-
1
-
-
0000874557
-
Theoretical foundations of the potential function method in pattern recognition learning
-
Aizerman A, Braverman EM, Rozoner L. 1964. Theoretical foundations of the potential function method in pattern recognition learning. Automat Remote Control 25:821-837.
-
(1964)
Automat Remote Control
, vol.25
, pp. 821-837
-
-
Aizerman, A.1
Braverman, E.M.2
Rozoner, L.3
-
2
-
-
80051732262
-
Accurate and comprehensive sequencing of personal genomes
-
Ajay SS, Parker SC, Abaan HO, Fajardo KVF,Margulies EH. 2011. Accurate and comprehensive sequencing of personal genomes. Genome Res. 21:1498-1505.
-
(2011)
Genome Res.
, vol.21
, pp. 1498-1505
-
-
Ajay, S.S.1
Parker, S.C.2
Abaan, H.O.3
Fajardo, K.V.F.4
Margulies, E.H.5
-
3
-
-
77049164783
-
Protection afforded by sickle-cell trait against subtertian malarial infection
-
Allison AC. 1954. Protection afforded by sickle-cell trait against subtertian malarial infection. Br Med J. 1:290-294.
-
(1954)
Br Med J.
, vol.1
, pp. 290-294
-
-
Allison, A.C.1
-
4
-
-
84975795680
-
An integrated map of genetic variation from 1,092 human genomes
-
Altshuler DM, et al. 2012. An integrated map of genetic variation from 1,092 human genomes. Nature 491:56-65.
-
(2012)
Nature
, vol.491
, pp. 56-65
-
-
Altshuler, D.M.1
-
5
-
-
4444291477
-
Maternal transmission disequilibrium of the glutamate receptor GRIK2 in schizophrenia
-
Bah J, et al. 2004. Maternal transmission disequilibrium of the glutamate receptor GRIK2 in schizophrenia. Neuroreport 15:1987-1991.
-
(2004)
Neuroreport
, vol.15
, pp. 1987-1991
-
-
Bah, J.1
-
6
-
-
34249026300
-
High-resolution profiling of histone methylations in the human genome
-
Barski A, et al. 2007. High-resolution profiling of histone methylations in the human genome. Cell 129:823-837.
-
(2007)
Cell
, vol.129
, pp. 823-837
-
-
Barski, A.1
-
8
-
-
34250305146
-
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
-
Birney E, et al. 2007. Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Nature 447:799-816.
-
(2007)
Nature
, vol.447
, pp. 799-816
-
-
Birney, E.1
-
9
-
-
0034646993
-
Regulation of area identity in the mammalian neocortex by Emx2 and Pax6
-
Bishop KM, Goudreau G, O'Leary DD. 2000. Regulation of area identity in the mammalian neocortex by Emx2 and Pax6. Science 288:344-349.
-
(2000)
Science
, vol.288
, pp. 344-349
-
-
Bishop, K.M.1
Goudreau, G.2
O'Leary, D.D.3
-
11
-
-
44949129000
-
Assessing the evolutionary impact of amino acid mutations in the human genome
-
Boyko AR, 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
-
12
-
-
38649099445
-
High-resolution mapping and characterization of open chromatin across the genome
-
Boyle AP, et al. 2008. High-resolution mapping and characterization of open chromatin across the genome. Cell 132:311-322.
-
(2008)
Cell
, vol.132
, pp. 311-322
-
-
Boyle, A.P.1
-
13
-
-
33747857635
-
Scan of human genome reveals no new loci under ancient balancing selection
-
Bubb KL, et al. 2006. Scan of human genome reveals no new loci under ancient balancing selection. Genetics 173:2165-2177.
-
(2006)
Genetics
, vol.173
, pp. 2165-2177
-
-
Bubb, K.L.1
-
14
-
-
0034606207
-
NURR1 mutations in cases of schizophrenia and manic-depressive disorder
-
Buervenich S, et al. 2000. NURR1 mutations in cases of schizophrenia and manic-depressive disorder. Am J Med Genet. 96:808-813.
-
(2000)
Am J Med Genet.
, vol.96
, pp. 808-813
-
-
Buervenich, S.1
-
15
-
-
85047700330
-
Association between a GABRB3 polymorphism and autism
-
Buxbaum J, et al. 2002. Association between a GABRB3 polymorphism and autism. Mol Psychiatry. 7:311-316.
-
(2002)
Mol Psychiatry.
, vol.7
, pp. 311-316
-
-
Buxbaum, J.1
-
16
-
-
0345040882
-
Support vector machine applications in bioinformatics
-
Byvatov E, Schneider G. 2003. Support vector machine applications in bioinformatics. Appl Bioinformatics 2:67-77.
-
(2003)
Appl Bioinformatics
, vol.2
, pp. 67-77
-
-
Byvatov, E.1
Schneider, G.2
-
17
-
-
80052978224
-
Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclasses
-
Cabili MN, et al. 2011. Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclasses. Genes Dev. 25:1915-1927.
-
(2011)
Genes Dev.
, vol.25
, pp. 1915-1927
-
-
Cabili, M.N.1
-
19
-
-
0027305597
-
The effect of deleterious mutations on neutral molecular variation
-
Charlesworth B, Morgan M, Charlesworth D. 1993. The effect of deleterious mutations on neutral molecular variation. Genetics 134:1289-1303.
-
(1993)
Genetics
, vol.134
, pp. 1289-1303
-
-
Charlesworth, B.1
Morgan, M.2
Charlesworth, D.3
-
20
-
-
0035829981
-
Mutation analysis of the human NR4A2 gene, an essential gene for midbrain dopaminergic neurogenesis, in schizophrenic patients
-
Chen YH, Tsai MT, Shaw CK, Chen CH. 2001. Mutation analysis of the human NR4A2 gene, an essential gene for midbrain dopaminergic neurogenesis, in schizophrenic patients. Am J Med Genet. 105:753-757.
-
(2001)
Am J Med Genet.
, vol.105
, pp. 753-757
-
-
Chen, Y.H.1
Tsai, M.T.2
Shaw, C.K.3
Chen, C.H.4
-
21
-
-
1542563409
-
Initial sequencing and comparative analysis of the mouse genome
-
Chinwalla AT, et al. 2002. Initial sequencing and comparative analysis of the mouse genome. Nature 420:520-562.
-
(2002)
Nature
, vol.420
, pp. 520-562
-
-
Chinwalla, A.T.1
-
22
-
-
0032578387
-
A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergence
-
Chou HH, et al. 1998. A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergence. Proc Natl Acad Sci U S A. 95:11751-11756.
-
(1998)
Proc Natl Acad Sci U S A.
, vol.95
, pp. 11751-11756
-
-
Chou, H.H.1
-
23
-
-
7244245762
-
Finishing the euchromatic sequence of the human genome
-
Collins F, Lander E, Rogers J, Waterston R, Conso I. 2004. Finishing the euchromatic sequence of the human genome. Nature 431:931-945.
-
(2004)
Nature
, vol.431
, pp. 931-945
-
-
Collins, F.1
Lander, E.2
Rogers, J.3
Waterston, R.4
Conso, I.5
-
24
-
-
34249753618
-
Support-vector networks
-
Cortes C, Vapnik V. 1995. Support-vector networks. Mach Learn. 20:273-297.
-
(1995)
Mach Learn.
, vol.20
, pp. 273-297
-
-
Cortes, C.1
Vapnik, V.2
-
25
-
-
84879911829
-
The evolution of lineage-specific regulatory activities in the human embryonic limb
-
Cotney J, et al. 2013. The evolution of lineage-specific regulatory activities in the human embryonic limb. Cell 154:185-196.
-
(2013)
Cell
, vol.154
, pp. 185-196
-
-
Cotney, J.1
-
26
-
-
78651237647
-
Identifying a high fraction of the human genome to be under selective constraint using GERP++
-
Davydov EV, 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
-
27
-
-
84855989774
-
Fast computation and applications of genome mappability
-
Derrien T, et al. 2012. Fast computation and applications of genome mappability. PLoS One 7:e30377.
-
(2012)
PLoS One
, vol.7
-
-
Derrien, T.1
-
28
-
-
33244465618
-
Marital status, alcohol dependence, and GABRA2: Evidence for gene-environment correlation and interaction
-
Dick DM, et al. 2006. Marital status, alcohol dependence, and GABRA2: evidence for gene-environment correlation and interaction. J Stud Alcohol. 67:185-194.
-
(2006)
J Stud Alcohol.
, vol.67
, pp. 185-194
-
-
Dick, D.M.1
-
29
-
-
84865790047
-
An integrated encyclopedia of DNA elements in the human genome
-
Dunham I, et al. 2012. An integrated encyclopedia of DNA elements in the human genome. Nature 489:57-74.
-
(2012)
Nature
, vol.489
, pp. 57-74
-
-
Dunham, I.1
-
30
-
-
12144288685
-
Variations in GABRA2, encoding the a2 subunit of the GABA(A) receptor, are associated with alcohol dependence and with brain oscillations
-
Edenberg HJ, et al. 2004. Variations in GABRA2, encoding the a2 subunit of the GABA(A) receptor, are associated with alcohol dependence and with brain oscillations. Am J Hum Genet. 74:705-714.
-
(2004)
Am J Hum Genet.
, vol.74
, pp. 705-714
-
-
Edenberg, H.J.1
-
31
-
-
34447546660
-
The distribution of fitness effects of new mutations
-
Eyre-Walker A, Keightley PD. 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
-
32
-
-
0030447981
-
The mouse Pax21Neu mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney
-
Favor J, et al. 1996. The mouse Pax21Neu mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney. Proc Natl Acad Sci U S A. 93:13870-13875.
-
(1996)
Proc Natl Acad Sci U S A.
, vol.93
, pp. 13870-13875
-
-
Favor, J.1
-
33
-
-
0033911640
-
Hitchhiking under positive Darwinian selection
-
Fay JC, Wu CI. 2000. Hitchhiking under positive Darwinian selection. Genetics 155:1405-1413.
-
(2000)
Genetics
, vol.155
, pp. 1405-1413
-
-
Fay, J.C.1
Wu, C.I.2
-
36
-
-
74049144147
-
A study of GluK1 kainate receptor polymorphisms in Down syndrome reveals allelic nondisjunction at 1173 (C/T)
-
Ghosh D, Sinha S, Chatterjee A, Nandagopal K. 2009. A study of GluK1 kainate receptor polymorphisms in Down syndrome reveals allelic nondisjunction at 1173 (C/T). Dis Markers. 27:45-54.
-
(2009)
Dis Markers.
, vol.27
, pp. 45-54
-
-
Ghosh, D.1
Sinha, S.2
Chatterjee, A.3
Nandagopal, K.4
-
37
-
-
34247352040
-
Evolutionary and biomedical insights from the rhesus macaque genome
-
Gibbs RA, et al. 2007. Evolutionary and biomedical insights from the rhesus macaque genome. Science 316:222-234.
-
(2007)
Science
, vol.316
, pp. 222-234
-
-
Gibbs, R.A.1
-
39
-
-
19344370697
-
Loss of olfactory receptor genes coincides with the acquisition of full trichromatic vision in primates
-
Gilad Y,Wiebe V, Przeworski M, Lancet D, Pääbo S. 2004. Loss of olfactory receptor genes coincides with the acquisition of full trichromatic vision in primates. PLoS Biol. 2:e5.
-
(2004)
PLoS Biol.
, vol.2
, pp. e5
-
-
Gilad, Y.1
Wiebe, V.2
Przeworski, M.3
Lancet, D.4
Pääbo, S.5
-
41
-
-
84875275808
-
On the immortality of television sets:"function" in the human genome according to the evolution-free gospel of ENCODE
-
Graur D, et al. 2013. On the immortality of television sets:"function" in the human genome according to the evolution-free gospel of ENCODE. Genome Biol Evol. 5:578-590.
-
(2013)
Genome Biol Evol.
, vol.5
, pp. 578-590
-
-
Graur, D.1
-
42
-
-
84877601741
-
Comment on "Evidence of abundant purifying selection in humans for recently acquired regulatory functions"
-
Green P, Ewing B. 2013. Comment on "Evidence of abundant purifying selection in humans for recently acquired regulatory functions". Science 340:682-682.
-
(2013)
Science
, vol.340
, pp. 682
-
-
Green, P.1
Ewing, B.2
-
43
-
-
38549087902
-
ORegAnno: An open-access communitydriven resource for regulatory annotation
-
Griffith OL, et al. 2008. ORegAnno: an open-access communitydriven resource for regulatory annotation. Nucleic Acids Res. 36:D107-D113.
-
(2008)
Nucleic Acids Res.
, vol.36
, pp. D107-D113
-
-
Griffith, O.L.1
-
44
-
-
33644750115
-
MiRBase: MicroRNA sequences, targets and gene nomenclature
-
Griffiths-Jones S, Grocock RJ, Van Dongen S, Bateman A, Enright AJ. 2006. miRBase: microRNA sequences, targets and gene nomenclature. Nucleic Acids Res. 34:D140-D144.
-
(2006)
Nucleic Acids Res.
, vol.34
, pp. D140-D144
-
-
Griffiths-Jones, S.1
Grocock, R.J.2
Van Dongen, S.3
Bateman, A.4
Enright, A.J.5
-
45
-
-
84924039302
-
A method for calculating probabilities of fitness consequences for point mutations across the human genome
-
Gulko B, Hubisz MJ, Gronau I, Siepel A. 2015. A method for calculating probabilities of fitness consequences for point mutations across the human genome. Nat Genet. 47:276-283.
-
(2015)
Nat Genet.
, vol.47
, pp. 276-283
-
-
Gulko, B.1
Hubisz, M.J.2
Gronau, I.3
Siepel, A.4
-
46
-
-
77952148742
-
Ab initio reconstruction of cell type-specific transcriptomes in mouse reveals the conserved multi-exonic structure of lincRNAs
-
Guttman M, et al. 2010. Ab initio reconstruction of cell type-specific transcriptomes in mouse reveals the conserved multi-exonic structure of lincRNAs. Nat Biotechnol. 28:503-510.
-
(2010)
Nat Biotechnol.
, vol.28
, pp. 503-510
-
-
Guttman, M.1
-
47
-
-
75149156576
-
A de novo 8.8-Mb deletion of 21q21.1-q21.3 in an autistic male with a complex rearrangement involving chromosomes 6, 10, and 21
-
Haldeman-Englert CR, et al. 2010. A de novo 8.8-Mb deletion of 21q21.1-q21.3 in an autistic male with a complex rearrangement involving chromosomes 6, 10, and 21. Am J Med Genet A. 152:196-202.
-
(2010)
Am J Med Genet A.
, vol.152
, pp. 196-202
-
-
Haldeman-Englert, C.R.1
-
48
-
-
4043118347
-
EMX2 regulates sizes and positioning of the primary sensory and motor areas in neocortex by direct specification of cortical progenitors
-
Hamasaki T, Leingärtner A, Ringstedt T, O'Leary DD. 2004. EMX2 regulates sizes and positioning of the primary sensory and motor areas in neocortex by direct specification of cortical progenitors. Neuron 43:359-372.
-
(2004)
Neuron
, vol.43
, pp. 359-372
-
-
Hamasaki, T.1
Leingärtner, A.2
Ringstedt, T.3
O'Leary, D.D.4
-
49
-
-
84865760395
-
GENCODE: The reference human genome annotation for the ENCODE Project
-
Harrow J, et al. 2012. GENCODE: the reference human genome annotation for The ENCODE Project. Genome Res. 22:1760-1774.
-
(2012)
Genome Res.
, vol.22
, pp. 1760-1774
-
-
Harrow, J.1
-
50
-
-
33644780854
-
Fixation of the human-specific CMP-N-acetylneuraminic acid hydroxylase pseudogene and implications of haplotype diversity for human evolution
-
Hayakawa T, Aki I, Varki A, Satta Y, Takahata N. 2006. Fixation of the human-specific CMP-N-acetylneuraminic acid hydroxylase pseudogene and implications of haplotype diversity for human evolution. Genetics 172:1139-1146.
-
(2006)
Genetics
, vol.172
, pp. 1139-1146
-
-
Hayakawa, T.1
Aki, I.2
Varki, A.3
Satta, Y.4
Takahata, N.5
-
51
-
-
0020961177
-
Evidence for balancing selection at HLA
-
Hedrick PW, Thomson G. 1983. Evidence for balancing selection at HLA. Genetics 104:449-456.
-
(1983)
Genetics
, vol.104
, pp. 449-456
-
-
Hedrick, P.W.1
Thomson, G.2
-
52
-
-
33748344952
-
A homeodomain-zinc finger protein, ZFHX4, is expressed in neuronal differentiation manner and suppressed in muscle differentiation manner
-
Hemmi K, et al. 2006. A homeodomain-zinc finger protein, ZFHX4, is expressed in neuronal differentiation manner and suppressed in muscle differentiation manner. Biol Pharma Bull. 29:1830-1835.
-
(2006)
Biol Pharma Bull.
, vol.29
, pp. 1830-1835
-
-
Hemmi, K.1
-
53
-
-
79951829399
-
Classic selective sweeps were rare in recent human evolution
-
Hernandez RD, et al. 2011. Classic selective sweeps were rare in recent human evolution. Science 331:920-924.
-
(2011)
Science
, vol.331
, pp. 920-924
-
-
Hernandez, R.D.1
-
54
-
-
84888222007
-
Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humans
-
Hills LB, et al. 2013. Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humans. Neurology 81:1378-1386.
-
(2013)
Neurology
, vol.81
, pp. 1378-1386
-
-
Hills, L.B.1
-
55
-
-
67249117049
-
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
-
Hindorff LA, et al. 2009. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc Natl Acad Sci. 106:9362-9367.
-
(2009)
Proc Natl Acad Sci.
, vol.106
, pp. 9362-9367
-
-
Hindorff, L.A.1
-
56
-
-
33750599989
-
A new paradigm of channelopathy in epilepsy syndromes: Intracellular trafficking abnormality of channel molecules
-
Hirose S. 2006. A new paradigm of channelopathy in epilepsy syndromes: intracellular trafficking abnormality of channel molecules. Epilepsy Res. 70(Suppl 1):S206-S217.
-
(2006)
Epilepsy Res.
, vol.70
, pp. S206-S217
-
-
Hirose, S.1
-
57
-
-
0034016043
-
Profound obesity associated with a balanced translocation that disrupts the SIM1 gene
-
Holder JL, Butte NF, Zinn AR. 2000. Profound obesity associated with a balanced translocation that disrupts the SIM1 gene. Hum Mol Genet. 9:101-108.
-
(2000)
Hum Mol Genet.
, vol.9
, pp. 101-108
-
-
Holder, J.L.1
Butte, N.F.2
Zinn, A.R.3
-
58
-
-
33646133653
-
The UCSC known genes
-
Hsu F, et al. 2006. The UCSC known genes. Bioinformatics 22:1036-1046.
-
(2006)
Bioinformatics
, vol.22
, pp. 1036-1046
-
-
Hsu, F.1
-
59
-
-
0032546785
-
Themolecular basis for the absence of N-glycolylneuraminic acid in humans
-
Irie A, Koyama S, Kozutsumi Y, Kawasaki T, Suzuki A. 1998. Themolecular basis for the absence of N-glycolylneuraminic acid in humans. J Biol Chem. 273:15866-15871.
-
(1998)
J Biol Chem.
, vol.273
, pp. 15866-15871
-
-
Irie, A.1
Koyama, S.2
Kozutsumi, Y.3
Kawasaki, T.4
Suzuki, A.5
-
60
-
-
85047695028
-
Linkage and association of the glutamate receptor 6 gene with autism
-
Jamain S, et al. 2002. Linkage and association of the glutamate receptor 6 gene with autism. Mol Psychiatry. 7:302-310.
-
(2002)
Mol Psychiatry.
, vol.7
, pp. 302-310
-
-
Jamain, S.1
-
61
-
-
34250159524
-
Genome-wide mapping of in vivo protein-DNA interactions
-
Johnson DS, Mortazavi A, Myers RM, Wold B. 2007. Genome-wide mapping of in vivo protein-DNA interactions. Science 316:1497-1502.
-
(2007)
Science
, vol.316
, pp. 1497-1502
-
-
Johnson, D.S.1
Mortazavi, A.2
Myers, R.M.3
Wold, B.4
-
62
-
-
0347755531
-
The UCSC Table Browser data retrieval tool
-
Karolchik D, et al. 2004. The UCSC Table Browser data retrieval tool. Nucleic Acids Res. 32:D493-D496.
-
(2004)
Nucleic Acids Res.
, vol.32
, pp. D493-D496
-
-
Karolchik, D.1
-
63
-
-
0036079158
-
The human genome browser at UCSC
-
Kent WJ, et al. 2002. The human genome browser at UCSC. Genome Res. 12:996-1006.
-
(2002)
Genome Res.
, vol.12
, pp. 996-1006
-
-
Kent, W.J.1
-
64
-
-
65349168919
-
Correcting the site frequency spectrum for divergencebased ascertainment
-
Kern AD. 2009. Correcting the site frequency spectrum for divergencebased ascertainment. PLoS One 4:e5152.
-
(2009)
PLoS One
, vol.4
, pp. e5152
-
-
Kern, A.D.1
-
65
-
-
33847748974
-
Association of GABRB3 polymorphisms with autism spectrum disorders in Korean trios
-
Kim SA, Kim JH, Park M, Cho IH, Yoo HJ. 2007. Association of GABRB3 polymorphisms with autism spectrum disorders in Korean trios. Neuropsychobiology 54:160-165.
-
(2007)
Neuropsychobiology
, vol.54
, pp. 160-165
-
-
Kim, S.A.1
Kim, J.H.2
Park, M.3
Cho, I.H.4
Yoo, H.J.5
-
66
-
-
0016669094
-
Evolultion at two levels in humans and chimpanzees
-
King MC, Wilson AC. 1975. Evolultion at two levels in humans and chimpanzees. Science 188:107-116.
-
(1975)
Science
, vol.188
, pp. 107-116
-
-
King, M.C.1
Wilson, A.C.2
-
67
-
-
70349645640
-
Recent de novo origin of human protein-coding genes
-
Knowles DG, McLysaght A. 2009. Recent de novo origin of human protein-coding genes. Genome Res. 19:1752-1759.
-
(2009)
Genome Res.
, vol.19
, pp. 1752-1759
-
-
Knowles, D.G.1
McLysaght, A.2
-
68
-
-
0037474257
-
Heteromer formation of d2 glutamate receptorswith AMPA or kainate receptors
-
Kohda K, et al. 2003. Heteromer formation of d2 glutamate receptorswith AMPA or kainate receptors. Mol Brain Research 110:27-37.
-
(2003)
Mol Brain Research
, vol.110
, pp. 27-37
-
-
Kohda, K.1
-
69
-
-
78049354879
-
Fine-scale recombination rate differences between sexes, populations and individuals
-
Kong A, et al. 2010. Fine-scale recombination rate differences between sexes, populations and individuals. Nature 467:1099-1103.
-
(2010)
Nature
, vol.467
, pp. 1099-1103
-
-
Kong, A.1
-
70
-
-
84857214297
-
The role of GC-biased gene conversion in shaping the fastest evolving regions of the human genome
-
Kostka D, Hubisz MJ, Siepel A, Pollard KS. 2012. The role of GC-biased gene conversion in shaping the fastest evolving regions of the human genome. Mol Biol Evol. 29:1047-1057.
-
(2012)
Mol Biol Evol.
, vol.29
, pp. 1047-1057
-
-
Kostka, D.1
Hubisz, M.J.2
Siepel, A.3
Pollard, K.S.4
-
71
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
Lander ES, et al. 2001. Initial sequencing and analysis of the human genome. Nature 409:860-921.
-
(2001)
Nature
, vol.409
, pp. 860-921
-
-
Lander, E.S.1
-
72
-
-
0027074637
-
Identification of a new brain-specific transcription factor, NURR1
-
Law SW, Conneely O, DeMayo F, O'malley B. 1992. Identification of a new brain-specific transcription factor, NURR1. Mol Endocrinol 6:2129-2135.
-
(1992)
Mol Endocrinol
, vol.6
, pp. 2129-2135
-
-
Law, S.W.1
Conneely, O.2
DeMayo, F.3
O'Malley, B.4
-
73
-
-
0037226797
-
Mutations in NR4A2 associated with familial Parkinson disease
-
Le WD, et al. 2002. Mutations in NR4A2 associated with familial Parkinson disease. Nat Genet. 33:85-89.
-
(2002)
Nat Genet.
, vol.33
, pp. 85-89
-
-
Le, W.D.1
-
74
-
-
84875508254
-
Multiple instances of ancient balancing selection shared between humans and chimpanzees
-
Leffler EM, et al. 2013. Multiple instances of ancient balancing selection shared between humans and chimpanzees. Science 339:1578-1582.
-
(2013)
Science
, vol.339
, pp. 1578-1582
-
-
Leffler, E.M.1
-
75
-
-
33644875300
-
SnoRNA-LBME-db, a comprehensive database of human H/ACA and C/D box snoRNAs
-
Lestrade L, Weber MJ. 2006. snoRNA-LBME-db, a comprehensive database of human H/ACA and C/D box snoRNAs. Nucleic Acids Res. 34:D158-D162.
-
(2006)
Nucleic Acids Res.
, vol.34
, pp. D158-D162
-
-
Lestrade, L.1
Weber, M.J.2
-
76
-
-
78951472188
-
Distinguishing positive selection from neutral evolution: Boosting the performance of summary statistics
-
Lin K, Li H, Schlötterer C, Futschik A. 2011. Distinguishing positive selection from neutral evolution: boosting the performance of summary statistics. Genetics 187:229-244.
-
(2011)
Genetics
, vol.187
, pp. 229-244
-
-
Lin, K.1
Li, H.2
Schlötterer, C.3
Futschik, A.4
-
77
-
-
80054973803
-
A high-resolution map of human evolutionary constraint using 29 mammals
-
Lindblad-Toh K, et al. 2011. A high-resolution map of human evolutionary constraint using 29 mammals. Nature 478:476-482.
-
(2011)
Nature
, vol.478
, pp. 476-482
-
-
Lindblad-Toh, K.1
-
78
-
-
84859541449
-
Extension of cortical synaptic development distinguishes humans from chimpanzees and macaques
-
Liu X, et al. 2012. Extension of cortical synaptic development distinguishes humans from chimpanzees and macaques. Genome Res. 22:611-622.
-
(2012)
Genome Res.
, vol.22
, pp. 611-622
-
-
Liu, X.1
-
79
-
-
80055095261
-
Natural selection affects multiple aspects of genetic variation at putatively neutral sites across the human genome
-
Lohmueller KE, et al. 2011. Natural selection affects multiple aspects of genetic variation at putatively neutral sites across the human genome. PLoS Genet. 7:e1002326.
-
(2011)
PLoS Genet.
, vol.7
-
-
Lohmueller, K.E.1
-
80
-
-
10044257458
-
Glutamate and GABA receptor signalling in the developing brain
-
Lujan R, Shigemoto R, Lopez-Bendito G. 2005. Glutamate and GABA receptor signalling in the developing brain. Neuroscience 130:567-580.
-
(2005)
Neuroscience
, vol.130
, pp. 567-580
-
-
Lujan, R.1
Shigemoto, R.2
Lopez-Bendito, G.3
-
81
-
-
33645798112
-
Genome-wide identification of human functional DNA using a neutral indel model
-
Lunter G, Ponting CP, Hein J. 2006. Genome-wide identification of human functional DNA using a neutral indel model. PLoS Comput Biol. 2:e5.
-
(2006)
PLoS Comput Biol.
, vol.2
, pp. e5
-
-
Lunter, G.1
Ponting, C.P.2
Hein, J.3
-
82
-
-
0037422542
-
Sequence variations in the public human genome data reflect a bottlenecked population history
-
Marth G, et al. 2003. Sequence variations in the public human genome data reflect a bottlenecked population history. Proc Natl Acad Sci U S A. 100:376-381.
-
(2003)
Proc Natl Acad Sci U S A.
, vol.100
, pp. 376-381
-
-
Marth, G.1
-
83
-
-
0016220238
-
The hitch-hiking effect of a favourable gene
-
Maynard Smith J, Haigh J. 1974. The hitch-hiking effect of a favourable gene. Genet Res. 23:23-35.
-
(1974)
Genet Res.
, vol.23
, pp. 23-35
-
-
Maynard Smith, J.1
Haigh, J.2
-
84
-
-
77952214662
-
GREAT improves functional interpretation of cisregulatory regions
-
McLean CY, et al. 2010. GREAT improves functional interpretation of cisregulatory regions. Nat Biotechnol. 28:495-501.
-
(2010)
Nat Biotechnol.
, vol.28
, pp. 495-501
-
-
McLean, C.Y.1
-
85
-
-
79952386187
-
Human-specific loss of regulatory DNA and the evolution of human-specific traits
-
McLean CY, et al. 2011. Human-specific loss of regulatory DNA and the evolution of human-specific traits. Nature 471:216-219.
-
(2011)
Nature
, vol.471
, pp. 216-219
-
-
McLean, C.Y.1
-
86
-
-
2142773942
-
The fine-scale structure of recombination rate variation in the human genome
-
McVean GA, et al. 2004. The fine-scale structure of recombination rate variation in the human genome. Science 304:581-584.
-
(2004)
Science
, vol.304
, pp. 581-584
-
-
McVean, G.A.1
-
87
-
-
67149096366
-
Widespread genomic signatures of natural selection in hominid evolution
-
McVicker G, Gordon D, Davis C, Green P. 2009. Widespread genomic signatures of natural selection in hominid evolution. PLoS Genet. 5:e1000471.
-
(2009)
PLoS Genet.
, vol.5
-
-
McVicker, G.1
Gordon, D.2
Davis, C.3
Green, P.4
-
89
-
-
84875404794
-
The UCSC Genome Browser database: Extensions and updates 2013
-
Meyer LR, et al. 2013. The UCSC Genome Browser database: extensions and updates 2013. Nucleic Acids Res. 41:D64-D69.
-
(2013)
Nucleic Acids Res.
, vol.41
, pp. D64-D69
-
-
Meyer, L.R.1
-
90
-
-
0035393437
-
Sim1 haploinsufficiency causes hyperphagia, obesity and reduction of the paraventricular nucleus of the hypothalamus
-
Michaud JL, et al. 2001. Sim1 haploinsufficiency causes hyperphagia, obesity and reduction of the paraventricular nucleus of the hypothalamus. Hum Mol Genet. 10:1465-1473.
-
(2001)
Hum Mol Genet.
, vol.10
, pp. 1465-1473
-
-
Michaud, J.L.1
-
91
-
-
0032532480
-
Development of neuroendocrine lineages requires the bHLH-PAS transcription factor SIM1
-
Michaud JL, Rosenquist T, May NR, Fan CM. 1998. Development of neuroendocrine lineages requires the bHLH-PAS transcription factor SIM1. Genes Dev. 12:3264-3275.
-
(1998)
Genes Dev.
, vol.12
, pp. 3264-3275
-
-
Michaud, J.L.1
Rosenquist, T.2
May, N.R.3
Fan, C.M.4
-
92
-
-
24344500211
-
Initial sequence of the chimpanzee genome and comparison with the human genome
-
Mikkelsen TS, et al. 2005. Initial sequence of the chimpanzee genome and comparison with the human genome. Nature 437:69-87.
-
(2005)
Nature
, vol.437
, pp. 69-87
-
-
Mikkelsen, T.S.1
-
93
-
-
70349123821
-
Overlapping function of Lmx1a and Lmx1b in anterior hindbrain roof plate formation and cerebellar growth
-
Mishima Y, Lindgren AG, Chizhikov VV, Johnson RL, Millen KJ. 2009. Overlapping function of Lmx1a and Lmx1b in anterior hindbrain roof plate formation and cerebellar growth. J Neurosci 29:11377-11384.
-
(2009)
J Neurosci
, vol.29
, pp. 11377-11384
-
-
Mishima, Y.1
Lindgren, A.G.2
Chizhikov, V.V.3
Johnson, R.L.4
Millen, K.J.5
-
94
-
-
0028892358
-
Cloning and characterization of an ATBF1 isoform that expresses in a neuronal differentiation-dependent manner
-
Miura Y, et al. 1995. Cloning and characterization of an ATBF1 isoform that expresses in a neuronal differentiation-dependent manner. J Biol Chem. 270:26840-26848.
-
(1995)
J Biol Chem.
, vol.270
, pp. 26840-26848
-
-
Miura, Y.1
-
95
-
-
33644861212
-
ORegAnno: An open access database and curation system for literature-derived promoters, transcription factor binding sites and regulatory variation
-
Montgomery S, et al. 2006. ORegAnno: an open access database and curation system for literature-derived promoters, transcription factor binding sites and regulatory variation. Bioinformatics 22:637-640.
-
(2006)
Bioinformatics
, vol.22
, pp. 637-640
-
-
Montgomery, S.1
-
96
-
-
34547784323
-
A defect in the ionotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardation
-
Motazacker MM, et al. 2007. A defect in the ionotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardation. Am J Hum Genet. 81:792-798.
-
(2007)
Am J Hum Genet.
, vol.81
, pp. 792-798
-
-
Motazacker, M.M.1
-
97
-
-
1242284406
-
Myelin transcription factor 1 (Myt1) modulates the proliferation and differentiation of oligodendrocyte lineage cells
-
Nielsen JA, Berndt JA, Hudson LD, Armstrong RC. 2004. Myelin transcription factor 1 (Myt1) modulates the proliferation and differentiation of oligodendrocyte lineage cells. Mol Cell Neurosci 25:111-123.
-
(2004)
Mol Cell Neurosci
, vol.25
, pp. 111-123
-
-
Nielsen, J.A.1
Berndt, J.A.2
Hudson, L.D.3
Armstrong, R.C.4
-
98
-
-
0042970462
-
Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13
-
Nurmi EL, et al. 2003. Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13. J Am Acad Child Adolesc Psychiatry. 42:856-863.
-
(2003)
J Am Acad Child Adolesc Psychiatry.
, vol.42
, pp. 856-863
-
-
Nurmi, E.L.1
-
99
-
-
0033360995
-
When less is more: Gene loss as an engine of evolutionary change
-
OlsonMV. 1999. When less is more: gene loss as an engine of evolutionary change. Am J Hum Genet. 64:18-23.
-
(1999)
Am J Hum Genet.
, vol.64
, pp. 18-23
-
-
Olson, M.V.1
-
100
-
-
77955759338
-
Searching for footprints of positive selection in whole-genome SNP data from nonequilibrium populations
-
Pavlidis P, Jensen JD, StephanW. 2010. Searching for footprints of positive selection in whole-genome SNP data from nonequilibrium populations. Genetics 185:907-922.
-
(2010)
Genetics
, vol.185
, pp. 907-922
-
-
Pavlidis, P.1
Jensen, J.D.2
Stephan, W.3
-
101
-
-
0036892023
-
Book review: GABA and glutamate in the human brain
-
Petroff OA. 2002. Book review: GABA and glutamate in the human brain. Neuroscientist 8:562-573.
-
(2002)
Neuroscientist
, vol.8
, pp. 562-573
-
-
Petroff, O.A.1
-
102
-
-
84873087047
-
Current relaxation of selection on the human genome: Tolerance of deleterious mutations on olfactory receptors
-
Pierron D, Cortés NG, Letellier T, Grossman LI. 2012. Current relaxation of selection on the human genome: tolerance of deleterious mutations on olfactory receptors. Mol Phylogenet Evol. 66:558-564.
-
(2012)
Mol Phylogenet Evol.
, vol.66
, pp. 558-564
-
-
Pierron, D.1
Cortés, N.G.2
Letellier, T.3
Grossman, L.I.4
-
104
-
-
33750428182
-
Forces shaping the fastest evolving regions in the human genome
-
Pollard KS, Salama SR, King B, et al. 2006. Forces shaping the fastest evolving regions in the human genome. PLoS Genet. 2:e168.
-
(2006)
PLoS Genet.
, vol.2
, pp. e168
-
-
Pollard, K.S.1
Salama, S.R.2
King, B.3
-
105
-
-
33748675254
-
An RNA gene expressed during cortical development evolved rapidly in humans
-
Pollard KS, Salama SR, Lambert N, et al. 2006. An RNA gene expressed during cortical development evolved rapidly in humans. Nature 443:167-172.
-
(2006)
Nature
, vol.443
, pp. 167-172
-
-
Pollard, K.S.1
Salama, S.R.2
Lambert, N.3
-
106
-
-
11844262032
-
Haplotype-based localization of an alcohol dependence gene to the 5q34 {gamma}-aminobutyric acid type A gene cluster
-
Radel M, et al. 2005. Haplotype-based localization of an alcohol dependence gene to the 5q34 {gamma}-aminobutyric acid type A gene cluster. Arch Gen Psychiatry. 62:47-55.
-
(2005)
Arch Gen Psychiatry.
, vol.62
, pp. 47-55
-
-
Radel, M.1
-
107
-
-
33646679655
-
Human and nonhuman primate brains: Are they allometrically scaled versions of the same design?
-
Rilling JK. 2006. Human and nonhuman primate brains: are they allometrically scaled versions of the same design? Evol Anthropol 15:65-77.
-
(2006)
Evol Anthropol
, vol.15
, pp. 65-77
-
-
Rilling, J.K.1
-
108
-
-
84883794892
-
Learning natural selection from the site frequency spectrum
-
Ronen R, Udpa N, Halperin E, Bafna V. 2013. Learning natural selection from the site frequency spectrum. Genetics 195:181-193.
-
(2013)
Genetics
, vol.195
, pp. 181-193
-
-
Ronen, R.1
Udpa, N.2
Halperin, E.3
Bafna, V.4
-
109
-
-
0031883174
-
Distribution of olfactory receptor genes in the human genome
-
Rouquier S, et al. 1998. Distribution of olfactory receptor genes in the human genome. Nat Genet. 18:243-250.
-
(1998)
Nat Genet.
, vol.18
, pp. 243-250
-
-
Rouquier, S.1
-
110
-
-
0030930981
-
Evolution of primate ABO blood group genes and their homologous genes
-
Saitou N, Yamamoto FI. 1997. Evolution of primate ABO blood group genes and their homologous genes. Mol Biol Evol. 14:399-411.
-
(1997)
Mol Biol Evol.
, vol.14
, pp. 399-411
-
-
Saitou, N.1
Yamamoto, F.I.2
-
111
-
-
0030757806
-
Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphism
-
Sander T, et al. 1997. Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphism. Am J Med Genet. 74:416-421.
-
(1997)
Am J Med Genet.
, vol.74
, pp. 416-421
-
-
Sander, T.1
-
112
-
-
0032584085
-
Nurr1 is essential for the induction of the dopaminergic phenotype and the survival of ventral mesencephalic late dopaminergic precursor neurons
-
Saucedo-Cardenas O, et al. 1998. Nurr1 is essential for the induction of the dopaminergic phenotype and the survival of ventral mesencephalic late dopaminergic precursor neurons. Proc Natl Acad Sci U S A. 95:4013-4018.
-
(1998)
Proc Natl Acad Sci U S A.
, vol.95
, pp. 4013-4018
-
-
Saucedo-Cardenas, O.1
-
113
-
-
70349811327
-
All human-specific gene losses are present in the genome as pseudogenes
-
Schrider DR, Costello JC, Hahn MW. 2009. All human-specific gene losses are present in the genome as pseudogenes. J Comput Biol. 16:1419-1427.
-
(2009)
J Comput Biol.
, vol.16
, pp. 1419-1427
-
-
Schrider, D.R.1
Costello, J.C.2
Hahn, M.W.3
-
114
-
-
84926133266
-
Discovering functional DNA elements using population genomic information: A proof of concept using human mtDNA
-
Schrider DR, Kern AD. 2014. Discovering functional DNA elements using population genomic information: a proof of concept using human mtDNA. Genome Biol Evol. 6:1542-1548.
-
(2014)
Genome Biol Evol.
, vol.6
, pp. 1542-1548
-
-
Schrider, D.R.1
Kern, A.D.2
-
115
-
-
84929000155
-
Soft shoulders ahead: Spurious signatures of soft and partial selective sweeps result from linked hard sweeps
-
Schrider DR,Mendes FK, Hahn MW, Kern AD. 2015. Soft shoulders ahead: spurious signatures of soft and partial selective sweeps result from linked hard sweeps. Genetics 200:267-284.
-
(2015)
Genetics
, vol.200
, pp. 267-284
-
-
Schrider, D.R.1
Mendes, F.K.2
Hahn, M.W.3
Kern, A.D.4
-
116
-
-
0037267806
-
Human-mouse alignments with BLASTZ
-
Schwartz S, et al. 2003. Human-mouse alignments with BLASTZ. Genome Res. 13:103-107.
-
(2003)
Genome Res.
, vol.13
, pp. 103-107
-
-
Schwartz, S.1
-
118
-
-
0033166657
-
The diversity of cadherins and implications for a synaptic adhesive code in the CNS
-
Shapiro L, Colman DR. 1999. The diversity of cadherins and implications for a synaptic adhesive code in the CNS. Neuron 23:427-430.
-
(1999)
Neuron
, vol.23
, pp. 427-430
-
-
Shapiro, L.1
Colman, D.R.2
-
119
-
-
23744458086
-
Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes
-
Siepel A, et al. 2005. Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes. Genome Res. 15:1034-1050.
-
(2005)
Genome Res.
, vol.15
, pp. 1034-1050
-
-
Siepel, A.1
-
120
-
-
0026749964
-
Two vertebrate homeobox genes related to the Drosophila empty spiracles gene are expressed in the embryonic cerebral cortex
-
Simeone A, et al. 1992. Two vertebrate homeobox genes related to the Drosophila empty spiracles gene are expressed in the embryonic cerebral cortex. EMBO J. 11:2541-2550.
-
(1992)
EMBO J.
, vol.11
, pp. 2541-2550
-
-
Simeone, A.1
-
121
-
-
84894332450
-
A scan for human-specific relaxation of negative selection reveals unexpected polymorphism in proteasome genes
-
Somel M, et al. 2013. A scan for human-specific relaxation of negative selection reveals unexpected polymorphism in proteasome genes.Mol Biol Evol. 30:1808-1815.
-
(2013)
Mol Biol Evol
, vol.30
, pp. 1808-1815
-
-
Somel, M.1
-
122
-
-
0030268113
-
Neurogenins, a novel family of atonal-related bHLH transcription factors, are putativemammalian neuronal determination genes that reveal progenitor cell heterogeneity in the developing CNS and PNS
-
Sommer L, Ma Q, Anderson DJ. 1996. neurogenins, a novel family of atonal-related bHLH transcription factors, are putativemammalian neuronal determination genes that reveal progenitor cell heterogeneity in the developing CNS and PNS. Mol Cell Neurosci 8:221-241.
-
(1996)
Mol Cell Neurosci
, vol.8
, pp. 221-241
-
-
Sommer, L.1
Ma, Q.2
Anderson, D.J.3
-
123
-
-
10344221021
-
Disentangling the effects of demography and selection in human history
-
Stajich JE, Hahn MW. 2005. Disentangling the effects of demography and selection in human history. Mol Biol Evol. 22:63-73.
-
(2005)
Mol Biol Evol.
, vol.22
, pp. 63-73
-
-
Stajich, J.E.1
Hahn, M.W.2
-
124
-
-
12144288568
-
Myosin gene mutation correlates with anatomical changes in the human lineage
-
Stedman HH, et al. 2004. Myosin gene mutation correlates with anatomical changes in the human lineage. Nature 428:415-418.
-
(2004)
Nature
, vol.428
, pp. 415-418
-
-
Stedman, H.H.1
-
125
-
-
0024313579
-
Statisticalmethod for testing the neutral mutation hypothesis by DNA polymorphism
-
Tajima F. 1989. Statisticalmethod for testing the neutral mutation hypothesis by DNA polymorphism. Genetics 123:585-595.
-
(1989)
Genetics
, vol.123
, pp. 585-595
-
-
Tajima, F.1
-
126
-
-
44449134576
-
Hyperglycosylation and reduced GABA currents of mutated GABRB3 polypeptide in remitting childhood absence epilepsy
-
Tanaka M, et al. 2008. Hyperglycosylation and reduced GABA currents of mutated GABRB3 polypeptide in remitting childhood absence epilepsy. Am J Hum Genet. 82:1249-1261.
-
(2008)
Am J Hum Genet.
, vol.82
, pp. 1249-1261
-
-
Tanaka, M.1
-
127
-
-
84863556835
-
Evolution and functional impact of rare coding variation from deep sequencing of human exomes
-
Tennessen JA, et al. 2012. Evolution and functional impact of rare coding variation from deep sequencing of human exomes. Science 337:64-69.
-
(2012)
Science
, vol.337
, pp. 64-69
-
-
Tennessen, J.A.1
-
128
-
-
0023857831
-
Molecular genetics of the single-minded locus: A gene involved in the development of the Drosophila nervous system
-
Thomas JB, Crews ST, Goodman CS. 1988. Molecular genetics of the single-minded locus: a gene involved in the development of the Drosophila nervous system. Cell 52:133-141.
-
(1988)
Cell
, vol.52
, pp. 133-141
-
-
Thomas, J.B.1
Crews, S.T.2
Goodman, C.S.3
-
129
-
-
77952123055
-
Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation
-
Trapnell C, et al. 2010. Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation. Nat Biotechnol. 28:511-515.
-
(2010)
Nat Biotechnol.
, vol.28
, pp. 511-515
-
-
Trapnell, C.1
-
130
-
-
0036389517
-
The murine BTB/POZ zinc finger gene ZNF131: Predominant expression in the developing central nervous system, in adult brain, testis, and thymus
-
Trappe R, et al. 2002. The murine BTB/POZ zinc finger gene ZNF131: predominant expression in the developing central nervous system, in adult brain, testis, and thymus. Biochem Biophys Res Commun. 296:319-327.
-
(2002)
Biochem Biophys Res Commun.
, vol.296
, pp. 319-327
-
-
Trappe, R.1
-
131
-
-
84879381158
-
A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophy
-
Utine GE, et al. 2013. A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophy. J Child Neurol. 28:926-932.
-
(2013)
J Child Neurol.
, vol.28
, pp. 926-932
-
-
Utine, G.E.1
-
132
-
-
0035917818
-
The human and murine protocadherin-beta one-exon gene families show high evolutionary conservation, despite the difference in gene number
-
Vanhalst K, Kools P, Vanden E, van Roy F. 2001. The human and murine protocadherin-beta one-exon gene families show high evolutionary conservation, despite the difference in gene number. FEBS Lett. 495:120-125.
-
(2001)
FEBS Lett.
, vol.495
, pp. 120-125
-
-
Vanhalst, K.1
Kools, P.2
Vanden, E.3
Van Roy, F.4
-
133
-
-
0010864753
-
Pattern recognition using generalized portrait method
-
Vapnik V, Lerner A. 1963. Pattern recognition using generalized portrait method. Automat Remote Control. 24:774-780.
-
(1963)
Automat Remote Control.
, vol.24
, pp. 774-780
-
-
Vapnik, V.1
Lerner, A.2
-
134
-
-
0026581289
-
Empty spiracles, a gap gene containing a homeobox involved in Drosophila head development
-
Walldorf U, Gehring W. 1992. Empty spiracles, a gap gene containing a homeobox involved in Drosophila head development. EMBO J. 11:2247-2259.
-
(1992)
EMBO J.
, vol.11
, pp. 2247-2259
-
-
Walldorf, U.1
Gehring, W.2
-
136
-
-
84866775366
-
Evidence of abundant purifying selection in humans for recently acquired regulatory functions
-
Ward LD, Kellis M. 2012. Evidence of abundant purifying selection in humans for recently acquired regulatory functions. Science 337:1675-1678.
-
(2012)
Science
, vol.337
, pp. 1675-1678
-
-
Ward, L.D.1
Kellis, M.2
-
137
-
-
34848836316
-
Differential alterations of kainate receptor subunits in inhibitory interneurons in the anterior cingulate cortex in schizophrenia and bipolar disorder
-
Woo TU, et al. 2007. Differential alterations of kainate receptor subunits in inhibitory interneurons in the anterior cingulate cortex in schizophrenia and bipolar disorder. Schizophr Res. 96:46-61.
-
(2007)
Schizophr Res.
, vol.96
, pp. 46-61
-
-
Woo, T.U.1
-
138
-
-
51349159085
-
Probability estimates for multi-class classification by pairwise coupling
-
Wu TF, Lin CJ, Weng RC. 2004. Probability estimates for multi-class classification by pairwise coupling. J Mach Learn Res. 5:975-1005.
-
(2004)
J Mach Learn Res.
, vol.5
, pp. 975-1005
-
-
Wu, T.F.1
Lin, C.J.2
Weng, R.C.3
-
139
-
-
33645462359
-
Spread of an inactive form of caspase-12 in humans is due to recent positive selection
-
Xue Y, et al. 2006. Spread of an inactive form of caspase-12 in humans is due to recent positive selection. Am J Hum Genet. 78:659-670.
-
(2006)
Am J Hum Genet.
, vol.78
, pp. 659-670
-
-
Xue, Y.1
-
140
-
-
0036501461
-
Different evolutionary processes shaped the mouse and human olfactory receptor gene families
-
Young JM, et al. 2002. Different evolutionary processes shaped the mouse and human olfactory receptor gene families. Hum Mol Genet. 11:535-546.
-
(2002)
Hum Mol Genet.
, vol.11
, pp. 535-546
-
-
Young, J.M.1
-
141
-
-
0036163689
-
The olfactory receptor gene superfamily of the mouse
-
Zhang X, Firestein S. 2002. The olfactory receptor gene superfamily of the mouse. Nat Neurosci. 5:124-133.
-
(2002)
Nat Neurosci.
, vol.5
, pp. 124-133
-
-
Zhang, X.1
Firestein, S.2
|