-
1
-
-
77956230065
-
Cortical thickness or grey matter volume? the importance of selecting the phenotype for imaging genetics studies
-
Winkler AM, Kochunov P, Blangero J, Almasy L, Zilles K, Fox PT et al. Cortical thickness or grey matter volume? The importance of selecting the phenotype for imaging genetics studies. NeuroImage 2010; 53: 1135-1146.
-
(2010)
NeuroImage
, vol.53
, pp. 1135-1146
-
-
Winkler, A.M.1
Kochunov, P.2
Blangero, J.3
Almasy, L.4
Zilles, K.5
Fox, P.T.6
-
2
-
-
84860351742
-
Identification of common variants associated with human hippocampal and intracranial volumes
-
Stein JL, Medland SE, Vasquez AA, Hibar DP, Senstad RE, Winkler AM et al. Identification of common variants associated with human hippocampal and intracranial volumes. Nat Genet 2012; 44: 552-561.
-
(2012)
Nat Genet
, vol.44
, pp. 552-561
-
-
Stein, J.L.1
Medland, S.E.2
Vasquez, A.A.3
Hibar, D.P.4
Senstad, R.E.5
Winkler, A.M.6
-
3
-
-
84871398141
-
Genetic and environmental influences on neuroimaging phenotypes: A meta-analytical perspective on twin imaging studies
-
Blokland GAM, de Zubicaray GI, McMahon KL, Wright MJ. Genetic and Environmental Influences on Neuroimaging Phenotypes: A Meta-Analytical Perspective on Twin Imaging Studies. Twin Res Hum Genet 2012; 15: 351-371.
-
(2012)
Twin Res Hum Genet
, vol.15
, pp. 351-371
-
-
Blokland, G.A.M.1
De Zubicaray, G.I.2
McMahon, K.L.3
Wright, M.J.4
-
4
-
-
77953715731
-
Genetic influences on brain asymmetry: A DTI study of 374 twins and siblings
-
Jahanshad N, Lee AD, Barysheva M, McMahon KL, de Zubicaray GI, Martin NG et al. Genetic influences on brain asymmetry: a DTI study of 374 twins and siblings. NeuroImage 2010; 52: 455-469.
-
(2010)
NeuroImage
, vol.52
, pp. 455-469
-
-
Jahanshad, N.1
Lee, A.D.2
Barysheva, M.3
McMahon, K.L.4
De Zubicaray, G.I.5
Martin, N.G.6
-
6
-
-
33744901419
-
Brain volume in first-episode schizophrenia: Systematic review and meta-analysis of magnetic resonance imaging studies
-
Steen RG, Mull C, Mcclure R, Hamer RM, Jeffrey A, Steen ANT et al. Brain volume in first-episode schizophrenia: Systematic review and meta-analysis of magnetic resonance imaging studies. Br J Psychiatry 2012, 188: 510-518.
-
(2012)
Br J Psychiatry
, vol.188
, pp. 510-518
-
-
Steen, R.G.1
Mull, C.2
McClure, R.3
Hamer, R.M.4
Jeffrey, A.5
Steen, A.N.T.6
-
7
-
-
84860326795
-
Common variants at 12q14 and 12q24 are associated with hippocampal volume
-
Bis JC, DeCarli C, Smith AV, van der Lijn F, Crivello F, Fornage M et al. Common variants at 12q14 and 12q24 are associated with hippocampal volume. Nat Genet 2012; 44: 545-551.
-
(2012)
Nat Genet
, vol.44
, pp. 545-551
-
-
Bis, J.C.1
DeCarli, C.2
Smith, A.V.3
Van Der Lijn, F.4
Crivello, F.5
Fornage, M.6
-
8
-
-
84860342407
-
Common variants at 6q22 and 17q21 are associated with intracranial volume
-
Ikram MA, Fornage M, Smith AV, Seshadri S, Schmidt R, Debette S et al. Common variants at 6q22 and 17q21 are associated with intracranial volume. Nat Genet 2012; 44: 539-544.
-
(2012)
Nat Genet
, vol.44
, pp. 539-544
-
-
Ikram, M.A.1
Fornage, M.2
Smith, A.V.3
Seshadri, S.4
Schmidt, R.5
Debette, S.6
-
9
-
-
77954140531
-
Common SNPs explain a large proportion of the heritability for human height
-
Yang J, Benyamin B, McEvoy BP, Gordon S, Henders AK, Nyholt DR et al. Common SNPs explain a large proportion of the heritability for human height. Nat Genet 2010; 42: 565-569.
-
(2010)
Nat Genet
, vol.42
, pp. 565-569
-
-
Yang, J.1
Benyamin, B.2
McEvoy, B.P.3
Gordon, S.4
Henders, A.K.5
Nyholt, D.R.6
-
10
-
-
79957588287
-
Genome partitioning of genetic variation for complex traits using common SNPs
-
Yang J, Manolio TA, Pasquale LR, Boerwinkle E, Caporaso N, Cunningham JM et al. Genome partitioning of genetic variation for complex traits using common SNPs. Nat Genet 2011; 43: 519-525.
-
(2011)
Nat Genet
, vol.43
, pp. 519-525
-
-
Yang, J.1
Manolio, T.A.2
Pasquale, L.R.3
Boerwinkle, E.4
Caporaso, N.5
Cunningham, J.M.6
-
11
-
-
78649336132
-
The IMAGEN study: Reinforcement-related behaviour in normal brain function and psychopathology
-
Schumann G, Loth E, Banaschewski T, Barbot A, Barker G, Büchel C et al. The IMAGEN study: reinforcement-related behaviour in normal brain function and psychopathology. Mol Psychiatry 2010; 15: 1128-1139.
-
(2010)
Mol Psychiatry
, vol.15
, pp. 1128-1139
-
-
Schumann, G.1
Loth, E.2
Banaschewski, T.3
Barbot, A.4
Barker, G.5
Büchel, C.6
-
12
-
-
0036425968
-
Improved optimization for the robust and accurate linear registration and motion correction of brain images
-
Jenkinson M, Bannister P, Brady M, Smith S. Improved optimization for the robust and accurate linear registration and motion correction of brain images. Neuro-Image 2002; 17: 825-841.
-
(2002)
Neuro-Image
, vol.17
, pp. 825-841
-
-
Jenkinson, M.1
Bannister, P.2
Brady, M.3
Smith, S.4
-
13
-
-
7044260964
-
Advances in functional and structural MR image analysis and implementation as FSL
-
Smith SM, Jenkinson M, Woolrich MW, Beckmann CF, Behrens TEJ, Johansen-Berg H et al. Advances in functional and structural MR image analysis and implementation as FSL. NeuroImage 2004; 23(Suppl 1): S208-S219.
-
(2004)
NeuroImage
, vol.23
, pp. S208-S219
-
-
Smith, S.M.1
Jenkinson, M.2
Woolrich, M.W.3
Beckmann, C.F.4
Behrens, T.E.J.5
Johansen Berg, H.6
-
14
-
-
5644271407
-
A unified approach for morphometric and functional data analysis in young, old, and demented adults using automated atlas-based head size normalization: Reliability and validation against manual measurement of total intracranial volume
-
Buckner RL, Head D, Parker J, Fotenos AF, Marcus D, Morris JC et al. A unified approach for morphometric and functional data analysis in young, old, and demented adults using automated atlas-based head size normalization: reliability and validation against manual measurement of total intracranial volume. NeuroImage 2004; 23: 724-738.
-
(2004)
NeuroImage
, vol.23
, pp. 724-738
-
-
Buckner, R.L.1
Head, D.2
Parker, J.3
Fotenos, A.F.4
Marcus, D.5
Morris, J.C.6
-
15
-
-
0030175198
-
AFNI: Software for analysis and visualization of functional magnetic resonance neuroimages
-
Cox RW. AFNI: software for analysis and visualization of functional magnetic resonance neuroimages. Comput Biomed Res 1996; 29: 162-173.
-
(1996)
Comput Biomed Res
, vol.29
, pp. 162-173
-
-
Cox, R.W.1
-
16
-
-
0034745001
-
Segmentation of brain MR images through a hidden Markov random field model and the expectation-maximization algorithm
-
Zhang Y, Brady M, Smith S. Segmentation of brain MR images through a hidden Markov random field model and the expectation-maximization algorithm. IEEE Trans Med Imaging 2001; 20: 45-57.
-
(2001)
IEEE Trans Med Imaging
, vol.20
, pp. 45-57
-
-
Zhang, Y.1
Brady, M.2
Smith, S.3
-
17
-
-
79955484518
-
A Bayesian model of shape and appearance for subcortical brain segmentation
-
Patenaude B, Smith SM, Kennedy DN, Jenkinson M. A Bayesian model of shape and appearance for subcortical brain segmentation. NeuroImage 2011; 56: 907-922.
-
(2011)
NeuroImage
, vol.56
, pp. 907-922
-
-
Patenaude, B.1
Smith, S.M.2
Kennedy, D.N.3
Jenkinson, M.4
-
18
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MAR, Bender D et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 2007; 81: 559-575.
-
(2007)
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.R.5
Bender, D.6
-
19
-
-
84867284056
-
Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood
-
Lee SH, Yang J, Goddard ME, Visscher PM, Wray NR. Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood. Bioinforma Oxf Engl 2012; 28: 2540-2542.
-
(2012)
Bioinforma Oxf Engl
, vol.28
, pp. 2540-2542
-
-
Lee, S.H.1
Yang, J.2
Goddard, M.E.3
Visscher, P.M.4
Wray, N.R.5
-
21
-
-
69749099417
-
Fast model-based estimation of ancestry in unrelated individuals
-
Alexander DH, Novembre J, Lange K. Fast model-based estimation of ancestry in unrelated individuals. Genome Res 2009; 19: 1655-1664.
-
(2009)
Genome Res
, vol.19
, pp. 1655-1664
-
-
Alexander, D.H.1
Novembre, J.2
Lange, K.3
-
22
-
-
79959503826
-
-
International HapMap Consortium The International HapMap Project
-
International HapMap Consortium. The International HapMap Project. Nature 2003; 426: 789-796.
-
(2003)
Nature
, vol.426
, pp. 789-796
-
-
-
23
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D. Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 2006; 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
-
24
-
-
38949212271
-
Analysis and application of European genetic substructure using 300K SNP information
-
Tian C, Plenge RM, Ransom M, Lee A, Villoslada P, Selmi C et al. Analysis and application of European genetic substructure using 300K SNP information. PLoS Genet 2008; 4: e4-e4.
-
(2008)
PLoS Genet
, vol.4
, pp. e4-e4
-
-
Tian, C.1
Plenge, R.M.2
Ransom, M.3
Lee, A.4
Villoslada, P.5
Selmi, C.6
-
25
-
-
84901380413
-
Statistical Power to Detect Genetic (Co)Variance of Complex Traits Using SNP Data in Unrelated Samples
-
Visscher PM, Hemani G, Vinkhuyzen AAE, Chen G-B, Lee SH, Wray NR et al. Statistical Power to Detect Genetic (Co)Variance of Complex Traits Using SNP Data in Unrelated Samples. PLoS Genet 2014; 10: e1004269.
-
(2014)
PLoS Genet
, vol.10
, pp. e1004269
-
-
Visscher, P.M.1
Hemani, G.2
Vinkhuyzen, A.A.E.3
Chen, G.-B.4
Lee, S.H.5
Wray, N.R.6
-
26
-
-
80053132878
-
Genome-wide association studies establish that human intelligence is highly heritable and polygenic
-
Davies G, Tenesa A, Payton A, Yang J, Harris SE, Liewald D et al. Genome-wide association studies establish that human intelligence is highly heritable and polygenic. Mol Psychiatry 2011; 16: 996-1005.
-
(2011)
Mol Psychiatry
, vol.16
, pp. 996-1005
-
-
Davies, G.1
Tenesa, A.2
Payton, A.3
Yang, J.4
Harris, S.E.5
Liewald, D.6
-
27
-
-
78049450213
-
Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function
-
Raychaudhuri S, Korn J, McCarroll S. ,Altshuler D, Sklar P. Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. PLoS Genet 2010; 6: e1001097.
-
(2010)
PLoS Genet
, vol.6
, pp. e1001097
-
-
Raychaudhuri, S.1
Korn, J.2
McCarroll, S.3
Altshuler, D.4
Sklar, P.5
-
28
-
-
84862777863
-
Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs
-
Lee SH, DeCandia TR, Ripke S, Yang J, Sullivan PF, Goddard ME et al. Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. Nat Genet 2012; 44: 247-250.
-
(2012)
Nat Genet
, vol.44
, pp. 247-250
-
-
Lee, S.H.1
DeCandia, T.R.2
Ripke, S.3
Yang, J.4
Sullivan, P.F.5
Goddard, M.E.6
-
29
-
-
70749085568
-
Genetic and environmental influences on the size of specific brain regions in midlife: The VETSA MRI study
-
Kremen WS, Prom-Wormley E, Panizzon MS, Eyler LT, Fischl B, Neale MC et al. Genetic and environmental influences on the size of specific brain regions in midlife: the VETSA MRI study. NeuroImage 2010; 49: 1213-1223.
-
(2010)
NeuroImage
, vol.49
, pp. 1213-1223
-
-
Kremen, W.S.1
Prom-Wormley, E.2
Panizzon, M.S.3
Eyler, L.T.4
Fischl, B.5
Neale, M.C.6
-
30
-
-
79952624304
-
Genetic and environmental influences on structural variability of the brain in pediatric twin: Deformation based morphometry
-
Yoon U, Perusse D, Lee J-M, Evans AC. Genetic and environmental influences on structural variability of the brain in pediatric twin: deformation based morphometry. Neurosci Lett 2011; 493: 8-13.
-
(2011)
Neurosci Lett
, vol.493
, pp. 8-13
-
-
Yoon, U.1
Perusse, D.2
Lee, J.-M.3
Evans, A.C.4
-
31
-
-
84880965027
-
Heritability of subcortical brain measures: A perspective for future genome-wide association studies
-
Den Braber A, Bohlken MM, Brouwer RM, van 't Ent D, Kanai R, Kahn RS et al. Heritability of subcortical brain measures: a perspective for future genome-wide association studies. Neuro Image 2013; 83: 98-102.
-
(2013)
Neuro Image
, vol.83
, pp. 98-102
-
-
Den Braber, A.1
Bohlken, M.M.2
Brouwer, R.M.3
Van 'T Ent, D.4
Kanai, R.5
Kahn, R.S.6
-
32
-
-
84893904007
-
A polygenic burden of rare disruptive mutations in schizophrenia
-
Purcell SM, Moran JL, Fromer M, Ruderfer D, Solovieff N, Roussos P et al. A polygenic burden of rare disruptive mutations in schizophrenia. Nature 2014; 506: 185-190.
-
(2014)
Nature
, vol.506
, pp. 185-190
-
-
Purcell, S.M.1
Moran, J.L.2
Fromer, M.3
Ruderfer, D.4
Solovieff, N.5
Roussos, P.6
-
33
-
-
84897058188
-
Explaining additional genetic variation in complex traits
-
Robinson MR, Wray NR, Visscher PM. Explaining additional genetic variation in complex traits. Trends Genet 2014; 30: 124-132.
-
(2014)
Trends Genet
, vol.30
, pp. 124-132
-
-
Robinson, M.R.1
Wray, N.R.2
Visscher, P.M.3
-
35
-
-
54049144653
-
Copy-number variations associated with neuropsychiatric conditions
-
Cook EH Jr, Scherer SW. Copy-number variations associated with neuropsychiatric conditions. Nature 2008; 455: 919-923.
-
(2008)
Nature
, vol.455
, pp. 919-923
-
-
Cook, Jr.E.H.1
Scherer, S.W.2
-
36
-
-
84883465830
-
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
-
Cross-Disorder Group of the Psychiatric Genomics Consortium.
-
Cross-Disorder Group of the Psychiatric Genomics Consortium. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet 2013; 45: 984-994.
-
(2013)
Nat Genet
, vol.45
, pp. 984-994
-
-
-
37
-
-
84873031286
-
Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis
-
Lee SH, Harold D, Nyholt DR, Goddard ME, Zondervan KT, Williams J et al. Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis. Hum Mol Genet 2013; 22: 832-841.
-
(2013)
Hum Mol Genet
, vol.22
, pp. 832-841
-
-
Lee, S.H.1
Harold, D.2
Nyholt, D.R.3
Goddard, M.E.4
Zondervan, K.T.5
Williams, J.6
-
38
-
-
84871298155
-
Common genetic variants, acting additively, are a major source of risk for autism
-
Klei L, Sanders SJ, Murtha MT, Hus V, Lowe JK, Willsey AJ et al. Common genetic variants, acting additively, are a major source of risk for autism. Mol Autism 2012; 3: 9.
-
(2012)
Mol Autism
, vol.3
, pp. 9
-
-
Klei, L.1
Sanders, S.J.2
Murtha, M.T.3
Hus, V.4
Lowe, J.K.5
Willsey, A.J.6
-
39
-
-
77954133026
-
Estimation of effect size distribution from genome-wide association studies and implications for future discoveries
-
Park J-H, Wacholder S, Gail MH, Peters U, Jacobs KB, Chanock SJ et al. Estimation of effect size distribution from genome-wide association studies and implications for future discoveries. Nat Genet 2010; 42: 570-575.
-
(2010)
Nat Genet
, vol.42
, pp. 570-575
-
-
Park, J.-H.1
Wacholder, S.2
Gail, M.H.3
Peters, U.4
Jacobs, K.B.5
Chanock, S.J.6
-
40
-
-
33748924655
-
Intermediate phenotypes and genetic mechanisms of psychiatric disorders
-
Meyer-Lindenberg A, Weinberger DR. Intermediate phenotypes and genetic mechanisms of psychiatric disorders. Nat Rev Neurosci 2006; 7: 818-827.
-
(2006)
Nat Rev Neurosci
, vol.7
, pp. 818-827
-
-
Meyer-Lindenberg, A.1
Weinberger, D.R.2
|