-
1
-
-
0004235298
-
-
American Psychiatric Association. (DSM-IV). Washington, DC: American Psychiatric Association
-
American Psychiatric Association. 1994. Diagnostic and statistical manual of mental disorders. 4th edition. (DSM-IV). Washington, DC: American Psychiatric Association.
-
(1994)
Diagnostic and Statistical Manual of Mental Disorders. 4th Edition
-
-
-
2
-
-
12444258372
-
Candidate genes for anorexia nervosa in the 1p33-36 linkage region: Serotonin 1D and delta opioid receptor loci exhibit significant association to anorexia nervosa
-
Bergen AW, van den Bree MB, Yeager M, Welch R, Ganjei JK, Haque K, Bacanu S, Berrettini WH, Grice DE, Goldman D, Bulik CM, Klump K, Fichter M, Halmi K, Kaplan A, Strober M, Treasure J, Woodside B, Kaye WH. 2003. Candidate genes for anorexia nervosa in the 1p33-36 linkage region: Serotonin 1D and delta opioid receptor loci exhibit significant association to anorexia nervosa. Mol Psychiatry 4:397-406.
-
(2003)
Mol Psychiatry
, vol.4
, pp. 397-406
-
-
Bergen, A.W.1
Van Den Bree, M.B.2
Yeager, M.3
Welch, R.4
Ganjei, J.K.5
Haque, K.6
Bacanu, S.7
Berrettini, W.H.8
Grice, D.E.9
Goldman, D.10
Bulik, C.M.11
Klump, K.12
Fichter, M.13
Halmi, K.14
Kaplan, A.15
Strober, M.16
Treasure, J.17
Woodside, B.18
Kaye, W.H.19
-
3
-
-
0018225877
-
Psychopathology in adopted-away offspring of biologic parents with antisocial behavior
-
Cadoret RJ. 1978. Psychopathology in adopted-away offspring of biologic parents with antisocial behavior. Arch Gen Psychiatry 2:176-184.
-
(1978)
Arch Gen Psychiatry
, vol.2
, pp. 176-184
-
-
Cadoret, R.J.1
-
5
-
-
20444412281
-
Molecular genetics of attention deficit hyperactivity disorder
-
Faraone SV, Perlis RH, Doyle AE, Smoller JW, Goralnick J, Holmgren MA, et al. 2005. Molecular genetics of attention deficit hyperactivity disorder. Biol Psychiatry 57:1313-1323.
-
(2005)
Biol Psychiatry
, vol.57
, pp. 1313-1323
-
-
Faraone, S.V.1
Perlis, R.H.2
Doyle, A.E.3
Smoller, J.W.4
Goralnick, J.5
Holmgren, M.A.6
-
6
-
-
0036239098
-
A genomewide scan for loci involved in attention-deficit/hyperactivity disorder
-
Fisher SE, Francks C, McCracken JT, McGough JJ, Marlow AJ, MacPhie IL, Newbury DF, Palmer CGS, Woodward JA, Del'Homme M, Cantwell DP, Nelson SF, Monaco AP, Smalley SL. 2002. A genomewide scan for loci involved in attention-deficit/hyperactivity disorder. Am J Hum Genet 70:1183-1196.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1183-1196
-
-
Fisher, S.E.1
Francks, C.2
McCracken, J.T.3
McGough, J.J.4
Marlow, A.J.5
MacPhie, I.L.6
Newbury, D.F.7
Palmer, C.G.S.8
Woodward, J.A.9
Del'Homme, M.10
Cantwell, D.P.11
Nelson, S.F.12
Monaco, A.P.13
Smalley, S.L.14
-
7
-
-
0033555898
-
Role of serotonin in the paradoxical calming effect of psychostimulants on hyperactivity
-
Gainetdinov RR, Wetsel WC, Jones SR, et al. 1999. Role of serotonin in the paradoxical calming effect of psychostimulants on hyperactivity. Science 285(15):397-401.
-
(1999)
Science
, vol.285
, Issue.15
, pp. 397-401
-
-
Gainetdinov, R.R.1
Wetsel, W.C.2
Jones, S.R.3
-
9
-
-
0036364966
-
Serotonergic system and attention deficit hyperactivity disorder (ADHD): A potential susceptibility locus at the 5-HT(1B) receptor gene in 273 nuclear families from a multi-centre sample
-
Hawi Z, Dring M, Kirley A, Foley D, Kent L, Craddock N, Asherson P, Curran S, Gould A, Richards S, Lawson D, Pay H, Turic D, Langley K, Owen M, O'Donovan M, Thapar A, Fitzgerald M, Gill M. 2002. Serotonergic system and attention deficit hyperactivity disorder (ADHD): A potential susceptibility locus at the 5-HT(1B) receptor gene in 273 nuclear families from a multi-centre sample. Mol Psychiatry 7:718-725.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 718-725
-
-
Hawi, Z.1
Dring, M.2
Kirley, A.3
Foley, D.4
Kent, L.5
Craddock, N.6
Asherson, P.7
Curran, S.8
Gould, A.9
Richards, S.10
Lawson, D.11
Pay, H.12
Turic, D.13
Langley, K.14
Owen, M.15
O'Donovan, M.16
Thapar, A.17
Fitzgerald, M.18
Gill, M.19
-
10
-
-
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, Parmar R, Gingell K, Hawi Z, Kirley A, Lowe N, Fitzgerald M, Gill M, Craddock N. 2002. Evidence that variation at the serotonin transporter gene influences susceptibility to attention deficit hyperactivity disorder (ADHD): Analysis and pooled analysis. Mol Psychiatry 7:908-912.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 908-912
-
-
Kent, L.1
Doerry, U.2
Hardy, E.3
Parmar, R.4
Gingell, K.5
Hawi, Z.6
Kirley, A.7
Lowe, N.8
Fitzgerald, M.9
Gill, M.10
Craddock, N.11
-
11
-
-
0029896472
-
The diagnosis and prevalence of hyperactivity in Chinese schoolboys
-
Leung PWL, Luk SL, Ho TP, Taylor E, Mak FL, Bacon-Shone J. 1996. The diagnosis and prevalence of hyperactivity in Chinese schoolboys. Br J Psychiatry 168:486-496.
-
(1996)
Br J Psychiatry
, vol.168
, pp. 486-496
-
-
Leung, P.W.L.1
Luk, S.L.2
Ho, T.P.3
Taylor, E.4
Mak, F.L.5
Bacon-Shone, J.6
-
12
-
-
11244315275
-
Serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder in Chinese Han subjects
-
Li J, Wang Y, Zhou R, Zhang H, Yang L, Wang B, Khan S, Faraone SV. 2005. Serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder in Chinese Han subjects. Am J Med Genet Part B Neuropsychiatr Genet 132B:59-63.
-
(2005)
Am J Med Genet Part B Neuropsychiatr Genet
, vol.132 B
, pp. 59-63
-
-
Li, J.1
Wang, Y.2
Zhou, R.3
Zhang, H.4
Yang, L.5
Wang, B.6
Khan, S.7
Faraone, S.V.8
-
13
-
-
32244445001
-
Association between tryptophan hydroxylase gene polymorphisms and attention deficit hyperactivity disorder in Chinese Han population
-
Li J, Wang Y, Zhou R, Zhang H, Yang L, Wang B, Faraone SV. 2006. Association between tryptophan hydroxylase gene polymorphisms and attention deficit hyperactivity disorder in Chinese Han population. Am J Med Genet B Neuropsychiatr Genet 41:126-129.
-
(2006)
Am J Med Genet B Neuropsychiatr Genet
, vol.41
, pp. 126-129
-
-
Li, J.1
Wang, Y.2
Zhou, R.3
Zhang, H.4
Yang, L.5
Wang, B.6
Faraone, S.V.7
-
14
-
-
0021025533
-
Low cerebrospinal fluid 5-hydroxyindoleacetic acid concentration differentiates impulsive from nonimpulsive violent behavior
-
Linnoila M, Virkkunen M, Scheinin M, et al. 1983. Low cerebrospinal fluid 5-hydroxyindoleacetic acid concentration differentiates impulsive from nonimpulsive violent behavior. Life Sci 33:2609-2614.
-
(1983)
Life Sci
, vol.33
, pp. 2609-2614
-
-
Linnoila, M.1
Virkkunen, M.2
Scheinin, M.3
-
15
-
-
0035825205
-
Family-based association study of the serotonin transporter promoter region polymorphism (5-HTTLPR) in attention deficit hyperactivity disorder
-
Manor I, Eisenberg J, Tyano S, Sever Y, Cohen H, Ebstein RP, Kotler M. 2001. Family-based association study of the serotonin transporter promoter region polymorphism (5-HTTLPR) in attention deficit hyperactivity disorder. Am J Med Genet 105:91-95.
-
(2001)
Am J Med Genet
, vol.105
, pp. 91-95
-
-
Manor, I.1
Eisenberg, J.2
Tyano, S.3
Sever, Y.4
Cohen, H.5
Ebstein, R.P.6
Kotler, M.7
-
16
-
-
0027474153
-
Release-regulating serotonin 5-HT1D autoreceptors in human cerebral cortex
-
Maura G, Thellung S, Andrioli GC, Ruelle A, Raiteri M. 1993. Release-regulating serotonin 5-HT1D autoreceptors in human cerebral cortex. J Neurochem 3:1179-1182.
-
(1993)
J Neurochem
, vol.3
, pp. 1179-1182
-
-
Maura, G.1
Thellung, S.2
Andrioli, G.C.3
Ruelle, A.4
Raiteri, M.5
-
17
-
-
0015196013
-
A family study of the hyperactive child syndrome
-
Morrison JR, Stewart MA. 1971. A family study of the hyperactive child syndrome. Biol Psychiatry 3:189-195.
-
(1971)
Biol Psychiatry
, vol.3
, pp. 189-195
-
-
Morrison, J.R.1
Stewart, M.A.2
-
18
-
-
0028904290
-
Mapping of the serotonin 5-HT1D alpha autoreceptor gene (HTR1D) on chromosome 1 using a silent polymorphism in the coding region
-
Ozaki N, Lappalainen J, Dean M, Virkkunen M, Linnoila M, Goldman D. 1995. Mapping of the serotonin 5-HT1D alpha autoreceptor gene (HTR1D) on chromosome 1 using a silent polymorphism in the coding region. Am J Med Genet 2:162-164.
-
(1995)
Am J Med Genet
, vol.2
, pp. 162-164
-
-
Ozaki, N.1
Lappalainen, J.2
Dean, M.3
Virkkunen, M.4
Linnoila, M.5
Goldman, D.6
-
19
-
-
12244292661
-
The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder
-
Quist JF, Barr CL, Schachar R, Roberts W, Malone M, Tannock R, Basile VS, Beitchman J, Kennedy JL. 2003. The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder. Mol Psychiatry 8:98-102.
-
(2003)
Mol Psychiatry
, vol.8
, pp. 98-102
-
-
Quist, J.F.1
Barr, C.L.2
Schachar, R.3
Roberts, W.4
Malone, M.5
Tannock, R.6
Basile, V.S.7
Beitchman, J.8
Kennedy, J.L.9
-
20
-
-
0016189915
-
Platelet serotonin of hyperactive school age boys
-
Rapoport J, Quinn P, Scribanu N, et al. 1974. Platelet serotonin of hyperactive school age boys. Br J Psychiatry 125:138-140.
-
(1974)
Br J Psychiatry
, vol.125
, pp. 138-140
-
-
Rapoport, J.1
Quinn, P.2
Scribanu, N.3
-
21
-
-
27144480407
-
Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD
-
Sheehan K, Lowe N, Kirley A, Mullins C, Fitzgerald M, Gill M, Hawi Z. 2005. Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD. Mol Psychiatry 10:944-949.
-
(2005)
Mol Psychiatry
, vol.10
, pp. 944-949
-
-
Sheehan, K.1
Lowe, N.2
Kirley, A.3
Mullins, C.4
Fitzgerald, M.5
Gill, M.6
Hawi, Z.7
-
22
-
-
0021927097
-
An epidemiological investigation of minimal brain dysfunction in six elementary schools in Beijing
-
Shen YC, Wang YF, Yang XL. 1985. An epidemiological investigation of minimal brain dysfunction in six elementary schools in Beijing. J Child Psychol Psychiatry 26:777-788.
-
(1985)
J Child Psychol Psychiatry
, vol.26
, pp. 777-788
-
-
Shen, Y.C.1
Wang, Y.F.2
Yang, X.L.3
-
23
-
-
33344457837
-
Association between the 5HT1B receptor gene (HTR1B) and the inattentive subtype of ADHD
-
Smoller JW, Biederman J, Arbeitman L, Doyle AE, Fagerness J, Perlis RH, Sklar P, Faraone SV. 2006. Association between the 5HT1B receptor gene (HTR1B) and the inattentive subtype of ADHD. Biol Psychiatry 59:460-467.
-
(2006)
Biol Psychiatry
, vol.59
, pp. 460-467
-
-
Smoller, J.W.1
Biederman, J.2
Arbeitman, L.3
Doyle, A.E.4
Fagerness, J.5
Perlis, R.H.6
Sklar, P.7
Faraone, S.V.8
-
24
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
Spielman RS, McGinnis RE, Ewens WJ. 1993. Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet 3:506-516.
-
(1993)
Am J Hum Genet
, vol.3
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
25
-
-
0035828091
-
Lack of association between the tryptophan hydroxylase gene A218C polymorphism and attention-deficit hyperactivity disorder in Chinese Han population
-
Tang G, Ren D, Xin R, Qian Y, Wang D, Jiang S. 2001. Lack of association between the tryptophan hydroxylase gene A218C polymorphism and attention-deficit hyperactivity disorder in Chinese Han population. Am J Med Genet 105:485-488.
-
(2001)
Am J Med Genet
, vol.105
, pp. 485-488
-
-
Tang, G.1
Ren, D.2
Xin, R.3
Qian, Y.4
Wang, D.5
Jiang, S.6
-
26
-
-
0028884659
-
Childhood hyperactivity scores are highly heritable and show sibling competition effects: Twin study evidence
-
Thapar A, Hervas A, McGuffin P. 1995. Childhood hyperactivity scores are highly heritable and show sibling competition effects: Twin study evidence. Behav Genet 6:537-544.
-
(1995)
Behav Genet
, vol.6
, pp. 537-544
-
-
Thapar, A.1
Hervas, A.2
McGuffin, P.3
-
27
-
-
27144538430
-
Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in attention-deficit/hyperactivity disorder
-
Walitza S, Renner TJ, Dempfle A, Konrad K, Wewetzer Ch, Halbach A, Herpertz-Dahlmann B, Remschmidt H, Smidt J, Linder M, Flierl L, Knolker U, Friedel S, Schafer H, Gross C, Hebebrand J, Warnke A, Lesch KP. 2005. Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in attention-deficit/hyperactivity disorder. Mol Psychiatry 10:1126-1132.
-
(2005)
Mol Psychiatry
, vol.10
, pp. 1126-1132
-
-
Walitza, S.1
Renner, T.J.2
Dempfle, A.3
Konrad, K.4
Wewetzer, C.5
Halbach, A.6
Herpertz-Dahlmann, B.7
Remschmidt, H.8
Smidt, J.9
Linder, M.10
Flierl, L.11
Knolker, U.12
Friedel, S.13
Schafer, H.14
Gross, C.15
Hebebrand, J.16
Warnke, A.17
Kp, L.18
-
28
-
-
0036315096
-
Significance of serotonin transporter gene 5-HTTLPR and variable number of tandem repeat polymorphism in attention deficit hyperactivity disorder
-
Zoroglu SS, Erdal ME, Alasehirli B, Erdal N, Sivasli E, Tutkun H, Savas HA, Herken H. 2002. Significance of serotonin transporter gene 5-HTTLPR and variable number of tandem repeat polymorphism in attention deficit hyperactivity disorder. Neuropsychobiology 45:176-181.
-
(2002)
Neuropsychobiology
, vol.45
, pp. 176-181
-
-
Zoroglu, S.S.1
Erdal, M.E.2
Alasehirli, B.3
Erdal, N.4
Sivasli, E.5
Tutkun, H.6
Savas, H.A.7
Herken, H.8
|