-
1
-
-
0142258997
-
Genetic and environmental contributions to stability and change in children’s internalizing and externalizing problems
-
PID: 14560171
-
van der Valk JC, van den Oord EJ, Verhulst FC, Boomsma DI (2003) Genetic and environmental contributions to stability and change in children’s internalizing and externalizing problems. J Am Acad Child Adolesc Psychiatry 42:1212–1220
-
(2003)
J Am Acad Child Adolesc Psychiatry
, vol.42
, pp. 1212-1220
-
-
van der Valk, J.C.1
van den Oord, E.J.2
Verhulst, F.C.3
Boomsma, D.I.4
-
2
-
-
0032611687
-
An adoption study of the etiology of teacher and parent reports of externalizing behavior problems in middle childhood
-
COI: 1:STN:280:DyaK1M3gslansQ%3D%3D, PID: 10191519
-
Deater-Deckard K, Plomin R (1999) An adoption study of the etiology of teacher and parent reports of externalizing behavior problems in middle childhood. Child Dev 70:144–154
-
(1999)
Child Dev
, vol.70
, pp. 144-154
-
-
Deater-Deckard, K.1
Plomin, R.2
-
3
-
-
0029047944
-
A twin study of competence and problem behavior in childhood and early adolescence
-
COI: 1:STN:280:DyaK28%2FitlKrug%3D%3D, PID: 7559844
-
Edelbrock C, Rende R, Plomin R, Thompson LA (1995) A twin study of competence and problem behavior in childhood and early adolescence. J Child Psychol Psychiatry 36:775–785
-
(1995)
J Child Psychol Psychiatry
, vol.36
, pp. 775-785
-
-
Edelbrock, C.1
Rende, R.2
Plomin, R.3
Thompson, L.A.4
-
4
-
-
0030118689
-
Genetic and environmental influences on temperament in middle childhood: analyses of teacher and tester ratings
-
COI: 1:STN:280:DyaK283gvFalug%3D%3D, PID: 8625721
-
Schmitz S, Saudino KJ, Plomin R, Fulker DW, DeFries JC (1996) Genetic and environmental influences on temperament in middle childhood: analyses of teacher and tester ratings. Child Dev 67:409–422
-
(1996)
Child Dev
, vol.67
, pp. 409-422
-
-
Schmitz, S.1
Saudino, K.J.2
Plomin, R.3
Fulker, D.W.4
DeFries, J.C.5
-
5
-
-
0028200074
-
A study of problem behaviors in 10- to 15-year-old biologically related and unrelated international adoptees
-
PID: 7945150
-
van den Oord EJ, Boomsma DI, Verhulst FC (1994) A study of problem behaviors in 10- to 15-year-old biologically related and unrelated international adoptees. Behav Genet 24:193–205
-
(1994)
Behav Genet
, vol.24
, pp. 193-205
-
-
van den Oord, E.J.1
Boomsma, D.I.2
Verhulst, F.C.3
-
6
-
-
0026471247
-
Academic underachievement, attention deficits, and aggression: comorbidity and implications for intervention
-
COI: 1:STN:280:DyaK3s%2FpsVChtA%3D%3D, PID: 1460150
-
Hinshaw SP (1992) Academic underachievement, attention deficits, and aggression: comorbidity and implications for intervention. J Consult Clin Psychol 60:893–903
-
(1992)
J Consult Clin Psychol
, vol.60
, pp. 893-903
-
-
Hinshaw, S.P.1
-
7
-
-
1642285537
-
Learning disabilities and the risk of psychiatric disorders in children and adolescents
-
Greenhill LL, (ed), American Psychiatric Press Inc, Washington:
-
Osman BB (2000) Learning disabilities and the risk of psychiatric disorders in children and adolescents. In: Greenhill LL (ed) Learning disabilities. Implications for psychiatric treatment. American Psychiatric Press Inc, Washington
-
(2000)
Learning disabilities. Implications for psychiatric treatment
-
-
Osman, B.B.1
-
9
-
-
0016806105
-
Attainment and adjustment in two geographical areas. II. The prevalence of specific reading retardation
-
COI: 1:STN:280:DyaE28%2FhvFOitg%3D%3D, PID: 1174768
-
Berger M, Yule W, Rutter M (1975) Attainment and adjustment in two geographical areas. II. The prevalence of specific reading retardation. Br J Psychiatry 126:510–519
-
(1975)
Br J Psychiatry
, vol.126
, pp. 510-519
-
-
Berger, M.1
Yule, W.2
Rutter, M.3
-
10
-
-
0002950082
-
Reading retardation and antisocial behavior—the nature of the association
-
Rutter M, Tizard J, Whitmore K, (eds), Longmans, London:
-
Rutter M, Yule W (1970) Reading retardation and antisocial behavior—the nature of the association. In: Rutter M, Tizard J, Whitmore K (eds) Education, health and behavior. Longmans, London, pp 240–255
-
(1970)
Education, health and behavior
, pp. 240-255
-
-
Rutter, M.1
Yule, W.2
-
11
-
-
0033803521
-
Adolescents with learning disabilities: risk and protective factors associated with emotional well-being: findings from the National Longitudinal Study of Adolescent Health
-
COI: 1:STN:280:DC%2BD3M%2FivFWmtQ%3D%3D, PID: 11044706
-
Svetaz MV, Ireland M, Blum R (2000) Adolescents with learning disabilities: risk and protective factors associated with emotional well-being: findings from the National Longitudinal Study of Adolescent Health. J Adolesc Health 27:340–348
-
(2000)
J Adolesc Health
, vol.27
, pp. 340-348
-
-
Svetaz, M.V.1
Ireland, M.2
Blum, R.3
-
12
-
-
33749362972
-
The role of learning to read in the development of problem behaviour: a cross-lagged longitudinal study
-
PID: 16953960
-
Halonen A, Aunola K, Ahonen T, Nurmi JE (2006) The role of learning to read in the development of problem behaviour: a cross-lagged longitudinal study. Br J Educ Psychol 76:517–534
-
(2006)
Br J Educ Psychol
, vol.76
, pp. 517-534
-
-
Halonen, A.1
Aunola, K.2
Ahonen, T.3
Nurmi, J.E.4
-
13
-
-
33748266068
-
Literacy and mental disorders
-
PID: 16721162
-
Maughan B, Carroll J (2006) Literacy and mental disorders. Curr Opin Psychiatry. 19:350–354
-
(2006)
Curr Opin Psychiatry.
, vol.19
, pp. 350-354
-
-
Maughan, B.1
Carroll, J.2
-
14
-
-
0034804070
-
Separating attention deficit hyperactivity disorder and learning disabilities in girls: a familial risk analysis
-
COI: 1:STN:280:DC%2BD3MrjtF2nsg%3D%3D, PID: 11579000
-
Doyle AE, Faraone SV, DuPre EP, Biederman J (2001) Separating attention deficit hyperactivity disorder and learning disabilities in girls: a familial risk analysis. Am J Psychiatry 158:1666–1672
-
(2001)
Am J Psychiatry
, vol.158
, pp. 1666-1672
-
-
Doyle, A.E.1
Faraone, S.V.2
DuPre, E.P.3
Biederman, J.4
-
15
-
-
77958150289
-
Etiology and neuropsychology of comorbidity between RD and ADHD: the case for multiple-deficit models
-
PID: 20828676
-
Willcutt EG, Betjemann RS, McGrath LM, Chhabildas NA, Olson RK, DeFries JC, Pennington BF (2010) Etiology and neuropsychology of comorbidity between RD and ADHD: the case for multiple-deficit models. Cortex. 46:1345–1361
-
(2010)
Cortex.
, vol.46
, pp. 1345-1361
-
-
Willcutt, E.G.1
Betjemann, R.S.2
McGrath, L.M.3
Chhabildas, N.A.4
Olson, R.K.5
DeFries, J.C.6
Pennington, B.F.7
-
16
-
-
0026530258
-
A twin study of the etiology of comorbidity: attention-deficit hyperactivity disorder and dyslexia
-
COI: 1:STN:280:DyaK383is1Wjsw%3D%3D, PID: 1564037
-
Gilger JW, Pennington BF, DeFries JC (1992) A twin study of the etiology of comorbidity: attention-deficit hyperactivity disorder and dyslexia. J Am Acad Child Adolesc Psychiatry 31:343–348
-
(1992)
J Am Acad Child Adolesc Psychiatry
, vol.31
, pp. 343-348
-
-
Gilger, J.W.1
Pennington, B.F.2
DeFries, J.C.3
-
17
-
-
0000307915
-
Reading disability and hyperactivity disorder: evidence for a common genetic etiology
-
Light JG, Pennington BF, Gilger JW, DeFries JC (1995) Reading disability and hyperactivity disorder: evidence for a common genetic etiology. Dev Neuropsychol 11:323–335
-
(1995)
Dev Neuropsychol
, vol.11
, pp. 323-335
-
-
Light, J.G.1
Pennington, B.F.2
Gilger, J.W.3
DeFries, J.C.4
-
18
-
-
34548676377
-
Understanding comorbidity: a twin study of reading disability and attention-deficit/hyperactivity disorder
-
PID: 17440942
-
Willcutt EG, Pennington BF, Olson RK, DeFries JC (2007) Understanding comorbidity: a twin study of reading disability and attention-deficit/hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet. 144B:709–714
-
(2007)
Am J Med Genet B Neuropsychiatr Genet.
, vol.144B
, pp. 709-714
-
-
Willcutt, E.G.1
Pennington, B.F.2
Olson, R.K.3
DeFries, J.C.4
-
19
-
-
0033928210
-
Chromosome 6p influences on different dyslexia-related cognitive processes: further confirmation
-
COI: 1:CAS:528:DC%2BD3cXitFyitbo%3D, PID: 10677331
-
Grigorenko EL, Wood FB, Meyer MS, Pauls DL (2000) Chromosome 6p influences on different dyslexia-related cognitive processes: further confirmation. Am J Hum Genet 66:715–723
-
(2000)
Am J Hum Genet
, vol.66
, pp. 715-723
-
-
Grigorenko, E.L.1
Wood, F.B.2
Meyer, M.S.3
Pauls, D.L.4
-
20
-
-
0035828096
-
Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia
-
COI: 1:STN:280:DC%2BD3MvltVWjsw%3D%3D, PID: 11496366
-
Petryshen TL, Kaplan BJ, Fu Liu M, de French NS, Tobias R, Hughes ML, Field LL (2001) Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia. Am J Med Genet 105:507–517
-
(2001)
Am J Med Genet
, vol.105
, pp. 507-517
-
-
Petryshen, T.L.1
Kaplan, B.J.2
Fu Liu, M.3
de French, N.S.4
Tobias, R.5
Hughes, M.L.6
Field, L.L.7
-
21
-
-
0028030006
-
Quantitative trait locus for reading disability on chromosome 6
-
COI: 1:CAS:528:DyaK2cXmslemurw%3D, PID: 7939663
-
Cardon LR, Smith SD, Fulker DW, Kimberling WJ, Pennington BF, DeFries JC (1994) Quantitative trait locus for reading disability on chromosome 6. Science 266:276–279
-
(1994)
Science
, vol.266
, pp. 276-279
-
-
Cardon, L.R.1
Smith, S.D.2
Fulker, D.W.3
Kimberling, W.J.4
Pennington, B.F.5
DeFries, J.C.6
-
22
-
-
18344374003
-
Evidence for linkage and association with reading disability on 6p21.3-22
-
COI: 1:CAS:528:DC%2BD38XjsFGnsL8%3D, PID: 11951179
-
Kaplan DE, Gayan J, Ahn J, Won TW, Pauls D, Olson RK, DeFries JC, Wood F, Pennington BF, Page GP, Smith SD, Gruen JR (2002) Evidence for linkage and association with reading disability on 6p21.3-22. Am J Hum Genet 70:1287–1298
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1287-1298
-
-
Kaplan, D.E.1
Gayan, J.2
Ahn, J.3
Won, T.W.4
Pauls, D.5
Olson, R.K.6
DeFries, J.C.7
Wood, F.8
Pennington, B.F.9
Page, G.P.10
Smith, S.D.11
Gruen, J.R.12
-
23
-
-
3543029197
-
Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses
-
COI: 1:CAS:528:DC%2BD2cXltVSms7w%3D, PID: 15138886
-
Deffenbacher KE, Kenyon JB, Hoover DM, Olson RK, Pennington BF, DeFries JC, Smith SD (2004) Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses. Hum Genet 115:128–138
-
(2004)
Hum Genet
, vol.115
, pp. 128-138
-
-
Deffenbacher, K.E.1
Kenyon, J.B.2
Hoover, D.M.3
Olson, R.K.4
Pennington, B.F.5
DeFries, J.C.6
Smith, S.D.7
-
24
-
-
8844258018
-
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States
-
COI: 1:CAS:528:DC%2BD2cXhtVegsrnE, PID: 15514892
-
Francks C, Paracchini S, Smith SD, Richardson AJ, Scerri TS, Cardon LR, Marlow AJ, MacPhie IL, Walter J, Pennington BF, Fisher SE, Olson RK, DeFries JC, Stein JF, Monaco AP (2004) A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. Am J Hum Genet 75:1046–1058
-
(2004)
Am J Hum Genet
, vol.75
, pp. 1046-1058
-
-
Francks, C.1
Paracchini, S.2
Smith, S.D.3
Richardson, A.J.4
Scerri, T.S.5
Cardon, L.R.6
Marlow, A.J.7
MacPhie, I.L.8
Walter, J.9
Pennington, B.F.10
Fisher, S.E.11
Olson, R.K.12
DeFries, J.C.13
Stein, J.F.14
Monaco, A.P.15
-
25
-
-
0037041301
-
Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention-deficit/hyperactivity disorder
-
PID: 11920845
-
Willcutt EG, Pennington BF, Smith SD, Cardon LR, Gayan J, Knopik VS, Olson RK, DeFries JC (2002) Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention-deficit/hyperactivity disorder. Am J Med Genet 114:260–268
-
(2002)
Am J Med Genet
, vol.114
, pp. 260-268
-
-
Willcutt, E.G.1
Pennington, B.F.2
Smith, S.D.3
Cardon, L.R.4
Gayan, J.5
Knopik, V.S.6
Olson, R.K.7
DeFries, J.C.8
-
26
-
-
34250810249
-
Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia
-
COI: 1:CAS:528:DC%2BD2sXnsVSlurk%3D, PID: 17450541
-
Brkanac Z, Chapman NH, Matsushita MM, Chun L, Nielsen K, Cochrane E, Berninger VW, Wijsman EM, Raskind WH (2007) Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia. Am J Med Genet B Neuropsychiatr Genet. 144B:556–560
-
(2007)
Am J Med Genet B Neuropsychiatr Genet.
, vol.144B
, pp. 556-560
-
-
Brkanac, Z.1
Chapman, N.H.2
Matsushita, M.M.3
Chun, L.4
Nielsen, K.5
Cochrane, E.6
Berninger, V.W.7
Wijsman, E.M.8
Raskind, W.H.9
-
27
-
-
28044465597
-
DCDC2 is associated with reading disability and modulates neuronal development in the brain
-
COI: 1:CAS:528:DC%2BD2MXht1yksLnO, PID: 16278297
-
Meng H, Smith SD, Hager K, Held M, Liu J, Olson RK, Pennington BF, DeFries JC, Gelernter J, O’Reilly-Pol T, Somlo S, Skudlarski P, Shaywitz SE, Shaywitz BA, Marchione K, Wang Y, Paramasivam M, LoTurco JJ, Page GP, Gruen JR (2005) DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc Natl Acad Sci USA 102:17053–17058
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 17053-17058
-
-
Meng, H.1
Smith, S.D.2
Hager, K.3
Held, M.4
Liu, J.5
Olson, R.K.6
Pennington, B.F.7
DeFries, J.C.8
Gelernter, J.9
O’Reilly-Pol, T.10
Somlo, S.11
Skudlarski, P.12
Shaywitz, S.E.13
Shaywitz, B.A.14
Marchione, K.15
Wang, Y.16
Paramasivam, M.17
LoTurco, J.J.18
Page, G.P.19
Gruen, J.R.20
more..
-
28
-
-
29244468273
-
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia
-
COI: 1:CAS:528:DC%2BD28XhslKktQ%3D%3D, PID: 16385449
-
Schumacher J, Anthoni H, Dahdouh F, Konig IR, Hillmer AM, Kluck N, Manthey M, Plume E, Warnke A, Remschmidt H, Hulsmann J, Cichon S, Lindgren CM, Propping P, Zucchelli M, Ziegler A, Peyrard-Janvid M, Schulte-Korne G, Nothen MM, Kere J (2006) Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. Am J Hum Genet 78:52–62
-
(2006)
Am J Hum Genet
, vol.78
, pp. 52-62
-
-
Schumacher, J.1
Anthoni, H.2
Dahdouh, F.3
Konig, I.R.4
Hillmer, A.M.5
Kluck, N.6
Manthey, M.7
Plume, E.8
Warnke, A.9
Remschmidt, H.10
Hulsmann, J.11
Cichon, S.12
Lindgren, C.M.13
Propping, P.14
Zucchelli, M.15
Ziegler, A.16
Peyrard-Janvid, M.17
Schulte-Korne, G.18
Nothen, M.M.19
Kere, J.20
more..
-
29
-
-
84880278604
-
Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment
-
COI: 1:CAS:528:DC%2BC3sXptFOlsb8%3D, PID: 23746548
-
Powers NR, Eicher JD, Butter F, Kong Y, Miller LL, Ring SM, Mann M, Gruen JR (2013) Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment. Am J Hum Genet 93:19–28
-
(2013)
Am J Hum Genet
, vol.93
, pp. 19-28
-
-
Powers, N.R.1
Eicher, J.D.2
Butter, F.3
Kong, Y.4
Miller, L.L.5
Ring, S.M.6
Mann, M.7
Gruen, J.R.8
-
30
-
-
60549095658
-
The role of gene DCDC2 in German dyslexics
-
COI: 1:STN:280:DC%2BD1MzksVegsQ%3D%3D, PID: 19238550
-
Wilcke A, Weissfuss J, Kirsten H, Wolfram G, Boltze J, Ahnert P (2009) The role of gene DCDC2 in German dyslexics. Ann Dyslexia. 59:1–11
-
(2009)
Ann Dyslexia.
, vol.59
, pp. 1-11
-
-
Wilcke, A.1
Weissfuss, J.2
Kirsten, H.3
Wolfram, G.4
Boltze, J.5
Ahnert, P.6
-
31
-
-
84655169217
-
DCDC2 genetic variants and susceptibility to developmental dyslexia
-
COI: 1:CAS:528:DC%2BC38XktVKgu7k%3D, PID: 21881542
-
Marino C, Meng H, Mascheretti S, Rusconi M, Cope N, Giorda R, Molteni M, Gruen JR (2012) DCDC2 genetic variants and susceptibility to developmental dyslexia. Psychiatr Genet 22:25–30
-
(2012)
Psychiatr Genet
, vol.22
, pp. 25-30
-
-
Marino, C.1
Meng, H.2
Mascheretti, S.3
Rusconi, M.4
Cope, N.5
Giorda, R.6
Molteni, M.7
Gruen, J.R.8
-
32
-
-
79952443636
-
Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects
-
COI: 1:STN:280:DC%2BC3M7kslCgtw%3D%3D, PID: 21165691
-
Newbury DF, Paracchini S, Scerri TS, Winchester L, Addis L, Richardson AJ, Walter J, Stein JF, Talcott JB, Monaco AP (2011) Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. Behav Genet 41:90–104
-
(2011)
Behav Genet
, vol.41
, pp. 90-104
-
-
Newbury, D.F.1
Paracchini, S.2
Scerri, T.S.3
Winchester, L.4
Addis, L.5
Richardson, A.J.6
Walter, J.7
Stein, J.F.8
Talcott, J.B.9
Monaco, A.P.10
-
33
-
-
84864415162
-
Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability
-
COI: 1:CAS:528:DC%2BC38Xht1GktrjK, PID: 22750057
-
Cope N, Eicher JD, Meng H, Gibson CJ, Hager K, Lacadie C, Fulbright RK, Constable RT, Page GP, Gruen JR (2012) Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability. Neuroimage. 63:148–156
-
(2012)
Neuroimage.
, vol.63
, pp. 148-156
-
-
Cope, N.1
Eicher, J.D.2
Meng, H.3
Gibson, C.J.4
Hager, K.5
Lacadie, C.6
Fulbright, R.K.7
Constable, R.T.8
Page, G.P.9
Gruen, J.R.10
-
34
-
-
33845246158
-
Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia
-
COI: 1:CAS:528:DC%2BD28Xht1ClsLzE, PID: 17033633, (1061)
-
Harold D, Paracchini S, Scerri T, Dennis M, Cope N, Hill G, Moskvina V, Walter J, Richardson AJ, Owen MJ, Stein JF, Green ED, O’Donovan MC, Williams J, Monaco AP (2006) Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Mol Psychiatry. 11:1085–1091 (1061)
-
(2006)
Mol Psychiatry.
, vol.11
, pp. 1085-1091
-
-
Harold, D.1
Paracchini, S.2
Scerri, T.3
Dennis, M.4
Cope, N.5
Hill, G.6
Moskvina, V.7
Walter, J.8
Richardson, A.J.9
Owen, M.J.10
Stein, J.F.11
Green, E.D.12
O’Donovan, M.C.13
Williams, J.14
Monaco, A.P.15
-
35
-
-
84872489568
-
Meta-analysis of the association between DCDC2 polymorphisms and risk of dyslexia
-
COI: 1:CAS:528:DC%2BC3sXjvVGjtg%3D%3D, PID: 23229871
-
Zhong R, Yang B, Tang H, Zou L, Song R, Zhu LQ, Miao X (2013) Meta-analysis of the association between DCDC2 polymorphisms and risk of dyslexia. Mol Neurobiol 47:435–442
-
(2013)
Mol Neurobiol
, vol.47
, pp. 435-442
-
-
Zhong, R.1
Yang, B.2
Tang, H.3
Zou, L.4
Song, R.5
Zhu, L.Q.6
Miao, X.7
-
36
-
-
55349131289
-
Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample
-
PID: 18810304
-
Ludwig KU, Roeske D, Schumacher J, Schulte-Korne G, Konig IR, Warnke A, Plume E, Ziegler A, Remschmidt H, Muller-Myhsok B, Nothen MM, Hoffmann P (2008) Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample. J Neural Transm. 115:1587–1589
-
(2008)
J Neural Transm.
, vol.115
, pp. 1587-1589
-
-
Ludwig, K.U.1
Roeske, D.2
Schumacher, J.3
Schulte-Korne, G.4
Konig, I.R.5
Warnke, A.6
Plume, E.7
Ziegler, A.8
Remschmidt, H.9
Muller-Myhsok, B.10
Nothen, M.M.11
Hoffmann, P.12
-
37
-
-
79951807749
-
Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population
-
COI: 1:CAS:528:DC%2BC3MXks1Kgt78%3D, PID: 20846247
-
Paracchini S, Ang QW, Stanley FJ, Monaco AP, Pennell CE, Whitehouse AJ (2011) Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population. Genes Brain Behav. 10:158–165
-
(2011)
Genes Brain Behav.
, vol.10
, pp. 158-165
-
-
Paracchini, S.1
Ang, Q.W.2
Stanley, F.J.3
Monaco, A.P.4
Pennell, C.E.5
Whitehouse, A.J.6
-
38
-
-
84898824897
-
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort
-
COI: 1:CAS:528:DC%2BC3sXhsVCqu77I, PID: 24022301
-
Becker J, Czamara D, Scerri TS, Ramus F, Csepe V, Talcott JB, Stein J, Morris A, Ludwig KU, Hoffmann P, Honbolygo F, Toth D, Fauchereau F, Bogliotti C, Iannuzzi S, Chaix Y, Valdois S, Billard C, George F, Soares-Boucaud I, Gerard CL, van der Mark S, Schulz E, Vaessen A, Maurer U, Lohvansuu K, Lyytinen H, Zucchelli M, Brandeis D, Blomert L, Leppanen PH, Bruder J, Monaco AP, Muller-Myhsok B, Kere J, Landerl K, Nothen MM, Schulte-Korne G, Paracchini S, Peyrard-Janvid M, Schumacher J (2014) Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. Eur J Hum Genet 22:675–680
-
(2014)
Eur J Hum Genet
, vol.22
, pp. 675-680
-
-
Becker, J.1
Czamara, D.2
Scerri, T.S.3
Ramus, F.4
Csepe, V.5
Talcott, J.B.6
Stein, J.7
Morris, A.8
Ludwig, K.U.9
Hoffmann, P.10
Honbolygo, F.11
Toth, D.12
Fauchereau, F.13
Bogliotti, C.14
Iannuzzi, S.15
Chaix, Y.16
Valdois, S.17
Billard, C.18
George, F.19
Soares-Boucaud, I.20
Gerard, C.L.21
van der Mark, S.22
Schulz, E.23
Vaessen, A.24
Maurer, U.25
Lohvansuu, K.26
Lyytinen, H.27
Zucchelli, M.28
Brandeis, D.29
Blomert, L.30
Leppanen, P.H.31
Bruder, J.32
Monaco, A.P.33
Muller-Myhsok, B.34
Kere, J.35
Landerl, K.36
Nothen, M.M.37
Schulte-Korne, G.38
Paracchini, S.39
Peyrard-Janvid, M.40
Schumacher, J.41
more..
-
39
-
-
67651048992
-
Association of attention-deficit/hyperactivity disorder with a candidate region for reading disabilities on chromosome 6p
-
COI: 1:CAS:528:DC%2BD1MXptlWks7k%3D, PID: 19362708
-
Couto JM, Gomez L, Wigg K, Ickowicz A, Pathare T, Malone M, Kennedy JL, Schachar R, Barr CL (2009) Association of attention-deficit/hyperactivity disorder with a candidate region for reading disabilities on chromosome 6p. Biol Psychiatry 66:368–375
-
(2009)
Biol Psychiatry
, vol.66
, pp. 368-375
-
-
Couto, J.M.1
Gomez, L.2
Wigg, K.3
Ickowicz, A.4
Pathare, T.5
Malone, M.6
Kennedy, J.L.7
Schachar, R.8
Barr, C.L.9
-
40
-
-
40949114128
-
Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog DCDC2 in the rat
-
COI: 1:CAS:528:DC%2BD1cXktFCntLk%3D, PID: 18313856
-
Burbridge TJ, Wang Y, Volz AJ, Peschansky VJ, Lisann L, Galaburda AM, Lo Turco JJ, Rosen GD (2008) Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog DCDC2 in the rat. Neuroscience 152:723–733
-
(2008)
Neuroscience
, vol.152
, pp. 723-733
-
-
Burbridge, T.J.1
Wang, Y.2
Volz, A.J.3
Peschansky, V.J.4
Lisann, L.5
Galaburda, A.M.6
Lo Turco, J.J.7
Rosen, G.D.8
-
41
-
-
79952443927
-
A dyslexia-associated variant in DCDC2 changes gene expression
-
PID: 21042874
-
Meng H, Powers NR, Tang L, Cope NA, Zhang PX, Fuleihan R, Gibson C, Page GP, Gruen JR (2011) A dyslexia-associated variant in DCDC2 changes gene expression. Behav Genet 41:58–66
-
(2011)
Behav Genet
, vol.41
, pp. 58-66
-
-
Meng, H.1
Powers, N.R.2
Tang, L.3
Cope, N.A.4
Zhang, P.X.5
Fuleihan, R.6
Gibson, C.7
Page, G.P.8
Gruen, J.R.9
-
42
-
-
0027989796
-
Prospective investigation of the effects of socioeconomic disadvantage, life stress, and social support on early adolescent adjustment
-
COI: 1:STN:280:DyaK2M%2FhsFaluw%3D%3D, PID: 7930051
-
DuBois DL, Felner RD, Meares H, Krier M (1994) Prospective investigation of the effects of socioeconomic disadvantage, life stress, and social support on early adolescent adjustment. J Abnorm Psychol 103:511–522
-
(1994)
J Abnorm Psychol
, vol.103
, pp. 511-522
-
-
DuBois, D.L.1
Felner, R.D.2
Meares, H.3
Krier, M.4
-
43
-
-
0037438651
-
Socioeconomic inequalities in depression: a meta-analysis
-
COI: 1:STN:280:DC%2BD3s%2FhsFemuw%3D%3D, PID: 12522017
-
Lorant V, Deliege D, Eaton W, Robert A, Philippot P, Ansseau M (2003) Socioeconomic inequalities in depression: a meta-analysis. Am J Epidemiol 157:98–112
-
(2003)
Am J Epidemiol
, vol.157
, pp. 98-112
-
-
Lorant, V.1
Deliege, D.2
Eaton, W.3
Robert, A.4
Philippot, P.5
Ansseau, M.6
-
44
-
-
79951813841
-
Cross-national comparison of the link between socioeconomic status and emotional and behavioral problems in youths
-
PID: 20165830
-
van Oort FV, van der Ende J, Wadsworth ME, Verhulst FC, Achenbach TM (2011) Cross-national comparison of the link between socioeconomic status and emotional and behavioral problems in youths. Soc Psychiatry Psychiatr Epidemiol 46:167–172
-
(2011)
Soc Psychiatry Psychiatr Epidemiol
, vol.46
, pp. 167-172
-
-
van Oort, F.V.1
van der Ende, J.2
Wadsworth, M.E.3
Verhulst, F.C.4
Achenbach, T.M.5
-
45
-
-
31544452078
-
Explaining the link between low socioeconomic status and psychopathology: testing two mechanisms of the social causation hypothesis
-
PID: 16392987
-
Wadsworth ME, Achenbach TM (2005) Explaining the link between low socioeconomic status and psychopathology: testing two mechanisms of the social causation hypothesis. J Consult Clin Psychol 73:1146–1153
-
(2005)
J Consult Clin Psychol
, vol.73
, pp. 1146-1153
-
-
Wadsworth, M.E.1
Achenbach, T.M.2
-
47
-
-
33745429086
-
The Italian preadolescent mental health project (PrISMA): rationale and methods
-
PID: 16676683
-
Frigerio A, Vanzin L, Pastore V, Nobile M, Giorda R, Marino C, Molteni M, Rucci P, Ammaniti M, Lucarelli L, Lenti C, Walder M, Martinuzzi A, Carlet O, Muratori F, Milone A, Zuddas A, Cavolina P, Nardocci F, Tullini A, Morosini P, Polidori G, De Girolamo G (2006) The Italian preadolescent mental health project (PrISMA): rationale and methods. Int J Methods Psychiatr Res. 15:22–35
-
(2006)
Int J Methods Psychiatr Res.
, vol.15
, pp. 22-35
-
-
Frigerio, A.1
Vanzin, L.2
Pastore, V.3
Nobile, M.4
Giorda, R.5
Marino, C.6
Molteni, M.7
Rucci, P.8
Ammaniti, M.9
Lucarelli, L.10
Lenti, C.11
Walder, M.12
Martinuzzi, A.13
Carlet, O.14
Muratori, F.15
Milone, A.16
Zuddas, A.17
Cavolina, P.18
Nardocci, F.19
Tullini, A.20
Morosini, P.21
Polidori, G.22
De Girolamo, G.23
more..
-
48
-
-
40449112527
-
Multicultural assessment of child and adolescent psychopathology with ASEBA and SDQ instruments: research findings, applications, and future directions
-
PID: 18333930
-
Achenbach TM, Becker A, Dopfner M, Heiervang E, Roessner V, Steinhausen HC, Rothenberger A (2008) Multicultural assessment of child and adolescent psychopathology with ASEBA and SDQ instruments: research findings, applications, and future directions. J Child Psychol Psychiatry 49:251–275
-
(2008)
J Child Psychol Psychiatry
, vol.49
, pp. 251-275
-
-
Achenbach, T.M.1
Becker, A.2
Dopfner, M.3
Heiervang, E.4
Roessner, V.5
Steinhausen, H.C.6
Rothenberger, A.7
-
50
-
-
72449140613
-
A conceptual and empirical examination of justifications for dichotomization
-
PID: 19968397
-
DeCoster J, Iselin AM, Gallucci M (2009) A conceptual and empirical examination of justifications for dichotomization. Psychol Methods 14:349–366
-
(2009)
Psychol Methods
, vol.14
, pp. 349-366
-
-
DeCoster, J.1
Iselin, A.M.2
Gallucci, M.3
-
51
-
-
35348901386
-
Socioeconomic status mediates the genetic contribution of the dopamine receptor D4 and serotonin transporter linked promoter region repeat polymorphisms to externalization in preadolescence
-
PID: 17931440
-
Nobile M, Giorda R, Marino C, Carlet O, Pastore V, Vanzin L, Bellina M, Molteni M, Battaglia M (2007) Socioeconomic status mediates the genetic contribution of the dopamine receptor D4 and serotonin transporter linked promoter region repeat polymorphisms to externalization in preadolescence. Dev Psychopathol 19:1147–1160
-
(2007)
Dev Psychopathol
, vol.19
, pp. 1147-1160
-
-
Nobile, M.1
Giorda, R.2
Marino, C.3
Carlet, O.4
Pastore, V.5
Vanzin, L.6
Bellina, M.7
Molteni, M.8
Battaglia, M.9
-
52
-
-
77956974398
-
COMT Val158Met polymorphism and socioeconomic status interact to predict attention deficit/hyperactivity problems in children aged 10–14
-
PID: 19946720
-
Nobile M, Rusconi M, Bellina M, Marino C, Giorda R, Carlet O, Vanzin L, Molteni M, Battaglia M (2010) COMT Val158Met polymorphism and socioeconomic status interact to predict attention deficit/hyperactivity problems in children aged 10–14. Eur Child Adolesc Psychiatry 19:549–557
-
(2010)
Eur Child Adolesc Psychiatry
, vol.19
, pp. 549-557
-
-
Nobile, M.1
Rusconi, M.2
Bellina, M.3
Marino, C.4
Giorda, R.5
Carlet, O.6
Vanzin, L.7
Molteni, M.8
Battaglia, M.9
-
53
-
-
84890471620
-
Testing Hardy–Weinberg equilibrium with a simple root-mean-square statistic
-
PID: 23975799
-
Ward R, Carroll RJ (2014) Testing Hardy–Weinberg equilibrium with a simple root-mean-square statistic. Biostatistics. 15:74–86
-
(2014)
Biostatistics.
, vol.15
, pp. 74-86
-
-
Ward, R.1
Carroll, R.J.2
-
54
-
-
79952442429
-
Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia
-
PID: 21046216
-
Marino C, Mascheretti S, Riva V, Cattaneo F, Rigoletto C, Rusconi M, Gruen JR, Giorda R, Lazazzera C, Molteni M (2011) Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia. Behav Genet 41:67–76
-
(2011)
Behav Genet
, vol.41
, pp. 67-76
-
-
Marino, C.1
Mascheretti, S.2
Riva, V.3
Cattaneo, F.4
Rigoletto, C.5
Rusconi, M.6
Gruen, J.R.7
Giorda, R.8
Lazazzera, C.9
Molteni, M.10
-
55
-
-
0027244611
-
An epidemiological study of disorders in late childhood and adolescence. I. Age- and gender-specific prevalence
-
COI: 1:STN:280:DyaK2c%2FhtlWrsA%3D%3D, PID: 8408371
-
Cohen P, Cohen J, Kasen S, Velez CN, Hartmark C, Johnson J, Rojas M, Brook J, Streuning EL (1993) An epidemiological study of disorders in late childhood and adolescence. I. Age- and gender-specific prevalence. J Child Psychol Psychiatry 34:851–867
-
(1993)
J Child Psychol Psychiatry
, vol.34
, pp. 851-867
-
-
Cohen, P.1
Cohen, J.2
Kasen, S.3
Velez, C.N.4
Hartmark, C.5
Johnson, J.6
Rojas, M.7
Brook, J.8
Streuning, E.L.9
-
56
-
-
0033194456
-
A multivariate model of gender differences in adolescents’ internalizing and externalizing problems
-
COI: 1:STN:280:DyaK1MvitFeqtA%3D%3D, PID: 10493653
-
Leadbeater BJ, Kuperminc GP, Blatt SJ, Hertzog C (1999) A multivariate model of gender differences in adolescents’ internalizing and externalizing problems. Dev Psychol 35:1268–1282
-
(1999)
Dev Psychol
, vol.35
, pp. 1268-1282
-
-
Leadbeater, B.J.1
Kuperminc, G.P.2
Blatt, S.J.3
Hertzog, C.4
-
57
-
-
0034105851
-
Developmental brain anomalies in children with attention-deficit hyperactivity disorder
-
COI: 1:STN:280:DC%2BD3c7lvVCnsA%3D%3D, PID: 10695895
-
Nopoulos P, Berg S, Castellenos FX, Delgado A, Andreasen NC, Rapoport JL (2000) Developmental brain anomalies in children with attention-deficit hyperactivity disorder. J Child Neurol 15:102–108
-
(2000)
J Child Neurol
, vol.15
, pp. 102-108
-
-
Nopoulos, P.1
Berg, S.2
Castellenos, F.X.3
Delgado, A.4
Andreasen, N.C.5
Rapoport, J.L.6
-
58
-
-
0036512920
-
Economic pressure in African American families: a replication and extension of the family stress model
-
PID: 11881755
-
Conger RD, Wallace LE, Sun Y, Simons RL, McLoyd VC, Brody GH (2002) Economic pressure in African American families: a replication and extension of the family stress model. Dev Psychol 38:179–193
-
(2002)
Dev Psychol
, vol.38
, pp. 179-193
-
-
Conger, R.D.1
Wallace, L.E.2
Sun, Y.3
Simons, R.L.4
McLoyd, V.C.5
Brody, G.H.6
-
59
-
-
29544431601
-
Animal models that elucidate basic principles of the developmental origins of adult diseases
-
COI: 1:CAS:528:DC%2BD2MXht12nu7nN, PID: 16391433
-
Nathanielsz PW (2006) Animal models that elucidate basic principles of the developmental origins of adult diseases. ILAR J 47:73–82
-
(2006)
ILAR J
, vol.47
, pp. 73-82
-
-
Nathanielsz, P.W.1
-
60
-
-
77951256752
-
Progress towards a cellular neurobiology of reading disability
-
COI: 1:CAS:528:DC%2BC3cXksFCmtrg%3D, PID: 19616627
-
Gabel LA, Gibson CJ, Gruen JR, LoTurco JJ (2010) Progress towards a cellular neurobiology of reading disability. Neurobiol Dis 38:173–180
-
(2010)
Neurobiol Dis
, vol.38
, pp. 173-180
-
-
Gabel, L.A.1
Gibson, C.J.2
Gruen, J.R.3
LoTurco, J.J.4
-
61
-
-
33745745579
-
Why sex matters for neuroscience
-
COI: 1:CAS:528:DC%2BD28Xkslelu7g%3D, PID: 16688123
-
Cahill L (2006) Why sex matters for neuroscience. Nat Rev Neurosci 7:477–484
-
(2006)
Nat Rev Neurosci
, vol.7
, pp. 477-484
-
-
Cahill, L.1
|