-
1
-
-
0034060459
-
Twin studies of schizophrenia: From bow-And-Arrow concordances to star wars Mx and functional genomics
-
Cardno AG, Gottesman II. Twin studies of schizophrenia: From bow-And-Arrow concordances to star wars Mx and functional genomics. Am J Med Genet 2000; 97: 12-17
-
(2000)
Am J Med Genet
, vol.97
, pp. 12-17
-
-
Cardno, A.G.1
Gottesman, I.I.2
-
2
-
-
54249166128
-
Gene-environment interactions in schizophrenia: Review of epidemiological findings and future directions
-
van Os J, Rutten BP, Poulton R. Gene-environment interactions in schizophrenia: Review of epidemiological findings and future directions. Schizophr Bull 2008; 34: 1066-1082
-
(2008)
Schizophr Bull
, vol.34
, pp. 1066-1082
-
-
Van Os, J.1
Rutten, B.P.2
Poulton, R.3
-
3
-
-
77955426959
-
Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort
-
Athanasiu L, Mattingsdal M, Kahler AK, Brown A, Gustafsson O, Agartz I et al. Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort. J Psychiatr Res 2010; 44: 748-753
-
(2010)
J Psychiatr Res
, Issue.44
, pp. 748-753
-
-
Athanasiu, L.1
Mattingsdal, M.2
Kahler, A.K.3
Brown, A.4
Gustafsson, O.5
Agartz, I.6
-
4
-
-
80053159517
-
Common variants at VRK2 and TCF4 conferring risk of schizophrenia
-
Steinberg S, de Jong S, Andreassen OA, Werge T, Borglum AD, Mors O et al. Common variants at VRK2 and TCF4 conferring risk of schizophrenia. Hum Mol Genet 2011; 20: 4076-4081
-
(2011)
Hum Mol Genet
, Issue.20
, pp. 4076-4081
-
-
Steinberg, S.1
De Jong, S.2
Andreassen, O.A.3
Werge, T.4
Borglum, A.D.5
Mors, O.6
-
5
-
-
84866427260
-
Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe
-
Rietschel M, Mattheisen M, Degenhardt F, Kahn RS, Linszen DH, Os JV et al. Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe. Mol Psychiatry 2012; 17: 906-917
-
(2012)
Mol Psychiatry
, Issue.17
, pp. 906-917
-
-
Rietschel, M.1
Mattheisen, M.2
Degenhardt, F.3
Kahn, R.S.4
Linszen, D.H.5
Os, J.V.6
-
6
-
-
61449229353
-
A genome-wide investigation of SNPs and CNVs in schizophrenia
-
Need AC, Ge D, Weale ME, Maia J, Feng S, Heinzen EL et al. A genome-wide investigation of SNPs and CNVs in schizophrenia. PLoS Genet 2009; 5: E1000373
-
(2009)
PLoS Genet
, vol.5
-
-
Need, A.C.1
Ge, D.2
Weale, M.E.3
Maia, J.4
Feng, S.5
Heinzen, E.L.6
-
7
-
-
77349127597
-
Support of association between BRD1 and both schizophrenia and bipolar affective disorder
-
Nyegaard M, Severinsen JE, Als TD, Hedemand A, Straarup S, Nordentoft M et al. Support of association between BRD1 and both schizophrenia and bipolar affective disorder. Am J Med Genet B Neuropsychiatr Genet 2010; 153B: 582-591
-
(2010)
Am J Med Genet B Neuropsychiatr Genet
, vol.153
, pp. 582-591
-
-
Nyegaard, M.1
Severinsen, J.E.2
Als, T.D.3
Hedemand, A.4
Straarup, S.5
Nordentoft, M.6
-
8
-
-
67651177454
-
Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms
-
Holmans PA, Riley B, Pulver AE, Owen MJ, Wildenauer DB, Gejman PV et al. Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms. Mol Psychiatry 2009; 14: 786-795
-
(2009)
Mol Psychiatry
, vol.14
, pp. 786-795
-
-
Holmans, P.A.1
Riley, B.2
Pulver, A.E.3
Owen, M.J.4
Wildenauer, D.B.5
Gejman, P.V.6
-
9
-
-
68449090594
-
Common variants conferring risk of schizophrenia
-
Stefansson H, Ophoff RA, Steinberg S, Andreassen OA, Cichon S, Rujescu D et al. Common variants conferring risk of schizophrenia. Nature 2009; 460: 744-747
-
(2009)
Nature
, vol.460
, pp. 744-747
-
-
Stefansson, H.1
Ophoff, R.A.2
Steinberg, S.3
Andreassen, O.A.4
Cichon, S.5
Rujescu, D.6
-
10
-
-
68449096727
-
Common variants on chromosome 6p22.1 are associated with schizophrenia
-
Shi J, Levinson DF, Duan J, Sanders AR, Zheng Y, Péer I et al. Common variants on chromosome 6p22.1 are associated with schizophrenia. Nature 2009; 460: 753-757
-
(2009)
Nature
, vol.460
, pp. 753-757
-
-
Shi, J.1
Levinson, D.F.2
Duan, J.3
Sanders, A.R.4
Zheng, Y.5
Péer, I.6
-
11
-
-
80053384370
-
Genome-wide association study identifies five new schizophrenia loci
-
Ripke S, Sanders AR, Kendler KS, Levinson DF, Sklar P, Holmans PA et al. Genome-wide association study identifies five new schizophrenia loci. Nat Genet 2011; 43: 969-976
-
(2011)
Nat Genet
, Issue.43
, pp. 969-976
-
-
Ripke, S.1
Sanders, A.R.2
Kendler, K.S.3
Levinson, D.F.4
Sklar, P.5
Holmans, P.A.6
-
12
-
-
68449086236
-
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
-
Purcell SM, Wray NR, Stone JL, Visscher PM, O'Donovan MC, Sullivan PF et al. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 2009; 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
-
13
-
-
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
, Issue.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
-
14
-
-
49949085933
-
Large recurrent microdeletions associated with schizophrenia
-
Stefansson H, Rujescu D, Cichon S, Pietilainen OP, Ingason A, Steinberg S et al. Large recurrent microdeletions associated with schizophrenia. Nature 2008; 455: 232-236
-
(2008)
Nature
, vol.455
, pp. 232-236
-
-
Stefansson, H.1
Rujescu, D.2
Cichon, S.3
Pietilainen, O.P.4
Ingason, A.5
Steinberg, S.6
-
15
-
-
79959938953
-
Genome-wide analysis shows increased frequency of copy number variation deletions in dutch schizophrenia patients
-
Buizer-Voskamp JE, Muntjewerff JW, Strengman E, Sabatti C, Stefansson H, Vorstman JA et al. Genome-wide analysis shows increased frequency of copy number variation deletions in dutch schizophrenia patients. Biol Psychiatry 2011; 70: 655-662
-
(2011)
Biol Psychiatry
, Issue.70
, pp. 655-662
-
-
Buizer-Voskamp, J.E.1
Muntjewerff, J.W.2
Strengman, E.3
Sabatti, C.4
Stefansson, H.5
Vorstman, J.A.6
-
16
-
-
78249281977
-
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia
-
Moreno-De-Luca D, Mulle JG, Kaminsky EB, Sanders SJ, Myers SM, Adam MP et al. Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia. Am J Hum Genet 2010; 87: 618-630
-
(2010)
Am J Hum Genet
, Issue.87
, pp. 618-630
-
-
Moreno-De-Luca, D.1
Mulle, J.G.2
Kaminsky, E.B.3
Sanders, S.J.4
Myers, S.M.5
Adam, M.P.6
-
17
-
-
80051617030
-
Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a Northern Swedish population
-
Moens LN, De Rijk P, Reumers J, Van Den Bossche MJ, Glassee W, De Zutter S et al. Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a Northern Swedish population. PLoS One 2011; 6: E23450
-
(2011)
PLoS One
, Issue.6
-
-
Moens, L.N.1
De Rijk, P.2
Reumers, J.3
Van Den Bossche, M.J.4
Glassee, W.5
De Zutter, S.6
-
18
-
-
80052273655
-
Exome sequencing supports a de novo mutational paradigm for schizophrenia
-
Xu B, Roos JL, Dexheimer P, Boone B, Plummer B, Levy S et al. Exome sequencing supports a de novo mutational paradigm for schizophrenia. Nat Genet 2011; 43: 864-868
-
(2011)
Nat Genet
, Issue.43
, pp. 864-868
-
-
Xu, B.1
Roos, J.L.2
Dexheimer, P.3
Boone, B.4
Plummer, B.5
Levy, S.6
-
19
-
-
79955841697
-
Evaluating the heritability explained by known susceptibility variants: A survey of ten complex diseases
-
So HC, Gui AH, Cherny SS, Sham PC. Evaluating the heritability explained by known susceptibility variants: A survey of ten complex diseases. Genet Epidemiol 2011; 35: 310-317
-
(2011)
Genet Epidemiol
, Issue.35
, pp. 310-317
-
-
So, H.C.1
Gui, A.H.2
Cherny, S.S.3
Sham, P.C.4
-
20
-
-
79953058290
-
The missing genes: What happened to the heritability of psychiatric disorders?
-
Crow TJ. 'The missing genes: What happened to the heritability of psychiatric disorders?'. Mol Psychiatry 2011; 16: 362-364
-
(2011)
Mol Psychiatry
, Issue.16
, pp. 362-364
-
-
Crow, T.J.1
-
21
-
-
0344305525
-
Schizophrenia as a complex trait: Evidence from a meta-Analysis of twin studies
-
Sullivan PF, Kendler KS, Neale MC. Schizophrenia as a complex trait: Evidence from a meta-Analysis of twin studies. Arch Gen Psychiatry 2003; 60: 1187-1192
-
(2003)
Arch Gen Psychiatry
, vol.60
, pp. 1187-1192
-
-
Sullivan, P.F.1
Kendler, K.S.2
Neale, M.C.3
-
22
-
-
40849145994
-
Maternal exposure to herpes simplex virus and risk of psychosis among adult offspring
-
Buka SL, Cannon TD, Torrey EF, Yolken RH. Maternal exposure to herpes simplex virus and risk of psychosis among adult offspring. Biol Psychiatry 2008; 63: 809-815
-
(2008)
Biol Psychiatry
, vol.63
, pp. 809-815
-
-
Buka, S.L.1
Cannon, T.D.2
Torrey, E.F.3
Yolken, R.H.4
-
23
-
-
77956188326
-
A Danish National Birth Cohort study of maternal HSV-2 antibodies as a risk factor for schizophrenia in their offspring
-
Mortensen PB, Pedersen CB, Hougaard DM, Norgaard-Petersen B, Mors O, Borglum AD et al. A Danish National Birth Cohort study of maternal HSV-2 antibodies as a risk factor for schizophrenia in their offspring. Schizophr Res 2010; 122: 257-263
-
(2010)
Schizophr Res
, Issue.122
, pp. 257-263
-
-
Mortensen, P.B.1
Pedersen, C.B.2
Hougaard, D.M.3
Norgaard-Petersen, B.4
Mors, O.5
Borglum, A.D.6
-
24
-
-
3543093977
-
Serologic evidence of prenatal influenza in the etiology of schizophrenia
-
Brown AS, Begg MD, Gravenstein S, Schaefer CA, Wyatt RJ, Bresnahan M et al. Serologic evidence of prenatal influenza in the etiology of schizophrenia. Arch Gen Psychiatry 2004; 61: 774-780
-
(2004)
Arch Gen Psychiatry
, vol.61
, pp. 774-780
-
-
Brown, A.S.1
Begg, M.D.2
Gravenstein, S.3
Schaefer, C.A.4
Wyatt, R.J.5
Bresnahan, M.6
-
25
-
-
16844364265
-
Maternal exposure to toxoplasmosis and risk of schizophrenia in adult offspring
-
Brown AS, Schaefer CA, Quesenberry Jr. CP, Liu L, Babulas VP, Susser ES. Maternal exposure to toxoplasmosis and risk of schizophrenia in adult offspring. Am J Psychiatry 2005; 162: 767-773
-
(2005)
Am J Psychiatry
, vol.162
, pp. 767-773
-
-
Brown, A.S.1
Schaefer, C.A.2
Quesenberry Jr., C.P.3
Liu, L.4
Babulas, V.P.5
Susser, E.S.6
-
26
-
-
80054862386
-
Association of GRIN1 and GRIN2A-D with schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk
-
Demontis D, Nyegaard M, Buttenschøn HN, Hedemand A, Pedersen CP, Grove J et al. Association of GRIN1 and GRIN2A-D with schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk. Am J Med Genet B Neuropsychiatr Genet 2011; 156B: 913-922
-
(2011)
Am J Med Genet B Neuropsychiatr Genet
, vol.156
, pp. 913-922
-
-
Demontis, D.1
Nyegaard, M.2
Buttenschøn, H.N.3
Hedemand, A.4
Pedersen, C.P.5
Grove, J.6
-
27
-
-
34548485304
-
Storage policies and use of the Danish Newborn Screening Biobank
-
Nørgaard-Pedersen B, Hougaard DM. Storage policies and use of the Danish Newborn Screening Biobank. J Inherit Metab Dis 2007; 30: 530-536
-
(2007)
J Inherit Metab Dis
, vol.30
, pp. 530-536
-
-
Nørgaard-Pedersen, B.1
Hougaard, D.M.2
-
29
-
-
34247161352
-
Are exposure to cytomegalovirus and genetic variation on chromosome 6p joint risk factors for schizophrenia?
-
Kim JJ, Shirts BH, Dayal M, Bacanu SA, Wood J, Xie W et al. Are exposure to cytomegalovirus and genetic variation on chromosome 6p joint risk factors for schizophrenia? Ann Med 2007; 39: 145-153
-
(2007)
Ann Med
, vol.39
, pp. 145-153
-
-
Kim, J.J.1
Shirts, B.H.2
Dayal, M.3
Bacanu, S.A.4
Wood, J.5
Xie, W.6
-
30
-
-
34447130839
-
Polymorphisms in MICB are associated with human herpes virus seropositivity and schizophrenia risk
-
Shirts BH, Kim JJ, Reich S, Dickerson FB, Yolken RH, Devlin B et al. Polymorphisms in MICB are associated with human herpes virus seropositivity and schizophrenia risk. Schizophr Res 2007; 94: 342-353
-
(2007)
Schizophr Res
, vol.94
, pp. 342-353
-
-
Shirts, B.H.1
Kim, J.J.2
Reich, S.3
Dickerson, F.B.4
Yolken, R.H.5
Devlin, B.6
-
31
-
-
31744435871
-
Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies
-
Skol AD, Scott LJ, Abecasis GR, Boehnke M. Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies. Nat Genet 2006; 38: 209-213
-
(2006)
Nat Genet
, vol.38
, pp. 209-213
-
-
Skol, A.D.1
Scott, L.J.2
Abecasis, G.R.3
Boehnke, M.4
-
32
-
-
55549115654
-
Genes mirror geography within Europe
-
Novembre J, Johnson T, Bryc K, Kutalik Z, Boyko AR, Auton A et al. Genes mirror geography within Europe. Nature 2008; 456: 98-101
-
(2008)
Nature
, vol.456
, pp. 98-101
-
-
Novembre, J.1
Johnson, T.2
Bryc, K.3
Kutalik, Z.4
Boyko, A.R.5
Auton, A.6
-
34
-
-
67749098061
-
Genome-wide scans using archived neonatal dried blood spot samples
-
Hollegaard MV, Grauholm J, Borglum A, Nyegaard M, Norgaard-Pedersen B, Orntoft T et al. Genome-wide scans using archived neonatal dried blood spot samples. BMC Genomics 2009; 10: 297
-
(2009)
BMC Genomics
, vol.10
, pp. 297
-
-
Hollegaard, M.V.1
Grauholm, J.2
Borglum, A.3
Nyegaard, M.4
Norgaard-Pedersen, B.5
Orntoft, T.6
-
36
-
-
40849145994
-
Maternal exposure to herpes simplex virus and risk of psychosis among adult offspring
-
group TCS
-
Buka SL, Cannon TD, Torrey EF, Yolken RH. group TCS. Maternal exposure to herpes simplex virus and risk of psychosis among adult offspring. Biol Psychiatry 2008; 63: 809-815
-
(2008)
Biol Psychiatry
, vol.63
, pp. 809-815
-
-
Buka, S.L.1
Cannon, T.D.2
Torrey, E.F.3
Yolken, R.H.4
-
38
-
-
66649103750
-
Epidemiological impact and disease burden of congenital cytomegalovirus infection in Europe
-
Ludwig A, Hengel H. Epidemiological impact and disease burden of congenital cytomegalovirus infection in Europe. Euro Surveill 2009; 14: 26-32
-
(2009)
Euro Surveill
, vol.14
, pp. 26-32
-
-
Ludwig, A.1
Hengel, H.2
-
39
-
-
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 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.5
Bender, D.6
-
41
-
-
79959241413
-
Genomic inflation factors under polygenic inheritance
-
Yang J, Weedon MN, Purcell S, Lettre G, Estrada K, Willer CJ et al. Genomic inflation factors under polygenic inheritance. Eur J Hum Genet 2011; 19: 807-812
-
(2011)
Eur J Hum Genet
, Issue.19
, pp. 807-812
-
-
Yang, J.1
Weedon, M.N.2
Purcell, S.3
Lettre, G.4
Estrada, K.5
Willer, C.J.6
-
43
-
-
58449107994
-
Gene-environment interaction in genome- wide association studies
-
Murcray CE, Lewinger JP, Gauderman WJ. Gene-environment interaction in genome- wide association studies. Am J Epidemiol 2009; 169: 219-226
-
(2009)
Am J Epidemiol
, vol.169
, pp. 219-226
-
-
Murcray, C.E.1
Lewinger, J.P.2
Gauderman, W.J.3
-
44
-
-
37549064336
-
Mach 1.0: Rapid haplotype reconstruction and missing genotype inference
-
Li Y, Abecasis GR. Mach 1.0: Rapid haplotype reconstruction and missing genotype inference. Am J Hum Genet 2006; S79: 2290
-
(2006)
Am J Hum Genet
, vol.S79
, pp. 2290
-
-
Li, Y.1
Abecasis, G.R.2
-
45
-
-
79953281764
-
Circadian clock gene expression in brain regions of Alzheimer 's disease patients and control subjects
-
Cermakian N, Lamont EW, Boudreau P, Boivin DB. Circadian clock gene expression in brain regions of Alzheimer 's disease patients and control subjects. J Biol Rhythms 2011; 26: 160-170
-
(2011)
J Biol Rhythms
, Issue.26
, pp. 160-170
-
-
Cermakian, N.1
Lamont, E.W.2
Boudreau, P.3
Boivin, D.B.4
-
46
-
-
33646687759
-
The suitability of actigraphy, diary data, and urinary melatonin profiles for quantitative assessment of sleep disturbances in schizophrenia: A case report
-
Wulff K, Joyce E, Middleton B, Dijk DJ, Foster RG. The suitability of actigraphy, diary data, and urinary melatonin profiles for quantitative assessment of sleep disturbances in schizophrenia: A case report. Chronobiol Int 2006; 23: 485-495
-
(2006)
Chronobiol Int
, vol.23
, pp. 485-495
-
-
Wulff, K.1
Joyce, E.2
Middleton, B.3
Dijk, D.J.4
Foster, R.G.5
-
47
-
-
0025034582
-
Electroencephalographic sleep in schizophrenia: A critical review
-
Keshavan MS, Reynolds CF, Kupfer DJ. Electroencephalographic sleep in schizophrenia: A critical review. Compr Psychiatry 1990; 31: 34-47
-
(1990)
Compr Psychiatry
, vol.31
, pp. 34-47
-
-
Keshavan, M.S.1
Reynolds, C.F.2
Kupfer, D.J.3
-
48
-
-
0001540749
-
Influence of sleep-wake and circadian rhythm disturbances in psychiatric disorders
-
Boivin DB. Influence of sleep-wake and circadian rhythm disturbances in psychiatric disorders. J Psychiatry Neurosci 2000; 25: 446-458
-
(2000)
J Psychiatry Neurosci
, vol.25
, pp. 446-458
-
-
Boivin, D.B.1
-
49
-
-
0028224344
-
Circadian rhythm of tryptophan, serotonin, melatonin, and pituitary hormones in schizophrenia
-
Rao ML, Gross G, Strebel B, Halaris A, Huber G, Braunig P et al. Circadian rhythm of tryptophan, serotonin, melatonin, and pituitary hormones in schizophrenia. Biol Psychiatry 1994; 35: 151-163
-
(1994)
Biol Psychiatry
, vol.35
, pp. 151-163
-
-
Rao, M.L.1
Gross, G.2
Strebel, B.3
Halaris, A.4
Huber, G.5
Braunig, P.6
-
50
-
-
33645999344
-
Suggestive evidence for association of the circadian genes PERIOD3 and ARNTL with bipolar disorder
-
Nievergelt CM, Kripke DF, Barrett TB, Burg E, Remick RA, Sadovnick AD et al. Suggestive evidence for association of the circadian genes PERIOD3 and ARNTL with bipolar disorder. Am J Med Genet B Neuropsychiatr Genet 2006; 141B: 234-241
-
(2006)
Am J Med Genet B Neuropsychiatr Genet
, vol.141
, pp. 234-241
-
-
Nievergelt, C.M.1
Kripke, D.F.2
Barrett, T.B.3
Burg, E.4
Remick, R.A.5
Sadovnick, A.D.6
-
51
-
-
33644790985
-
Association study of eight circadian genes with bipolar I disorder, schizoaffective disorder and schizophrenia
-
Mansour HA, Wood J, Logue T, Chowdari KV, Dayal M, Kupfer DJ et al. Association study of eight circadian genes with bipolar I disorder, schizoaffective disorder and schizophrenia. Genes Brain Behav 2006; 5: 150-157
-
(2006)
Genes Brain Behav
, vol.5
, pp. 150-157
-
-
Mansour, H.A.1
Wood, J.2
Logue, T.3
Chowdari, K.V.4
Dayal, M.5
Kupfer, D.J.6
-
52
-
-
77951113131
-
Differential association of circadian genes with mood disorders: CRY1 and NPAS2 are associated with unipolar major depression and CLOCK and VIP with bipolar disorder
-
Soria V, Martinez-Amoros E, Escaramis G, Valero J, Perez-Egea R, Garcia C et al. Differential association of circadian genes with mood disorders: CRY1 and NPAS2 are associated with unipolar major depression and CLOCK and VIP with bipolar disorder. Neuropsychopharmacology 2010; 35: 1279-1289
-
(2010)
Neuropsychopharmacology
, Issue.35
, pp. 1279-1289
-
-
Soria, V.1
Martinez-Amoros, E.2
Escaramis, G.3
Valero, J.4
Perez-Egea, R.5
Garcia, C.6
-
53
-
-
70350548087
-
Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophrenia
-
Mansour HA, Talkowski ME, Wood J, Chowdari KV, McClain L, Prasad K et al. Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophrenia. Bipolar Disord 2009; 11: 701-710
-
(2009)
Bipolar Disord
, vol.11
, pp. 701-710
-
-
Mansour, H.A.1
Talkowski, M.E.2
Wood, J.3
Chowdari, K.V.4
McClain, L.5
Prasad, K.6
-
54
-
-
61449223631
-
Convergent functional genomics of genome-wide association data for bipolar disorder: Comprehensive identification of candidate genes, pathways and mechanisms
-
Le-Niculescu H, Patel SD, Bhat M, Kuczenski R, Faraone SV, Tsuang MT et al. Convergent functional genomics of genome-wide association data for bipolar disorder: Comprehensive identification of candidate genes, pathways and mechanisms. Am J Med Genet B Neuropsychiatr Genet 2009; 150B: 155-181
-
(2009)
Am J Med Genet B Neuropsychiatr Genet
, vol.150
, pp. 155-181
-
-
Le-Niculescu, H.1
Patel, S.D.2
Bhat, M.3
Kuczenski, R.4
Faraone, S.V.5
Tsuang, M.T.6
-
55
-
-
23144442645
-
Regulation of cadherin-mediated adhesion in morphogenesis
-
Gumbiner BM. Regulation of cadherin-mediated adhesion in morphogenesis. Nat Rev Mol Cell Biol 2005; 6: 622-634
-
(2005)
Nat Rev Mol Cell Biol
, vol.6
, pp. 622-634
-
-
Gumbiner, B.M.1
-
56
-
-
0029160437
-
Morphogenetic roles of classic cadherins
-
Takeichi M. Morphogenetic roles of classic cadherins. Curr Opin Cell Biol 1995; 7: 619-627
-
(1995)
Curr Opin Cell Biol
, vol.7
, pp. 619-627
-
-
Takeichi, M.1
-
57
-
-
33845727992
-
The cadherin superfamily in neuronal connections and interactions
-
Takeichi M. The cadherin superfamily in neuronal connections and interactions. Nat Rev Neurosci 2007; 8: 11-20
-
(2007)
Nat Rev Neurosci
, vol.8
, pp. 11-20
-
-
Takeichi, M.1
-
58
-
-
0034066303
-
Expression of T-cadherin (CDH13, H-Cadherin) in human brain and its characteristics as a negative growth regulator of epidermal growth factor in neuroblastoma cells
-
Takeuchi T, Misaki A, Liang SB, Tachibana A, Hayashi N, Sonobe H et al. Expression of T-cadherin (CDH13, H-Cadherin) in human brain and its characteristics as a negative growth regulator of epidermal growth factor in neuroblastoma cells. J Neurochem 2000; 74: 1489-1497
-
(2000)
J Neurochem
, vol.74
, pp. 1489-1497
-
-
Takeuchi, T.1
Misaki, A.2
Liang, S.B.3
Tachibana, A.4
Hayashi, N.5
Sonobe, H.6
-
59
-
-
0029832383
-
Inhibition of motor axon growth by T-cadherin substrata
-
Fredette BJ, Miller J, Ranscht B. Inhibition of motor axon growth by T-cadherin substrata. Development 1996; 122: 3163-3171
-
(1996)
Development
, vol.122
, pp. 3163-3171
-
-
Fredette, B.J.1
Miller, J.2
Ranscht, B.3
-
60
-
-
77949261544
-
T-cadherin structures reveal a novel adhesive binding mechanism
-
Ciatto C, Bahna F, Zampieri N, VanSteenhouse HC, Katsamba PS, Ahlsen G et al. T-cadherin structures reveal a novel adhesive binding mechanism. Nat Struct Mol Biol 2010; 17: 339-347
-
(2010)
Nat Struct Mol Biol
, Issue.17
, pp. 339-347
-
-
Ciatto, C.1
Bahna, F.2
Zampieri, N.3
VanSteenhouse, H.C.4
Katsamba, P.S.5
Ahlsen, G.6
-
61
-
-
57349087863
-
Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations
-
Lasky-Su J, Neale BM, Franke B, Anney RJ, Zhou K, Maller JB et al. Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. Am J Med Genet B Neuropsychiatr Genet 2008; 147B: 1345-1354
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147
, pp. 1345-1354
-
-
Lasky-Su, J.1
Neale, B.M.2
Franke, B.3
Anney, R.J.4
Zhou, K.5
Maller, J.B.6
-
62
-
-
55349128167
-
Molecular genetics of adult ADHD: Converging evidence from genome-wide association and extended pedigree linkage studies
-
Lesch KP, Timmesfeld N, Renner TJ, Halperin R, Roser C, Nguyen TT et al. Molecular genetics of adult ADHD: Converging evidence from genome-wide association and extended pedigree linkage studies. J Neural Transm 2008; 115: 1573-1585
-
(2008)
J Neural Transm
, vol.115
, pp. 1573-1585
-
-
Lesch, K.P.1
Timmesfeld, N.2
Renner, T.J.3
Halperin, R.4
Roser, C.5
Nguyen, T.T.6
-
63
-
-
57349166006
-
Genome-wide association scan of attention deficit hyperactivity disorder
-
Neale BM, Lasky-Su J, Anney R, Franke B, Zhou K, Maller JB et al. Genome-wide association scan of attention deficit hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet 2008; 147B: 1337-1344
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147
, pp. 1337-1344
-
-
Neale, B.M.1
Lasky-Su, J.2
Anney, R.3
Franke, B.4
Zhou, K.5
Maller, J.B.6
-
64
-
-
77956180603
-
Case-control genome-wide association study of attention-deficit/ hyperactivity disorder
-
Neale BM, Medland S, Ripke S, Anney RJ, Asherson P, Buitelaar J et al. Case-control genome-wide association study of attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry 2010; 49: 906-920
-
(2010)
J Am Acad Child Adolesc Psychiatry
, Issue.49
, pp. 906-920
-
-
Neale, B.M.1
Medland, S.2
Ripke, S.3
Anney, R.J.4
Asherson, P.5
Buitelaar, J.6
-
65
-
-
57349131186
-
Meta-Analysis of genome-wide linkage scans of attention deficit hyperactivity disorder
-
Zhou K, Dempfle A, Arcos-Burgos M, Bakker SC, Banaschewski T, Biederman J et al. Meta-Analysis of genome-wide linkage scans of attention deficit hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet 2008; 147B: 1392-1398
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147
, pp. 1392-1398
-
-
Zhou, K.1
Dempfle, A.2
Arcos-Burgos, M.3
Bakker, S.C.4
Banaschewski, T.5
Biederman, J.6
-
66
-
-
77957914573
-
Genome-wide association scan of trait depression
-
Terracciano A, Tanaka T, Sutin AR, Sanna S, Deiana B, Lai S et al. Genome-wide association scan of trait depression. Biol Psychiatry 2010; 68: 811-817
-
(2010)
Biol Psychiatry
, Issue.68
, pp. 811-817
-
-
Terracciano, A.1
Tanaka, T.2
Sutin, A.R.3
Sanna, S.4
Deiana, B.5
Lai, S.6
-
67
-
-
67349112868
-
Common genetic variants on 5p14.1 associate with autism spectrum disorders
-
Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS et al. Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature 2009; 459: 528-533
-
(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
-
68
-
-
79958074870
-
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism
-
Sanders SJ, Ercan-Sencicek AG, Hus V, Luo R, Murtha MT, Moreno-De-Luca D et al. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron 2011; 70: 863-885
-
(2011)
Neuron
, Issue.70
, pp. 863-885
-
-
Sanders, S.J.1
Ercan-Sencicek, A.G.2
Hus, V.3
Luo, R.4
Murtha, M.T.5
Moreno-De-Luca, D.6
-
69
-
-
33745166261
-
Complementary expression pattern of Zfhx1 genes Sip1 and deltaEF1 in the mouse embryo and their genetic interaction revealed by compound mutants
-
Miyoshi T, Maruhashi M, Van De Putte T, Kondoh H, Huylebroeck D, Higashi Y. Complementary expression pattern of Zfhx1 genes Sip1 and deltaEF1 in the mouse embryo and their genetic interaction revealed by compound mutants. Dev Dyn 2006; 235: 1941-1952
-
(2006)
Dev Dyn
, vol.235
, pp. 1941-1952
-
-
Miyoshi, T.1
Maruhashi, M.2
Van De Putte, T.3
Kondoh, H.4
Huylebroeck, D.5
Higashi, Y.6
-
70
-
-
77952550259
-
Transcriptional inhibition of REST by NeuroD2 during neuronal differentiation
-
Ravanpay AC, Hansen SJ, Olson JM. Transcriptional inhibition of REST by NeuroD2 during neuronal differentiation. Mol Cell Neurosci 2010; 44: 178-189
-
(2010)
Mol Cell Neurosci
, Issue.44
, pp. 178-189
-
-
Ravanpay, A.C.1
Hansen, S.J.2
Olson, J.M.3
-
71
-
-
66849104147
-
The class I bHLH factors E2-2A and E2-2B regulate EMT
-
Sobrado VR, Moreno-Bueno G, Cubillo E, Holt LJ, Nieto MA, Portillo F et al. The class I bHLH factors E2-2A and E2-2B regulate EMT. J Cell Sci 2009; 122: 1014-1024
-
(2009)
J Cell Sci
, vol.122
, pp. 1014-1024
-
-
Sobrado, V.R.1
Moreno-Bueno, G.2
Cubillo, E.3
Holt, L.J.4
Nieto, M.A.5
Portillo, F.6
-
72
-
-
77956521660
-
E2-2 protein and Fuchs's corneal dystrophy
-
Baratz KH, Tosakulwong N, Ryu E, Brown WL, Branham K, Chen W et al. E2-2 protein and Fuchs's corneal dystrophy. N Engl J Med 2010; 363: 1016-1024
-
(2010)
N Engl J Med
, Issue.363
, pp. 1016-1024
-
-
Baratz, K.H.1
Tosakulwong, N.2
Ryu, E.3
Brown, W.L.4
Branham, K.5
Chen, W.6
-
73
-
-
73149085311
-
Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p.
-
Riazuddin SA, Zaghloul NA, Al-Saif A, Davey L, Diplas BH, Meadows DN et al. Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p. Am J Hum Genet 2010; 86: 45-53
-
(2010)
Am J Hum Genet
, Issue.86
, pp. 45-53
-
-
Riazuddin, S.A.1
Zaghloul, N.A.2
Al-Saif, A.3
Davey, L.4
Diplas, B.H.5
Meadows, D.N.6
-
74
-
-
58149529709
-
Zeb1-mediated T-cadherin repression increases the invasive potential of gallbladder cancer
-
Adachi Y, Takeuchi T, Nagayama T, Ohtsuki Y, Furihata M. Zeb1-mediated T-cadherin repression increases the invasive potential of gallbladder cancer. FEBS Lett 2009; 583: 430-436
-
(2009)
FEBS Lett
, vol.583
, pp. 430-436
-
-
Adachi, Y.1
Takeuchi, T.2
Nagayama, T.3
Ohtsuki, Y.4
Furihata, M.5
-
75
-
-
2342574965
-
Alpha-Tcatenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease
-
Busby V, Goossens S, Nowotny P, Hamilton G, Smemo S, Harold D et al. Alpha-Tcatenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease. Neuromolecular Med 2004; 5: 133-146
-
(2004)
Neuromolecular Med
, vol.5
, pp. 133-146
-
-
Busby, V.1
Goossens, S.2
Nowotny, P.3
Hamilton, G.4
Smemo, S.5
Harold, D.6
-
76
-
-
0031440104
-
Molecular and functional analysis of cadherinbased adherens junctions
-
Yap AS, Brieher WM, Gumbiner BM. Molecular and functional analysis of cadherinbased adherens junctions. Annu Rev Cell Dev Biol 1997; 13: 119-146
-
(1997)
Annu Rev Cell Dev Biol
, vol.13
, pp. 119-146
-
-
Yap, A.S.1
Brieher, W.M.2
Gumbiner, B.M.3
-
77
-
-
0034741031
-
Alphatcatenin: A novel tissue-specific beta-catenin-binding protein mediating strong cell-cell adhesion
-
Janssens B, Goossens S, Staes K, Gilbert B, van Hengel J, Colpaert C et al. alphaTcatenin: A novel tissue-specific beta-catenin-binding protein mediating strong cell-cell adhesion. J Cell Sci 2001; 114: 3177-3188
-
(2001)
J Cell Sci
, vol.114
, pp. 3177-3188
-
-
Janssens, B.1
Goossens, S.2
Staes, K.3
Gilbert, B.4
Van Hengel, J.5
Colpaert, C.6
-
78
-
-
0343986307
-
Cytomegalovirus-induced transendothelial cell migration a closer look at intercellular communication mechanisms
-
Scholz M, Blaheta RA, Vogel J, Doerr HW, Cinatl Jr. J. Cytomegalovirus-induced transendothelial cell migration. a closer look at intercellular communication mechanisms. Intervirology 1999; 42: 350-356
-
(1999)
Intervirology
, vol.42
, pp. 350-356
-
-
Scholz, M.1
Blaheta, R.A.2
Vogel, J.3
Doerr, H.W.4
Cinatl Jr., J.5
-
79
-
-
37549009966
-
Human cytomegalovirus immediate-early-gene expression disrupts embryogenesis in transgenic Drosophila
-
Steinberg R, Shemer-Avni Y, Adler N, Neuman-Silberberg S. Human cytomegalovirus immediate-early-gene expression disrupts embryogenesis in transgenic Drosophila. Transgenic Res 2008; 17: 105-119
-
(2008)
Transgenic Res
, vol.17
, pp. 105-119
-
-
Steinberg, R.1
Shemer-Avni, Y.2
Adler, N.3
Neuman-Silberberg, S.4
-
80
-
-
33845202373
-
LRRTM3 promotes processing of amyloid-precursor protein by BACE1 and is a positional candidate gene for late-onset Alzheimer's disease
-
Majercak J, Ray WJ, Espeseth A, Simon A, Shi XP, Wolffe C et al. LRRTM3 promotes processing of amyloid-precursor protein by BACE1 and is a positional candidate gene for late-onset Alzheimer's disease. Proc Natl Acad Sci USA 2006; 103: 17967-17972
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 17967-17972
-
-
Majercak, J.1
Ray, W.J.2
Espeseth, A.3
Simon, A.4
Shi, X.P.5
Wolffe, C.6
-
81
-
-
35648975571
-
Effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer disease
-
Liang X, Martin ER, Schnetz-Boutaud N, Bartlett J, Anderson B, Zuchner S et al. Effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer disease. Hum Mutat 2007; 28: 1065-1073
-
(2007)
Hum Mutat
, vol.28
, pp. 1065-1073
-
-
Liang, X.1
Martin, E.R.2
Schnetz-Boutaud, N.3
Bartlett, J.4
Anderson, B.5
Zuchner, S.6
-
82
-
-
35748957469
-
Genetic association of CTNNA3 with late-onset Alzheimer's disease in females
-
Miyashita A, Arai H, Asada T, Imagawa M, Matsubara E, Shoji M et al. Genetic association of CTNNA3 with late-onset Alzheimer's disease in females. Hum Mol Genet 2007; 16: 2854-2869
-
(2007)
Hum Mol Genet
, vol.16
, pp. 2854-2869
-
-
Miyashita, A.1
Arai, H.2
Asada, T.3
Imagawa, M.4
Matsubara, E.5
Shoji, M.6
-
83
-
-
51449109314
-
Association analysis of 528 intra-genic SNPs in a region of chromosome 10 linked to late onset Alzheimer's disease
-
Morgan AR, Hamilton G, Turic D, Jehu L, Harold D, Abraham R et al. Association analysis of 528 intra-genic SNPs in a region of chromosome 10 linked to late onset Alzheimer's disease. Am J Med Genet B Neuropsychiatr Genet 2008; 147B: 727-731
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147
, pp. 727-731
-
-
Morgan, A.R.1
Hamilton, G.2
Turic, D.3
Jehu, L.4
Harold, D.5
Abraham, R.6
-
84
-
-
67649432541
-
An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3
-
Edwards TL, Pericak-Vance M, Gilbert JR, Haines JL, Martin ER, Ritchie MD. An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3. Am J Med Genet B Neuropsychiatr Genet 2009; 150B: 721-735
-
(2009)
Am J Med Genet B Neuropsychiatr Genet
, vol.150
, pp. 721-735
-
-
Edwards, T.L.1
Pericak-Vance, M.2
Gilbert, J.R.3
Haines, J.L.4
Martin, E.R.5
Ritchie, M.D.6
-
85
-
-
77954646843
-
Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry
-
Sousa I, Clark TG, Holt R, Pagnamenta AT, Mulder EJ, Minderaa RB et al. Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry. Mol Autism 2010; 1: 7
-
(2010)
Mol Autism
, Issue.1
, pp. 7
-
-
Sousa, I.1
Clark, T.G.2
Holt, R.3
Pagnamenta, A.T.4
Mulder, E.J.5
Minderaa, R.B.6
-
86
-
-
0022411324
-
Association of cytomegalovirus and herpes simplex virus infections of the cervix in four clinic populations
-
Embil JA, Garner JB, Pereira LH, White FM, Manuel FR. Association of cytomegalovirus and herpes simplex virus infections of the cervix in four clinic populations. Sex Transm Dis 1985; 12: 224-228
-
(1985)
Sex Transm Dis
, vol.12
, pp. 224-228
-
-
Embil, J.A.1
Garner, J.B.2
Pereira, L.H.3
White, F.M.4
Manuel, F.R.5
-
87
-
-
33750128821
-
Seroprevalence of cytomegalovirus infection in the United States 1988 1994
-
Staras SA, Dollard SC, Radford KW, Flanders WD, Pass RF, Cannon MJ. Seroprevalence of cytomegalovirus infection in the United States, 1988-1994. Clin Infect Dis 2006; 43: 1143-1151.
-
(2006)
Clin Infect Dis
, vol.43
, pp. 1143-1151
-
-
Staras, S.A.1
Dollard, S.C.2
Radford, K.W.3
Flanders, W.D.4
Pass, R.F.5
Cannon, M.J.6
|