-
1
-
-
1642514265
-
The worldwide prevalence of ADHD: Is it an American condition?
-
Faraone SV, Sergeant J, Gillberg C, Biederman J. The worldwide prevalence of ADHD: Is it an American condition? World Psychiatry. 2003;2(2):104-113.
-
(2003)
World Psychiatry
, vol.2
, Issue.2
, pp. 104-113
-
-
Faraone, S.V.1
Sergeant, J.2
Gillberg, C.3
Biederman, J.4
-
2
-
-
0002795435
-
Developmental epidemiology of the disruptive behavior disorders
-
Quay HC, Hogan AE, editors. New York: Kluwer Acedemic/Plenum Publishers
-
Lahey BB, Miller TL, Gordon RA, et al. Developmental epidemiology of the disruptive behavior disorders. In: Quay HC, Hogan AE, editors. Handbook of Disruptive Behavior Disorders. New York: Kluwer Acedemic/Plenum Publishers; 1999. p. 23-48.
-
(1999)
Handbook of Disruptive Behavior Disorders
, pp. 23-48
-
-
Lahey, B.B.1
Miller, T.L.2
Gordon, R.A.3
-
3
-
-
0032533256
-
Neurobiology of attention-deficit hyperactivity disorder
-
Faraone SV, Biederman J. Neurobiology of attention-deficit hyperactivity disorder. Soc Biol Psychiatry. 1998;44(10):951-958.
-
(1998)
Soc Biol Psychiatry
, vol.44
, Issue.10
, pp. 951-958
-
-
Faraone, S.V.1
Biederman, J.2
-
4
-
-
0004235298
-
-
American Psychiatric Association (APA). 4th ed. Washington DC: American Psychiatric Association
-
American Psychiatric Association (APA). Diagnostic and Statistical Manual of Mental Disorders: DSM-IV-TR, 4th ed. Washington DC: American Psychiatric Association; 2000.
-
(2000)
Diagnostic and Statistical Manual of Mental Disorders: DSM-IV-TR
-
-
-
5
-
-
33746860422
-
Pervasive developmental disorders in Montreal, Quebec, Canada: Prevalence and links with immunizations
-
DOI 10.1542/peds.2005-2993
-
Fombonne E. Zakarian R, Bennett A, Meng L, McLean-Heywood D. Pervasive developmental disorders in Montreal, Quebec, Canada: Prevalence and Links with Immunizations. Pediatrics. 2006;118(1): e139-e150. (Pubitemid 46071129)
-
(2006)
Pediatrics
, vol.118
, Issue.1
-
-
Fombonne, E.1
Zakarian, R.2
Bennett, A.3
Meng, L.4
McLean-Heywood, D.5
-
6
-
-
56549098966
-
Autism Overflows: Increasing prevalence and proliferating theories
-
Waterhouse L. Autism Overflows: Increasing prevalence and proliferating theories. Neuropsychol Rev. 2008;18(4):273-286.
-
(2008)
Neuropsychol Rev
, vol.18
, Issue.4
, pp. 273-286
-
-
Waterhouse, L.1
-
7
-
-
0033790652
-
Heritability and the comorbidity of attention deficit hyperactivity disorder with behavioral disorders and executive function deficits: A preliminary investigation
-
Coolidge FL, Thede LL, Young SE. Heritability and the comorbidity of attention deficit hyperactivity disorder with behavioral disorders and executive function deficits: a preliminary investigation. Dev Neuropsychol. 2000;17(3):237-287.
-
(2000)
Dev Neuropsychol
, vol.17
, Issue.3
, pp. 237-287
-
-
Coolidge, F.L.1
Thede, L.L.2
Young, S.E.3
-
8
-
-
0034126980
-
A twin study of inattentive, aggressive, and anxious/depressed behaviors
-
Hudziak JJ, Rudiger LP, Neale MC, Heath AC, Todd RD. A twin study of inattentive, aggressive, and anxious/depressed behaviors. J Am Acad Child Adolesc Psychiatry. 2000;39(4):469-476.
-
(2000)
J Am Acad Child Adolesc Psychiatry
, vol.39
, Issue.4
, pp. 469-476
-
-
Hudziak, J.J.1
Rudiger, L.P.2
Neale, M.C.3
Heath, A.C.4
Todd, R.D.5
-
9
-
-
0036511712
-
Observer effects and heritability of childhood attention-deficit hyperactivity disorder symptoms
-
Martin N, Scourfield J, McGUffin P. Observer effects and heritability of childhood attention-deficit hyperactivity disorder symptoms. Br J Psychiatry. 2002;180:260-265.
-
(2002)
Br J Psychiatry
, vol.180
, pp. 260-265
-
-
Martin, N.1
Scourfield, J.2
McGuffin, P.3
-
10
-
-
0042823889
-
Heritability of attention problems in children: Cross-sectional results from a study of twins, age 3-12 years
-
Rietveld MJ, Hudziak JJ, Bartels M, van Beijsterveldt CE, Boomsma. Heritability of attention problems in children: cross-sectional results from a study of twins, age 3-12 years. Am J Med Genet B Neuropsychiatr Genet. 2003;117B(1):102-113.
-
(2003)
Am J Med Genet B Neuropsychiatr Genet
, vol.117 B
, Issue.1
, pp. 102-113
-
-
Rietveld, M.J.1
Hudziak, J.J.2
Bartels, M.3
Van Beijsterveldt, C.E.4
Boomsma5
-
11
-
-
0033653256
-
Does the definition of ADHD affect heritability?
-
Thapar A, Harrington R, Ross K, McGuffin P. Does the definition of ADHD affect heritability? J Am Acad Child Adolesc Psychiatry. 2000;39(12):1528-1536.
-
(2000)
J Am Acad Child Adolesc Psychiatry
, vol.39
, Issue.12
, pp. 1528-1536
-
-
Thapar, A.1
Harrington, R.2
Ross, K.3
McGuffin, P.4
-
12
-
-
0034028878
-
Etiology of inattention and hyperactivity/impulsivity in a community sample of twins with learning difficulties
-
Wilcutt EG, Penington BF, De Fries JC. Etiology of inattention and hyperactivity/impulsivity in a community sample of twins with learning difficulties. J Abnorm Child Psychol. 2000;28(2):149-159.
-
(2000)
J Abnorm Child Psychol
, vol.28
, Issue.2
, pp. 149-159
-
-
Wilcutt, E.G.1
Penington, B.F.2
De Fries, J.C.3
-
13
-
-
20444412281
-
Molecular genetics of attention-deficit/hyperactivity disorder
-
Faraone SV, Perlis RH, Doyle AE, et al. Molecular genetics of attention-deficit/hyperactivity disorder. Soc Biol Psychiatry. 2005;57: 1313-1323.
-
(2005)
Soc Biol Psychiatry
, vol.57
, pp. 1313-1323
-
-
Faraone, S.V.1
Perlis, R.H.2
Doyle, A.E.3
-
14
-
-
33845797961
-
The genetics of autistic disorders and its clinical relevance: A review of the literature
-
DOI 10.1038/sj.mp.4001896, PII 4001896
-
Freitag CM. The genetics of autistic disorders and its clinical relevance: a review of the literature. Mol Psychiatry. 2007;12(1):2-22. (Pubitemid 44973659)
-
(2007)
Molecular Psychiatry
, vol.12
, Issue.1
, pp. 2-22
-
-
Freitag, C.M.1
-
16
-
-
33947421697
-
Attention deficit hyperactivity disorder symptoms in pervasive developmental disorders: Association with autistic behavior domains and coexisting psychopathology
-
DOI 10.1159/000100007
-
Holtmann M, Bölte S, Pousta F. Attention deficit hyperactivity disorder symptoms in pervasive developmental disorders: association with autistic behavior domains and coexisting psychopathology. Psychopathology. 2007;40(3):172-177. (Pubitemid 46457598)
-
(2007)
Psychopathology
, vol.40
, Issue.3
, pp. 172-177
-
-
Holtmann, M.1
Bolte, S.2
Poustka, F.3
-
17
-
-
19044394761
-
Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism
-
Smalley SL, Kustanovich V, Minassian SL, et al. Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism. Am J Hum Genet. 2002;71(4):959-963. (Pubitemid 135750527)
-
(2002)
American Journal of Human Genetics
, vol.71
, Issue.4
, pp. 959-963
-
-
Smalley, S.L.1
Kustanovich, V.2
Minassian, S.L.3
Stone, J.L.4
Ogdie, M.N.5
McGough, J.J.6
McCracken, J.T.7
MacPhie, I.L.8
Francks, C.9
Fisher, S.E.10
Cantor, R.M.11
Monaco, A.P.12
Nelson, S.F.13
-
18
-
-
0038414643
-
A whole-genome scan in 164 Dutch sib pairs with attention-deficit/ hyperactivity disorder: Suggestive evidence for linkage on chromosome 7p and 15q
-
Bakker SC, van der Meulen EM, Buitelaar JK, et al. A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosome 7p and 15q. Am J Hum Genet. 2003;72(5):1251-1260.
-
(2003)
Am J Hum Genet
, vol.72
, Issue.5
, pp. 1251-1260
-
-
Bakker, S.C.1
Van Der Meulen, E.M.2
Buitelaar, J.K.3
-
19
-
-
6344272220
-
The clinical necessity for assessing Attention Dificit/Hyperactivity Disorder (AD/HD) symptoms in children with high-functioning Pervasive Developmental Disorder (PDD)
-
DOI 10.1007/s00787-004-0391-1
-
Yoshida Y, Uchiyama T. The clinical necessity for assessing attention deficit/hyperactivity disorder (AD/HD) symptoms in children with high-functioning Pervasive Developmental Disorder (PDD). Eur Child Adolesc Psychiatry. 2004;13(5):307-314. (Pubitemid 39390322)
-
(2004)
European Child and Adolescent Psychiatry
, vol.13
, Issue.5
, pp. 307-314
-
-
Yoshida, Y.1
Uchiyama, T.2
-
20
-
-
33846585912
-
Attention-deficit hyperactivity disorder symptoms in a clinic sample of children and adolescents with pervasive developmental disorders
-
Lee DO, Ousley OY. Attention-deficit hyperactivity disorder symptoms in a clinical sample of children and adolescents with pervasive developmental disorders. J Child Adolesc Psychopharmacol. 2006;16(6):737-746. (Pubitemid 46175429)
-
(2006)
Journal of Child and Adolescent Psychopharmacology
, vol.16
, Issue.6
, pp. 737-746
-
-
Lee, D.O.1
Ousley, O.Y.2
-
21
-
-
33748978440
-
Comorbid psychiatric disorders in children with autism: Interview development and rates of disorders
-
DOI 10.1007/s10803-006-0123-0
-
Leyfer OT, Folstein SE, Bacalman S, et al. Comorbid psychiatric disorders in children with autism: interview development and rates of disorders. J Autism Dev Disord. 2006;36(7):849-861. (Pubitemid 44440104)
-
(2006)
Journal of Autism and Developmental Disorders
, vol.36
, Issue.7
, pp. 849-861
-
-
Leyfer, O.T.1
Folstein, S.E.2
Bacalman, S.3
Davis, N.O.4
Dinh, E.5
Morgan, J.6
Tager-Flusberg, H.7
Lainhart, J.E.8
-
22
-
-
41849124886
-
Evidence for overlapping genetic influences on autistic and ADHD behaviours in a community twin sample
-
Ronald A, Simonoff E, Kuntsi J, Asherson P, Plomin R. Evidence for overlapping genetic influences on autistic and ADHD behaviours in a community twin sample. J Child Psychol Psychiatry. 2008;49(5): 535-542.
-
(2008)
J Child Psychol Psychiatry
, vol.49
, Issue.5
, pp. 535-542
-
-
Ronald, A.1
Simonoff, E.2
Kuntsi, J.3
Asherson, P.4
Plomin, R.5
-
23
-
-
44849116640
-
Co-occurrence of motor problems and autistic symptoms in attention-deficit/hyperactivity disorder
-
Reiersen AM, Constantino JN, Todd RD. Co-occurrence of motor problems and autistic symptoms in attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry. 2008;47(6):662-672.
-
(2008)
J Am Acad Child Adolesc Psychiatry
, vol.47
, Issue.6
, pp. 662-672
-
-
Reiersen, A.M.1
Constantino, J.N.2
Todd, R.D.3
-
24
-
-
58549084760
-
Autism symptoms in attention-deficit//hyperactivity disorder: A familiar trait which correlates with conduct, oppositional defiant, language and motor disorders
-
Epub Jul 19
-
Mulligan A, Anney RJL, O'Regan M, et al. Autism symptoms in attention-deficit//hyperactivity disorder: a familiar trait which correlates with conduct, oppositional defiant, language and motor disorders. J Autism Dev Disord. Epub 2008 Jul 19.
-
(2008)
J Autism Dev Disord
-
-
Mulligan, A.1
Anney, R.J.L.2
O'Regan, M.3
-
25
-
-
34249943502
-
Autistic traits in a population-based ADHD twin sample
-
Reiersen AM, Constatino JN, Volke HE, Todd RD. Autistic traits in a population-based ADHD twin sample. J Child Psychol Psychiatry. 2007;48(5):464-472.
-
(2007)
J Child Psychol Psychiatry
, vol.48
, Issue.5
, pp. 464-472
-
-
Reiersen, A.M.1
Constatino, J.N.2
Volke, H.E.3
Todd, R.D.4
-
26
-
-
57349100444
-
Evidence for shared genetic influences on self-reported ADHD and autistic symptoms in young adult Autralian twins
-
Reiersen AM, Constantino JN, Grimmer M, Martin NG, Todd RD. Evidence for shared genetic influences on self-reported ADHD and autistic symptoms in young adult Autralian twins. Twin Res Hum Genet. 2008;11(6):579-585.
-
(2008)
Twin Res Hum Genet
, vol.11
, Issue.6
, pp. 579-585
-
-
Reiersen, A.M.1
Constantino, J.N.2
Grimmer, M.3
Martin, N.G.4
Todd, R.D.5
-
27
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander E, Kruglyak L. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet. 1995;11(3): 241-247.
-
(1995)
Nat Genet
, vol.11
, Issue.3
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
28
-
-
42349098697
-
Genome-wide linkage analysis of ADHD using high-density SNP arrays: Novel loci at 5q13.1 and 14q12
-
DOI 10.1038/mp.2008.12, PII MP200812
-
Romanos M, Freitag C, Jacob C, et al. Genome-wide linkage analysis of ADHD using high-density SNP arrays: nocel loci at 5q31.1 and 14q12. Mol Psychiatry. 2008;13(5):522-530. (Pubitemid 351556035)
-
(2008)
Molecular Psychiatry
, vol.13
, Issue.5
, pp. 522-530
-
-
Romanos, M.1
Freitag, C.2
Jacob, C.3
Craig, D.W.4
Dempfle, A.5
Nguyen, T.T.6
Halperin, R.7
Walitza, S.8
Renner, T.J.9
Seitz, C.10
Romanos, J.11
Palmason, H.12
Reif, A.13
Heine, M.14
Windemuth-Kieselbach, C.15
Vogler, C.16
Sigmund, J.17
Warnke, A.18
Schafer, H.19
Meyer, J.20
Stephan, D.A.21
Lesch, K.P.22
more..
-
29
-
-
10744231297
-
Chromosome 2 deletion encompassing the MAP2 gene in a patient with autism and Rett-like features
-
DOI 10.1046/j.1399-0004.2003.00176.x
-
Pescucci C, Meloni I, Bruttini M, et al. Chromosome 2 deletion encompassing the MAP2 gene in a patient with autism and Rett-like features. Clin Genet. 2003;64(6):497-501. (Pubitemid 37493120)
-
(2003)
Clinical Genetics
, vol.64
, Issue.6
, pp. 497-501
-
-
Pescucci, C.1
Meloni, I.2
Bruttini, M.3
Ariani, F.4
Longo, I.5
Mari, F.6
Canitano, R.7
Hayek, G.8
Zappella, M.9
Renieri, A.10
-
30
-
-
0142178047
-
Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype
-
de Silva MG, Elliott K, Dahl HH, et al. Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype. J Med Genet. 2003;40(10):733-740. (Pubitemid 37311071)
-
(2003)
Journal of Medical Genetics
, vol.40
, Issue.10
, pp. 733-740
-
-
De Silva, M.G.1
Elliott, K.2
Dahl, H.-H.3
Fitzpatrick, E.4
Wilcox, S.5
Delatycki, M.6
Williamson, R.7
Efron, D.8
Lynch, M.9
Forrest, S.10
-
31
-
-
0022863056
-
Autism, mental retardation, and chromosomal abnormalities
-
Mariner R, Jackson AW 3rd, Levitas A, et al. Autism, mental retardation, and chromosomal abnormalities. J Autism Dev Disord. 1986;16(4):425-440.
-
(1986)
J Autism Dev Disord
, vol.16
, Issue.4
, pp. 425-440
-
-
Mariner, R.1
Jackson III, A.W.2
Levitas, A.3
-
32
-
-
0035313922
-
First known microdeletion within the Wolf-Hirschhorn syndrome critical region refines genotypephenotype correlation
-
Rauch A, Schellmoser S, Kraus C, et al. First known microdeletion within the Wolf-Hirschhorn syndrome critical region refines genotypephenotype correlation. Am J Med Genet. 2001;99(4):338-342.
-
(2001)
Am J Med Genet
, vol.99
, Issue.4
, pp. 338-342
-
-
Rauch, A.1
Schellmoser, S.2
Kraus, C.3
-
33
-
-
77953437536
-
Subtelomeric FISH analysis in 108 autistic patients as adjunct to chromosome analysis and fragile X testing
-
Medne L, Russel K, Ming J, et al. Subtelomeric FISH analysis in 108 autistic patients as adjunct to chromosome analysis and fragile X testing. ASHG. 2003;(847).
-
(2003)
ASHG
, Issue.847
-
-
Medne, L.1
Russel, K.2
Ming, J.3
-
34
-
-
77953471982
-
Is autism caused by numerous genetic and cytogenetic syndromes?
-
Lucchese S, Takahashi N, Miles J. Is autism caused by numerous genetic and cytogenetic syndromes? ASHG. 2003;(589).
-
(2003)
ASHG
, Issue.589
-
-
Lucchese, S.1
Takahashi, N.2
Miles, J.3
-
35
-
-
10744231602
-
Joint anakysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypes
-
Lowe N, Kirley A, Hawi Z, et al. Joint anakysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypes. Am J Hum Genet. 2004;74:348-356.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 348-356
-
-
Lowe, N.1
Kirley, A.2
Hawi, Z.3
-
36
-
-
38749143965
-
Investigation of the dopamine D5 receptor gene (DRD5) in adult attention deficit hyperactivity disorder
-
Squassina A, Lanktree M, De Luca V, et al. Investigation of the dopamine D5 receptor gene (DRD5) in adult attention deficit hyperactivity disorder. Neurosci Lett. 2008;432(1):50-53.
-
(2008)
Neurosci Lett
, vol.432
, Issue.1
, pp. 50-53
-
-
Squassina, A.1
Lanktree, M.2
De Luca, V.3
-
37
-
-
34748902277
-
Association and linkage of allelic variants of the dopamine transporter gene in ADHD
-
DOI 10.1038/sj.mp.4001986, PII 4001986
-
Friedel S, Saar K, Sauer S, et al. Association and linkage of allelic variants of the dopamine transporter gene in ADHD. Mol Psychiatry. 2007;12:923-933 (Pubitemid 47482693)
-
(2007)
Molecular Psychiatry
, vol.12
, Issue.10
, pp. 923-933
-
-
Friedel, S.1
Saar, K.2
Sauer, S.3
Dempfle, A.4
Walitza, S.5
Renner, T.6
Romanos, M.7
Freitag, C.8
Seitz, C.9
Palmason, H.10
Scherag, A.11
Windemuth-Kieselbach, C.12
Schimmelmann, B.G.13
Wewetzer, C.14
Meyer, J.15
Warnke, A.16
Lesch, K.P.17
Reinhardt, R.18
Herpertz-Dahlmann, B.19
Linder, M.20
Hinney, A.21
Remschmidt, H.22
Schafer, H.23
Konrad, K.24
Hubner, N.25
Hebebrand, J.26
more..
-
38
-
-
0028987091
-
Association of attention-deficit disorder and the dopamine transporter gene
-
Cook EH Jr, Stein MA, Krasowski MD, et al. Association of attention-deficit disorder and the dopamine transporter gene. Am J Hum Genet. 1995;56(4):993-998.
-
(1995)
Am J Hum Genet
, vol.56
, Issue.4
, pp. 993-998
-
-
Cook Jr., E.H.1
Stein, M.A.2
Krasowski, M.D.3
-
39
-
-
0030844034
-
Confirmation of association between attention deficit hyperactivity disorder and a dopamine transporter polymorphism
-
Gill M, Daly G, Heron S, Hawi Z, Fitzgerald M. Confirmation of association between attention defecit hyperactivity disorder and a dopamine transporter polymorphism. Mol Psychiatry. 1997;2(4):311-313. (Pubitemid 27450313)
-
(1997)
Molecular Psychiatry
, vol.2
, Issue.4
, pp. 311-313
-
-
Gill, M.1
Daly, G.2
Heron, S.3
Hawi, Z.4
Fitzgerald, M.5
-
40
-
-
3042849035
-
Family-based and case-control association studies of DRD4 and DAT1 polymorphisms in Chinese attention deficit hyperactivity disorder patients suggests long repeats contribute to genetic risk for the disorder
-
Qian Q, Wang Y, Zhou R, Yang L, Faraone SV. Family-based and case-control association studies of DRD4 and DAT1 polymorphisms in Chinese attention deficit hyperactivity disorder patients suggests long repeats contribute to genetic risk for the disorder. Am J Med Genet B Neuropsuchiatr Genet. 2004;128B(1):84-89.
-
(2004)
Am J Med Genet B Neuropsuchiatr Genet
, vol.128 B
, Issue.1
, pp. 84-89
-
-
Qian, Q.1
Wang, Y.2
Zhou, R.3
Yang, L.4
Faraone, S.V.5
-
41
-
-
33644690357
-
Collaboratuve analysis of DRD4 and DAT genotypes in population-defined ADHD subtypes
-
Todd RD, Huang H, Smalley SL, et al. Collaboratuve analysis of DRD4 and DAT genotypes in population-defined ADHD subtypes. J Child Psychol Psychiatry. 2005;46(10):1067-1073.
-
(2005)
J Child Psychol Psychiatry
, vol.46
, Issue.10
, pp. 1067-1073
-
-
Todd, R.D.1
Huang, H.2
Smalley, S.L.3
-
42
-
-
27644464349
-
Sequence variation in the 3′-untranslated region of the dopamine transporter gene and attention-defecit hyperactivity disorder (ADHD)
-
Feng Y, Wigg KG, Makkar R, et al. Sequence variation in the 3′-untranslated region of the dopamine transporter gene and attention-defecit hyperactivity disorder (ADHD). Am J Med Genet B Neuropsychiatr Genet. 2005;139B(1):1-6.
-
(2005)
Am J Med Genet B Neuropsychiatr Genet
, vol.139 B
, Issue.1
, pp. 1-6
-
-
Feng, Y.1
Wigg, K.G.2
Makkar, R.3
-
43
-
-
21844447826
-
Association of the dopamine transporter (DAT1) 10/10-repeat genotype with ADHD symptoms and response inhibition in a general population sample
-
DOI 10.1038/sj.mp.4001641
-
Cornish KM, Manly T, Savage R, et al. Association of the dopamine transporter (DAT1) 10/10-repeat genotype with ADHD symptoms and response inhibition in a general population sample. Mol Psychiatry. 2005;10(7):686-698. (Pubitemid 40961739)
-
(2005)
Molecular Psychiatry
, vol.10
, Issue.7
, pp. 686-698
-
-
Cornish, K.M.1
Manly, T.2
Savage, R.3
Swanson, J.4
Morisano, D.5
Butler, N.6
Grant, C.7
Cross, G.8
Bentley, L.9
Hollis, C.P.10
-
44
-
-
33748646825
-
The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: Association signals in DRD4, DAT1 and 16 other genes
-
DOI 10.1038/sj.mp.4001869, PII 4001869
-
Brookes K, Xu X, Chen W, et al. The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes. Mol Psychiatry. 2006;11(10):934-953. (Pubitemid 44470216)
-
(2006)
Molecular Psychiatry
, vol.11
, Issue.10
, pp. 934-953
-
-
Brookes, K.1
Xu, X.2
Chen, W.3
Zhou, K.4
Neale, B.5
Lowe, N.6
Aneey, R.7
Franke, B.8
Gill, M.9
Ebstein, R.10
Buitelaar, J.11
Sham, P.12
Campbell, D.13
Knight, J.14
Andreou, P.15
Altink, M.16
Arnold, R.17
Boer, F.18
Buschgens, C.19
Butler, L.20
Christiansen, H.21
Feldman, L.22
Fleischman, K.23
Fliers, E.24
Howe-Forbes, R.25
Goldfarb, A.26
Heise, A.27
Gabriels, I.28
Korn-Lubetzki, I.29
Marco, R.30
Medad, S.31
Minderaa, R.32
Mulas, F.33
Muller, U.34
Mulligan, A.35
Rabin, K.36
Rommelse, N.37
Sethna, V.38
Sorohan, J.39
Uebel, H.40
Psychogiou, L.41
Weeks, A.42
Barrett, R.43
Craig, I.44
Banaschewski, T.45
Sonuga-Barke, E.46
Eisenberg, J.47
Kuntsi, J.48
Manor, I.49
McGuffin, P.50
Miranda, A.51
Oades, R.D.52
Plomin, R.53
Roeyers, H.54
Rothenberger, A.55
Sergeant, J.56
Steinhausen, H.-C.57
Taylor, E.58
Thompson, M.59
Faraone, S.V.60
Asherson, P.61
Johansson, L.62
more..
-
45
-
-
33745946035
-
Attention-deficit/hyperactivity disorder (ADHD) association with the DAT1 core promoter -67 T allele
-
DOI 10.1016/j.brainres.2006.05.024, PII S0006899306014016
-
Ohadi M, Shirazi E, Tehranidoosti M, et al. Attention-deficit/ hyperactivity disorder (ADHD) association with the DAT1 core promoter-67 T allele. Brain Res. 2006;1101(1):1-4. (Pubitemid 44055926)
-
(2006)
Brain Research
, vol.1101
, Issue.1
, pp. 1-4
-
-
Ohadi, M.1
Shirazi, E.2
Tehranidoosti, M.3
Moghimi, N.4
Keikhaee, M.R.5
Ehssani, S.6
Aghajani, A.7
Najmabadi, H.8
-
46
-
-
29844456031
-
A common haplotype of the dopamine transporter gene associated with attention-deficit/hyperactivity disorder and interacting with maternal use of alcohol during pregnancy
-
DOI 10.1001/archpsyc.63.1.74
-
Brookes KJ, Mill J, Guindalani C, et al. A common haplotype of the dopamine transporter gene associated with attention-deficit/hyperactivity disorder and interacting with maternal use of alcohol during pregnancy. Arch Gen Psychiatry. 2006;63(1):74-81. (Pubitemid 43037471)
-
(2006)
Archives of General Psychiatry
, vol.63
, Issue.1
, pp. 74-81
-
-
Brookes, K.-J.1
Mill, J.2
Guindalini, C.3
Curran, S.4
Xu, X.5
Knight, J.6
Chen, C.-K.7
Huang, Y.-S.8
Sethna, V.9
Taylor, E.10
Chen, W.11
Breen, G.12
Asherson, P.13
-
47
-
-
33745710365
-
The dopamine transporter gene and the impulsivity phenotype in attention deficit hyperactivity disorder: A case-control association study in a Korean sample
-
DOI 10.1016/j.jpsychires.2005.11.002, PII S002239560500138X
-
Kim JW, Kim BN, Cho SC. The dopamine transporter gene and the impulsivity phenotype in attention deficit hyperactivity disorder: a case-control association study in a Korean sample. J Psychiatr Res. 2006;40(8):730-737. (Pubitemid 44486245)
-
(2006)
Journal of Psychiatric Research
, vol.40
, Issue.8
, pp. 730-737
-
-
Kim, J.-W.1
Kim, B.-N.2
Cho, S.-C.3
-
48
-
-
67149133854
-
Association of the dopamine transporter gene and ADHD symptoms in a Canadian population-based sample of same-age twins
-
Epub Dec 28
-
Quellet-Morin I, Wigg KG, Feng Y, et al. Association of the dopamine transporter gene and ADHD symptoms in a Canadian population-based sample of same-age twins. Am J Med Genet B Neuropsychiatr Genet. Epub 2007 Dec 28.
-
(2007)
Am J Med Genet B Neuropsychiatr Genet
-
-
Quellet-Morin, I.1
Wigg, K.G.2
Feng, Y.3
-
49
-
-
34248172347
-
Interacting effects of the dopamine transporter gene and psychosocial adversity on attention-deficit/hyperactivity disorder symptoms among 15-year-olds from a high-risk community sample
-
DOI 10.1001/archpsyc.64.5.585
-
Laucht M, Skowronek MH, Becker K, et al. Interacting effects of the dopamine transporter gene and psychosocial adversity on attention-deficit/ hyperactivity disorder symptoms among 15-year-olds from a high-risk community sample. Arch Gen Psychiatry. 2007;64(5):585-590. (Pubitemid 46718291)
-
(2007)
Archives of General Psychiatry
, vol.64
, Issue.5
, pp. 585-590
-
-
Laucht, M.1
Skowronek, M.H.2
Becker, K.3
Schmidt, M.H.4
Esser, G.5
Schulze, T.G.6
Rietschel, M.7
-
50
-
-
34247463477
-
Confirmation that a specific haplotype of the dopamine transporter gene is associated with combined-type ADHD
-
DOI 10.1176/appi.ajp.164.4.674
-
Asherson P, Brookes K, Franke B, et al. Confirmation that a specific haplotype of the dopamine transporter gene is associated with combined-type ADHD. Am J Psychiatry. 2007;164(4):674-677. (Pubitemid 46650201)
-
(2007)
American Journal of Psychiatry
, vol.164
, Issue.4
, pp. 674-677
-
-
Asherson, P.1
Brookes, K.2
Franke, B.3
Chen, W.4
Gill, M.5
Ebstein, R.P.6
Buitelaar, J.7
Banaschewski, T.8
Sonuga-Barke, E.9
Eisenberg, J.10
Manor, I.11
Miranda, A.12
Oades, R.D.13
Roeyers, H.14
Rothenberger, A.15
Sergeant, J.16
Steinhausen, H.-C.17
Faraone, S.V.18
-
51
-
-
34247342088
-
Association of dopamine transporter genotype with disruptive behavior disorders in an eightyear longitudinal study of children and adolescents
-
Lee SS, Lahey BB, Waldman I, et al. Association of dopamine transporter genotype with disruptive behavior disorders in an eightyear longitudinal study of children and adolescents. Am J Med Genet B Neuropsychiatr Genet. 2007;144B(3):310-317.
-
(2007)
Am J Med Genet B Neuropsychiatr Genet
, vol.144 B
, Issue.3
, pp. 310-317
-
-
Lee, S.S.1
Lahey, B.B.2
Waldman, I.3
-
52
-
-
34047249904
-
A promoter polymorphism (-839 C>T) at the dopamine transporter gene is associated with attention deficit/hyperactivity disorder in Brazilian children
-
DOI 10.1002/ajmg.b.30428
-
Genro JP, Zeni C, Polanczyk GV, et al. A promoter polymorphism (-839 C > T) at the dopamine transporter gene is associated with attention deficit/hyperactivity disorder in Brazilian children. Am J Med Genet B Neuropsychiatr Genet. 2007;144B(2):215-219. (Pubitemid 46606646)
-
(2007)
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
, vol.144
, Issue.2
, pp. 215-219
-
-
Genro, J.P.1
Zeni, C.2
Polanczyk, G.V.3
Roman, T.4
Rohde, L.A.5
Hutz, M.H.6
-
53
-
-
0025141468
-
Cytogenetic survey for autistic fragile X carriers in a mental retardation center
-
Cantú ES, Stone JW, Wing AA, Langee HR, Williams CA. Cytogenetic survey for autistic fragile X carriers in a mental retardation center. Am J Ment Retard. 1990;94(4):442-447.
-
(1990)
Am J Ment Retard
, vol.94
, Issue.4
, pp. 442-447
-
-
Cantú, E.S.1
Stone, J.W.2
Wing, A.A.3
Langee, H.R.4
Williams, C.A.5
-
54
-
-
0027968086
-
Case reports of autism with interstitial deletion of chromosome 17 (p11.2 p11.2) and monosomy of chromosome 5 (5 pter->5p15.3)
-
Vostanis P, Harrington R, Prendergast M, Farndon P. Case reports of autism with interstitial deletion of chromosome 17 (p11.2 p11.2) and monosomy of chromosome 5 (5 pter->5p15.3). Psychiatr Genet. 1994;4(2):109-111.
-
(1994)
Psychiatr Genet
, vol.4
, Issue.2
, pp. 109-111
-
-
Vostanis, P.1
Harrington, R.2
Prendergast, M.3
Farndon, P.4
-
55
-
-
31544439114
-
A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs
-
DOI 10.1038/sj.mp.4001761, PII 4001761
-
Hebebrand J, Dempfle A, Saar K, et al. A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs. Mol Psychiatry. 2006;11(2):196-205. (Pubitemid 43164621)
-
(2006)
Molecular Psychiatry
, vol.11
, Issue.2
, pp. 196-205
-
-
Hebebrand, J.1
Dempfle, A.2
Saar, K.3
Thiele, H.4
Herpertz-Dahlmann, B.5
Linder, M.6
Kiefl, H.7
Remschmidt, H.8
Hemminger, U.9
Warnke, A.10
Knolker, U.11
Heiser, P.12
Friedel, S.13
Hinney, A.14
Schafer, H.15
Nurnberg, P.16
Konrad, K.17
-
56
-
-
33750340554
-
Developmental, behavioral and genetic factors in correlation with attention deficit hyperactivity disorder in Egyptian children
-
Menabbawy KA, Gerzawy AE, Ezzat A, Mottawie H. Developmental, behavioral and genetic factors in correlation with attention deficit hyperactivity disorder in Egyptian children. J Med Sci. 2006;6(4):569-576. (Pubitemid 44613170)
-
(2006)
Journal of Medical Sciences
, vol.6
, Issue.4
, pp. 569-576
-
-
Al-Menabbawy, K.1
El-Gerzawy, A.2
Ezzat, A.3
Mottawie, H.4
-
57
-
-
0027913991
-
Infantile autism among children in the county of Nordland. Prevalence and etiology
-
Herder GA. Infantile autism among children in the county of Nordland. Prevalence and etiology. Tidsskr Nor Laegeforen. 1993;113(18): 2247-2249.
-
(1993)
Tidsskr Nor Laegeforen
, vol.113
, Issue.18
, pp. 2247-2249
-
-
Herder, G.A.1
-
58
-
-
0032454027
-
Chromosomal disorders and autism
-
Gillberg C. Chromosomal disorders and autism. J Autism Dev Disord. 1998;28(5):415-425.
-
(1998)
J Autism Dev Disord
, vol.28
, Issue.5
, pp. 415-425
-
-
Gillberg, C.1
-
59
-
-
18444371140
-
Presence of large deletions in kindreds with autism
-
DOI 10.1086/341291
-
Yu CE, Dawson G, Munson J, et al. Presence of large deletions in kindreds with autism. Am J Hum Genet. 2002;71(1):100-115. (Pubitemid 34734711)
-
(2002)
American Journal of Human Genetics
, vol.71
, Issue.1
, pp. 100-115
-
-
Yu, C.-E.1
Dawson, G.2
Munson, J.3
D'Souza, I.4
Osterling, J.5
Estes, A.6
Leutenegger, A.-L.7
Flodman, P.8
Smith, M.9
Raskind, W.H.10
Spence, M.A.11
McMahon, W.12
Wijsman, E.M.13
Schellenberg, G.D.14
-
60
-
-
0035826462
-
De novo partial duplication of chromosome 7p in a male with autistic disorder
-
Wolpert CM, Donnelly SL, Cuccaro ML, et al. De novo partial duplication of chromosome 7p in a male with autistic disorder. Am J Med Genet. 2001;105(3):222-225.
-
(2001)
Am J Med Genet
, vol.105
, Issue.3
, pp. 222-225
-
-
Wolpert, C.M.1
Donnelly, S.L.2
Cuccaro, M.L.3
-
61
-
-
0033013602
-
Infantile autism and associated autosomal chromosome abnormalities: A register-based study and a literature survey
-
Lauritsen M , Mors O, Mortensen PB, Ewald H. Infantile autism and associated autosomal chromosome abnormalities: a register-based study and a literature survey. J Child Psychol Psychiatry. 1999;40(3):335-345.
-
(1999)
J Child Psychol Psychiatry
, vol.40
, Issue.3
, pp. 335-345
-
-
Lauritsen, M.1
Mors, O.2
Mortensen, P.B.3
Ewald, H.4
-
62
-
-
0033746705
-
Disease associated balanced chromosome rearragements: A resource for large scale genotype-phenotype delineation in man
-
Bugge M, Bruun-Petersen G, Brondum-Nielsen K, et al. Disease associated balanced chromosome rearrangements: a resource for large scale genotype-phenotype delineation in man. J Med Genet. 2000;37(11):858-865. (Pubitemid 30843795)
-
(2000)
Journal of Medical Genetics
, vol.37
, Issue.11
, pp. 858-865
-
-
Bugge, M.1
Bruun-Petersen, G.2
Brondum-Nielsen, K.3
Friedrich, U.4
Hansen, J.5
Jensen, G.6
Jensen, P.K.A.7
Kristoffersson, U.8
Lundsteen, C.9
Niebuhr, E.10
Rasmussen, K.R.11
Rasmussen, K.12
Tommerup, N.13
-
63
-
-
0031827203
-
Chromosomes in autism and related pervasive developmental disorders: A cytogenetic study
-
DOI 10.1046/j.1365-2788.1998.00091.x
-
Weidmer-Mikhail E, Sheldon S, Ghaziuddin M. Chromosomes in autism and related pervasive developmental disorders: a cytogenetic study. J Intellect Disabil Res. 1998;42(Pt 1):8-12. (Pubitemid 28349719)
-
(1998)
Journal of Intellectual Disability Research
, vol.42
, Issue.1
, pp. 8-12
-
-
Weidmer-Mikhail, E.1
Sheldon, S.2
Ghaziuddin, M.3
-
64
-
-
0038238370
-
The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism
-
Castermans D, Wilquet V, Parthoens, et al. The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism. J Med Genet. 2003;40(5):352-356. (Pubitemid 36613473)
-
(2003)
Journal of Medical Genetics
, vol.40
, Issue.5
, pp. 352-356
-
-
Castermans, D.1
Wilquet, V.2
Parthoens, E.3
Huysmans, C.4
Steyaert, J.5
Swinnen, L.6
Fryns, J.-P.7
Van De Ven, W.8
Devriendt, K.9
-
65
-
-
0041320864
-
Genetic and clinical characterization of patients with an interstitial duplication 15q11-q13, emphasizing behavioral phenotype and response to treatment
-
Thomas JA, Johnson J, Peterson Kraai TL, et al. Genetic and clinical characterization of patients with an interstitial duplication 15q11-q13, emphasizing behavioral phenotype and response to treatment. Am J Med Genet A. 2003;119A(2):111-120. (Pubitemid 37063879)
-
(2003)
American Journal of Medical Genetics
, vol.119 A
, Issue.2
, pp. 111-120
-
-
Thomas, J.A.1
Johnson, J.2
Peterson Kraai, T.L.3
Wilson, R.4
Tartaglia, N.5
Leroux, J.6
Beischel, L.7
McGavran, L.8
Hagerman, R.J.9
-
66
-
-
18344413881
-
Autism and maternally derived aberrations of chromosome 15q
-
Schroer RJ, Phelan MC, Michaelis RC, et al. Autism and maternally derived aberrations of chromosome 15q. Am J Med Genet. 1998;76(4): 327-336.
-
(1998)
Am J Med Genet
, vol.76
, Issue.4
, pp. 327-336
-
-
Schroer, R.J.1
Phelan, M.C.2
Michaelis, R.C.3
-
67
-
-
0035057465
-
Relationship between clinical and genetic features in "inverted duplicated chromosome 15" patients
-
Borgatti R, Piccinelli P, Passoni, et al. Relationship between clinical and genetic features in "inverted duplicated chromosome 15" patients. Pediatr Neurol. 2001;24(2):111-116.
-
(2001)
Pediatr Neurol
, vol.24
, Issue.2
, pp. 111-116
-
-
Borgatti, R.1
Piccinelli, P.2
Passoni3
-
68
-
-
0036481198
-
Molecular and Cytogenetic Analyses on Brazilian Youths with Pervasive Developmental Disorders
-
DOI 10.1023/A:1017952123258
-
Estecio MRH, Fett-Conte AC, Varella-Garcia M, Fridman C, Silva AE. Molecular and cytogenetic analyses on Brazilian youths with pervasive developmental disorders. J Autism Dev Disord. 2002;32(1):35-41. (Pubitemid 37486144)
-
(2002)
Journal of Autism and Developmental Disorders
, vol.32
, Issue.1
, pp. 35-41
-
-
Higino Estecio, M.R.1
Fett-Conte, A.C.2
Varella-Garcia, M.3
Fridman, C.4
Silva, A.E.5
-
69
-
-
0036593135
-
Tetrasomy 15q11-q13 identified by fluorescence in situ hybridization in a patient with autistic disorder
-
Silva AE, Veyego-Lourenço SA, Fett-Conte AC, Goloni-Bertollo EM, Verella-Garcia M. Tetrasomy 15q11-q13 identified by fluorescence in situ hybridization in a patient with autistic disorder. Arq Neuropsiquiatr. 2002;60(2A):290-294.
-
(2002)
Arq Neuropsiquiatr
, vol.60
, Issue.2 A
, pp. 290-294
-
-
Silva, A.E.1
Veyego-Lourenço, S.A.2
Fett-Conte, A.C.3
Goloni-Bertollo, E.M.4
Verella-Garcia, M.5
-
70
-
-
0037766224
-
Mitochondrial dysfunction in autistic patients with 15q inverted duplication
-
DOI 10.1002/ana.10596
-
Filipek PA, Juranek J, Smith M, et al. Mitochondrial dysfunction in autistic patients with 15q inverted duplication. Ann Neurol. 2003;53(6):801-804. (Pubitemid 36622519)
-
(2003)
Annals of Neurology
, vol.53
, Issue.6
, pp. 801-804
-
-
Filipek, P.A.1
Juranek, J.2
Smith, M.3
Mays, L.Z.4
Ramos, E.R.5
Bocian, M.6
Masser-Frye, D.7
Laulhere, T.M.8
Modahl, C.9
Spence, M.A.10
Gargus, J.J.11
-
71
-
-
21644462077
-
Autistic spectrum disorder associated with partial duplication of chromosome 15; three case reports
-
DOI 10.1007/s00787-004-0414-y
-
Simic M, Turk J. Autistic spectrum disorder associated with partial duplication of chromosome 15; three case reports. Eur Child Adolesc Psychiatry. 2004;13(6):389-393. (Pubitemid 40933130)
-
(2004)
European Child and Adolescent Psychiatry
, vol.13
, Issue.6
, pp. 389-393
-
-
Simic, M.1
Turk, J.2
-
72
-
-
0034640701
-
Three probands with autistic disorder and isodicentric chromosome 15
-
Wolpert CM, Menold MM, Bass MP, et al. Three probands with autistic disorder and isodicentric chromosome 15. Am J Med Genet. 2000;96(3):365-372.
-
(2000)
Am J Med Genet
, vol.96
, Issue.3
, pp. 365-372
-
-
Wolpert, C.M.1
Menold, M.M.2
Bass, M.P.3
-
74
-
-
0028959478
-
A case of autism associated with partial tetrasomy 15
-
Hotopf M, Bolton P. A case of autism associated with partial tetrasomy 15. J Autism Dev Disord. 1995;25(1):41-49.
-
(1995)
J Autism Dev Disord
, vol.25
, Issue.1
, pp. 41-49
-
-
Hotopf, M.1
Bolton, P.2
-
75
-
-
0032794689
-
Chromosomal abnormalities in a series of children with autistic disorder
-
DOI 10.1023/A:1022155201662
-
Konstantareas MM, Homatidis S. Chromosomal abnormalities in a series of children with autistic disorder. J Autism Dev Disord. 1999;29(4):275-285. (Pubitemid 29400356)
-
(1999)
Journal of Autism and Developmental Disorders
, vol.29
, Issue.4
, pp. 275-285
-
-
Konstantareas, M.M.1
Homatidis, S.2
-
76
-
-
0031660251
-
Autistic symptoms among children and young adults with isodicentric chromosome 15
-
Rineer S, Finucane B, Simon EW. Autistic symptoms among children and young adults with isodicentric chromosome 15. Am J Med Genet. 1998;81(5):428-433.
-
(1998)
Am J Med Genet
, vol.81
, Issue.5
, pp. 428-433
-
-
Rineer, S.1
Finucane, B.2
Simon, E.W.3
-
77
-
-
77953453715
-
Characterization of maternally derived aberration of chromosome 15q in a patient with autism
-
Kwasnicka D, Roberts W, Li M, Rusell S, Choufani S, Scherer S. Characterization of maternally derived aberration of chromosome 15q in a patient with autism. ASHG. 2004;(962).
-
(2004)
ASHG
, Issue.962
-
-
Kwasnicka, D.1
Roberts, W.2
Li, M.3
Rusell, S.4
Choufani, S.5
Scherer, S.6
-
78
-
-
0029916624
-
Autism in Angelman syndrome: A population-based study
-
DOI 10.1016/0887-8994(96)00011-2
-
Steffenburg S, Gillberg CL, Steffenburg U, Kyllerman M. Autism in Angelman syndrome: a population-based study. Pediatr Neurol. 1996;14(2):131-136. (Pubitemid 26104417)
-
(1996)
Pediatric Neurology
, vol.14
, Issue.2
, pp. 131-136
-
-
Steffenburg, S.1
Gillberg, C.L.2
Steffenburg, U.3
Kyllerman, M.4
-
79
-
-
0031859763
-
Chromosome 15q11-13 region and the autistic disorder
-
Sabry MA, Farag TI. Chromosome 15q11-13 region and the autistic disorder. J Intellect Disabil Res. 1998;42(Pt 3):259.
-
(1998)
J Intellect Disabil Res
, vol.42
, Issue.PART 3
, pp. 259
-
-
Sabry, M.A.1
Farag, T.I.2
-
80
-
-
0035829969
-
The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders
-
Bolton PF, Dennis NR, Browne CE, et al. The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders. Am J Med Genet. 2001;105(8):675-685.
-
(2001)
Am J Med Genet
, vol.105
, Issue.8
, pp. 675-685
-
-
Bolton, P.F.1
Dennis, N.R.2
Browne, C.E.3
-
81
-
-
0041413297
-
Routine cytogenetic and FISH studies for 17p11/15q11 duplications and subtelomeric rearrangement studies in children with autism spectrum disorders
-
Keller K, Williams C, Wharton P, et al. Routine cytogenetic and FISH studies for 17p11/15q11 duplications and subtelomeric rearrangement studies in children with autism spectrum disorders. Am J Med Genet. 2003;117A(2):105-111. (Pubitemid 37069231)
-
(2003)
American Journal of Medical Genetics
, vol.117 A
, Issue.2
, pp. 105-111
-
-
Keller, K.1
Williams, C.2
Wharton, P.3
Paulk, M.4
Bent-Williams, A.5
Gray, B.6
Ward, A.7
Stalker, H.8
Wallace, M.9
Carter, R.10
Zori, R.11
-
82
-
-
77953390941
-
Identification of Chromosomal Abnormalities and Susceptibility Loci on Chromosome 15q in Autism Families
-
Kashork CD, Stockton DW, SahooT, Bercovich D, Shaffer LG, Beaudet AL. Identification of Chromosomal Abnormalities and Susceptibility Loci on Chromosome 15q in Autism Families. ASHG. 2003;(1793).
-
(2003)
ASHG
, Issue.1793
-
-
Kashork, C.D.1
Stockton, D.W.2
Sahoo, T.3
Bercovich, D.4
Shaffer, L.G.5
Beaudet, A.L.6
-
83
-
-
16944364326
-
Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
-
Cook EH Jr, Lindgren V, Leventhal BL, et al. Autism or atypical autism in maternally but not paternally derived proximal 15q duplication. Am J Hum Genet. 1997;60(4):928-934. (Pubitemid 27146502)
-
(1997)
American Journal of Human Genetics
, vol.60
, Issue.4
, pp. 928-934
-
-
Cook Jr., E.H.1
Lindgren, V.2
Leventhal, B.L.3
Courchesne, R.4
Lincoln, A.5
Shulman, C.6
Lord, C.7
Courchesne, E.8
-
84
-
-
0033549034
-
Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13
-
Gurrieri F, Battaglia A, Torrisi L, et al. Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13. Neurology. 1999;52(8):1694-1697. (Pubitemid 29220651)
-
(1999)
Neurology
, vol.52
, Issue.8
, pp. 1694-1697
-
-
Gurrieri, F.1
Battaglia, A.2
Torrisi, L.3
Tancredi, R.4
Cavallaro, C.5
Sangiorgi, E.6
Neri, G.7
-
85
-
-
77953415437
-
Paternally derived 15q12-q13 duplication associated with Autism Spectrum Disorder
-
Smith M, Hanouni M, Spence MA, Gargus JJ, LeRoux J. Paternally derived 15q12-q13 duplication associated with Autism Spectrum Disorder. ASHG. 2004;(1015/W).
-
(2004)
ASHG
, Issue.1015 W
-
-
Smith, M.1
Hanouni, M.2
Spence, M.A.3
Gargus, J.J.4
LeRoux, J.5
-
86
-
-
19044394761
-
Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism
-
Smalley SL, Kustanovich V, Minassian SL, et al. Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism. Am J Hum Genet. 2002;71(4):959-963. (Pubitemid 135750527)
-
(2002)
American Journal of Human Genetics
, vol.71
, Issue.4
, pp. 959-963
-
-
Smalley, S.L.1
Kustanovich, V.2
Minassian, S.L.3
Stone, J.L.4
Ogdie, M.N.5
McGough, J.J.6
McCracken, J.T.7
MacPhie, I.L.8
Francks, C.9
Fisher, S.E.10
Cantor, R.M.11
Monaco, A.P.12
Nelson, S.F.13
-
87
-
-
0038752692
-
A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: Suggestive linkage on 17p11
-
Ogdie MN, Macphie IL, Minassian SL, et al. A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11. Am J Hum Genet. 2003;72(5):1268-1279.
-
(2003)
Am J Hum Genet
, vol.72
, Issue.5
, pp. 1268-1279
-
-
Ogdie, M.N.1
Macphie, I.L.2
Minassian, S.L.3
-
88
-
-
4544293448
-
Attention deficit hyperactivity disorder: Fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11
-
DOI 10.1086/424387
-
Ogdie MN, Fisher SE, Yang M, et al. Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13 and 17p11. Am J Hum Genet. 2004;75(4):661-668. (Pubitemid 39244780)
-
(2004)
American Journal of Human Genetics
, vol.75
, Issue.4
, pp. 661-668
-
-
Ogdie, M.N.1
Fisher, S.E.2
Yang, M.3
Ishii, J.4
Francks, C.5
Loo, S.K.6
Cantor, R.M.7
McCracken, J.T.8
McGough, J.J.9
Smalley, S.L.10
Nelson, S.F.11
-
89
-
-
0027989527
-
Partial trisomy 16p in an adolescent with autistic disorder and Tourette's syndrome
-
Hebebrand J, Martin M, Körner J, et al. Partial trisomy 16p in an adolescent with autistic disorder and Tourette's syndrome. Am J Med Genet. 1994;54(3):268-270. (Pubitemid 24292190)
-
(1994)
American Journal of Medical Genetics
, vol.54
, Issue.3
, pp. 268-270
-
-
Hebebrand, J.1
Martin, M.2
Korner, J.3
Roitzheim, B.4
De Braganca, K.5
Werner, W.6
Remschmidt, H.7
-
90
-
-
0035825205
-
Family-based association study of the serotonin transporter promoter region polymorphism (5-HTTLPR) in attention deficit hyperactivity disorder
-
DOI 10.1002/1096-8628(20010108)105:1<91::AID-AJMG1069>3.0.CO;2-V
-
Manor I, Eisenberg J, Tyano S, et al. Family-based association study of the serotonin transporter promoter region polymorphism (5-HTTLPR) in attention deficit hyperactivity disorder. Am J Med Genet. 2001;105(1):91-95. (Pubitemid 32105208)
-
(2001)
American Journal of Medical Genetics - Neuropsychiatric Genetics
, vol.105
, Issue.1
, pp. 91-95
-
-
Levinson, D.F.1
Kirby, A.2
Slepner, S.3
Nolte, I.4
Spijker, G.T.5
Meerman, G.T.6
-
91
-
-
0036384203
-
Evidence that variation at the serotonin transporter gene influences susceptibility to attention deficit hyperactivity disorder (ADHD): Analysis and pooled analysis
-
Kent L, Doerry U, Hardy E, et al. Evidence that variation at the serotonin transporter gene influences susceptibility to attention deficit hyperactivity disorder (ADHD): analysis and pooled analysis. Mol Psychiatry. 2002;7(8):908-912.
-
(2002)
Mol Psychiatry
, vol.7
, Issue.8
, pp. 908-912
-
-
Kent, L.1
Doerry, U.2
Hardy, E.3
-
92
-
-
0347926319
-
Associations of the serotonin transporter promoter polymorphism with aggressivity, attention deficit, and conduct disorder in an adoptee population
-
DOI 10.1053/comp.2003.50018
-
Cadoret RJ, Langbehn D, Caspers K, et al. Associations of the serotonin transporter promoter polymorphism with aggressivity, attention deficit, and conduct disorder in an adoptee population. Compr Psychiatry. 2003;44(2):88-101. (Pubitemid 36359141)
-
(2003)
Comprehensive Psychiatry
, vol.44
, Issue.2
, pp. 88-101
-
-
Cadoret, R.J.1
Langbehn, D.2
Caspers, K.3
Troughton, E.P.4
Yucuis, R.5
Sandhu, H.K.6
Philibert, R.7
-
93
-
-
27644579502
-
Family-based associated study of the serotonin transporter gene polymorphism in Korean ADHD trios
-
Kim SJ, Badner J, Cheon KA, et al. Family-based associated study of the serotonin transporter gene polymorphism in Korean ADHD trios. Am J Med Genet B Neuropsychiatr Genet. 2005;139B(1):14-18.
-
(2005)
Am J Med Genet B Neuropsychiatr Genet
, vol.139 B
, Issue.1
, pp. 14-18
-
-
Kim, S.J.1
Badner, J.2
Cheon, K.A.3
-
94
-
-
33745028902
-
A family-based study of Indian subjects from Kolkata reveals allelic association of the serotonin transporter intron-2 (STin2) polymorphism and attention-deficit-hyperactivity disorder (ADHD)
-
DOI 10.1002/ajmg.b.30296
-
Banerjee E, Sinha S, Chatterjee A, Gangopadhyay PK, Singh M, Nandagopal K. A family-based study of Indian subjects from Kolkata reveals allelic association of the serotonin transporter intron-2 (STin2) polymorphism and attention-deficit-hyperactivity disorder (ADHD). Am J Med Genet B Neuropsychiatr Genet. 2006;141B(4):361-366. (Pubitemid 43872887)
-
(2006)
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
, vol.141
, Issue.4
, pp. 361-366
-
-
Banerjee, E.1
Sinha, S.2
Chatterjee, A.3
Gangopadhyay, P.K.4
Singh, M.5
Nandagopal, K.6
-
95
-
-
8244234472
-
Evidence of linkage between the serotonin transporter and autistic disorder
-
Cook EH Jr, Courchesne R, Lord C, et al. Evidence of linkage between the serotonin transporter and autistic disorder. Mol Psychiatry. 1997;2(3):247-250. (Pubitemid 27217689)
-
(1997)
Molecular Psychiatry
, vol.2
, Issue.3
, pp. 247-250
-
-
Cook Jr., E.H.1
Courchesne, R.2
Lord, C.3
Cox, N.J.4
Van, S.5
Lincoln, A.6
Haas, R.7
Courchesne, E.8
Leventhal, B.L.9
-
96
-
-
0030830590
-
Serotonin transporter (5-HTT) gene variants associated with autism?
-
Klauck SM, Poustka F, Benner A, Lesch A, Lesch KP, Poustka A. Serotonin transporter (5-HTT) gene variants associated with autism? Hum Mol Genet. 1997;6(13):2233-2238. (Pubitemid 27501073)
-
(1997)
Human Molecular Genetics
, vol.6
, Issue.13
, pp. 2233-2238
-
-
Klauck, S.M.1
Poustka, F.2
Benner, A.3
Lesch, K.-P.4
Poustka, A.5
-
97
-
-
0035826536
-
Evidence for an association with the serotonin transporter promoter region polymorphism and autism
-
DOI 10.1002/ajmg.1365
-
Yirmiya N, Pilowsky T, Nemanov L, et al. Evidence for an association with the serotonin transporter promoter region polymorphism and autism. Am J Med Genet. 2001;105(4):381-386. (Pubitemid 32578238)
-
(2001)
American Journal of Medical Genetics - Neuropsychiatric Genetics
, vol.105
, Issue.4
, pp. 381-386
-
-
Yirmiya, N.1
Pilowsky, T.2
Nemanov, L.3
Arbelle, S.4
Feinsilver, T.5
Fried, I.6
Ebstein, R.P.7
-
98
-
-
85047695697
-
Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder
-
DOI 10.1038/sj/mp/4001033
-
Kim SJ, Cox N, Courchesne R, et al. Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder. Mol Psychiatry. 2002;7(3):278-288. (Pubitemid 34280636)
-
(2002)
Molecular Psychiatry
, vol.7
, Issue.3
, pp. 278-288
-
-
Kim, S.-J.1
Cox, N.2
Courchesne, R.3
Lord, C.4
Corsello, C.5
Akshoomoff, N.6
Guter, S.7
Leventhal, B.L.8
Courchesne, E.9
Cook Jr., E.H.10
-
99
-
-
2342520299
-
Serotonin transporter gene and autism: A haplotype analysis in an Irish autistic population
-
DOI 10.1038/sj.mp.4001459
-
Conroy J, Meally E, Kearney G, Fitzgerald M, Gill M, Gallagher L. Serotonin transporter gene and autism: a haplotype analysis in an Irish autistic population. Mol Psychiatry. 2004;9(6):587-593. (Pubitemid 38850438)
-
(2004)
Molecular Psychiatry
, vol.9
, Issue.6
, pp. 587-593
-
-
Conroy, J.1
Meally, E.2
Kearney, G.3
Fitzgerald, M.4
Gill, M.5
Gallagher, L.6
-
100
-
-
22544446444
-
Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors
-
Sutcliffe JS, Delahanty RJ, Prasad HC, et al. Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors. Am J Hum Genet. 2005;77(2):265-279.
-
(2005)
Am J Hum Genet
, vol.77
, Issue.2
, pp. 265-279
-
-
Sutcliffe, J.S.1
Delahanty, R.J.2
Prasad, H.C.3
-
101
-
-
33847300921
-
Family-based association study of 5-HTTLPR and the 5-HT2A receptor gene polymorphisms with autism spectrum disorder in Korean trios
-
DOI 10.1016/j.brainres.2007.01.002, PII S000689930700008X
-
Cho IH, Yoo HJ, Park M, Lee YS, Kim SA. Family-based association study of 5-HTTLPR and the 5-HT2A receptor gene polymorphisms with autism spectrum disorder in Korean trios. Brain Res. 2007; 1139:34-41. (Pubitemid 46319040)
-
(2007)
Brain Research
, vol.1139
, Issue.1
, pp. 34-41
-
-
Cho, I.H.1
Yoo, H.J.2
Park, M.3
Lee, Y.S.4
Kim, S.A.5
-
102
-
-
12244261615
-
18q-syndrome and ectodermal dysplasia syndrome: Description of a child and his family
-
Zannolli R, Pierluigi M, Pucci L, et al. 18q-syndrome and ectodermal dysplasia syndrome: description of a child and his family. Am J Med Genet A. 2003;116(2):192-199. (Pubitemid 36043395)
-
(2003)
American Journal of Medical Genetics
, vol.116
, Issue.2
, pp. 192-199
-
-
Zannolli, R.1
Pierluigi, M.2
Pucci, L.3
Lagrasta, N.4
Gasparre, O.5
Matera, M.R.6
Di Bartolo, R.M.7
Mazzei, M.A.8
Sacco, P.9
Miracco, C.10
De Santi, M.M.11
Aitiani, P.12
Cavani, S.13
Pellegrini, L.14
Fimiani, M.15
Alessandrini, C.16
Galluzzi, P.17
Livi, W.18
Gonnelli, S.19
Terrosi-Vagnoli, P.20
Zappella, M.21
Morgese, G.22
more..
-
103
-
-
0026465705
-
18q- chromosomal abnormality in a phenotypically normal 2 1/2-year-old male with autism
-
Seshadri K, Wallerstein R, Burack.18q- chromosomal abnormality in a phenotypically normal 2 1/2-year-old male with autism. Dev Med Child Neurol. 1992;34(11):1005-1009.
-
(1992)
Dev Med Child Neurol
, vol.34
, Issue.11
, pp. 1005-1009
-
-
Seshadri, K.1
Wallerstein, R.2
Burack3
-
105
-
-
0036143742
-
Chromosome 22q11 deletion syndrome (CATCH 22): Neuropsychiatric and neuropsychological aspects
-
Niklasson L, Rasmussen P, Oskarsdóttir S, Gillberg C. Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects. Dev Med Child Neurol. 2002;44(1):44-50. (Pubitemid 34051460)
-
(2002)
Developmental Medicine and Child Neurology
, vol.44
, Issue.1
, pp. 44-50
-
-
Niklasson, L.1
Rasmussen, P.2
Oskarsdottir, S.3
Gillberg, C.4
-
106
-
-
12144290440
-
Genetic, Developmental, and Physical Factors Associated with Attention Deficit Hyperactivity Disorder in Patients with Velocardiofacial Syndrome
-
Gothelf D, Presburger G, Levy D, et al. Genetic, developmental, and physical factors associated with attention deficit hyperactivity disorder in patients with velocardiofacial syndrome. Am J Med Genet B Neuropsychiatr Genet. 2004;126B(1):116-121. (Pubitemid 38420133)
-
(2004)
American Journal of Medical Genetics - Neuropsychiatric Genetics
, vol.126 B
, Issue.1
, pp. 116-121
-
-
Gothelf, D.1
Presburger, G.2
Levy, D.3
Nahmani, A.4
Burg, M.5
Berant, M.6
Blieden, L.C.7
Finkelstein, Y.8
Frisch, A.9
Apter, A.10
Weizman, A.11
-
107
-
-
33646755589
-
ADHD, major depressive disorder, and simple phobias are prevalent psychiatric conditions in youth with velocardofacial syndrome
-
Antshel KM, Fremont W, Roizen NJ, Shprintzen R, Higgins AM, Dhamoon A, Kates WR. ADHD, major depressive disorder, and simple phobias are prevalent psychiatric conditions in youth with velocardofacial syndrome. J Am Acad Child Adolesc Psychiatry. 2006;45(5):596-603.
-
(2006)
J Am Acad Child Adolesc Psychiatry
, vol.45
, Issue.5
, pp. 596-603
-
-
Antshel, K.M.1
Fremont, W.2
Roizen, N.J.3
Shprintzen, R.4
Higgins, A.M.5
Dhamoon, A.6
Kates, W.R.7
-
108
-
-
30944438660
-
The neuropsychological phenotype of velocardiofacial syndrome (VCFS): Relationship to psychopathology
-
DOI 10.1016/j.acn.2005.09.001, PII S0887617705001472
-
Lajiness-O'Neill R, Beaulieu I, Asamoah A, et al. The neuropsychological phenotype of velocardiofacial syndrome (VCFS): relationship to psychopathology. Arch Clin Neuropsychol. 2006;21(2):175-184. (Pubitemid 43117193)
-
(2006)
Archives of Clinical Neuropsychology
, vol.21
, Issue.2
, pp. 175-184
-
-
Lajiness-O'Neill, R.1
Beaulieu, I.2
Asamoah, A.3
Titus, J.B.4
Bawle, E.5
Ahmad, S.6
Kirk, J.W.7
Pollack, R.8
-
109
-
-
33645559153
-
Prevalence of ADHD in children with velocardiofacial syndrome: A preliminary report
-
Zagursky K, Weller RA, Jessani N, Abbas J, Weller EB. Prevalence of ADHD in children with velocardiofacial syndrome: a preliminary report. Curr Psychiatry Rep. 2006;8(2):102-107
-
(2006)
Curr Psychiatry Rep
, vol.8
, Issue.2
, pp. 102-107
-
-
Zagursky, K.1
Weller, R.A.2
Jessani, N.3
Abbas, J.4
Weller, E.B.5
-
110
-
-
0035826540
-
Velo-cardiofacial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders
-
Arnold PD, Siegel-Bartelt J, Cytrynbaum C, Teshima I, Schachar R. Velo-cardiofacial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders. Am J Med Genet. 2001;105(4): 354-362
-
(2001)
Am J Med Genet
, vol.105
, Issue.4
, pp. 354-362
-
-
Arnold, P.D.1
Siegel-Bartelt, J.2
Cytrynbaum, C.3
Teshima, I.4
Schachar, R.5
-
111
-
-
0029853761
-
Bipolar spectrum disorders in patients diagnosed with velo-cardio- Facial syndrome: Does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?
-
Papolos DF, Faedda GL, Veit S, et al. Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizyggous deletion of chromosome 22q11 result in bipolar affective disorder? Am J Psychiatry. 1996;153(12):1541-1547. (Pubitemid 26406163)
-
(1996)
American Journal of Psychiatry
, vol.153
, Issue.12
, pp. 1541-1547
-
-
Papolos, D.F.1
Faedda, G.L.2
Veit, S.3
Goldberg, R.4
Morrow, B.5
Kucherlapati, R.6
Shprintzen, R.J.7
-
112
-
-
0032175387
-
Outcomes of Genetic Evaluation in Children with Pervasive Developmental Disorder
-
Chudley AE, Gutierrez E, Jocelyn LJ, Chodirker BN. Outcomes of genetic evaluation in children with pervasive developmental disorder. J Dev Behav Pediatr. 1998;19(5):321-325. (Pubitemid 128454082)
-
(1998)
Journal of Developmental and Behavioral Pediatrics
, vol.19
, Issue.5
, pp. 321-325
-
-
Chudley, A.E.1
Gutierrez, E.2
Jocelyn, L.J.3
Chodirker, B.N.4
-
113
-
-
0343952988
-
Young children with Velo-Cardio-Facial syndrome (CATCH-22). Psychological and language phenotypes
-
Eliez S, Palacio-Espasa F, Spira A, et al. Young children with Velo-Cardio-Facial syndrome (CATCH-22). Psychological and language phenotypes. Eur Child Adolesc Psychiatry. 2000;9(2):109-114.
-
(2000)
Eur Child Adolesc Psychiatry
, vol.9
, Issue.2
, pp. 109-114
-
-
Eliez, S.1
Palacio-Espasa, F.2
Spira, A.3
-
114
-
-
0035746376
-
Neuropsychiatric disorders in the 22q11 deletion syndrome
-
Niklasson L, Rasmussen P, Oskarsdottir S, Gillberg C. Neuropsychiatric disorders in the 22q11 deletion syndrome. Genet Med. 2001; 3(1):79-84. (Pubitemid 34884521)
-
(2001)
Genetics in Medicine
, vol.3
, Issue.1
, pp. 79-84
-
-
Niklasson, L.1
Rasmussen, P.2
Oskarsdottir, S.3
Gillberg, C.4
-
115
-
-
0035201119
-
Neurological presentation of three patients with 22q11 deletion (CATCH 22 syndrome)
-
DOI 10.1016/S0387-7604(01)00258-3, PII S0387760401002583
-
Roubertie A, Semprino M, Chaze AM, et al. Neurological presentation of three patients with 22q11 deletion (CATCH 22 syndrome). Brain Dev. 2001;23(8):810-814. (Pubitemid 33101872)
-
(2001)
Brain and Development
, vol.23
, Issue.8
, pp. 810-814
-
-
Roubertie, A.1
Semprino, M.2
Chaze, A.M.3
Rivier, F.4
Humbertclaude, V.5
Cheminal, R.6
Lefort, G.7
Echenne, B.8
-
116
-
-
34447504783
-
Contiguous gene syndrome due to an interstitial deletion in Xp22.3 in a boy with ichthyosis, chondrodysplasia punctata, mental retardation and ADHD
-
DOI 10.1016/j.ejmg.2007.04.005, PII S1769721207000511
-
Lonardo F, Parenti G, Luquetti DV, et al. Contiguous gene syndrome due to an interstitial deletion in Xp22.3 in a boy with ichthyosis, chondrodysplacia punctata, mental retardation and ADHD. Eur J Med Genet. 2007;50(4):301-308. (Pubitemid 47064449)
-
(2007)
European Journal of Medical Genetics
, vol.50
, Issue.4
, pp. 301-308
-
-
Lonardo, F.1
Parenti, G.2
Luquetti, D.V.3
Annunziata, I.4
Della Monica, M.5
Perone, L.6
De Gregori, M.7
Zuffardi, O.8
Brunetti-Pierri, N.9
Andria, G.10
Scarano, G.11
-
117
-
-
0141680209
-
A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHD
-
Boycott KM, Parslow MI, Ross JL, Miller IP, Bech-Hansen NT, MacLeod PM. A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHD. Am J Med Genet A. 2003;122(2):139-147
-
(2003)
Am J Med Genet A
, vol.122
, Issue.2
, pp. 139-147
-
-
Boycott, K.M.1
Parslow, M.I.2
Ross, J.L.3
Miller, I.P.4
Bech-Hansen, N.T.5
MacLeod, P.M.6
-
118
-
-
0032971826
-
Xp deletions associated with autism in three females
-
DOI 10.1007/s004390050908
-
Thomas NS, Sharp AJ, Browne CE, Skuse D, Hardie C, Dennis NR. Xp deletions associated with autism in three females. Hum Genet. 1999;104(1):43-48. (Pubitemid 29134640)
-
(1999)
Human Genetics
, vol.104
, Issue.1
, pp. 43-48
-
-
Thomas, N.S.1
Sharp, A.J.2
Browne, C.E.3
Skuse, D.4
Hardie, C.5
Dennis, N.R.6
-
119
-
-
30344447674
-
Genes for schizophrenia and bipolar disorder? Implications for psychiatric nosology
-
DOI 10.1093/schbul/sbj033
-
Craddock N, O'Donovan MC, Owen MJ. Genes for schizophrenia and bipolar disorder? Implications for psychiatric nosology. Schizophr Bull. 2006;32(1):9-16. (Pubitemid 43063811)
-
(2006)
Schizophrenia Bulletin
, vol.32
, Issue.1
, pp. 9-16
-
-
Craddock, N.1
O'Donovan, M.C.2
Owen, M.J.3
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