-
1
-
-
42349088634
-
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
-
T. Walsh, J.M. McClellan, S.E. McCarthy, A.M. Addington, S.B. Pierce, G.M. Cooper Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia Science 320 2008 539 543
-
(2008)
Science
, vol.320
, pp. 539-543
-
-
Walsh, T.1
McClellan, J.M.2
McCarthy, S.E.3
Addington, A.M.4
Pierce, S.B.5
Cooper, G.M.6
-
2
-
-
51649107017
-
Rare chromosomal deletions and duplications increase risk of schizophrenia
-
International Schizophrenia Consortium
-
International Schizophrenia Consortium Rare chromosomal deletions and duplications increase risk of schizophrenia Nature 455 2008 237 241
-
(2008)
Nature
, vol.455
, pp. 237-241
-
-
-
3
-
-
49949085933
-
Large recurrent microdeletions associated with schizophrenia
-
H. Stefansson, D. Rujescu, S. Cichon, O.P. Pietiläinen, A. Ingason, S. Steinberg Large recurrent microdeletions associated with schizophrenia Nature 455 2008 232 236
-
(2008)
Nature
, vol.455
, pp. 232-236
-
-
Stefansson, H.1
Rujescu, D.2
Cichon, S.3
Pietiläinen, O.P.4
Ingason, A.5
Steinberg, S.6
-
4
-
-
46249093584
-
Strong association of de novo copy number mutations with sporadic schizophrenia
-
B. Xu, J.L. Roos, S. Levy, E.J. van Rensburg, J.A. Gogos, M. Karayiorgou Strong association of de novo copy number mutations with sporadic schizophrenia Nat Genet 40 2008 880 885
-
(2008)
Nat Genet
, vol.40
, pp. 880-885
-
-
Xu, B.1
Roos, J.L.2
Levy, S.3
Van Rensburg, E.J.4
Gogos, J.A.5
Karayiorgou, M.6
-
5
-
-
78049450213
-
Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function
-
International Schizophrenia Consortium
-
S. Raychaudhuri, J.M. Korn, S.A. McCarroll, D. Altshuler, P. Sklar International Schizophrenia Consortium Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function PLoS Genet 6 2010 e1001097
-
(2010)
PLoS Genet
, vol.6
, pp. 1001097
-
-
Raychaudhuri, S.1
Korn, J.M.2
McCarroll, S.A.3
Altshuler, D.4
Sklar, P.5
-
6
-
-
79952710338
-
Copy number variants in schizophrenia: Confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications
-
D.F. Levinson, J. Duan, S. Oh, K. Wang, A.R. Sanders, J. Shi Copy number variants in schizophrenia: Confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications Am J Psychiatry 168 2011 302 316
-
(2011)
Am J Psychiatry
, vol.168
, pp. 302-316
-
-
Levinson, D.F.1
Duan, J.2
Oh, S.3
Wang, K.4
Sanders, A.R.5
Shi, J.6
-
7
-
-
79958035893
-
Rare de novo variants associated with autism implicate a large functional network of genes
-
S.R. Gilman, IossifovI, D. Levy, M. Ronemus, M. Wigler, D. Vitkup Rare de novo variants associated with autism implicate a large functional network of genes Neuron 70 2011 898 907
-
(2011)
Neuron
, vol.70
, pp. 898-907
-
-
Gilman, S.R.1
Iossifov, I.2
Levy, D.3
Ronemus, M.4
Wigler, M.5
Vitkup, D.6
-
8
-
-
79952289176
-
Ontogenetic de novo copy number variations (CNVs) as a source of genetic individuality: Studies on two families with MZD twins for schizophrenia
-
S. Mahti, K. Kumar, C. Castellani, R. O'Riley, S. Singh Ontogenetic de novo copy number variations (CNVs) as a source of genetic individuality: Studies on two families with MZD twins for schizophrenia PLoS One 6 2011 e17125
-
(2011)
PLoS One
, vol.6
, pp. 17125
-
-
Mahti, S.1
Kumar, K.2
Castellani, C.3
O'Riley, R.4
Singh, S.5
-
9
-
-
33748745764
-
Critical factors in gene expression in postmortem human brain: Focus on studies in schizophrenia
-
B.K. Lipska, A. Deep-Soboslay, C.S. Weickert, T.M. Hyde, C.E. Martin, M.M. Herman, J.E. Kleinman Critical factors in gene expression in postmortem human brain: Focus on studies in schizophrenia Biol Psychiatry 60 2006 650 658
-
(2006)
Biol Psychiatry
, vol.60
, pp. 650-658
-
-
Lipska, B.K.1
Deep-Soboslay, A.2
Weickert, C.S.3
Hyde, T.M.4
Martin, C.E.5
Herman, M.M.6
Kleinman, J.E.7
-
10
-
-
35948984173
-
PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
-
K. Wang, M. Li, D. Hadley, R. Liu, J. Glessner, S.F. Grant PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data Genome Res 17 2007 1665 1674
-
(2007)
Genome Res
, vol.17
, pp. 1665-1674
-
-
Wang, K.1
Li, M.2
Hadley, D.3
Liu, R.4
Glessner, J.5
Grant, S.F.6
-
11
-
-
34247877877
-
QuantiSNP: An Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data
-
S. Colella, C. Yau, J.M. Taylor, G. Mirza, H. Butler, P. Clouston QuantiSNP: An Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data Nucleic Acids Res 35 2007 2013 2025
-
(2007)
Nucleic Acids Res
, vol.35
, pp. 2013-2025
-
-
Colella, S.1
Yau, C.2
Taylor, J.M.3
Mirza, G.4
Butler, H.5
Clouston, P.6
-
12
-
-
46249088370
-
Lumi: A pipeline for processing Illumina microarray
-
P. Du, W.A. Kibbe, S.M. Lin Lumi: A pipeline for processing Illumina microarray Bioinformatics 24 2008 1547 1548
-
(2008)
Bioinformatics
, vol.24
, pp. 1547-1548
-
-
Du, P.1
Kibbe, W.A.2
Lin, S.M.3
-
13
-
-
33845432928
-
Adjusting batch effects in microarray expression data using Empirical Bayes methods
-
W.E. Johnson, A. Rabinovic, C. Li Adjusting batch effects in microarray expression data using Empirical Bayes methods Biostatistics 8 2007 118 127
-
(2007)
Biostatistics
, vol.8
, pp. 118-127
-
-
Johnson, W.E.1
Rabinovic, A.2
Li, C.3
-
14
-
-
34848914038
-
Capturing heterogeneity in gene expression studies by surrogate variable analysis
-
J.T. Leek, J.D. Storey Capturing heterogeneity in gene expression studies by surrogate variable analysis PLoS Genet 3 2007 1724 1735
-
(2007)
PLoS Genet
, vol.3
, pp. 1724-1735
-
-
Leek, J.T.1
Storey, J.D.2
-
15
-
-
80054848222
-
Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: A susceptibility region for neurological dysfunction including developmental and language delay
-
R.D. Burnside, R. Pasion, F.M. Mikhail, A.J. Carroll, N.H. Robin, E.L. Youngs Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: A susceptibility region for neurological dysfunction including developmental and language delay Hum Genet 130 2011 517 528
-
(2011)
Hum Genet
, vol.130
, pp. 517-528
-
-
Burnside, R.D.1
Pasion, R.2
Mikhail, F.M.3
Carroll, A.J.4
Robin, N.H.5
Youngs, E.L.6
-
16
-
-
33847327313
-
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
-
Autism Genome Project Consortium
-
Autism Genome Project Consortium P. Szatmari, A.D. Paterson, L. Zwaigenbaum, W. Roberts, J. Brian et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nat Genet 39 2007 319 328
-
(2007)
Nat Genet
, vol.39
, pp. 319-328
-
-
Szatmari, P.1
Paterson, A.D.2
Zwaigenbaum, L.3
Roberts, W.4
Brian, J.5
-
17
-
-
80055015161
-
Temporal dynamics and genetic control of the human neocortical transcriptome across the lifespan
-
C. Colantuoni, B.K. Lipska, T. Ye, T.M. Hyde, R. Tao, J.T. Leek Temporal dynamics and genetic control of the human neocortical transcriptome across the lifespan Nature 478 2011 519 524
-
(2011)
Nature
, vol.478
, pp. 519-524
-
-
Colantuoni, C.1
Lipska, B.K.2
Ye, T.3
Hyde, T.M.4
Tao, R.5
Leek, J.T.6
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