-
1
-
-
51349141278
-
A genome screen for quantitative trait loci influencing schizophrenia and neurocognitive phenotypes
-
Almasy L, Gur RC, Haack K, Cole SA, Calkins ME, Peralta JM, Hare E, Prasad K, Pogue-Geile MF, Nimgaonkar V. et al. 2008. A genome screen for quantitative trait loci influencing schizophrenia and neurocognitive phenotypes. Am J Psychiatry 165:1185-1192.
-
(2008)
Am J Psychiatry
, vol.165
, pp. 1185-1192
-
-
Almasy, L.1
Gur, R.C.2
Haack, K.3
Cole, S.A.4
Calkins, M.E.5
Peralta, J.M.6
Hare, E.7
Prasad, K.8
Pogue-Geile, M.F.9
Nimgaonkar, V.10
-
2
-
-
84868121906
-
Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development
-
Anderson GR, Galfin T, Xu W, Aoto J, Malenka RC, Südhof TC. 2012. Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development. Proc Natl Acad Sci 109:18120-18125.
-
(2012)
Proc Natl Acad Sci
, vol.109
, pp. 18120-18125
-
-
Anderson, G.R.1
Galfin, T.2
Xu, W.3
Aoto, J.4
Malenka, R.C.5
Südhof, T.C.6
-
3
-
-
0035704343
-
Genetic structure of spatial and verbal working memory
-
Ando J, Ono Y, Wright MJ. 2001. Genetic structure of spatial and verbal working memory. Behavr Genet 31:615-624.
-
(2001)
Behavr Genet
, vol.31
, pp. 615-624
-
-
Ando, J.1
Ono, Y.2
Wright, M.J.3
-
4
-
-
60349127006
-
Genetic overlap among intelligence and other candidate endophenotypes for schizophrenia
-
Aukes MF, Alizadeh BZ, Sitskoorn MM, Kemner C, Ophoff RA, Kahn RS. 2009. Genetic overlap among intelligence and other candidate endophenotypes for schizophrenia. Biol Psychiatry 65:527-534.
-
(2009)
Biol Psychiatry
, vol.65
, pp. 527-534
-
-
Aukes, M.F.1
Alizadeh, B.Z.2
Sitskoorn, M.M.3
Kemner, C.4
Ophoff, R.A.5
Kahn, R.S.6
-
5
-
-
79960953774
-
Heritability of working memory brain activation
-
Blokland GA, McMahon KL, Thompson PM, Martin NG, de Zubicaray GI, Wright MJ. 2011. Heritability of working memory brain activation. J Neuroscience 31:10882-10890.
-
(2011)
J Neuroscience
, vol.31
, pp. 10882-10890
-
-
Blokland, G.A.1
McMahon, K.L.2
Thompson, P.M.3
Martin, N.G.4
de Zubicaray, G.I.5
Wright, M.J.6
-
6
-
-
84902588653
-
Meta-analysis of Cognitive Deficits in Ultra-high Risk to Psychosis and First-Episode Psychosis: Do the Cognitive Deficits Progress Over, or After, the Onset of Psychosis?
-
Bora E, Murray RM. 2013. Meta-analysis of Cognitive Deficits in Ultra-high Risk to Psychosis and First-Episode Psychosis: Do the Cognitive Deficits Progress Over, or After, the Onset of Psychosis? Schizophr Bull 40:744-755.
-
(2013)
Schizophr Bull
, vol.40
, pp. 744-755
-
-
Bora, E.1
Murray, R.M.2
-
7
-
-
33845870419
-
Deconstructing schizophrenia: An overview of the use of endophenotypes in order to understand a complex disorder
-
Braff DL, Freedman R, Schork NJ, Gottesman II. 2007. Deconstructing schizophrenia: An overview of the use of endophenotypes in order to understand a complex disorder. Schizophr Bull 33:21-32.
-
(2007)
Schizophr Bull
, vol.33
, pp. 21-32
-
-
Braff, D.L.1
Freedman, R.2
Schork, N.J.3
Gottesman, I.I.4
-
8
-
-
84893654179
-
Childhood intelligence is heritable, highly polygenic and associated with FNBP1L
-
Benyamin B, Pourcain B, Davis OS, Davies G, Hansell NK, Brion MJ, Kirkpatrick RM, Cents RA, Franić S, Miller MB, et al. 2014. Childhood intelligence is heritable, highly polygenic and associated with FNBP1L. Molecular Psychiatry 19:253-258.
-
(2014)
Molecular Psychiatry
, vol.19
, pp. 253-258
-
-
Benyamin, B.1
Pourcain, B.2
Davis, O.S.3
Davies, G.4
Hansell, N.K.5
Brion, M.J.6
Kirkpatrick, R.M.7
Cents, R.A.8
Franić, S.9
Miller, M.B.10
-
9
-
-
33744478880
-
Endophenotypes in the genetic analyses of mental disorders
-
Cannon TD, Keller MC. 2006. Endophenotypes in the genetic analyses of mental disorders. Annu Rev Clin Psychol 2:267-290.
-
(2006)
Annu Rev Clin Psychol
, vol.2
, pp. 267-290
-
-
Cannon, T.D.1
Keller, M.C.2
-
10
-
-
84883465830
-
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
-
Cross-Disorder Group of the Psychiatric Genomics Consortium, Lee SH, Ripke S, Neale BM, Faraone SV, Purcell SM. 2013. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet 45:984-994.
-
(2013)
Nat Genet
, vol.45
, pp. 984-994
-
-
Lee, S.H.1
Ripke, S.2
Neale, B.M.3
Faraone, S.V.4
Purcell, S.M.5
-
11
-
-
58249091398
-
A possible association between schizophrenia and GRIK3 polymorphisms in a multicenter sample of Scandinavian origin (SCOPE)
-
Djurovic S, Kähler AK, Kulle B, Jönsson EG, Agartz I, Le Hellard S, Hall H, Jakobsen KD, Hansen T, Melle I. et al. 2009. A possible association between schizophrenia and GRIK3 polymorphisms in a multicenter sample of Scandinavian origin (SCOPE). Schizophr Res 107:242-248.
-
(2009)
Schizophr Res
, vol.107
, pp. 242-248
-
-
Djurovic, S.1
Kähler, A.K.2
Kulle, B.3
Jönsson, E.G.4
Agartz, I.5
Le Hellard, S.6
Hall, H.7
Jakobsen, K.D.8
Hansen, T.9
Melle, I.10
-
12
-
-
77956262527
-
A genome-wide association study of bipolar disorder in Norwegian individuals, followed by replication in Icelandic sample
-
Djurovic S, Gustafsson O, Mattingsdal M, Athanasiu L, Bjella T, Tesli M, Agartz I, Lorentzen S, Melle I, Morken G. et al. 2010. A genome-wide association study of bipolar disorder in Norwegian individuals, followed by replication in Icelandic sample. J Affect Disord 126:312-316.
-
(2010)
J Affect Disord
, vol.126
, pp. 312-316
-
-
Djurovic, S.1
Gustafsson, O.2
Mattingsdal, M.3
Athanasiu, L.4
Bjella, T.5
Tesli, M.6
Agartz, I.7
Lorentzen, S.8
Melle, I.9
Morken, G.10
-
13
-
-
84883313538
-
Neurocognitive phenomics: Examining the genetic basis of cognitive abilities
-
Donohoe G, Deary IJ, Glahn DC, Malhotra AK, Burdick KE. 2013. Neurocognitive phenomics: Examining the genetic basis of cognitive abilities. Psychol Med 43:2027-2036.
-
(2013)
Psychol Med
, vol.43
, pp. 2027-2036
-
-
Donohoe, G.1
Deary, I.J.2
Glahn, D.C.3
Malhotra, A.K.4
Burdick, K.E.5
-
14
-
-
84893725555
-
Arguments for the sake of endophenotypes: Examining common misconceptions about the use of endophenotypes in psychiatric genetics
-
Glahn DC, Knowles EE, McKay DR, Sprooten E, Raventós H, Blangero J, Gottesman II, Almasy L. 2014. Arguments for the sake of endophenotypes: Examining common misconceptions about the use of endophenotypes in psychiatric genetics. Am J Med Genet Part B Neuropsychiatr Genet 165B:122-130.
-
(2014)
Am J Med Genet Part B Neuropsychiatr Genet
, vol.165B
, pp. 122-130
-
-
Glahn, D.C.1
Knowles, E.E.2
McKay, D.R.3
Sprooten, E.4
Raventós, H.5
Blangero, J.6
Gottesman, I.I.7
Almasy, L.8
-
15
-
-
0038823525
-
The endophenotype concept in psychiatry: Etymology and strategic intentions
-
Gottesman II, Gould TD. 2003. The endophenotype concept in psychiatry: Etymology and strategic intentions. Am J Psychiatry 160:636-645.
-
(2003)
Am J Psychiatry
, vol.160
, pp. 636-645
-
-
Gottesman, I.I.1
Gould, T.D.2
-
16
-
-
84878258578
-
Substantial genetic link between IQ and working memory: Implications for molecular genetic studies on schizophrenia. the European twin study of schizophrenia (EUTwinsS)
-
Goldberg X, Alemany S, Rosa A, Picchioni M, Nenadic I, Owens SF, Rijsdijk F, Rebollo I, Sauer H, Murray RM. et al. 2013. Substantial genetic link between IQ and working memory: Implications for molecular genetic studies on schizophrenia. the European twin study of schizophrenia (EUTwinsS). Am J Med Genet B Neuropsychiatr Genetics 162B:413-418.
-
(2013)
Am J Med Genet B Neuropsychiatr Genetics
, vol.162 B
, pp. 413-418
-
-
Goldberg, X.1
Alemany, S.2
Rosa, A.3
Picchioni, M.4
Nenadic, I.5
Owens, S.F.6
Rijsdijk, F.7
Rebollo, I.8
Sauer, H.9
Murray, R.M.10
-
17
-
-
35948991435
-
Initial heritability analyses of endophenotypic measures for schizophrenia: The consortium on the genetics of schizophrenia
-
Greenwood TA, Braff DL, Light GA, Cadenhead KS, Calkins ME, Dobie DJ, Freedman R, Green MF, Gur RE, Gur RC. et al. 2007. Initial heritability analyses of endophenotypic measures for schizophrenia: The consortium on the genetics of schizophrenia. Archives General Psychiatry 64:1242-1250.
-
(2007)
Archives General Psychiatry
, vol.64
, pp. 1242-1250
-
-
Greenwood, T.A.1
Braff, D.L.2
Light, G.A.3
Cadenhead, K.S.4
Calkins, M.E.5
Dobie, D.J.6
Freedman, R.7
Green, M.F.8
Gur, R.E.9
Gur, R.C.10
-
18
-
-
80051953863
-
Analysis of 94 candidate genes and 12 endophenotypes for schizophrenia from the Consortium on the Genetics of Schizophrenia
-
Greenwood TA, Lazzeroni LC, Murray SS, Cadenhead KS, Calkins ME, Dobie DJ, Green MF, Gur RE, Gur RC, Hardiman G. et al. 2011. Analysis of 94 candidate genes and 12 endophenotypes for schizophrenia from the Consortium on the Genetics of Schizophrenia. Am J Psychiatry 168:930-946.
-
(2011)
Am J Psychiatry
, vol.168
, pp. 930-946
-
-
Greenwood, T.A.1
Lazzeroni, L.C.2
Murray, S.S.3
Cadenhead, K.S.4
Calkins, M.E.5
Dobie, D.J.6
Green, M.F.7
Gur, R.E.8
Gur, R.C.9
Hardiman, G.10
-
19
-
-
84879446191
-
Genome-wide linkage analyses of 12 endophenotypes for schizophrenia from the Consortium on the Genetics of Schizophrenia
-
Greenwood TA, Swerdlow NR, Gur RE, Cadenhead KS, Calkins ME, Dobie DJ, Freedman R, Green MF, Gur RC, Lazzeroni LC. et al. 2013. Genome-wide linkage analyses of 12 endophenotypes for schizophrenia from the Consortium on the Genetics of Schizophrenia. Am J Psychiatry 170:521-532.
-
(2013)
Am J Psychiatry
, vol.170
, pp. 521-532
-
-
Greenwood, T.A.1
Swerdlow, N.R.2
Gur, R.E.3
Cadenhead, K.S.4
Calkins, M.E.5
Dobie, D.J.6
Freedman, R.7
Green, M.F.8
Gur, R.C.9
Lazzeroni, L.C.10
-
20
-
-
84898640959
-
Neurocognitive Growth Charting in Psychosis Spectrum Youths
-
Gur RC, Calkins ME, Satterthwaite TD, Ruparel K, Bilker WB, Moore TM, Savitt AP, Hakonarson H, Gur RE. 2014. Neurocognitive Growth Charting in Psychosis Spectrum Youths. JAMA Psychiatry DOI: 10.1001/jamapsychiatry.2013.4190.
-
(2014)
JAMA Psychiatry
-
-
Gur, R.C.1
Calkins, M.E.2
Satterthwaite, T.D.3
Ruparel, K.4
Bilker, W.B.5
Moore, T.M.6
Savitt, A.P.7
Hakonarson, H.8
Gur, R.E.9
-
21
-
-
34249331344
-
Neurocognitive endophenotypes in a multiplex multigenerational family study of schizophrenia
-
Gur RE, Nimgaonkar VL, Almasy L, Calkins ME, Ragland JD, Pogue-Geile MF, Kanes S, Blangero J, Gur RC. 2007. Neurocognitive endophenotypes in a multiplex multigenerational family study of schizophrenia. Am J Psychiatry 164:813-819.
-
(2007)
Am J Psychiatry
, vol.164
, pp. 813-819
-
-
Gur, R.E.1
Nimgaonkar, V.L.2
Almasy, L.3
Calkins, M.E.4
Ragland, J.D.5
Pogue-Geile, M.F.6
Kanes, S.7
Blangero, J.8
Gur, R.C.9
-
22
-
-
84863474958
-
Bipolar disorder ANK3 risk variant effect on sustained attention is replicated in a large healthy population
-
Hatzimanolis A, Smyrnis N, Avramopoulos D, Stefanis CN, Evdokimidis I, Stefanis NC. 2012. Bipolar disorder ANK3 risk variant effect on sustained attention is replicated in a large healthy population. Psychiatr Genet 22:210-213.
-
(2012)
Psychiatr Genet
, vol.22
, pp. 210-213
-
-
Hatzimanolis, A.1
Smyrnis, N.2
Avramopoulos, D.3
Stefanis, C.N.4
Evdokimidis, I.5
Stefanis, N.C.6
-
23
-
-
77958499255
-
The heritability of general cognitive ability increases linearly from childhood to young adulthood
-
Haworth CM, Wright MJ, Luciano M, Martin NG, de Geus EJ, van Beijsterveldt CE, Bartels M, Posthuma D, Boomsma DI, Davis OS. et al. 2010. The heritability of general cognitive ability increases linearly from childhood to young adulthood. Mol Psychiatry 15:1112-1120.
-
(2010)
Mol Psychiatry
, vol.15
, pp. 1112-1120
-
-
Haworth, C.M.1
Wright, M.J.2
Luciano, M.3
Martin, N.G.4
de Geus, E.J.5
van Beijsterveldt, C.E.6
Bartels, M.7
Posthuma, D.8
Boomsma, D.I.9
Davis, O.S.10
-
24
-
-
48949116172
-
Verbal working memory impairments in individuals with schizophrenia and their first- degree relatives: Findings from the Consortium on the Genetics of Schizophrenia
-
Horan WP, Braff DL, Nuechterlein KH, Sugar CA, Cadenhead KS, Calkins ME, Dobie DJ, Freedman R, Greenwood TA, Gur RE. et al. 2008. Verbal working memory impairments in individuals with schizophrenia and their first- degree relatives: Findings from the Consortium on the Genetics of Schizophrenia. Schizophrenia Research 103:218-228.
-
(2008)
Schizophrenia Research
, vol.103
, pp. 218-228
-
-
Horan, W.P.1
Braff, D.L.2
Nuechterlein, K.H.3
Sugar, C.A.4
Cadenhead, K.S.5
Calkins, M.E.6
Dobie, D.J.7
Freedman, R.8
Greenwood, T.A.9
Gur, R.E.10
-
25
-
-
67651222400
-
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies
-
Howie BN, Donnelly P, Marchini J. 2009. A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet 5(6):e1000529.
-
(2009)
PLoS Genet
, vol.5
, Issue.6
, pp. e1000529
-
-
Howie, B.N.1
Donnelly, P.2
Marchini, J.3
-
26
-
-
68449086236
-
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.
-
International Schizophrenia Consortium, Purcell SM, Wray NR, Stone JL, Visscher PM, O'Donovan MC, Sullivan PF, Sklar P. 2009. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 460:748-752.
-
(2009)
Nature
, vol.460
, pp. 748-752
-
-
Purcell, S.M.1
Wray, N.R.2
Stone, J.L.3
Visscher, P.M.4
O'Donovan, M.C.5
Sullivan, P.F.6
Sklar, P.7
-
27
-
-
84885210127
-
Schizophrenia is a cognitive illness: Time for a change in focus
-
Kahn RS, Keefe RS. 2013. Schizophrenia is a cognitive illness: Time for a change in focus. JAMA Psychiatry 70:1107-1112.
-
(2013)
JAMA Psychiatry
, vol.70
, pp. 1107-1112
-
-
Kahn, R.S.1
Keefe, R.S.2
-
28
-
-
84904264255
-
Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission
-
Karayannis T, Au E, Patel JC, Kruglikov I, Markx S, Delorme R, Héron D, Salomon D, Glessner J, Restituito S. et al. 2014. Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission. Nature 511:236-240.
-
(2014)
Nature
, vol.511
, pp. 236-240
-
-
Karayannis, T.1
Au, E.2
Patel, J.C.3
Kruglikov, I.4
Markx, S.5
Delorme, R.6
Héron, D.7
Salomon, D.8
Glessner, J.9
Restituito, S.10
-
29
-
-
84858785307
-
Schizophrenia-related RGS4 gene variations specifically disrupt prefrontal control of saccadic eye movements
-
Kattoulas E, Stefanis NC, Avramopoulos D, Stefanis CN, Evdokimidis I, Smyrnis N. 2012. Schizophrenia-related RGS4 gene variations specifically disrupt prefrontal control of saccadic eye movements. Psychol Med 42:757-767.
-
(2012)
Psychol Med
, vol.42
, pp. 757-767
-
-
Kattoulas, E.1
Stefanis, N.C.2
Avramopoulos, D.3
Stefanis, C.N.4
Evdokimidis, I.5
Smyrnis, N.6
-
30
-
-
84930925715
-
Polygenic Risk for Schizophrenia Associated With Working Memory-related Prefrontal Brain Activation in Patients With Schizophrenia and Healthy Controls
-
Kauppi K, Westlye LT, Tesli M, Bettella F, Brandt CL, Mattingsdal M, Ueland T, Espeseth T, Agartz I, Melle I. et al. 2014. Polygenic Risk for Schizophrenia Associated With Working Memory-related Prefrontal Brain Activation in Patients With Schizophrenia and Healthy Controls. Schizophr Bull 41: 736-743.
-
(2014)
Schizophr Bull
, vol.41
, pp. 736-743
-
-
Kauppi, K.1
Westlye, L.T.2
Tesli, M.3
Bettella, F.4
Brandt, C.L.5
Mattingsdal, M.6
Ueland, T.7
Espeseth, T.8
Agartz, I.9
Melle, I.10
-
31
-
-
84893661023
-
Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: A report from the Cognitive Genomics consorTium (COGENT)
-
Lencz T, Knowles E, Davies G, Guha S, Liewald DC, Starr JM, Djurovic S, Melle I, Sundet K, Christoforou A. et al. 2014. Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: A report from the Cognitive Genomics consorTium (COGENT). Mol Psychiatry 19:168-174.
-
(2014)
Mol Psychiatry
, vol.19
, pp. 168-174
-
-
Lencz, T.1
Knowles, E.2
Davies, G.3
Guha, S.4
Liewald, D.C.5
Starr, J.M.6
Djurovic, S.7
Melle, I.8
Sundet, K.9
Christoforou, A.10
-
32
-
-
84864619695
-
OATS Research Team. 2012. Genetic influences on four measures of executive functions and their covariation with general cognitive ability: The Older Australian Twins Study
-
Lee T, Mosing MA, Henry JD, Trollor JN, Ames D, Martin NG, Wright MJ, Sachdev PS. OATS Research Team. 2012. Genetic influences on four measures of executive functions and their covariation with general cognitive ability: The Older Australian Twins Study. Behav Genet 42:528-538.
-
Behav Genet
, vol.42
, pp. 528-538
-
-
Lee, T.1
Mosing, M.A.2
Henry, J.D.3
Trollor, J.N.4
Ames, D.5
Martin, N.G.6
Wright, M.J.7
Sachdev, P.S.8
-
33
-
-
77953808087
-
Genotype imputation for genome-wide association studies
-
Marchini J, Howie B. 2010. Genotype imputation for genome-wide association studies. Nat Rev Genet 11:499-511.
-
(2010)
Nat Rev Genet
, vol.11
, pp. 499-511
-
-
Marchini, J.1
Howie, B.2
-
34
-
-
84876936728
-
Polygenic risk for schizophrenia is associated with cognitive change between childhood and old age
-
McIntosh AM, Gow A, Luciano M, Davies G, Liewald DC, Harris SE, Corley J, Hall J, Starr JM, Porteous DJ. et al. 2013. Polygenic risk for schizophrenia is associated with cognitive change between childhood and old age. Biol Psychiatry 73:938-943.
-
(2013)
Biol Psychiatry
, vol.73
, pp. 938-943
-
-
McIntosh, A.M.1
Gow, A.2
Luciano, M.3
Davies, G.4
Liewald, D.C.5
Harris, S.E.6
Corley, J.7
Hall, J.8
Starr, J.M.9
Porteous, D.J.10
-
35
-
-
84891722130
-
Neuropsychological decline in schizophrenia from the premorbid to the postonset period: Evidence from a population-representative longitudinal study
-
Meier MH, Caspi A, Reichenberg A, Keefe RS, Fisher HL, Harrington H, Houts R, Poulton R, Moffitt TE. 2014. Neuropsychological decline in schizophrenia from the premorbid to the postonset period: Evidence from a population-representative longitudinal study. Am J Psychiatry 171:91-101.
-
(2014)
Am J Psychiatry
, vol.171
, pp. 91-101
-
-
Meier, M.H.1
Caspi, A.2
Reichenberg, A.3
Keefe, R.S.4
Fisher, H.L.5
Harrington, H.6
Houts, R.7
Poulton, R.8
Moffitt, T.E.9
-
36
-
-
77956180603
-
Case-control genome-wide association study of attention-deficit/hyperactivity disorder
-
Neale BM, Medland S, Ripke S, Anney RJ, Asherson P, Buitelaar J, Franke B, Gill M, Kent L, Holmans P. et al. 2010. Case-control genome-wide association study of attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry 49:06-20.
-
(2010)
J Am Acad Child Adolesc Psychiatry
, vol.49
, pp. 06-20
-
-
Neale, B.M.1
Medland, S.2
Ripke, S.3
Anney, R.J.4
Asherson, P.5
Buitelaar, J.6
Franke, B.7
Gill, M.8
Kent, L.9
Holmans, P.10
-
37
-
-
77951439152
-
Trait-associated SNPs are more likely to be eQTLs: Annotation to enhance discovery from GWAS
-
Nicolae DL, Gamazon E, Zhang W, Duan S, Dolan ME, Cox NJ. 2010. Trait-associated SNPs are more likely to be eQTLs: Annotation to enhance discovery from GWAS. PLoS Genet 6(4):e1000888.
-
(2010)
PLoS Genet
, vol.6
, Issue.4
, pp. e1000888
-
-
Nicolae, D.L.1
Gamazon, E.2
Zhang, W.3
Duan, S.4
Dolan, M.E.5
Cox, N.J.6
-
38
-
-
79952315009
-
Genetic overlap between episodic memory deficits and schizophrenia: Results from the Maudsley Twin Study
-
Owens SF, Picchioni MM, Rijsdijk FV, Stahl D, Vassos E, Rodger AK, Collier DA, Murray RM, Toulopoulou T. 2011. Genetic overlap between episodic memory deficits and schizophrenia: Results from the Maudsley Twin Study. Psychol Med 41:521-532.
-
(2011)
Psychol Med
, vol.41
, pp. 521-532
-
-
Owens, S.F.1
Picchioni, M.M.2
Rijsdijk, F.V.3
Stahl, D.4
Vassos, E.5
Rodger, A.K.6
Collier, D.A.7
Murray, R.M.8
Toulopoulou, T.9
-
39
-
-
77955694150
-
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia
-
Pagnamenta AT, Bacchelli E, de Jonge MV, Mirza G, Scerri TS, Minopoli F, Chiocchetti A, Ludwig KU, Hoffmann P, Paracchini S. et al. 2010. Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. Biol Psychiatry 15:320-328.
-
(2010)
Biol Psychiatry
, vol.15
, pp. 320-328
-
-
Pagnamenta, A.T.1
Bacchelli, E.2
de Jonge, M.V.3
Mirza, G.4
Scerri, T.S.5
Minopoli, F.6
Chiocchetti, A.7
Ludwig, K.U.8
Hoffmann, P.9
Paracchini, S.10
-
40
-
-
84873060948
-
A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene
-
Papassotiropoulos A, Stefanova E, Vogler C, Gschwind L, Ackermann S, Spalek K, Rasch B, Heck A, Aerni A, Hanser E. et al. 2013. A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene. Mol Psychiatry 18:255-263.
-
(2013)
Mol Psychiatry
, vol.18
, pp. 255-263
-
-
Papassotiropoulos, A.1
Stefanova, E.2
Vogler, C.3
Gschwind, L.4
Ackermann, S.5
Spalek, K.6
Rasch, B.7
Heck, A.8
Aerni, A.9
Hanser, E.10
-
41
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D. 2006. Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 38:904-909.
-
(2006)
Nat Genet
, vol.38
, pp. 904-909
-
-
Price, A.L.1
Patterson, N.J.2
Plenge, R.M.3
Weinblatt, M.E.4
Shadick, N.A.5
Reich, D.6
-
42
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ. et al. 2010. PLINK: A tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81:559-575.
-
(2010)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.5
Bender, D.6
Maller, J.7
Sklar, P.8
de Bakker, P.I.9
Daly, M.J.10
-
44
-
-
84926180596
-
The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort
-
Robinson EB, Kirby A, Ruparel K, Yang J, McGrath L, Anttila V, Neale BM, Merikangas K, Lehner T, Sleiman PM. et al. 2014. The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort. Mol Psychiatry DOI: 10.1038/mp.2014.65.
-
(2014)
Mol Psychiatry
-
-
Robinson, E.B.1
Kirby, A.2
Ruparel, K.3
Yang, J.4
McGrath, L.5
Anttila, V.6
Neale, B.M.7
Merikangas, K.8
Lehner, T.9
Sleiman, P.M.10
-
45
-
-
79959249145
-
The CACNA1C and ANK3 risk alleles impact on affective personality traits and startle reactivity but not on cognition or gating in healthy males
-
Roussos P, Giakoumaki SG, Georgakopoulos A, Robakis NK, Bitsios P. 2011. The CACNA1C and ANK3 risk alleles impact on affective personality traits and startle reactivity but not on cognition or gating in healthy males. Bipolar Disord 13:250-259.
-
(2011)
Bipolar Disord
, vol.13
, pp. 250-259
-
-
Roussos, P.1
Giakoumaki, S.G.2
Georgakopoulos, A.3
Robakis, N.K.4
Bitsios, P.5
-
46
-
-
84904804929
-
Biological Insights from 108 Schizophrenia-associated genetic loci
-
Schizophrenia Working Group of the Psychiatric Genomics Consortium
-
Schizophrenia Working Group of the Psychiatric Genomics Consortium Ripke S, Neale BM, Corvin A, Walters JT, Farh KH, Holmans PA, Lee P, Bulik- Sullivan B, Collier DA, Huang H. et al. 2014. Biological Insights from 108 Schizophrenia-associated genetic loci. Nature 511:421-427.
-
(2014)
Nature
, vol.511
, pp. 421-427
-
-
Ripke, S.1
Neale, B.M.2
Corvin, A.3
Walters, J.T.4
Farh, K.H.5
Holmans, P.A.6
Lee, P.7
Bulik-Sullivan, B.8
Collier, D.A.9
Huang, H.10
-
47
-
-
2542479951
-
Active eye fixation performance in 940 young men: Effects of IQ, schizotypy, anxiety and depression
-
Smyrnis N, Kattoulas E, Evdokimidis I, Stefanis NC, Avramopoulos D, Pantes G, Theleritis C, Stefanis CN. 2004. Active eye fixation performance in 940 young men: Effects of IQ, schizotypy, anxiety and depression. Exp Brain Res 156:1-10.
-
(2004)
Exp Brain Res
, vol.156
, pp. 1-10
-
-
Smyrnis, N.1
Kattoulas, E.2
Evdokimidis, I.3
Stefanis, N.C.4
Avramopoulos, D.5
Pantes, G.6
Theleritis, C.7
Stefanis, C.N.8
-
48
-
-
67349220748
-
Larger variability of saccadic reaction times in schizophrenia patients
-
Smyrnis N, Karantinos T, Malogiannis I, Theleritis C, Mantas A, Stefanis NC, Hatzimanolis J, Evdokimidis I, . 2009. Larger variability of saccadic reaction times in schizophrenia patients. Psychiatr Res 168:129-136.
-
(2009)
Psychiatr Res
, vol.168
, pp. 129-136
-
-
Smyrnis, N.1
Karantinos, T.2
Malogiannis, I.3
Theleritis, C.4
Mantas, A.5
Stefanis, N.C.6
Hatzimanolis, J.7
Evdokimidis, I.8
-
49
-
-
33947158684
-
Effect of schizotypy on cognitive performance and its tuning by COMT val158 met genotype variations in a large population of young men
-
Smyrnis N, Avramopoulos D, Evdokimidis I, Stefanis CN, Tsekou H, Stefanis NC. 2007. Effect of schizotypy on cognitive performance and its tuning by COMT val158 met genotype variations in a large population of young men. Biol Psychiatry 61:845-853.
-
(2007)
Biol Psychiatry
, vol.61
, pp. 845-853
-
-
Smyrnis, N.1
Avramopoulos, D.2
Evdokimidis, I.3
Stefanis, C.N.4
Tsekou, H.5
Stefanis, N.C.6
-
50
-
-
79959769831
-
Schizophrenia-related neuregulin-1 single-nucleotide polymorphisms lead to deficient smooth eye pursuit in a large sample of young men
-
Smyrnis N, Kattoulas E, Stefanis NC, Avramopoulos D, Stefanis CN, Evdokimidis I, . 2011. Schizophrenia-related neuregulin-1 single-nucleotide polymorphisms lead to deficient smooth eye pursuit in a large sample of young men. Schizophr Bull 37:822-831.
-
(2011)
Schizophr Bull
, vol.37
, pp. 822-831
-
-
Smyrnis, N.1
Kattoulas, E.2
Stefanis, N.C.3
Avramopoulos, D.4
Stefanis, C.N.5
Evdokimidis, I.6
-
51
-
-
34548499070
-
Impact of schizophrenia candidate genes on schizotypy and cognitive endophenotypes at the population level
-
Stefanis NC, Trikalinos TA, Avramopoulos D, Smyrnis N, Evdokimidis I, Ntzani EE, Ioannidis JP, Stefanis CN. 2007. Impact of schizophrenia candidate genes on schizotypy and cognitive endophenotypes at the population level. Biol Psychiatry 62:784-792.
-
(2007)
Biol Psychiatry
, vol.62
, pp. 784-792
-
-
Stefanis, N.C.1
Trikalinos, T.A.2
Avramopoulos, D.3
Smyrnis, N.4
Evdokimidis, I.5
Ntzani, E.E.6
Ioannidis, J.P.7
Stefanis, C.N.8
-
52
-
-
84892838679
-
1p34.3 deletion involving GRIK3: Further clinical implication of GRIK family glutamate receptors in the pathogenesis of developmental delay
-
Takenouchi T, Hashida N, Torii C, Kosaki R, Takahashi T, Kosaki K. 2014. 1p34.3 deletion involving GRIK3: Further clinical implication of GRIK family glutamate receptors in the pathogenesis of developmental delay. Am J Med Genet B Neuropsychiatr Genet 164:456-460.
-
(2014)
Am J Med Genet B Neuropsychiatr Genet
, vol.164
, pp. 456-460
-
-
Takenouchi, T.1
Hashida, N.2
Torii, C.3
Kosaki, R.4
Takahashi, T.5
Kosaki, K.6
-
53
-
-
84895733925
-
Bipolar and schizophrenia network for intermediate phenotypes: outcomes across the psychosis continuum
-
Tamminga CA, Pearlson G, Keshavan M, Sweeney J, Clementz B, Thaker G. 2014. Bipolar and schizophrenia network for intermediate phenotypes: outcomes across the psychosis continuum. Schizophr Bull 2:S131-S137.
-
(2014)
Schizophr Bull
, vol.2
, pp. S131-S137
-
-
Tamminga, C.A.1
Pearlson, G.2
Keshavan, M.3
Sweeney, J.4
Clementz, B.5
Thaker, G.6
-
54
-
-
84874542049
-
Genetic schizophrenia risk variants jointly modulate total brain and white matter volume
-
Terwisscha van Scheltinga AF, Bakker SC, van Haren NE, Derks EM, Buizer- Voskamp JE, Boos HB, Cahn W, Hulshoff Pol HE, Ripke S, Ophoff RA, Kahn RS. et al. 2013. Genetic schizophrenia risk variants jointly modulate total brain and white matter volume. Biol Psychiatry 73:525-531.
-
(2013)
Biol Psychiatry
, vol.73
, pp. 525-531
-
-
Terwisscha van Scheltinga, A.F.1
Bakker, S.C.2
van Haren, N.E.3
Derks, E.M.4
Buizer-Voskamp, J.E.5
Boos, H.B.6
Cahn, W.7
Hulshoff Pol, H.E.8
Ripke, S.9
Ophoff, R.A.10
Kahn, R.S.11
-
55
-
-
84897669665
-
Variability in the decision process leading to saccades: A specific marker for schizophrenia?
-
Theleritis C, Evdokimidis I, Smyrnis N. 2014. Variability in the decision process leading to saccades: A specific marker for schizophrenia? Psychophysiology 51:327-336.
-
(2014)
Psychophysiology
, vol.51
, pp. 327-336
-
-
Theleritis, C.1
Evdokimidis, I.2
Smyrnis, N.3
-
56
-
-
36849056624
-
Substantial genetic overlap between neurocognition and schizophrenia: Genetic modeling in twin samples
-
Toulopoulou T, Picchioni M, Rijsdijk F, Hua-Hall M, Ettinger U, Sham P, Murray R. 2007. Substantial genetic overlap between neurocognition and schizophrenia: Genetic modeling in twin samples. Arch Gen Psychiatry 64:1348-1355.
-
(2007)
Arch Gen Psychiatry
, vol.64
, pp. 1348-1355
-
-
Toulopoulou, T.1
Picchioni, M.2
Rijsdijk, F.3
Hua-Hall, M.4
Ettinger, U.5
Sham, P.6
Murray, R.7
-
57
-
-
77956355318
-
Impaired intellect and memory: A missing link between genetic risk and schizophrenia?
-
Toulopoulou T, Goldberg TE, Mesa IR, Picchioni M, Rijsdijk F, Stahl D, Cherny SS, Sham P, Faraone SV, Tsuang M. et al. 2010. Impaired intellect and memory: A missing link between genetic risk and schizophrenia? Arch Gen Psychiatry 67:905-913.
-
(2010)
Arch Gen Psychiatry
, vol.67
, pp. 905-913
-
-
Toulopoulou, T.1
Goldberg, T.E.2
Mesa, I.R.3
Picchioni, M.4
Rijsdijk, F.5
Stahl, D.6
Cherny, S.S.7
Sham, P.8
Faraone, S.V.9
Tsuang, M.10
-
58
-
-
84894540542
-
DNA evidence for strong genetic stability and increasing heritability of intelligence from age 7 to 12
-
Trzaskowski M, Yang J, Visscher PM, Plomin R. 2014. DNA evidence for strong genetic stability and increasing heritability of intelligence from age 7 to 12. Mol Psychiatry 19:380-384.
-
(2014)
Mol Psychiatry
, vol.19
, pp. 380-384
-
-
Trzaskowski, M.1
Yang, J.2
Visscher, P.M.3
Plomin, R.4
-
59
-
-
84925958019
-
Heritability and molecular genetic basis of antisaccade eye tracking error rate: A genome-wide association study
-
Vaidyanathan U, Malone SM, Donnelly JM, Hammer MA, Miller MB, McGue M, Iacono WG. 2014. Heritability and molecular genetic basis of antisaccade eye tracking error rate: A genome-wide association study. Psychophysiology 51:1272-1284.
-
(2014)
Psychophysiology
, vol.51
, pp. 1272-1284
-
-
Vaidyanathan, U.1
Malone, S.M.2
Donnelly, J.M.3
Hammer, M.A.4
Miller, M.B.5
McGue, M.6
Iacono, W.G.7
-
60
-
-
84901380413
-
Statistical power to detect genetic (co) variance of complex traits using SNP data in unrelated samples
-
Visscher PM, Hemani G, Vinkhuyzen AA, Chen GB, Lee SH, Wray NR, Goddard ME, Yang J. 2014. Statistical power to detect genetic (co) variance of complex traits using SNP data in unrelated samples. PLoS Genet 10(4):e1004269.
-
(2014)
PLoS Genet
, vol.10
, Issue.4
, pp. e1004269
-
-
Visscher, P.M.1
Hemani, G.2
Vinkhuyzen, A.A.3
Chen, G.B.4
Lee, S.H.5
Wray, N.R.6
Goddard, M.E.7
Yang, J.8
-
61
-
-
84927800658
-
Substantial SNP-based heritability estimates for working memory performance
-
Vogler C, Gschwind L, Coynel D, Freytag V, Milnik A, Egli T, Heck A, de Quervain DJ, Papassotiropoulos A. 2014. Substantial SNP-based heritability estimates for working memory performance. Transl Psychiatry 4:e438. DOI: 10.1038/tp.2014.81.
-
(2014)
Transl Psychiatry
, vol.4
, pp. e438
-
-
Vogler, C.1
Gschwind, L.2
Coynel, D.3
Freytag, V.4
Milnik, A.5
Egli, T.6
Heck, A.7
de Quervain, D.J.8
Papassotiropoulos, A.9
-
62
-
-
84883312273
-
The role of the major histocompatibility complex region in cognition and brain structure: A schizophrenia GWAS follow- up
-
Walters JT, Rujescu D, Franke B, Giegling I, Vásquez AA, Hargreaves A, Russo G, Morris DW, Hoogman M, Da Costa A, et al. 2013. The role of the major histocompatibility complex region in cognition and brain structure: A schizophrenia GWAS follow- up. Am J Psychiatry 170:877-885.
-
(2013)
Am J Psychiatry
, vol.170
, pp. 877-885
-
-
Walters, J.T.1
Rujescu, D.2
Franke, B.3
Giegling, I.4
Vásquez, A.A.5
Hargreaves, A.6
Russo, G.7
Morris, D.W.8
Hoogman, M.9
Da Costa, A.10
|