-
1
-
-
0016669094
-
Evolution at two levels in humans and chimpanzees
-
King M.C., Wilson A.C. Evolution at two levels in humans and chimpanzees. Science (New York, NY) 1975, 188:107-116.
-
(1975)
Science (New York, NY)
, vol.188
, pp. 107-116
-
-
King, M.C.1
Wilson, A.C.2
-
2
-
-
84864126183
-
Emerging roles of non-coding RNAs in brain evolution, development, plasticity and disease
-
Qureshi I.A., Mehler M.F. Emerging roles of non-coding RNAs in brain evolution, development, plasticity and disease. Nat Rev Neurosci 2012, 13:528.
-
(2012)
Nat Rev Neurosci
, vol.13
, pp. 528
-
-
Qureshi, I.A.1
Mehler, M.F.2
-
3
-
-
61849140663
-
Signatures of purifying and local positive selection in human miRNAs
-
Quach H., Barreiro L.B., Laval G., Zidane N., Patin E., Kidd K.K., Kidd J.R., Bouchier C., Veuille M., Antoniewski C., et al. Signatures of purifying and local positive selection in human miRNAs. Am J Hum Genet 2009, 84:316-327.
-
(2009)
Am J Hum Genet
, vol.84
, pp. 316-327
-
-
Quach, H.1
Barreiro, L.B.2
Laval, G.3
Zidane, N.4
Patin, E.5
Kidd, K.K.6
Kidd, J.R.7
Bouchier, C.8
Veuille, M.9
Antoniewski, C.10
-
4
-
-
84859248536
-
Evidence for positive selection on a number of microRNA regulatory interactions during recent human evolution
-
Li J., Liu Y., Xin X., Kim T.S., Cabeza E.A., Ren J., Nielsen R., Wrana J.L., Zhang Z. Evidence for positive selection on a number of microRNA regulatory interactions during recent human evolution. PLoS Genet 2012, 8:e1002578.
-
(2012)
PLoS Genet
, vol.8
, pp. e1002578
-
-
Li, J.1
Liu, Y.2
Xin, X.3
Kim, T.S.4
Cabeza, E.A.5
Ren, J.6
Nielsen, R.7
Wrana, J.L.8
Zhang, Z.9
-
5
-
-
84863571375
-
An ancestral miR-1304 allele present in Neanderthals regulates genes involved in enamel formation and could explain dental differences with modern humans
-
Lopez-Valenzuela M., Ramírez O., Rosas A., García-Vargas S., de la Rasilla M., Lalueza-Fox C., Espinosa-Parrilla Y. An ancestral miR-1304 allele present in Neanderthals regulates genes involved in enamel formation and could explain dental differences with modern humans. Mol Biol Evol 2012, 29:1797.
-
(2012)
Mol Biol Evol
, vol.29
, pp. 1797
-
-
Lopez-Valenzuela, M.1
Ramírez, O.2
Rosas, A.3
García-Vargas, S.4
de la Rasilla, M.5
Lalueza-Fox, C.6
Espinosa-Parrilla, Y.7
-
6
-
-
77950574586
-
Genome-wide comparative analysis of microRNAs in three non-human primates
-
Brameier M. Genome-wide comparative analysis of microRNAs in three non-human primates. BMC Res Notes 2010, 3:64.
-
(2010)
BMC Res Notes
, vol.3
, pp. 64
-
-
Brameier, M.1
-
7
-
-
84855175650
-
MicroRNA-driven developmental remodeling in the brain distinguishes humans from other primates
-
Somel M., Xie G., Li N., Hu Y., Chen W., Pääbo S., Khaitovich P., Liu X., Tang L., Yan Z., et al. MicroRNA-driven developmental remodeling in the brain distinguishes humans from other primates. PLoS Biol 2011, 9:e1001214.
-
(2011)
PLoS Biol
, vol.9
, pp. e1001214
-
-
Somel, M.1
Xie, G.2
Li, N.3
Hu, Y.4
Chen, W.5
Pääbo, S.6
Khaitovich, P.7
Liu, X.8
Tang, L.9
Yan, Z.10
-
8
-
-
80055092199
-
MicroRNA expression and regulation in human, chimpanzee, and macaque brains
-
Hu H.Y., Zhao M., Zeng R., Chen W., Pääbo S., Khaitovich P., Guo S., Xi J., Yan Z., Fu N., et al. MicroRNA expression and regulation in human, chimpanzee, and macaque brains. PLoS Genet 2011, 7:e1002327.
-
(2011)
PLoS Genet
, vol.7
, pp. e1002327
-
-
Hu, H.Y.1
Zhao, M.2
Zeng, R.3
Chen, W.4
Pääbo, S.5
Khaitovich, P.6
Guo, S.7
Xi, J.8
Yan, Z.9
Fu, N.10
-
9
-
-
84864101947
-
Transcription factors are targeted by differentially expressed miRNAs in primates
-
Dannemann M., Prüfer K., Lizano E., Nickel B., Burbano H.A., Kelso J. Transcription factors are targeted by differentially expressed miRNAs in primates. Genome Biol Evol 2012, 4:552-564.
-
(2012)
Genome Biol Evol
, vol.4
, pp. 552-564
-
-
Dannemann, M.1
Prüfer, K.2
Lizano, E.3
Nickel, B.4
Burbano, H.A.5
Kelso, J.6
-
10
-
-
84898810409
-
Human-specific microRNA regulation of FOXO1: implications for microRNA recognition element evolution
-
McLoughlin H.S., Wan J., Spengler R.M., Xing Y., Davidson B.L. Human-specific microRNA regulation of FOXO1: implications for microRNA recognition element evolution. Hum Mol Genet 2014, 23:2593-2603.
-
(2014)
Hum Mol Genet
, vol.23
, pp. 2593-2603
-
-
McLoughlin, H.S.1
Wan, J.2
Spengler, R.M.3
Xing, Y.4
Davidson, B.L.5
-
11
-
-
35349012592
-
Genome-wide detection and characterization of positive selection in human populations
-
Sabeti P.C., Varilly P., Fry B., Lohmueller J., Hostetter E., Cotsapas C., Xie X., Byrne E.H., McCarroll S.A., Gaudet R., et al. Genome-wide detection and characterization of positive selection in human populations. Nature 2007, 449:913-918.
-
(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
-
12
-
-
66049157487
-
Signals of recent positive selection in a worldwide sample of human populations
-
Pickrell J.K., Feldman M.W., Pritchard J.K., Coop G., Novembre J., Kudaravalli S., Li J.Z., Absher D., Srinivasan B.S., Barsh G.S., et al. Signals of recent positive selection in a worldwide sample of human populations. Genome Res 2009, 19:826-837.
-
(2009)
Genome Res
, vol.19
, pp. 826-837
-
-
Pickrell, J.K.1
Feldman, M.W.2
Pritchard, J.K.3
Coop, G.4
Novembre, J.5
Kudaravalli, S.6
Li, J.Z.7
Absher, D.8
Srinivasan, B.S.9
Barsh, G.S.10
-
13
-
-
83455188178
-
Shared and unique components of human population structure and genome-wide signals of positive selection in South Asia
-
Metspalu M., Remm M., Pitchappan R., Singh L., Thangaraj K., Villems R., Kivisild T., Romero I.G., Yunusbayev B., Chaubey G., et al. Shared and unique components of human population structure and genome-wide signals of positive selection in South Asia. Am J Hum Genet 2011, 89:731-744.
-
(2011)
Am J Hum Genet
, vol.89
, pp. 731-744
-
-
Metspalu, M.1
Remm, M.2
Pitchappan, R.3
Singh, L.4
Thangaraj, K.5
Villems, R.6
Kivisild, T.7
Romero, I.G.8
Yunusbayev, B.9
Chaubey, G.10
-
14
-
-
84874069538
-
Identifying recent adaptations in large-scale genomic data
-
Grossman S.R., Wong S.H., Cabili M., Adegbola R.A., Bamezai R.N.K., Hill A.V.S., Vannberg F.O., Rinn J.L., Lander E.S., Schaffner S.F., et al. Identifying recent adaptations in large-scale genomic data. Cell 2013, 152:703-713.
-
(2013)
Cell
, vol.152
, pp. 703-713
-
-
Grossman, S.R.1
Wong, S.H.2
Cabili, M.3
Adegbola, R.A.4
Bamezai, R.N.K.5
Hill, A.V.S.6
Vannberg, F.O.7
Rinn, J.L.8
Lander, E.S.9
Schaffner, S.F.10
-
15
-
-
0033647653
-
An overview of the structures of protein-DNA complexes
-
REVIEWS001-REVIEWS001.037
-
Luscombe N.M., Austin S.E., Berman H.M., Thornton J.M. An overview of the structures of protein-DNA complexes. Genome Biol 2000, 1. REVIEWS001-REVIEWS001.037.
-
(2000)
Genome Biol
, vol.1
-
-
Luscombe, N.M.1
Austin, S.E.2
Berman, H.M.3
Thornton, J.M.4
-
16
-
-
84876529769
-
TFClass: an expandable hierarchical classification of human transcription factors
-
Wingender E., Schoeps T., Dönitz J. TFClass: an expandable hierarchical classification of human transcription factors. Nucleic Acids Res 2013, 41:D165-D170.
-
(2013)
Nucleic Acids Res
, vol.41
, pp. D165-D170
-
-
Wingender, E.1
Schoeps, T.2
Dönitz, J.3
-
17
-
-
84874805342
-
Criteria for an updated classification of human transcription factor DNA-binding domains
-
Wingender E. Criteria for an updated classification of human transcription factor DNA-binding domains. J Bioinformat Comput Biol 2013, 11:1340007.
-
(2013)
J Bioinformat Comput Biol
, vol.11
, pp. 1340007
-
-
Wingender, E.1
-
18
-
-
81355142141
-
Non-coding RNAs in human disease
-
Esteller M. Non-coding RNAs in human disease. Nat Rev Genet 2011, 12:861.
-
(2011)
Nat Rev Genet
, vol.12
, pp. 861
-
-
Esteller, M.1
-
19
-
-
84865727393
-
The GENCODE v7 catalog of human long noncoding RNAs: analysis of their gene structure, evolution, and expression
-
Derrien T., Knowles D.G., Lagarde J., Veeravalli L., Ruan X., Ruan Y., Lassmann T., Carninci P., Brown J.B., Lipovich L., et al. The GENCODE v7 catalog of human long noncoding RNAs: analysis of their gene structure, evolution, and expression. Genome Res 2012, 22:1775-1789.
-
(2012)
Genome Res
, vol.22
, pp. 1775-1789
-
-
Derrien, T.1
Knowles, D.G.2
Lagarde, J.3
Veeravalli, L.4
Ruan, X.5
Ruan, Y.6
Lassmann, T.7
Carninci, P.8
Brown, J.B.9
Lipovich, L.10
-
20
-
-
80052978224
-
Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclasses
-
Cabili M.N., Trapnell C., Goff L., Koziol M., Tazon-Vega B., Regev A., Rinn J.L. Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclasses. Genes Dev 2011, 25:1915-1927.
-
(2011)
Genes Dev
, vol.25
, pp. 1915-1927
-
-
Cabili, M.N.1
Trapnell, C.2
Goff, L.3
Koziol, M.4
Tazon-Vega, B.5
Regev, A.6
Rinn, J.L.7
-
21
-
-
78651325932
-
LncRNAdb: a reference database for long noncoding RNAs
-
Amaral P.P., Clark M.B., Gascoigne D.K., Dinger M.E., Mattick J.S. lncRNAdb: a reference database for long noncoding RNAs. Nucleic Acids Res 2011, 39:D146-D151.
-
(2011)
Nucleic Acids Res
, vol.39
, pp. D146-D151
-
-
Amaral, P.P.1
Clark, M.B.2
Gascoigne, D.K.3
Dinger, M.E.4
Mattick, J.S.5
-
22
-
-
84884953564
-
Function of lncRNAs and approaches to lncRNA-protein interactions
-
Zhu J., Fu H., Wu Y., Zheng X. Function of lncRNAs and approaches to lncRNA-protein interactions. Sci China Life Sci 2013, 56:876-885.
-
(2013)
Sci China Life Sci
, vol.56
, pp. 876-885
-
-
Zhu, J.1
Fu, H.2
Wu, Y.3
Zheng, X.4
-
23
-
-
34248162440
-
Functionality or transcriptional noise? Evidence for selection within long noncoding RNAs
-
Ponjavic J., Ponting C.P., Lunter G. Functionality or transcriptional noise? Evidence for selection within long noncoding RNAs. Genome Res 2007, 17:556-565.
-
(2007)
Genome Res
, vol.17
, pp. 556-565
-
-
Ponjavic, J.1
Ponting, C.P.2
Lunter, G.3
-
24
-
-
79957580288
-
Long noncoding RNAs in cell biology
-
Clark M.B., Mattick J.S. Long noncoding RNAs in cell biology. Semin Cell Dev Biol 2011, 22:366-376.
-
(2011)
Semin Cell Dev Biol
, vol.22
, pp. 366-376
-
-
Clark, M.B.1
Mattick, J.S.2
-
25
-
-
84897993537
-
Regulation of metabolism by long, non-coding RNAs
-
Kornfeld J.-W., Brüning J.C. Regulation of metabolism by long, non-coding RNAs. Front Genet 2014, 5:57.
-
(2014)
Front Genet
, vol.5
, pp. 57
-
-
Kornfeld, J.-W.1
Brüning, J.C.2
-
27
-
-
84895908120
-
The evolution of lncRNA repertoires and expression patterns in tetrapods
-
Necsulea A., Soumillon M., Warnefors M., Liechti A., Daish T., Zeller U., Baker J.C., Grützner F., Kaessmann H. The evolution of lncRNA repertoires and expression patterns in tetrapods. Nature 2014, 505:635.
-
(2014)
Nature
, vol.505
, pp. 635
-
-
Necsulea, A.1
Soumillon, M.2
Warnefors, M.3
Liechti, A.4
Daish, T.5
Zeller, U.6
Baker, J.C.7
Grützner, F.8
Kaessmann, H.9
-
28
-
-
84898747543
-
Evolutionary dynamics and tissue specificity of human long noncoding RNAs in six mammals
-
Washietl S., Kellis M., Garber M. Evolutionary dynamics and tissue specificity of human long noncoding RNAs in six mammals. Genome Res 2014, 24:616-628.
-
(2014)
Genome Res
, vol.24
, pp. 616-628
-
-
Washietl, S.1
Kellis, M.2
Garber, M.3
-
29
-
-
84879671055
-
Pervasive transcription of the human genome produces thousands of previously unidentified long intergenic noncoding RNAs
-
Hangauer M.J., Vaughn I.W., McManus M.T. Pervasive transcription of the human genome produces thousands of previously unidentified long intergenic noncoding RNAs. PLoS Genet 2013, 9:e1003569.
-
(2013)
PLoS Genet
, vol.9
, pp. e1003569
-
-
Hangauer, M.J.1
Vaughn, I.W.2
McManus, M.T.3
-
30
-
-
80055025720
-
Accelerated recruitment of new brain development genes into the human genome
-
Zhang Y.E., Landback P., Vibranovski M.D., Long M. Accelerated recruitment of new brain development genes into the human genome. PLoS Biol 2011, 9:e1001179.
-
(2011)
PLoS Biol
, vol.9
, pp. e1001179
-
-
Zhang, Y.E.1
Landback, P.2
Vibranovski, M.D.3
Long, M.4
-
31
-
-
79959668884
-
Gain, loss and divergence in primate zinc-finger genes: a rich resource for evolution of gene regulatory differences between species
-
Nowick K., Fields C., Gernat T., Caetano-Anolles D., Kholina N., Stubbs L. Gain, loss and divergence in primate zinc-finger genes: a rich resource for evolution of gene regulatory differences between species. PLoS ONE 2011, 6:e21553.
-
(2011)
PLoS ONE
, vol.6
, pp. e21553
-
-
Nowick, K.1
Fields, C.2
Gernat, T.3
Caetano-Anolles, D.4
Kholina, N.5
Stubbs, L.6
-
32
-
-
18744385495
-
The SYT-SSX1 fusion type of synovial sarcoma is associated with increased expression of cyclin A and D1. A link between t(X;18)(p11.2; q11.2) and the cell cycle machinery
-
Xie Y., Larsson O., Skytting B., Nilsson G., Grimer R.J., Mangham C.D., Fisher C., Shipley J., Bjerkehagen B., Myklebost O. The SYT-SSX1 fusion type of synovial sarcoma is associated with increased expression of cyclin A and D1. A link between t(X;18)(p11.2; q11.2) and the cell cycle machinery. Oncogene 2002, 21:5791-5796.
-
(2002)
Oncogene
, vol.21
, pp. 5791-5796
-
-
Xie, Y.1
Larsson, O.2
Skytting, B.3
Nilsson, G.4
Grimer, R.J.5
Mangham, C.D.6
Fisher, C.7
Shipley, J.8
Bjerkehagen, B.9
Myklebost, O.10
-
33
-
-
0036927009
-
New BAGE (B melanoma antigen) genes mapping to the juxtacentromeric regions of human chromosomes 13 and 21 have a cancer/testis expression profile
-
Ruault M., van der Bruggen P., Brun M.-E., Boyle S., Roizès G., De Sario A. New BAGE (B melanoma antigen) genes mapping to the juxtacentromeric regions of human chromosomes 13 and 21 have a cancer/testis expression profile. Eur J Hum Genet 2002, 10:833-840.
-
(2002)
Eur J Hum Genet
, vol.10
, pp. 833-840
-
-
Ruault, M.1
van der Bruggen, P.2
Brun, M.-E.3
Boyle, S.4
Roizès, G.5
De Sario, A.6
-
34
-
-
84867538540
-
FOXO3 gene variants and human aging: coding variants may not be key players
-
Donlon T.A., Curb J.D., He Q., Grove J.S., Masaki K.H., Rodriguez B., Elliott A., Willcox D.C., Willcox B.J. FOXO3 gene variants and human aging: coding variants may not be key players. J Gerontol Series A Biol Sci Med Sci 2012, 67:1132-1139.
-
(2012)
J Gerontol Series A Biol Sci Med Sci
, vol.67
, pp. 1132-1139
-
-
Donlon, T.A.1
Curb, J.D.2
He, Q.3
Grove, J.S.4
Masaki, K.H.5
Rodriguez, B.6
Elliott, A.7
Willcox, D.C.8
Willcox, B.J.9
-
35
-
-
0037158715
-
Molecular evolution of FOXP2, a gene involved in speech and language
-
Enard W., Przeworski M., Fisher S.E., Lai C.S.L., Wiebe V., Kitano T., Monaco A.P., Pääbo S. Molecular evolution of FOXP2, a gene involved in speech and language. Nature 2002, 418:869-872.
-
(2002)
Nature
, vol.418
, pp. 869-872
-
-
Enard, W.1
Przeworski, M.2
Fisher, S.E.3
Lai, C.S.L.4
Wiebe, V.5
Kitano, T.6
Monaco, A.P.7
Pääbo, S.8
-
36
-
-
0035807360
-
A forkhead-domain gene is mutated in a severe speech and language disorder
-
Lai C.S.L., Fisher S.E., Hurst J.A., Vargha-Khadem F., Monaco A.P. A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 2001, 413:519-523.
-
(2001)
Nature
, vol.413
, pp. 519-523
-
-
Lai, C.S.L.1
Fisher, S.E.2
Hurst, J.A.3
Vargha-Khadem, F.4
Monaco, A.P.5
-
37
-
-
70449653431
-
Human-specific transcriptional regulation of CNS development genes by FOXP2
-
Konopka G., Geschwind D.H., Bomar J.M., Winden K., Coppola G., Jonsson Z.O., Gao F., Peng S., Preuss T.M., Wohlschlegel J.A. Human-specific transcriptional regulation of CNS development genes by FOXP2. Nature 2009, 462:213-217.
-
(2009)
Nature
, vol.462
, pp. 213-217
-
-
Konopka, G.1
Geschwind, D.H.2
Bomar, J.M.3
Winden, K.4
Coppola, G.5
Jonsson, Z.O.6
Gao, F.7
Peng, S.8
Preuss, T.M.9
Wohlschlegel, J.A.10
-
38
-
-
78951481923
-
Humanized Foxp2 specifically affects cortico-basal ganglia circuits
-
Reimers-Kipping S., Hevers W., Pääbo S., Enard W. Humanized Foxp2 specifically affects cortico-basal ganglia circuits. Neuroscience 2011, 175:75-84.
-
(2011)
Neuroscience
, vol.175
, pp. 75-84
-
-
Reimers-Kipping, S.1
Hevers, W.2
Pääbo, S.3
Enard, W.4
-
39
-
-
76049088399
-
Differences in human and chimpanzee gene expression patterns define an evolving network of transcription factors in brain
-
Nowick K., Gernat T., Almaas E., Stubbs L., Robinson G.E. Differences in human and chimpanzee gene expression patterns define an evolving network of transcription factors in brain. Proc Natl Acad Sci U S A 2009, 106:22358-22363.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 22358-22363
-
-
Nowick, K.1
Gernat, T.2
Almaas, E.3
Stubbs, L.4
Robinson, G.E.5
-
40
-
-
77958130019
-
Rapid sequence and expression divergence suggest selection for novel function in primate-specific KRAB-ZNF genes
-
Nowick K., Hamilton A.T., Zhang H., Stubbs L. Rapid sequence and expression divergence suggest selection for novel function in primate-specific KRAB-ZNF genes. Mol Biol Evol 2010, 27:2606-2617.
-
(2010)
Mol Biol Evol
, vol.27
, pp. 2606-2617
-
-
Nowick, K.1
Hamilton, A.T.2
Zhang, H.3
Stubbs, L.4
-
41
-
-
84875254039
-
A prominent role of KRAB-ZNF transcription factors in mammalian speciation?
-
Nowick K., Carneiro M., Faria R. A prominent role of KRAB-ZNF transcription factors in mammalian speciation?. Trends Genet 2012, 3:130-139.
-
(2012)
Trends Genet
, vol.3
, pp. 130-139
-
-
Nowick, K.1
Carneiro, M.2
Faria, R.3
-
42
-
-
80053906761
-
Deep sequencing reveals 50 novel genes for recessive cognitive disorders
-
Najmabadi H., Jamali P., Zecha A., Mohseni M., Püttmann L., Vahid L.N., Jensen C., Moheb L.A., Bienek M., Larti F., et al. Deep sequencing reveals 50 novel genes for recessive cognitive disorders. Nature 2011, 478:57-63.
-
(2011)
Nature
, vol.478
, pp. 57-63
-
-
Najmabadi, H.1
Jamali, P.2
Zecha, A.3
Mohseni, M.4
Püttmann, L.5
Vahid, L.N.6
Jensen, C.7
Moheb, L.A.8
Bienek, M.9
Larti, F.10
-
43
-
-
79952313620
-
Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting
-
Betancur C. Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting. Brain Res 2011, 1380:42-77.
-
(2011)
Brain Res
, vol.1380
, pp. 42-77
-
-
Betancur, C.1
-
44
-
-
84891157201
-
Genetics of recessive cognitive disorders
-
Musante L., Ropers H.H. Genetics of recessive cognitive disorders. Trends Genet 2014, 30:32.
-
(2014)
Trends Genet
, vol.30
, pp. 32
-
-
Musante, L.1
Ropers, H.H.2
-
45
-
-
77954061801
-
Extraordinary molecular evolution in the PRDM9 fertility gene
-
Thomas J.H., Emerson R.O., Shendure J. Extraordinary molecular evolution in the PRDM9 fertility gene. PLoS ONE 2009, 4:e8505.
-
(2009)
PLoS ONE
, vol.4
, pp. e8505
-
-
Thomas, J.H.1
Emerson, R.O.2
Shendure, J.3
-
46
-
-
76749170346
-
PRDM9 is a major determinant of meiotic recombination hotspots in humans and mice
-
Baudat F., Buard J., Grey C., Fledel-Alon A., Ober C., Przeworski M., Coop G., de Massy B. PRDM9 is a major determinant of meiotic recombination hotspots in humans and mice. Science 2010, 327:836-840.
-
(2010)
Science
, vol.327
, pp. 836-840
-
-
Baudat, F.1
Buard, J.2
Grey, C.3
Fledel-Alon, A.4
Ober, C.5
Przeworski, M.6
Coop, G.7
de Massy, B.8
-
47
-
-
84859636918
-
A fine-scale chimpanzee genetic map from population sequencing
-
Auton A., Broxholme J., Humburg P., Iqbal Z., Lunter G., Maller J., Hernandez R.D., Melton C., Venkat A., Nobrega M.A., et al. A fine-scale chimpanzee genetic map from population sequencing. Science (New York, NY) 2012, 336:193.
-
(2012)
Science (New York, NY)
, vol.336
, pp. 193
-
-
Auton, A.1
Broxholme, J.2
Humburg, P.3
Iqbal, Z.4
Lunter, G.5
Maller, J.6
Hernandez, R.D.7
Melton, C.8
Venkat, A.9
Nobrega, M.A.10
-
48
-
-
84887094704
-
Great ape genomics
-
Wall J.D. Great ape genomics. ILAR J 2013, 54:82-90.
-
(2013)
ILAR J
, vol.54
, pp. 82-90
-
-
Wall, J.D.1
-
49
-
-
84887376115
-
ANRIL/CDKN2B-AS shows two-stage clade-specific evolution and becomes conserved after transposon insertions in simians
-
He S., Gu W., Li Y., Zhu H. ANRIL/CDKN2B-AS shows two-stage clade-specific evolution and becomes conserved after transposon insertions in simians. BMC Evol Biol 2013, 13:247.
-
(2013)
BMC Evol Biol
, vol.13
, pp. 247
-
-
He, S.1
Gu, W.2
Li, Y.3
Zhu, H.4
-
50
-
-
84876864345
-
Transposable elements are major contributors to the origin, diversification, and regulation of vertebrate long noncoding RNAs
-
Kapusta A., Kronenberg Z., Lynch V.J., Zhuo X., Ramsay L., Bourque G., Yandell M., Feschotte C. Transposable elements are major contributors to the origin, diversification, and regulation of vertebrate long noncoding RNAs. PLoS Genet 2013, 9:e1003470.
-
(2013)
PLoS Genet
, vol.9
, pp. e1003470
-
-
Kapusta, A.1
Kronenberg, Z.2
Lynch, V.J.3
Zhuo, X.4
Ramsay, L.5
Bourque, G.6
Yandell, M.7
Feschotte, C.8
-
51
-
-
84878522936
-
The majority of primate-specific regulatory sequences are derived from transposable elements
-
Jacques P.-É., Jeyakani J., Bourque G. The majority of primate-specific regulatory sequences are derived from transposable elements. PLoS Genet 2013, 9:e1003504.
-
(2013)
PLoS Genet
, vol.9
, pp. e1003504
-
-
Jacques, P.-É.1
Jeyakani, J.2
Bourque, G.3
-
52
-
-
45749112954
-
Distinctive structures between chimpanzee and human in a brain noncoding RNA
-
Beniaminov A., Westhof E., Krol A. Distinctive structures between chimpanzee and human in a brain noncoding RNA. RNA (New York, NY) 2008, 14:1270-1275.
-
(2008)
RNA (New York, NY)
, vol.14
, pp. 1270-1275
-
-
Beniaminov, A.1
Westhof, E.2
Krol, A.3
-
53
-
-
84866437197
-
NMR studies of HAR1 RNA secondary structures reveal conformational dynamics in the human RNA
-
Ziegeler M., Cevec M., Richter C., Schwalbe H. NMR studies of HAR1 RNA secondary structures reveal conformational dynamics in the human RNA. ChemBioChem 2012, 13:2100.
-
(2012)
ChemBioChem
, vol.13
, pp. 2100
-
-
Ziegeler, M.1
Cevec, M.2
Richter, C.3
Schwalbe, H.4
-
55
-
-
79955088437
-
The sequence, structure and evolutionary features of HOTAIR in mammals
-
He S., Liu S., Zhu H. The sequence, structure and evolutionary features of HOTAIR in mammals. BMC Evol Biol 2011, 11:102.
-
(2011)
BMC Evol Biol
, vol.11
, pp. 102
-
-
He, S.1
Liu, S.2
Zhu, H.3
-
56
-
-
34250729138
-
Functional demarcation of active and silent chromatin domains in human HOX loci by noncoding RNAs
-
Rinn J.L., Segal E., Chang H.Y., Kertesz M., Wang J.K., Squazzo S.L., Xu X., Brugmann S.A., Goodnough L.H., Helms J.A., et al. Functional demarcation of active and silent chromatin domains in human HOX loci by noncoding RNAs. Cell 2007, 129:1311-1323.
-
(2007)
Cell
, vol.129
, pp. 1311-1323
-
-
Rinn, J.L.1
Segal, E.2
Chang, H.Y.3
Kertesz, M.4
Wang, J.K.5
Squazzo, S.L.6
Xu, X.7
Brugmann, S.A.8
Goodnough, L.H.9
Helms, J.A.10
-
57
-
-
84921944464
-
Overexpression of long noncoding RNA HOTAIR predicts a poor prognosis in patients with cervical cancer
-
Huang L., Liao L.-M., Liu A.-W., Wu J.-B., Cheng X.-L., Lin J.-X., Zheng M. Overexpression of long noncoding RNA HOTAIR predicts a poor prognosis in patients with cervical cancer. Arch Gynecol Obstet 2014, 4:1-7.
-
(2014)
Arch Gynecol Obstet
, vol.4
, pp. 1-7
-
-
Huang, L.1
Liao, L.-M.2
Liu, A.-W.3
Wu, J.-B.4
Cheng, X.-L.5
Lin, J.-X.6
Zheng, M.7
-
58
-
-
78651397147
-
Large non-coding RNAs: missing links in cancer?
-
Huarte M., Rinn J.L. Large non-coding RNAs: missing links in cancer?. Human Mol Genet 2010, 19:R152-R161.
-
(2010)
Human Mol Genet
, vol.19
, pp. R152-R161
-
-
Huarte, M.1
Rinn, J.L.2
-
59
-
-
84885740857
-
Targeted disruption of Hotair leads to homeotic transformation and gene derepression
-
Li L., Gupta R.A., Helms J.A., Chang H.Y., Liu B., Wapinski O.L., Tsai M.-C., Qu K., Zhang J., Carlson J.C., et al. Targeted disruption of Hotair leads to homeotic transformation and gene derepression. Cell Rep 2013, 5:3.
-
(2013)
Cell Rep
, vol.5
, pp. 3
-
-
Li, L.1
Gupta, R.A.2
Helms, J.A.3
Chang, H.Y.4
Liu, B.5
Wapinski, O.L.6
Tsai, M.-C.7
Qu, K.8
Zhang, J.9
Carlson, J.C.10
-
60
-
-
35548955882
-
The derived FOXP2 variant of modern humans was shared with Neandertals
-
Krause J., Lalueza-Fox C., Orlando L., Enard W., Green R.E., Burbano H.A., Hublin J.-J., Hänni C., Fortea J., de la Rasilla M., et al. The derived FOXP2 variant of modern humans was shared with Neandertals. Curr Biol 2007, 17:1908-1912.
-
(2007)
Curr Biol
, vol.17
, pp. 1908-1912
-
-
Krause, J.1
Lalueza-Fox, C.2
Orlando, L.3
Enard, W.4
Green, R.E.5
Burbano, H.A.6
Hublin, J.-J.7
Hänni, C.8
Fortea, J.9
de la Rasilla, M.10
-
61
-
-
77952136530
-
A draft sequence of the Neandertal genome
-
Green R.E., Fritz M.H.-Y., Hansen N.F., Durand E.Y., Malaspinas A.-S., Jensen J.D., Marques-Bonet T., Alkan C., Prüfer K., Meyer M., et al. A draft sequence of the Neandertal genome. Science (New York, NY) 2010, 328:710-722.
-
(2010)
Science (New York, NY)
, vol.328
, pp. 710-722
-
-
Green, R.E.1
Fritz, M.H.-Y.2
Hansen, N.F.3
Durand, E.Y.4
Malaspinas, A.-S.5
Jensen, J.D.6
Marques-Bonet, T.7
Alkan, C.8
Prüfer, K.9
Meyer, M.10
-
62
-
-
78650850475
-
Genetic history of an archaic hominin group from Denisova Cave in Siberia
-
Reich D., Johnson P.L.F., Maricic T., Good J.M., Marques-Bonet T., Alkan C., Fu Q., Mallick S., Li H., Meyer M., et al. Genetic history of an archaic hominin group from Denisova Cave in Siberia. Nature 2010, 468:1053-1060.
-
(2010)
Nature
, vol.468
, pp. 1053-1060
-
-
Reich, D.1
Johnson, P.L.F.2
Maricic, T.3
Good, J.M.4
Marques-Bonet, T.5
Alkan, C.6
Fu, Q.7
Mallick, S.8
Li, H.9
Meyer, M.10
-
63
-
-
84875614116
-
A recent evolutionary change affects a regulatory element in the human FOXP2 gene
-
Maricic T., Lalueza-Fox C., de la Rasilla M., Rosas A., Gajovic S., Kelso J., Enard W., Schaffner W., Pääbo S., Günther V., et al. A recent evolutionary change affects a regulatory element in the human FOXP2 gene. Mol Biol Evol 2013, 30:844-852.
-
(2013)
Mol Biol Evol
, vol.30
, pp. 844-852
-
-
Maricic, T.1
Lalueza-Fox, C.2
de la Rasilla, M.3
Rosas, A.4
Gajovic, S.5
Kelso, J.6
Enard, W.7
Schaffner, W.8
Pääbo, S.9
Günther, V.10
-
64
-
-
45849086837
-
The timing of selection at the human FOXP2 gene
-
Coop G., Bullaughey K., Luca F., Przeworski M. The timing of selection at the human FOXP2 gene. Mol Biol Evol 2008, 25:1257-1259.
-
(2008)
Mol Biol Evol
, vol.25
, pp. 1257-1259
-
-
Coop, G.1
Bullaughey, K.2
Luca, F.3
Przeworski, M.4
-
65
-
-
84872506987
-
Phenotypic impact of genomic structural variation: insights from and for human disease
-
Weischenfeldt J., Symmons O., Spitz F., Korbel J.O. Phenotypic impact of genomic structural variation: insights from and for human disease. Nat Rev Genet 2013, 14:125-138.
-
(2013)
Nat Rev Genet
, vol.14
, pp. 125-138
-
-
Weischenfeldt, J.1
Symmons, O.2
Spitz, F.3
Korbel, J.O.4
-
66
-
-
84883682103
-
Evolution and diversity of copy number variation in the great ape lineage
-
Sudmant P.H., Persengiev S., Antonacci F., Ventura M., Prado-Martinez J., Marques-Bonet T., Eichler E.E., Huddleston J., Catacchio C.R., Malig M., et al. Evolution and diversity of copy number variation in the great ape lineage. Genome Res 2013, 23:1373-1382.
-
(2013)
Genome Res
, vol.23
, pp. 1373-1382
-
-
Sudmant, P.H.1
Persengiev, S.2
Antonacci, F.3
Ventura, M.4
Prado-Martinez, J.5
Marques-Bonet, T.6
Eichler, E.E.7
Huddleston, J.8
Catacchio, C.R.9
Malig, M.10
-
67
-
-
84892365780
-
The complete genome sequence of a Neanderthal from the Altai Mountains
-
Prüfer K., de Filippo C., Li H., Mallick S., Dannemann M., Fu Q., Kircher M., Kuhlwilm M., Lachmann M., Meyer M., et al. The complete genome sequence of a Neanderthal from the Altai Mountains. Nature 2014, 505:43-49.
-
(2014)
Nature
, vol.505
, pp. 43-49
-
-
Prüfer, K.1
de Filippo, C.2
Li, H.3
Mallick, S.4
Dannemann, M.5
Fu, Q.6
Kircher, M.7
Kuhlwilm, M.8
Lachmann, M.9
Meyer, M.10
-
68
-
-
84864276520
-
Association and mutation analyses of 16p11.2 autism candidate genes
-
Kumar R.A., Karamohamed S., Sutcliffe J.S., Cook E.H., Geschwind D.H., Dobyns W.B., Scherer S.W., Christian S.L., Marshall C.R., Badner J.A., et al. Association and mutation analyses of 16p11.2 autism candidate genes. PLoS ONE 2009, 4:e4582.
-
(2009)
PLoS ONE
, vol.4
, pp. e4582
-
-
Kumar, R.A.1
Karamohamed, S.2
Sutcliffe, J.S.3
Cook, E.H.4
Geschwind, D.H.5
Dobyns, W.B.6
Scherer, S.W.7
Christian, S.L.8
Marshall, C.R.9
Badner, J.A.10
-
69
-
-
72949122159
-
Association between microdeletion and microduplication at 16p11.2 and autism
-
Weiss L.A., Green T., Platt O.S., Ruderfer D.M., Walsh C.A., Altshuler D., Chakravarti A., Tanzi R.E., Stefansson K., Santangelo S.L., et al. Association between microdeletion and microduplication at 16p11.2 and autism. Obstet Gynecol Surv 2008, 63:361-363.
-
(2008)
Obstet Gynecol Surv
, vol.63
, pp. 361-363
-
-
Weiss, L.A.1
Green, T.2
Platt, O.S.3
Ruderfer, D.M.4
Walsh, C.A.5
Altshuler, D.6
Chakravarti, A.7
Tanzi, R.E.8
Stefansson, K.9
Santangelo, S.L.10
-
70
-
-
84892596990
-
Identification of putative target genes of the transcription factor RUNX2
-
Kuhlwilm M., Davierwala A., Pääbo S. Identification of putative target genes of the transcription factor RUNX2. PLoS ONE 2013, 8:e83218.
-
(2013)
PLoS ONE
, vol.8
, pp. e83218
-
-
Kuhlwilm, M.1
Davierwala, A.2
Pääbo, S.3
-
71
-
-
84555206233
-
On characterizing adaptive events unique to modern humans
-
Crisci J.L., Wong A., Good J.M., Jensen J.D. On characterizing adaptive events unique to modern humans. Genome Biol Evol 2011, 3:791-798.
-
(2011)
Genome Biol Evol
, vol.3
, pp. 791-798
-
-
Crisci, J.L.1
Wong, A.2
Good, J.M.3
Jensen, J.D.4
-
72
-
-
0031062972
-
Developmental functions of mammalian Hox genes
-
Favier B., Dollé P. Developmental functions of mammalian Hox genes. Mol Hum Reprod 1997, 3:115-131.
-
(1997)
Mol Hum Reprod
, vol.3
, pp. 115-131
-
-
Favier, B.1
Dollé, P.2
-
73
-
-
84900442346
-
Reconstructing the DNA methylation maps of the Neandertal and the Denisovan
-
Gokhman D., Lavi E., Prüfer K., Fraga M.F., Riancho J.A., Kelso J., Pääbo S., Meshorer E., Carmel L. Reconstructing the DNA methylation maps of the Neandertal and the Denisovan. Science (New York, NY) 2014, 344:523.
-
(2014)
Science (New York, NY)
, vol.344
, pp. 523
-
-
Gokhman, D.1
Lavi, E.2
Prüfer, K.3
Fraga, M.F.4
Riancho, J.A.5
Kelso, J.6
Pääbo, S.7
Meshorer, E.8
Carmel, L.9
-
74
-
-
74249088732
-
Accelerated evolution of the Prdm9 speciation gene across diverse metazoan taxa
-
Oliver P.L., Ponting C.P., Goodstadt L., Bayes J.J., Birtle Z., Roach K.C., Phadnis N., Beatson S.A., Lunter G., Malik H.S. Accelerated evolution of the Prdm9 speciation gene across diverse metazoan taxa. PLoS Genet 2009, 5:e1000753.
-
(2009)
PLoS Genet
, vol.5
, pp. e1000753
-
-
Oliver, P.L.1
Ponting, C.P.2
Goodstadt, L.3
Bayes, J.J.4
Birtle, Z.5
Roach, K.C.6
Phadnis, N.7
Beatson, S.A.8
Lunter, G.9
Malik, H.S.10
-
75
-
-
57349102927
-
Two single nucleotide polymorphisms in PRDM9 (MEISETZ) gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest
-
Miyamoto T., Koh E., Sakugawa N., Sato H., Hayashi H., Namiki M., Sengoku K. Two single nucleotide polymorphisms in PRDM9 (MEISETZ) gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest. J Assis Reprod Genet 2008, 25:553-557.
-
(2008)
J Assis Reprod Genet
, vol.25
, pp. 553-557
-
-
Miyamoto, T.1
Koh, E.2
Sakugawa, N.3
Sato, H.4
Hayashi, H.5
Namiki, M.6
Sengoku, K.7
-
76
-
-
84901393253
-
Genome-wide signals of positive selection in human evolution
-
Enard D., Messer P.W., Petrov D.A. Genome-wide signals of positive selection in human evolution. Genome Res 2014, 6:885-895.
-
(2014)
Genome Res
, vol.6
, pp. 885-895
-
-
Enard, D.1
Messer, P.W.2
Petrov, D.A.3
-
77
-
-
77957818072
-
WWOX gene is associated with HDL cholesterol and triglyceride levels
-
Sáez M.E., González-Pérez A., Martínez-Larrad M.T., Gayán J., Real L.M., Serrano-Ríos M., Ruiz A. WWOX gene is associated with HDL cholesterol and triglyceride levels. BMC Med Genet 2010, 11:148.
-
(2010)
BMC Med Genet
, vol.11
, pp. 148
-
-
Sáez, M.E.1
González-Pérez, A.2
Martínez-Larrad, M.T.3
Gayán, J.4
Real, L.M.5
Serrano-Ríos, M.6
Ruiz, A.7
-
78
-
-
84925298996
-
The WWOX gene modulates HDL and lipid metabolism
-
Iatan I., Choi H.Y., Ruel I., Reddy M.V.P.L., Kil H., Lee J., Abu Odeh M., Salah Z., Abu-Remaileh M., Weissglas-Volkov D., et al. The WWOX gene modulates HDL and lipid metabolism. Circ Cardiovasc Genet 2014, 7:491-504.
-
(2014)
Circ Cardiovasc Genet
, vol.7
, pp. 491-504
-
-
Iatan, I.1
Choi, H.Y.2
Ruel, I.3
Reddy, M.V.P.L.4
Kil, H.5
Lee, J.6
Abu Odeh, M.7
Salah, Z.8
Abu-Remaileh, M.9
Weissglas-Volkov, D.10
-
79
-
-
84893833543
-
The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation
-
Mallaret M., Synofzik M., Lee J., Sagum C.A., Mahajnah M., Sharkia R., Drouot N., Renaud M., Klein F.A.C., Anheim M., et al. The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation. Brain 2014, 137:411-419.
-
(2014)
Brain
, vol.137
, pp. 411-419
-
-
Mallaret, M.1
Synofzik, M.2
Lee, J.3
Sagum, C.A.4
Mahajnah, M.5
Sharkia, R.6
Drouot, N.7
Renaud, M.8
Klein, F.A.C.9
Anheim, M.10
|