-
1
-
-
0032533256
-
Neurobiology of attention-deficit hyperactivity disorder
-
Faraone SV, Biederman J. Neurobiology of attention-deficit hyperactivity disorder. Biol Psychiatry 1998; 44: 951-958.
-
(1998)
Biol Psychiatry
, vol.44
, pp. 951-958
-
-
Faraone, S.V.1
Biederman, J.2
-
2
-
-
7444263504
-
Molecular genetic aspects of attention-deficit/hyperactivity disorder
-
Heiser P, Friedel S, Dempfle A, Konrad K, Smidt J, Grabarkiewicz J et al. Molecular genetic aspects of attention-deficit/hyperactivity disorder. Neurosci Biobehav Rev 2004; 28: 625-641.
-
(2004)
Neurosci Biobehav Rev
, vol.28
, pp. 625-641
-
-
Heiser, P.1
Friedel, S.2
Dempfle, A.3
Konrad, K.4
Smidt, J.5
Grabarkiewicz, J.6
-
3
-
-
31544439114
-
A genome-wide scan for attention-deficit/ hyperactivity disorder in 155 German sib-pairs
-
Hebebrand J, Dempfle A, Saar K, Thiele H, Herpertz-Dahlmann B, Linder M et al. A genome-wide scan for attention-deficit/ hyperactivity disorder in 155 German sib-pairs. Mol Psychiatry 2006; 11: 196-205.
-
(2006)
Mol Psychiatry
, vol.11
, pp. 196-205
-
-
Hebebrand, J.1
Dempfle, A.2
Saar, K.3
Thiele, H.4
Herpertz-Dahlmann, B.5
Linder, M.6
-
4
-
-
0036239098
-
A genomewide scan for loci involved in attention-deficit/ hyperactivity disorder
-
Fisher SE, Francks C, McCracken JT, McGough JJ, Marlow AJ, MacPhie IL et al. A genomewide scan for loci involved in attention-deficit/ hyperactivity disorder. Am J Hum Genet 2002; 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
-
5
-
-
0038752692
-
A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: Suggestive linkage on 17p11
-
Ogdie MN, Macphie IL, Minassian SL, Yang M, Fisher SE, Francks C et al. A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11. Am J Hum Genet 2003; 72: 1268-1279.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1268-1279
-
-
Ogdie, M.N.1
Macphie, I.L.2
Minassian, S.L.3
Yang, M.4
Fisher, S.E.5
Francks, C.6
-
6
-
-
4544293448
-
Attention deficit hyperactivity disorder: Fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11
-
Ogdie MN, Fisher SE, Yang M, Ishii J, Francks C, Loo SK et al. Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11. Am J Hum Genet 2004; 75: 661-668.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 661-668
-
-
Ogdie, M.N.1
Fisher, S.E.2
Yang, M.3
Ishii, J.4
Francks, C.5
Loo, S.K.6
-
7
-
-
32844459495
-
Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13
-
Ogdie MN, Bakker SC, Fisher SE, Francks C, Yang MH, Cantor RM et al. Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13. Mol Psychiatry 2006; 11: 5-8.
-
(2006)
Mol Psychiatry
, vol.11
, pp. 5-8
-
-
Ogdie, M.N.1
Bakker, S.C.2
Fisher, S.E.3
Francks, C.4
Yang, M.H.5
Cantor, R.M.6
-
8
-
-
33644797485
-
Recognition of psychostimulants, antidepressants, and other inhibitors of synaptic neurotransmitter uptake by the plasma membrane monoamine transporters
-
Surratt CK, Ukairo OT, Ramanujapuram S. Recognition of psychostimulants, antidepressants, and other inhibitors of synaptic neurotransmitter uptake by the plasma membrane monoamine transporters. AAPS J 2005; 7: E739-51.
-
(2005)
AAPS J
, vol.7
-
-
Surratt, C.K.1
Ukairo, O.T.2
Ramanujapuram, S.3
-
9
-
-
0033770381
-
Attention deficit hyperactivity disorder: Binding of [99mTc]TRODAT-1 to the dopamine transporter before and after methylphenidate treatment
-
Dresel S, Krause J, Krause KH, LaFougere C, Brinkbauer K, Kung HF et al. Attention deficit hyperactivity disorder: binding of [99mTc]TRODAT-1 to the dopamine transporter before and after methylphenidate treatment. Eur J Nucl Med 2000; 27: 1518-1524.
-
(2000)
Eur J Nucl Med
, vol.27
, pp. 1518-1524
-
-
Dresel, S.1
Krause, J.2
Krause, K.H.3
LaFougere, C.4
Brinkbauer, K.5
Kung, H.F.6
-
10
-
-
0033582097
-
Dopamine transporter density in patients with attention deficit hyperactivity disorder
-
Dougherty DD, Bonab AA, Spencer TJ, Rauch SL, Madras BK, Fischman AJ. Dopamine transporter density in patients with attention deficit hyperactivity disorder. Lancet 1999; 354: 2132-2133.
-
(1999)
Lancet
, vol.354
, pp. 2132-2133
-
-
Dougherty, D.D.1
Bonab, A.A.2
Spencer, T.J.3
Rauch, S.L.4
Madras, B.K.5
Fischman, A.J.6
-
11
-
-
0034640146
-
Increased striatal dopamine transporter in adult patients with attention deficit hyperactivity disorder: Effects of methylphenidate as measured by single photon emission computed tomography
-
Krause KH, Dresel SH, Krause J, Kung HF, Tatsch K. Increased striatal dopamine transporter in adult patients with attention deficit hyperactivity disorder: effects of methylphenidate as measured by single photon emission computed tomography. Neurosci Lett 2000; 285: 107-110.
-
(2000)
Neurosci Lett
, vol.285
, pp. 107-110
-
-
Krause, K.H.1
Dresel, S.H.2
Krause, J.3
Kung, H.F.4
Tatsch, K.5
-
12
-
-
0038515241
-
Dopamine transporter density in the basal ganglia assessed with [123I]IPT SPET in children with attention deficit hyperactivity disorder
-
Cheon KA, Ryu YH, Kim YK, Namkoong K, Kim CH, Lee JD. Dopamine transporter density in the basal ganglia assessed with [123I]IPT SPET in children with attention deficit hyperactivity disorder. Eur J Nucl Med Mol Imaging 2003; 30: 306-311.
-
(2003)
Eur J Nucl Med Mol Imaging
, vol.30
, pp. 306-311
-
-
Cheon, K.A.1
Ryu, Y.H.2
Kim, Y.K.3
Namkoong, K.4
Kim, C.H.5
Lee, J.D.6
-
13
-
-
0036164416
-
Unaltered dopamine transporter availability in adult attention deficit hyperactivity disorder
-
van Dyck CH, Quinlan DM, Cretella LM, Staley JK, Malison RT, Baldwin RM et al. Unaltered dopamine transporter availability in adult attention deficit hyperactivity disorder. Am J Psychiatry 2002; 159: 309-312.
-
(2002)
Am J Psychiatry
, vol.159
, pp. 309-312
-
-
van Dyck, C.H.1
Quinlan, D.M.2
Cretella, L.M.3
Staley, J.K.4
Malison, R.T.5
Baldwin, R.M.6
-
14
-
-
20444424891
-
The dopamine transporter and attention-deficit/hyperactivity disorder
-
Madras BK, Miller GM, Fischman AJ. The dopamine transporter and attention-deficit/hyperactivity disorder. Biol Psychiatry 2005; 57: 1397-1409.
-
(2005)
Biol Psychiatry
, vol.57
, pp. 1397-1409
-
-
Madras, B.K.1
Miller, G.M.2
Fischman, A.J.3
-
15
-
-
0030071106
-
Hyperlocomotion and indifference to cocaine and amphetamine in mice lacking the dopamine transporter
-
Giros B, Jaber M, Jones SR, Wightman RM, Caron MG. Hyperlocomotion and indifference to cocaine and amphetamine in mice lacking the dopamine transporter. Nature 1996; 379: 606-612.
-
(1996)
Nature
, vol.379
, pp. 606-612
-
-
Giros, B.1
Jaber, M.2
Jones, S.R.3
Wightman, R.M.4
Caron, M.G.5
-
16
-
-
0035125656
-
Genetics of childhood disorders: XXIV. ADHD, part 8: hyperdopaminergic mice as an animal model of ADHD
-
Gainetdinov RR, Caron MG. Genetics of childhood disorders: XXIV. ADHD, part 8: hyperdopaminergic mice as an animal model of ADHD. J Am Acad Child Adolesc Psychiatry 2001; 40: 380-382.
-
(2001)
J Am Acad Child Adolesc Psychiatry
, vol.40
, pp. 380-382
-
-
Gainetdinov, R.R.1
Caron, M.G.2
-
17
-
-
0033936633
-
Behavioural disturbances associated with hyperdopaminergia in dopamine-transporter knockout mice
-
Spielewoy C, Roubert C, Hamon M, Nosten-Bertrand M, Betancur C, Giros B. Behavioural disturbances associated with hyperdopaminergia in dopamine-transporter knockout mice. Behav Pharmacol 2000; 11: 279-290.
-
(2000)
Behav Pharmacol
, vol.11
, pp. 279-290
-
-
Spielewoy, C.1
Roubert, C.2
Hamon, M.3
Nosten-Bertrand, M.4
Betancur, C.5
Giros, B.6
-
18
-
-
0033555898
-
Role of serotonin in the paradoxical calming effect of psychostimulants on hyperactivity
-
Gainetdinov RR, Wetsel WC, Jones SR, Levin ED, Jaber M, Caron MG. Role of serotonin in the paradoxical calming effect of psychostimulants on hyperactivity. Science 1999; 283: 397-401.
-
(1999)
Science
, vol.283
, pp. 397-401
-
-
Gainetdinov, R.R.1
Wetsel, W.C.2
Jones, S.R.3
Levin, E.D.4
Jaber, M.5
Caron, M.G.6
-
19
-
-
0347626244
-
Aberrant responses in social interaction of dopamine transporter knockout mice
-
Rodriguiz RM, Chu R, Caron MG, Wetsel WC. Aberrant responses in social interaction of dopamine transporter knockout mice. Behav Brain Res 2004; 148: 185-198.
-
(2004)
Behav Brain Res
, vol.148
, pp. 185-198
-
-
Rodriguiz, R.M.1
Chu, R.2
Caron, M.G.3
Wetsel, W.C.4
-
20
-
-
0035846827
-
The human dopamine transporter gene: The 5′-flanking region reveals five diallelic polymorphic sites in a Caucasian population sample
-
Rubie C, Schmidt F, Knapp M, Sprandel J, Wiegand C, Meyer J et al. The human dopamine transporter gene: the 5′-flanking region reveals five diallelic polymorphic sites in a Caucasian population sample. Neurosci Lett 2001; 297: 125-128.
-
(2001)
Neurosci Lett
, vol.297
, pp. 125-128
-
-
Rubie, C.1
Schmidt, F.2
Knapp, M.3
Sprandel, J.4
Wiegand, C.5
Meyer, J.6
-
21
-
-
0035091751
-
Nurr1 enhances transcription of the human dopamine transporter gene through a novel mechanism
-
Sacchetti P, Mitchell TR, Granneman JG, Bannon MJ. Nurr1 enhances transcription of the human dopamine transporter gene through a novel mechanism. J Neurochem 2001; 76: 1565-1572.
-
(2001)
J Neurochem
, vol.76
, pp. 1565-1572
-
-
Sacchetti, P.1
Mitchell, T.R.2
Granneman, J.G.3
Bannon, M.J.4
-
22
-
-
17444398973
-
Sp1 and Sp3 activate transcription of the human dopamine transporter gene
-
Wang J, Bannon MJ. Sp1 and Sp3 activate transcription of the human dopamine transporter gene. J Neurochem 2005; 93: 474-482.
-
(2005)
J Neurochem
, vol.93
, pp. 474-482
-
-
Wang, J.1
Bannon, M.J.2
-
23
-
-
0141992020
-
Promoter and intronic variants affect the transcriptional regulation of the human dopamine transporter gene
-
Greenwood TA, Kelsoe JR. Promoter and intronic variants affect the transcriptional regulation of the human dopamine transporter gene. Genomics 2003; 82: 511-520.
-
(2003)
Genomics
, vol.82
, pp. 511-520
-
-
Greenwood, T.A.1
Kelsoe, J.R.2
-
24
-
-
31544431742
-
Identification of additional variants within the human dopamine transporter gene provides further evidence for an association with bipolar disorder in two independent samples
-
Greenwood TA, Schork NJ, Eskin E, Kelsoe JR. Identification of additional variants within the human dopamine transporter gene provides further evidence for an association with bipolar disorder in two independent samples. Mol Psychiatry 2006; 11: 125-133.
-
(2006)
Mol Psychiatry
, vol.11
, pp. 125-133
-
-
Greenwood, T.A.1
Schork, N.J.2
Eskin, E.3
Kelsoe, J.R.4
-
25
-
-
23444458557
-
Dopamine transporter (SLC6A3) 5′ region haplotypes significantly affect transcriptional activity in vitro but are not associated with Parkinson's disease
-
Kelada SN, Costa-Mallen P, Checkoway H, Carlson CS, Weller TS, Swanson PD et al. Dopamine transporter (SLC6A3) 5′ region haplotypes significantly affect transcriptional activity in vitro but are not associated with Parkinson's disease. Pharmacogenet Genomics 2005; 15: 659-668.
-
(2005)
Pharmacogenet Genomics
, vol.15
, pp. 659-668
-
-
Kelada, S.N.1
Costa-Mallen, P.2
Checkoway, H.3
Carlson, C.S.4
Weller, T.S.5
Swanson, P.D.6
-
26
-
-
33749552018
-
Common human 5′ dopamine transporter (SLC6A3) haplotypes yield varying expression levels in vivo
-
Drgon T, Lin Z, Wang GJ, Fowler J, Pablo J, Mash DC et al. Common human 5′ dopamine transporter (SLC6A3) haplotypes yield varying expression levels in vivo. Cell Mol Neurobiol 2006; 26: 875-889.
-
(2006)
Cell Mol Neurobiol
, vol.26
, pp. 875-889
-
-
Drgon, T.1
Lin, Z.2
Wang, G.J.3
Fowler, J.4
Pablo, J.5
Mash, D.C.6
-
27
-
-
0032991552
-
Characterization of single-nucleotide polymorphisms in coding regions of human genes
-
Cargill M, Altshuler D, Ireland J, Sklar P, Ardlie K, Patil N et al. Characterization of single-nucleotide polymorphisms in coding regions of human genes. Nat Genet 1999; 22: 231-238.
-
(1999)
Nat Genet
, vol.22
, pp. 231-238
-
-
Cargill, M.1
Altshuler, D.2
Ireland, J.3
Sklar, P.4
Ardlie, K.5
Patil, N.6
-
28
-
-
0033946739
-
Systematic screening for DNA sequence variation in the coding region of the human dopamine transporter gene (DAT1)
-
Grunhage F, Schulze TG, Muller DJ, Lanczik M, Franzek E, Albus M et al. Systematic screening for DNA sequence variation in the coding region of the human dopamine transporter gene (DAT1). Mol Psychiatry 2000; 5: 275-282.
-
(2000)
Mol Psychiatry
, vol.5
, pp. 275-282
-
-
Grunhage, F.1
Schulze, T.G.2
Muller, D.J.3
Lanczik, M.4
Franzek, E.5
Albus, M.6
-
29
-
-
0004883390
-
Human dopamine transporter gene: Coding region conservation among normal, Tourette's disorder, alcohol dependence and attention-deficit hyperactivity disorder populations
-
Vandenbergh DJ, Thompson MD, Cook EH, Bendahhou E, Nguyen T, Krasowski MD et al. Human dopamine transporter gene: coding region conservation among normal, Tourette's disorder, alcohol dependence and attention-deficit hyperactivity disorder populations. Mol Psychiatry 2000; 5: 283-292.
-
(2000)
Mol Psychiatry
, vol.5
, pp. 283-292
-
-
Vandenbergh, D.J.1
Thompson, M.D.2
Cook, E.H.3
Bendahhou, E.4
Nguyen, T.5
Krasowski, M.D.6
-
30
-
-
26944484406
-
Sequence variation in the human dopamine transporter gene in children with attention deficit hyperactivity disorder
-
Mazei-Robison MS, Couch RS, Shelton RC, Stein MA, Blakely RD. Sequence variation in the human dopamine transporter gene in children with attention deficit hyperactivity disorder. Neuropharmacology 2005; 49: 724-736.
-
(2005)
Neuropharmacology
, vol.49
, pp. 724-736
-
-
Mazei-Robison, M.S.1
Couch, R.S.2
Shelton, R.C.3
Stein, M.A.4
Blakely, R.D.5
-
31
-
-
0028987091
-
Association of attention-deficit disorder and the dopamine transporter gene
-
Cook Jr EH, Stein MA, Krasowski MD, Cox NJ, Olkon DM, Kieffer JE et al. Association of attention-deficit disorder and the dopamine transporter gene. Am J Hum Genet 1995; 56: 993-998.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 993-998
-
-
Cook Jr, E.H.1
Stein, M.A.2
Krasowski, M.D.3
Cox, N.J.4
Olkon, D.M.5
Kieffer, J.E.6
-
32
-
-
0032217057
-
Association and linkage of the dopamine transporter gene and attention-deficit hyperactivity disorder in children: Heterogeneity owing to diagnostic subtype and severity
-
Waldman ID, Rowe DC, Abramowitz A, Kozel ST, Mohr JH, Sherman SL et al. Association and linkage of the dopamine transporter gene and attention-deficit hyperactivity disorder in children: heterogeneity owing to diagnostic subtype and severity. Am J Hum Genet 1998; 63: 1767-1776.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1767-1776
-
-
Waldman, I.D.1
Rowe, D.C.2
Abramowitz, A.3
Kozel, S.T.4
Mohr, J.H.5
Sherman, S.L.6
-
33
-
-
0032910655
-
Mapping susceptibility loci in attention deficit hyperactivity disorder: Preferential transmission of parental alleles at DAT1, DBH and DRD5 to affected children
-
Daly G, Hawi Z, Fitzgerald M, Gill M. Mapping susceptibility loci in attention deficit hyperactivity disorder: preferential transmission of parental alleles at DAT1, DBH and DRD5 to affected children. Mol Psychiatry 1999; 4: 192-196.
-
(1999)
Mol Psychiatry
, vol.4
, pp. 192-196
-
-
Daly, G.1
Hawi, Z.2
Fitzgerald, M.3
Gill, M.4
-
34
-
-
11244264176
-
DAT1, DRD4, and DRD5 polymorphisms are not associated with ADHD in Dutch families
-
Bakker SC, van der Meulen EM, Oteman N, Schelleman H, Pearson PL, Buitelaar JK et al. DAT1, DRD4, and DRD5 polymorphisms are not associated with ADHD in Dutch families. Am J Med Genet B Neuropsychiatr Genet 2005; 132: 50-52.
-
(2005)
Am J Med Genet B Neuropsychiatr Genet
, vol.132
, pp. 50-52
-
-
Bakker, S.C.1
van der Meulen, E.M.2
Oteman, N.3
Schelleman, H.4
Pearson, P.L.5
Buitelaar, J.K.6
-
35
-
-
27644570110
-
No support for association between the dopamine transporter (DAT1) gene and ADHD
-
Langley K, Turic D, Peirce TR, Mills S, Van Den Bree MB, Owen MJ et al. No support for association between the dopamine transporter (DAT1) gene and ADHD. Am J Med Genet B Neuropsychiatr Genet 2005; 139: 7-10.
-
(2005)
Am J Med Genet B Neuropsychiatr Genet
, vol.139
, pp. 7-10
-
-
Langley, K.1
Turic, D.2
Peirce, T.R.3
Mills, S.4
Van Den Bree, M.B.5
Owen, M.J.6
-
36
-
-
27644464349
-
Sequence variation in the 3′-untranslated region of the dopamine transporter gene and attention-deficit hyperactivity disorder (ADHD)
-
Feng Y, Wigg KG, Makkar R, Ickowicz A, Pathare T, Tannock R et al. Sequence variation in the 3′-untranslated region of the dopamine transporter gene and attention-deficit hyperactivity disorder (ADHD). Am J Med Genet B Neuropsychiatr Genet 2005; 139: 1-6.
-
(2005)
Am J Med Genet B Neuropsychiatr Genet
, vol.139
, pp. 1-6
-
-
Feng, Y.1
Wigg, K.G.2
Makkar, R.3
Ickowicz, A.4
Pathare, T.5
Tannock, R.6
-
37
-
-
15744386142
-
Meta-analysis of family-based association studies between the dopamine transporter gene and attention deficit hyperactivity disorder
-
Purper-Ouakil D, Wohl M, Mouren MC, Verpillat P, Ades J, Gorwood P. Meta-analysis of family-based association studies between the dopamine transporter gene and attention deficit hyperactivity disorder. Psychiatr Genet 2005; 15: 53-59.
-
(2005)
Psychiatr Genet
, vol.15
, pp. 53-59
-
-
Purper-Ouakil, D.1
Wohl, M.2
Mouren, M.C.3
Verpillat, P.4
Ades, J.5
Gorwood, P.6
-
38
-
-
33745700886
-
Meta-analysis shows significant association between dopamine system genes and attention deficit hyperactivity disorder (ADHD)
-
Li D, Sham PC, Owen MJ, He L. Meta-analysis shows significant association between dopamine system genes and attention deficit hyperactivity disorder (ADHD). Hum Mol Genet 2006; 15: 2276-2284.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 2276-2284
-
-
Li, D.1
Sham, P.C.2
Owen, M.J.3
He, L.4
-
39
-
-
0037499734
-
Linkage disequilibrium mapping at DAT1, DRD5 and DBH narrows the search for ADHD susceptibility alleles at these loci
-
Hawi Z, Lowe N, Kirley A, Gruenhage F, Nothen M, Greenwood T et al. Linkage disequilibrium mapping at DAT1, DRD5 and DBH narrows the search for ADHD susceptibility alleles at these loci. Mol Psychiatry 2003; 8: 299-308.
-
(2003)
Mol Psychiatry
, vol.8
, pp. 299-308
-
-
Hawi, Z.1
Lowe, N.2
Kirley, A.3
Gruenhage, F.4
Nothen, M.5
Greenwood, T.6
-
40
-
-
0242365681
-
Dopamine transporter: Basic science and human variation of a key molecule for dopaminergic function, locomotion, and parkinsonism
-
Uhl GR. Dopamine transporter: basic science and human variation of a key molecule for dopaminergic function, locomotion, and parkinsonism. Mov Disord 2003; S7: S71-S80.
-
(2003)
Mov Disord
, vol.S7
-
-
Uhl, G.R.1
-
41
-
-
33748646825
-
The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: Association signals in DRD4, DAT1 and 16 other genes
-
Brookes K, Xu X, Chen W, Zhou K, Neale B, Lowe N 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: 934-953.
-
(2006)
Mol Psychiatry
, vol.11
, pp. 934-953
-
-
Brookes, K.1
Xu, X.2
Chen, W.3
Zhou, K.4
Neale, B.5
Lowe, N.6
-
42
-
-
0004235298
-
-
American Psychiatric Association, 4th edn. The American Psychiatric Association APA, Washington, DC
-
American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, 4th edn. The American Psychiatric Association (APA): Washington, DC, 1994.
-
(1994)
Diagnostic and Statistical Manual of Mental Disorders
-
-
-
43
-
-
0028989093
-
Diagnosis of psychiatric disorders in children and adolescents using structured interviews]
-
Unnewehr S. Diagnosis of psychiatric disorders in children and adolescents using structured interviews]. Z Kinder Jugendpsychiatr 1995; 23: 121-132.
-
(1995)
Z Kinder Jugendpsychiatr
, vol.23
, pp. 121-132
-
-
Unnewehr, S.1
-
44
-
-
0035865564
-
Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder
-
Barr CL, Xu C, Kroft J, Feng Y, Wigg K, Zai G et al. Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder. Biol Psychiatry 2001; 49: 333-339.
-
(2001)
Biol Psychiatry
, vol.49
, pp. 333-339
-
-
Barr, C.L.1
Xu, C.2
Kroft, J.3
Feng, Y.4
Wigg, K.5
Zai, G.6
-
45
-
-
17144461485
-
A novel procedure for efficient genotyping of single nucleotide polymorphisms
-
Sauer S, Lechner D, Berlin K, Lehrach H, Escary JL, Fox N et al. A novel procedure for efficient genotyping of single nucleotide polymorphisms. Nucleic Acids Res 2000; 28: E13.
-
(2000)
Nucleic Acids Res
, vol.28
-
-
Sauer, S.1
Lechner, D.2
Berlin, K.3
Lehrach, H.4
Escary, J.L.5
Fox, N.6
-
46
-
-
0037930756
-
Extension of the GOOD assay for genotyping single nucleotide polymorphisms by matrix-assisted laser desorption/ ionization mass spectrometry
-
Sauer S, Gut IG. Extension of the GOOD assay for genotyping single nucleotide polymorphisms by matrix-assisted laser desorption/ ionization mass spectrometry. Rapid Commun Mass Spectrom 2003; 17: 1265-1272.
-
(2003)
Rapid Commun Mass Spectrom
, vol.17
, pp. 1265-1272
-
-
Sauer, S.1
Gut, I.G.2
-
47
-
-
0038606971
-
MALDI mass spectrometry analysis of single nucleotide polymorphisms by photo-cleavage and charge-tagging
-
Sauer S, Lehrach H, Reinhardt R. MALDI mass spectrometry analysis of single nucleotide polymorphisms by photo-cleavage and charge-tagging. Nucleic Acids Res 2003; 31: e63.
-
(2003)
Nucleic Acids Res
, vol.31
-
-
Sauer, S.1
Lehrach, H.2
Reinhardt, R.3
-
48
-
-
4444242792
-
Automated solid-phase extraction for purification of single nucleotide polymorphism genotyping products prior to matrix-assisted laser desorption/ionisation time-of-flight mass spectrometric analysis
-
Sauer S, Kepper P, Smyra A, Dahl A, Ferse FT, Lehrach H et al. Automated solid-phase extraction for purification of single nucleotide polymorphism genotyping products prior to matrix-assisted laser desorption/ionisation time-of-flight mass spectrometric analysis. J Chromatogr A 2004; 1049: 9-16.
-
(2004)
J Chromatogr A
, vol.1049
, pp. 9-16
-
-
Sauer, S.1
Kepper, P.2
Smyra, A.3
Dahl, A.4
Ferse, F.T.5
Lehrach, H.6
-
49
-
-
0030872838
-
PolyPhred: Automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing
-
Nickerson DA, Tobe VO, Taylor SL. PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing. Nucleic Acids Res 1997; 25: 2745-2751.
-
(1997)
Nucleic Acids Res
, vol.25
, pp. 2745-2751
-
-
Nickerson, D.A.1
Tobe, V.O.2
Taylor, S.L.3
-
50
-
-
0032231941
-
PedCheck: A program for identification of genotype incompatibilities in linkage analysis
-
O'Connell JR, Weeks DE. PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet 1998; 63: 259-266.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 259-266
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
51
-
-
24044550689
-
PEDSTATS: Descriptive statistics, graphics and quality assessment for gene mapping data
-
Wigginton JE, Abecasis GR. PEDSTATS: descriptive statistics, graphics and quality assessment for gene mapping data. Bioinformatics 2005; 21: 3445-3447.
-
(2005)
Bioinformatics
, vol.21
, pp. 3445-3447
-
-
Wigginton, J.E.1
Abecasis, G.R.2
-
52
-
-
33646175930
-
Identification of probable genotyping errors by consideration of haplotypes
-
Becker T, Valentonyte R, Croucher PJ, Strauch K, Schreiber S, Hampe J et al. Identification of probable genotyping errors by consideration of haplotypes. Eur J Hum Genet 2006; 14: 450-458.
-
(2006)
Eur J Hum Genet
, vol.14
, pp. 450-458
-
-
Becker, T.1
Valentonyte, R.2
Croucher, P.J.3
Strauch, K.4
Schreiber, S.5
Hampe, J.6
-
53
-
-
13444269543
-
Haploview: Analysis and visualization of LD and haplotype maps
-
Barrett JC, Fry B, Maller J, Daly MJ. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 2005; 21: 263-265.
-
(2005)
Bioinformatics
, vol.21
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
54
-
-
0033794971
-
Transmission/disequilibrium tests using multiple tightly linked markers
-
Zhao H, Zhang S, Merikangas KR, Trixler M, Wildenauer DB, Sun F et al. Transmission/disequilibrium tests using multiple tightly linked markers. Am J Hum Genet 2000; 67: 936-946.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 936-946
-
-
Zhao, H.1
Zhang, S.2
Merikangas, K.R.3
Trixler, M.4
Wildenauer, D.B.5
Sun, F.6
-
55
-
-
4544387440
-
A powerful strategy to account for multiple testing in the context of haplotype analysis
-
Becker T, Knapp M. A powerful strategy to account for multiple testing in the context of haplotype analysis. Am J Hum Genet 2004; 75: 561-570.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 561-570
-
-
Becker, T.1
Knapp, M.2
-
56
-
-
0038315385
-
Confidence intervals for genotype relative risks and allele frequencies from the case parent trio design for candidate-gene studies
-
Scherag A, Dempfle A, Hinney A, Hebebrand J, Schafer H. Confidence intervals for genotype relative risks and allele frequencies from the case parent trio design for candidate-gene studies. Hum Hered 2002; 54: 210-217.
-
(2002)
Hum Hered
, vol.54
, pp. 210-217
-
-
Scherag, A.1
Dempfle, A.2
Hinney, A.3
Hebebrand, J.4
Schafer, H.5
-
57
-
-
0028301661
-
A class of tests for linkage using affected pedigree members
-
Whittemore AS, Halpern J. A class of tests for linkage using affected pedigree members. Biometrics 1994; 50: 118-127.
-
(1994)
Biometrics
, vol.50
, pp. 118-127
-
-
Whittemore, A.S.1
Halpern, J.2
-
58
-
-
0030728925
-
Allele-sharing models: LOD scores and accurate linkage tests
-
Kong A, Cox NJ. Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet 1997; 61: 1179-1188.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1179-1188
-
-
Kong, A.1
Cox, N.J.2
-
59
-
-
0036338150
-
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR. Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 2002; 30: 97-101.
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
60
-
-
0036077215
-
Powerful regression-based quantitative-trait linkage analysis of general pedigrees
-
Sham PC, Purcell S, Cherny SS, Abecasis GR. Powerful regression-based quantitative-trait linkage analysis of general pedigrees. Am J Hum Genet 2002; 71: 238-253.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 238-253
-
-
Sham, P.C.1
Purcell, S.2
Cherny, S.S.3
Abecasis, G.R.4
-
61
-
-
0000408893
-
Der Fremdbeurteilungsbogen für hyperkinetische Störungen (FBB-HKS) - Prävalenz hyperkinetischer Störungen im Elternurteil und psychometrische Kriterien
-
Bruehl B, Doepfner M, Lehmkuhl G. Der Fremdbeurteilungsbogen für hyperkinetische Störungen (FBB-HKS) - Prävalenz hyperkinetischer Störungen im Elternurteil und psychometrische Kriterien. Kindheit und Entwicklung 2000; 9: 115-125.
-
(2000)
Kindheit und Entwicklung
, vol.9
, pp. 115-125
-
-
Bruehl, B.1
Doepfner, M.2
Lehmkuhl, G.3
-
62
-
-
1542374068
-
Assessing whether an allele can account in part for a linkage signal: The Genotype-IBD Sharing Test (GIST)
-
Li C, Scott LJ, Boehnke M. Assessing whether an allele can account in part for a linkage signal: the Genotype-IBD Sharing Test (GIST). Am J Hum Genet 2004; 74: 418-431.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 418-431
-
-
Li, C.1
Scott, L.J.2
Boehnke, M.3
-
63
-
-
18944361861
-
Joint modeling of linkage and association: Identifying SNPs responsible for a linkage signal
-
Li M, Boehnke M, Abecasis GR. Joint modeling of linkage and association: identifying SNPs responsible for a linkage signal. Am J Hum Genet 2005; 76: 934-949.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 934-949
-
-
Li, M.1
Boehnke, M.2
Abecasis, G.R.3
-
64
-
-
0038414643
-
-
Bakker SC, van der Meulen EM, Buitelaar JK, Sandkuijl LA, Pauls DL, Monsuur AJ et al. Awhole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q. Am J Hum Genet 2003; 72: 1251-1260.
-
Bakker SC, van der Meulen EM, Buitelaar JK, Sandkuijl LA, Pauls DL, Monsuur AJ et al. Awhole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q. Am J Hum Genet 2003; 72: 1251-1260.
-
-
-
-
65
-
-
0035208755
-
Sample size requirements to control for stochastic variation in magnitude and location of allele-sharing linkage statistics in affected sibling pairs
-
Cordell HJ. Sample size requirements to control for stochastic variation in magnitude and location of allele-sharing linkage statistics in affected sibling pairs. Ann Hum Genet 2001; 65: 491-502.
-
(2001)
Ann Hum Genet
, vol.65
, pp. 491-502
-
-
Cordell, H.J.1
-
66
-
-
0034917133
-
Mapping genes that regulate density of dopamine transporters and correlated behaviors in recombinant inbred mice
-
Janowsky A, Mah C, Johnson RA, Cunningham CL, Phillips TJ, Crabbe JC et al. Mapping genes that regulate density of dopamine transporters and correlated behaviors in recombinant inbred mice. J Pharmacol Exp Ther 2001; 298: 634-643.
-
(2001)
J Pharmacol Exp Ther
, vol.298
, pp. 634-643
-
-
Janowsky, A.1
Mah, C.2
Johnson, R.A.3
Cunningham, C.L.4
Phillips, T.J.5
Crabbe, J.C.6
-
67
-
-
33646840707
-
Family based association analysis of statistically derived quantitative traits for drug use in ADHD and the dopamine transporter gene
-
Lasky-Su J, Biederman J, Doyle AE, Wilens T, Monuteaux M, Smoller JW et al. Family based association analysis of statistically derived quantitative traits for drug use in ADHD and the dopamine transporter gene. Addict Behav 2006; 31: 1088-1099.
-
(2006)
Addict Behav
, vol.31
, pp. 1088-1099
-
-
Lasky-Su, J.1
Biederman, J.2
Doyle, A.E.3
Wilens, T.4
Monuteaux, M.5
Smoller, J.W.6
-
68
-
-
32544456772
-
Characterization and prediction of alternative splice sites
-
Wang M, Marin A. Characterization and prediction of alternative splice sites. Gene 2006; 366: 219-227.
-
(2006)
Gene
, vol.366
, pp. 219-227
-
-
Wang, M.1
Marin, A.2
-
69
-
-
0037208166
-
TRANSFAC: Transcriptional regulation, from patterns to profiles
-
Matys V, Fricke E, Geffers R, Gossling E, Haubrock M, Hehl R et al. TRANSFAC: transcriptional regulation, from patterns to profiles. Nucleic Acids Res 2003; 31: 374-378.
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 374-378
-
-
Matys, V.1
Fricke, E.2
Geffers, R.3
Gossling, E.4
Haubrock, M.5
Hehl, R.6
-
70
-
-
0141541805
-
Investigating single nucleotide polymorphism (SNP) density in the human genome and its implications for molecular evolution
-
Zhao Z, Fu YX, Hewett-Emmett D, Boerwinkle E. Investigating single nucleotide polymorphism (SNP) density in the human genome and its implications for molecular evolution. Gene 2003; 312: 207-213.
-
(2003)
Gene
, vol.312
, pp. 207-213
-
-
Zhao, Z.1
Fu, Y.X.2
Hewett-Emmett, D.3
Boerwinkle, E.4
|