.M.1
-
11
-
-
84856084252
-
Implications for health and disease in the genetic signature of the Ashkenazi Jewish population
-
Guha, S. et al. Implications for health and disease in the genetic signature of the Ashkenazi Jewish population. Genome. Biol. 13, R2 (2012).
-
(2012)
Genome. Biol.
, vol.13
, pp. R2
-
-
Guha, S.1
-
12
-
-
84855900920
-
The architecture of long-range haplotypes shared within and across populations
-
Gusev, A. et al. The architecture of long-range haplotypes shared within and across populations. Mol. Biol. Evol. 29, 473-486 (2012).
-
(2012)
Mol. Biol. Evol.
, vol.29
, pp. 473-486
-
-
Gusev, A.1
-
13
-
-
40349093195
-
Analysis of genetic variation in Ashkenazi Jews by high density SNP genotyping
-
Olshen, A. B. et al. Analysis of genetic variation in Ashkenazi Jews by high density SNP genotyping. BMC Genet. 9, 14 (2008).
-
(2008)
BMC Genet.
, vol.9
, pp. 14
-
-
Olshen, A.B.1
-
14
-
-
84868450328
-
Length distributions of identity by descent reveal fine-scale demographic history
-
Palamara, P. F., Lencz, T., Darvasi, A. & Pe'er, I. Length distributions of identity by descent reveal fine-scale demographic history. Am. J. Hum. Genet. 91, 809-822 (2012).
-
(2012)
Am. J. Hum. Genet.
, vol.91
, pp. 809-822
-
-
Palamara, P.F.1
Lencz, T.2
Darvasi, A.3
Pe'Er, I.4
-
15
-
-
11244279011
-
An Icelandic example of the impact of population structure on association studies
-
Helgason, A., Yngvadottir, B., Hrafnkelsson, B., Gulcher, J. & Stefansson, K. An Icelandic example of the impact of population structure on association studies. Nat. Genet. 37, 90-95 (2005).
-
(2005)
Nat. Genet.
, vol.37
, pp. 90-95
-
-
Helgason, A.1
Yngvadottir, B.2
Hrafnkelsson, B.3
Gulcher, J.4
Stefansson, K.5
-
16
-
-
84878143904
-
Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits
-
Styrkarsdottir, U. et al. Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits. Nature 497, 517-520 (2013).
-
(2013)
Nature
, vol.497
, pp. 517-520
-
-
Styrkarsdottir, U.1
-
17
-
-
74949138753
-
Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays
-
Drmanac, R. et al. Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays. Science 327, 78-81 (2010).
-
(2010)
Science
, vol.327
, pp. 78-81
-
-
Drmanac, R.1
-
18
-
-
84975795680
-
An integrated map of genetic variation from 1, 092 human genomes
-
Genomes Project C et al. An integrated map of genetic variation from 1, 092 human genomes. Nature 491, 56-65 (2012).
-
(2012)
Nature
, vol.491
, pp. 56-65
-
-
-
19
-
-
12144291681
-
Contrasting patterns of y chromosome variation in Ashkenazi Jewish and host non-Jewish European populations
-
Behar, D. M. et al. Contrasting patterns of Y chromosome variation in Ashkenazi Jewish and host non-Jewish European populations. Hum. Genet. 114, 354-365 (2004).
-
(2004)
Hum. Genet.
, vol.114
, pp. 354-365
-
-
Behar, D.M.1
-
20
-
-
59949088494
-
Whole population, genome-wide mapping of hidden relatedness
-
Gusev, A. et al. Whole population, genome-wide mapping of hidden relatedness. Genome Res. 19, 318-326 (2009).
-
(2009)
Genome Res.
, vol.19
, pp. 318-326
-
-
Gusev, A.1
-
21
-
-
84876442367
-
The variance of identity-by-descent sharing in the wright-fisher model
-
Carmi, S. et al. The variance of identity-by-descent sharing in the wright-fisher model. Genetics 193, 911-928 (2013).
-
(2013)
Genetics
, vol.193
, pp. 911-928
-
-
Carmi, S.1
-
22
-
-
84863117175
-
Low-pass genome-wide sequencing and variant inference using identity-by-descent in an isolated human population
-
Gusev, A. et al. Low-pass genome-wide sequencing and variant inference using identity-by-descent in an isolated human population. Genetics 190, 679-689 (2012).
-
(2012)
Genetics
, vol.190
, pp. 679-689
-
-
Gusev, A.1
-
23
-
-
62649089065
-
Genotype-imputation accuracy across worldwide human populations
-
Huang, L. et al. Genotype-imputation accuracy across worldwide human populations. Am. J. Hum. Genet. 84, 235-250 (2009).
-
(2009)
Am. J. Hum. Genet.
, vol.84
, pp. 235-250
-
-
Huang, L.1
-
24
-
-
84864417548
-
Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
-
Howie, B., Fuchsberger, C., Stephens, M., Marchini, J. & Abecasis, G. R. Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. Nat. Genet. 44, 955-959 (2012).
-
(2012)
Nat. Genet.
, vol.44
, pp. 955-959
-
-
Howie, B.1
Fuchsberger, C.2
Stephens, M.3
Marchini, J.4
Abecasis, G.R.5
-
25
-
-
84860817223
-
Recent explosive human population growth has resulted in an excess of rare genetic variants
-
Keinan, A. & Clark, A. G. Recent explosive human population growth has resulted in an excess of rare genetic variants. Science 336, 740-743 (2012).
-
(2012)
Science
, vol.336
, pp. 740-743
-
-
Keinan, A.1
Clark, A.G.2
-
26
-
-
73449149044
-
Inferring the joint demographic history of multiple populations from multidimensional SNP frequency data
-
Gutenkunst, R. N., Hernandez, R. D., Williamson, S. H. & Bustamante, C. D. Inferring the joint demographic history of multiple populations from multidimensional SNP frequency data. PLoS Genet. 5, e1000695 (2009).
-
(2009)
PLoS Genet.
, vol.5
, pp. e1000695
-
-
Gutenkunst, R.N.1
Hernandez, R.D.2
Williamson, S.H.3
Bustamante, C.D.4
-
27
-
-
84860740251
-
Mitochondrial DNA signals of late glacial recolonization of Europe from near eastern refugia
-
Pala, M. et al. Mitochondrial DNA signals of late glacial recolonization of Europe from near eastern refugia. Am. J. Hum. Genet. 90, 915-924 (2012).
-
(2012)
Am. J. Hum. Genet.
, vol.90
, pp. 915-924
-
-
Pala, M.1
-
28
-
-
84865856910
-
Revising the human mutation rate: Implications for understanding human evolution
-
Scally, A. & Durbin, R. Revising the human mutation rate: implications for understanding human evolution. Nat. Rev. Genet. 13, 745-753 (2012).
-
(2012)
Nat. Rev. Genet.
, vol.13
, pp. 745-753
-
-
Scally, A.1
Durbin, R.2
-
29
-
-
84884413307
-
Properties and rates of germline mutations in humans
-
Campbell, C. D. & Eichler, E. E. Properties and rates of germline mutations in humans. Trends Genet 29, 575-584 (2013).
-
(2013)
Trends Genet
, vol.29
, pp. 575-584
-
-
Campbell, C.D.1
Eichler, E.E.2
-
30
-
-
84892684329
-
Reconstructing native american migrations from whole-genome and whole-exome data
-
Gravel, S. et al. Reconstructing native american migrations from whole-genome and whole-exome data. PLoS Genet. 9, e1004023 (2013).
-
(2013)
PLoS Genet.
, vol.9
, pp. e1004023
-
-
Gravel, S.1
-
31
-
-
84865208871
-
Rate of de novo mutations and the importance of father's age to disease risk
-
Kong, A. et al. Rate of de novo mutations and the importance of father's age to disease risk. Nature 488, 471-475 (2012).
-
(2012)
Nature
, vol.488
, pp. 471-475
-
-
Kong, A.1
-
32
-
-
84906855270
-
Determinants of mutation rate variation in the human germline
-
Ségurel, L., Wyman, M. J. & Przeworski, M. Determinants of mutation rate variation in the human germline. Annu. Rev. Genomics Hum. Genet. 15, 11-19.24 (2014).
-
(2014)
Annu. Rev. Genomics Hum. Genet.
, vol.15
, pp. 1119-1124
-
-
Ségurel, L.1
Wyman, M.J.2
Przeworski, M.3
-
33
-
-
79961091828
-
Demographic history and rare allele sharing among human populations
-
Gravel, S. et al. Demographic history and rare allele sharing among human populations. Proc. Natl Acad. Sci. USA 108, 11983-11988 (2011).
-
(2011)
Proc. Natl Acad. Sci. USA
, vol.108
, pp. 11983-11988
-
-
Gravel, S.1
-
34
-
-
34748819978
-
Measurement of the human allele frequency spectrum demonstrates greater genetic drift in East Asians than in Europeans
-
Keinan, A., Mullikin, J. C., Patterson, N. & Reich, D. Measurement of the human allele frequency spectrum demonstrates greater genetic drift in East Asians than in Europeans. Nat. Genet. 39, 1251-1255 (2007).
-
(2007)
Nat. Genet.
, vol.39
, pp. 1251-1255
-
-
Keinan, A.1
Mullikin, J.C.2
Patterson, N.3
Reich, D.4
-
35
-
-
81855164876
-
The earliest evidence for anatomically modern humans in northwestern Europe
-
Higham, T. et al. The earliest evidence for anatomically modern humans in northwestern Europe. Nature 479, 521-524 (2011).
-
(2011)
Nature
, vol.479
, pp. 521-524
-
-
Higham, T.1
-
36
-
-
84874762618
-
Genome-wide diversity in the levant reveals recent structuring by culture
-
Haber, M. et al. Genome-wide diversity in the levant reveals recent structuring by culture. PLoS Genet. 9, e1003316 (2013).
-
(2013)
PLoS Genet.
, vol.9
, pp. e1003316
-
-
Haber, M.1
-
37
-
-
84868692234
-
A calibrated human Y-chromosomal phylogeny based on resequencing
-
Wei, W. et al. A calibrated human Y-chromosomal phylogeny based on resequencing. Genome Res. 23, 388-395 (2013).
-
(2013)
Genome Res.
, vol.23
, pp. 388-395
-
-
Wei, W.1
-
38
-
-
84860132302
-
Origins and genetic legacy of Neolithic farmers and hunter-gatherers in Europe
-
Skoglund, P. et al. Origins and genetic legacy of Neolithic farmers and hunter-gatherers in Europe. Science 336, 466-469 (2012).
-
(2012)
Science
, vol.336
, pp. 466-469
-
-
Skoglund, P.1
-
39
-
-
78649929790
-
Ancient DNA from European early neolithic farmers reveals their near eastern affinities
-
Haak, W. et al. Ancient DNA from European early neolithic farmers reveals their near eastern affinities. PLoS Biol. 8, e1000536 (2010).
-
(2010)
PLoS Biol.
, vol.8
, pp. e1000536
-
-
Haak, W.1
-
40
-
-
84885625204
-
Ancient DNA reveals key stages in the formation of central European mitochondrial genetic diversity
-
Brandt, G. et al. Ancient DNA reveals key stages in the formation of central European mitochondrial genetic diversity. Science 342, 257-261 (2013).
-
(2013)
Science
, vol.342
, pp. 257-261
-
-
Brandt, G.1
-
42
-
-
84901614381
-
Population genomic analysis of ancient and modern genomes yields new insights into the genetic ancestry of the Tyrolean Iceman and the genetic structure of Europe
-
Sikora, M. et al. Population genomic analysis of ancient and modern genomes yields new insights into the genetic ancestry of the Tyrolean Iceman and the genetic structure of Europe. PLoS Genet. 10, e1004353 (2014).
-
(2014)
PLoS Genet.
, vol.10
, pp. e1004353
-
-
Sikora, M.1
-
43
-
-
84884681237
-
Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans
-
Casals, F. et al. 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).
-
(2013)
PLoS Genet.
, vol.9
, pp. e1003815
-
-
Casals, F.1
-
44
-
-
39749139577
-
Proportionally more deleterious genetic variation in European than in African populations
-
Lohmueller, K. E. et al. Proportionally more deleterious genetic variation in European than in African populations. Nature 451, 994-997 (2008).
-
(2008)
Nature
, vol.451
, pp. 994-997
-
-
Lohmueller, K.E.1
-
45
-
-
84863556835
-
Evolution and functional impact of rare coding variation from deep sequencing of human exomes
-
Tennessen, J. A. et al. Evolution and functional impact of rare coding variation from deep sequencing of human exomes. Science 337, 64-69 (2012).
-
(2012)
Science
, vol.337
, pp. 64-69
-
-
Tennessen, J.A.1
-
46
-
-
84895867277
-
The deleterious mutation load is insensitive to recent population history
-
Simons, Y. B., Turchin, M. C., Pritchard, J. K. & Sella, G. The deleterious mutation load is insensitive to recent population history. Nat. Genet. 46, 220-224 (2014).
-
(2014)
Nat. Genet.
, vol.46
, pp. 220-224
-
-
Simons, Y.B.1
Turchin, M.C.2
Pritchard, J.K.3
Sella, G.4
-
47
-
-
79952186533
-
Global analysis of disease-related DNA sequence variation in 10 healthy individuals: Implications for whole genome-based clinical diagnostics
-
Moore, B. et al. Global analysis of disease-related DNA sequence variation in 10 healthy individuals: implications for whole genome-based clinical diagnostics. Genet. Med. 13, 210-217 (2011).
-
(2011)
Genet. Med.
, vol.13
, pp. 210-217
-
-
Moore, B.1
-
48
-
-
84893361550
-
Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder
-
Lencz, T. et al. Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder. Nat. Commun. 4, 2739 (2013).
-
(2013)
Nat. Commun.
, vol.4
, pp. 2739
-
-
Lencz, T.1
-
49
-
-
84859253322
-
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci
-
Kenny, E. E. et al. A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. PLoS Genet. 8, e1002559 (2012).
-
(2012)
PLoS Genet.
, vol.8
, pp. e1002559
-
-
Kenny, E.E.1
-
50
-
-
84890690821
-
A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates
-
Tachmazidou, I. et al. A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates. Nat. Commun. 4, 2872 (2013).
-
(2013)
Nat. Commun.
, vol.4
, pp. 2872
-
-
Tachmazidou, I.1
-
51
-
-
84896718035
-
High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms
-
Kurki, M. I. et al. High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms. PLoS Genet. 10, e1004134 (2014).
-
(2014)
PLoS Genet.
, vol.10
, pp. e1004134
-
-
Kurki, M.I.1
-
52
-
-
84867487903
-
Distinguishing between longevity and buffered-deleterious genotypes for exceptional human longevity: The case of the MTP gene
-
Huffman, D. M. et al. Distinguishing between longevity and buffered-deleterious genotypes for exceptional human longevity: the case of the MTP gene. J. Gerontol. A. Biol. Sci. Med. Sci. 67, 1153-1160 (2012).
-
(2012)
J. Gerontol. A. Biol. Sci. Med. Sci.
, vol.67
, pp. 1153-1160
-
-
Huffman, D.M.1
-
53
-
-
0141535355
-
Familial aggregation of early-and late-onset Parkinson's disease
-
Marder, K. et al. Familial aggregation of early-and late-onset Parkinson's disease. Ann. Neurol. 54, 507-513 (2003).
-
(2003)
Ann. Neurol.
, vol.54
, pp. 507-513
-
-
Marder, K.1
-
54
-
-
79960981876
-
Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population
-
Liu, X. et al. Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population. BMC Med. Genet. 12, 104 (2011).
-
(2011)
BMC Med. Genet.
, vol.12
, pp. 104
-
-
Liu, X.1
-
55
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
Purcell, S. et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am. J. Hum. Genet. 81, 559-575 (2007).
-
(2007)
Am. J. Hum. Genet.
, vol.81
, pp. 559-575
-
-
Purcell, S.1
-
56
-
-
39749181521
-
Worldwide human relationships inferred from genome-wide patterns of variation
-
Li, J. Z. et al. Worldwide human relationships inferred from genome-wide patterns of variation. Science 319, 1100-1104 (2008).
-
(2008)
Science
, vol.319
, pp. 1100-1104
-
-
Li, J.Z.1
-
57
-
-
33846006923
-
Population structure and eigenanalysis
-
Patterson, N., Price, A. L. & Reich, D. Population structure and eigenanalysis. PLoS Genet. 2, e190 (2006).
-
(2006)
PLoS Genet.
, vol.2
, pp. e190
-
-
Patterson, N.1
Price, A.L.2
Reich, D.3
-
58
-
-
84871952176
-
Improved whole-chromosome phasing for disease and population genetic studies
-
Delaneau, O., Zagury, J. F. & Marchini, J. Improved whole-chromosome phasing for disease and population genetic studies. Nat. Methods. 10, 5-6 (2013).
-
(2013)
Nat. Methods.
, vol.10
, pp. 5-6
-
-
Delaneau, O.1
Zagury, J.F.2
Marchini, J.3
-
59
-
-
0036079158
-
The human genome browser at UCSC
-
Kent, W. J. et al. The human genome browser at UCSC. Genome Res. 12, 996-1006 (2002).
-
(2002)
Genome Res.
, vol.12
, pp. 996-1006
-
-
Kent, W.J.1
-
60
-
-
77956534324
-
ANNOVAR: Functional annotation of genetic variants from high-throughput sequencing data
-
Wang, K., Li, M. & Hakonarson, H. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res. 38, e164 (2010).
-
(2010)
Nucleic Acids Res.
, vol.38
, pp. e164
-
-
Wang, K.1
Li, M.2
Hakonarson, H.3
-
62
-
-
79955475534
-
Analytical results on the neutral non-equilibrium allele frequency spectrum based on diffusion theory
-
Zivkovic, D. & Stephan, W. Analytical results on the neutral non-equilibrium allele frequency spectrum based on diffusion theory. Theor. Popul. Biol. 79, 184-191 (2011).
-
(2011)
Theor. Popul. Biol.
, vol.79
, pp. 184-191
-
-
Zivkovic, D.1
Stephan, W.2
-
63
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
International HapMap C et al. A second generation human haplotype map of over 3.1 million SNPs. Nature 449, 851-861 (2007).
-
(2007)
Nature
, vol.449
, pp. 851-861
-
-
International Hapmap, C.1
-
64
-
-
67651222400
-
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies
-
Howie, B. N., Donnelly, P. & Marchini, J. A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet. 5, e1000529 (2009).
-
(2009)
PLoS Genet.
, vol.5
, pp. e1000529
-
-
Howie, B.N.1
Donnelly, P.2
Marchini, J.3
-
65
-
-
61449135985
-
Fast and flexible simulation of DNA sequence data
-
Chen, G. K., Marjoram, P. & Wall, J. D. Fast and flexible simulation of DNA sequence data. Genome Res. 19, 136-142 (2009).
-
(2009)
Genome Res.
, vol.19
, pp. 136-142
-
-
Chen, G.K.1
Marjoram, P.2
Wall, J.D.3
-
66
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
Adzhubei, I. A. et al. A method and server for predicting damaging missense mutations. Nat. Methods 7, 248-249 (2010).
-
(2010)
Nat. Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
-
67
-
-
78651237647
-
Identifying a high fraction of the human genome to be under selective constraint using GERP + +
-
Davydov, E. V. et al. Identifying a high fraction of the human genome to be under selective constraint using GERP + +. PLoS Comput. Biol. 6, e1001025 (2010).
-
(2010)
PLoS Comput. Biol.
, vol.6
, pp. e1001025
-
-
Davydov, E.V.1
-
68
-
-
27344435774
-
Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles
-
Subramanian, A. et al. Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles. Proc. Natl Acad. Sci. USA 102, 15545-15550 (2005).
-
(2005)
Proc. Natl Acad. Sci. USA
, vol.102
, pp. 15545-15550
-
-
Subramanian, A.1
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