-
2
-
-
77149136734
-
Molecular genetics of attention deficit hyperactivity disorder
-
Faraone SV, Mick E: Molecular genetics of attention deficit hyperactivity disorder. Psychiatr Clin North Am 2010; 33: 159-180
-
(2010)
Psychiatr Clin North Am
, vol.33
, pp. 159-180
-
-
Faraone, S.V.1
Mick, E.2
-
3
-
-
0034237530
-
Attention-deficit disorder and conduct disorder in girls: Evidence for a familial subtype
-
Faraone SV, Biederman J, Monuteaux MC: Attention-deficit disorder and conduct disorder in girls: evidence for a familial subtype. Biol Psychiatry 2000; 48: 21-29
-
(2000)
Biol Psychiatry
, vol.48
, pp. 21-29
-
-
Faraone, S.V.1
Biederman, J.2
Monuteaux, M.C.3
-
4
-
-
84863116701
-
Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: The role of rare variants and duplications at 15q13.3
-
Williams NM, Franke B, Mick E, Anney RJL, Freitag CM, Gill M, Thapar A, O'Donovan MC, Owen MJ, Holmans P, Kent L,Middleton F, Zhang-James Y, Liu L, Meyer J, Nguyen TT, Romanos J, Romanos M, Seitz C, Renner TJ, Walitza S, Warnke A, Palmason H, Buitelaar J, Rommelse N, Vasquez AA, Hawi Z, Langley K, Sergeant J, Steinhausen HC, Roeyers H, Biederman J, Zaharieva I, Hakonarson H, Elia J, Lionel AC, Crosbie J, Marshall CR, Schachar R, Scherer SW, Todorov A, Smalley SL, Loo S, Nelson S, Shtir C, Asherson P, Reif A, Lesch KP, Faraone SV: Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. Am J Psychiatry 2012; 169: 195-204
-
(2012)
Am J Psychiatry
, vol.169
, pp. 195-204
-
-
Williams, N.M.1
Franke, B.2
Mick, E.3
Anney, R.J.L.4
Freitag, C.M.5
Gill, M.6
Thapar, A.7
O'Donovan, M.C.8
Owen, M.J.9
Holmans, P.10
Kent Lmiddleton, F.11
Zhang-James, Y.12
Liu, L.13
Meyer, J.14
Nguyen, T.T.15
Romanos, J.16
Romanos, M.17
Seitz, C.18
Renner, T.J.19
Walitza, S.20
Warnke, A.21
Palmason, H.22
Buitelaar, J.23
Rommelse, N.24
Vasquez, A.A.25
Hawi, Z.26
Langley, K.27
Sergeant, J.28
Steinhausen, H.C.29
Roeyers, H.30
Biederman, J.31
Zaharieva, I.32
Hakonarson, H.33
Elia, J.34
Lionel, A.C.35
Crosbie, J.36
Marshall, C.R.37
Schachar, R.38
Scherer, S.W.39
Todorov, A.40
Smalley, S.L.41
Loo, S.42
Nelson, S.43
Shtir, C.44
Asherson, P.45
Reif, A.46
Lesch, K.P.47
Faraone, S.V.48
more..
-
5
-
-
84863116416
-
Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD
-
deCODE Genetics; Psychiatric GWAS Consortium
-
Stergiakouli E, Hamshere M, Holmans P, Langley K, Zaharieva I, Hawi Z, Kent L, Gill M, Williams N, Owen MJ, O'Donovan M, Thapar A; deCODE Genetics; Psychiatric GWAS Consortium: Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. Am J Psychiatry 2012; 169: 186-194
-
(2012)
Am J Psychiatry
, vol.169
, pp. 186-194
-
-
Stergiakouli, E.1
Hamshere, M.2
Holmans, P.3
Langley, K.4
Zaharieva, I.5
Hawi, Z.6
Kent, L.7
Gill, M.8
Williams, N.9
Owen, M.J.10
O'Donovan, M.11
Thapar, A.12
-
6
-
-
78049303903
-
Rare chromosomal deletions and duplications in attentiondeficit hyperactivity disorder: A genome-wide analysis
-
Williams NM, Zaharieva I, Martin A, Langley K, Mantripragada K, Fossdal R, Stefansson H, Stefansson K,Magnusson P, Gudmundsson OO, Gustafsson O, Holmans P, Owen MJ, O'Donovan M, Thapar A: Rare chromosomal deletions and duplications in attentiondeficit hyperactivity disorder: a genome-wide analysis. Lancet 2010; 376: 1401-1408
-
(2010)
Lancet
, vol.376
, pp. 1401-1408
-
-
Williams, N.M.1
Zaharieva, I.2
Martin, A.3
Langley, K.4
Mantripragada, K.5
Fossdal, R.6
Stefansson, H.7
Stefansson, K.8
Magnusson, P.9
Gudmundsson, O.O.10
Gustafsson, O.11
Holmans, P.12
Owen, M.J.13
O'Donovan, M.14
Thapar, A.15
-
7
-
-
79955470881
-
Genome-wide copy number variation analysis in attention-deficit/ hyperactivity disorder: Association with neuropeptide y gene dosage in an extended pedigree
-
Lesch KP, Selch S, Renner TJ, Jacob C, Nguyen TT, Hahn T, Romanos M, Walitza S, Shoichet S, Dempfle A, Heine M, Boreatti- Hümmer A, Romanos J, Gross-Lesch S, Zerlaut H, Wultsch T, Heinzel S, Fassnacht M, Fallgatter A, Allolio B, Schäfer H, Warnke A, Reif A, Ropers HH, Ullmann R: Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree. Mol Psychiatry 2011; 16: 491-503
-
(2011)
Mol Psychiatry
, vol.16
, pp. 491-503
-
-
Lesch, K.P.1
Selch, S.2
Renner, T.J.3
Jacob, C.4
Nguyen, T.T.5
Hahn, T.6
Romanos, M.7
Walitza, S.8
Shoichet, S.9
Dempfle, A.10
Heine, M.11
Boreatti-Hümmer, A.12
Romanos, J.13
Gross-Lesch, S.14
Zerlaut, H.15
Wultsch, T.16
Heinzel, S.17
Fassnacht, M.18
Fallgatter, A.19
Allolio, B.20
Schäfer, H.21
Warnke, A.22
Reif, A.23
Ropers, H.H.24
Ullmann, R.25
more..
-
8
-
-
77956178166
-
Meta-analysis of genome-wide association studies of attention-deficit/ hyperactivity disorder
-
Psychiatric GWAS Consortium ADHD Subgroup
-
Neale BM, Medland SE, Ripke S, Asherson P, Franke B, Lesch KP, Faraone SV, Nguyen TT, Schäfer H, Holmans P, Daly M, Steinhausen HC, Freitag C, Reif A, Renner TJ, Romanos M, Romanos J, Walitza S, Warnke A, Meyer J, Palmason H, Buitelaar J, Vasquez AA, Lambregts-Rommelse N, Gill M, Anney RJ, Langely K, O'Donovan M, Williams N, Owen M, Thapar A, Kent L, Sergeant J, Roeyers H, Mick E, Biederman J, Doyle A, Smalley S, Loo S, Hakonarson H, Elia J, Todorov A, Miranda A, Mulas F, Ebstein RP, Rothenberger A, Banaschewski T, Oades RD, Sonuga-Barke E, McGough J, Nisenbaum L, Middleton F, Hu X, Nelson S; Psychiatric GWAS Consortium, ADHD Subgroup: Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry 2010; 49: 884-897
-
(2010)
J Am Acad Child Adolesc Psychiatry
, vol.49
, pp. 884-897
-
-
Neale, B.M.1
Medland, S.E.2
Ripke, S.3
Asherson, P.4
Franke, B.5
Lesch, K.P.6
Faraone, S.V.7
Nguyen, T.T.8
Schäfer, H.9
Holmans, P.10
Daly, M.11
Steinhausen, H.C.12
Freitag, C.13
Reif, A.14
Renner, T.J.15
Romanos, M.16
Romanos, J.17
Walitza, S.18
Warnke, A.19
Meyer, J.20
Palmason, H.21
Buitelaar, J.22
Vasquez, A.A.23
Lambregts-Rommelse, N.24
Gill, M.25
Anney, R.J.26
Langely, K.27
O'Donovan, M.28
Williams, N.29
Owen, M.30
Thapar, A.31
Kent, L.32
Sergeant, J.33
Roeyers, H.34
Mick, E.35
Biederman, J.36
Doyle, A.37
Smalley, S.38
Loo, S.39
Hakonarson, H.40
Elia, J.41
Todorov, A.42
Miranda, A.43
Mulas, F.44
Ebstein, R.P.45
Rothenberger, A.46
Banaschewski, T.47
Oades, R.D.48
Sonuga-Barke, E.49
McGough, J.50
Nisenbaum, L.51
Middleton, F.52
Hu, X.53
Nelson, S.54
more..
-
9
-
-
67651113905
-
Genome-wide association studies in ADHD
-
Franke B, Neale BM, Faraone SV: Genome-wide association studies in ADHD. Hum Genet 2009; 126: 13-50
-
(2009)
Hum Genet
, vol.126
, pp. 13-50
-
-
Franke, B.1
Neale, B.M.2
Faraone, S.V.3
-
10
-
-
84863980709
-
Genetic architectures of psychiatric disorders: The emerging picture and its implications
-
Sullivan PF, Daly MJ, O'Donovan M: Genetic architectures of psychiatric disorders: the emerging picture and its implications. Nat Rev Genet 2012; 13: 537-551
-
(2012)
Nat Rev Genet
, vol.13
, pp. 537-551
-
-
Sullivan, P.F.1
Daly, M.J.2
O'Donovan, M.3
-
11
-
-
77953867567
-
Genomic analysis of mental illness: A changing landscape
-
McClellan J, King MC: Genomic analysis of mental illness: a changing landscape. JAMA 2010; 303: 2523-2524
-
(2010)
JAMA
, vol.303
, pp. 2523-2524
-
-
McClellan, J.1
King, M.C.2
-
12
-
-
84860712363
-
Patterns and rates of exonic de novo mutations in autism spectrum disorders
-
Neale BM, Kou Y, Liu L, Ma'ayan A, Samocha KE, Sabo A, Lin CF, Stevens C, Wang LS, Makarov V, Polak P, Yoon S, Maguire J, Crawford EL, Campbell NG, Geller ET, Valladares O, Schafer C, Liu H, Zhao T, Cai G, Lihm J, Dannenfelser R, Jabado O, Peralta Z, Nagaswamy U, Muzny D, Reid JG, Newsham I, Wu Y, Lewis L, Han Y, Voight BF, Lim E, Rossin E, Kirby A, Flannick J, Fromer M, Shakir K, Fennell T, Garimella K, Banks E, Poplin R, Gabriel S, DePristo M,Wimbish JR, Boone BE, Levy SE, Betancur C, Sunyaev S, Boerwinkle E, BuxbaumJD, Cook EH Jr, Devlin B, Gibbs RA, Roeder K, Schellenberg GD, Sutcliffe JS, Daly MJ: Patterns and rates of exonic de novo mutations in autism spectrum disorders. Nature 2012; 485: 242-245
-
(2012)
Nature
, vol.485
, pp. 242-245
-
-
Neale, B.M.1
Kou, Y.2
Liu, L.3
Ma'Ayan, A.4
Samocha, K.E.5
Sabo, A.6
Lin, C.F.7
Stevens, C.8
Wang, L.S.9
Makarov, V.10
Polak, P.11
Yoon, S.12
Maguire, J.13
Crawford, E.L.14
Campbell, N.G.15
Geller, E.T.16
Valladares, O.17
Schafer, C.18
Liu, H.19
Zhao, T.20
Cai, G.21
Lihm, J.22
Dannenfelser, R.23
Jabado, O.24
Peralta, Z.25
Nagaswamy, U.26
Muzny, D.27
Reid, J.G.28
Newsham, I.29
Wu, Y.30
Lewis, L.31
Han, Y.32
Voight, B.F.33
Lim, E.34
Rossin, E.35
Kirby, A.36
Flannick, J.37
Fromer, M.38
Shakir, K.39
Fennell, T.40
Garimella, K.41
Banks, E.42
Poplin, R.43
Gabriel, S.44
Depristo, M.45
Wimbish, J.R.46
Boone, B.E.47
Levy, S.E.48
Betancur, C.49
Sunyaev, S.50
Boerwinkle, E.51
Buxbaum, J.D.52
Cook Jr., E.H.53
Devlin, B.54
Gibbs, R.A.55
Roeder, K.56
Schellenberg, G.D.57
Sutcliffe, J.S.58
Daly, M.J.59
more..
-
13
-
-
84860780495
-
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
-
Sanders SJ, Murtha MT, Gupta AR, Murdoch JD, Raubeson MJ, Willsey AJ, Ercan-Sencicek AG, DiLullo NM, Parikshak NN, Stein JL, Walker MF, Ober GT, Teran NA, Song Y, El-Fishawy P, Murtha RC, Choi M, Overton JD, Bjornson RD, Carriero NJ, Meyer KA, Bilguvar K, Mane SM, Sestan N, Lifton RP, Günel M, Roeder K, Geschwind DH, Devlin B, State MW: De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Nature 2012; 485: 237-241
-
(2012)
Nature
, vol.485
, pp. 237-241
-
-
Sanders, S.J.1
Murtha, M.T.2
Gupta, A.R.3
Murdoch, J.D.4
Raubeson, M.J.5
Willsey, A.J.6
Ercan-Sencicek, A.G.7
Dilullo, N.M.8
Parikshak, N.N.9
Stein, J.L.10
Walker, M.F.11
Ober, G.T.12
Teran, N.A.13
Song, Y.14
El-Fishawy, P.15
Murtha, R.C.16
Choi, M.17
Overton, J.D.18
Bjornson, R.D.19
Carriero, N.J.20
Meyer, K.A.21
Bilguvar, K.22
Mane, S.M.23
Sestan, N.24
Lifton, R.P.25
Günel, M.26
Roeder, K.27
Geschwind, D.H.28
Devlin, B.29
State, M.W.30
more..
-
14
-
-
84860741138
-
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
-
O'Roak BJ, Vives L, Girirajan S, Karakoc E, Krumm N, Coe BP, Levy R, Ko A, Lee C, Smith JD, Turner EH, Stanaway IB, Vernot B, Malig M, Baker C, Reilly B, Akey JM, Borenstein E, Rieder MJ, Nickerson DA, Bernier R, Shendure J, Eichler EE: Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Nature 2012; 485: 246-250
-
(2012)
Nature
, vol.485
, pp. 246-250
-
-
O'Roak, B.J.1
Vives, L.2
Girirajan, S.3
Karakoc, E.4
Krumm, N.5
Coe, B.P.6
Levy, R.7
Ko, A.8
Lee, C.9
Smith, J.D.10
Turner, E.H.11
Stanaway, I.B.12
Vernot, B.13
Malig, M.14
Baker, C.15
Reilly, B.16
Akey, J.M.17
Borenstein, E.18
Rieder, M.J.19
Nickerson, D.A.20
Bernier, R.21
Shendure, J.22
Eichler, E.E.23
more..
-
15
-
-
77950859884
-
Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder
-
Rommelse NNJ, Franke B, Geurts HM, Hartman CA, Buitelaar JK: Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder. Eur Child Adolesc Psychiatry 2010; 19: 281-295
-
(2010)
Eur Child Adolesc Psychiatry
, vol.19
, pp. 281-295
-
-
Rommelse, N.N.J.1
Franke, B.2
Geurts, H.M.3
Hartman, C.A.4
Buitelaar, J.K.5
-
16
-
-
79955135758
-
Integrated genome-wide association study findings: Identification of a neurodevelopmental network for attention deficit hyperactivity disorder
-
Poelmans G, Pauls DL, Buitelaar JK, Franke B: Integrated genome-wide association study findings: identification of a neurodevelopmental network for attention deficit hyperactivity disorder. Am J Psychiatry 2011; 168: 365-377
-
(2011)
Am J Psychiatry
, vol.168
, pp. 365-377
-
-
Poelmans, G.1
Pauls, D.L.2
Buitelaar, J.K.3
Franke, B.4
-
18
-
-
0033986057
-
Toward guidelines for pedigree selection in genetic studies of attention deficit hyperactivity disorder
-
Faraone SV, Biederman J, Monuteaux MC: Toward guidelines for pedigree selection in genetic studies of attention deficit hyperactivity disorder. Genet Epidemiol 2000; 18: 1-16
-
(2000)
Genet Epidemiol
, vol.18
, pp. 1-16
-
-
Faraone, S.V.1
Biederman, J.2
Monuteaux, M.C.3
-
19
-
-
0034843635
-
Examining the comorbidity of ADHD-related behaviours and conduct problems using a twin study design
-
Thapar A, Harrington R, McGuffin P: Examining the comorbidity of ADHD-related behaviours and conduct problems using a twin study design. Br J Psychiatry 2001; 179: 224-229
-
(2001)
Br J Psychiatry
, vol.179
, pp. 224-229
-
-
Thapar, A.1
Harrington, R.2
McGuffin, P.3
-
20
-
-
10244265949
-
Genetic and environmental influences on the covariation between hyperactivity and conduct disturbance in juvenile twins
-
Silberg J, Rutter M, Meyer J, Maes H, Hewitt J, Simonoff E, Pickles A, Loeber R, Eaves L: Genetic and environmental influences on the covariation between hyperactivity and conduct disturbance in juvenile twins. J Child Psychol Psychiatry 1996; 37: 803-816
-
(1996)
J Child Psychol Psychiatry
, vol.37
, pp. 803-816
-
-
Silberg, J.1
Rutter, M.2
Meyer, J.3
Maes, H.4
Hewitt, J.5
Simonoff, E.6
Pickles, A.7
Loeber, R.8
Eaves, L.9
-
21
-
-
41149172350
-
Test of alternative hypotheses explaining the comorbidity between attention-deficit/hyperactivity disorder and conduct disorder
-
Rhee SH, Willcutt EG, Hartman CA, Pennington BF, DeFries JC: Test of alternative hypotheses explaining the comorbidity between attention-deficit/ hyperactivity disorder and conduct disorder. J Abnorm Child Psychol 2008; 36: 29-40
-
(2008)
J Abnorm Child Psychol
, vol.36
, pp. 29-40
-
-
Rhee, S.H.1
Willcutt, E.G.2
Hartman, C.A.3
Pennington, B.F.4
Defries, J.C.5
-
23
-
-
80053385384
-
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
-
Psychiatric GWAS Consortium Bipolar Disorder Working Group
-
Sklar P, Ripke S, Scott LJ, Andreassen OA, Cichon S, Craddock N, et al; Psychiatric GWAS Consortium Bipolar Disorder Working Group: Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4. Nat Genet 2011; 43: 977-983
-
(2011)
Nat Genet
, vol.43
, pp. 977-983
-
-
Sklar, P.1
Ripke, S.2
Scott, L.J.3
Andreassen, O.A.4
Cichon, S.5
Craddock, N.6
-
24
-
-
80053384370
-
Genome-wide association study identifies five new schizophrenia loci
-
Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium
-
Ripke S, Sanders AR, Kendler KS, Levinson DF, Sklar P, Holmans PA, et al; Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium: Genome-wide association study identifies five new schizophrenia loci. Nat Genet 2011; 43: 969-976
-
(2011)
Nat Genet
, vol.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
-
25
-
-
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; International Schizophrenia Consortium: 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
Sklar, P.7
-
26
-
-
0029119813
-
The Child and Adolescent Psychiatric Assessment (CAPA)
-
Angold A, Prendergast M, Cox A, Harrington R, Simonoff E, Rutter M: The Child and Adolescent Psychiatric Assessment (CAPA). Psychol Med 1995; 25: 739-753
-
(1995)
Psychol Med
, vol.25
, pp. 739-753
-
-
Angold, A.1
Prendergast, M.2
Cox, A.3
Harrington, R.4
Simonoff, E.5
Rutter, M.6
-
28
-
-
0003860186
-
-
4th ed (WISC-IV): Administration and Scoring Manual. San Antonio, Tex, Psychological Corp
-
Wechsler D: Wechsler Intelligence Scale for Children, 4th ed (WISC-IV): Administration and Scoring Manual. San Antonio, Tex, Psychological Corp, 2003
-
(2003)
Wechsler Intelligence Scale for Children
-
-
Wechsler, D.1
-
29
-
-
0345742555
-
The Child Attention-Deficit Hyperactivity Disorder Teacher Telephone Interview (CHATTI): Reliability and validity
-
Holmes J, Lawson D, Langley K, Fitzpatrick H, Trumper A, Pay H, Harrington R, Thapar A: The Child Attention-Deficit Hyperactivity Disorder Teacher Telephone Interview (CHATTI): reliability and validity. Br J Psychiatry 2004; 184: 74-78
-
(2004)
Br J Psychiatry
, vol.184
, pp. 74-78
-
-
Holmes, J.1
Lawson, D.2
Langley, K.3
Fitzpatrick, H.4
Trumper, A.5
Pay, H.6
Harrington, R.7
Thapar, A.8
-
30
-
-
0000003137
-
Parent and teacher ratings of ADHD symptoms: Psychometric properties in a community-based sample
-
DuPaul G: Parent and teacher ratings of ADHD symptoms: psychometric properties in a community-based sample. J Clin Child Psychol 1991; 20: 245-253
-
(1991)
J Clin Child Psychol
, vol.20
, pp. 245-253
-
-
Dupaul, G.1
-
31
-
-
0014637765
-
A teacher rating scale for use in drug studies with children
-
Conners CK: A teacher rating scale for use in drug studies with children. Am J Psychiatry 1969; 126: 884-888
-
(1969)
Am J Psychiatry
, vol.126
, pp. 884-888
-
-
Conners, C.K.1
-
32
-
-
68749099496
-
Genetic risk for conduct disorder symptom subtypes in an ADHD sample: Specificity to aggressive symptoms
-
Monuteaux MC, Biederman J, Doyle AE, Mick E, Faraone SV: Genetic risk for conduct disorder symptom subtypes in an ADHD sample: specificity to aggressive symptoms. J Am Acad Child Adolesc Psychiatry 2009; 48: 757-764
-
(2009)
J Am Acad Child Adolesc Psychiatry
, vol.48
, pp. 757-764
-
-
Monuteaux, M.C.1
Biederman, J.2
Doyle, A.E.3
Mick, E.4
Faraone, S.V.5
-
33
-
-
0027222817
-
Oppositional defiant disorder and conduct disorder: A meta-analytic review of factor analyses and cross-validation in a clinic sample
-
Frick PJ, Lahey BB, Loeber R, Tannenbaum L, Van Horn Y, Christ MAG, Hart EA, Hanson K: Oppositional defiant disorder and conduct disorder: a meta-analytic review of factor analyses and cross-validation in a clinic sample. Clin Psychol Rev 1993; 13: 319-340
-
(1993)
Clin Psychol Rev
, vol.13
, pp. 319-340
-
-
Frick, P.J.1
Lahey, B.B.2
Loeber, R.3
Tannenbaum, L.4
Van Horn, Y.5
Christ, M.A.G.6
Hart, E.A.7
Hanson, K.8
-
34
-
-
34548292504
-
PLINK: A tool set for whole-genome association and populationbased linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC: PLINK: a tool set for whole-genome association and populationbased 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
Maller, J.7
Sklar, P.8
De Bakker, P.I.9
Daly, M.J.10
Sham, P.C.11
-
36
-
-
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
-
37
-
-
3342933010
-
Do aggressive and non-aggressive antisocial behaviors in adolescents result from the same genetic and environmental effects?
-
Button TMM, Scourfield J, Martin N, McGuffin P: Do aggressive and non-aggressive antisocial behaviors in adolescents result from the same genetic and environmental effects? Am J Med Genet B Neuropsychiatr Genet 2004; 129B: 59-63
-
(2004)
Am J Med Genet B Neuropsychiatr Genet
, vol.129 B
, pp. 59-63
-
-
Button, T.M.M.1
Scourfield, J.2
Martin, N.3
McGuffin, P.4
-
38
-
-
58549109197
-
Autism symptoms in attention-deficit/hyperactivity disorder: A familial trait which correlates with conduct, oppositional defiant, language, and motor disorders
-
Mulligan A, Anney RJ, O'Regan M, Chen W, Butler L, Fitzgerald M, Buitelaar J, Steinhausen HC, Rothenberger A, Minderaa R, Nijmeijer J, Hoekstra PJ, Oades RD, Roeyers H, Buschgens C, Christiansen H, Franke B, Gabriels I, Hartman C, Kuntsi J, Marco R, Meidad S, Mueller U, Psychogiou L, Rommelse N, Thompson M, Uebel H, Banaschewski T, Ebstein R, Eisenberg J, Manor I, Miranda A, Mulas F, Sergeant J, Sonuga-Barke E, Asherson P, Faraone SV, Gill M: Autism symptoms in attention-deficit/hyperactivity disorder: a familial trait which correlates with conduct, oppositional defiant, language, and motor disorders. J Autism Dev Disord 2009; 39: 197-209
-
(2009)
J Autism Dev Disord
, vol.39
, pp. 197-209
-
-
Mulligan, A.1
Anney, R.J.2
O'Regan, M.3
Chen, W.4
Butler, L.5
Fitzgerald, M.6
Buitelaar, J.7
Steinhausen, H.C.8
Rothenberger, A.9
Minderaa, R.10
Nijmeijer, J.11
Hoekstra, P.J.12
Oades, R.D.13
Roeyers, H.14
Buschgens, C.15
Christiansen, H.16
Franke, B.17
Gabriels, I.18
Hartman, C.19
Kuntsi, J.20
Marco, R.21
Meidad, S.22
Mueller, U.23
Psychogiou, L.24
Rommelse, N.25
Thompson, M.26
Uebel, H.27
Banaschewski, T.28
Ebstein, R.29
Eisenberg, J.30
Manor, I.31
Miranda, A.32
Mulas, F.33
Sergeant, J.34
Sonuga-Barke, E.35
Asherson, P.36
Faraone, S.V.37
Gill, M.38
more..
-
39
-
-
39549113876
-
Co-transmission of conduct problems with attention-deficit/hyperactivity disorder: Familial evidence for a distinct disorder
-
Christiansen H, Chen W, Oades RD, Asherson P, Taylor EA, Lasky- Su J, Zhou K, Banaschewski T, Buschgens C, Franke B, Gabriels I, Manor I, Marco R, Müller UC, Mulligan A, Psychogiou L, Rommelse NN, Uebel H, Buitelaar J, Ebstein RP, Eisenberg J, Gill M, Miranda A,Mulas F, Roeyers H, Rothenberger A, Sergeant JA, Sonuga-Barke EJ, Steinhausen HC, Thompson M, Faraone SV: Co-transmission of conduct problems with attention-deficit/hyperactivity disorder: familial evidence for a distinct disorder. J Neural Transm 2008; 115: 163-175
-
(2008)
J Neural Transm
, vol.115
, pp. 163-175
-
-
Christiansen, H.1
Chen, W.2
Oades, R.D.3
Asherson, P.4
Taylor, E.A.5
Lasky-Su, J.6
Zhou, K.7
Banaschewski, T.8
Buschgens, C.9
Franke, B.10
Gabriels, I.11
Manor, I.12
Marco, R.13
Müller, U.C.14
Mulligan, A.15
Psychogiou, L.16
Rommelse, N.N.17
Uebel, H.18
Buitelaar, J.19
Ebstein, R.P.20
Eisenberg, J.21
Gill, M.22
Miranda Amulas, F.23
Roeyers, H.24
Rothenberger, A.25
Sergeant, J.A.26
Sonuga-Barke, E.J.27
Steinhausen, H.C.28
Thompson, M.29
Faraone, S.V.30
more..
-
40
-
-
27744534613
-
Catechol O-methyltransferase gene variant and birth weight predict earlyonset antisocial behavior in children with attention-deficit/hyperactivity disorder
-
Thapar A, Langley K, Fowler T, Rice F, Turic D, Whittinger N, Aggleton J, Van den Bree M, Owen M, O'Donovan M: Catechol O-methyltransferase gene variant and birth weight predict earlyonset antisocial behavior in children with attention-deficit/hyperactivity disorder. Arch Gen Psychiatry 2005; 62: 1275-1278
-
(2005)
Arch Gen Psychiatry
, vol.62
, pp. 1275-1278
-
-
Thapar, A.1
Langley, K.2
Fowler, T.3
Rice, F.4
Turic, D.5
Whittinger, N.6
Aggleton, J.7
Van Den Bree, M.8
Owen, M.9
O'Donovan, M.10
-
41
-
-
38949113693
-
A replicated molecular genetic basis for subtyping antisocial behavior in children with attention-deficit/hyperactivity disorder
-
Caspi A, Langley K, Milne B, Moffitt TE, O'Donovan MC, Owen MJ, Polo Tomas M, Poulton R, Rutter M, Taylor A, Williams B, Thapar A: A replicated molecular genetic basis for subtyping antisocial behavior in children with attention-deficit/hyperactivity disorder. Arch Gen Psychiatry 2008; 65: 203-210
-
(2008)
Arch Gen Psychiatry
, vol.65
, pp. 203-210
-
-
Caspi, A.1
Langley, K.2
Milne, B.3
Moffitt, T.E.4
O'Donovan, M.C.5
Owen, M.J.6
Polo Tomas, M.7
Poulton, R.8
Rutter, M.9
Taylor, A.10
Williams, B.11
Thapar, A.12
-
42
-
-
75149138337
-
Variation in the catechol-O-methyltransferase Val 158 Met polymorphism associated with conduct disorder and ADHD symptoms, among adolescent male delinquents
-
DeYoung CG, Getchell M, Koposov RA, Yrigollen CM, Haeffel GJ, af Klinteberg B, Oreland L, Ruchkin VV, Pakstis AJ, Grigorenko EL: Variation in the catechol-O-methyltransferase Val 158 Met polymorphism associated with conduct disorder and ADHD symptoms, among adolescent male delinquents. Psychiatr Genet 2010; 20: 20-24
-
(2010)
Psychiatr Genet
, vol.20
, pp. 20-24
-
-
Deyoung, C.G.1
Getchell, M.2
Koposov, R.A.3
Yrigollen, C.M.4
Haeffel, G.J.5
Af Klinteberg, B.6
Oreland, L.7
Ruchkin, V.V.8
Pakstis, A.J.9
Grigorenko, E.L.10
-
43
-
-
78649952834
-
Genotype link with extreme antisocial behavior: The contribution of cognitive pathways
-
Langley K, Heron J, O'Donovan MC, Owen MJ, Thapar A: Genotype link with extreme antisocial behavior: the contribution of cognitive pathways. Arch Gen Psychiatry 2010; 67: 1317-1323
-
(2010)
Arch Gen Psychiatry
, vol.67
, pp. 1317-1323
-
-
Langley, K.1
Heron, J.2
O'Donovan, M.C.3
Owen, M.J.4
Thapar, A.5
-
44
-
-
67651121684
-
Candidate gene studies of ADHD: A meta-analytic review
-
Gizer IR, Ficks C, Waldman ID: Candidate gene studies of ADHD: a meta-analytic review. Hum Genet 2009; 126: 51-90
-
(2009)
Hum Genet
, vol.126
, pp. 51-90
-
-
Gizer, I.R.1
Ficks, C.2
Waldman, I.D.3
-
45
-
-
0030917457
-
Child and family factors influencing the clinical referral of children with hyperactivity: A research note
-
Woodward LJ, Dowdney L, Taylor E: Child and family factors influencing the clinical referral of children with hyperactivity: a research note. J Child Psychol Psychiatry 1997; 38: 479-485
-
(1997)
J Child Psychol Psychiatry
, vol.38
, pp. 479-485
-
-
Woodward, L.J.1
Dowdney, L.2
Taylor, E.3
-
46
-
-
79953703116
-
Polygenic dissection of the bipolar phenotype
-
Hamshere ML, O'Donovan MC, Jones IR, Jones L, Kirov G, Green EK, Moskvina V, Grozeva D, Bass N, McQuillin A, Gurling H, St Clair D, Young AH, Ferrier IN, Farmer A, McGuffin P, Sklar P, Purcell S, Holmans PA, Owen MJ, Craddock N: Polygenic dissection of the bipolar phenotype. Br J Psychiatry 2011; 198: 284-288
-
(2011)
Br J Psychiatry
, vol.198
, pp. 284-288
-
-
Hamshere, M.L.1
O'Donovan, M.C.2
Jones, I.R.3
Jones, L.4
Kirov, G.5
Green, E.K.6
Moskvina, V.7
Grozeva, D.8
Bass, N.9
McQuillin, A.10
Gurling, H.11
St Clair, D.12
Young, A.H.13
Ferrier, I.N.14
Farmer, A.15
McGuffin, P.16
Sklar, P.17
Purcell, S.18
Holmans, P.A.19
Owen, M.J.20
Craddock, N.21
more..
-
47
-
-
84865839935
-
Schizophrenia Psychiatric GWAS Consortium: Genome-wide association study of multiplex schizophrenia pedigrees
-
Levinson DF, Shi J, Wang K, Oh S, Riley B, Pulver AE, Wildenauer DB, Laurent C, Mowry BJ, Gejman PV, Owen MJ, Kendler KS, Nestadt G, Schwab SG, Mallet J, Nertney D, Sanders AR, Williams NM,Wormley B, Lasseter VK, Albus M, Godard-Bauché S, Alexander M, Duan J, O'Donovan MC, Walsh D, O'Neill A, Papadimitriou GN, Dikeos D, Maier W, Lerer B, Campion D, Cohen D, Jay M, Fanous A, Eichhammer P, Silverman JM, Norton N, Zhang N, Hakonarson H, Gao C, Citri A, Hansen M, Ripke S, Dudbridge F, Holmans PA; Schizophrenia Psychiatric GWAS Consortium: Genome-wide association study of multiplex schizophrenia pedigrees. Am J Psychiatry 2012; 169: 963-973
-
(2012)
Am J Psychiatry
, vol.169
, pp. 963-973
-
-
Levinson, D.F.1
Shi, J.2
Wang, K.3
Oh, S.4
Riley, B.5
Pulver, A.E.6
Wildenauer, D.B.7
Laurent, C.8
Mowry, B.J.9
Gejman, P.V.10
Owen, M.J.11
Kendler, K.S.12
Nestadt, G.13
Schwab, S.G.14
Mallet, J.15
Nertney, D.16
Sanders, A.R.17
Williams, N.M.18
Wormley, B.19
Lasseter, V.K.20
Albus, M.21
Godard-Bauché, S.22
Alexander, M.23
Duan, J.24
O'Donovan, M.C.25
Walsh, D.26
O'Neill, A.27
Papadimitriou, G.N.28
Dikeos, D.29
Maier, W.30
Lerer, B.31
Campion, D.32
Cohen, D.33
Jay, M.34
Fanous, A.35
Eichhammer, P.36
Silverman, J.M.37
Norton, N.38
Zhang, N.39
Hakonarson, H.40
Gao, C.41
Citri, A.42
Hansen, M.43
Ripke, S.44
Dudbridge, F.45
Holmans, P.A.46
more..
|