-
1
-
-
42349095075
-
Advances in autism genetics: On the threshold of a new neurobiology
-
CrossRef Medline
-
Abrahams BS, Geschwind DH (2008) Advances in autism genetics: on the threshold of a new neurobiology. Nat Rev Genet 9:341-355. CrossRef Medline
-
(2008)
Nat Rev Genet
, vol.9
, pp. 341-355
-
-
Abrahams, B.S.1
Geschwind, D.H.2
-
2
-
-
58149178561
-
AutDB: A gene reference resource for autism research
-
CrossRef Medline
-
Basu SN, Kollu R, Banerjee-Basu S (2009) AutDB: a gene reference resource for autism research. Nucleic Acids Res 37:D832-D836. CrossRef Medline
-
(2009)
Nucleic Acids Res
, vol.37
-
-
Basu, S.N.1
Kollu, R.2
Banerjee-Basu, S.3
-
3
-
-
0001677717
-
Controlling the false discovery rate-a practical and powerful approach to multiple testing
-
Benjamini Y, Hochberg Y (1995) Controlling the false discovery rate-a practical and powerful approach to multiple testing. J R Stat Soc Ser B 57:289-300.
-
(1995)
J R Stat Soc Ser B
, vol.57
, pp. 289-300
-
-
Benjamini, Y.1
Hochberg, Y.2
-
4
-
-
0030070333
-
Copper/zinc superoxide dismutase expression in the human central nervous system-correlation with selective neuronal vulnerability
-
Medline
-
Bergeron C, Petrunka C, Weyer L (1996) Copper/zinc superoxide dismutase expression in the human central nervous system-correlation with selective neuronal vulnerability. Am J Pathol 148:273-279. Medline
-
(1996)
Am J Pathol
, vol.148
, pp. 273-279
-
-
Bergeron, C.1
Petrunka, C.2
Weyer, L.3
-
5
-
-
67651010456
-
Genetic advances in autism: Heterogeneity and convergence on shared pathways
-
CrossRef Medline
-
Bill BR, Geschwind DH (2009) Genetic advances in autism: heterogeneity and convergence on shared pathways. Curr Opin Genet Dev 19:271-278. CrossRef Medline
-
(2009)
Curr Opin Genet Dev
, vol.19
, pp. 271-278
-
-
Bill, B.R.1
Geschwind, D.H.2
-
7
-
-
24244469447
-
Mutations in the parkin gene are a common cause for autosomal recessive early onset parkinsonism in Europe
-
Brice A, Lucking CB, Abbas N, Durr A, Ricard S, Bonifati V, De Michele G, Wood NW, Gasser T, Breteler M, Harhangi S, Oostra B, Filla A, Meco G, Denefle P, Agid Y (1999) Mutations in the parkin gene are a common cause for autosomal recessive early onset parkinsonism in Europe. Neurology 52:A554-A555.
-
(1999)
Neurology
, vol.52
-
-
Brice, A.1
Lucking, C.B.2
Abbas, N.3
Durr, A.4
Ricard, S.5
Bonifati, V.6
De Michele, G.7
Wood, N.W.8
Gasser, T.9
Breteler, M.10
Harhangi, S.11
Oostra, B.12
Filla, A.13
Meco, G.14
Denefle, P.15
Agid, Y.16
-
8
-
-
84888286336
-
Brain-reactive IgG correlates with autoimmunity in mothers of a child with an autism spectrum disorder
-
CrossRef Medline
-
Brimberg L, Sadiq A, Gregersen PK, Diamond B (2013) Brain-reactive IgG correlates with autoimmunity in mothers of a child with an autism spectrum disorder. Mol Psychiatry 18:1171-1177. CrossRef Medline
-
(2013)
Mol Psychiatry
, vol.18
, pp. 1171-1177
-
-
Brimberg, L.1
Sadiq, A.2
Gregersen, P.K.3
Diamond, B.4
-
9
-
-
38149129457
-
A transcriptome database for astrocytes, neurons, and oligodendrocytes: A new resource for understanding brain development and function
-
CrossRef Medline
-
Cahoy JD, Emery B, Kaushal A, Foo LC, Zamanian JL, Christopherson KS, Xing Y, Lubischer JL, Krieg PA, Krupenko SA, Thompson WJ, Barres BA (2008) A transcriptome database for astrocytes, neurons, and oligodendrocytes: a new resource for understanding brain development and function. J Neurosci 28:264-278. CrossRef Medline
-
(2008)
J Neurosci
, vol.28
, pp. 264-278
-
-
Cahoy, J.D.1
Emery, B.2
Kaushal, A.3
Foo, L.C.4
Zamanian, J.L.5
Christopherson, K.S.6
Xing, Y.7
Lubischer, J.L.8
Krieg, P.A.9
Krupenko, S.A.10
Thompson, W.J.11
Barres, B.A.12
-
10
-
-
78149431869
-
Dysfunction in GABA signalling mediates autismlike stereotypies and Rett syndrome phenotypes
-
CrossRef Medline
-
Chao HT, Chen H, Samaco RC, Xue M, Chahrour M, Yoo J, Neul JL, Gong S, Lu HC, Heintz N, Ekker M, Rubenstein JL, Noebels JL, Rosenmund C, Zoghbi HY (2010) Dysfunction in GABA signalling mediates autismlike stereotypies and Rett syndrome phenotypes. Nature 468:263-269. CrossRef Medline
-
(2010)
Nature
, vol.468
, pp. 263-269
-
-
Chao, H.T.1
Chen, H.2
Samaco, R.C.3
Xue, M.4
Chahrour, M.5
Yoo, J.6
Neul, J.L.7
Gong, S.8
Lu, H.C.9
Heintz, N.10
Ekker, M.11
Rubenstein, J.L.12
Noebels, J.L.13
Rosenmund, C.14
Zoghbi, H.Y.15
-
11
-
-
84859220108
-
Age-dependent brain gene expression and copy number anomalies in autism suggest distinct pathological processes at young versus mature ages
-
CrossRef Medline
-
Chow ML, Pramparo T, Winn ME, Barnes CC, Li HR, Weiss L, Fan JB, Murray S, April C, Belinson H, Fu XD, Wynshaw-Boris A, Schork NJ, Courchesne E (2012) Age-dependent brain gene expression and copy number anomalies in autism suggest distinct pathological processes at young versus mature ages. PLoS Genet 8:e1002592. CrossRef Medline
-
(2012)
PLoS Genet
, vol.8
-
-
Chow, M.L.1
Pramparo, T.2
Winn, M.E.3
Barnes, C.C.4
Li, H.R.5
Weiss, L.6
Fan, J.B.7
Murray, S.8
April, C.9
Belinson, H.10
Fu, X.D.11
Wynshaw-Boris, A.12
Schork, N.J.13
Courchesne, E.14
-
12
-
-
34547498486
-
A typology of photoreceptor gene expression patterns in the mouse
-
CrossRef Medline
-
Corbo JC, Myers CA, Lawrence KA, Jadhav AP, Cepko CL (2007) A typology of photoreceptor gene expression patterns in the mouse. Proc Natl Acad Sci U S A 104:12069-12074. CrossRef Medline
-
(2007)
Proc Natl Acad Sci U S A
, vol.104
, pp. 12069-12074
-
-
Corbo, J.C.1
Myers, C.A.2
Lawrence, K.A.3
Jadhav, A.P.4
Cepko, C.L.5
-
13
-
-
29144535372
-
Evolving gene/transcript definitions significantly alter the interpretation of GeneChip data
-
CrossRef Medline
-
Dai M, Wang P, Boyd AD, Kostov G, Athey B, Jones EG, Bunney WE, Myers RM, Speed TP, Akil H, Watson SJ, Meng F (2005) Evolving gene/transcript definitions significantly alter the interpretation of GeneChip data. Nucleic Acids Res 33:e175. CrossRef Medline
-
(2005)
Nucleic Acids Res
, vol.33
-
-
Dai, M.1
Wang, P.2
Boyd, A.D.3
Kostov, G.4
Athey, B.5
Jones, E.G.6
Bunney, W.E.7
Myers, R.M.8
Speed, T.P.9
Akil, H.10
Watson, S.J.11
Meng, F.12
-
15
-
-
84874827375
-
Translational profiling of hypocretin neurons identifies candidate molecules for sleep regulation
-
CrossRef Medline
-
Dalal J, Roh JH, Maloney SE, Akuffo A, Shah S, Yuan H, Wamsley B, Jones WB, Strong Cde G, Gray PA, Holtzman DM, Heintz N, Dougherty JD (2013) Translational profiling of hypocretin neurons identifies candidate molecules for sleep regulation. Genes Dev 27:565-578. CrossRef Medline
-
(2013)
Genes Dev
, vol.27
, pp. 565-578
-
-
Dalal, J.1
Roh, J.H.2
Maloney, S.E.3
Akuffo, A.4
Shah, S.5
Yuan, H.6
Wamsley, B.7
Jones, W.B.8
Strong Cde, G.9
Gray, P.A.10
Holtzman, D.M.11
Heintz, N.12
Dougherty, J.D.13
-
16
-
-
0038005018
-
DAVID: Database for annotation, visualization, and integrated discovery
-
CrossRef Medline
-
DennisGJr, Sherman BT, Hosack DA, Yang J, Gao W, Lane HC, LempickiRA (2003) DAVID: database for annotation, visualization, and integrated discovery. Genome Biol 4:P3. CrossRef Medline
-
(2003)
Genome Biol
, vol.4
-
-
Dennis Jr., G.1
Sherman, B.T.2
Hosack, D.A.3
Yang, J.4
Gao, W.5
Lane, H.C.6
Lempicki, R.A.7
-
17
-
-
84862493260
-
Genetic architecture in autism spectrum disorder
-
CrossRef Medline
-
Devlin B, Scherer SW (2012) Genetic architecture in autism spectrum disorder. Curr Opin Genet Dev 22:229-237. CrossRef Medline
-
(2012)
Curr Opin Genet Dev
, vol.22
, pp. 229-237
-
-
Devlin, B.1
Scherer, S.W.2
-
18
-
-
77955256931
-
Analytical approaches to RNA profiling data for the identification of genes enriched in specific cells
-
CrossRef Medline
-
Dougherty JD, Schmidt EF, Nakajima M, Heintz N (2010) Analytical approaches to RNA profiling data for the identification of genes enriched in specific cells. Nucleic Acids Res 38:4218-4230. CrossRef Medline
-
(2010)
Nucleic Acids Res
, vol.38
, pp. 4218-4230
-
-
Dougherty, J.D.1
Schmidt, E.F.2
Nakajima, M.3
Heintz, N.4
-
19
-
-
84866369083
-
Candidate pathways for promoting differentiation or quiescence of oligodendrocyte progenitorlike cells in glioma
-
CrossRef Medline
-
Dougherty JD, Fomchenko EI, Akuffo AA, Schmidt E, Helmy KY, Bazzoli E, Brennan CW, Holland EC, Milosevic A (2012) Candidate pathways for promoting differentiation or quiescence of oligodendrocyte progenitorlike cells in glioma. Cancer Res 72:4856-4868. CrossRef Medline
-
(2012)
Cancer Res
, vol.72
, pp. 4856-4868
-
-
Dougherty, J.D.1
Fomchenko, E.I.2
Akuffo, A.A.3
Schmidt, E.4
Helmy, K.Y.5
Bazzoli, E.6
Brennan, C.W.7
Holland, E.C.8
Milosevic, A.9
-
20
-
-
84873641538
-
The disruption of Celf6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviors
-
CrossRef Medline
-
Dougherty JD, Maloney SE, Wozniak DF, Rieger MA, Sonnenblick L, Coppola G, Mahieu NG, Zhang J, Cai J, Patti GJ, Abrahams BS, Geschwind DH, HeintzN (2013) The disruption of Celf6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviors. J Neurosci 33:2732-2753. CrossRef Medline
-
(2013)
J Neurosci
, vol.33
, pp. 2732-2753
-
-
Dougherty, J.D.1
Maloney, S.E.2
Wozniak, D.F.3
Rieger, M.A.4
Sonnenblick, L.5
Coppola, G.6
Mahieu, N.G.7
Zhang, J.8
Cai, J.9
Patti, G.J.10
Abrahams, B.S.11
Geschwind, D.H.12
Heintz, N.13
-
21
-
-
55449103144
-
Application of a translational profiling approach for the comparative analysis of CNS cell types
-
CrossRef Medline
-
Doyle JP, Dougherty JD, Heiman M, Schmidt EF, Stevens TR, Ma G, Bupp S, Shrestha P, Shah RD, Doughty ML, Gong S, Greengard P, Heintz N (2008) Application of a translational profiling approach for the comparative analysis of CNS cell types. Cell 135:749-762. CrossRef Medline
-
(2008)
Cell
, vol.135
, pp. 749-762
-
-
Doyle, J.P.1
Dougherty, J.D.2
Heiman, M.3
Schmidt, E.F.4
Stevens, T.R.5
Ma, G.6
Bupp, S.7
Shrestha, P.8
Shah, R.D.9
Doughty, M.L.10
Gong, S.11
Greengard, P.12
Heintz, N.13
-
22
-
-
77952629167
-
L-histidine decarboxylase and Tourette's syndrome
-
CrossRef Medline
-
Ercan-Sencicek AG, Stillman AA, Ghosh AK, Bilguvar K, O'Roak BJ, Mason CE, Abbott T, Gupta A, King RA, Pauls DL, Tischfield JA, Heiman GA, Singer HS, Gilbert DL, Hoekstra PJ, Morgan TM, Loring E, Yasuno K, Fernandez T, Sanders S, et al. (2010) L-histidine decarboxylase and Tourette's syndrome. N Engl J Med 362:1901-1908. CrossRef Medline
-
(2010)
N Engl J Med
, vol.362
, pp. 1901-1908
-
-
Ercan-Sencicek, A.G.1
Stillman, A.A.2
Ghosh, A.K.3
Bilguvar, K.4
O'Roak, B.J.5
Mason, C.E.6
Abbott, T.7
Gupta, A.8
King, R.A.9
Pauls, D.L.10
Tischfield, J.A.11
Heiman, G.A.12
Singer, H.S.13
Gilbert, D.L.14
Hoekstra, P.J.15
Morgan, T.M.16
Loring, E.17
Yasuno, K.18
Fernandez, T.19
Sanders, S.20
more..
-
23
-
-
0002386913
-
On the interpretation of χ2 from contingency tables, and the calculation of P
-
CrossRef
-
Fisher RA (1922) On the interpretation of χ2 from contingency tables, and the calculation of P. J R Stat Soc Ser B 85:87-94. CrossRef
-
(1922)
J R Stat Soc Ser B
, vol.85
, pp. 87-94
-
-
Fisher, R.A.1
-
24
-
-
0030669568
-
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor
-
CrossRef Medline
-
Freund CL, Gregory-Evans CY, Furukawa T, Papaioannou M, Looser J, Ploder L, Bellingham J, Ng D, Herbrick JA, Duncan A, Scherer SW, Tsui LC, Loutradis-Anagnostou A, Jacobson SG, Cepko CL, Bhattacharya SS, McInnes RR (1997) Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor. Cell 91:543-553. CrossRef Medline
-
(1997)
Cell
, vol.91
, pp. 543-553
-
-
Freund, C.L.1
Gregory-Evans, C.Y.2
Furukawa, T.3
Papaioannou, M.4
Looser, J.5
Ploder, L.6
Bellingham, J.7
Ng, D.8
Herbrick, J.A.9
Duncan, A.10
Scherer, S.W.11
Tsui, L.C.12
Loutradis-Anagnostou, A.13
Jacobson, S.G.14
Cepko, C.L.15
Bhattacharya, S.S.16
McInnes, R.R.17
-
25
-
-
0028128535
-
Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal-dominant stationary night blindness
-
Medline
-
Gal A, Orth U, Baehr W, Schwinger E, Rosenberg T (1994) Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal-dominant stationary night blindness. Nat Genet 7:551. Medline
-
(1994)
Nat Genet
, vol.7
, pp. 551
-
-
Gal, A.1
Orth, U.2
Baehr, W.3
Schwinger, E.4
Rosenberg, T.5
-
26
-
-
33645790701
-
LRRK2 expression linked to dopamine-innervated areas
-
CrossRef Medline
-
Galter D, Westerlund M, Carmine A, Lindqvist E, Sydow O, Olson L (2006) LRRK2 expression linked to dopamine-innervated areas. Ann Neurol 59: 714-719. CrossRef Medline
-
(2006)
Ann Neurol
, vol.59
, pp. 714-719
-
-
Galter, D.1
Westerlund, M.2
Carmine, A.3
Lindqvist, E.4
Sydow, O.5
Olson, L.6
-
27
-
-
43849112803
-
Immune transcriptome alterations in the temporal cortex of subjects with autism
-
CrossRef Medline
-
Garbett K, Ebert PJ, Mitchell A, Lintas C, Manzi B, Mirnics K, Persico AM (2008) Immune transcriptome alterations in the temporal cortex of subjects with autism. Neurobiol Dis 30:303-311. CrossRef Medline
-
(2008)
Neurobiol Dis
, vol.30
, pp. 303-311
-
-
Garbett, K.1
Ebert, P.J.2
Mitchell, A.3
Lintas, C.4
Manzi, B.5
Mirnics, K.6
Persico, A.M.7
-
28
-
-
67349182343
-
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
-
CrossRef Medline
-
Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, Zhang H, Estes A, Brune CW, Bradfield JP, Imielinski M, Frackelton EC, Reichert J, Crawford EL, Munson J, Sleiman PM, Chiavacci R, Annaiah K, Thomas K, Hou C, et al (2009) Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature 459:569-573. CrossRef Medline
-
(2009)
Nature
, vol.459
, pp. 569-573
-
-
Glessner, J.T.1
Wang, K.2
Cai, G.3
Korvatska, O.4
Kim, C.E.5
Wood, S.6
Zhang, H.7
Estes, A.8
Brune, C.W.9
Bradfield, J.P.10
Imielinski, M.11
Frackelton, E.C.12
Reichert, J.13
Crawford, E.L.14
Munson, J.15
Sleiman, P.M.16
Chiavacci, R.17
Annaiah, K.18
Thomas, K.19
Hou, C.20
more..
-
29
-
-
84885783699
-
Reexposure to nicotine during withdrawal increases the pacemaking activity of cholinergic habenular neurons
-
CrossRef Medline
-
Görlich A, Antolin-Fontes B, Ables JL, Frahm S, Slimak MA, Dougherty JD, Ibañez-Tallon I (2013) Reexposure to nicotine during withdrawal increases the pacemaking activity of cholinergic habenular neurons. Proc Natl Acad Sci U S A 110:17077-17082. CrossRef Medline
-
(2013)
Proc Natl Acad Sci U S A
, vol.110
, pp. 17077-17082
-
-
Görlich, A.1
Antolin-Fontes, B.2
Ables, J.L.3
Frahm, S.4
Slimak, M.A.5
Dougherty, J.D.6
Ibañez-Tallon, I.7
-
30
-
-
48749095219
-
Expression of the LRRK2 gene in the midbrain dopaminergic neurons of the substantia nigra
-
CrossRef Medline
-
Han BS, Iacovitti L, Katano T, Hattori N, Seol W, Kim KS (2008) Expression of the LRRK2 gene in the midbrain dopaminergic neurons of the substantia nigra. Neurosci Lett 442:190-194. CrossRef Medline
-
(2008)
Neurosci Lett
, vol.442
, pp. 190-194
-
-
Han, B.S.1
Iacovitti, L.2
Katano, T.3
Hattori, N.4
Seol, W.5
Kim, K.S.6
-
31
-
-
64249130693
-
IGFBP3 colocalizes with and regulates hypocretin (orexin)
-
CrossRef Medline
-
Honda M, Eriksson KS, Zhang S, Tanaka S, Lin L, Salehi A, Hesla PE, Maehlen J, Gaus SE, Yanagisawa M, Sakurai T, Taheri S, Tsuchiya K, Honda Y, Mignot E (2009) IGFBP3 colocalizes with and regulates hypocretin (orexin). PLoS One 4:e4254. CrossRef Medline
-
(2009)
PLoS One
, vol.4
-
-
Honda, M.1
Eriksson, K.S.2
Zhang, S.3
Tanaka, S.4
Lin, L.5
Salehi, A.6
Hesla, P.E.7
Maehlen, J.8
Gaus, S.E.9
Yanagisawa, M.10
Sakurai, T.11
Taheri, S.12
Tsuchiya, K.13
Honda, Y.14
Mignot, E.15
-
32
-
-
84892695635
-
Evaluation of TRAP-sequencing technology with a versatile conditional mouse model
-
Advance online publication. Retrieved December 18, 2013. doi:10.1093/nar/gkt995. CrossRef Medline
-
Hupe M, Li MX, Gertow Gillner K, Adams RH, Stenman JM (2013) Evaluation of TRAP-sequencing technology with a versatile conditional mouse model. Nucleic Acids Res. Advance online publication. Retrieved December 18, 2013. doi:10.1093/nar/gkt995. CrossRef Medline
-
(2013)
Nucleic Acids Res.
-
-
Hupe, M.1
Li, M.X.2
Gertow Gillner, K.3
Adams, R.H.4
Stenman, J.M.5
-
33
-
-
84860297457
-
De novo gene disruptions in children on the autistic spectrum
-
CrossRef Medline
-
Iossifov I, Ronemus M, Levy D, Wang Z, Hakker I, Rosenbaum J, Yamrom B, Lee YH, Narzisi G, Leotta A, Kendall J, Grabowska E, Ma B, Marks S, Rodgers L, Stepansky A, Troge J, Andrews P, Bekritsky M, Pradhan K, et al (2012) De novo gene disruptions in children on the autistic spectrum. Neuron 74:285-299. CrossRef Medline
-
(2012)
Neuron
, vol.74
, pp. 285-299
-
-
Iossifov, I.1
Ronemus, M.2
Levy, D.3
Wang, Z.4
Hakker, I.5
Rosenbaum, J.6
Yamrom, B.7
Lee, Y.H.8
Narzisi, G.9
Leotta, A.10
Kendall, J.11
Grabowska, E.12
Ma, B.13
Marks, S.14
Rodgers, L.15
Stepansky, A.16
Troge, J.17
Andrews, P.18
Bekritsky, M.19
Pradhan, K.20
more..
-
34
-
-
80054993342
-
Spatio-temporal transcriptome of the human brain
-
CrossRef Medline
-
Kang HJ, Kawasawa YI, Cheng F, Zhu Y, Xu X, Li M, Sousa AM, Pletikos M, Meyer KA, Sedmak G, Guennel T, Shin Y, Johnson MB, Krsnik Z, Mayer S, Fertuzinhos S, Umlauf S, Lisgo SN, Vortmeyer A, Weinberger DR, et al (2011) Spatio-temporal transcriptome of the human brain. Nature 478: 483-489. CrossRef Medline
-
(2011)
Nature
, vol.478
, pp. 483-489
-
-
Kang, H.J.1
Kawasawa, Y.I.2
Cheng, F.3
Zhu, Y.4
Xu, X.5
Li, M.6
Sousa, A.M.7
Pletikos, M.8
Meyer, K.A.9
Sedmak, G.10
Guennel, T.11
Shin, Y.12
Johnson, M.B.13
Krsnik, Z.14
Mayer, S.15
Fertuzinhos, S.16
Umlauf, S.17
Lisgo, S.N.18
Vortmeyer, A.19
Weinberger, D.R.20
more..
-
35
-
-
0032499264
-
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
-
CrossRef Medline
-
Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, Minoshima S, Yokochi M, Mizuno Y, Shimizu N (1998) Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 392:605-608. CrossRef Medline
-
(1998)
Nature
, vol.392
, pp. 605-608
-
-
Kitada, T.1
Asakawa, S.2
Hattori, N.3
Matsumine, H.4
Yamamura, Y.5
Minoshima, S.6
Yokochi, M.7
Mizuno, Y.8
Shimizu, N.9
-
36
-
-
84870040446
-
Molecular profiling of activated neurons by phosphorylated ribosome capture
-
CrossRef Medline
-
Knight ZA, Tan K, Birsoy K, Schmidt S, Garrison JL, Wysocki RW, Emiliano A, Ekstrand MI, Friedman JM (2012) Molecular profiling of activated neurons by phosphorylated ribosome capture. Cell 151:1126-1137. CrossRef Medline
-
(2012)
Cell
, vol.151
, pp. 1126-1137
-
-
Knight, Z.A.1
Tan, K.2
Birsoy, K.3
Schmidt, S.4
Garrison, J.L.5
Wysocki, R.W.6
Emiliano, A.7
Ekstrand, M.I.8
Friedman, J.M.9
-
37
-
-
80255135608
-
Populationspecific expression analysis (PSEA) reveals molecular changes in diseased brain
-
CrossRef Medline
-
Kuhn A, Thu D, Waldvogel HJ, Faull RL, Luthi-CarterR (2011) Populationspecific expression analysis (PSEA) reveals molecular changes in diseased brain. Nat Methods 8:945-947. CrossRef Medline
-
(2011)
Nat Methods
, vol.8
, pp. 945-947
-
-
Kuhn, A.1
Thu, D.2
Waldvogel, H.J.3
Faull, R.L.4
Luthi-Carter, R.5
-
38
-
-
60549111634
-
WGCNA: An R package for weighted correlation network analysis
-
CrossRef Medline
-
Langfelder P, Horvath S (2008) WGCNA: an R package for weighted correlation network analysis. BMC Bioinformatics 9:559. CrossRef Medline
-
(2008)
BMC Bioinformatics
, vol.9
, pp. 559
-
-
Langfelder, P.1
Horvath, S.2
-
39
-
-
77957947562
-
Hundreds of variants clustered in genomic loci and biological pathways affect human height
-
CrossRef Medline
-
Lango Allen H, Estrada K, Lettre G, Berndt SI, Weedon MN, Rivadeneira F, Willer CJ, Jackson AU, Vedantam S, Raychaudhuri S, Ferreira T, Wood AR, Weyant RJ, Segrè AV, Speliotes EK, Wheeler E, Soranzo N, Park JH, Yang J, Gudbjartsson D, et al. (2010) Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature 467: 832-838. CrossRef Medline
-
(2010)
Nature
, vol.467
, pp. 832-838
-
-
Lango Allen, H.1
Estrada, K.2
Lettre, G.3
Berndt, S.I.4
Weedon, M.N.5
Rivadeneira, F.6
Willer, C.J.7
Jackson, A.U.8
Vedantam, S.9
Raychaudhuri, S.10
Ferreira, T.11
Wood, A.R.12
Weyant, R.J.13
Segrè, A.V.14
Speliotes, E.K.15
Wheeler, E.16
Soranzo, N.17
Park, J.H.18
Yang, J.19
Gudbjartsson, D.20
more..
-
40
-
-
33846252240
-
Genome-wide atlas of gene expression in the adult mouse brain
-
CrossRef Medline
-
Lein ES, Hawrylycz MJ, Ao N, Ayres M, Bensinger A, Bernard A, Boe AF, Boguski MS, Brockway KS, Byrnes EJ, Chen L, Chen L, Chen TM, Chin MC, Chong J, Crook BE, Czaplinska A, Dang CN, Datta S, Dee NR, et al (2007) Genome-wide atlas of gene expression in the adult mouse brain. Nature 445:168-176. CrossRef Medline
-
(2007)
Nature
, vol.445
, pp. 168-176
-
-
Lein, E.S.1
Hawrylycz, M.J.2
Ao, N.3
Ayres, M.4
Bensinger, A.5
Bernard, A.6
Boe, A.F.7
Boguski, M.S.8
Brockway, K.S.9
Byrnes, E.J.10
Chen, L.11
Chen, L.12
Chen, T.M.13
Chin, M.C.14
Chong, J.15
Crook, B.E.16
Czaplinska, A.17
Dang, C.N.18
Datta, S.19
Dee, N.R.20
more..
-
41
-
-
24044440971
-
BiNGO: A Cytoscape plugin to assess overrepresentation of gene ontology categories in biological networks
-
CrossRef Medline
-
Maere S, Heymans K, KuiperM (2005) BiNGO: a Cytoscape plugin to assess overrepresentation of gene ontology categories in biological networks. Bioinformatics 21:3448-3449. CrossRef Medline
-
(2005)
Bioinformatics
, vol.21
, pp. 3448-3449
-
-
Maere, S.1
Heymans, K.2
Kuiper, M.3
-
42
-
-
84856046439
-
Interneuron dysfunction in psychiatric disorders
-
CrossRef Medline
-
Marín O (2012) Interneuron dysfunction in psychiatric disorders. Nat Rev Neurosci 13:107-120. CrossRef Medline
-
(2012)
Nat Rev Neurosci
, vol.13
, pp. 107-120
-
-
Marín, O.1
-
43
-
-
84860712363
-
Patterns and rates of exonic de novo mutations in autism spectrum disorders
-
CrossRef Medline
-
Neale BM, Kou Y, Liu L, Ma'ayan A, Samocha KE, Sabo A, Lin CF, Stevens C, Wang LS, Makarov V, Polak P, Yoon S, Maguire J, Crawford EL, Campbell NG, Geller ET, Valladares O, Schafer C, Liu H, Zhao T, et al. (2012) Patterns and rates of exonic de novo mutations in autism spectrum disorders. Nature 485:242-245. CrossRef Medline
-
(2012)
Nature
, vol.485
, pp. 242-245
-
-
Neale, B.M.1
Kou, Y.2
Liu, L.3
Ma'Ayan, A.4
Samocha, K.E.5
Sabo, A.6
Lin, C.F.7
Stevens, C.8
Wang, L.S.9
Makarov, V.10
Polak, P.11
Yoon, S.12
Maguire, J.13
Crawford, E.L.14
Campbell, N.G.15
Geller, E.T.16
Valladares, O.17
Schafer, C.18
Liu, H.19
Zhao, T.20
more..
-
44
-
-
54949113578
-
Functional organization of the transcriptome in human brain
-
CrossRef Medline
-
Oldham MC, Konopka G, Iwamoto K, Langfelder P, Kato T, Horvath S, Geschwind DH (2008) Functional organization of the transcriptome in human brain. Nat Neurosci 11:1271-1282. CrossRef Medline
-
(2008)
Nat Neurosci
, vol.11
, pp. 1271-1282
-
-
Oldham, M.C.1
Konopka, G.2
Iwamoto, K.3
Langfelder, P.4
Kato, T.5
Horvath, S.6
Geschwind, D.H.7
-
45
-
-
84860741138
-
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
-
CrossRef Medline
-
O'Roak BJ, Vives L, Girirajan S, Karakoc E, Krumm N, Coe BP, Levy R, Ko A, Lee C, Smith JD, Turner EH, Stanaway IB, Vernot B, Malig M, Baker C, Reilly B, Akey JM, Borenstein E, Rieder MJ, Nickerson DA, et al. (2012) Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Nature 485:246-250. CrossRef Medline
-
(2012)
Nature
, vol.485
, pp. 246-250
-
-
O'Roak, B.J.1
Vives, L.2
Girirajan, S.3
Karakoc, E.4
Krumm, N.5
Coe, B.P.6
Levy, R.7
Ko, A.8
Lee, C.9
Smith, J.D.10
Turner, E.H.11
Stanaway, I.B.12
Vernot, B.13
Malig, M.14
Baker, C.15
Reilly, B.16
Akey, J.M.17
Borenstein, E.18
Rieder, M.J.19
Nickerson, D.A.20
more..
-
46
-
-
80051608305
-
Exome sequencing and cis-regulatory mapping identify mutations in MAK, a gene encoding a regulator of ciliary length, as a cause of retinitis pigmentosa
-
CrossRef Medline
-
Ozgül RK, Siemiatkowska AM, Yücel D, Myers CA, Collin RW, Zonneveld MN, Beryozkin A, Banin E, Hoyng CB, van den Born LI, Bose R, Shen W, Sharon D, Cremers FPM, Klevering BJ, den Hollander AI, Corbo JC, Consortium ERD (2011) Exome sequencing and cis-regulatory mapping identify mutations in MAK, a gene encoding a regulator of ciliary length, as a cause of retinitis pigmentosa. Am J Hum Genet 89:253-264. CrossRef Medline
-
(2011)
Am J Hum Genet
, vol.89
, pp. 253-264
-
-
Ozgül, R.K.1
Siemiatkowska, A.M.2
Yücel, D.3
Myers, C.A.4
Collin, R.W.5
Zonneveld, M.N.6
Beryozkin, A.7
Banin, E.8
Hoyng, C.B.9
van den Born, L.I.10
Bose, R.11
Shen, W.12
Sharon, D.13
Cremers, F.P.M.14
Klevering, B.J.15
den Hollander, A.I.16
Corbo, J.C.17
Consortium, E.R.D.18
-
47
-
-
84859789501
-
Neural stem cells and transplantation studies in Parkinson's disease
-
CrossRef Medline
-
Pardal R, López-Barneo J (2012) Neural stem cells and transplantation studies in Parkinson's disease. Adv Exp Med Biol 741:206-216. CrossRef Medline
-
(2012)
Adv Exp Med Biol
, vol.741
, pp. 206-216
-
-
Pardal, R.1
López-Barneo, J.2
-
48
-
-
0028815433
-
Superoxide-dismutase is an abundant component in cell-bodies, dendrites, and axons of motor-neurons and in a subset of other neurons
-
CrossRef Medline
-
Pardo CA, Xu Z, Borchelt DR, Price DL, Sisodia SS, Cleveland DW (1995) Superoxide-dismutase is an abundant component in cell-bodies, dendrites, and axons of motor-neurons and in a subset of other neurons. Proc Natl Acad Sci U S A 92:954-958. CrossRef Medline
-
(1995)
Proc Natl Acad Sci U S A
, vol.92
, pp. 954-958
-
-
Pardo, C.A.1
Xu, Z.2
Borchelt, D.R.3
Price, D.L.4
Sisodia, S.S.5
Cleveland, D.W.6
-
49
-
-
84889561601
-
Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism
-
CrossRef Medline
-
Parikshak NN, Luo R, Zhang A, Won H, Lowe JK, Chandran V, Horvath S, Geschwind DH (2013) Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism. Cell 155:1008-1021. CrossRef Medline
-
(2013)
Cell
, vol.155
, pp. 1008-1021
-
-
Parikshak, N.N.1
Luo, R.2
Zhang, A.3
Won, H.4
Lowe, J.K.5
Chandran, V.6
Horvath, S.7
Geschwind, D.H.8
-
50
-
-
0033826856
-
A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains
-
CrossRef Medline
-
Peyron C, Faraco J, Rogers W, Ripley B, Overeem S, Charnay Y, Nevsimalova S, Aldrich M, Reynolds D, Albin R, Li R, Hungs M, Pedrazzoli M, Padigaru M, Kucherlapati M, Fan J, Maki R, Lammers GJ, Bouras C, Kucherlapati R, et al. (2000) A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains. Nat Med 6:991-997. CrossRef Medline
-
(2000)
Nat Med
, vol.6
, pp. 991-997
-
-
Peyron, C.1
Faraco, J.2
Rogers, W.3
Ripley, B.4
Overeem, S.5
Charnay, Y.6
Nevsimalova, S.7
Aldrich, M.8
Reynolds, D.9
Albin, R.10
Li, R.11
Hungs, M.12
Pedrazzoli, M.13
Padigaru, M.14
Kucherlapati, M.15
Fan, J.16
Maki, R.17
Lammers, G.J.18
Bouras, C.19
Kucherlapati, R.20
more..
-
51
-
-
77954657070
-
Functional impact of global rare copy number variation in autism spectrum disorders
-
CrossRef Medline
-
Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bölte S, Bolton PF, et al. (2010) Functional impact of global rare copy number variation in autism spectrum disorders. Nature 466:368-372. CrossRef Medline
-
(2010)
Nature
, vol.466
, pp. 368-372
-
-
Pinto, D.1
Pagnamenta, A.T.2
Klei, L.3
Anney, R.4
Merico, D.5
Regan, R.6
Conroy, J.7
Magalhaes, T.R.8
Correia, C.9
Abrahams, B.S.10
Almeida, J.11
Bacchelli, E.12
Bader, G.D.13
Bailey, A.J.14
Baird, G.15
Battaglia, A.16
Berney, T.17
Bolshakova, N.18
Bölte, S.19
Bolton, P.F.20
more..
-
52
-
-
79952051533
-
Levodopa in the treatment of Parkinson's disease: An old drug still going strong
-
CrossRef Medline
-
Poewe W, Antonini A, Zijlmans JC, Burkhard PR, Vingerhoets F (2010) Levodopa in the treatment of Parkinson's disease: an old drug still going strong. Clin Interv Aging 5:229-238. CrossRef Medline
-
(2010)
Clin Interv Aging
, vol.5
, pp. 229-238
-
-
Poewe, W.1
Antonini, A.2
Zijlmans, J.C.3
Burkhard, P.R.4
Vingerhoets, F.5
-
53
-
-
74549125753
-
An abundance of ubiquitously expressed genes revealed by tissue transcriptome sequence data
-
CrossRef Medline
-
Ramsköld D, Wang ET, Burge CB, Sandberg R (2009) An abundance of ubiquitously expressed genes revealed by tissue transcriptome sequence data. PLoS Comput Biol 5:e1000598. CrossRef Medline
-
(2009)
PLoS Comput Biol
, vol.5
-
-
Ramsköld, D.1
Wang, E.T.2
Burge, C.B.3
Sandberg, R.4
-
54
-
-
77952323515
-
Deep brain stimulation for advanced Parkinson's disease
-
CrossRef Medline
-
Rodriguez-Oroz MC (2010) Deep brain stimulation for advanced Parkinson's disease. Lancet Neurol 9:558-559. CrossRef Medline
-
(2010)
Lancet Neurol
, vol.9
, pp. 558-559
-
-
Rodriguez-Oroz, M.C.1
-
55
-
-
84860780495
-
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
-
CrossRef Medline
-
Sanders SJ, Murtha MT, Gupta AR, Murdoch JD, Raubeson MJ, Willsey AJ, Ercan-Sencicek AG, DiLullo NM, Parikshak NN, Stein JL, Walker MF, Ober GT, Teran NA, Song Y, El-Fishawy P, Murtha RC, Choi M, Overton JD, Bjornson RD, Carriero NJ, et al. (2012) De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Nature 485:237-241. CrossRef Medline
-
(2012)
Nature
, vol.485
, pp. 237-241
-
-
Sanders, S.J.1
Murtha, M.T.2
Gupta, A.R.3
Murdoch, J.D.4
Raubeson, M.J.5
Willsey, A.J.6
Ercan-Sencicek, A.G.7
DiLullo, N.M.8
Parikshak, N.N.9
Stein, J.L.10
Walker, M.F.11
Ober, G.T.12
Teran, N.A.13
Song, Y.14
El-Fishawy, P.15
Murtha, R.C.16
Choi, M.17
Overton, J.D.18
Bjornson, R.D.19
Carriero, N.J.20
more..
-
56
-
-
84876796759
-
Knockout of NMDA receptors in parvalbumin interneurons recreates autism-like phenotypes
-
CrossRef Medline
-
Saunders JA, Tatard-Leitman VM, Suh J, Billingslea EN, Roberts TP, Siegel SJ (2013) Knockout of NMDA receptors in parvalbumin interneurons recreates autism-like phenotypes. Autism Res 6:69-77. CrossRef Medline
-
(2013)
Autism Res
, vol.6
, pp. 69-77
-
-
Saunders, J.A.1
Tatard-Leitman, V.M.2
Suh, J.3
Billingslea, E.N.4
Roberts, T.P.5
Siegel, S.J.6
-
57
-
-
84881378088
-
Loss of GABAergic neurons in the hippocampus and cerebral cortex of Engrailed-2 null mutant mice: Implications for autism spectrum disorders
-
CrossRef Medline
-
Sgadò P, Genovesi S, Kalinovsky A, Zunino G, Macchi F, Allegra M, Murenu E, Provenzano G, Tripathi PP, Casarosa S, Joyner AL, Bozzi Y (2013) Loss of GABAergic neurons in the hippocampus and cerebral cortex of Engrailed-2 null mutant mice: implications for autism spectrum disorders. Exp Neurol 247:496-505. CrossRef Medline
-
(2013)
Exp Neurol
, vol.247
, pp. 496-505
-
-
Sgadò, P.1
Genovesi, S.2
Kalinovsky, A.3
Zunino, G.4
Macchi, F.5
Allegra, M.6
Murenu, E.7
Provenzano, G.8
Tripathi, P.P.9
Casarosa, S.10
Joyner, A.L.11
Bozzi, Y.12
-
58
-
-
77951634577
-
Cell type-specific gene expression differences in complex tissues
-
CrossRef Medline
-
Shen-Orr SS, Tibshirani R, Khatri P, Bodian DL, Staedtler F, Perry NM, Hastie T, Sarwal MM, Davis MM, Butte AJ (2010) Cell type-specific gene expression differences in complex tissues. Nat Methods 7:287-289. CrossRef Medline
-
(2010)
Nat Methods
, vol.7
, pp. 287-289
-
-
Shen-Orr, S.S.1
Tibshirani, R.2
Khatri, P.3
Bodian, D.L.4
Staedtler, F.5
Perry, N.M.6
Hastie, T.7
Sarwal, M.M.8
Davis, M.M.9
Butte, A.J.10
-
59
-
-
34249317298
-
Gene set enrichment analysis (GSEA) for interpreting gene expression profiles
-
CrossRef
-
Shi J, Walker MG (2007) Gene set enrichment analysis (GSEA) for interpreting gene expression profiles. Curr Bioinform 2:133-137. CrossRef
-
(2007)
Curr Bioinform
, vol.2
, pp. 133-137
-
-
Shi, J.1
Walker, M.G.2
-
60
-
-
0034515773
-
Parkin expression in the adult mouse brain
-
CrossRef Medline
-
Stichel CC, Augustin M, Kühn K, Zhu XR, Engels P, Ullmer C, Lübbert H (2000) Parkin expression in the adult mouse brain. Eur J Neurosci 12: 4181-4194. CrossRef Medline
-
(2000)
Eur J Neurosci
, vol.12
, pp. 4181-4194
-
-
Stichel, C.C.1
Augustin, M.2
Kühn, K.3
Zhu, X.R.4
Engels, P.5
Ullmer, C.6
Lübbert, H.7
-
61
-
-
84871939639
-
Microglial activation in young adults with autism spectrum disorder
-
CrossRef Medline
-
Suzuki K, Sugihara G, Ouchi Y, Nakamura K, Futatsubashi M, Takebayashi K, Yoshihara Y, Omata K, Matsumoto K, Tsuchiya KJ, Iwata Y, Tsujii M, Sugiyama T, Mori N (2013) Microglial activation in young adults with autism spectrum disorder. JAMA Psychiatry 70:49-58. CrossRef Medline
-
(2013)
JAMA Psychiatry
, vol.70
, pp. 49-58
-
-
Suzuki, K.1
Sugihara, G.2
Ouchi, Y.3
Nakamura, K.4
Futatsubashi, M.5
Takebayashi, K.6
Yoshihara, Y.7
Omata, K.8
Matsumoto, K.9
Tsuchiya, K.J.10
Iwata, Y.11
Tsujii, M.12
Sugiyama, T.13
Mori, N.14
-
62
-
-
0036302041
-
The role of hypocretins (orexins) in sleep regulation and narcolepsy
-
CrossRef Medline
-
Taheri S, Zeitzer JM, Mignot E (2002) The role of hypocretins (orexins) in sleep regulation and narcolepsy. Annu Rev Neurosci 25:283-313. CrossRef Medline
-
(2002)
Annu Rev Neurosci
, vol.25
, pp. 283-313
-
-
Taheri, S.1
Zeitzer, J.M.2
Mignot, E.3
-
63
-
-
0035942271
-
Significance analysis of microarrays applied to the ionizing radiation response
-
CrossRef Medline
-
Tusher VG, Tibshirani R, ChuG (2001) Significance analysis of microarrays applied to the ionizing radiation response. Proc Natl Acad Sci U S A 98: 5116-5121. CrossRef Medline
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 5116-5121
-
-
Tusher, V.G.1
Tibshirani, R.2
Chu, G.3
-
64
-
-
79959262465
-
Transcriptomic analysis of autistic brain reveals convergent molecular pathology
-
CrossRef Medline
-
Voineagu I, Wang X, Johnston P, Lowe JK, Tian Y, Horvath S, Mill J, Cantor RM, Blencowe BJ, Geschwind DH (2011) Transcriptomic analysis of autistic brain reveals convergent molecular pathology. Nature 474:380-384. CrossRef Medline
-
(2011)
Nature
, vol.474
, pp. 380-384
-
-
Voineagu, I.1
Wang, X.2
Johnston, P.3
Lowe, J.K.4
Tian, Y.5
Horvath, S.6
Mill, J.7
Cantor, R.M.8
Blencowe, B.J.9
Geschwind, D.H.10
-
65
-
-
67349112868
-
Commongenetic variants on 5p14.1 associate with autism spectrum disorders
-
CrossRef Medline
-
Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PM, Kim CE, Hou C, Frackelton E, Chiavacci R, Takahashi N, Sakurai T, Rappaport E, Lajonchere CM, Munson J, Estes A, et al. (2009) Commongenetic variants on 5p14.1 associate with autism spectrum disorders. Nature 459:528-533. CrossRef Medline
-
(2009)
Nature
, vol.459
, pp. 528-533
-
-
Wang, K.1
Zhang, H.2
Ma, D.3
Bucan, M.4
Glessner, J.T.5
Abrahams, B.S.6
Salyakina, D.7
Imielinski, M.8
Bradfield, J.P.9
Sleiman, P.M.10
Kim, C.E.11
Hou, C.12
Frackelton, E.13
Chiavacci, R.14
Takahashi, N.15
Sakurai, T.16
Rappaport, E.17
Lajonchere, C.M.18
Munson, J.19
Estes, A.20
more..
-
66
-
-
84855922674
-
Further characterization of autoantibodies to GABAergic neurons in the central nervous system produced by a subset of children with autism
-
CrossRef Medline
-
Wills S, Rossi CC, Bennett J, Martinez Cerdeño V, Ashwood P, Amaral DG, Van de Water J (2011) Further characterization of autoantibodies to GABAergic neurons in the central nervous system produced by a subset of children with autism. Mol Autism 2:5. CrossRef Medline
-
(2011)
Mol Autism
, vol.2
, pp. 5
-
-
Wills, S.1
Rossi, C.C.2
Bennett, J.3
Martinez Cerdeño, V.4
Ashwood, P.5
Amaral, D.G.6
Van de Water, J.7
-
67
-
-
84889583293
-
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism
-
CrossRef Medline
-
Willsey AJ, Sanders SJ, Li M, Dong S, Tebbenkamp AT, Muhle RA, Reilly SK, Lin L, Fertuzinhos S, Miller JA, Murtha MT, Bichsel C, Niu W, Cotney J, Ercan-Sencicek AG, Gockley J, Gupta AR, Han W, He X, Hoffman EJ, et al (2013) Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. Cell 155:997-1007. CrossRef Medline
-
(2013)
Cell
, vol.155
, pp. 997-1007
-
-
Willsey, A.J.1
Sanders, S.J.2
Li, M.3
Dong, S.4
Tebbenkamp, A.T.5
Muhle, R.A.6
Reilly, S.K.7
Lin, L.8
Fertuzinhos, S.9
Miller, J.A.10
Murtha, M.T.11
Bichsel, C.12
Niu, W.13
Cotney, J.14
Ercan-Sencicek, A.G.15
Gockley, J.16
Gupta, A.R.17
Han, W.18
He, X.19
Hoffman, E.J.20
more..
-
68
-
-
84991981413
-
Cell type specific analysis of human brain transcriptome data to predict alterations in cellular composition
-
CrossRef
-
Xu X, Nehorai A, Dougherty JD. (2013) Cell type specific analysis of human brain transcriptome data to predict alterations in cellular composition. Syst Biomed 1:1-10. CrossRef
-
(2013)
Syst Biomed
, vol.1
, pp. 1-10
-
-
Xu, X.1
Nehorai, A.2
Dougherty, J.D.3
-
69
-
-
84859744583
-
Large-scale cellular-resolution gene profiling in human neocortex reveals species-specific molecular signatures
-
CrossRef Medline
-
Zeng H, Shen EH, Hohmann JG, Oh SW, Bernard A, Royall JJ, Glattfelder KJ, Sunkin SM, Morris JA, Guillozet-Bongaarts AL, Smith KA, Ebbert AJ, Swanson B, Kuan L, Page DT, Overly CC, Lein ES, Hawrylycz MJ, Hof PR, Hyde TM, et al. (2012) Large-scale cellular-resolution gene profiling in human neocortex reveals species-specific molecular signatures. Cell 149: 483-496. CrossRef Medline
-
(2012)
Cell
, vol.149
, pp. 483-496
-
-
Zeng, H.1
Shen, E.H.2
Hohmann, J.G.3
Oh, S.W.4
Bernard, A.5
Royall, J.J.6
Glattfelder, K.J.7
Sunkin, S.M.8
Morris, J.A.9
Guillozet-Bongaarts, A.L.10
Smith, K.A.11
Ebbert, A.J.12
Swanson, B.13
Kuan, L.14
Page, D.T.15
Overly, C.C.16
Lein, E.S.17
Hawrylycz, M.J.18
Hof, P.R.19
Hyde, T.M.20
more..
-
70
-
-
84884306810
-
Interrogating translational efficiency and lineagespecific transcriptomes using ribosome affinity purification
-
CrossRef Medline
-
Zhou P, Zhang Y, Ma Q, Gu F, Day DS, He A, Zhou B, Li J, Stevens SM, Romo D, Pu WT (2013) Interrogating translational efficiency and lineagespecific transcriptomes using ribosome affinity purification. Proc Natl Acad Sci U S A 110:15395-15400. CrossRef Medline
-
(2013)
Proc Natl Acad Sci U S A
, vol.110
, pp. 15395-15400
-
-
Zhou, P.1
Zhang, Y.2
Ma, Q.3
Gu, F.4
Day, D.S.5
He, A.6
Zhou, B.7
Li, J.8
Stevens, S.M.9
Romo, D.10
Pu, W.T.11
|